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1. Development of a high-throughput SARS-CoV-2 antibody testing pathway using dried blood spot specimens

Author

Wiola M. Zelek, Rachael Steven, Matthew J. Wise, B.P. Morgan, Sara Jones, Stuart J. Moat, Kathyryn Bramhall, Chloe George, Christopher Fegan, Stephen Jolles, Mark J. Ponsford, Emily Carne, Annette Thomas, Ian Weeks, Russell Webb, and Tariq El-Shanawany

Subjects
0301 basic medicine, medicine.medical_specialty, Clinical Biochemistry, Blood volume, Enzyme-Linked Immunosorbent Assay, Antibodies, Viral, Gastroenterology, Serology, COVID-19 Serological Testing, 03 medical and health sciences, 0302 clinical medicine, Dried blood spots, Internal medicine, medicine, Humans, antibodies, 030212 general & internal medicine, Newborn screening, Venipuncture, biology, medicine.diagnostic_test, business.industry, SARS-CoV-2, COVID-19, General Medicine, Phlebotomy, Dried blood spot, 030104 developmental biology, Immunoassay, Immunoglobulin G, Spike Glycoprotein, Coronavirus, biology.protein, Dried Blood Spot Testing, Antibody, business, Research Article
Abstract

Background Serological assays for Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) have roles in seroepidemiology, convalescent plasma-testing, antibody durability and vaccine studies. Currently, SARS-CoV-2 serology is performed using serum/plasma collected by venepuncture. Dried blood spot (DBS) testing offers significant advantages as it is minimally invasive, avoids venepuncture with specimens being mailed to the laboratory. Methods A pathway utilizing a newborn screening laboratory infrastructure was developed using an enzyme-linked immunosorbent assay to detect IgG antibodies against the receptor-binding domain of the SARS-CoV-2 spike protein in DBS specimens. Paired plasma and DBS specimens from SARS-CoV-2 antibody-positive and -negative subjects and polymerase chain reaction positive subjects were tested. DBS specimen stability, effect of blood volume and punch location were also evaluated. Results DBS specimens from antibody-negative ( n = 85) and -positive ( n = 35) subjects and polymerase chain reaction positive subjects ( n = 11) had a mean (SD; range) optical density (OD) of 0.14 (0.046; 0.03–0.27), 0.98 (0.41; 0.31–1.64) and 1.12 (0.37; 0.49–1.54), respectively. An action value OD >0.28 correctly assigned all cases. The weighted Deming regression for comparison of the DBS and the plasma assay yielded: y = 0.004041 + 1.005 x, r = 0.991, Sy/ x 0.171, n = 82. Extraction efficiency of antibodies from DBS specimens was >99%. DBS specimens were stable for at least 28 days at ambient room temperature and humidity. Conclusions SARS-CoV-2 IgG receptor-binding domain antibodies can be reliably detected in DBS specimens. DBS serological testing offers lower costs than either point of care or serum/plasma assays that require patient travel, phlebotomy and hospital/clinic resources; the development of a DBS assay may be particularly important for resource poor settings.

Published
2020

2. Thrombomodulin enhances complement regulation through strong affinity interactions with factor H and C3b-Factor H complex

Author

Valerie B. O'Donnell, Meike Heurich, Peter William Collins, Roger J. S. Preston, and B.P. Morgan

Subjects
0301 basic medicine, Chemistry, Thrombomodulin, Hematology, Complement factor I, Surface Plasmon Resonance, R1, Complement factor B, Complement system, 03 medical and health sciences, Classical complement pathway, 030104 developmental biology, Biochemistry, Complement Factor H, Lectin pathway, Factor H, Alternative complement pathway, Humans, Complement Activation, Protein Binding, circulatory and respiratory physiology
Abstract

