29 results on '"F., Ae"'
Search Results
2. Subcellular localization and nucleocytoplasmic transport of the chromosomal passenger proteins before nuclear envelope breakdown
- Author
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Rodriguez, J A, Lens, S MA, Span, S W, Vader, G, Medema, R H, Kruyt, F AE, and Giaccone, G
- Published
- 2006
3. Transverse momentum spectra of charged particles in proton–proton collisions at s=900 GeV with ALICE at the LHC
- Author
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Aamodt, By, K., Abel, Aq, N., Abeysekara, Bw, U., Abrahantes, Quintana, Ap, A., Abramyan, Dh, A., Adamová, Cg, D., Aggarwal, M. M. y., Aglieri, Rinella, An, G., Agocs, A. G. r., Aguilar, Salazar, Bk, S., Ahammed, Ba, Z., Ahmad, A. b., Ahmad, N. b., Ahn, S. U., Al, Akimoto, Cu, R., Akindinov, Bn, A., Aleksandrov, Bp, D., Alessandro, Cz, B., Alfaro, Molina, Bk, R., Alici, A. m., Almaráz, Aviña, Bk, E., Alme, J. h., Alt, Aq, T., Altini, V. e., Altinpinar, Ae, S., Andrei, C. q., Andronic, Ae, A., Anelli, Angelov, Aq, V., Anson, Aa, C., Antičić, Di, T., Antinori, An, F., Antinori, S. m., Antipin, Aj, K., Antończyk, Aj, D., Antonioli, P. n., Anzo, Bk, A., Aphecetche, Bs, L., Appelshäuser, Aj, H., Arcelli, S. m., Arceo, Arend, Aj, A., Armesto, Cm, N., Arnaldi, Cz, R., Aronsson, Bt, T., Arsene, I. C., By, Asryan, Cs, A., Augustinus, An, A., Averbeck, Ae, R., Awes, T. C., Bv, Äystö, Aw, J., Azmi, M. D. b., Bablok, S. h., Bach, Ai, M., Badalà, A. x., Baek, Y. W., Al, Bagnasco, Cz, S., Bailhache, Bala, Cy, R., Baldisseri, Cj, A., Baldit, A. z., Bán, Bd, J., Barbera, R. w., Barnaföldi, G. G. r., Barnby, L. l., Barret, V. z., Bartke, Ac, J., Barile, F. e., Basile, M. m., Basmanov, Co, V., Bastid, N. z., Bathen, Br, B., Batigne, Bs, G., Batyunya, Ah, B., Baumann, Br, C., Bearden, I. G., Ab, Becker, B. t., Belikov, Ct, I., Bellwied, Ag, R., Belmont, Moreno, Belogianni, A. d., Benhabib, Beole, Cy, S., Berceanu, I. q., Bercuci, Berdermann, Ae, E., Berdnikov, Am, Y., Betev, An, L., Bhasin, Av, A., Bhati, A. K. y., Bianchi, Cy, L., Ak, N., Bianchin, Bz, C., Bielčík, Cb, J., Bielčíková, Cg, J., Bilandzic, A. c., Bimbot, Bx, L., Biolcati, Cy, E., Blanc, A. z., Blanco, F. w., Blanco, Bi, F., Blau, Blume, Aj, C., Boccioli, An, M., Bock, Aa, N., Bogdanov, Bo, A., Bøggild, Ab, H., Bogolyubsky, Cd, M., Bohm, Cq, J., Boldizsár, L. r., Bombara, Bc, M., Bombonati, Bondila, Aw, M., Borel, Cj, H., Borisov, Ax, A., Bortolin, Bose, Az, S., Bosisio, Luciano, Bossú, Cy, F., Botje, M. c., Böttger, Aq, S., Bourdaud, Boyer, Bx, B., Braun, Cs, M., Braun, Munzinger, ae af, P., Bravina, By, L., Bregant, Marco, Breitner, Bruckner, Brun, An, R., Bruna, Bt, E., Bruno, G. E. e., Budnikov, Co, D., Buesching, Buncic, An, P., Busch, Ar, O., Buthelezi, Z. v., Caffarri, Bz, D., Cai, Dg, X., Caines, Bt, H., Calvo, Bf, E., Camacho, Bl, E., Camerini, Paolo, Campbell, Canoa, Roman, An, V., Capitani, G. P., Ak, Cara, Romeo, G. n., Carena, Carena, An, W., Carminati, Casanova, Díaz, Ak, A., Caselle, Castillo, Castellanos, Cj, J., Castillo, Hernandez, J. F., Ae, Catanescu, V. q., Cattaruzza, Enrico, Cavicchioli, An, C., Cerello, Cz, P., Chambert, Bx, V., Chang, Cq, B., Chapeland, An, S., Charpy, Bx, A., Charvet, J. L., Cj, Chattopadhyay, Ba, S., Cherney, Bw, M., Cheshkov, Cheynis, Db, B., Chiavassa, Chibante, Barroso, Chinellato, D. D. u., Chochula, Choi, Cf, K., Chojnacki, Da, M., Christakoglou, Da, P., Christensen, C. H., Ab, Christiansen, Bh, P., Chujo, Cx, T., Chuman, As, F., Cicalo, C. t., Cifarelli, L. m., Cindolo, F. n., Cleymans, J. v., Cobanoglu, Cy, O., Coffin, J. P., Ct, Coli, Colla, Conesa, Balbastre, Ak, G., Conesa del Valle, Bs, Z., Conner, E. S., Df, Constantin, Ar, P., Contin, Giacomo, Contreras, J. G., Bl, Corrales, Morales, Cy, Y., Cormier, T. M., Ag, Cortese, P. a., Cortés, Maldonado, Ce, I., Cosentino, M. R. u., Costa, Cotallo, M. E., Bi, Crescio, Crochet, P. z., Cuautle, Bj, E., Cunqueiro, Ak, L., Cussonneau, Bs, J., Dainese, Ca, A., Dalsgaard, H. H., Ab, Danu, A. p., Das, Az, I., Dash, A. k., Dash, S. k., Barros, De, G. O. V., Cn, Caro, De, Ck, A., Cataldo, De, G. f., Cuveland, De, Aq, J., Falco, De, A. s., Gaspari, De, Ar, M., Groot, De, An, J., Gruttola, De, Ck, D., Marco, De, Cz, N., Pasquale, De, Ck, S., Remigis, De, Rooij, De, Da, R., Vaux, De, G. v., Delagrange, Bs, H., Delgado, Bf, Y., Dellacasa, G. a., Deloff, Dc, A., Demanov, Dénes, E. r., Deppman, Cn, A., D'Erasmo, G. e., Derkach, Cs, D., Devaux, A. z., Bari, Di, D. e., Giglio, Di, C. e., Liberto, Di, Ci, S., Mauro, Di, Nezza, Di, Ak, P., Dialinas, Bs, M., Díaz, Bj, L., Aw, R., Dietel, Br, T., Divià, Djuvsland, Ø. h., Dobretsov, Bp, V., Dobrin, Bh, A., Dobrowolski, Dc, T., Dönigus, Ae, B., Domínguez, Bj, I., Don, D. M. M., At, Dordic, By, O., Dubey, A. K., Ba, Dubuisson, Ducroux, Db, L., Dupieux, P. z., Dutta, Majumdar, A. K., Az, M. R., Ba, Elia, D. f., Emschermann, Ar, D., Enokizono, Bv, A., Espagnon, Estienne, Esumi, Cx, S., Evans, D. l., Evrard, Eyyubova, By, G., Fabjan, C. W., An, Fabris, Ca, D., Faivre, Ao, J., Falchieri, D. m., Fantoni, Fasel, Ae, M., Fateev, Ah, O., Fearick, R. v., Fedunov, Ah, A., Fehlker, D. h., Fekete, V. o., Felea, D. p., Fenton, Olsen, Ab, B., Feofilov, Cs, G., Fernández, Téllez, Ce, A., Ferreiro, E. G., Cm, Ferretti, Cy, A., Ferretti, R. a., Figueredo, M. A. S., Cn, Filchagin, Co, S., Fini, R. f., Fionda, F. M. e., Fiore, E. M. e., Floris, M. s., Fodor, Z. r., Foertsch, S. v., Foka, Ae, P., Fokin, Bp, S., Formenti, Fragiacomo, Enrico, Fragkiadakis, M. d., Frankenfeld, Ae, U., Frolov, Bu, A., Fuchs, An, U., Furano, Furget, Ao, C., Fusco, Girard, Ck, M., Gaardhøje, J. J., Ab, Gadrat, Ao, S., Gagliardi, Cy, M., Gago, Bf, A., Gallio, Ganoti, P. d., Ganti, M. S., Ba, Garabatos, Ae, C., García, Trapaga, Cy, C., Gebelein, Gemme, R. a., Germain, Gheata, Ghidini, B. e., Ghosh, Ba, P., Giraudo, Cz, G., Giubellino, Gladysz, Dziadus, Ac, E., Glasow, Br, R., Glässel, Glenn, Bg, A., Gómez, Jiménez, Ad, R., González, Santos, Ce, H., González, Trueba, L. H., Bk, González, Zamora, Bi, P., Gorbunov, Bw, Y., Gotovac, Cr, S., Gottschlag, Br, H., Grabski, Bk, V., Grajcarek, Ar, R., Grelli, Da, A., Grigoras, Grigoriev, Bo, V., Grigoryan, Ah, S., Grinyov, Ax, B., Grion, Cw, N., Gros, Grosse, Oetringhaus, J. F., An, Grossiord, J. Y., Db, Grosso, Raffaele, Guber, Bm, F., Guernane, Ao, R., Guerra, Bf, C., Guerzoni, B. m., Gulbrandsen, Ab, K., Gulkanyan, Dh, H., Gunji, Cu, T., Gupta, Av, R., Gustafsson, H. A., Bh, Gutbrod, Ae, H., Haaland, Ø. h., Hadjidakis, Bx, C., Haiduc, M. p., Hamagaki, Cu, H., Hamar, G. r., Hamblen, Ay, J., Han, B. H., Cp, Harris, J. W., Bt, Hartig, Aj, M., Harutyunyan, Hasch, Ak, D., Hasegan, D. p., Hatzifotiadou, D. n., Hayrapetyan, Heide, Br, M., Heinz, Bt, M., Helstrup, H. i., Herghelegiu, A. q., Hernández, Herrera, Corral, Bl, G., Herrmann, Ar, N., Hetland, K. F. i., Hicks, Bt, B., Hiei, As, A., Hille, P. T., By, Hippolyte, Ct, B., Horaguchi, As, T., Hori, Cu, Y., Hristov, Hřivnáčová, Bx, I., S. g., Hu, Huang, M. h., Huber, Humanic, T. J., Aa, Hutter, Ai, D., Hwang, D. S., Cp, Ichou, Bs, R., Ilkaev, Co, R., Ilkiv, Dc, I., Inaba, Cx, M., Innocenti, P. G., An, Ippolitov, Bp, M., Irfan, M. b., Ivan, Da, C., Ivanov, Am, V., Iwasaki, Jachołkowski, Jacobs, P. j., Jančurová, Ah, L., Jangal, Ct, S., Janik, R. o., Jena, C. k., Jena, Bq, S., Jirden, Jones, G. T. l., Jones, P. G. l., Jovanović, P. l., Jung, Al, H., Al, W., Jusko, A. l., Kaidalov, A. B., Bn, Kalcher, Kalićák, Bd, P., Kalisky, Kalliokoski, Aw, T., Kalweit, Af, A., Kamal, A. b., Kamermans, Kanaki, K. h., Kang, Al, E., J. H., Cq, Kapitan, Kaplin, Kapusta, Karavichev, Bm, O., Karavicheva, Bm, T., Karpechev, Bm, E., Kazantsev, Bp, A., Kebschull, Aq, U., Keidel, Df, R., Khan, M. M. b., Khan, S. A., Ba, Khanzadeev, Am, A., Kharlov, Cd, Y., Kikola, Dd, D., Kileng, B. i., Kim, D. J., Aw, D. S., Al, D. W., Al, H. N., Al, Cd, J., J. H., Cp, J. S., Al, Al, M., Cq, M., S. H., Al, Cp, S., Cq, Y., Kirsch, Kisel, Aq, I., Kiselev, Bn, S., Kisiel, Aa, A., Klay, J. L., Cl, Klein, Ar, J., Klein, Bösing, Kliemant, Klovning, A. h., Kluge, Knichel, M. L., Ae, Kniege, Aj, S., Koch, Ar, K., Kolevatov, By, R., Kolojvari, Kondratiev, Cs, V., Kondratyeva, Bo, N., Konevskih, Bm, A., Kornać, Kour, R. l., Kowalski, Ac, M., Kox, Kozlov, Bp, K., Kral, Králik, Bd, I., Kramer, Aj, F., Kraus, Af, I., Kravćáková, Bc, A., Krawutschke, Bb, T., Krivda, M. l., Krumbhorn, Krus, Cb, M., Kryshen, Am, E., Krzewicki, M. c., Kucheriaev, Bp, Y., Kuhn, Ct, C., Kuijer, P. G. c., Kumar, L. y., Kumar, N. y., Kupczak, Dd, R., Kurashvili, Dc, P., Kurepin, A. N., Bm, Kuryakin, Co, A., Kushpil, Cg, S., Cg, V., Kutouski, Ah, M., Kvaerno, By, H., Kweon, M. J., Ar, Kwon, Rocca, La, P. w., Lackner, Ladrón