Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Tracie L Miner"'
Autor:
Jenifer L Marks, Michael D McLellan, Maureen F Zakowski, Alex E Lash, Yumi Kasai, Stephen Broderick, Inderpal S Sarkaria, Duykhanh Pham, Bhuvanesh Singh, Tracie L Miner, Ginger A Fewell, Lucinda L Fulton, Elaine R Mardis, Richard K Wilson, Mark G Kris, Valerie W Rusch, Harold Varmus, William Pao
Publikováno v:
PLoS ONE, Vol 2, Iss 5, p e426 (2007)
Fifty percent of lung adenocarcinomas harbor somatic mutations in six genes that encode proteins in the EGFR signaling pathway, i.e., EGFR, HER2/ERBB2, HER4/ERBB4, PIK3CA, BRAF, and KRAS. We performed mutational profiling of a large cohort of lung ad
Externí odkaz:
https://doaj.org/article/1109a4064a2f4bbe902c334cb072ed5d
Autor:
Lincoln D Stein, Zhirong Bao, Darin Blasiar, Thomas Blumenthal, Michael R Brent, Nansheng Chen, Asif Chinwalla, Laura Clarke, Chris Clee, Avril Coghlan, Alan Coulson, Peter D'Eustachio, David H A Fitch, Lucinda A Fulton, Robert E Fulton, Sam Griffiths-Jones, Todd W Harris, LaDeana W Hillier, Ravi Kamath, Patricia E Kuwabara, Elaine R Mardis, Marco A Marra, Tracie L Miner, Patrick Minx, James C Mullikin, Robert W Plumb, Jane Rogers, Jacqueline E Schein, Marc Sohrmann, John Spieth, Jason E Stajich, C Wei, David Willey, Richard K Wilson, Richard Durbin, Robert H Waterston
Publikováno v:
PLoS Biology, Vol 1, Iss 2, p E45 (2003)
The soil nematodes Caenorhabditis briggsae and Caenorhabditis elegans diverged from a common ancestor roughly 100 million years ago and yet are almost indistinguishable by eye. They have the same chromosome number and genome sizes, and they occupy th
Externí odkaz:
https://doaj.org/article/103ed0f984d9479e8740763c1a2676dc
Autor:
Bob Fulton, Scott Abbott, Lisa Cook, Tracie L. Miner, Yu Zhao, Jacqueline E. Payton, David E. Larson, Rhonda E. Ries, Mark A. Watson, Scott M. Smith, Vincent Magrini, John F. DiPersio, Peter Westervelt, Brian H. Dunford-Shore, Sean McGrath, Jennifer Ivanovich, Michael D. McLellan, Matthew J. Walter, Nathan Sander, Timothy J. Ley, Craig Pohl, Matthew T. Hickenbotham, Jarret Glasscock, Daniel C. Koboldt, Amy Hawkins, Devin P. Locke, Rakesh Nagarajan, David Gordon, Li Ding, William D. Shannon, Elaine R. Mardis, Michael H. Tomasson, LaDeana W. Hillier, Ken Chen, Daniel C. Link, Richard K. Wilson, Patrick Minx, John R. Osborne, Sharon Heath, Rachel Abbott, Lucinda Fulton, Joshua J. Conyers, Asif T. Chinwalla, David J. Dooling, Timothy A. Graubert, Todd Wylie, Jack Baty, Xiaoqi Shi
Publikováno v:
Nature
Lay Summary Acute myeloid leukemia is a highly malignant hematopoietic tumor that affects about 13,000 adults yearly in the United States. The treatment of this disease has changed little in the past two decades, since most of the genetic events that
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:
Tracie L. Miner, James W. Vardiman, Daniel C. Link, Christine Bellanné-Chantelot, Audrey Anna Bolyard, Yumi Kasai, Deepak Kapur, Ghada M Kunter, Jean Donadieu, Michael A. Caligiuri, Elaine R. Mardis, Rakesh Nagarajan, Richard K. Wilson, Timothy J. Ley, Karl Welte, David C. Dale, William D. Shannon, John F. DiPersio, Clara D. Bloomfield, Rhonda E. Ries, Cornelia Zeidler, Timothy A. Graubert, Laurence A. Boxer, Peter Westervelt, Jack Baty, Michael H. Tomasson, Yu Zhao, Michael D. McLellan, Mark A. Watson