Introduction Coagulation and complement systems are simultaneously activated at sites of tissue injury, leading to thrombin generation and opsonisation with C3b. Thrombomodulin (TM) is a cell-bound regulator of thrombin activation, but can also enhance the regulatory activity of complement factor H (FH), thus accelerating the degradation of C3b into inactive iC3b. Objectives This study sought to determine the biophysical interaction affinities of two recombinant TM analogs with thrombin, FH and C3b in order to analyze their ability to regulate serum complement activity. Methods Surface plasmon resonance (SPR) analysis was used to determine binding affinities of TM analogs with FH and C3b, and compared to thrombin as positive control. The capacity of the two recombinant TM analogs to regulate complement in serum was tested in standard complement hemolytic activity assays. Results SPR analysis showed that both TM analogs bind FH and C3b-Factor H with nanomolar and C3b with micromolar affinity; binding affinity for its natural ligand thrombin was several fold higher than for FH. At a physiological relevant concentration, TM inhibits complement hemolytic activity in serum via FH dependent and independent mechanisms. Conclusions TM exhibits significant binding affinity for complement protein FH and C3b-FH complex and its soluble form is capable at physiologically relevant concentrations of inhibiting complement activation in serum.

Published
2016

3. A Wiki for Classroom Writing

Author

B.P. Morgan and Richard D. Smith

Subjects
Pharmacology, Linguistics and Language, Access to information, Multimedia, Writing instruction, Early adolescence, Pharmacology (medical), computer.software_genre, Psychology, computer, Humanities, Language and Linguistics
Abstract

Wikis can be a very useful addition to any classroom. They are engaging to students, easy to use, and focus on literacy whenever students genuinely interact with them. Wikipedia, the online encyclopedia (www.wikipedia.org), is the most famous example of a wiki. But today, teachers and students are beginning to engage with this technology more and more, creating a variety of wiki types, which are engaging to students, easy to use, and focus on literacy whenever students genuinely interact with them. قد تكون الويكيات تكملة مفيدة لأي صف فإنها شيقة للطلاب وسهلة الاستخدام ومركزة على معرفة القراءة والكتابة كلما يتعامل معها الطلاب بجدية. فإن موسوعة يكيبيديا الحرة على الشكبة العالمية www.wikipedia.org أشهر مثال على الويكيات ولكن اليوم صار الأساتذة والطلاب يشتغلون مع هذه التقنية أكثر فأكثر كي يخلقوا عدة أنواع من الويكيات التي تجذب الطلاب وتسهل الاستخدام وتركز على معرفة القراءة والكتابة كلما يتعاملون معها بجدية. 维基可以作为任何教室里一种很有用的附加教学活动。每当学生与维基认真地互动时，维基能吸引学生的学习兴趣，容易使用，又能集中于读写能力的培养。维基百科─网上百科全书 (www.wikipedia.org)─就是最著名的一个维基例子。然而，现今教师与学生正开始深入了解这信息科技，并创制出多样化的维基教学活动。每当学生与这些教学活动认真地互动时，这些维基教学活动能吸引学生的学习兴趣，容易使用，又能集中于读写能力的培养。 Les wikis peuvent etre un tres utile complement dans n'importe quelle classe. Ils sont seduisants pour les eleves, faciles a utiliser, et centrent l'attention sur la lecture-ecriture chaque fois que les eleves interagissent veritablement avec eux. Wikipedia, l'encyclopedie en ligne (www.wikipedia.org), est l'exemple de wiki le plus celebre. Aujourd'hui, les enseignants et les eleves commencent a s'investir de plus en plus dans cette technologie, en creant differents types de wikis, seduisants pour les eleves, faciles a utiliser, et centrant l'attention sur la lecture-ecriture chaque fois que les eleves interagissent veritablement avec eux. Так называемые “вики”, то есть различные он-лайн ресурсы, развиваемые самими пользователями – очень полезное дополнение к любому уроку. Это занимательные и легкие в использовании источники информации, взаимодействуя с которыми ученики неизменно совершенствуют уровень грамотности. Википедия, или он-лайн энциклопедия (www.wikipedia.org; www.wikipedia.ru), самый известный “вики”-ресурс. Но сегодня и учителя, и сами школьники все шире знакомятся с этой технологией, создавая разнообразные “вики”. И всякий раз это расширяет список доступных им видов грамотности и благоприятно влияет на ее общий уровень. Wikis pueden ser de gran beneficio en cualquier salon de clase. Los wikis atraen a los estudiantes, son faciles de utilizar, y enfocan a los estudiantes en el aprendizaje cada vez que interactuan genuinamente con ellos. Wikipedia, la enciclopedia en la red (www.wikipedia.org), es el ejemplo mas conocido de un wiki. Hoy dia, los maestros y los estudiantes participan mas y mas en esta tecnologia, creando una variedad de tipos wiki, que atraen a los estudiantes, son faciles de usar, y los enfoca en el aprendizaje al interactuar genuinamente con ellos.