de Guevara, Lafage, Lal, Av, C., Lara, Aq, C., Larsen, D. T. h., Laurenti, G. n., Lazzeroni, C. l., Bornec, Le, Bx, Y., Bris, Le, Bs, N., Lee, Cf, H., K. S., Al, S. C., Al, Lefèvre, Bs, F., Lenhardt, Leistam, Lehnert, Aj, J., Lenti, V. f., León, Bk, H., León, Monzón, Ad, I., León, Vargas, Lévai, P. r., X. g., Li, Y. g., Li, Lietava, R. l., Lindal, By, S., Lindenstruth, Lippmann, Lisa, M. A., Aa, Liu, L. h., Loginov, Lohn, Lopez, X. z., López, Noriega, Bx, M., López, Ramírez, Ce, R., López, Torres, Ap, E., Løvhøiden, Lozea Feijo Soares, S. g., Lu, Luettig, Aj, P., Lunardon, Bz, M., Luparello, Cy, G., Luquin, Lutz, J. R., Ct, Dg, K., Bt, R., Madagodahettige, Don, D. M., At, Maevskaya, Mager, Af, M., Mahapatra, D. P. k., Maire, Ct, A., Makhlyueva, An, I., Mal'Kevich, Bn, D., Malaev, Am, M., Malagalage, K. J., Bw, Maldonado, Cervantes, Malek, Malkiewicz, Malzacher, Mamonov, Manceau, L. z., Mangotra, Av, L., Manko, Manso, F. z., Manzari, V. f., Mao, Dg, Y., Mareš, Cc, J., Margagliotti, Giacomo, Margotti, A. n., Marín, Martashvili, Ay, I., Martinengo, Martínez, Hernández, M. I., Ce, Martínez, Davalos, Martínez, García, Maruyama, As, Y., Marzari, Chiesa, Masciocchi, Masera, Masetti, M. m., Masoni, A. t., Massacrier, Mastromarco, M. f., Mastroserio, A. e., Matthews, Z. L. l., Matyja, Ac, A., Mayani, Bj, D., Mazza, Mazzoni, M. A., Ci, Meddi, Ch, F., Menchaca, Rocha, Mendez, Lorenzo, Meoni, Mercado, Pérez, Mereu, Miake, Cx, Y., Michalon, Miftakhov, Am, N., Milano, Milosevic, By, J., Minafra, F. e., Mischke, Mićkowiec, Ae, D., Mitu, C. p., Mizoguchi, As, K., Mlynarz, Ag, J., Mohanty, Ba, B., Molnar, L. r., Mondal, M. M., Ba, Montaño, Zetina, Bl, L., Monteno, Cz, M., Montes, Bi, E., Morando, Moretto, Bz, S., Morsch, Moukhanova, Bp, T., Muccifora, Ak, V., Mudnic, Cr, E., Muhuri, Müller, An, H., Munhoz, M. G., Cn, Munoz, Ce, J., Musa, Musso, Cz, A., Nandi, B. K., Bq, Nania, R. n., Nappi, E. f., Navach, F. e., Navin, S. l., Nayak, T. K., Ba, Nazarenko, Nazarov, Co, G., Nedosekin, Nendaz, Db, F., Newby, Bg, J., Nianine, Nicassio, M. f., Nielsen, B. S., Ab, Nikolaev, Nikolic, Di, V., Nikulin, Nilsen, B. S., Bw, Nilsson, M. S., By, Noferini, F. n., Nomokonov, Ah, P., Nooren, Da, G., Novitzky, Aw, N., Nyatha, Bq, A., Nygaard, Ab, C., Nyiri, By, A., Nystrand, J. h., Ochirov, Odyniec, G. j., Oeschler, Af, H., Oinonen, Okada, Cu, K., Oldenburg, Oleniacz, Dd, J., Oppedisano, Cz, C., Orsini, Cj, F., Ortiz, Velasquez, Bj, A., Ortona, Oskarsson, Osmic, Österman, Bh, L., Ostrowski, Dd, P., Otterlund, Bh, I., Otwinowski, Ae, J., Øvrebekk, G. h., Oyama, Ozawa, Pachmayer, Ar, Y., Pachr, Padilla, Pagano, Ck, P., Paić, Bj, G., Painke, Aq, F., Pajares, Cm, C., Pal, S. K., Ba, Palaha, A. l., Palmeri, A. x., Panse, Aq, R., Papikyan, Dh, V., Pappalardo, G. S. x., Park, W. J., Ae, Pastirćák, Bd, B., Pastore, C. f., Paticchio, V. f., Pavlinov, Ag, A., Pawlak, Dd, T., Peitzmann, Da, T., Pepato, Pereira, Peressounko, Pérez, Perini, An, D., Perrino, D. e., Peryt, Dd, W., Peschek, Pesci, A. n., Peskov, Bj, V., Pestov, Bu, Y., Peters, A. J., An, Petráćek, Cb, V., Petridis, A. d., Petris, M. q., Petrov, P. l., Petrovici, M. q., Petta, C. w., Peyré, Bx, J., Piano, Stefano, Piccotti, Pikna, M. o., Pillot, Bs, P., Pinazza, O. n., Pinsky, At, L., Pitz, Aj, N., Piuz, Platt, R. l., Pćoskoć, M. j., Pluta, Pocheptsov, Ah, T., Pochybova, S. r., Podesta, Lerma, P. L. M., Ad, Poggio, Poghosyan, M. G., Cy, Polák, Cc, K., Polichtchouk, Cd, B., Polozov, Bn, P., Polyakov, Pommeresch, B. h., Pop, A. q., Posa, F. e., Pospíšil, Potukuchi, Av, B., Pouthas, Prasad, Preghenella, R. m., Prino, Cz, F., Pruneau, C. A., Ag, Pshenichnov, Bm, I., Puddu, G. s., Pujahari, Bq, P., Pulvirenti, A. w., Punin, Putiš, Putschke, Bt, J., Quercigh, An, E., Rachevski, Cw, A., Rademakers, Radomski, Ar, S., Räihä, T. S., Aw, Rak, Rakotozafindrabe, Ramello, L. a., Ramírez, Reyes, Bl, A., Rammler, Raniwala, Au, R., Au, S., Räsänen, S. S., Aw, Rashevskaya, Cw, I., Rath, S. k., Read, K. F., Ay, Real, J. S., Ao, Redlich, Dc, K., Renfordt, Aj, R., Reolon, A. R., Ak, Reshetin, Rettig, Revol, J. P., An, Reygers, Br, K., Ricaud, Riccati, Cz, L., Ricci, R. A., Be, Richter, M. h., Riedler, Riegler, Riggi, F. w., Rivetti, Rodriguez, Cahuantzi, Ce, M., Røed, K. i., Röhrich, Román, López, Ce, S., Romita, R. e., Ronchetti, Ak, F., Rosinskỳ, Rosnet, P. z., Rossegger, Rossi, Cv, A., Roukoutakis, Rousseau, Bx, S., Roy, Bs, C., Az, P., Rubio, Montero, A. J., Bi, Rui, Rinaldo, Rusanov, Ar, I., Russo, Ck, G., Ryabinkin, Bp, E., Rybicki, Sadovsky, Cd, S., Šafaćík, An, K., Sahoo, Bz, R., Saini, Ba, J., Saiz, Sakata, Cx, D., Salgado, C. A., Cm, Salgueiro Domingues da Silva, Salur, S. j., Samanta, Ba, T., Sambyal, Av, S., Samsonov, Šándor, Bd, L., Sandoval, Sano, Cu, S., Santo, Santoro, R. e., Sarkamo, Saturnini, P. z., Scapparone, E. n., Scarlassara, Bz, F., Scharenberg, R. P., De, Schiaua, C. q., Schicker, Schindler, Schmidt, H. R., Ae, Schossmaier, Schreiner, Schuchmann, Schukraft, Schutz, Bs, Y., Schwarz, Ae, K., Schweda, Scioli, G. m., Scomparin, Cz, E., Scott, P. A. l., Segato, Bz, G., Semenov, Senyukov, S. a., Seo, Al, J., Serci, S. s., Serkin, Serradilla, Sevcenco, A. p., Sgura, I. e., Shabratova, Ah, G., Shahoyan, Sharkov, Bn, G., Sharma, N. y., Sharma, Shigaki, Shimomura, Shtejer, Ap, K., Sibiriak, Siciliano, Sicking, Siddi, E. t., Siemiarczuk, Silenzi, A. m., Silvermyr, Bv, D., Simili, Da, E., Simonetti, G. e., Singaraju, Ba, R., Singh, Singhal, Ba, V., Sinha, B. C., Ba, Az, T., Sitar, B. o., Sitta, M. a., Skaali, T. B., By, Skjerdal, K. h., Smakal, Cb, R., Smirnov, Bt, N., Snellings, R. c., Snow, H. l., Søgaard, Soloviev, Cd, A., Soltveit, H. K., Ar, Soltz, Bg, R., Sommer, Aj, W., Son, C. W., Cf, Cp, H., Song, Soos, Soramel, Soyk, Spyropoulou, Stassinaki, M. d., Srivastava, B. K., De, Stachel, Staley, Stan, E. p., Stefanek, Dc, G., Stefanini, Steinbeck, Stenlund, Bh, E., Steyn, G. v., Stocco, Cy, D., Stock, Stolpovsky, Cd, P., Strmen, P. o., Suaide, A. A. P., Cn, Subieta, Vásquez, M. A., Cy, Sugitate, Suire, Šumbera, Cg, M., Susa, Swoboda, Symons, J. j., Szanto de Toledo, Szarka, I. o., Szostak, A. t., Szuba, Dd, M., Tadel, Tagridis, C. d., Takahara, Cu, A., Takahashi, J. u., Tanabe, Cx, R., Tapia, Takaki, J. D., Bx, Taureg, Tauro, Tavlet, Tejeda, Muñoz, Ce, G., Telesca, Terrevoli, C. e., Thäder, Tieulent, Db, R., Tlusty, Cb, D., Toia, Tolyhy, T. r., Torcato de Matos, Torii, As, H., Torralba, Aq, G., Toscano, Tosello, Tournaire, Bs, A., Traczyk, Tribedy, Tröger, Truesdale, Aa, D., Trzaska, W. H., Aw, Tsiledakis, Ar, G., Tsilis, E. d., Tsuji, Tumkin, Turrisi, Ca, R., Turvey, Bw, A., Tveter, T. S., By, Tydesjö, Tywoniuk, Ulery, Ullaland, K. h., Uras, A. s., Urbán, Bc, J., Urciuoli, G. M., Ci, Usai, G. L. s., Vacchi, Vala, Valencia, Palomo, Bk, L., Vallero, van der