Publikováno v:
Blood. 110:1648-1655
Severe congenital neutropenia (SCN) is an inborn disorder of granulopoiesis. Like most other bone marrow failure syndromes, it is associated with a marked propensity to transform into a myelodysplastic syndrome (MDS) or acute leukemia, with a cumulat
Autor:
Gudrun A. Rappold, Claudia Münch, Evan E. Eichler, Stefan Kirsch, Birgit Weiß, Robert H. Waterston, Royden A. Clark, Tracie L. Miner, Werner Schempp
Publikováno v:
Genome Research. 15:195-204
Basic medical research critically depends on the finished human genome sequence. Two types of gaps are known to exist in the human genome: those associated with heterochromatic sequences and those embedded within euchromatin. We identified and analyz
Autor:
Jason Carter, Shawn Leonard, Lucinda Fulton, John Spieth, Liliana Florea, Cindy Strong, Phil Latreille, Aniko Sabo, Michael McClelland, C Richard Harkins, Chunyan Wang, Christine Nguyen, Steffen Porwollik, Kenneth E. Sanderson, Sandra W. Clifton, Sara Kohlberg, Glendoria Elliott, Catrina Fronick, William E. Nash, Michael D. McLellan, Kim D. Delehaunty, Wesley C. Warren, Vincent Magrini, Richard K. Wilson, Patrick Minx, Hui Sun, Amy Berghoff, Tamberlyn Bieri, Tracie L. Miner, Rekha Meyer, Feiyu Du, Dan Layman, Phil Ozersky, Colin Kremizki, Michael Nhan
Publikováno v:
Nature Genetics. 36:1268-1274
Salmonella enterica serovars often have a broad host range, and some cause both gastrointestinal and systemic disease. But the serovars Paratyphi A and Typhi are restricted to humans and cause only systemic disease. It has been estimated that Typhi a
Autor:
Robert Baertsch, Karen A. Phelps, Lisa Cook, Joelle Kalicki, Michelle O'Laughlin, Kerry L. Bubb, David Torrents, Kristine M. Wylie, Andrew Vanbrunt, Mark E. Schaller, Dan Layman, Kelsi Scott, LaDeana W. Hillier, Marco A. Marra, Caryn Wagner-McPherson, Cindy Strong, Phil Latreille, Hui Sun, Maynard V. Olson, Holland Bradshaw-Cordum, Amanda Abbott, Robert S. Fulton, Nicolas Berkowicz, Richard Harkins, Asif T. Chinwalla, Rajinder Kaul, William E. Nash, Chad Tomlinson, Susan M. Rock, Patricia Wohldmann, Paul Flicek, Elaine R. Mardis, Catrina Strowmatt, James M. Eldred, Betty Lamar, Christopher K. Raymond, Michael C. Wendl, Lauren Bielicki, Shawn Leonard, John Douglas Mcpherson, Christine Nguyen, Jennifer Murray, Michael C. Becker, Lucinda Fulton, Amber Isak, Will Gillett, Matt Cordes, James B. Clendenning, Kymberlie H. Pepin, Mandeep Sekhon, Eric Haugen, Feiyu Du, Theresa Rohlfing, Kimberly D. Delehaunty, Nancy Miller, Amy Kozlowicz-Reilly, Eric D. Green, W. James Kent, Tamberlyn Bieri, Peer Bork, Richard K. Wilson, Patrick Minx, John Spieth, Evan E. Eichler, Shawn Iadanoto, Terrence S. Furey, Matthew E. Portnoy, Shunfang Hou, R. James, Warren Gish, Brian Schultz, Doug Johnson, Philip Ozersky, Jennifer Edwards, Stephanie L. Chissoe, Jeffrey