Published
2008

5. Contents Vol. 89, 2000

Author

B. Rosenbusch, M.-T. Bihoreau, J. Satrústegui, J. Browne, B.P. Morgan, C. Niehrs, V.A. Valentine, L.Z. Topol, K. Rader, S.-Y. Li, S. Seino, T. Ono, M.L. Ramírez-Dueñas, K.C Arden, T.-H. Hsu, M. Schmid, S. Rensen, S.H. Park, M.J. Pettenati, H. Yano, W. Van Hul, J.L Vernon, K. Ellington, S. Yonezawa, M.A. Sims, A. Dutra, G. Kandala, S. Paradisi, N.A. Jenkins, F. Gruetzner, C. Dixkens, A.I. Protopopov, N.G. Copeland, A. Glinka, L. Ferretti, H.-U.G. Weier, S. Zabel, Y.-C. Li, S. Sonta, R.A. White, E. Roessler, C. Von Kap-Herr, D. Incarnato, M. Osaki, A. Solans, A.V. Zelenin, E. Petek, G.P. Zambetti, K. Wagner, D.S. Holt, P.M. Richardson, N.D. Rendtorff, T.A. Lister, D. Taruscio, L. Iannuzzi, A. Buck, N.A. Jensen, M.G. Foti, M.A. Hyatt, I. Nanda, M.R. James, P. Doevendans, L. Cai, Y. Du, C.X. George, S. Doerr, M. Athanasiou, G.J.J.M. van Eys, Y. Yokoyama, M.R. Barnes, C.E. Samuel, W. Wuyts, R.S. Bora, M.G. Farquhar, F. Sablitzky, L. Archangelo, M.-G. Mattéi, E.R. Zabarovsky, Q. Zhang, M.-J. Pébusque, M.L. Ayala-Madrigal, L.M. Pasztor, M.-C. Hernandez, R.A. Lersch, S. Yamashita, N. Spurr, G.K. Zoraqi, Y.M. Heng, P.M. Kroisel, M.J. Neat, P. Zambonelli, S. Comincini, R.K. Gupta, G.P. Di Meo, P. Musilová, H. Vissing, Z. Shan, E. Kalm, X. Estivill, S.S. Mann, C. Hansen, I. Hansmann, V. Setaluri, A. Stratil, V.I. Kashuba, R. Davoli, M. Fox, C.C. Lin, H. Egger, J.E. Wiley, Y. Wang, Z. Gu, A. Oohira, A.S. Hill, R. Sanz, V. Falbo, J. Fitzgibbon, P.D. Thomsen, A. Perucatti, J.B. Rattner, G. Merkx, H. Kim, S. Masaki, S. de la Luna, T.L. Harboe, L. Schibler, M.A. Israel, S. Paul, O. Bögler, R.Z. Gizatullin, O.V. Muravenko, B. Brenig, S. Ichikawa, M. Muenke, M.B. Powell, J.-F. Cheng, J. Rubeš, C. Looft, A. Vortkamp, P.C. Burr, T.C. Hart, C. Ramos, N. Tommerup, D.A. Campbell, C.M. Owczarek, B.U. Koelsch, L. Jones, Y. Hirabayashi, K.J. Portbury, S. Aono, C.-Z. Wang, S.D. Field, V. Russo, T. Haaf, P.J. Andres-Barquin, W. Emberger, S. Hirano, C. Lee, A. Kindler-Röhrborn, C. Ayuso, T. Tsukasaki, C. Windpassinger, P.J. Hertzog, A. Kanamori, C. Popovici, A.D. Boyer, M.A. Farwell, N. Foot, L.I. Zon, S. Cepica, D. Birnbaum, A. Silahtaroglu, I. Kola, B. Castiglioni, J. Kohlhase, A. Geurts van Kessel, D.J. Gilbert, M. Yerle, V.W. Sykes, K.E. Murphy, A. del Arco, M. Schneider, E.P. Cribiu, N.K. Rushmere, S.T. Suzuki, S. Breitweser, D.G. Blair, Y.K. Jung, N. Shaikh, Z. Tümer, N. Yokoi, K. Lindpaintner, and D.G. Jo

