Zobrazeno 1 - 10
of 78
pro vyhledávání: '"Oliver A Hampton"'
Autor:
Xuefeng Wang, Igor Puzanov, Abdul Rafeh Naqash, Ahmad A Tarhini, George J Weiner, Phaedra Agius, Margaret E Gatti-Mays, Howard Colman, Aik Choon Tan, Issam El Naqa, Timothy I Shaw, Aakrosh Ratan, Martin D McCarter, John Carpten, Susanne M Arnold, Michelle Churchman, Michael D Radmacher, Oliver A Hampton, David M McKean, Daniel R Elgort, Robert J Rounbehler, Donghai Dai, Tingyi Li, William S Dalton
Publikováno v:
Journal for ImmunoTherapy of Cancer, Vol 11, Iss Suppl 1 (2023)
Externí odkaz:
https://doaj.org/article/801cbc91062449379d40afd58c6cfbc8
Autor:
McKayla J Riggs, Nan Lin, Chi Wang, Dava W Piecoro, Rachel W Miller, Oliver A Hampton, Mahadev Rao, Frederick R Ueland, Jill M Kolesar
Publikováno v:
PLoS ONE, Vol 15, Iss 12, p e0244558 (2020)
ObjectiveDACH1 is a transcriptional repressor and tumor suppressor gene frequently mutated in melanoma, bladder, and prostate cancer. Loss of DACH1 expression is associated with poor prognostic features and reduced overall survival in uterine cancer.
Externí odkaz:
https://doaj.org/article/88001314a2504f16a427bf8864988a90
Autor:
Oliver A. Hampton, Adam C. English, Mark Wang, William J. Salerno, Yue Liu, Donna M. Muzny, Yi Han, David A. Wheeler, Kim C. Worley, James R. Lupski, Richard A. Gibbs
Publikováno v:
BMC Genomics, Vol 18, Iss S6, Pp 31-36 (2017)
Abstract Background Characterization of genomic structural variation (SV) is essential to expanding the research and clinical applications of genome sequencing. Reliance upon short DNA fragment paired end sequencing has yielded a wealth of single nuc
Externí odkaz:
https://doaj.org/article/c2af46ca18934c6ba68187e64ea94585
Autor:
Soheil Meshinchi, Daniela S. Gerhard, Malcolm A. Smith, David A. Wheeler, Alan S. Gamis, Lora R. Lewis, Navin Rustagi, Ninad Dewal, Donna M. Muzny, Leandro Hermida, Patee Gesuwan, Tanja M. Davidsen, Jaime M. Guidry Auvil, Todd A. Alonzo, Lisa R. Trevino, Oliver A. Hampton, Daniel Wai, Rhonda E. Ries, Heather L. Schuback, Jason E. Farrar
Demographic Information of Patient Cohort. A) Age category of patients. B) Cytogenetic category.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5073cf6db09b01277dbc1eb3e614631c
https://doi.org/10.1158/0008-5472.22410521.v1
https://doi.org/10.1158/0008-5472.22410521.v1
Autor:
Soheil Meshinchi, Daniela S. Gerhard, Malcolm A. Smith, David A. Wheeler, Alan S. Gamis, Lora R. Lewis, Navin Rustagi, Ninad Dewal, Donna M. Muzny, Leandro Hermida, Patee Gesuwan, Tanja M. Davidsen, Jaime M. Guidry Auvil, Todd A. Alonzo, Lisa R. Trevino, Oliver A. Hampton, Daniel Wai, Rhonda E. Ries, Heather L. Schuback, Jason E. Farrar
Patient Characteristics
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e1730c4808a820a6068d5be1f2e47d6
https://doi.org/10.1158/0008-5472.22410509
https://doi.org/10.1158/0008-5472.22410509
Autor:
Elizabeth J. Perlman, Julie M. Gastier-Foster, Nicole Ross, Ronald R. de Krijger, Marry M. van den Heuvel-Eibrink, Amy L. Walz, Oliver A. Hampton, David A. Wheeler, Jing Ma, Charles G. Mullighan, James I. Geller, Jing Tian, Yueh-Yun Chi, Jeffrey S. Dome, Vicki Huff, Marco A. Marra, Richard A. Moore, Andrew J. Mungall, Zusheng Zong, Yussanne Ma, Ying Hu, Cu Nguyen, Chunhua Yan, Chih Hao Hsu, Qing-Rong Chen, Daoud Meerzaman, Jaime M. Guidry Auvil, Malcolm A. Smith, Daniela S. Gerhard, Samantha Gadd, Ariadne H.A.G. Ooms
