Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Gary W. Swift"'
Autor:
Jasreet Hundal, Jacqueline E. Payton, Chris Harris, Timothy J. Ley, Jason Walker, Mark A. Watson, Cyriac Kandoth, Rakesh Nagarajan, Qunyuan Zhang, Ling Lin, Elaine R. Mardis, Joshua J. Conyers, Patricia A. Alldredge, Cheryl F. Lichti, Michael D. McLellan, Robert S. Fulton, John S. Welch, Daniel C. Link, Sean McGrath, William D. Shannon, Vincent Magrini, John R. Osborne, Sharon Heath, Joshua F. McMichael, Richard K. Wilson, Peter Westervelt, Li Ding, Tammi L. Vickery, Jack Baty, R. Reid Townsend, Tamara Lamprecht, Lisa Cook, Timothy A. Graubert, David J. Dooling, Nobish Varghese, Matthew J. Walter, Todd Wylie, Lucinda Fulton, Daniel C. Koboldt, John F. DiPersio, Joelle Kalicki, Gary W. Swift, Michelle O'Laughlin, Jerry P. Reed, Michael H. Tomasson, Kim D. Delehaunty, Heather Schmidt, David E. Larson
Publikováno v:
New England Journal of Medicine. 363:2424-2433
BACKGROUND The genetic alterations responsible for an adverse outcome in most patients with acute myeloid leukemia (AML) are unknown. METHODS Using massively parallel DNA sequencing, we identified a somatic mutation in DNMT3A, encoding a DNA methyltr
Autor:
Sandy Aronson, Leslie Cope, Michael L. Bittner, Daniel C. Koboldt, Alex E. Lash, W. K. Alfred Yung, Margaret Morgan, Devin Absher, Carl F. Schaefer, Roger E. McLendon, Michael D. Prados, Josh Gould, Ju Han, Stacey Gabriel, Scott R. VandenBerg, Ilana Perna, Troy Shelton, Junyuan Wu, Sacha Scott, Steve Scherer, Michael J. T. O’Kelly, Li Ding, Erin Hickey, Elizabeth J. Thomson, Bahram Parvin, Kim D. Delehaunty, Gi Choi Yoon, Mark D. Robinson, Oliver Bogler, Darrell D. Bigner, Michael R. Reich, Jianhua Zhang, Robert S. Fulton, Allan H. Friedman, Tammi L. Vickery, Amita Aggarwal, Subhashree Madhavan, Liuda Ziaugra, Yuan Qi, Vandita Joshi, Eric Van Name, Jane Wilkinson, W. Ruprecht Wiedemeyer, Xiaoqi Shi, Richard A. Gibbs, Lynda Chin, Jessica Chen, Stefano Monti, Erwin G. Van Meir, John Ngai, Amy Hawkins, Elizabeth Lenkiewicz, Brad Ozenberger, Shannon Dorton, Georgia Ren, John N. Weinstein, Gena M. Mastrogianakis, Asif T. Chinwalla, Scott L. Carter, Nicholas D. Socci, Rachel Abbott, Gavin Sherlock, Lucinda Fulton, Hyun Soo Kim, Fei Pan, Magali Cavatore, Gabriele Alexe, Francis S. Collins, Narayanan Sathiamoorthy, Lakshmi Jakkula, Brian H. Dunford-Shore, Jireh Santibanez, Tom Mikkelsen, Huy V. Nguyen, Levi A. Garraway, Christopher A. Miller, Jinghui Zhang, Ken Chen, Timothy Fennell, Robert Sfeir, James A. Robinson, Alexey Stukalov, Richard K. Wilson, Matthew Meyerson, Daniel J. Weisenberger, Mi Yi Joo, Yevgeniy Antipin, Anna Lapuk, Gerald V. Fontenay, Nicolas Stransky, Adam B. Olshen, Elizabeth Purdom, Josh Korn, Huyen Dinh, Sai Balu, Victoria Wang, James G. Herman, Christie Kovar, Kristian Cibulskis, Tisha Chung, Agnes Viale, Paul T. Spellman, Supriya Gupta, Melissa Parkin, Peter J. Park, Maddy Wiechert, John W. Wallis, Peter W. Laird, Nikolaus Schultz, James D. Brooks, David Nassau, Jun Li, John R. Osborne, Anna D. Barker, Peter Fielding, Boris Reva, Karen Vranizan, D. Neil Hayes, Aleksandar Milosavljevic, Lawrence A. Donehower, Won Kong Sek, Daniela S. Gerhard, Otis Hall, Rameen Beroukhim, Audrey Southwick, George M. Weinstock, Chris Markovic, Roel G.W. Verhaak, David Van Den Berg, Joe W. Gray, Yanru Ren, Ethan Cerami, Yiming Zhu, Amrita Ray, Yonghong Xiao, Kristin G. Ardlie, William L. Gerald, Michael S. Lawrence, Gerald R. Fowler, Mark S. Guyer, Isaac S. Kohane, Kornel E. Schuebel, Mitchel S. Berger, Jeffrey J. Olson, Gary W. Swift, Lora Lewis, Sheri Sanders, Norman L. Lehman, Eric S. Lander, Robert Penny, Liliana Villafania, John G. Conboy, Ari B. Kahn, Henry Marr, Heidi S. Feiler, Lynn Nazareth, David J. Dooling, Katherine A. Hoadley, Alicia Hawes, Marc Ladanyi, Aniko Sabo, Wendy Winckler, Vivian Peng, Barbara A. Weir, Daniel J. Brat, Scott Morris, Carolyn C. Compton, Todd R. Golub, Scott Abbott, Michael D. McLellan, Jiqiang Yao, Shalini N. Jhangiani, Michael D. Topal, Michael C. Wendl, Gad Getz, Jun Yao, Derek Y. Chiang, Larry Feng, Steffen Durinck, David A. Wheeler, Yuzhu Tang, Benjamin Gross, Barry S. Taylor, Kenneth Aldape, Craig