Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Genevieve M Gould"'
Autor:
Genevieve M Gould, Peter V Grauman, Mark R Theilmann, Lindsay Spurka, Irving E Wang, Laura M Melroy, Robert G Chin, Dustin H Hite, Clement S Chu, Jared R Maguire, Gregory J Hogan, Dale Muzzey
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-13 (2018)
Abstract Background Hereditary cancer screening (HCS) for germline variants in the 3′ exons of PMS2, a mismatch repair gene implicated in Lynch syndrome, is technically challenging due to homology with its pseudogene PMS2CL. Sequences of PMS2 and P
Externí odkaz:
https://doaj.org/article/ccfcf68da84140cda2157d12caa3e872
Autor:
Valentina S. Vysotskaia, Gregory J. Hogan, Genevieve M. Gould, Xin Wang, Alex D. Robertson, Kevin R. Haas, Mark R. Theilmann, Lindsay Spurka, Peter V. Grauman, Henry H. Lai, Diana Jeon, Genevieve Haliburton, Matt Leggett, Clement S. Chu, Kevin Iori, Jared R. Maguire, Kaylene Ready, Eric A. Evans, Hyunseok P. Kang, Imran S. Haque
Publikováno v:
PeerJ, Vol 5, p e3046 (2017)
The past two decades have brought many important advances in our understanding of the hereditary susceptibility to cancer. Numerous studies have provided convincing evidence that identification of germline mutations associated with hereditary cancer
Externí odkaz:
https://doaj.org/article/2583b6401d394609b0e50fd51a04e636
Autor:
Boris Zinshteyn, Genevieve M. Gould, Joseph M. Paggi, Christopher B. Burge, Yuchun Guo, David V. Phizicky, David K. Gifford, Wendy V. Gilbert, Eric T. Wang
Publikováno v:
Cold Spring Harbor Laboratory Press
Spliced messages constitute one-fourth of expressed mRNAs in the yeast Saccharomyces cerevisiae, and most mRNAs in metazoans. Splicing requires 5′ splice site (5′SS), branch point (BP), and 3′ splice site (3′SS) elements, but the role of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7a6d9a9ce68b2d4e640b08cbe2f0ae9
https://doi.org/10.1261/rna.057216.116
https://doi.org/10.1261/rna.057216.116
Autor:
Genevieve M. Gould, Laura M. Melroy, Peter V. Grauman, Gregory J. Hogan, Clement Chu, Irving E Wang, Jared Maguire, Dustin H Hite, Robert Chin, Lindsay Spurka, Mark R. Theilmann, Dale Muzzey
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-13 (2018)
BMC Medical Genetics
BMC Medical Genetics
BackgroundHereditary cancer screening (HCS) for germline variants in the 3’ exons of PMS2, a mismatch repair gene implicated in Lynch syndrome, is technically challenging due to homology with its pseudogene PMS2CL. Sequences of PMS2 and PMS2CL are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89e0c33a7addd7498b8c887ffc679c23
Autor:
Alexander De Jong Robertson, Xin Wang, Diana Jeon, Valentina Vysotskaia, Imran S. Haque, Genevieve Haliburton, Matt Leggett, Lai Henry H, Clement Chu, Gregory J. Hogan, Kevin Iori, Kevin R. Haas, Peter V. Grauman, Genevieve M. Gould, Hyunseok Kang, Mark R. Theilmann, Jared Maguire, Lindsay Spurka, Eric A. Evans, Kaylene Ready
Publikováno v:
PeerJ, Vol 5, p e3046 (2017)
PeerJ
PeerJ
The past two decades have brought many important advances in our understanding of the hereditary susceptibility to cancer. Numerous studies have provided convincing evidence that identification of germline mutations associated with hereditary cancer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06304e18113fbf456d970d3d84a069c8
https://doi.org/10.1101/088252
https://doi.org/10.1101/088252
Autor:
Gabriel A. Lazarin, Genevieve M. Gould, Gregory J. Hogan, Kevin R. Haas, Dale Muzzey, Kyle A. Beauchamp, Eric A. Evans, Kenny K. Wong, Peter V. Grauman
Publikováno v:
American Journal of Obstetrics and Gynecology. 218:S166
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e4e71844185eabe34509cfdc5d7ba999
https://doi.org/10.1016/j.ajog.2017.10.187
https://doi.org/10.1016/j.ajog.2017.10.187
Autor:
Dale Muzzey, Gregory J. Hogan, Gabriel A. Lazarin, Kevin R. Haas, Genevieve M. Gould, Peter V. Grauman, Eric A. Evans, Kenny K. Wong, Kyle A. Beauchamp
Publikováno v:
Fertility and Sterility. 108:e282
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ec0823b99aa458f369335c0759e108a
https://doi.org/10.1016/j.fertnstert.2017.07.836
https://doi.org/10.1016/j.fertnstert.2017.07.836
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 108(38)
Variations in microRNA (miRNA) gene and/or target repertoire are likely to be key drivers of phenotypic differences between species. To better understand these changes, we developed a computational method that identifies signatures of species-specifi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09f470cde18dc51f42aef70fdd69afbb
https://pubmed.ncbi.nlm.nih.gov/21911408
https://pubmed.ncbi.nlm.nih.gov/21911408
Autor:
Gould, Genevieve M1 gould@counsyl.com, Grauman, Peter V1 pgrauman@counsyl.com, Theilmann, Mark R1 mark_theilmann@counsyl.com, Spurka, Lindsay1 lindsay@counsyl.com, Wang, Irving E1 iwang@counsyl.com, Melroy, Laura M1 lmelroy@counsyl.com, Chin, Robert G1 rchin@counsyl.com, Hite, Dustin H1 dustinhowardhite@gmail.com, Chu, Clement S1 clement@counsyl.com, Maguire, Jared R1 jared.maguire@gmail.com, Hogan, Gregory J1 hogan.greg@gmail.com, Muzzey, Dale1 research@counsyl.com
Publikováno v:
BMC Medical Genetics. 9/29/2018, Vol. 19 Issue 1, pN.PAG-N.PAG. 1p.