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16 results on '"Brooke A. Brown"'

1. Single-cell RNA sequencing reveals microenvironment context-specific routes for epithelial-mesenchymal transition in pancreas cancer cells

Author

Brooke A Brown and Matthew Lazzara

Subjects
Article
Abstract

In the PDAC tumor microenvironment, multiple factors initiate the epithelial-mesenchymal transition (EMT) that occurs heterogeneously among transformed ductal cells, but it is unclear if different drivers promote EMT through common or distinct signaling pathways. Here, we use single-cell RNA sequencing (scRNA-seq) to identify the transcriptional basis for EMT in pancreas cancer cells in response to hypoxia or EMT-inducing growth factors. Using clustering and gene set enrichment analysis, we find EMT gene expression patterns that are unique to the hypoxia or growth factor conditions or that are common between them. Among the inferences from the analysis, we find that the FAT1 cell adhesion protein is enriched in epithelial cells and suppresses EMT. Further, the receptor tyrosine kinase AXL is preferentially expressed in hypoxic mesenchymal cells in a manner correlating with YAP nuclear localization, which is suppressed by FAT1 expression. AXL inhibition prevents EMT in response to hypoxia but not growth factors. Relationships between FAT1 or AXL expression with EMT were confirmed through analysis of patient tumor scRNA-seq data. Further exploration of inferences from this unique dataset will reveal additional microenvironment context-specific signaling pathways for EMT that may represent novel drug targets for PDAC combination therapies.

Published
2023

2. A histone methylation-MAPK signaling axis drives durable epithelial-mesenchymal transition in hypoxic pancreas cancer

Author

Brooke A. Brown, Paul J. Myers, Sara J. Adair, Jason R. Pitarresi, Shiv K. Sah-Teli, William S. Hart, Michelle Barbeau, Kelsey Leong, Nicholas Seyler, William Kane, Kyoung Eun Lee, Edward Stelow, M. Celeste Simon, Peppi Koivunen, Todd W. Bauer, Ben Z. Stanger, and Matthew J. Lazzara

Abstract

Here, we show that hypoxia drives especially long-lasting epithelial-mesenchymal transition (EMT) in pancreatic ductal adenocarcinoma (PDAC) primarily through a positive-feedback histone methylation-MAPK signaling axis. We find that neoplastic PDAC cells preferentially undergo EMT in hypoxic tumor regions in multiple model systems and that hypoxia drives a cell-autonomous EMT in PDAC cells which, unlike EMT in response to growth factors, can last for weeks. We further demonstrate that hypoxia reduces histone demethylase KDM2A activity, suppresses PP2 family phosphatase expression, and activates MAPKs to post-translationally stabilize histone methyltransferase NSD2, leading to an H3K36me2-dependent EMT in which hypoxia-inducible factors play only a supporting role. This mechanism can be antagonizedin vivoby combinations of MAPK inhibitors that may be effective in multi-drug therapies designed to target EMT.

Published
2022

3. Charge Detection Mass Spectrometry Measurements of Exosomes and other Extracellular Particles Enriched from Bovine Milk

Author

Jonathan C. Trinidad, Xuyao Zeng, Brooke A. Brown, Lauren F. Barnes, Jonathan M. A. Winstone, David E. Clemmer, Aaron R. Todd, Martin F. Jarrold, and Milos V. Novotny

Subjects
Proteomics, Chemistry, 010401 analytical chemistry, Analytical chemistry, Extracellular vesicle, Exosomes, 010402 general chemistry, Mass spectrometry, 01 natural sciences, Exosome, Mass Spectrometry, Article, Charge detection, Microvesicles, 0104 chemical sciences, Analytical Chemistry, law.invention, Milk, law, Extracellular, Animals, Cattle, Electron microscope, Chromatography, Liquid
Abstract

The masses of particles in a bovine milk extracellular vesicle (EV) preparation enriched for exosomes were directly determined for the first time by charge detection mass spectrometry (CDMS). In CDMS, both the mass-to-charge ratio (m/z) and z are determined simultaneously for individual particles, enabling mass determinations for particles that are far beyond the mass limit (∼1.0 MDa) of conventional mass spectrometry (MS). Particle masses and charges span a wide range from m ∼ 2 to ∼90 MDa and z ∼ 50 to ∼1300 e (elementary charges) and are highly dependent upon the conditions used to extract and isolate the EVs. EV particles span a continuum of masses, reflecting the highly heterogeneous nature of these samples. However, evidence for unique populations of particles is obtained from correlation of the charges and masses. An analysis that uses a two-dimensional Gaussian model, provides evidence for six families of particles, four of which having masses in the range expected for exosomes. Complementary proteomics measurements and electron microscopy (EM) imaging are used to further characterize the EVs and confirm that these samples have been enriched in exosomes. The ability to characterize such extremely heterogeneous mixtures of large particles with rapid, sensitive, and high-resolution MS techniques is critical to ongoing analytical efforts to separate and purify exosomes and exosome subpopulations. Direct measurement of each particle's mass and charge is a new means of characterizing the physical and chemical properties of exosomes and other EVs.

