Resultats de la cerca - Colleen M. Cebulla
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Exceptional Response of Therapy-resistant SF3B1 Mutant Conjunctival Melanoma to Nivolumab/LAG3 Inhibitor Relatlimab Combination Therapy: A Case Report per Fernando M. Núñez, Salvador Méndez Gómez, Raymond J. Cho, Rebecca Kuennen, Colleen M. Cebulla, Richard C. Wu
Publicat 2025Artigo -
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Germline BAP1 mutation predisposes to uveal melanoma, lung adenocarcinoma, meningioma, and other cancers per Mohamed H. Abdel‐Rahman, Robert Pilarski, Colleen M. Cebulla, James B. Massengill, Benjamin Christopher, Getachew Boru, Peter Hovland, Frederick H. Davidorf
Publicat 2011Artigo -
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Patterns of BAP1 protein expression provide insights into prognostic significance and the biology of uveal melanoma per Neil Farquhar, Sophie Thornton, Sarah E. Coupland, Judy M. Coulson, Joseph J. Sacco, Yamini Krishna, Heinrich Heimann, Azzam Taktak, Colleen M. Cebulla, Mohamed H. Abdel‐Rahman, Helen Kalirai
Publicat 2017Artigo -
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Expanding the clinical phenotype of hereditary <i>BAP1</i> cancer predisposition syndrome, reporting three new cases per Robert Pilarski, Colleen M. Cebulla, James B. Massengill, Karan Rai, Thereasa A. Rich, Louise C. Strong, Barbara McGillivray, Mary‐Jill Asrat, Frederick H. Davidorf, Mohamed H. Abdel‐Rahman
Publicat 2013Artigo -
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Germline <i>BAP1</i> alterations in familial uveal melanoma per Karan Rai, Robert Pilarski, Getachew Boru, Muneeb U. Rehman, Ahmad H. Saqr, James B. Massengill, Arun D. Singh, Meghan J. Marino, Frederick H. Davidorf, Colleen M. Cebulla, Mohamed H. Abdel‐Rahman
Publicat 2016Artigo -
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Author Correction: Uveal melanoma per Martine J. Jager, Carol L. Shields, Colleen M. Cebulla, Mohamed H. Abdel‐Rahman, Hans E. Grossniklaus, Marc‐Henri Stern, Richard D. Carvajal, Rubens Belfort, Renbing Jia, Jerry A. Shields, Bertil Damato
Publicat 2022Revisão -
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Whole Exome Sequencing Identifies Candidate Genes Associated with Hereditary Predisposition to Uveal Melanoma per Mohamed H. Abdel‐Rahman, Klarke M. Sample, Robert Pilarski, Tom Walsh, Timothy W. Grosel, Daniel D. Kinnamon, Getachew Boru, James B. Massengill, Lynn Schoenfield, Ben Kelly, David Gordon, Peter A. Johansson, Meghan J. DeBenedictis, Arun D. Singh, Silvia Casadei, Frederick H. Davidorf, Peter White, Andrew W. Stacey, James A. Scarth, Eleanor Fewings, Marc Tischkowitz, Mary‐Claire King, Nicholas K. Hayward, Colleen M. Cebulla
Publicat 2019Artigo -
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Integrative Analysis Identifies Four Molecular and Clinical Subsets in Uveal Melanoma per A. Gordon Robertson, Juliann Shih, Christina Yau, Ewan A. Gibb, Junna Oba, Karen Mungall, Julian M. Hess, Vladislav Uzunangelov, Vonn Walter, Ludmila Danilova, Tara M. Lichtenberg, Melanie H. Kucherlapati, Patrick K. Kimes, Ming Tang, Alexander Penson, Özgün Babur, Rehan Akbani, Christopher A. Bristow, Katherine A. Hoadley, Lisa Iype, Matthew T. Chang, Andrew D. Cherniack, Christopher C. Benz, Gordon B. Mills, Roel G.W. Verhaak, Klaus Griewank, Ina Felau, Jean C. Zenklusen, Hui Shen, Lynn Schoenfield, Alexander J. Lazar, Mohamed H. Abdel‐Rahman, Sergio Román-Román, Marc‐Henri Stern, Colleen M. Cebulla, Michelle D. Williams, Martine J. Jager, Sarah E. Coupland, Bita Esmaeli, Cyriac Kandoth, Scott E. Woodman
Publicat 2018Errata/Corrigenda -