Kolk, N. c., Vande, Vyvre, Van, Leeuwen, Vannucci, Be, L., Vargas, Varma, Bq, R., Vasiliev, Vassiliev, Vasileiou, M. d., Vechernin, Venaruzzo, Massimo, Vercellin, Vergara, Vernet, R. w., Verweij, Vetlitskiy, Bn, I., Vickovic, Cr, L., Viesti, Vikhlyantsev, Co, O., Vilakazi, Z. v., Villalobos, Baillie, O. l., Vinogradov, Vinogradov, Cs, L., Co, Y., Virgili, Ck, T., Viyogi, Y. P., Ba, Vodopianov, Voloshin, Bn, K., Ag, S., Volpe, G. e., Von, Haller, An, B., Vranic, Vrláková, Vulpescu, B. z., Wagner, B. h., Wagner, Wallet, Wan, Dg, R., Wang, Dg, D., Watanabe, Cx, K., Wen, Q. g., Wessels, Br, J., Westerhoff, Br, U., Wiechula, Wikne, Wilk, Br, A., Williams, M. C. S. n., Willis, Bx, N., Windelband, Ar, B., Dg, C., Yang, Ar, H., Yasnopolskiy, Yermia, Cf, J., Yin, Dg, Z., Yokoyama, Cx, H., Yoo, I. K., Cf, Yuan, Yurevich, Ah, V., Yushmanov, Bp, I., Zabrodin, By, E., Zagreev, Bn, B., Zalite, Zampolli, Zanevsky, Ah, Y., Zaporozhets, Zarochentsev, Závada, Cc, P., Zbroszczyk, Dd, H., Zelnicek, Aq, P., Zenin, Zepeda, Zgura, I. p., Zhalov, Zhang, Zhou, Zhou, S. g., Zhu, Dg, J., Zichichi, A. m., Zinchenko, Zinovjev, Ax, G., Zoccarato, Db, Y., Zycháćek, Zynovyev, M., Aamodt, K., By, Abel, N., Aq, Abeysekara, U., Bw, Abrahantes, Quintana, A., Ap, Abramyan, A., Dh, Adamová, D., Cg, Aggarwal, M. M. y., Aglieri, Rinella, G., An, Agocs, A. G. r., Aguilar, Salazar, S., Bk, Ahammed, Z., Ba, Ahmad, A. b., Ahmad, N. b., Ahn, S. U., Al, Akimoto, R., Cu, Akindinov, A., Bn, Aleksandrov, D., Bp, Alessandro, B., Cz, Alfaro, Molina, R., Bk, Alici, A. m., Almaráz, Aviña, E., Bk, Alme, J. h., Alt, T., Aq, Altini, V. e., Altinpinar, S., Ae, Andrei, C. q., Andronic, A., Ae, Anelli, Angelov, V., Aq, Anson, C., Aa, Antičić, T., Di, Antinori, F., An, Antinori, S. m., Antipin, K., Aj, Antończyk, D., Aj, Antonioli, P. n., Anzo, A., Bk, Aphecetche, L., B, Appelshäuser, H., Aj, Arcelli, S. m., Arceo, Arend, A., Aj, Armesto, N., Cm, Arnaldi, R., Cz, Aronsson, T., Bt, Arsene, I. C., By, Asryan, A., C, Augustinus, A., An, Averbeck, R., Ae, Awes, T. C., Bv, Äystö, J., Aw, Azmi, M. D. b., Bablok, S. h., Bach, M., Ai, Badalà, A. x., Baek, Y. W., Al, Bagnasco, S., Cz, Bailhache, Bala, R., Cy, Baldisseri, A., Cj, Baldit, A. z., Bán, J., Bd, Barbera, R. w., Barnaföldi, G. G. r., Barnby, L. l., Barret, V. z., Bartke, J., Ac, Barile, F. e., Basile, M. m., Basmanov, V., Co, Bastid, N. z., Bathen, B., Br, Batigne, G., B, Batyunya, B., Ah, Baumann, C., Br, Bearden, I. G., Ab, Becker, B. t., Belikov, I., Ct, Bellwied, R., Ag, Belmont, Moreno, Belogianni, A. d., Benhabib, Beole, S., Cy, Berceanu, I. q., Bercuci, Berdermann, E., Ae, Berdnikov, Y., Am, Betev, L., An, Bhasin, A., Av, Bhati, A. K. y., Bianchi, L., Cy, N., Ak, Bianchin, C., Bz, Bielčík, J., Cb, Bielčíková, J., Cg, Bilandzic, A. c., Bimbot, L., Bx, Biolcati, E., Cy, Blanc, A. z., Blanco, F. w., Blanco, F., Bi, Blau, Blume, C., Aj, Boccioli, M., An, Bock, N., Aa, Bogdanov, A., Bo, Bøggild, H., Ab, Bogolyubsky, M., Cd, Bohm, J., Cq, Boldizsár, L. r., Bombara, M., Bc, Bombonati, Bondila, M., Aw, Borel, H., Cj, Borisov, A., Ax, Bortolin, Bose, S., Az, Bosisio, Luciano, Bossú, F., Cy, Botje, M. c., Böttger, S., Aq, Bourdaud, Boyer, B., Bx, Braun, M., C, Braun, Munzinger, P., ae af, Bravina, L., By, Bregant, Marco, Breitner, Bruckner, Brun, R., An, Bruna, E., Bt, Bruno, G. E. e., Budnikov, D., Co, Buesching, Buncic, P., An, Busch, O., Ar, Buthelezi, Z. v., Caffarri, D., Bz, Cai, X., Dg, Caines, H., Bt, Calvo, E., Bf, Camacho, E., Bl, Camerini, Paolo, Campbell, Canoa, Roman, V., An, Capitani, G. P., Ak, Cara, Romeo, G. n., Carena, Carena, W., An, Carminati, Casanova, Díaz, A., Ak, Caselle, Castillo, Castellano, J., Cj, Castillo, Hernandez, J. F., Ae, Catanescu, V. q., Cattaruzza, Enrico, Cavicchioli, C., An, Cerello, P., Cz, Chambert, V., Bx, Chang, B., Cq, Chapeland, S., An, Charpy, A., Bx, Charvet, J. L., Cj, Chattopadhyay, S., Ba, Cherney, M., Bw, Cheshkov, Cheynis, B., Db, Chiavassa, Chibante, Barroso, Chinellato, D. D. u., Chochula, Choi, K., Cf, Chojnacki, M., Da, Christakoglou, P., Da, Christensen, C. H., Ab, Christiansen, P., Bh, Chujo, T., Cx, Chuman, F., A, Cicalo, C. t., Cifarelli, L. m., Cindolo, F. n., Cleymans, J. v., Cobanoglu, O., Cy, Coffin, J. P., Ct, Coli, Colla, Conesa, Balbastre, G., Ak, Conesa del, Valle, Z., B, Conner, E. S., Df, Constantin, P., Ar, Contin, Giacomo, Contreras, J. G., Bl, Corrales, Morale, Y., Cy, Cormier, T. M., Ag, Cortese, P. a., Cortés, Maldonado, I., Ce, Cosentino, M. R. u., Costa, Cotallo, M. E., Bi, Crescio, Crochet, P. z., Cuautle, E., Bj, Cunqueiro, L., Ak, Cussonneau, J., B, Dainese, A., Ca, Dalsgaard, H. H., Ab, Danu, A. p., Das, I., Az, Dash, A. k., Dash, S. k., De, Barro, G. O. V., Cn, De, Caro, A., Ck, De, Cataldo, G., F., De, Cuveland, J., Aq, De, Falco, A., S., De, Gaspari, M., Ar, De, Groot, J., An, De, Gruttola, D., Ck, De, Marco, N., Cz, De, Pasquale, S., Ck, De, Remigi, De, Rooij, R., Da, De, Vaux, G. v., Delagrange, H., B, Delgado, Y., Bf, Dellacasa, G. a., Deloff, A., Dc, Demanov, Dénes, E. r., Deppman, A., Cn, D'Erasmo, G. e., Derkach, D., C, Devaux, A. z., Di, Bari, D., E., Di, Giglio, C., E., Di, Liberto, S., Ci, Di, Mauro, Di, Nezza, P., Ak, Dialinas, M., B, Díaz, L., Bj, R., Aw, Dietel, T., Br, Divià, Djuvsland, Ø. h., Dobretsov, V., Bp, Dobrin, A., Bh, Dobrowolski, T., Dc, Dönigus, B., Ae, Domínguez, I., Bj, Don, D. M. M., At, Dordic, O., By, Dubey, A. K., Ba, Dubuisson, Ducroux, L., Db, Dupieux, P. z., Dutta, Majumdar, A. K., Az, M. R., Ba, Elia, D. f., Emschermann, D., Ar, Enokizono, A., Bv, Espagnon, Estienne, Esumi, S., Cx, Evans, D. l., Evrard, Eyyubova, G., By, Fabjan, C. W., An, Fabris, D., Ca, Faivre, J., Ao, Falchieri, D. m., Fantoni, Fasel, M., Ae, Fateev, O., Ah, Fearick, R. v., Fedunov, A., Ah, Fehlker, D. h., Fekete, V. o., Felea, D. p., Fenton, Olsen, B., Ab, Feofilov, G., C, Fernández, Téllez, A., Ce, Ferreiro, E. G., Cm, Ferretti, A., Cy, Ferretti, R. a., Figueredo, M. A. S., Cn, Filchagin, S., Co, Fini, R. f., Fionda, F. M. e., Fiore, E. M. e., Floris, M. s., Fodor, Z. r., Foertsch, S. v., Foka, P., Ae, Fokin, S., Bp, Formenti, Fragiacomo, Enrico, Fragkiadakis, M. d., Frankenfeld, U., Ae, Frolov, A., Bu, Fuchs, U., An, Furano, Furget, C., Ao, Fusco, Girard, M., Ck, Gaardhøje, J. J., Ab, Gadrat, S., Ao, Gagliardi, M., Cy, Gago, A., Bf, Gallio, Ganoti, P. d., Ganti, M. S., Ba, Garabatos, C., Ae, García, Trapaga, C., Cy, Gebelein, Gemme, R. a., Germain, Gheata, Ghidini, B. e., Ghosh, P., Ba, Giraudo, G., Cz, Giubellino, Gladysz, Dziadu, E., Ac, Glasow, R., Br, Glässel, Glenn, A., Bg, Gómez, Jiménez, R., Ad, González, Santo, H., Ce, González, Trueba, L. H., Bk, González, Zamora, P., Bi, Gorbunov, Y., Bw, Gotovac, S., Cr, Gottschlag, H., Br, Grabski, V., Bk, Grajcarek, R., Ar, Grelli, A., Da, Grigoras, Grigoriev, V., Bo, Grigoryan, S., Ah, Grinyov, B., Ax, Grion, N., Cw, Gros, Grosse, Oetringhau, J. F., An, Grossiord, J. Y., Db, Grosso, Raffaele, Guber, F., Bm, Guernane, R., Ao, Guerra, C., Bf, Guerzoni, B. m., Gulbrandsen, K., Ab, Gulkanyan, H., Dh, Gunji, T., Cu, Gupta, R., Av, Gustafsson, H. A., Bh, Gutbrod, H., Ae, Haaland, Ø. h., Hadjidakis, C., Bx, Haiduc, M. p., Hamagaki, H., Cu, Hamar, G. r., Hamblen, J., Ay, Han, B. H., Cp, Harris, J. W., Bt, Hartig, M., Aj, Harutyunyan, Hasch, D., Ak, Hasegan, D. p., Hatzifotiadou, D. n., Hayrapetyan, Heide, M., Br, Heinz, M., Bt, Helstrup, H. i., Herghelegiu, A. q., Hernández, Herrera, Corral, G., Bl, Herrmann, N., Ar, Hetland, K. F. i., Hicks, B., Bt, Hiei, A., A, Hille, P. T., By, Hippolyte, B., Ct, Horaguchi, T., A, Hori, Y., Cu, Hristov, Hřivnáčová, I., Bx, Hu, S. g., Huang, M. h., Huber, Humanic, T. J., Aa, Hutter, D., Ai, Hwang, D. S., Cp, Ichou, R., B, Ilkaev, R., Co, Ilkiv, I., Dc, Inaba, M., Cx, Innocenti, P. G., An, Ippolitov, M., Bp, Irfan, M. b., Ivan, C., Da, Ivanov, V., Am, Iwasaki, Jachołkowski, Jacobs, P. j., Jančurová, L., Ah, Jangal, S., Ct, Janik, R. o., Jena, C. k., Jena, S., Bq, Jirden, Jones, G. T. l., Jones, P. G. l., Jovanović, P. l., Jung, H., Al, W., Al, Jusko, A. l., Kaidalov, A. B., Bn, Kalcher, Kalićák, P., Bd, Kalisky, Kalliokoski, T., Aw, Kalweit, A., Af, Kamal, A. b., Kamermans, Kanaki, K. h., Kang, E., Al, J. H., Cq, Kapitan, Kaplin, Kapusta, Karavichev, O., Bm, Karavicheva, T., Bm, Karpechev, E., Bm, Kazantsev, A., Bp, Kebschull, U., Aq, Keidel, R., Df, Khan, M. M. b., Khan, S. A., Ba, Khanzadeev, A., Am, Kharlov, Y., Cd, Kikola, D., Dd, Kileng, B. i., Kim, D. J., Aw, D. S., Al, D. W., Al, H. N., Al, J., Cd, J. H., Cp, J. S., Al, M., Al, M., Cq, S. H., Al, S., Cp, Y., Cq, Kirsch, Kisel, I., Aq, Kiselev, S., Bn, Kisiel, A., Aa, Klay, J. L., Cl, Klein, J., Ar, Klein, Bösing, Kliemant, Klovning, A. h., Kluge, Knichel, M. L., Ae, Kniege, S., Aj, Koch, K., Ar, Kolevatov, R., By, Kolojvari, Kondratiev, V., C, Kondratyeva, N., Bo, Konevskih, A., Bm, Kornać, Kour, R. l., Kowalski, M., Ac, Kox, Kozlov, K., Bp, Kral, Králik, I., Bd, Kramer, F., Aj, Kraus, I., Af, Kravćáková, A., Bc, Krawutschke, T., Bb, Krivda, M. l., Krumbhorn, Krus, M., Cb, Kryshen, E., Am, Krzewicki, M. c., Kucheriaev, Y., Bp, Kuhn, C., Ct, Kuijer, P. G. c., Kumar, L. y., Kumar, N. y., Kupczak, R., Dd, Kurashvili, P., Dc, Kurepin, A. N., Bm, Kuryakin, A., Co, Kushpil, S., Cg, V., Cg, Kutouski, M., Ah, Kvaerno, H., By, Kweon, M. J., Ar, Kwon, La, Rocca, P. w., Lackner, Ladrón