檢索結果 - Bernard J. Pope
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Risk of colorectal cancer for carriers of a germ-line mutation in POLE or POLD1 由 Daniel D. Buchanan, Jenna R. Stewart, Mark Clendenning, Christophe Rosty, Khalid Mahmood, Bernard J. Pope, Mark A. Jenkins, John L. Hopper, Melissa C. Southey, Finlay Macrae, Ingrid Winship, Aung Ko Win
出版 2017Artigo -
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MYRF Is a Membrane-Associated Transcription Factor That Autoproteolytically Cleaves to Directly Activate Myelin Genes 由 Helena Bujalka, Matthias Koenning, Stacey Jackson, Victoria M. Perreau, Bernard J. Pope, Curtis M. Hay, Stanislaw Mitew, Andrew F. Hill, Quanlong Lü, Michael Wegner, Rajini Srinivasan, John Svaren, Melanie Willingham, Ben A. Barres, Ben Emery
出版 2013Artigo -
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Long-read assembly and comparative evidence-based reanalysis of <i>Cryptosporidium</i> genome sequences reveal expanded transporter repertoire and duplication of entire chromosome... 由 Rodrigo P. Baptista, Yiran Li, Adam Sateriale, Mandy Sanders, Karen Brooks, Alan Tracey, Brendan R. E. Ansell, Aaron R. Jex, Garrett W. Cooper, Ethan D. Smith, R. Xiao, Jennifer E. Dumaine, Peter Georgeson, Bernard J. Pope, Matthew Berriman, Boris Striepen, James A. Cotton, Jessica C. Kissinger
出版 2021Artigo -
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Detection of ctDNA in plasma of patients with clinically localised prostate cancer is associated with rapid disease progression 由 Edmund Lau, Patrick J. McCoy, Fairleigh Reeves, Ken Chow, Michael J. Clarkson, Edmond M. Kwan, Kate Packwood, Helen Northen, Miao He, Zoya Kingsbury, Stefano Mangiola, Michael Kerger, Marc A. Furrer, Helen Crowe, Anthony J. Costello, David J. McBride, Mark T. Ross, Bernard J. Pope, Christopher M. Hovens, Niall M. Corcoran
出版 2020Artigo -
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Evaluating the utility of tumour mutational signatures for identifying hereditary colorectal cancer and polyposis syndrome carriers 由 Peter Georgeson, Bernard J. Pope, Christophe Rosty, Mark Clendenning, Khalid Mahmood, Jihoon E. Joo, Romy Walker, Ryan Hutchinson, Susan Preston, Julia Como, Sharelle Joseland, Aung Ko Win, Finlay Macrae, John L. Hopper, Dmitri Mouradov, Peter Gibbs, Oliver M. Sieber, Dylan E. O’Sullivan, Darren R. Brenner, Steve Gallinger, Mark A. Jenkins, Ingrid Winship, Daniel D. Buchanan
出版 2021Artigo -
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Rare Mutations in XRCC2 Increase the Risk of Breast Cancer 由 Daniel J. Park, Fabienne Lesueur, Tú Nguyen‐Dumont, Maroulio Pertesi, FA Odefrey, Fleur Hammet, Susan L. Neuhausen, Esther M. John, Irene L. Andrulis, Mary Beth Terry, M. Daly, Saundra S. Buys, Florence Le Calvez‐Kelm, Andrew Lonie, Bernard J. Pope, Helen Tsimiklis, Catherine Voegele, Florentine Hilbers, Nicoline Hoogerbrugge, A. Barroso, Ana Osório, Graham G. Giles, Peter Devilee, Javier Benı́tez, John L. Hopper, Sean V. Tavtigian, David E. Goldgar, Melissa C. Southey
出版 2012Artigo -
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Adenomas from individuals with pathogenic biallelic variants in the<i>MUTYH</i>and<i>NTHL1</i>genes demonstrate base excision repair tumour mutational signature profiles similar to... 由 Romy Walker, Jihoon E. Joo, Khalid Mahmood, Mark Clendenning, Julia Como, Susan Preston, Sharelle Joseland, Bernard J. Pope, Ana B. D. Medeiros, Brenely V. Murillo, Nicholas Pachter, Kevin Sweet, Allan D. Spigelman, Alexandra Groves, Margaret Gleeson, Krzysztof Bernatowicz, Nicola Poplawski, Lesley Andrews, Emma Healey, Steven Gallinger, Robert C. Grant, Aung Ko Win, John L. Hopper, Mark A. Jenkins, Giovana Tardin Torrezan, Christophe Rosty, Finlay Macrae, Ingrid Winship, Daniel D. Buchanan, Peter Georgeson
出版 2024Pré-impressão -