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Integrative Analysis Identifies Four Molecular and Clinical Subsets in Uveal Melanoma per A. Gordon Robertson, Juliann Shih, Christina Yau, Ewan A. Gibb, Junna Oba, Karen Mungall, Julian M. Hess, Vladislav Uzunangelov, Vonn Walter, Ludmila Danilova, Tara M. Lichtenberg, Melanie H. Kucherlapati, Patrick K. Kimes, Ming Tang, Alexander Penson, Özgün Babur, Rehan Akbani, Christopher A. Bristow, Katherine A. Hoadley, Lisa Iype, Matthew T. Chang, Andrew D. Cherniack, Christopher C. Benz, Gordon B. Mills, Roel G.W. Verhaak, Klaus Griewank, Ina Felau, Jean C. Zenklusen, Hui Shen, Lynn Schoenfield, Alexander J. Lazar, Mohamed H. Abdel‐Rahman, Sergio Román-Román, Marc‐Henri Stern, Colleen M. Cebulla, Michelle D. Williams, Martine J. Jager, Sarah E. Coupland, Bita Esmaeli, Cyriac Kandoth, Scott E. Woodman, Mohamed H. Abdel‐Rahman, Rehan Akbani, Adrian Ally, J. Todd Auman, Özgün Babur, Miruna Balasundaram, Saianand Balu, Christopher C. Benz, Rameen Beroukhim, İnanç Birol, Tom Bodenheimer, Jay Bowen, Reanne Bowlby, Christopher A. Bristow, Denise Brooks, Rebecca Carlsen, Colleen M. Cebulla, Matthew T. Chang, Andrew D. Cherniack, Lynda Chin, Juok Cho, Eric Chuah, Sudha Chudamani, Carrie Cibulskis, Kristian Cibulskis, Leslie Cope, Sarah E. Coupland, Ludmila Danilova, Timothy Defreitas, John A. Demchok, Laurence Desjardins, Noreen Dhalla, Bita Esmaeli, Ina Felau, Martin L. Ferguson, Scott Frazer, Stacey Gabriel, Julie M. Gastier‐Foster, Nils Gehlenborg, Mark Gerken, Hui Shen, Gad Getz, Ewan A. Gibb, Klaus Griewank, Elizabeth A. Grimm, D. Neil Hayes, Apurva M. Hegde, David I. Heiman, Carmen Helsel, Julian M. Hess, Katherine A. Hoadley, Shital Hobensack, Robert A. Holt, Alan P. Hoyle, Xin Hu, Carolyn M. Hutter, Martine J. Jager, Joshua M. Stuart, Corbin D. Jones
Publicat 2017Artigo -
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Comprehensive Study of the Clinical Phenotype of Germline<i>BAP1</i>Variant-Carrying Families Worldwide per Sebastian Walpole, Antonia L. Pritchard, Colleen M. Cebulla, Robert Pilarski, Meredith Stautberg, Frederick H. Davidorf, Arnaud de la Fouchardière, Odile Cabaret, Lisa Golmard, Dominique Stoppa‐Lyonnet, Erin M. Garfield, Ching-Ni Jenny Njauw, Mitchell Cheung, Joni A. Turunen, Pauliina Repo, Reetta-Stiina Järvinen, Remco van Doorn, Martine J. Jager, Gregorius P. M. Luyten, Marina Marinkovic, Cindy Chau, Míriam Potrony, Veronica Höiom, Hildur Helgadóttir, Lorenza Pastorino, William Bruno, Virginia Andreotti, Bruna Dalmasso, Giulia Ciccarese, Paola Queirolo, Luca Mastracci, Karin Wadt, Jens Folke Kiilgaard, Michael R. Speicher, Natasha van Poppelen, Emine Kılıç, Rana’a T. Al‐Jamal, Irma Dianzani, Marta Betti, Carsten Bergmann, Sandro Santagata, Sonika Dahiya, Saleem Taibjee, Jo Burke, Nicola Poplawski, Sally J. O’Shea, Julia Newton‐Bishop, Julian Adlard, David J. Adams, Anne-Marie Lane, Ivana K. Kim, Sonja Klebe, Hilary Racher, J. William Harbour, Michael L. Nickerson, Rajmohan Murali, Jane M. Palmer, Madeleine Howlie, Judith Symmons, Hayley R. Hamilton, Sunil Warrier, William Glasson, Peter A. Johansson, Carla Daniela Robles‐Espinoza, Raúl Ossio, Annelies de Klein, Susana Puig, Paola Ghiorzo, Maartje Nielsen, Tero Kivelä, Hensin Tsao, Joseph R. Testa, Pedram Gerami, Marc‐Henri Stern, Brigitte Bressac–de Paillerets, Mohamed H. Abdel‐Rahman, Nicholas K. Hayward
Publicat 2018Revisão
Eines de cerca:
Matèries relacionades
Medicine
Biology
Genetics
Cancer research
Gene
Melanoma
BAP1
Oncology
Cancer
Internal medicine
Mutation
Germline mutation
Germline
Pathology
Ophthalmology
Retinal
Dermatology
Disease
Family history
Phenotype
Proband
Cancer syndrome
Chromosome
Computational biology
Immunology
Immunotherapy
Karyotype
Monosomy
Neuroscience
Optometry