de, Guevara, Lafage, Lal, C., Av, Lara, C., Aq, Larsen, D. T. h., Laurenti, G. n., Lazzeroni, C. l., Le, Bornec, Y., Bx, Le, Bri, N., B, Lee, H., Cf, K. S., Al, S. C., Al, Lefèvre, F., B, Lenhardt, Leistam, Lehnert, J., Aj, Lenti, V. f., León, H., Bk, León, Monzón, I., Ad, León, Varga, Lévai, P. r., Li, X. g., Li, Y. g., Lietava, R. l., Lindal, S., By, Lindenstruth, Lippmann, Lisa, M. A., Aa, Liu, L. h., Loginov, Lohn, Lopez, X. z., López, Noriega, M., Bx, López, Ramírez, R., Ce, López, Torre, E., Ap, Løvhøiden, Lozea Feijo, Soare, Lu, S. g., Luettig, P., Aj, Lunardon, M., Bz, Luparello, G., Cy, Luquin, Lutz, J. R., Ct, Ma, K., Dg, R., Bt, Madagodahettige, Don, D. M., At, Maevskaya, Mager, M., Af, Mahapatra, D. P. k., Maire, A., Ct, Makhlyueva, I., An, Mal'Kevich, D., Bn, Malaev, M., Am, Malagalage, K. J., Bw, Maldonado, Cervante, Malek, Malkiewicz, Malzacher, Mamonov, Manceau, L. z., Mangotra, L., Av, Manko, Manso, F. z., Manzari, V. f., Mao, Y., Dg, Mareš, J., Cc, Margagliotti, Giacomo, Margotti, A. n., Marín, Martashvili, I., Ay, Martinengo, Martínez, Hernández, M. I., Ce, Martínez, Davalo, Martínez, García, Maruyama, Y., A, Marzari, Chiesa, Masciocchi, Masera, Masetti, M. m., Masoni, A. t., Massacrier, Mastromarco, M. f., Mastroserio, A. e., Matthews, Z. L. l., Matyja, A., Ac, Mayani, D., Bj, Mazza, Mazzoni, M. A., Ci, Meddi, F., Ch, Menchaca, Rocha, Mendez, Lorenzo, Meoni, Mercado, Pérez, Mereu, Miake, Y., Cx, Michalon, Miftakhov, N., Am, Milano, Milosevic, J., By, Minafra, F. e., Mischke, Mićkowiec, D., Ae, Mitu, C. p., Mizoguchi, K., A, Mlynarz, J., Ag, Mohanty, B., Ba, Molnar, L. r., Mondal, M. M., Ba, Montaño, Zetina, L., Bl, Monteno, M., Cz, Montes, E., Bi, Morando, Moretto, S., Bz, Morsch, Moukhanova, T., Bp, Muccifora, V., Ak, Mudnic, E., Cr, Muhuri, Müller, H., An, Munhoz, M. G., Cn, Munoz, J., Ce, Musa, Musso, A., Cz, Nandi, B. K., Bq, Nania, R. n., Nappi, E. f., Navach, F. e., Navin, S. l., Nayak, T. K., Ba, Nazarenko, Nazarov, G., Co, Nedosekin, Nendaz, F., Db, Newby, J., Bg, Nianine, Nicassio, M. f., Nielsen, B. S., Ab, Nikolaev, Nikolic, V., Di, Nikulin, Nilsen, B. S., Bw, Nilsson, M. S., By, Noferini, F. n., Nomokonov, P., Ah, Nooren, G., Da, Novitzky, N., Aw, Nyatha, A., Bq, Nygaard, C., Ab, Nyiri, A., By, Nystrand, J. h., Ochirov, Odyniec, G. j., Oeschler, H., Af, Oinonen, Okada, K., Cu, Oldenburg, Oleniacz, J., Dd, Oppedisano, C., Cz, Orsini, F., Cj, Ortiz, Velasquez, A., Bj, Ortona, Oskarsson, Osmic, Österman, L., Bh, Ostrowski, P., Dd, Otterlund, I., Bh, Otwinowski, J., Ae, Øvrebekk, G. h., Oyama, Ozawa, Pachmayer, Y., Ar, Pachr, Padilla, Pagano, P., Ck, Paić, G., Bj, Painke, F., Aq, Pajares, C., Cm, Pal, S. K., Ba, Palaha, A. l., Palmeri, A. x., Panse, R., Aq, Papikyan, V., Dh, Pappalardo, G. S. x., Park, W. J., Ae, Pastirćák, B., Bd, Pastore, C. f., Paticchio, V. f., Pavlinov, A., Ag, Pawlak, T., Dd, Peitzmann, T., Da, Pepato, Pereira, Peressounko, Pérez, Perini, D., An, Perrino, D. e., Peryt, W., Dd, Peschek, Pesci, A. n., Peskov, V., Bj, Pestov, Y., Bu, Peters, A. J., An, Petráćek, V., Cb, Petridis, A. d., Petris, M. q., Petrov, P. l., Petrovici, M. q., Petta, C. w., Peyré, J., Bx, Piano, Stefano, Piccotti, Pikna, M. o., Pillot, P., B, Pinazza, O. n., Pinsky, L., At, Pitz, N., Aj, Piuz, Platt, R. l., Pćoskoć, M. j., Pluta, Pocheptsov, T., Ah, Pochybova, S. r., Podesta, Lerma, P. L. M., Ad, Poggio, Poghosyan, M. G., Cy, Polák, K., Cc, Polichtchouk, B., Cd, Polozov, P., Bn, Polyakov, Pommeresch, B. h., Pop, A. q., Posa, F. e., Pospíšil, Potukuchi, B., Av, Pouthas, Prasad, Preghenella, R. m., Prino, F., Cz, Pruneau, C. A., Ag, Pshenichnov, I., Bm, Puddu, G. s., Pujahari, P., Bq, Pulvirenti, A. w., Punin, Putiš, Putschke, J., Bt, Quercigh, E., An, Rachevski, A., Cw, Rademakers, Radomski, S., Ar, Räihä, T. S., Aw, Rak, Rakotozafindrabe, Ramello, L. a., Ramírez, Reye, A., Bl, Rammler, Raniwala, R., Au, S., Au, Räsänen, S. S., Aw, Rashevskaya, I., Cw, Rath, S. k., Read, K. F., Ay, Real, J. S., Ao, Redlich, K., Dc, Renfordt, R., Aj, Reolon, A. R., Ak, Reshetin, Rettig, Revol, J. P., An, Reygers, K., Br, Ricaud, Riccati, L., Cz, Ricci, R. A., Be, Richter, M. h., Riedler, Riegler, Riggi, F. w., Rivetti, Rodriguez, Cahuantzi, M., Ce, Røed, K. i., Röhrich, Román, López, S., Ce, Romita, R. e., Ronchetti, F., Ak, Rosinskỳ, Rosnet, P. z., Rossegger, Rossi, A., Cv, Roukoutakis, Rousseau, S., Bx, Roy, C., B, P., Az, Rubio, Montero, A. J., Bi, Rui, Rinaldo, Rusanov, I., Ar, Russo, G., Ck, Ryabinkin, E., Bp, Rybicki, Sadovsky, S., Cd, Šafaćík, K., An, Sahoo, R., Bz, Saini, J., Ba, Saiz, Sakata, D., Cx, Salgado, C. A., Cm, Salgueiro Domingues da, Silva, Salur, S. j., Samanta, T., Ba, Sambyal, S., Av, Samsonov, Šándor, L., Bd, Sandoval, Sano, S., Cu, Santo, Santoro, R. e., Sarkamo, Saturnini, P. z., Scapparone, E. n., Scarlassara, F., Bz, Scharenberg, R. P., De, Schiaua, C. q., Schicker, Schindler, Schmidt, H. R., Ae, Schossmaier, Schreiner, Schuchmann, Schukraft, Schutz, Y., B, Schwarz, K., Ae, Schweda, Scioli, G. m., Scomparin, E., Cz, Scott, P. A. l., Segato, G., Bz, Semenov, Senyukov, S. a., Seo, J., Al, Serci, S. s., Serkin, Serradilla, Sevcenco, A. p., Sgura, I. e., Shabratova, G., Ah, Shahoyan, Sharkov, G., Bn, Sharma, N. y., Sharma, Shigaki, Shimomura, Shtejer, K., Ap, Sibiriak, Siciliano, Sicking, Siddi, E. t., Siemiarczuk, Silenzi, A. m., Silvermyr, D., Bv, Simili, E., Da, Simonetti, G. e., Singaraju, R., Ba, Singh, Singhal, V., Ba, Sinha, B. C., Ba, T., Az, Sitar, B. o., Sitta, M. a., Skaali, T. B., By, Skjerdal, K. h., Smakal, R., Cb, Smirnov, N., Bt, Snellings, R. c., Snow, H. l., Søgaard, Soloviev, A., Cd, Soltveit, H. K., Ar, Soltz, R., Bg, Sommer, W., Aj, Son, C. W., Cf, H., Cp, Song, Soos, Soramel, Soyk, Spyropoulou, Stassinaki, M. d., Srivastava, B. K., De, Stachel, Staley, Stan, E. p., Stefanek, G., Dc, Stefanini, Steinbeck, Stenlund, E., Bh, Steyn, G. v., Stocco, D., Cy, Stock, Stolpovsky, P., Cd, Strmen, P. o., Suaide, A. A. P., Cn, Subieta, Vásquez, M. A., Cy, Sugitate, Suire, Šumbera, M., Cg, Susa, Swoboda, Symons, J. j., Szanto de, Toledo, Szarka, I. o., Szostak, A. t., Szuba, M., Dd, Tadel, Tagridis, C. d., Takahara, A., Cu, Takahashi, J. u., Tanabe, R., Cx, Tapia, Takaki, J. D., Bx, Taureg, Tauro, Tavlet, Tejeda, Muñoz, G., Ce, Telesca, Terrevoli, C. e., Thäder, Tieulent, R., Db, Tlusty, D., Cb, Toia, Tolyhy, T. r., Torcato de, Mato, Torii, H., A, Torralba, G., Aq, Toscano, Tosello, Tournaire, A., B, Traczyk, Tribedy, Tröger, Truesdale, D., Aa, Trzaska, W. H., Aw, Tsiledakis, G., Ar, Tsilis, E. d., Tsuji, Tumkin, Turrisi, R., Ca, Turvey, A., Bw, Tveter, T. S., By, Tydesjö, Tywoniuk, Ulery, Ullaland, K. h., Uras, A. s., Urbán, J., Bc, Urciuoli, G. M., Ci, Usai, G. L. s., Vacchi, Vala, Valencia, Palomo, L., Bk, Vallero, van der, Kolk, N., C., Vande, Vyvre, Van, Leeuwen, Vannucci, L., Be, Vargas, Varma, R., Bq, Vasiliev, Vassiliev, Vasileiou, M. d., Vechernin, Venaruzzo, Massimo, Vercellin, Vergara, Vernet, R. w., Verweij, Vetlitskiy, I., Bn, Vickovic, L., Cr, Viesti, Vikhlyantsev, O., Co, Vilakazi, Z. v., Villalobos, Baillie, O. l., Vinogradov, Vinogradov, L., C, Y., Co, Virgili, T., Ck, Viyogi, Y. P., Ba, Vodopianov, Voloshin, K., Bn, S., Ag, Volpe, G. e., Von, Haller, B., An, Vranic, Vrláková, Vulpescu, B. z., Wagner, B. h., Wagner, Wallet, Wan, R., Dg, Wang, D., Dg, Watanabe, K., Cx, Wen, Q. g., Wessels, J., Br, Westerhoff, U., Br, Wiechula, Wikne, Wilk, A., Br, Williams, M. C. S. n., Willis, N., Bx, Windelband, B., Ar, Xu, C., Dg, Yang, H., Ar, Yasnopolskiy, Yermia, Yi, J., Cf, Yin, Z., Dg, Yokoyama, H., Cx, Yoo, I. K., Cf, Yuan, Yurevich, V., Ah, Yushmanov, I., Bp, Zabrodin, E., By, Zagreev, B., Bn, Zalite, Zampolli, Zanevsky, Y., Ah, Zaporozhets, Zarochentsev, Závada, P., Cc, Zbroszczyk, H., Dd, Zelnicek, P., Aq, Zenin, Zepeda, Zgura, I. p., Zhalov, Zhang, Zhou, Zhou, S. g., Zhu, J., Dg, Zichichi, A. m., Zinchenko, Zinovjev, G., Ax, Zoccarato, Y., Db, Zycháćek, and Zynovyev, M.