Subjects
Botany, Genetics, Biology, Molecular Biology, Genetics (clinical)
Published
2000

6. Functionally active complement proteins C6 and C7 detected in C6- and C7-deficient individuals

Author

B.P. Morgan, Paul C. Potter, P.J. Späth, Denise Ponard, Otto Götze, R. Würzner, Ann Orren, M. Brai, M. Schulze, and L. Happe

Subjects
Blood Bactericidal Activity, medicine.drug_class, Immunoblotting, Immunology, Enzyme-Linked Immunosorbent Assay, Biology, Monoclonal antibody, Complement Hemolytic Activity Assay, Specimen Handling, 03 medical and health sciences, 0302 clinical medicine, Terminal complement complex, Immunopathology, medicine, Humans, Immunology and Allergy, Complement Activation, Volume concentration, 030304 developmental biology, 0303 health sciences, Temperature, Zymosan, Antibodies, Monoclonal, Complement deficiency, Complement C9, Serum samples, medicine.disease, Molecular biology, Complement C7, Complement C6, 3. Good health, Complement (complexity), Complement system, Electrophoresis, Polyacrylamide Gel, Research Article, 030215 immunology
Abstract

SUMMARYTwo sensitive sandwich ELISAs based on monoclonal antibodies directed to native C6 and C7 allowed the detection and quantitation of these complement proteins in 20 out of 37 serum samples from individuals who had previously been classified as deficient in these proteins as assessed by immunochemical and/or functional assays. Furthermore, serum from four C6-deficient and one combined C6-/C7-deficient individual showed an increase in the terminal complement complex (TCC) and a decrease in native C6 and C7 after complement activation as assayed by specific ELISAs. Despite their (incomplete) deficiencies, these individuals therefore possess functionally active terminal complement proteins with respect to their ability to generate the TCC. As these individuals have no history of a susceptibility to neisserial infections, even low concentrations of functionally active C6 and C7 may provide sufficient protection against those micro-organisms whose destruction requires TCC formation.

Published
1991

7. Soluble complement receptor 1 protects the peripheral nerve from early axon loss after injury

Author

Rosalind H.M. King, Miriam Ann Vigar, Maryla de Kok, Ineke Wagenaar-Bos, Valeria Ramaglia, R. A. Wolterman, B.P. Morgan, Frank Baas, Genome Analysis, Human Genetics, Amsterdam Neuroscience, and Neurology

Subjects
Male, Wallerian degeneration, Nerve Crush, Complement receptor 1, Complement Pathway, Alternative, Biology, Pathology and Forensic Medicine, Classical complement pathway, Complement Receptor Type 1, medicine, Animals, Humans, Peripheral Nerves, Axon, Complement Activation, Myelin Sheath, Macrophages, Macrophage Activation, medicine.disease, Axons, Rats, Receptors, Complement, Complement system, Cell biology, Neuroprotective Agents, medicine.anatomical_structure, nervous system, Immunology, Sciatic nerve, biology.gene, Wallerian Degeneration, Complement membrane attack complex, Regular Articles
Abstract

Complement activation is a crucial early event in Wallerian degeneration. In this study we show that treatment of rats with soluble complement receptor 1 (sCR1), an inhibitor of all complement pathways, blocked both systemic and local complement activation after crush injury of the sciatic nerve. Deposition of membrane attack complex (MAC) in the nerve was inhibited, the nerve was protected from axonal and myelin breakdown at 3 days after injury, and macrophage infiltration and activation was strongly reduced. We show that both classical and alternative complement pathways are activated after acute nerve trauma. Inhibition of the classical pathway by C1 inhibitor (Cetor) diminished, but did not completely block, MAC deposition in the injured nerve, blocked myelin breakdown, inhibited macrophage infiltration, and prevented macrophage activation at 3 days after injury. However, in contrast to sCR1 treatment, early signs of axonal degradation were visible in the nerve, linking MAC deposition to axonal damage. We conclude that sCR1 protects the nerve from early axon loss after injury and propose complement inhibition as a potential therapy for the treatment of diseases in which axon loss is the main cause of disabilities.