Published
2020

4. Abstract C054: Hypoxia promotes a durable epithelial-mesenchymal transition in pancreas cancer through a histone methylation-MAPK signaling axis

Author

Brooke A. Brown, Paul J. Myers, Sara J. Adair, Jason R. Pitarresi, Shiv Sah Teli, Peppi Karppinen, Ben Z. Stanger, Todd W. Bauer, and Matthew J. Lazzara

Subjects
Cancer Research, Oncology
Abstract

Pancreatic ductal adenocarcinoma (PDAC) tumors are poorly vascularized and exhibit regions of hypoxia. Here, we demonstrate that this feature of the tumor microenvironment promotes epithelial-mesenchymal transition (EMT), which occurs early in PDAC and drives chemoresistance, and we identify the underlying signaling mechanism. Analysis of publicly-available human transcriptomics and proteomics demonstrated that PDAC cells or tumors enriched in mesenchymal markers were also enriched in markers of hypoxia or HIF activity. Furthermore, in lineage-traced autochthonous, orthotopic patient-derived xenograft, and orthotopic or subcutaneous implanted cell line models of PDAC, hypoxic tumor tissue regions were enriched for neoplastic cells that had undergone EMT. In cell culture experiments, PDAC cells from human and mouse tumors exhibited an ability to undergo EMT in response to 1% O2, with loss of membranous E-cadherin, increased vimentin protein expression, and transcriptional changes indicative of both hypoxia and EMT. Moreover, EMT in response to hypoxia was substantially more persistent than that observed in response to growth factors, and a hypoxia fate mapping system revealed that once-hypoxic cells could retain mesenchymal characteristics outside hypoxic tumor regions. To understand the mechanism for EMT in response to low oxygen tension, we constructed a multivariable linear regression model of the dependence of the hypoxic gene signature on different gene sets in PDAC ductal cells, which identified MAPK signaling as the most important feature. Consistent with the model inference, in both in vitro and in vivo settings, hypoxic cells showing evidence of EMT displayed elevated MAPK signaling. We further demonstrated that MAPK activation in hypoxia was potentiated by suppressed activity of a histone demethylase and concomitant loss of protein phosphatase expression, which reinforced the mechanism by stabilizing the expression of a histone methyltransferase. Thus, this study identifies a tumor microenvironment-initiated mechanism leading to EMT and nominates several potential drug targets whose antagonism may promote PDAC chemoresponse. Citation Format: Brooke A. Brown, Paul J. Myers, Sara J. Adair, Jason R. Pitarresi, Shiv Sah Teli, Peppi Karppinen, Ben Z. Stanger, Todd W. Bauer, Matthew J. Lazzara. Hypoxia promotes a durable epithelial-mesenchymal transition in pancreas cancer through a histone methylation-MAPK signaling axis [abstract]. In: Proceedings of the AACR Special Conference on Pancreatic Cancer; 2022 Sep 13-16; Boston, MA. Philadelphia (PA): AACR; Cancer Res 2022;82(22 Suppl):Abstract nr C054.

Published
2022

5. Exosome-Mediated Crosstalk between Keratinocytes and Macrophages in Cutaneous Wound Healing

Author

Lava Timsina, Puneet Khandelwal, Mohamed S. El Masry, Stephen C. Jacobson, Subhadip Ghatak, Amanda P. Siegel, Amitava Das, Mahadeo Gorain, David E. Clemmer, Xuyao Zeng, Sashwati Roy, Robert J. Lee, Brooke A. Brown, Xiaoju Zhou, Andrew G. Clark, Chandan K. Sen, Woran Song, Kanhaiya Singh, Yi Xuan, Mangilal Agarwal, Poornachander R. Guda, and Milos V. Novotny

Subjects
Keratinocytes, General Physics and Astronomy, 02 engineering and technology, 010402 general chemistry, Exosomes, 01 natural sciences, Exosome, Article, Mice, microRNA, Animals, General Materials Science, Skin, Wound Healing, Chemistry, Vesicle, Macrophages, General Engineering, 021001 nanoscience & nanotechnology, Microvesicles, 0104 chemical sciences, Cell biology, Crosstalk (biology), Cutaneous wound, 0210 nano-technology, Wound healing
Abstract