Purpose: To investigate the role and significance of TP53 mutation in diffusely anaplastic Wilms tumors (DAWTs).Experimental Design: All DAWTs registered on National Wilms Tumor Study-5 (n = 118) with available samples were analyzed for TP53 mutation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41e5ffc41c18b2d4c2506525d3dba9a1
https://doi.org/10.1158/1078-0432.c.6524982
https://doi.org/10.1158/1078-0432.c.6524982
Autor:
Elizabeth J. Perlman, Julie M. Gastier-Foster, Nicole Ross, Ronald R. de Krijger, Marry M. van den Heuvel-Eibrink, Amy L. Walz, Oliver A. Hampton, David A. Wheeler, Jing Ma, Charles G. Mullighan, James I. Geller, Jing Tian, Yueh-Yun Chi, Jeffrey S. Dome, Vicki Huff, Marco A. Marra, Richard A. Moore, Andrew J. Mungall, Zusheng Zong, Yussanne Ma, Ying Hu, Cu Nguyen, Chunhua Yan, Chih Hao Hsu, Qing-Rong Chen, Daoud Meerzaman, Jaime M. Guidry Auvil, Malcolm A. Smith, Daniela S. Gerhard, Samantha Gadd, Ariadne H.A.G. Ooms
This table shows the recurrent mutations that were identified as well as the gains/losses at previously reported chromosomal segments in the 39 DAWTs that were selected for in-depth analysis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3cc0f1178c491c1b33e2675cd9e5a8d5
https://doi.org/10.1158/1078-0432.22462011
https://doi.org/10.1158/1078-0432.22462011
Autor:
Soheil Meshinchi, Daniela S. Gerhard, Malcolm A. Smith, David A. Wheeler, Alan S. Gamis, Lora R. Lewis, Navin Rustagi, Ninad Dewal, Donna M. Muzny, Leandro Hermida, Patee Gesuwan, Tanja M. Davidsen, Jaime M. Guidry Auvil, Todd A. Alonzo, Lisa R. Trevino, Oliver A. Hampton, Daniel Wai, Rhonda E. Ries, Heather L. Schuback, Jason E. Farrar
List of all segment variations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d21d77850adb8344d7aeb4f0c594fc83
https://doi.org/10.1158/0008-5472.22410503
https://doi.org/10.1158/0008-5472.22410503
Autor:
Soheil Meshinchi, Daniela S. Gerhard, Malcolm A. Smith, David A. Wheeler, Alan S. Gamis, Lora R. Lewis, Navin Rustagi, Ninad Dewal, Donna M. Muzny, Leandro Hermida, Patee Gesuwan, Tanja M. Davidsen, Jaime M. Guidry Auvil, Todd A. Alonzo, Lisa R. Trevino, Oliver A. Hampton, Daniel Wai, Rhonda E. Ries, Heather L. Schuback, Jason E. Farrar
Clonal cluster analysis. Mutations were clustered using DBSCAN based on the VAF and graphed according to timepoint. Panels A-T illustrate possible scenarios of how individual mutations may originate, evolve, and resolve based on VAF.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fa9f69b815765f6fabdb41f9b5be176
https://doi.org/10.1158/0008-5472.22410512
https://doi.org/10.1158/0008-5472.22410512
Autor:
Elizabeth J. Perlman, Julie M. Gastier-Foster, Nicole Ross, Ronald R. de Krijger, Marry M. van den Heuvel-Eibrink, Amy L. Walz, Oliver A. Hampton, David A. Wheeler, Jing Ma, Charles G. Mullighan, James I. Geller, Jing Tian, Yueh-Yun Chi, Jeffrey S. Dome, Vicki Huff, Marco A. Marra, Richard A. Moore, Andrew J. Mungall, Zusheng Zong, Yussanne Ma, Ying Hu, Cu Nguyen, Chunhua Yan, Chih Hao Hsu, Qing-Rong Chen, Daoud Meerzaman, Jaime M. Guidry Auvil, Malcolm A. Smith, Daniela S. Gerhard, Samantha Gadd, Ariadne H.A.G. Ooms
This table shows all TP53 variant that were identified by Whole Genome or Exome Sequencing in all DAWTs included in this study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68f33114e201af8a81e3df21d845e274
https://doi.org/10.1158/1078-0432.22462017.v1
https://doi.org/10.1158/1078-0432.22462017.v1