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ALICE ,LHC ,Transverse momentum ,pp ,900 GeV ,PYTHIA ,High Energy Physics::Experiment ,Nuclear Experiment - Abstract
The inclusive charged particle transverse momentum distribution is measured in proton–proton collisions at s=900 GeV at the LHC using the ALICE detector. The measurement is performed in the central pseudorapidity region (|η
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4. Effects of a Supraseasonal Drought on the Ecological Attributes of Plagioscion squamosissimus (Heckel, 1840) (Pisces, Sciaenidae) in a Brazilian Reservoir.
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Souza AE, Oliveira JF, Peretti D, Fernandes R, Costa RS, and Novaes JL
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- Animals, Brazil, Diet veterinary, Ecology, Ecosystem, Droughts, Perciformes, Seasons
- Abstract
The aim of this study was to evaluate the effect of a supraseasonal drought on the ecological attributes of Plagioscion squamosissimus . The fish were caught quarterly from February 2010 to November 2014 using gill nets in the reservoir of Santa Cruz, Rio Grande do Norte, Brazil. The abundance of the species was evaluated with the catch per unit effort (CPUE) metric and then correlated with the accumulated rainfall and water volume of the reservoir. The diet of the fish was evaluated using the feeding index (IAi). The proportional similarity index (PS
i ) was used to evaluate the variation in the niches of the fish. The body condition was inferred through the relative condition factor, and its variation was assessed with ANOVA. A reduction in the abundance of the species that were positively correlated with the reservoir water volume was observed. The diet of the fish comprised shrimp, gastropods, fish, insects, shrimp larvae, and vegetable matter, with shrimp being the major component. PSi showed the occurrence of individual specialization during November 2013 and November 2014. The relative condition factor was not correlated with a reduction in the water volume of the reservoir. The supraseasonal drought did not affect the relative condition factor, diet, and the trophic niche, but it did affect the species abundance., Competing Interests: The authors declare that they have no competing interests.- Published
- 2017
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5. Prediction of the Carcinogenic Potential of Human Pharmaceuticals Using Repeated Dose Toxicity Data and Their Pharmacological Properties.
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van der Laan JW, Buitenhuis WH, Wagenaar L, Soffers AE, van Someren EP, Krul CA, and Woutersen RA
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In an exercise designed to reduce animal use, we analyzed the results of rat subchronic toxicity studies from 289 pharmaceutical compounds with the aim to predict the tumor outcome of carcinogenicity studies in this species. The results were obtained from the assessment reports available at the Medicines Evaluation Board of the Netherlands for 289 pharmaceutical compounds that had been shown to be non-genotoxic. One hundred forty-three of the 239 compounds not inducing putative preneoplastic lesions in the subchronic study did not induce tumors in the carcinogenicity study [true negatives (TNs)], whereas 96 compounds were categorized as false negatives (FNs) because tumors were observed in the carcinogenicity study. Of the remaining 50 compounds, 31 showed preneoplastic lesions in the subchronic study and tumors in the carcinogenicity study [true positives (TPs)], and 19 only showed preneoplastic lesions in subchronic studies but no tumors in the carcinogenicity study [false positives (FPs)]. In addition, we then re-assessed the prediction of the tumor outcome by integrating the pharmacological properties of these compounds. These pharmacological properties were evaluated with respect to the presence or absence of a direct or indirect proliferative action. We found support for the absence of cellular proliferation for 204 compounds (TN). For 67 compounds, the presence of cellular hyperplasia as evidence for proliferative action could be found (TP). Therefore, this approach resulted in an ability to predict non-carcinogens at a success rate of 92% and the ability to detect carcinogens at 98%. The combined evaluation of pharmacological and histopathological endpoints eventually led to only 18 unknown outcomes (17 categorized as FN and 1 as FP), thereby enhancing both the negative and positive predictivity of an evaluation based upon histopathological evaluation only. The data show the added value of a consideration of the pharmacological properties of compounds in relation to potential class effects, both in the negative and positive direction. A high negative and a high positive predictivity will both result in waiving the need for conducting 2-year rat carcinogenicity studies, if this is accepted by Regulatory Authorities, which will save large numbers of animals and reduce drug development costs and time.
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- 2016
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6. Biotransformation and Rearrangement of Laromustine.
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Nassar AE, Wisnewski AV, and King I
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- Animals, Antineoplastic Agents, Alkylating chemistry, Antineoplastic Agents, Alkylating toxicity, Biotransformation, Cytochrome P-450 CYP2B6 metabolism, Cytochrome P-450 CYP3A metabolism, Dogs, Haplorhini, Humans, Hydrazines chemistry, Hydrazines toxicity, Hydroxylation, Molecular Structure, Rats, Substrate Specificity, Sulfonamides chemistry, Sulfonamides toxicity, Antineoplastic Agents, Alkylating metabolism, Hydrazines metabolism, Microsomes, Liver enzymology, Sulfonamides metabolism
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This review highlights the recent research into the biotransformations and rearrangement of the sulfonylhydrazine-alkylating agent laromustine. Incubation of [(14)C]laromustine with rat, dog, monkey, and human liver microsomes produced eight radioactive components (C-1 to C-8). There was little difference in the metabolite profile among the species examined, partly because NADPH was not required for the formation of most components, which instead involved decomposition and/or hydrolysis. The exception was C-7, a hydroxylated metabolite, largely formed by CYP2B6 and CYP3A4/5. Liquid chromatography-multistage mass spectrometry (LC-MS(n)) studies determined that collision-induced dissociation, and not biotransformation or enzyme catalysis, produced the unique mass spectral rearrangement. Accurate mass measurements performed with a Fourier-transform ion cyclotron resonance mass spectrometer (FTICR-MS) significantly aided determination of the elemental compositions of the fragments and in the case of laromustine revealed the possibility of rearrangement. Further, collision-induced dissociation produced the loss of nitrogen (N2) and methylsulfonyl and methyl isocyanate moieties. The rearrangement, metabolite/decomposition products, and conjugation reactions were analyzed utilizing hydrogen-deuterium exchange, exact mass, (13)C-labeled laromustine, nuclear magnetic resonance spectroscopy (NMR), and LC-MS(n) experiments to assist with the assignments of these fragments and possible mechanistic rearrangement. Such techniques produced valuable insights into these functions: 1) Cytochrome P450 is involved in C-7 formation but plays little or no role in the conversion of [(14)C]laromustine to C-1 through C-6 and C-8; 2) the relative abundance of individual degradation/metabolite products was not species-dependent; and 3) laromustine produces several reactive intermediates that may produce the toxicities seen in the clinical trials., (Copyright © 2016 by The American Society for Pharmacology and Experimental Therapeutics.)
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- 2016
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7. Simultaneous purification of DNA and RNA from microbiota in a single colonic mucosal biopsy.
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Moen AE, Tannæs TM, Vatn S, Ricanek P, Vatn MH, and Jahnsen J
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- Biopsy, Colectomy, Colon pathology, Colonoscopy, DNA genetics, DNA Barcoding, Taxonomic methods, DNA, Complementary chemistry, DNA, Complementary genetics, Humans, Inflammatory Bowel Diseases microbiology, Inflammatory Bowel Diseases pathology, Intestinal Mucosa pathology, RNA genetics, RNA, Ribosomal, 16S genetics, Reproducibility of Results, Reverse Transcriptase Polymerase Chain Reaction, Sequence Analysis, DNA, Colon microbiology, DNA isolation & purification, Intestinal Mucosa microbiology, Microbiota genetics, RNA isolation & purification
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Background: Nucleic acid purification methods are of importance when performing microbiota studies and especially when analysing the intestinal microbiota as we here find a wide range of different microbes. Various considerations must be taken to lyse the microbial cell wall of each microbe. In the present article, we compare several tissue lysis steps and commercial purification kits, to achieve a joint RNA and DNA purification protocol for the purpose of investigating the microbiota and the microbiota-host interactions in a single colonic mucosal tissue sample., Results: A further optimised tissue homogenisation and lysis protocol comprising mechanical bead beating, lysis buffer replacement and enzymatic treatment, in combination with the AllPrep DNA/RNA Mini Kit (Qiagen, Hilden, Germany) resulted in efficient and simultaneous purification of microbial and human RNA and DNA from a single mucosal colonic tissue sample., Conclusions: The present work provides a unique possibility to study RNA and DNA from the same mucosal biopsy sample, making a direct comparison between metabolically active microbes and total microbial DNA. The protocol also offers an opportunity to investigate other members of a microbiota such as viruses, fungi and micro-eukaryotes, and moreover the possibility to extract data on microbiota and host interactions from one single mucosal biopsy.
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- 2016
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8. Mode of action based risk assessment of the botanical food-borne alkenylbenzene apiol from parsley using physiologically based kinetic (PBK) modelling and read-across from safrole.
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Alajlouni AM, Al Malahmeh AJ, Kiwamoto R, Wesseling S, Soffers AE, Al-Subeihi AA, Vervoort J, and Rietjens IM
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- Activation, Metabolic, Animals, Humans, Kinetics, Petroselinum, Rats, Dioxoles toxicity, Food Contamination, Models, Theoretical, Safrole pharmacokinetics
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The present study developed physiologically-based kinetic (PBK) models for the alkenylbenzene apiol in order to facilitate risk assessment based on read-across from the related alkenylbenzene safrole. Model predictions indicate that in rat liver the formation of the 1'-sulfoxy metabolite is about 3 times lower for apiol than for safrole. These data support that the lower confidence limit of the benchmark dose resulting in a 10% extra cancer incidence (BMDL10) that would be obtained in a rodent carcinogenicity study with apiol may be 3-fold higher for apiol than for safrole. These results enable a preliminary risk assessment for apiol, for which tumor data are not available, using a BMDL10 value of 3 times the BMDL10 for safrole. Based on an estimated BMDL10 for apiol of 5.7-15.3 mg/kg body wt per day and an estimated daily intake of 4 × 10(-5) mg/kg body wt per day, the margin of exposure (MOE) would amount to 140,000-385,000. This indicates a low priority for risk management. The present study shows how PBK modelling can contribute to the development of alternatives for animal testing, facilitating read-across from compounds for which in vivo toxicity studies on tumor formation are available to compounds for which these data are unavailable., (Copyright © 2016 The Authors. Published by Elsevier Ltd.. All rights reserved.)