Bidirectional cell-cell communication involving exosome-borne cargo such as miRNA, has emerged as a critical mechanism for wound healing. Unlike other shedding vesicles, exosomes selectively package miRNA by SUMOylation of heterogeneous nuclear ribonucleoproteinA2B1 (hnRNPA2B1). In this work, we elucidate the significance of exosome in keratinocyte-macrophage crosstalk following injury. Keratinocyte-derived exosomes were genetically labeled with GFP reporter (Exo(κ-GFP)) using tissue nanotransfection and were isolated from dorsal murine skin and wound-edge tissue by affinity selection using magnetic beads. Surface N-glycans of Exo(κ-GFP) were also characterized. Unlike skin exosome, wound-edge Exo(κ-GFP) demonstrated characteristic N-glycan ions with abundance of low base pair RNA and were selectively engulfed by wound-macrophages (ωmϕ) in granulation tissue. In vitro addition of wound-edge Exo(κ-GFP) to proinflammatory ωmϕ resulted in conversion to a proresolution phenotype. To selectively inhibit miRNA packaging within Exo(κ-GFP) in vivo, pH-responsive keratinocyte-targeted siRNA-hnRNPA2B1 functionalized lipid nanoparticles (TLNP(κ)) were designed with 94.3% encapsulation efficiency. Application of TLNP(κ/si-hnRNPA2B1) to murine dorsal wound-edge significantly inhibited expression of hnRNPA2B1 by 80% in epidermis compared to TLNP(κ/si-control) group. Although no significant difference in wound closure or re-epithelialization was observed, TLNP(κ/si-hnRNPA2B1) treated group showed significant increase in ωmϕ displaying proinflammatory markers in the granulation tissue at day 10 post-wounding compared to TLNP(κ/si-control) group. Furthermore, TLNP(κ/si-hnRNPA2B1) treated mice showed impaired barrier function with diminished expression of epithelial junctional proteins, lending credence to the notion that unresolved inflammation results in leaky skin. This work provides insight wherein Exo(κ-GFP) are recognized as a major contributor that regulates macrophage trafficking and epithelial barrier properties post-injury.

Published
2020

6. Outcomes Following Reinduction Therapy for Relapsed Acute Myeloid Leukemia Post Allogeneic Hematopoietic Cell Transplantation

Author

Brooke Laine Brown, LeAnne Kennedy, Brandi Anders, Rebecca Garcia Hunt, Dianna S. Howard, Maho Hibino, and Emily Johnson

Subjects
Oncology, Transplantation, medicine.medical_specialty, Hematopoietic cell, business.industry, Myeloid leukemia, Cell Biology, Hematology, Internal medicine, Molecular Medicine, Immunology and Allergy, Medicine, business
Published
2021

7. Prospective health students' perceptions of the pharmacist role in the interprofessional team

Author

Erika K. Dumke, Brooke L Brown, Erin Hickey, and Rollin L Ballentine

Subjects
Health Knowledge, Attitudes, Practice, Students, Health Occupations, Attitude of Health Personnel, media_common.quotation_subject, Interprofessional Relations, education, Pharmacist, Coding (therapy), Pharmacy, Pharmacists, 03 medical and health sciences, 0302 clinical medicine, Professional Role, Nursing, Perception, Health care, Medicine, Interprofessional teamwork, Humans, 030212 general & internal medicine, Prospective Studies, health care economics and organizations, media_common, Patient Care Team, Teamwork, Health professionals, business.industry, 030229 sport sciences, General Medicine, business
Abstract

Negative perceptions or underdeveloped understanding of healthcare team member roles can impact the functionality of the team and stunt innovations in interprofessional practice and education. Therefore, the intent of this study was to explore the perception of pharmacists' role on the healthcare team by future team members: prospective health professional students. The study utilised a survey to examine these perceptions in prospective health professional students (n = 34) nearing the application process to health professional school. A coding process was used to explore open-ended text responses through a line-by-line analysis and identify emerging themes regarding perception of pharmacists' roles, responsibilities, and practice settings. Quantitative data examined perception of pharmacists by intended prospective profession, healthcare experience, and pharmacy experience. Results indicate that while prospective health professional students find pharmacists to be an important part of the healthcare team, they lack a developed understanding of pharmacists' roles, responsibilities, and practice settings. Identifying and addressing prospective health professional students' misperceptions surrounding pharmacists' roles and responsibilities may encourage them to make informed career decisions and shape them into more knowledgeable future professionals with the ability to better impact patient care on interprofessional teams.

Published
2017

8. Automated peak width measurements for targeted analysis of ion mobility unresolved species

Author

Michael E. Pettit, Brooke A. Brown, Matthew R. Brantley, Touradj Solouki, and Brett Harper

Subjects
Chemistry, 010401 analytical chemistry, Statistics as Topic, Analytical chemistry, Peak fitting, 010402 general chemistry, Mass spectrometry, Software package, 01 natural sciences, Biochemistry, Rapid detection, Mass Spectrometry, 0104 chemical sciences, Analytical Chemistry, Ion, Chemometrics, Automation, User-Computer Interface, Traveling wave, Environmental Chemistry, Deconvolution, Spectroscopy, Software
Abstract

