Zobrazeno 1 - 5
of 5
pro vyhledávání: '"NCI DCEG Cancer Genomics Research Laboratory"'
Autor:
Melissa Rotunno, Mary L. McMaster, Joseph Boland, Sara Bass, Xijun Zhang, Laurie Burdett, Belynda Hicks, Sarangan Ravichandran, Brian T. Luke, Meredith Yeager, Laura Fontaine, Paula L. Hyland, Alisa M. Goldstein, NCI DCEG Cancer Sequencing Working Group, NCI DCEG Cancer Genomics Research Laboratory, Stephen J. Chanock, Neil E. Caporaso, Margaret A. Tucker, Lynn R. Goldin
Publikováno v:
Haematologica, Vol 101, Iss 7 (2016)
Hodgkin lymphoma shows strong familial aggregation but no major susceptibility genes have been identified to date. The goal of this study was to identify high-penetrance variants using whole exome sequencing in 17 Hodgkin lymphoma prone families with
Externí odkaz:
https://doaj.org/article/dd621d80caec49b2a120337287b92624
Autor:
Anand Pathak, Katja Seipel, Alexander Pemov, Ramita Dewan, Christina Brown, Sarangan Ravichandran, Brian T. Luke, Michael Malasky, Shalabh Suman, Meredith Yeager, NCI DCEG Cancer Genomics Research Laboratory, NCI DCEG Cancer Sequencing Working Group, Richard A. Gatti, Neil E. Caporaso, John J. Mulvihill, Lynn R. Goldin, Thomas Pabst, Mary L. McMaster, Douglas R. Stewart
Publikováno v:
Haematologica, Vol 101, Iss 7 (2016)
Familial acute myeloid leukemia is rare and linked to germline mutations in RUNX1, GATA2 or CCAAT/enhancer binding protein-α (CEBPA). We re-evaluated a large family with acute myeloid leukemia originally seen at NIH in 1969. We used whole exome sequ
Externí odkaz:
https://doaj.org/article/699212f3fc02497f9951f2dde63a1eb9
Autor:
Pemov, Alexander, Hansen, Nancy F, Sindiri, Sivasish, Patidar, Rajesh, Higham, Christine S, Dombi, Eva, Miettinen, Markku M, Fetsch, Patricia, Brems, Hilde, Chandrasekharappa, Settara, Jones, Kristine, Zhu, Bin, Wei, Jun S, NISC Comparative Sequencing Program, NCI DCEG Cancer Genomics Research Laboratory, Mullikin, James C, Wallace, Margaret R, Khan, Javed, Legius, Eric, Widemann, Brigitte C, Stewart, Douglas R
Background Neurofibromatosis type 1 (NF1) is a tumor-predisposition disorder caused by germline mutations in NF1. NF1 patients have an 8–16% lifetime risk of developing a malignant peripheral nerve sheath tumor (MPNST), a highly aggressive soft-tis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::086f235300438dd428cee4f51d85dec3
https://lirias.kuleuven.be/handle/123456789/636276
https://lirias.kuleuven.be/handle/123456789/636276
Autor:
Pathak, Anand, Seipel, Katja, Pemov, Alexander, Dewan, Ramita, Brown, Christina, Ravichandran, Sarangan, Luke, Brian T, Malasky, Michael, Suman, Shalabh, Yeager, Meredith, NCI DCEG Cancer Genomics Research Laboratory, NCI DCEG Cancer Sequencing Working Group, Gatti, Richard A, Caporaso, Neil E, Mulvihill, John J, Goldin, Lynn R, Pabst, Thomas, McMaster, Mary L, Stewart, Douglas R
Publikováno v:
Haematologica, vol 101, iss 7
Familial acute myeloid leukemia is rare and linked to germline mutations in RUNX1, GATA2 or CCAAT/enhancer binding protein-α (CEBPA). We re-evaluated a large family with acute myeloid leukemia originally seen at NIH in 1969. We used whole exome sequ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::a56e552fdec0db3d42f7531ea0ca8ba0
https://escholarship.org/uc/item/0qb236f6
https://escholarship.org/uc/item/0qb236f6
Autor:
Burris, Ashley M.1, Ballew, Bari J.2, Kentosh, Joshua B.3, Turner, Clesson E.3, Norton, Scott A.4, Giri, Neelam2, Alter, Blanche P.2, Nellan, Anandani5, Gamper, Christopher5, Hartman, Kip R.3, Savage, Sharon A.2 savagesh@mail.nih.gov, NCI DCEG Cancer Genomics Research Laboratory (CORPORATE AUTHOR), NCI DCEG Cancer Sequencing Working Group (CORPORATE AUTHOR)
Publikováno v:
Pediatric Neurology. Mar2016, Vol. 56, p62-68.e1. 1p.