Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Nicholas S. Davis"'
Autor:
Ryne C. Ramaker, Kevin M. Bowling, Brittany N. Lasseigne, Megan H. Hagenauer, Andrew A. Hardigan, Nicholas S. Davis, Jason Gertz, Preston M. Cartagena, David M. Walsh, Marquis P. Vawter, Edward G. Jones, Alan F. Schatzberg, Jack D. Barchas, Stanley J. Watson, Blynn G. Bunney, Huda Akil, William E. Bunney, Jun Z. Li, Sara J. Cooper, Richard M. Myers
Publikováno v:
Genome Medicine, Vol 9, Iss 1, Pp 1-12 (2017)
Abstract Background Psychiatric disorders are multigenic diseases with complex etiology that contribute significantly to human morbidity and mortality. Although clinically distinct, several disorders share many symptoms, suggesting common underlying
Externí odkaz:
https://doaj.org/article/29db10a441b94b67924cb7c4510ec9e2
Autor:
Marie K. Kirby, Ryne C. Ramaker, Brian S. Roberts, Brittany N. Lasseigne, David S. Gunther, Todd C. Burwell, Nicholas S. Davis, Zulfiqar G. Gulzar, Devin M. Absher, Sara J. Cooper, James D. Brooks, Richard M. Myers
Publikováno v:
BMC Cancer, Vol 17, Iss 1, Pp 1-10 (2017)
Abstract Background Current diagnostic tools for prostate cancer lack specificity and sensitivity for detecting very early lesions. DNA methylation is a stable genomic modification that is detectable in peripheral patient fluids such as urine and blo
Externí odkaz:
https://doaj.org/article/9a39d794a64a48a3a8bfb311493a6d59
Autor:
Marie K. Kirby, Ryne C. Ramaker, Jason Gertz, Nicholas S. Davis, Bobbi E. Johnston, Patsy G. Oliver, Katherine C. Sexton, Edward W. Greeno, John D. Christein, Martin J. Heslin, James A. Posey, William E. Grizzle, Selwyn M. Vickers, Donald J. Buchsbaum, Sara J. Cooper, Richard M. Myers
Publikováno v:
Molecular Oncology, Vol 10, Iss 8, Pp 1169-1182 (2016)
Background Pancreatic adenocarcinoma patients have low survival rates due to late‐stage diagnosis and high rates of cancer recurrence even after surgical resection. It is important to understand the molecular characteristics associated with surviva
Externí odkaz:
https://doaj.org/article/18b28309935b4450822c1557f59a1f5b
Autor:
Sandeep S. Davé, David B. Dunson, Jyotishka Datta, Yuan Zhuang, Shawn Levy, Cassandra Love, Anupama Reddy, Deepthi Rajagopalan, Jenny Zhang, Guojie Li, Nicholas S. Davis, Randy D. Gascoyne, Sandra Basic-Kinda, Igor Aurer, John R. Goodlad, William W. L. Choi, Gopesh Srivastava, Rex K.H. Au-Yeung, Amy Chadburn, Andrew M. Evens, Monika Pilichowska, Pierre Sujobert, Anne Moreau, Marie Parrens, Lucile Baseggio, Mayur Parihar, Anne W. Beaven, Christopher R. Flowers, Leon Bernal-Mizrachi, Steven Horwitz, Neha Mehta-Shah, Wing C. Chan, Dennis Weisenburger, Lawrence Low, Eric D. Hsi, Sarah L. Ondrejka, Yuri Fedoriw, Kristy L. Richards, Jennifer R. Chapman-Fredricks, Izidore S. Lossos, Magdalena B. Czader, Virginie Fataccioli, Marie Helene Delfau-Larue, Karim Belhadj, Javeed Iqbal, Tayla Heavican, Liqiang Xi, Stefania Pittaluga, Elaine S. Jaffe, Mark Raffeld, Alina Nicolae, Laurence De Leval, Marion Travert, Philippe Gaulard, Andrea B. Moffitt, Matthew McKinney
Supplementary Table S1. Sanger validated variants. Supplementary Table S2. Mutations in HSTL driver genes. Supplementary Table S3. Other mutations identified by exome sequencing. Supplementary Table S4. Copy number of HSTL patients and cell lines. Su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2977857d8e39de8241655319c2cafef
https://doi.org/10.1158/2159-8290.22532180
https://doi.org/10.1158/2159-8290.22532180
Autor:
Sandeep S. Davé, David B. Dunson, Jyotishka Datta, Yuan Zhuang, Shawn Levy, Cassandra Love, Anupama Reddy, Deepthi Rajagopalan, Jenny Zhang, Guojie Li, Nicholas S. Davis, Randy D. Gascoyne, Sandra Basic-Kinda, Igor Aurer, John R. Goodlad, William W. L. Choi, Gopesh Srivastava, Rex K.H. Au-Yeung, Amy Chadburn, Andrew M. Evens, Monika Pilichowska, Pierre Sujobert, Anne Moreau, Marie Parrens, Lucile Baseggio, Mayur Parihar, Anne W. Beaven, Christopher R. Flowers, Leon Bernal-Mizrachi, Steven Horwitz, Neha Mehta-Shah, Wing C. Chan, Dennis Weisenburger, Lawrence Low, Eric D. Hsi, Sarah L. Ondrejka, Yuri Fedoriw, Kristy L. Richards, Jennifer R. Chapman-Fredricks, Izidore S. Lossos, Magdalena B. Czader, Virginie Fataccioli, Marie Helene Delfau-Larue, Karim Belhadj, Javeed Iqbal, Tayla Heavican, Liqiang Xi, Stefania Pittaluga, Elaine S. Jaffe, Mark Raffeld, Alina Nicolae, Laurence De Leval, Marion Travert, Philippe Gaulard, Andrea B. Moffitt, Matthew McKinney