Peak broadening in ion mobility (IM) is a relatively predictable process and abnormally broad peaks can be indicative of the presence of unresolved species. Here, we introduce a new ion mobility peak fitting (IM_FIT) software package for automated and systematic determination of traveling wave ion mobility (TWIM) unresolved species. To identify IM unresolved species, the IM_FIT software generates a trend line by plotting ions' mobility peak widths as a function of their arrival times. Utilizing user-defined thresholds, IM_FIT allows for automated and rapid detection of ions that deviate from the peak width trend line. To demonstrate the advantages of IM_FIT for automated detection of IM unresolved species, IM-mass spectrometry (IM-MS) data from a sample mixture containing polypropylene glycol and multiple peptides were analyzed. A total of 14 out of the 34 observed singly-charged IM peaks above 5% relative abundance (i.e., signal-to-noise ratios above ∼200) were tagged as potentially co-eluting ions by IM_FIT. Subsequently, the 14 IM peaks tagged as potentially unresolved (presumably, peaks corresponding to co-eluting compounds), were further analyzed by automated IM deconvolution (AIMD), liquid chromatography-IM-MS (LC-IM-MS), and/or ultra-high resolution mass spectrometry. Using the aforementioned techniques, more than 85% of the tagged IM peaks (12 out of 14) were confirmed to contain co-eluting ions. As an additional new finding, IM_FIT facilitated the discovery of an unexpected sequence-scrambled y-type fragment ion.