Published
2008

8. Complement regulation at the molecular level: the structure of decay-accelerating factor

Author

Pauline M. Rudd, J. Billington, Susan M. Lea, Pietro Roversi, Petra Lukacik, B.P. Morgan, R A Dwek, David Harvey, Mark R. Wormald, Dirk Esser, Catherine M. Radcliffe, JoAnna White, Richard A. G. Smith, Max Crispin, Graham P. Smith, David J.A. Evans, and Pamela A. Williams

Subjects
Models, Molecular, Repetitive Sequences, Amino Acid, Glycosylation, Regulator, medicine.disease_cause, behavioral disciplines and activities, chemistry.chemical_compound, von Willebrand Factor, medicine, Molecule, Humans, Decay-accelerating factor, Mutation, Multidisciplinary, CD55 Antigens, Chemistry, Complement System Proteins, Biological Sciences, Complement (complexity), Solutions, Crystallography, Membrane, Biophysics, Crystallization, Linker, Hydrophobic and Hydrophilic Interactions
Abstract

The human complement regulator CD55 is a key molecule protecting self-cells from complement-mediated lysis. X-ray diffraction and analytical ultracentrifugation data reveal a rod-like arrangement of four short consensus repeat (SCR) domains in both the crystal and solution. The stalk linking the four SCR domains to the glycosylphosphatidylinositol anchor is extended by the addition of 11 highly charged O-glycans and positions the domains an estimated 177 Å above the membrane. Mutation mapping and hydrophobic potential analysis suggest that the interaction with the convertase, and thus complement regulation, depends on the burial of a hydrophobic patch centered on the linker between SCR domains 2 and 3.

Published
2004

9. Subject Index Vol. 89, 2000

Author

C.-Z. Wang, M.A. Sims, T.A. Lister, J.L Vernon, S.S. Mann, C. Popovici, C. Hansen, D. Taruscio, L. Iannuzzi, S. Paradisi, T.C. Hart, Y. Wang, B. Castiglioni, J. Kohlhase, A. Geurts van Kessel, M. Yerle, E.R. Zabarovsky, F. Gruetzner, W. Van Hul, N. Tommerup, S. Aono, N.G. Copeland, C. Ayuso, P.J. Hertzog, M. Muenke, N.A. Jenkins, M.R. Barnes, H.-U.G. Weier, R.Z. Gizatullin, M.-J. Pébusque, L.M. Pasztor, O.V. Muravenko, N.A. Jensen, G.P. Di Meo, Y. Du, V.W. Sykes, R.A. Lersch, M.J. Neat, D.G. Jo, D.S. Holt, A. Buck, I. Nanda, L. Schibler, T. Haaf, W. Emberger, H. Vissing, D.J. Gilbert, S. Hirano, G.P. Zambetti, T. Tsukasaki, J. Fitzgibbon, J.-F. Cheng, A.S. Hill, C.E. Samuel, S. Paul, F. Sablitzky, S. Yonezawa, A.I. Protopopov, R. Davoli, C.X. George, M.L. Ayala-Madrigal, C. Windpassinger, S. Cepica, C. Looft, B. Rosenbusch, K.C Arden, A. Solans, K.E. Murphy, K. Wagner, S. Breitweser, Z. Tümer, R.K. Gupta, N. Yokoi, M. Schmid, O. Bögler, V. Russo, X. Estivill, N.K. Rushmere, P.M. Richardson, P.J. Andres-Barquin, P. Musilová, C. Lee, S. Seino, M.A. Hyatt, M. Fox, C.C. Lin, H. Yano, A. Vortkamp, S. Ichikawa, L. Jones, S.-Y. Li, M.G. Farquhar, V. Falbo, G.J.J.M. van Eys, Y. Yokoyama, M. Schneider, E.P. Cribiu, S. Masaki, M.B. Powell, P. Zambonelli, S. Comincini, W. Wuyts, R.S. Bora, P. Doevendans, E. Petek, P.M. Kroisel, M.-T. Bihoreau, J. Satrústegui, S. Rensen, M.J. Pettenati, B. Brenig, J. Browne, Y.K. Jung, N. Shaikh, S. Yamashita, N. Spurr, A. Oohira, L.Z. Topol, M.A. Israel, L.I. Zon, A.V. Zelenin, T.L. Harboe, K. Rader, D.A. Campbell, C.M. Owczarek, B.U. Koelsch, S.D. Field, R.A. White, A. Kindler-Röhrborn, R. Sanz, E. Roessler, G.K. Zoraqi, H. Egger, Y.M. Heng, P.D. Thomsen, I. Hansmann, G. Merkx, A. Kanamori, H. Kim, K.J. Portbury, C. Ramos, J. Rubeš, P.C. Burr, A. Glinka, S.T. Suzuki, S. Zabel, M. Osaki, Y.-C. Li, S. Sonta, L. Archangelo, M.-G. Mattéi, M.A. Farwell, S.H. Park, A. Dutra, D. Birnbaum, C. Dixkens, M.G. Foti, D.G. Blair, M.R. James, C. Von Kap-Herr, D. Incarnato, K. Lindpaintner, G. Kandala, N.D. Rendtorff, Q. Zhang, Z. Shan, V. Setaluri, A. Stratil, Z. Gu, E. Kalm, J.E. Wiley, J.B. Rattner, S. de la Luna, B.P. Morgan, C. Niehrs, V.A. Valentine, T.-H. Hsu, Y. Hirabayashi, A.D. Boyer, L. Ferretti, L. Cai, S. Doerr, M.L. Ramírez-Dueñas, K. Ellington, T. Ono, M. Athanasiou, N. Foot, A. Silahtaroglu, I. Kola, A. del Arco, M.-C. Hernandez, V.I. Kashuba, and A. Perucatti

