Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Trenell Mosley"'
Autor:
Yulia Mostovoy, Umamaheswaran Gurusamy, Feyza Yilmaz, Jennifer G. Mulle, Pui-Yan Kwok, Charles Lee, Michael Edward Zwick, Trenell Mosley, Tamim H. Shaikh
Chromosomal rearrangements that alter the copy number of dosage-sensitive genes can result in genomic disorders, such as the 3q29 deletion syndrome. At the 3q29 region, non-allelic homologous recombination (NAHR) between paralogous copies of segmenta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d73355fa4d780f867a3482b6043b870
https://doi.org/10.1101/2021.11.10.21266197
https://doi.org/10.1101/2021.11.10.21266197
Publikováno v:
BMC Medical Genomics
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-12 (2021)
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-12 (2021)
Background Structural rearrangements of the genome, which generally occur during meiosis and result in large-scale (> 1 kb) copy number variants (CNV; deletions or duplications ≥ 1 kb), underlie genomic disorders. Recurrent pathogenic CNVs harbor s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfd2b56be49139b22d53c29b12c4bf9f
https://doi.org/10.1186/s12920-021-00999-8
https://doi.org/10.1186/s12920-021-00999-8
Autor:
Rossana Sanchez Russo, Michael J. Gambello, Melissa M. Murphy, Katrina Aberizk, Emily Black, T. Lindsey Burrell, Grace Carlock, Joseph F. Cubells, Michael T. Epstein, Roberto Espana, Katrina Goines, Ryan M. Guest, Cheryl Klaiman, Sookyong Koh, Elizabeth J. Leslie, Longchuan Li, Derek M. Novacek, Celine A. Saulnier, Esra Sefik, Sarah Shultz, Elaine Walker, Stormi Pulver White, Hallie Averbach, Gary J. Bassell, Shanthi Cambala, Tamara Caspary, David Cutler, Paul A. Dawson, Michael P. Epstein, Henry R. Johnston, Bryan Mak, Tamika Malone, Trenell Mosley, Ava Papetti, Rebecca M. Pollak, Ryan Purcell, Nikisha Sisodoya, Steven Sloan, Stephen T. Warren, David Weinshenker, Zhexing Wen, Mike Zwick, Jennifer Gladys Mulle
Publikováno v:
Genetics in Medicine
Purpose To understand the consequences of the 3q29 deletion on medical, neurodevelopmental, psychiatric, brain structural, and neurological sequalae by systematic evaluation of affected individuals. To develop evidence-based recommendations using the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6656a927bbf69f7078f18a7f3143e244
https://pubmed.ncbi.nlm.nih.gov/33564151
https://pubmed.ncbi.nlm.nih.gov/33564151
SUMMARYGenomic disorders are caused by structural rearrangements of the genome that generally occur during meiosis1. Often the rearrangements result in large-scale (> 1 kb) copy number variants (CNV; deletions or duplications ≥ 1 kb)2,3. Recurrent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::523d83d9843cd7b9b7c09f19dcb636ff
https://doi.org/10.21203/rs.3.rs-50150/v1
https://doi.org/10.21203/rs.3.rs-50150/v1
Autor:
Logan R. Myler, Tanya T. Paull, Ji-Hoon Lee, Trenell Mosley, Yi Zhou, Jonghwan Kim, Soo Hyun Yang, Tanya E. Johnson, Nadima Uprety
Publikováno v:
Cell Reports, Vol 24, Iss 6, Pp 1471-1483 (2018)
Cell reports
Cell reports
SUMMARY Ataxia-telangiectasia mutated (ATM) is a serine/threonine kinase that coordinates the response to DNA double-strand breaks and oxidative stress. NKX3.1, a prostate-specific transcription factor, was recently shown to directly stimulate ATM ki
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5758b29baf87c6816d2940a4b85dbba2
http://www.sciencedirect.com/science/article/pii/S2211124718310313
http://www.sciencedirect.com/science/article/pii/S2211124718310313
Autor:
Tyler M. Smith, Annabelle Campbell, Huy Nguyen, Joshua A. Moore, Trenell Mosley, Greg Hatlestad, Juan Resendez, David Montes, Duncan Sudarshan, Alan M Lloyd, Lyndsey Wilson, Neda Akhavan, Antonio Gonzalez, Austin Hembd, Matthew Brown
Publikováno v:
Developmental Biology. 419:54-63
The brown color of Arabidopsis seeds is caused by the deposition of proanthocyanidins (PAs or condensed tannins) in their inner testa layer. A transcription factor complex consisting of TT2, TT8 and TTG1 controls expression of PA biosynthetic genes,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4db084fda5da16bad603a9615eb774d0
https://doi.org/10.1016/j.ydbio.2016.03.031
https://doi.org/10.1016/j.ydbio.2016.03.031