A. Bailey, Tracie L. Miner, Jason Maas, Andrea Holmes, Sandra W. Clifton, Sara Jaeger, Tina Graves, Ruth Levy, Joseph A. Bedell, Ginger A. Fewell, Mikita Suyama, Shiaw-Pyng Yang, Sean R. Eddy, Rebecca S. Walker, Aye-Mon Tin-Wollam, Hui Du, Evan Keibler, Matthew T. Hickenbotham, Sara Dauphin-Kohlberg, Robert H. Waterston, Yang Zhou, Stephanie Andrews, Johar Ali, John W. Wallis, Michael R. Brent, Rachel Maupin, Donald Williams, Elizabeth Simms, Laura Courtney, Anthony R. Harris, Jeffrey Woessner, Joanne O. Nelson
Publikováno v:
Nature. 424:157-164
Human chromosome 7 has historically received prominent attention in the human genetics community, primarily related to the search for the cystic fibrosis gene and the frequent cytogenetic changes associated with various forms of cancer. Here we prese
Autor:
Seth D. Crosby, Lionel Willatt, Elena Rossi, N. Van der Aa, Orsetta Zuffardi, Michael D. McLellan, Ana Cristina Victorino Krepischi-Santos, Lisenka E.L.M. Vissers, H. Stewart, Angela Maria Vianna-Morgante, Michael Field, Susan Price, Jane A. Hurst, Bernard Grisart, Andrew J. Sharp, J. Wagenstaller, Anne Destree, L. L. Antonacci-Fulton, Liesbeth Rooms, Alice Goldenberg, Swaroop Aradhya, Pino J. Poddighe, Evan E. Eichler, B. B. A. de Vries, M. A. Wiechert, Pascale Saugier-Veber, Roberto Ciccone, J. M. Garrett, Andrew O.M. Wilkie, Melanie A. Manning, R. Pfundt, Helen V. Firth, M. De Gregori, Tracie L. Miner, Joris A. Veltman, Samantha J. L. Knight, Martin Zenker, Charles Shaw-Smith, Kathleen Bell, Carla Rosenberg, Han G. Brunner, David A. Koolen, Małgorzata J.M. Nowaczyk, Anna Hackett, Anita Rauch, Grazia M.S. Mancini, C. E. Schwartz, T. M. Strom
Publikováno v:
Journal of Medical Genetics, 45, 11, pp. 710-20
Journal of medical genetics
Journal of Medical Genetics, 45, 710-20
Journal of Medical Genetics, 45(11), 710-720. BMJ Publishing Group
Journal of medical genetics
Journal of Medical Genetics, 45, 710-20
Journal of Medical Genetics, 45(11), 710-720. BMJ Publishing Group
Contains fulltext : 69531.pdf (Publisher’s version ) (Closed access) BACKGROUND: The chromosome 17q21.31 microdeletion syndrome is a novel genomic disorder that has originally been identified using high resolution genome analyses in patients with u
Autor:
Sharon Heath, Daved H. Fremont, Richard A. Walgren, Peter Westervelt, Rakesh Nagarajan, Rick K. Wilson, William D. Shannon, Clara D. Bloomfield, Daniel C. Link, Timothy J. Ley, Yu Zhao, Michael D. McLellan, John F. DiPersio, Elaine R. Mardis, Jacqueline E. Payton, Tracie L. Miner, Rhonda E. Ries, Matthew J. Walter, Mark F. Watson, Michael H. Tomasson, Zhifu Xiang, Olga Y. Lubman, Yumi Kasai, Jack Baty, Timothy A. Graubert
Activating mutations in tyrosine kinase (TK) genes (eg, FLT3 and KIT) are found in more than 30% of patients with de novo acute myeloid leukemia (AML); many groups have speculated that mutations in other TK genes may be present in the remaining 70%.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e9264712c91bd8c1eb04348f6dd706a
https://europepmc.org/articles/PMC2343607/
https://europepmc.org/articles/PMC2343607/