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- 2016
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9. tRNA-dependent alanylation of diacylglycerol and phosphatidylglycerol in Corynebacterium glutamicum.
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Smith AM, Harrison JS, Grube CD, Sheppe AE, Sahara N, Ishii R, Nureki O, and Roy H
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- Aminoacylation, Aminoacyltransferases genetics, Aminoacyltransferases metabolism, Bacterial Proteins genetics, Bacterial Proteins metabolism, Corynebacterium glutamicum chemistry, Corynebacterium glutamicum growth & development, Genetic Fitness, Molecular Sequence Data, Phylogeny, RNA, Bacterial genetics, RNA, Bacterial metabolism, RNA, Transfer metabolism, Corynebacterium glutamicum genetics, Corynebacterium glutamicum metabolism, Diglycerides metabolism, Phosphatidylglycerols metabolism, RNA, Transfer genetics
- Abstract
Aminoacyl-phosphatidylglycerol synthases (aaPGSs) are membrane proteins that utilize aminoacylated tRNAs to modify membrane lipids with amino acids. Aminoacylation of membrane lipids alters the biochemical properties of the cytoplasmic membrane and enables bacteria to adapt to changes in environmental conditions. aaPGSs utilize alanine, lysine and arginine as modifying amino acids, and the primary lipid recipients have heretofore been defined as phosphatidylglycerol (PG) and cardiolipin. Here we identify a new pathway for lipid aminoacylation, conserved in many Actinobacteria, which results in formation of Ala-PG and a novel alanylated lipid, Alanyl-diacylglycerol (Ala-DAG). Ala-DAG formation in Corynebacterium glutamicum is dependent on the activity of an aaPGS homolog, whereas formation of Ala-PG requires the same enzyme acting in concert with a putative esterase encoded upstream. The presence of alanylated lipids is sufficient to enhance the bacterial fitness of C. glutamicum cultured in the presence of certain antimicrobial agents, and elucidation of this system expands the known repertoire of membrane lipids acting as substrates for amino acid modification in bacterial cells., (© 2015 John Wiley & Sons Ltd.)
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- 2015
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10. Brucella melitensis Biovar 1 and Brucella abortus S19 Vaccine Strain Infections in Milkers Working at Cattle Farms in the Khartoum Area, Sudan.
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Osman AE, Hassan AN, Ali AE, Abdoel TH, and Smits HL
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- Adult, Animals, Cattle, Humans, Male, Middle Aged, Risk Factors, Sudan, Workforce, Agriculture, Brucella Vaccine immunology, Brucella abortus immunology, Brucella melitensis immunology, Brucellosis immunology, Brucellosis microbiology
- Abstract
Background: Human brucellosis is a preventable zoonoses that may become persistent, causing, if left untreated, severe localized disease. Occupational exposure to infected animals or animal products and consumption of fresh contaminated dairy are main risk factors., Methods: One hundred farmworkers employed at two cattle farms one in Khartoum North and one in Omdurman were screened for the presence of specific antibodies and seropositive workers were invited to donate a blood sample for blood culture. Molecular typing was used to characterize Brucella isolates., Results: Ten percent of farmworkers tested seropositive and while Brucella melitensis biovar 1 was isolated from the blood of three individuals, an isolate identical to the B. abortus S19 vaccine strain was isolated from a fourth person. All four bacteremic individuals were employed as milkers and did not have obvious disease., Conclusions: The isolation of the highly infectious pathogen B. melitensis from seropositive workers is consistent with the notion that the pathogen may persist in the blood without causing overt disease. While vaccination with strain S19 is essential for the control of bovine brucellosis the vaccine strain may be transmitted to the human population and protective measures remain important to prevent exposure also in view of the presence of B. melitensis. To create awareness for this potentially severe disease more information on the prevalence of the pathogen in different risk groups and in livestock in the Sudan is needed.
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- 2015
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11. Intraparietal sulcus activity and functional connectivity supporting spatial working memory manipulation.
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Bray S, Almas R, Arnold AE, Iaria G, and MacQueen G
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- Adolescent, Adult, Brain Mapping methods, Female, Humans, Image Processing, Computer-Assisted, Male, Mathematics, Prefrontal Cortex physiology, Young Adult, Attention physiology, Magnetic Resonance Imaging, Memory, Short-Term physiology, Parietal Lobe physiology, Pattern Recognition, Visual physiology, Spatial Memory physiology
- Abstract
The intraparietal sulcus (IPS) is recruited during tasks requiring attention, maintenance and manipulation of information in working memory (WM). While WM tasks often show broad bilateral engagement along the IPS, topographic maps of contralateral (CL) visual space have been identified along the IPS, similar to retinotopic maps in visual cortex. In the present study, we asked how these visuotopic IPS regions are differentially involved in the maintenance and manipulation of spatial information in WM. Visuotopic mapping was performed in 26 participants to define regions of interest along the IPS, corresponding to previously described IPS0-4. In a separate task, we showed that while maintaining the location of a briefly flashed target in WM preferentially engaged CL IPS, manipulation of spatial information by mentally rotating the target around a circle engaged bilateral IPS, peaking in IPS1 in most participants. Functional connectivity analyses showed increased interaction between the IPS and prefrontal regions during manipulation, as well as interhemispheric interactions. Two control tasks demonstrated that covert attention shifts, and nonspatial manipulation (arithmetic), engaged patterns of IPS activation and connectivity that were distinct from WM manipulation. These findings add to our understanding of the role of IPS in spatial WM maintenance and manipulation., (© The Author 2013. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.)
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- 2015
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12. Spatial and temporal functional connectivity changes between resting and attentive states.
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Bray S, Arnold AE, Levy RM, and Iaria G
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- Adolescent, Adult, Brain Mapping, Female, Humans, Magnetic Resonance Imaging, Male, Neural Pathways physiology, Signal Processing, Computer-Assisted, Time Factors, Visual Perception physiology, Young Adult, Attention physiology, Brain physiology, Rest physiology
- Abstract
Remote brain regions show correlated spontaneous activity at rest within well described intrinsic connectivity networks (ICNs). Meta-analytic coactivation studies have uncovered networks similar to resting ICNs, suggesting that in task states connectivity modulations may occur principally within ICNs. However, it has also been suggested that specific "hub" regions dynamically link networks under different task conditions. Here, we used functional magnetic resonance imaging at rest and a continuous visual attention task in 16 participants to investigate whether a shift from rest to attention was reflected by within-network connectivity modulation, or changes in network topography. Our analyses revealed evidence for both modulation of connectivity within the default-mode (DMN) and dorsal attention networks (DAN) between conditions, and identified a set of regions including the temporoparietal junction (TPJ) and posterior middle frontal gyrus (MFG) that switched between the DMN and DAN depending on the task. We further investigated the temporal nonstationarity of flexible (TPJ and MFG) regions during both attention and rest. This showed that moment-to-moment differences in connectivity at rest mirrored the variation in connectivity between tasks. Task-dependent changes in functional connectivity of flexible regions may, therefore, be understood as shifts in the proportion of time specific connections are engaged, rather than a switch between networks per se. This ability of specific regions to dynamically link ICNs under different task conditions may play an important role in behavioral flexibility., (© 2014 Wiley Periodicals, Inc.)
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- 2015
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13. A critical review of the allocentric spatial representation and its neural underpinnings: toward a network-based perspective.
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Ekstrom AD, Arnold AE, and Iaria G
- Abstract
While the widely studied allocentric spatial representation holds a special status in neuroscience research, its exact nature and neural underpinnings continue to be the topic of debate, particularly in humans. Here, based on a review of human behavioral research, we argue that allocentric representations do not provide the kind of map-like, metric representation one might expect based on past theoretical work. Instead, we suggest that almost all tasks used in past studies involve a combination of egocentric and allocentric representation, complicating both the investigation of the cognitive basis of an allocentric representation and the task of identifying a brain region specifically dedicated to it. Indeed, as we discuss in detail, past studies suggest numerous brain regions important to allocentric spatial memory in addition to the hippocampus, including parahippocampal, retrosplenial, and prefrontal cortices. We thus argue that although allocentric computations will often require the hippocampus, particularly those involving extracting details across temporally specific routes, the hippocampus is not necessary for all allocentric computations. We instead suggest that a non-aggregate network process involving multiple interacting brain areas, including hippocampus and extra-hippocampal areas such as parahippocampal, retrosplenial, prefrontal, and parietal cortices, better characterizes the neural basis of spatial representation during navigation. According to this model, an allocentric representation does not emerge from the computations of a single brain region (i.e., hippocampus) nor is it readily decomposable into additive computations performed by separate brain regions. Instead, an allocentric representation emerges from computations partially shared across numerous interacting brain regions. We discuss our non-aggregate network model in light of existing data and provide several key predictions for future experiments.
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- 2014
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14. Differential neural network configuration during human path integration.
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Arnold AE, Burles F, Bray S, Levy RM, and Iaria G
- Abstract
Path integration is a fundamental skill for navigation in both humans and animals. Despite recent advances in unraveling the neural basis of path integration in animal models, relatively little is known about how path integration operates at a neural level in humans. Previous attempts to characterize the neural mechanisms used by humans to visually path integrate have suggested a central role of the hippocampus in allowing accurate performance, broadly resembling results from animal data. However, in recent years both the central role of the hippocampus and the perspective that animals and humans share similar neural mechanisms for path integration has come into question. The present study uses a data driven analysis to investigate the neural systems engaged during visual path integration in humans, allowing for an unbiased estimate of neural activity across the entire brain. Our results suggest that humans employ common task control, attention and spatial working memory systems across a frontoparietal network during path integration. However, individuals differed in how these systems are configured into functional networks. High performing individuals were found to more broadly express spatial working memory systems in prefrontal cortex, while low performing individuals engaged an allocentric memory system based primarily in the medial occipito-temporal region. These findings suggest that visual path integration in humans over short distances can operate through a spatial working memory system engaging primarily the prefrontal cortex and that the differential configuration of memory systems recruited by task control networks may help explain individual biases in spatial learning strategies.
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- 2014
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15. Neural network configuration and efficiency underlies individual differences in spatial orientation ability.
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Arnold AE, Protzner AB, Bray S, Levy RM, and Iaria G
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- Adolescent, Adult, Brain Mapping, Cerebral Cortex anatomy & histology, Cerebral Cortex physiology, Data Interpretation, Statistical, Female, Functional Laterality physiology, Hippocampus physiology, Humans, Individuality, Magnetic Resonance Imaging, Male, Motor Cortex anatomy & histology, Motor Cortex physiology, Nerve Net anatomy & histology, Young Adult, Nerve Net physiology, Orientation physiology, Psychomotor Performance physiology, Space Perception physiology
- Abstract
Spatial orientation is a complex cognitive process requiring the integration of information processed in a distributed system of brain regions. Current models on the neural basis of spatial orientation are based primarily on the functional role of single brain regions, with limited understanding of how interaction among these brain regions relates to behavior. In this study, we investigated two sources of variability in the neural networks that support spatial orientation--network configuration and efficiency--and assessed whether variability in these topological properties relates to individual differences in orientation accuracy. Participants with higher accuracy were shown to express greater activity in the right supramarginal gyrus, the right precentral cortex, and the left hippocampus, over and above a core network engaged by the whole group. Additionally, high-performing individuals had increased levels of global efficiency within a resting-state network composed of brain regions engaged during orientation and increased levels of node centrality in the right supramarginal gyrus, the right primary motor cortex, and the left hippocampus. These results indicate that individual differences in the configuration of task-related networks and their efficiency measured at rest relate to the ability to spatially orient. Our findings advance systems neuroscience models of orientation and navigation by providing insight into the role of functional integration in shaping orientation behavior.
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- 2014
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16. Consumer and farmer safety evaluation of application of botanical pesticides in black pepper crop protection.