Pohl, Rick Meyer, Peter J. Good, Ling Lin, Elaine R. Mardis, Robert C. Onofrio, Jane Peterson, Stephen B. Baylin, Li-Xuan Qin, Andrew Cree, Cameron Brennan, Charles M. Perou, William Courtney, Omar Alvi, Donna M. Muzny, Joseph G. Vockley, Jill P. Mesirov, Yan Shi, Alexei Protopopov, Jim Vaught, Craig H. Mermel, Scott Mahan, Laetitia Borsu, Heather Schmidt, Jennifer Baldwin, Tracie L. Miner, Toby Bloom, David E. Larson, Leander Van Neste, Nicholas J. Wang, Kenneth H. Buetow, Raju Kucherlapati, Anthony San Lucas, Martin L. Ferguson, Terence P. Speed, Venkatraman E. Seshan, Debbie Beasley, Carrie Sougnez, Carrie A. Haipek, Richard M. Myers, Chris Sander, Qing Wang Wei, Jon G. Seidman, Rob Nicol, Manuel L. Gonzalez-Garay, Shin Leong, Shannon T. Brady
Publikováno v:
Nature
Nature, 455(7216), 1061-1068. Nature Publishing Group
Nature, 455(7216), 1061-1068. Nature Publishing Group
Human cancer cells typically harbour multiple chromosomal aberrations, nucleotide substitutions and epigenetic modifications that drive malignant transformation. The Cancer Genome Atlas ( TCGA) pilot project aims to assess the value of large- scale m
Autor:
Heather Schmidt, Ling Lin, Elaine R. Mardis, Daniel R. George, Ken Chen, David E. Larson, Christopher A. Miller, Li Ding, Chiao-Wang Sun, Ryan Demeter, Tim M. Townes, Gary W. Swift, Mark S. Sands, Richard K. Wilson, Kevin M. Pawlik, Michael C. Wendl, Xian Fan, Joelle Kalicki-Veizer, Timothy J. Ley, Margaret A. Young, Lisa Cook
SummaryTo assess the genetic consequences of induced pluripotent stem cell (iPSC) reprogramming, we sequenced the genomes of ten murine iPSC clones derived from three independent reprogramming experiments, and compared them to their parental cell gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b16f9875438d56415b13f9d8f9d043e
https://europepmc.org/articles/PMC3348423/
https://europepmc.org/articles/PMC3348423/
Autor:
Ken Chen, Jeffery M. Klco, Shashikant Kulkarni, Cyriac Kandoth, Jun Xia, Jacqueline E. Payton, Gary W. Swift, Michelle O'Laughlin, Sharon Heath, John S. Welch, Chris Harris, Daniel C. Link, Lucinda Fulton, Charles Lu, Sean McGrath, David J. Dooling, Joelle Kalicki-Veizer, Matthew J. Walter, Tammi L. Vickery, Fulu Liu, Lukas D. Wartman, Daniel C. Koboldt, Jason Walker, John F. DiPersio, Mark A. Watson, Jerry P. Reed, Kim D. Delehaunty, Rakesh Nagarajan, Ling Lin, Elaine R. Mardis, Nobish Varghese, John W. Wallis, Todd Wylie, Joshua F. McMichael, Michael H. Tomasson, William D. Shannon, Li Ding, Vincent Magrini, Tamara Lamprecht, Richard K. Wilson, Ryan Demeter, Jack Baty, Jasreet Hundal, Christopher A. Miller, Lisa Cook, Patricia A. Alldredge, Timothy J. Ley, Peter Westervelt, Timothy A. Graubert, Robert S. Fulton, Michael D. McLellan, Heather Schmidt, David E. Larson, Qunyuan Zhang
Publikováno v:
Cell. 150(2)
SummaryMost mutations in cancer genomes are thought to be acquired after the initiating event, which may cause genomic instability and drive clonal evolution. However, for acute myeloid leukemia (AML), normal karyotypes are common, and genomic instab
Autor:
Qunyuan Zhang, Joshua F. McMichael, Matthew J. Walter, Kim D. Delehaunty, Lisa Cook, Rakesh Nagarajan, Vincent Magrini, Joshua J. Conyers, Raymond R. Townsend, Nobish Varghese, Todd Wylie, Daniel C. Koboldt, Jasreet Hundal, Cyriac Kandoth, William D. Shannon, Ling Lin, Elaine R. Mardis, Timothy J. Ley, Heather Schmidt, Jacqueline E. Payton, Timothy A. Graubert, Li Ding, Patricia A. Alldredge, David E. Larson, Tamara Lamprecht, Lucinda Fulton, Robert S. Fulton, Michael D. McLellan, Jack Baty, David J. Dooling, John S. Welch, Daniel C. Link, Jason Walker, Tammi L. Vickery, John R. Osborne, Michael H. Tomasson, Sharon Heath, Chris Harris, Mark A. Watson, Joelle Kalicki-Veizer, Jerry P. Reed, Sean McGrath, Gary W. Swift, Michelle O'Laughlin, John F. DiPersio, Peter Westervelt, Cheryl F. Lichti, Richard K. Wilson
Publikováno v:
Blood. 116:99-99
Abstract 99 Whole genome sequencing with next generation technologies represents a new, unbiased approach for discovering somatic variations in cancer genomes. Our group recently reported the DNA sequence and analysis of the genomes of two patients w