Published
2016

9. CMS Collaboration

Author

Aarrestad, T.K. Abbaneo, D. Abbiendi, G. Abbrescia, M. Abdelalim, A.A. Abdullin, S. Abdulsalam, A. Abu Zeid, S. Ackert, A. Acosta, D. Acosta, J.G. Adair, A. Adam, W. Adams, J.R. Adams, M.R. Adams, T. Adiguzel, A. Adzic, P. Afanasiev, S. Agapitos, A. Aggleton, R. Agram, J.-L. Ahmad, A. Ahmad, M. Ahmad, M. Ahmed, I. Ahuja, S. Akbiyik, M. Akchurin, N. Akgun, B. Akin, I.V. Albajar, C. Albrow, M. Alcaraz Maestre, J. Aldá Júnior, W.L. Aldaya Martin, M. Alderweireldt, S. Aleksandrov, A. Alexander, J. Alimena, J. Alunni Solestizi, L. Alverson, G. Alves, F.L. Alves, G.A. Alyari, M. Amapane, N. Amsler, C. Anagnostou, G. Anderson, D. Anderson, I. Andrea, J. Andreev, V. Andreev, Y. Andrews, M.B. Androsov, K. Anelli, C. Antonelli, L. Antropov, I. Antunovic, Z. Apanasevich, L. Apollinari, G. Appelt, E. Apresyan, A. Apyan, A. Arcaro, D. Arcidiacono, R. Arenton, M.W. Argiro, S. Arneodo, M. Arora, S. Asavapibhop, B. Asawatangtrakuldee, C. Asilar, E. Asin, I. Askew, A. Ata, M. Attikis, A. Aubin, A. Auffray, E. Autermann, C. Auzinger, G. Avdeeva, E. Avery, P. Avetisyan, A. Avila, C. Awad, A. Azarkin, M. Azhgirey, I. Aziz, T. Azzi, P. Azzolini, V. Azzurri, P. Baarmand, M.M. Baber, M. Bacchetta, N. Bachmair, F. Bachtis, M. Baden, A. Baffioni, S. Bagliesi, G. Baillon, P. Bainbridge, R. Bakhshiansohi, H. Ball, A.H. Ball, F. Ban, Y. Banerjee, S. Banerjee, S. Bäni, L. Bansal, S. Barbagli, G. Barberis, E. Barbieri, R. Bargassa, P. Baringer, P. Barker, A. Barnes, V.E. Barnett, B.A. Barney, D. Baron, O. Barone, L. Barria, P. Bartek, R. Barth, C. Bartók, M. Bartosik, N. Basegmez, S. Baskakov, A. Battilana, C. Baty, A. Bauerdick, L.A.T. Baumgartel, D. Baus, C. Bayshev, I. Bean, A. Beauceron, S. Beaudette, F. Beck, L. Beernaert, K. Behnamian, H. Behnke, O. Behrens, U. Bein, S. Beirão Da Cruz E Silva, C. Belchior Batista Das Chagas, E. Belforte, S. Beliy, N. Belknap, D.A. Bell, A.J. Bellan, R. Belloni, A. Beluffi, C. Belyaev, A. Belyaev, A. Benaglia, A. Benato, L. Bencze, G. Bendavid, J. Benedetti, D. Benelli, G. Benhabib, L. Beni, N. Benitez, J.F. Benucci, L. Benussi, L. Benvenuti, A.C. Beranek, S. Beretvas, A. Bergauer, T. Berger, J. Beri, S.B. Bernardes, C.A. Bernardini, J. Bernet, C. Berruti, G.M. Berry, D. Berry, E. Berryhill, J. Bertl, W. Besancon, M. Betchart, B. Betts, R.R. Bhardwaj, A. Bhat, P.C. Bhatnagar, V. Bhattacharya, S. Bhattacharya, S. Bhopatkar, V. Bhowmik, S. Bialkowska, H. Bian, J.G. Bianchini, L. Bianco, S. Biasini, M. Bierwagen, K. Biino, C. Bilei, G.M. Bilin, B. Bilki, B. Bilmis, S. Bitioukov, S. Blekman, F. Blobel, V. Bloch, D. Bloch, P. Bloom, K. Bluj, M. Blumenfeld, B. Boccali, T. Bocci, A. Bochenek, J. Bodek, A. Bodlak, M. Boimska, B. Boletti, A. Bolla, G. Bonacorsi, D. Bonato, A. Bondu, O. Boos, E. Bornheim, A. Borras, K. Bortignon, P. Bortoletto, D. Borzou, A. Bose, S. Bose, T. Böser, C. Botta, C. Boudoul, G. Bouhali, O. Bourilkov, D. Bouvier, E. Bradmiller-Feld, J. Braghieri, A. Braibant-Giacomelli, S. Branca, A. Brandstetter, J. Brandt, S. Branson, J.G. Breedon, R. Breto, G. Breuker, H. Brew, C. Brianza, L. Brigliadori, L. Brigljevic, V. Brinkerhoff, A. Brinson, J. Brito, L. Brochero Cifuentes, J.A. Brochet, S. Brodski, M. Brom, J.-M. Brona, G. Brondolin, E. Brooke, J.J. Brown, R.M. Brun, H. Bruner, C. Bruno, G. Buchmuller, O. Bucinskaite, I. Bundock, A. Bunin, P. Bunkowski, K. Bunn, J. Buontempo, S. Burgmeier, A. Burkett, K. Burt, K. Burton, D. Busson, P. Busza, W. Butler, J.N. Butler, P.H. Buttignol, M. Butz, E. Bylinkin, A. Bylsma, B. Byszuk, A. Cabrera, A. Cabrillo, I.J. Cadamuro, L. Caillol, C. Cakir, A. Calabria, C. Calamba, A. Calderon, A. Calderon De La Barca Sanchez, M. Cali, I.A. Call, K. Calligaris, L. Calpas, B. Calvelli, V. Calvert, B. Calvo, E. Caminada, L. Campagnari, C. Campanini, R. Campbell, A. Camporesi, T. Candelise, V. Canelli, M.F. Cankocak, K. Capiluppi, P. Cappello, G. Caputo, C. Cardaci, M. Carlsmith, D. Carlson, B. Carnes, A. Carrillo Montoya, C.A. Carrillo Moreno, S. Cartiglia, N. Carvalho, W. Carver, M. Casal, B. Casarsa, M. Casasso, S. Casimiro Linares, E. Castaldi, R. Castaneda Hernandez, A. Castello, R. Castiñeiras De Saa, J.R. Castilla-Valdez, H. Castro, A. Caudron, A. Cavallari, F. Cavallo, F.R. Cavallo, N. Cavanaugh, R. Ceard, L. Celik, A. Centis Vignali, M. Cepeda, M. Cerati, G.B. Cerci, S. Cerminara, G. Cerrada, M. Chabert, E.C. Chamizo Llatas, M. Chang, P. Chang, Y.H. Chang, Y.W. Chanon, N. Chao, Y. Chaparro