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Hernández-Moreno D, Soffers AE, Wiratno, Falke HE, Rietjens IM, and Murk AJ
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- Acorus chemistry, Allylbenzene Derivatives, Anisoles toxicity, Chrysanthemum cinerariifolium chemistry, Derris chemistry, Eugenol toxicity, Evaluation Studies as Topic, Humans, Plant Roots chemistry, Pyrethrins toxicity, Risk Assessment, Rotenone toxicity, Syzygium chemistry, Consumer Product Safety, Crops, Agricultural, Environmental Exposure analysis, Pest Control, Biological methods, Pesticides pharmacology, Piper nigrum
- Abstract
This study presents a consumer and farmer safety evaluation on the use of four botanical pesticides in pepper berry crop protection. The pesticides evaluated include preparations from clove, tuba root, sweet flag and pyrethrum. Their safety evaluation was based on their active ingredients being eugenol, rotenone, β-asarone and pyrethrins, respectively. Botanical pesticides from Acorus calamus are of possible concern because of the genotoxic and carcinogenic ingredient β-asarone although estimated margins of exposure (MOE) for consumers indicate a low priority for risk management. For the other three botanical pesticides the margin of safety (MOS) between established acute reference doses and/or acceptable daily intake values and intake estimates for the consumer, resulting from their use as a botanical pesticide are not of safety concern, with the exception for levels of rotenone upon use of tuba root extracts on stored berries. Used levels of clove and pyrethrum as botanical pesticides in pepper berry crop production is not of safety concern for consumers or farmers, whereas for use of tuba root and sweet flag some risk factors were defined requiring further evaluation and/or risk management. It seems prudent to look for alternatives for use of sweet flag extracts containing β-asarone., (Copyright © 2013 Elsevier Ltd. All rights reserved.)
- Published
- 2013
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17. Specificity in the symbiotic association between fungus-growing ants and protective Pseudonocardia bacteria.
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Cafaro MJ, Poulsen M, Little AE, Price SL, Gerardo NM, Wong B, Stuart AE, Larget B, Abbot P, and Currie CR
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- Actinomycetales genetics, Actinomycetales physiology, Animals, Bacterial Proteins genetics, Biodiversity, Hypocreales physiology, Peptide Elongation Factor Tu genetics, RNA, Ribosomal, 16S genetics, Sequence Analysis, DNA, Species Specificity, Actinomycetales classification, Ants microbiology, Biological Evolution, Phylogeny, Symbiosis
- Abstract
Fungus-growing ants (tribe Attini) engage in a mutualism with a fungus that serves as the ants' primary food source, but successful fungus cultivation is threatened by microfungal parasites (genus Escovopsis). Actinobacteria (genus Pseudonocardia) associate with most of the phylogenetic diversity of fungus-growing ants; are typically maintained on the cuticle of workers; and infection experiments, bioassay challenges and chemical analyses support a role of Pseudonocardia in defence against Escovopsis through antibiotic production. Here we generate a two-gene phylogeny for Pseudonocardia associated with 124 fungus-growing ant colonies, evaluate patterns of ant-Pseudonocardia specificity and test Pseudonocardia antibiotic activity towards Escovopsis. We show that Pseudonocardia associated with fungus-growing ants are not monophyletic: the ants have acquired free-living strains over the evolutionary history of the association. Nevertheless, our analysis reveals a significant pattern of specificity between clades of Pseudonocardia and groups of related fungus-growing ants. Furthermore, antibiotic assays suggest that despite Escovopsis being generally susceptible to inhibition by diverse Actinobacteria, the ant-derived Pseudonocardia inhibit Escovopsis more strongly than they inhibit other fungi, and are better at inhibiting this pathogen than most environmental Pseudonocardia strains tested. Our findings support a model that many fungus-growing ants maintain specialized Pseudonocardia symbionts that help with garden defence.
- Published
- 2011
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18. Head orientation in CBCT-generated cephalograms.
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Cevidanes L, Oliveira AE, Motta A, Phillips C, Burke B, and Tyndall D
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- Head physiology, Humans, Imaging, Three-Dimensional, Malocclusion, Angle Class II diagnostic imaging, Malocclusion, Angle Class III diagnostic imaging, Observer Variation, Posture, Radiographic Image Enhancement, Cephalometry methods, Cone-Beam Computed Tomography, Head diagnostic imaging, Patient Positioning, Skull diagnostic imaging
- Abstract
Objective: To determine the reliability of obtaining two-dimensional cephalometric measurements using two virtual head orientations from cone-beam computed tomography (CBCT) models., Materials and Methods: CBCT scans of 12 patients (6 class II and 6 class III) were randomly selected from a pool of 159 patients. An orthodontist, a dental radiologist, and a third-year dental student independently oriented CBCT three-dimensional (3D) renderings in either visual natural head position (simulated NHP) or 3D intracranial reference planes (3D IRP). Each observer created and digitized four CBCT-generated lateral cephalograms per patient, two using simulated NHP and two using 3D IRP at intervals of at least 3 days. Mixed-effects analysis of variance was used to calculate intraclass correlation coefficients (ICCs) and to test the difference between the orientations for each measure., Results: ICC indicated good reliability both within each head orientation and between orientations. Of the 50 measurements, the reliability coefficients were > or =0.9 for 45 measurements obtained with 3D IRP orientation and 36 measurements with simulated NHP. The difference in mean values of the two orientations exceeded 2 mm or 2 degrees for 14 (28%) of the measurements., Conclusions: The reliability of both virtual head orientations was acceptable, although the percentage of measurements with ICC >0.9 was greater for 3D IRP. This may reflect the ease of using the guide planes to position the head in the 3D IRP during the simulation process.
- Published
- 2009
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19. Parasites may help stabilize cooperative relationships.
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Little AE and Currie CR
- Subjects
- Animals, Models, Biological, Ants microbiology, Host-Parasite Interactions, Hypocreales physiology, Symbiosis
- Abstract
Background: The persistence of cooperative relationships is an evolutionary paradox; selection should favor those individuals that exploit their partners (cheating), resulting in the breakdown of cooperation over evolutionary time. Our current understanding of the evolutionary stability of mutualisms (cooperation between species) is strongly shaped by the view that they are often maintained by partners having mechanisms to avoid or retaliate against exploitation by cheaters. In contrast, we empirically and theoretically examine how additional symbionts, specifically specialized parasites, potentially influence the stability of bipartite mutualistic associations. In our empirical work we focus on the obligate mutualism between fungus-growing ants and the fungi they cultivate for food. This mutualism is exploited by specialized microfungal parasites (genus Escovopsis) that infect the ant's fungal gardens. Using sub-colonies of fungus-growing ants, we investigate the interactions between the fungus garden parasite and cooperative and experimentally-enforced uncooperative ("cheating") pairs of ants and fungi. To further examine if parasites have the potential to help stabilize some mutualisms we conduct Iterative Prisoner's Dilemma (IPD) simulations, a common framework for predicting the outcomes of cooperative/non-cooperative interactions, which incorporate parasitism as an additional factor., Results: In our empirical work employing sub-colonies of fungus-growing ants, we found that Escovopsis-infected sub-colonies composed of cheating populations of ants or fungi lost significantly more garden biomass than sub-colonies subjected to infection or cheating (ants or fungi) alone. Since the loss of fungus garden compromises the fitness of both mutualists, our findings suggest that the potential benefit received by the ants or fungi for cheating is outweighed by the increased concomitant cost of parasitism engendered by non-cooperation (cheating). IPD simulations support our empirical results by confirming that a purely cooperative strategy, which is unsuccessful in the classic IPD model, becomes stable when parasites are included., Conclusion: Here we suggest, and provide evidence for, parasitism being an external force that has the potential to help stabilize cooperation by aligning the selfish interests of cooperative partners in opposition to a common enemy. Specifically, our empirical results and IPD simulations suggest that when two mutualists share a common enemy selection can favor cooperation over cheating, which may help explain the evolutionary stability of some mutualisms.
- Published
- 2009
- Full Text
- View/download PDF
20. Quantitative structure-activity relationship modeling of the toxicity of organothiophosphate pesticides to Daphnia magna and Cyprinus carpio.
- Author
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Zvinavashe E, Du T, Griff T, van den Berg HH, Soffers AE, Vervoort J, Murk AJ, and Rietjens IM
- Subjects
- Animals, Models, Biological, Models, Chemical, Organothiophosphorus Compounds chemistry, Pesticide Residues chemistry, Quantitative Structure-Activity Relationship, Toxicity Tests, Acute, Water Pollutants, Chemical chemistry, Carps physiology, Daphnia drug effects, Organothiophosphorus Compounds toxicity, Pesticide Residues toxicity, Water Pollutants, Chemical toxicity
- Abstract
Within the REACH regulatory framework in the EU, quantitative structure-activity relationships (QSAR) models are expected to help reduce the number of animals used for experimental testing. The objective of this study was to develop QSAR models to describe the acute toxicity of organothiophosphate pesticides to aquatic organisms. Literature data sets for acute toxicity data of organothiophosphates to fish and one data set from experiments with 15 organothiophosphates on Daphniamagna performed in the present study were used to establish QSARs based on quantum mechanically derived molecular descriptors. The logarithm of the octanol/water partition coefficient, logK(ow,) the energy of the lowest unoccupied molecular orbital, E(lumo), and the energy of the highest occupied molecular orbital, E(homo) were used as descriptors. Additionally, it was investigated if toxicity data for the invertebrate D. magna could be used to build a QSAR model to predict toxicity to fish. Suitable QSAR models (0.80
- Published
- 2009
- Full Text
- View/download PDF
21. Black yeast symbionts compromise the efficiency of antibiotic defenses in fungus-growing ants.
- Author
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Little AE and Currie CR
- Subjects
- Actinomycetales physiology, Animals, Anti-Bacterial Agents metabolism, Ants microbiology, Biological Assay, Biological Evolution, Ecosystem, Hypocreales physiology, Random Allocation, Ants physiology, Behavior, Animal physiology, Symbiosis physiology, Yeasts physiology
- Abstract
Multiplayer symbioses are common in nature, but our understanding of the ecological dynamics occurring in complex symbioses is limited. The tripartite mutualism between fungus-growing ants, their fungal cultivars, and antibiotic-producing bacteria exemplifies symbiotic complexity. Here we reveal how black yeasts, newly described symbionts of the ant-microbe system, compromise the efficiency of bacteria-derived antibiotic defense in fungus-growing ants. We found that symbiotic black yeasts acquire nutrients from the ants' bacterial mutualist, and suppress bacterial growth. Experimental manipulation of ant colonies and their symbionts shows that ants infected with black yeasts are significantly less effective at defending their fungus garden from Escovopsis, a prevalent and specialized pathogen. The reduction of mutualistic bacterial biomass on ants, likely caused by black yeast symbionts, apparently reduces the quantity of antibiotics available to inhibit the garden pathogen. Success of the ant-fungal mutualism is directly dependent on fungus garden health. Thus our finding that black yeasts compromise the ants' ability to deal with the garden parasite indicates that it is an integral component of the symbiosis. This is further evidence that a full understanding of symbiotic associations requires examining the direct and indirect interactions of symbionts in their ecological community context.
- Published
- 2008
- Full Text
- View/download PDF
22. Symbiotic complexity: discovery of a fifth symbiont in the attine ant-microbe symbiosis.
- Author
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Little AE and Currie CR
- Subjects
- Animals, Phylogeny, Ants microbiology, Ascomycota classification, Symbiosis
- Abstract
The fungus-growing ant-microbe mutualism is a classic example of organismal complexity generated through symbiotic association. The ants have an ancient obligate mutualism with fungi they cultivate for food. The success of the mutualism is threatened by specialized fungal parasites (Escovopsis) that consume the cultivated fungus. To defend their nutrient-rich garden against infection, the ants have a second mutualism with bacteria (Pseudonocardia), which produce antibiotics that inhibit the garden parasite Escovopsis. Here we reveal the presence of a fourth microbial symbiont associated with fungus-growing ants: black yeasts (Ascomycota; Phialophora). We show that black yeasts are commonly associated with fungus-growing ants, occurring throughout their geographical distribution. Black yeasts grow on the ants' cuticle, specifically localized to where the mutualistic bacteria are cultured. Molecular phylogenetic analyses reveal that the black yeasts form a derived monophyletic lineage associated with the phylogenetic diversity of fungus growers. The prevalence, distribution, localization and monophyly indicate that the black yeast is a fifth symbiont within the attine ant-microbe association, further exemplifying the complexity of symbiotic associations.