Subjects
Genetics, Index (economics), Subject (documents), Social science, Biology, Molecular Biology, Genetics (clinical)
Published
2000

10. Subject Index Vol. 85, 1999

Author

O. Bartsch, M. Vaiman, M.R. Matarazzo, M.P. Hande, L. Vieten, P. Marynen, T.D. Bunch, A.A. Bosma, R.A. Veitia, Marijo Kent-First, J.E. Womack, H. Aburatani, C.R. Lopes, A. Törnsten, H. Kusakabe, P.D. Pearce, N. Tanaka, A. Gelhaus, A. Wagner, H.E. McDermid, G.V.N. Velagaleti, M. Hirai, F. Apiou, P.R. Martens, C. Rogel-Gaillard, T. Ishida, N. Bourgeaux, C. Ottolenghi, L.J. Peelman, H.A. Ansari, M. Svelto, T. Antonevich, Giovanna Grimaldi, M.F. Rothschild, M. Yerle, K. Hashimoto, T. Takahashi, Y. Nakahori, R. Taneja, L. Blottière, Y. Koshizuka, M. Horie, G. Gupta, Y. Itoh, J. Schütte, W. Kreß, C.K. Tuggle, H. Hameister, K. Kikuchi, Mariano Rocchi, J.-C. Amé, P. Chardon, M. Isomura, T. Goldammer, M. Kinebuchi, I. Dunham, A. Aventin, M.D. Bishop, J. Kusuda, N. Werner, D.W. Maher, P. Laurent, P. Slijepcevic, J.M. Perez de la Lastra, T.E. Broad, Y. Hippo, D. Ferbus, D. Beare, D. Michael, G. Goubin, M.R.V. Amarante, H. Hayes, S.A. Tharapel, N. Sato, M.-T. Prospéri, B.P. Chowdhary, R.C. Michaelis, R.S. Danziger, F. Bröcker, A. Billault, A. Eggen, K. Jülicher, K. Kasai, J. Vanselow, M.-C. Bissery, M. Mattheeuws, R.D. Horstmann, M. Rosati, N.K. Rushmere, R. Hong, S. Ikegawa, B.S. Klein, B.P. Morgan, R.S. Wilroy, G. Calamita, M. Hirata, M. Bishop, A. Matsuura, M. Heß, K.E. Teague, C. Spalluto, R. Tanuma, R.M. Schmid, J. Sohal, Annamaria Franzè, A. van Zeveren, A. Zsolnai, T. Kodama, J.F. Taylor, A. Fellous, H. Levéziel, A.T. Tharapel, E.L. Jacobson, B. Dutrillaux, D.B. Zimonjic, D.S. Gallagher, P. Peeters, S.K. Davis, S.E. Long, I. Matsushita, A. Malterer, E. Seemanova, A. Mazzone, S. Liptay, B. Grandchamp, M. Schwerin, S. Nishimura, G. Rappold, M.K. Jacobson, J.D. Burzlaff, P.D. Buchanan, Y. Nakamura, B. Opalka, W. Bardenheuer, M. Vozdová, M.C. Yoshida, T. Voet, M. Van Poucke, R. Fürbass, J.T. Woitach, V. Trichet, C. Mecucci, K. Ried, K. Yamada, N.C. Popescu, A. Chase, P. Pinton, R.M. Brunner, C.L. Keck, C. Guenzi, D. Shkolny, S.S. Thorgeirsson, S. Kubíčková, J. Cools, N.C.P. Cross, J.M. Goldman, C.W. Ernst, G. Marquitan, J. Rubeš, H.-F.S. Sun, C.P. Popescu, and C.H. Laundon