Sierra, L.F. Chapon, E. Charaf, O. Charlot, C. Chasco, M. Chatterjee, A. Chatterjee, K. Chatterjee, R.M. Chauhan, S. Chauhan, S. Chaves, J. Chawla, R. Chen, G.M. Chen, H.S. Chen, K.F. Chen, K.H. Chen, M. Chen, P.H. Chen, Y. Chen, Z. Cheng, T. Cherepanov, V. Chertok, M. Cheung, H.W.K. Chhibra, S.S. Chierici, R. Chinellato, J. Chiochia, V. Chiorboli, M. Chlebana, F. Choi, M. Choi, S. Choi, Y. Chou, J.P. Choudhary, B.C. Choudhury, S. Chu, J. Chudasama, R. Chwalek, T. Ciangottini, D. Cieri, D. Cihangir, S. Cimmino, A. Ciocci, M.A. Cirkovic, P. Citron, M. Cittolin, S. Ciulli, V. Civinini, C. Claes, D.R. Clare, R. Clarida, W. Clarke, C. Clement, E. Clerbaux, B. Cockerill, D.J.A. Codispoti, G. Colafranceschi, S. Colaleo, A. Cole, J.E. Colino, N. Collard, C. Colling, D. Colombo, F. Contardo, D. Conte, E. Contreras-Campana, C. Contreras-Campana, E. Conway, J. Conway, R. Cooper, S.I. Cornelis, T. Corpe, L. Correa Martins Junior, M. Cossutti, F. Costa, M. Costa, S. Costanza, F. Coubez, X. Couderc, F. Coughlan, J.A. Courbon, B. Cousins, R. Covarelli, R. Cowden, C. Cox, B. Cox, P.T. Creanza, D. Cripps, N. Cristella, L. Crucy, S. Cuevas, J. Cuffiani, M. Cumalat, J.P. Curry, D. Cussans, D. Custódio, A. Cutts, D. Czellar, S. D'Agnolo, R.T. D'Alessandro, R. D'Alfonso, M. D'Hondt, J. Da Costa, E.M. Da Silveira, G.G. Dabrowski, A. Daci, N. Dahmes, B. Dahms, T. Dalchenko, M. Dall'Osso, M. Dallavalle, G.M. Damgov, J. Daponte, V. Das, S. Daskalakis, G. Dasu, S. Dauncey, P. David, A. Davies, G. Davignon, O. De Roeck, A. De Souza Santos, A. De Wit, A. De Cosa, A. De La Cruz, B. De Oliveira Martins, C. De Jesus Damiao, D. De La Cruz-Burelo, E. De Wolf, E.A. De Guio, F. De Lentdecker, G. De Bruyn, I. De Gruttola, M. De Mattia, M. De Palma, M. De Filippis, N. De Castro Manzano, P. De Visscher, S. De Boer, W. Degano, A. Deiters, K. Dejardin, M. Del Re, D. Delaere, C. Delannoy, A.G. Delgado, A. Delgado Peris, A. Dell'Orso, R. Della Ricca, G. Della Negra, M. Demaria, N. Demina, R. Demiragli, Z. Demiroglu, Z.S. Denegri, D. Depasse, P. Derdzinski, M. Dermenev, A. Deroover, K. Descroix, A. Dev, N. Dewanjee, R.K. Dey, S. Dhingra, N. Di Francesco, A. Di Mattia, A. Di Marco, E. Di Matteo, L. Di Guida, S. Diamond, B. Diemoz, M. Dierlamm, A. Dietz, C. Dietz-Laursonn, E. Diez Pardos, C. Dildick, S. Dilsiz, K. Dimitrov, A. D'imperio, G. Dinardo, M.E. Dishaw, A. Dissertori, G. Dittmann, J. Dittmar, M. Dittmer, S. Doan, T.H. Dobson, M. Dobur, D. Dodd, L. Dogra, S. Dolen, J. Dolinska, G. Dominguez, A. Domínguez Vázquez, D. Donato, S. Donegà, M. Dooling, S. Dordevic, M. Dorigo, T. Dorland, T. Dorney, B. Doroba, K. Dozen, C. Draeger, A.R. Dragicevic, M. Dragoiu, C. Dremin, I. Driga, O. Du, R. Duarte, J. Dube, S. Duchardt, D. Dudenas, V. Dudero, P.R. Dugad, S. Duggan, D. Dumanoglu, I. Dunne, P. Dünser, M. Dupont, N. Durgut, S. Duric, S. Durkin, L.S. Dutta, D. Dutta, S. Dutta, V. Eckerlin, G. Ecklund, K.M. Eckstein, D. Edelhoff, M. Eerola, P. Eggert, N. Eichhorn, T. El Mamouni, H. El Sawy, M. Eller, P. Elliott-Peisert, A. Ellison, J. Elmer, P. Elvira, V.D. Elwood, A. Eminizer, N. Endres, M. Eno, S.C. Epshteyn, V. Erbacher, R. Erdmann, M. Erdmann, W. Erdogan, Y. Erdweg, S. Erfle, J. Erö, J. Ershov, A. Escalante Del Valle, A. Esch, T. Eshaq, Y. Esposito, M. Etesami, S.M. Eusebi, R. Evangelou, I. Evans, A. Evdokimov, O. Everaerts, P. Fabbri, F. Fabbri, F. Fabbro, B. Fabozzi, F. Faccioli, P. Fagot, A. Fahim, A. Fan, J. Fanfani, A. Fangmeier, C. Fanò, L. Fantasia, C. Fanzago, F. Farrell, C. Fasanella, D. Fasanella, G. Faulkner, J. Faure, J.L. Favaro, C. Favart, D. Favart, L. Fay, J. Fedi, G. Fehling, D. Felcini, M. Feld, L. Feng, L. Ferapontov, A. Ferbel, T. Ferencek, D. Ferguson, T. Ferguson, W. Fernandez Bedoya, C. Fernandez Menendez, J. Fernández Ramos, J.P. Fernandez, M. Fernandez Perez Tomei, T.R. Ferraioli, C. Ferreira Parracho, P.G. Ferri, F. Ferro, F. Field, R.D. Filipovic, N. Finco, L. Finger, M., Jr. Finger, M. Fink, S. Finkel, A. Fiore, L. Fiorendi, S. Fiori, F. Fischer, R. Fisk, I. Flacher, H. Flechl, M. Flix, J. Florent, A. Florez, C. Flouris, G. Flowers, K. Flowers, S. Flucke, G. Flügge, G. Foà, L. Focardi, E. Foerster, M. Folgueras, S. Fonseca De Souza, S. Fontaine, J.-C. Ford, W.T. Forthomme, L. Foudas, C. Fouz, M.C. Francis, B. Franco Sevilla, M. Franzoni, G. Freeman, J. Frensch, F. Friedl, M. Friese, R. Frueboes, T. Frühwirth, R. Fulcher, J. Funk, W. Furic, I.K. Futyan, D. Gadrat, S. Galanti, M. Gallinaro, M. Gallo, E. Galloni, C. Gandrajula, R.P. Ganguly, S. Ganjour, S. 