Supplementary Figure S1. Sanger sequencing chromatograms. Supplementary Figure S2. Cancer cell fraction for driver genes. Supplementary Figure S3. Ideogram with chromosome 7 alterations. Supplementary Figure S4. Examples of Exome Copy Number. Supplem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1096702833396e08e883c3e0ac18c2a4
https://doi.org/10.1158/2159-8290.22532186
https://doi.org/10.1158/2159-8290.22532186
Publikováno v:
Physical Review B. 103
One of the long-standing goals of quantum transport is to use the noise, rather than the average current, for information processing. However, achieving this requires on-demand control of quantum fluctuations in the electric current. In this paper, w
Autor:
Eileen Smith, Jennifer R. Shingleton, Sandeep S. Dave, Jie Wang, Razvan Panea, Qiu Qin, Cassandra Love, Othmane Jadi, Nicholas S. Davis, Rachel Kositsky, Lanie Happ, Carolyn H. Baloh, Anupama Reddy, Naina Singhi, Devang Thakkar, Tushar Dave, Xiang Li
Publikováno v:
Cold Spring Harb Perspect Med
Non-Hodgkin lymphomas (NHLs) are a diverse group of entities, both clinically and molecularly. Here, we review the evolution of classification schemes in B-cell lymphoma, noting the now standard WHO classification system that is based on immune cell-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f3788f0f1a1ba7ed697a229096793c6
https://europepmc.org/articles/PMC7919396/
https://europepmc.org/articles/PMC7919396/
Autor:
Catherine Leites, Gang Zeng, Leslie Ryan, Helicia Paz, Erika Von Euw, Nathaniel Magilnick, Nicholas S. Davis, Christian S. Hinrichs
Publikováno v:
Cancer Research. 81:1496-1496
Introduction: As T cell receptor (TCR) therapy emerges as a powerful therapy in cancer treatment, the field is still limited by a relatively small number of targets that are expressed widely in tumor cells but not expressed healthy normal tissues. Ki
Autor:
Katherine C. Sexton, Sara J. Cooper, Martin J. Heslin, Nicholas S. Davis, Donald J. Buchsbaum, Ryne C. Ramaker, James Posey, Edward W Greeno, John D. Christein, Patsy G. Oliver, Selwyn M. Vickers, Jason Gertz, William E. Grizzle, Marie K. Kirby, Bobbi E Johnston, Richard M. Myers
Publikováno v:
Molecular Oncology. 10:1169-1182
Background Pancreatic adenocarcinoma patients have low survival rates due to late-stage diagnosis and high rates of cancer recurrence even after surgical resection. It is important to understand the molecular characteristics associated with survival
Autor:
Sirpa Leppä, Kikkeri N. Naresh, Tiffany Tzeng, Eric Tse, Yok-Lam Kwong, Chun Huat Teh, Javeed Iqbal, Yuan Zhuang, Rex Au-Yeung, Kristy L. Richards, Jonathan W. Said, Susanna Mannisto, Panu E. Kovanen, Diego Villa, Nicholas S. Davis, John R. Goodlad, Brooke C. Palus, David B. Dunson, Magdalena Czader, Rachel E. Rempel, Andrea B. Moffitt, Shawn Levy, Matthew McKinney, Sarah L. Ondrejka, Deepthi Rajagopalan, Sandeep S. Dave, Patricia L. Lugar, Cassandra Love, Eric D. Hsi, Jyotishka Datta, Jane Healy, Amy Chadburn, Randy D. Gascoyne, Jiayu Yu, Gopesh Srivastava, Eileen Smith
Publikováno v:
The Journal of experimental medicine, vol 214, iss 5
The Journal of Experimental Medicine
The Journal of Experimental Medicine
Enteropathy-associated T cell lymphoma (EATL) is the most common oncologic complication of celiac disease. Moffitt and colleagues identify novel EATL-defining mutations in SETD2, as well as clinically relevant mutations in the JAK-STAT pathway.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3fad0b34d3a8557351ce6d73b230c0d
https://escholarship.org/uc/item/5246q5xg
https://escholarship.org/uc/item/5246q5xg