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Adenomas from individuals with pathogenic biallelic variants in the MUTYH and NTHL1 genes demonstrate base excision repair tumour mutational signature profiles similar to colorecta... 由 Romy Walker, Jihoon E. Joo, Khalid Mahmood, Mark Clendenning, Julia Como, Susan Preston, Sharelle Joseland, Bernard J. Pope, Ana Beatriz Deleame Medeiros, Brenely V. Murillo, Nicholas Pachter, Kevin Sweet, Allan D. Spigelman, Alexandra Groves, Margaret Gleeson, Krzysztof Bernatowicz, Nicola Poplawski, Lesley Andrews, Emma Healey, Steven Gallinger, Robert C. Grant, Aung Ko Win, John L. Hopper, Mark A. Jenkins, Giovana Tardin Torrezan, Christophe Rosty, Finlay Macrae, Ingrid Winship, Daniel D. Buchanan, Peter Georgeson
出版 2025Artigo -
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Rare Mutations in <i>RINT1</i> Predispose Carriers to Breast and Lynch Syndrome–Spectrum Cancers 由 Daniel J. Park, Kayoko Tao, Florence Le Calvez‐Kelm, Tú Nguyen‐Dumont, Nivonirina Robinot, Fleur Hammet, Fabrice Odefrey, Helen Tsimiklis, Zhi L. Teo, Louise B. Thingholm, Erin L. Young, Catherine Voegele, Andrew Lonie, Bernard J. Pope, Terrell C. Roane, Russell Bell, Hao Hu, N.A. Shankaracharya, Chad Huff, Jonathan J. Ellis, Jun Li, Igor V. Makunin, Esther M. John, Irene L. Andrulis, Mary Beth Terry, Mary B. Daly, Saundra S. Buys, Carrie Snyder, Henry T. Lynch, Peter Devilee, Graham G. Giles, John L. Hopper, Bing Feng, Fabienne Lesueur, Sean V. Tavtigian, Melissa C. Southey, David E. Goldgar
出版 2014Artigo -
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Identifying colorectal cancer caused by biallelic MUTYH pathogenic variants using tumor mutational signatures 由 Peter Georgeson, Tabitha A. Harrison, Bernard J. Pope, Syed Hassan Ejaz Zaidi, Conghui Qu, Robert S. Steinfelder, Yi Lin, Jihoon E. Joo, Khalid Mahmood, Mark Clendenning, Romy Walker, Efrat L. Amitay, Sonja I. Berndt, Hermann Brenner, Peter T. Campbell, Yin Cao, Andrew T. Chan, Jenny Chang‐Claude, Kimberly F. Doheny, David A. Drew, Jane C. Figueiredo, Amy J. French, Steven Gallinger, Marios Giannakis, Graham G. Giles, Andrea Gsur, Marc J. Gunter, Michael Hoffmeister, Li Hsu, Wen‐Yi Huang, Paul J. Limburg, JoAnn E. Manson, Vı́ctor Moreno, Rami Nassir, Jonathan A. Nowak, Mireia Obón‐Santacana, Shuji Ogino, Amanda I. Phipps, John D. Potter, Robert E. Schoen, Wei Sun, Amanda E. Toland, Quang M. Trinh, Tomotaka Ugai, Finlay Macrae, Christophe Rosty, Thomas J. Hudson, Mark A. Jenkins, Stephen N. Thibodeau, Ingrid Winship, Ulrike Peters, Daniel D. Buchanan
出版 2022Artigo -
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The Germline and Somatic Origins of Prostate Cancer Heterogeneity 由 Takafumi N. Yamaguchi, Kathleen E. Houlahan, Helen Zhu, Natalie J. Kurganovs, Julie Livingstone, Natalie S. Fox, Jiapei Yuan, Jocelyn Sietsma Penington, Chol-Hee Jung, Tommer Schwarz, Weerachai Jaratlerdsiri, Job van Riet, Peter Georgeson, Stefano Mangiola, Kodi Taraszka, Robert Lesurf, Jue Jiang, Ken Chow, Lawrence E. Heisler, Yu-Jia Shiah, Susmita G. Ramanand, Michael J. Clarkson, Anne Nguyen, Shadrielle M. G. Espiritu, Ryan Stuchbery, Richard Jovelin, Vincent Huang, Connor Bell, Edward O’Connor, Patrick J. McCoy, Christopher M. Lalansingh, Marek Cmero, Adriana Salcedo, Eva K.F. Chan, Lydia Liu, Phillip D. Stricker, Vinayak Bhandari, Riana Bornman, Dorota H.S. Sendorek, Andrew Lonie, Stephenie D. Prokopec, Michael Fraser, Justin S. Peters, Adrien Foucal, Shingai B.A. Mutambirwa, Lachlan McIntosh, Michèle Orain, Matthew J. Wakefield, Valérie Picard, Daniel J. Park, Hélène Hovington, Michael Kerger, Alain Bergeron, Veronica Y. Sabelnykova, Ji-Heui Seo, Mark M. Pomerantz, Noah Zaitlen, Sebastian M. Waszak, Alexander Gusev, Louis Lacombe, Yves Fradet, Andrew Ryan, Amar U. Kishan, Martijn P. Lolkema, Joachim Weischenfeldt, Bernard Têtu, Anthony J. Costello, Vanessa M. Hayes, Rayjean J. Hung, Housheng Hansen He, John D. McPherson, Bogdan Paşaniuc, Theodorus van der Kwast, Anthony T. Papenfuss, Matthew L. Freedman, Bernard J. Pope, Robert G. Bristow, Ram S. Mani, Niall M. Corcoran, Jüri Reimand, Christopher M. Hovens, Paul C. Boutros
出版 2025Artigo
相關主題
Biology
Genetics
Gene
Cancer
Medicine
Cancer research
Colorectal cancer
Computational biology
Mutation
DNA mismatch repair
Germline mutation
Internal medicine
Oncology
MUTYH
Germline
Lynch syndrome
Base excision repair
Bioinformatics
Breast cancer
Cell biology
Central nervous system
Computer science
DNA repair
Genome
Genomics
Genotype
Neuroscience
Prostate cancer
Whole genome sequencing
Amplicon