Subjects
Genetics, Index (economics), Subject (documents), Social science, Biology, Molecular Biology, Genetics (clinical)
Published
1999

11. Contents Vol. 85, 1999

Author

T.D. Bunch, M. Hirai, D. Beare, G. Calamita, K. Hashimoto, M. Mattheeuws, O. Bartsch, A. Aventin, T. Takahashi, R.D. Horstmann, M. Heß, Annamaria Franzè, R. Tanuma, P. Marynen, B. Grandchamp, D. Shkolny, R.A. Veitia, M.P. Hande, H. Kusakabe, C.L. Keck, S.S. Thorgeirsson, A.T. Tharapel, H. Levéziel, N. Sato, M. Svelto, R.S. Danziger, A. Fellous, S. Kubíčková, E. Seemanova, D.W. Maher, Giovanna Grimaldi, Y. Itoh, D.S. Gallagher, P.D. Buchanan, T. Goldammer, S.A. Tharapel, L. Vieten, R.M. Brunner, C. Guenzi, H. Aburatani, B. Opalka, J. Kusuda, M. Bishop, C.R. Lopes, Y. Hippo, M. Kinebuchi, M. Horie, S.E. Long, I. Matsushita, J. Vanselow, T. Kodama, J.F. Taylor, A. Mazzone, J.D. Burzlaff, K. Ried, Y. Nakahori, H.E. McDermid, J.M. Perez de la Lastra, M. Vaiman, A. Törnsten, B. Dutrillaux, S. Liptay, M. Isomura, K. Yamada, M.D. Bishop, B.S. Klein, H.A. Ansari, N.K. Rushmere, R. Hong, S. Ikegawa, P.R. Martens, A. Zsolnai, J. Cools, Y. Nakamura, M.R. Matarazzo, A. Eggen, C. Ottolenghi, Mariano Rocchi, A. van Zeveren, W. Bardenheuer, M. Vozdová, D. Michael, M.C. Yoshida, J.-C. Amé, G. Gupta, C.W. Ernst, L.J. Peelman, N. Bourgeaux, R. Taneja, F. Bröcker, M.-C. Bissery, M. Rosati, H. Hayes, A. Billault, T.E. Broad, N. Werner, G. Marquitan, E.L. Jacobson, W. Kreß, D. Ferbus, M. Hirata, B.P. Chowdhary, M. Schwerin, R.M. Schmid, A.A. Bosma, K. Jülicher, P. Chardon, P. Peeters, K.E. Teague, F. Apiou, V. Trichet, C. Rogel-Gaillard, K. Kasai, A. Matsuura, N.C. Popescu, C. Spalluto, L. Blottière, A. Chase, I. Dunham, D.B. Zimonjic, G. Rappold, C.K. Tuggle, M.R.V. Amarante, N. Tanaka, A. Gelhaus, G.V.N. Velagaleti, T. Ishida, M.F. Rothschild, M.K. Jacobson, M. Van Poucke, N.C.P. Cross, J.M. Goldman, T. Antonevich, J. Schütte, R.C. Michaelis, B.P. Morgan, R.S. Wilroy, S. Nishimura, T. Voet, J.T. Woitach, C. Mecucci, J. Rubeš, H.-F.S. Sun, C.P. Popescu, C.H. Laundon, J.E. Womack, Y. Koshizuka, K. Kikuchi, H. Hameister, S.K. Davis, A. Malterer, P. Slijepcevic, M. Yerle, P. Laurent, G. Goubin, M.-T. Prospéri, R. Fürbass, P. Pinton, J. Sohal, Marijo Kent-First, P.D. Pearce, and A. Wagner

Subjects
Botany, Genetics, Biology, Molecular Biology, Genetics (clinical)
Published
1999

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