- Published
- 2007
- Full Text
- View/download PDF
23. Low host-pathogen specificity in the leaf-cutting ant-microbe symbiosis.
- Author
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Taerum SJ, Cafaro MJ, Little AE, Schultz TR, and Currie CR
- Subjects
- Animals, Biological Evolution, Fungi physiology, Geography, Host-Parasite Interactions, Phylogeny, Species Specificity, Ants microbiology, Hypocreales physiology, Symbiosis
- Abstract
Host-parasite associations are shaped by coevolutionary dynamics. One example is the complex fungus-growing ant-microbe symbiosis, which includes ancient host-parasite coevolution. Fungus-growing ants and the fungi they cultivate for food have an antagonistic symbiosis with Escovopsis, a specialized microfungus that infects the ants' fungus gardens. The evolutionary histories of the ant, cultivar and Escovopsis are highly congruent at the deepest phylogenetic levels, with specific parasite lineages exclusively associating with corresponding groups of ants and cultivar. Here, we examine host-parasite specificity at finer phylogenetic levels, within the most derived clade of fungus-growing ants, the leaf-cutters (Atta spp. and Acromyrmex spp.). Our molecular phylogeny of Escovopsis isolates from the leaf-cutter ant-microbe symbiosis confirms specificity at the broad phylogenetic level, but reveals frequent host-switching events between species and genera of leaf-cutter ants. Escovopsis strains isolated from Acromyrmex and Atta gardens occur together in the same clades, and very closely related strains can even infect the gardens of both ant genera. Experimental evidence supports low host-parasite specificity, with phylogenetically diverse strains of Escovopsis being capable of overgrowing all leaf-cutter cultivars examined. Thus, our findings indicate that this host-pathogen association is shaped by the farming ants having to protect their cultivated fungus from phylogenetically diverse Escovopsis garden pathogens.
- Published
- 2007
- Full Text
- View/download PDF
24. [Evaluation of the residual effect of pyrethroids on Anopheles in the Brazilian Amazon].
- Author
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Santos RL, Fayal Ada S, Aguiar AE, Vieira DB, and Póvoa MM
- Subjects
- Animals, Brazil, Housing, Humans, Time Factors, Urban Population, Anopheles, Insect Vectors, Insecticides, Mosquito Control methods, Pesticide Residues, Pyrethrins
- Abstract
Objective: To evaluate the residual effect of pyrethroids on the mortality rates of Anopheles in order to check their efficacy in indoor residual spraying in the Amazon Region, Brazil., Methods: The study was conducted in public housing units in the city of Belem, Northern Brazil, in 2003. Twelve houses were randomly chosen, three in each of the four established areas. Pyrethroids cypermethrin wettable powder, deltamethrin suspension concentrate, lambda-cyhalothrin wettable powder, and etofenprox wettable powder, were sprayed on the indoor wall surface of local houses. Their effects on the mortality of Anopheles were assessed from July to November. Wall bioassay was performed using plastic cones attached to insecticide and wild mosquitoes from the town of Peixe Boi., Results: Mortality rate varied according to the type of wall that received the insecticide. Those insecticides applied to wood and non-plastered brick surfaces were more stable and lasted longer. Lambda-cyhalothrin presented shorter effect than the other insecticides, and etofenprox had residual effects up to four months and was more effective in non-plastered brick surfaces. There was no statistical difference between the effect of deltamethrin and cypermethrin in all surfaces tested, and the duration of the residual effect was satisfactory up to three months after spraying., Conclusions: Deltamethrin and etofenprox presented greater performance when compared to the others. For these insecticides and formulations, a three-month interval between successive applications can be considered safe. In communities with predominance of houses with plastered brick surfaces, the smaller effectiveness of formulations should be considered, together with the importance of residual spraying as a vector control method in the area.
- Published
- 2007
- Full Text
- View/download PDF
25. Volume definition in radiotherapy planning for lung cancer: how the radiologist can help.
- Author
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Roy AE and Wells P
- Subjects
- Humans, Patient Selection, Lung Neoplasms radiotherapy, Radiotherapy Planning, Computer-Assisted, Radiotherapy, Conformal
- Abstract
Effective treatment for carcinoma of the lung remains one of the biggest challenges in oncology. Radical radiotherapy may be a curative option for patients who are unsuitable for radical surgery either because of disease stage or because of co-morbidity. Long-term disease control with radical radiotherapy is disappointing with only about 6% of patients treated being alive at 5 years. Technological advances involved in the planning and delivery of radiotherapy may improve this. The advent of conformal radiotherapy, utilizing computed tomography and three-dimensional planning systems, allows much more accurate shaping of the radiation fields. This greater accuracy of target volume definition facilitates a reduction in the radiation dose to normal tissues, allowing for dose escalation to the tumour. Delineation of the target volume can be problematic. Conventional CT has limitations in term of distinguishing between benign and malignant tissues, e.g. the size criteria for involved lymph nodes. The oncologist uses a combination of radiological and clinical information when defining the target volume but their radiological interpretation of imaging is inferior to that of a radiologist. The Royal College of Radiologists (RCR) issued guidance in 2004 on the optimal imaging strategies for common cancers. These guidelines address issues regarding the localisation and staging of cancers and treatment planning, and also reporting and training. They recommend the development of closer links between radiologists and oncologists to optimise the interpretation of imaging and target volume definition. This article aims to briefly explain the planning process involved in irradiating lung cancers, highlight problematic areas and suggest ways in which co-operation with radiologists may improve the delivery of radiotherapy and therefore the treatment outcomes for this group of patients., ((c) International Cancer Imaging Society.)
- Published
- 2006
- Full Text
- View/download PDF
26. Defending against parasites: fungus-growing ants combine specialized behaviours and microbial symbionts to protect their fungus gardens.
- Author
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Little AE, Murakami T, Mueller UG, and Currie CR
- Subjects
- Actinobacteria isolation & purification, Animals, Host-Parasite Interactions, Symbiosis, Actinobacteria physiology, Ants microbiology, Ants physiology, Hypocreales physiology
- Abstract
Parasites influence host biology and population structure, and thus shape the evolution of their hosts. Parasites often accelerate the evolution of host defences, including direct defences such as evasion and sanitation and indirect defences such as the management of beneficial microbes that aid in the suppression or removal of pathogens. Fungus-growing ants are doubly burdened by parasites, needing to protect their crops as well as themselves from infection. We show that parasite removal from fungus gardens is more complex than previously realized. In response to infection of their fungal gardens by a specialized virulent parasite, ants gather and compress parasitic spores and hyphae in their infrabuccal pockets, then deposit the resulting pellet in piles near their gardens. We reveal that the ants' infrabuccal pocket functions as a specialized sterilization device, killing spores of the garden parasite Escovopsis. This is apparently achieved through a symbiotic association with actinomycetous bacteria in the infrabuccal pocket that produce antibiotics which inhibit Escovopsis. The use of the infrabuccal pocket as a receptacle to sequester Escovopsis, and as a location for antibiotic administration by the ants' bacterial mutualist, illustrates how the combination of behaviour and microbial symbionts can be a successful defence strategy for hosts.
- Published
- 2006
- Full Text
- View/download PDF
27. Use of altered-specificity binding Oct-4 suggests an absence of pluripotent cell-specific cofactor usage.
- Author
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Smith AE and Ford KG
- Subjects
- Amino Acid Substitution, Animals, Binding Sites, Cell Differentiation, Cell Line, Cell Line, Tumor, DNA chemistry, DNA metabolism, DNA-Binding Proteins chemistry, DNA-Binding Proteins genetics, Humans, Male, Octamer Transcription Factor-3, Pluripotent Stem Cells metabolism, Protein Structure, Tertiary, Transcription Factors chemistry, Transcription Factors genetics, DNA-Binding Proteins metabolism, Transcription Factors metabolism, Transcriptional Activation
- Abstract
Oct-4 is a POU domain transcription factor that is critical for maintaining pluripotency and for stem cell renewal. Previous studies suggest that transcription regulation by Oct-4 at particular enhancers requires the input of a postulated E1A-like cofactor that is specific to pluripotent cells. However, such studies have been limited to the use of enhancer elements that bind other POU-protein family members in addition to Oct-4, thus preventing a 'clean' assessment of any Oct-4:cofactor relationships. Other attempts to study Oct-4 functionality in a more 'stand-alone' situation target Oct-4 transactivation domains to DNA using heterologous binding domains, a methodology which is known to generate artificial data. To circumvent these issues, an altered-specificity binding Oct-4 (Oct-4RR) and accompanying binding site, which binds Oct-4RR only, were generated. This strategy has previously been shown to maintain Oct-1:cofactor interactions that are highly binding-site and protein/binding conformation specific. This system therefore allows a stand-alone study of Oct-4 function in pluripotent versus differentiated cells, without interference from endogenous POU factors and with minimal deviation from bound wild-type protein characteristics. Subsequently, it was demonstrated that Oct-4RR and the highly transactive regions of its N-terminus determined here, and its C-terminus, have the same transactivation profile in pluripotent and differentiated cells, thus providing strong evidence against the existence of such a pluripotent cell-specific Oct-4 cofactor.
- Published
- 2005
- Full Text
- View/download PDF
28. Examining health equity through satisfaction and confidence of patients in primary healthcare in the Republic of Trinidad and Tobago.
- Author
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Rudzik AE
- Subjects
- Adolescent, Adult, Aged, Female, Health Services Research, Humans, Interviews as Topic, Male, Middle Aged, Primary Health Care statistics & numerical data, Private Sector standards, Private Sector statistics & numerical data, Public Sector statistics & numerical data, Quality of Health Care, Regression Analysis, Social Justice, Socioeconomic Factors, Trinidad and Tobago, Patient Satisfaction statistics & numerical data, Primary Health Care standards, Public Sector standards, Social Class
- Abstract
Surveys of patient satisfaction are widely used for identifying priorities and problems in healthcare reforms. The present study examined satisfaction and confidence of patients in public healthcare in Trinidad and Tobago. Data were gathered by interviewing a random sample (n = 280) of primary healthcare (PHC) patients. Level of patient satisfaction was high but not constant. Results of interviews showed that patients with a higher monthly income (p = 0.032) and patients who most recently used private medical care (p = 0.037) had lower levels of satisfaction with health services. Employment had an effect on satisfaction (p = 0.065), significant among patients who had recently accessed private medical care (p = 0.039). Patients using PHC clinics preferred private care to public care. Confidence in public care decreased with increasing complexity of the medical condition. These preliminary results support continued efforts in health-sector reforms and call for the enhancement of data on satisfaction through more comprehensive qualitative data-collection methods.
- Published
- 2003
29. Characterisation of site-biased DNA methyltransferases: specificity, affinity and subsite relationships.
- Author
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McNamara AR, Hurd PJ, Smith AE, and Ford KG
- Subjects
- Binding Sites genetics, Binding, Competitive, DNA genetics, DNA metabolism, DNA Methylation, DNA-Cytosine Methylases genetics, Deoxyribonuclease HpaII metabolism, Deoxyribonucleases, Type II Site-Specific metabolism, Kinetics, Oligonucleotides genetics, Oligonucleotides metabolism, Plasmids genetics, Protein Binding, Substrate Specificity, Time Factors, Zinc Fingers genetics, DNA-Cytosine Methylases metabolism
- Abstract
DNA methylation is now seen as a primary signal in the cell for mediating transcriptional repression through chromatin formation. The construction and evaluation of enzymes capable of influencing this process in vivo is therefore of significant interest. We have fused the C5-cytosine DNA methyltransferases, M.HhaI and M.HpaII, which both methylate 4 bp sequences containing a CpG dinucleotide, to a three zinc finger protein recognising a 9 bp DNA sequence. DNA methylation analyses demonstrate specific DNA methylation by both enzymes at target sites comprising adjacent methyltransferase and zinc finger subsites, targeted M.HpaII being the most specific. Binding analysis of the targeted M.HpaII enzyme reveals an 8-fold preference for binding to its target site, compared to binding to a zinc finger site alone, and an 18-fold preference over binding to a methyltransferase site alone, thereby demonstrating enhanced binding by the fusion protein, compared to its component proteins. Both DNA binding and methylation are specific for the target site up to separations of approximately 40 bp between the zinc finger and methyltransferase subsites. Ex vivo plasmid methylation experiments are also described that demonstrate targeted methylation. These targeted enzymes, however, are shown to be not fully mono-functional, retaining a significant non-targeted activity most evident at elevated protein concentrations.
- Published
- 2002
- Full Text
- View/download PDF
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