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Simonis, H.J. Singh, G. Singh, J.B. Sinthuprasith, T. Sirois, Y. Siroli, G.P. Sirunyan, A.M. Skatchkov, N. Skhirtladze, N. Skinnari, L. Skovpen, K. Skuja, A. Smirnov, I. Smirnov, V. Smith, D. Smith, G. Smith, J. Smith, N. Smith, V.J. Smith, W.H. Snigirev, A. Snook, B. Snow, G.R. Snowball, M. Snyder, C. Soares, M.S. Sobol, A. Soffi, L. Soha, A. Sola, V. Solano, A. Somalwar, S. Son, D.C. Song, S. Sonnenschein, L. Sordini, V. Sorokin, P. Spagnolo, P. Spalding, W.J. Spanier, S. Spannagel, S. Sperka, D. Sphicas, P. Spiegel, L. Spiezia, A. Spiridonov, A. Spiropulu, M. Squires, M. Srimanobhas, N. St. John, J. Stadie, H. Stahl, A. Staiano, A. Starodumov, A. Steggemann, J. Steinbrück, G. Stenson, K. Stephans, G.S.F. Stickland, D. Stieger, B. Stober, F.M. Stolp, D. Stone, R. Stoye, M. Stoykova, S. Stoynev, S. Strauss, J. Strebler, T. Stringer, R. Strobbe, N. Strologas, J. Strom, D. Stuart, D. Stupak, J. Sturdy, J. Suarez, I. Suarez Gonzalez, J. Sudic, L. Sulak, L. Sulimov, V. Sultanov, G. Sumorok, K. Sun, J. Sun, M. Sun, W. Sun, X. Sung, K. Sur, N. Sutar, B. Suwonjandee, N. Svyatkovskiy, A. Swain, S.K. Swartz, M. Syarif, R. Symonds, P. Szillasi, Z. Szleper, M. Sznajder, A. Tabarelli de Fatis, T. Tadel, M. Takahashi, M. Takahashi, Y. Takasugi, E. Tali, B. Talvitie, J. Tambe, N. Tan, P. Tan, S.M. Tao, J. Tapper, A. Taroni, S. Tatarinov, A. Tavernier, S. Tavolaro, V.R. Taylor, D. Taylor, L. Teixeira De Lima, R. Tenchini, R. Teo, W.D. Teodorescu, L. Terentyev, N. Teyssier, D. Thea, A. Theofilatos, K. Tholen, H. Thom, J. Thomas, L. Thomas, S. Thomassen, P. Thompson, J. Thüer, S. Thyssen, F. Tiko, A. Tiras, E. Titov, M. Tkaczyk, S. Tlisov, D. Toda, S. Toldaiev, O. Tomalin, I.R. Tonelli Manganote, E.J. Tonelli, G. Tonjes, M.B. Tonwar, S.C. Topakli, H. Topkar, A. Topsis-Giotis, I. Torassa, E. Toriashvili, T. Toropin, A. Tosi, M. Tosi, N. Tosi, S. Tourtchanovitch, L. Traczyk, P. Tran, N.V. Trauger, H. Travaglini, R. Treberer-Treberspurg, W. Treille, D. Trevisani, N. Tricomi, A. Triossi, A. Tripathi, M. Trippkewitz, K.D. Trocino, D. Trocsanyi, Z.L. Troendle, D. Tropiano, A. Troshin, S. Trovato, M. Tsai, J.F. Tsamalaidze, Z. Tsirou, A. Tu, Z. Tucker, J. Tully, C. Tumasyan, A. Tuo, S. Tuominen, E. Tuominiemi, J. Tuovinen, E. Turkewitz, J. Turner, M. Turner, P. Tuuva, T. Tuve, C. Tytgat, M. Tyurin, N. Tzeng, Y.M. Tziaferi, E. Bhawandeep, U. Uchida, K. Ujvari, B. Ulmer, K.A. Ulrich, R. Undleeb, S. Uplegger, L. Usai, E. Uvarov, L. Uzunian, A. Vaandering, E.W. Vadruccio, D. Vai, I. Vaitkus, J. Valls, N. Valuev, V. Van Spilbeeck, A. Van Onsem, G.P. Van Haevermaet, H. Van Parijs, I. Van De Klundert, M. Van Remortel, N. Van Mulders, P. Van Mechelen, P. Van Hove, P. Van Doninck, W. Van Driessche, W. Vander Velde, C. Vander Donckt, M. Vanelderen, L. Vanhoefer, A. Vanini, S. Vanlaer, P. Vardanyan, I. Vardarlı, F.I. Varela, J. Varelas, N. Varma, M. Vartak, A. Vavilov, S. Vazquez Valencia, F. Vazquez Acosta, M. Veelken, C. Velasco, M. Velicanu, D. Velkovska, J. Venditti, R. Ventura, S. Venturi, A. Verdier, P. Verdini, P.G. Veres, G.I. Vergili, M. Verlage, T. Vernieri, C. Verwilligen, P. Verzetti, M. Verzocchi, M. Veszpremi, V. Vesztergombi, G. Veverka, J. Vidal Marono, M. Vidal, R. Vila, I. Vilar Cortabitarte, R. Vilela Pereira, A. Viliani, L. Virdee, T. Viret, S. Vischia, P. Vitulo, P. Vizan Garcia, J.M. Vlasov, E. Vlimant, J.R. Vogel, H. Volkov, A. Volobouev, I. Vormwald, B. Vorobiev, I. Vorobyev, A. Voutilainen, M. Vutova, M. Wagner, S.R. Wagner-Kuhr, J. Walczak, M. Walia, G. Walker, M. Wallny, R. Walsh, R. Waltenberger, W. Wan Abdullah, W.A.T. Wang, C. Wang, D. Wang, F. Wang, J. Wang, J. Wang, Q. Wang, R.-J. Wang, S. Wang, T.W. Wang, Y. Wang, Z. Wardle, N. Wasserbaech, S. Wayand, S. Wayne, M. Weber, H. Weber, H.A. Weber, M. Weber, M. Wei, H. Weiler, T. Weinberg, M. Welke, C. Wendland, L. Weng, Y. West, C. Wetzel, J. Whitbeck, A. Wickramage, N. Wilbur, S. Williams, T. Wimpenny, S. Winer, B.L. Wissing, C. Wittich, P. Wittmer, B. Wöhri, H.K. Wöhrmann, C. Wolf, M. Wolf, R. Wolfe, E. Wood, D. Wood, J. Woodard, A. Woods, N. Worm, S.D. Wright, D. Wu, Z. Wulsin, H.W. Wulz, C.-E. Würthwein, F. Wyslouch, B. Xia, F. Xiao, M. Xie, S. Xie, W. Xin, Y. Xu, L. Xu, Q. Xu, Z. Yagil, A. Yalvac, M. Yang, F. Yang, M. Yang, Y. Yazgan, E. Yelton, J. Yetkin, E.A. Yetkin, T. Yi, K. Yilmaz, Y. Yohay, R. Yonamine, R. Yoo, H.D. Yoo, J. York, A. You, C. Yu, I. Yu, S.S. Yumiceva, F. Yusli, M.N. Zabel, J. Zabi, A. Zaganidis, N. Zagozdzinska, A. Zakaria, M. Zalewski, P. Zanetti, A. Zanetti, M. Zarubin, A. Zeinali, M. Zenoni, F. Zenz, S.C. Zeuner, W.D. Zevi Della Porta, G. Zeyrek, M. Zghiche, A. Zhang, F. Zhang, H. Zhang, J. Zhokin, A. Zhu, R.Y. Zhukov, V. Zhukova, V. Zorbilmez, C. Zotto, P. Zou, D. Zsigmond, A.J. Zucchetta, A. Zuranski, A. d'Enterria, D. de Trocóniz, J.F. de Barbaro, P. du Pree, T. CMS Collaboration

Published
2016

10. DON'T LET THEM SEE ME DIE.

Author

Chris Brooke ; Larisa Brown

Abstract

IN her last moments, Ann Maguire's thoughts were only for her pupils. [ABSTRACT FROM PUBLISHER]

Published
2014

11. STABBED TO DEATH IN FRONT OF HER CLASS.

Author

Chris Brooke; Larisa Brown

Abstract

A DEVOTED teacher was stabbed to death in front of her horrified class yesterday by a pupil said to have a grudge against her. [ABSTRACT FROM PUBLISHER]

Published
2014

12. Family in tearful vigil at shrine to stabbed teacher.

Author

Chris Brooke; Larisa Brown

Abstract

AS they filed past hundreds of floral tributes at the perimeter of Corpus Christi Catholic College, the tears began to flow for Ann Maguire's family. [ABSTRACT FROM PUBLISHER]

Published
2014

13. Family's vigil at shrine to stabbed teacher.

Author

Chris Brooke; Larisa Brown

Abstract

AS they filed past hundreds of floral tributes at the perimeter of Corpus Christi Catholic College, the tears began to flow for Ann Maguire's family. [ABSTRACT FROM PUBLISHER]

Published
2014

14. Murdered teacher's family moved to tears by tributes.

Author

Chris Brooke; Larisa Brown

Abstract

AS they walked alongside the hundreds of heartfelt floral tributes laid at the gates of the school where Ann Maguire was stabbed to death, the tears began to flow for the much-loved teacher's family. [ABSTRACT FROM PUBLISHER]

Published
2014

15. Stabbed to death in class 'by a pupil with grudge'.

Author

Chris Brooke; Larisa Brown

Abstract

A DEVOTED teacher was stabbed to death in front of her horrified class yesterday by a pupil said to have a grudge against her. [ABSTRACT FROM PUBLISHER]

Published
2014

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