Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Jessica T Williams"'
Autor:
Abigail T Fahim, Sara J Bowne, Lori S Sullivan, Kaylie D Webb, Jessica T Williams, Dianna K Wheaton, David G Birch, Stephen P Daiger
Publikováno v:
PLoS ONE, Vol 6, Iss 8, p e23021 (2011)
Mutations in RPGR account for over 70% of X-linked retinitis pigmentosa (XlRP), characterized by retinal degeneration and eventual blindness. The clinical consequences of RPGR mutations are highly varied, even among individuals with the same mutation
Externí odkaz:
https://doaj.org/article/1897dc779fbe4fb8a7ad8d493abb4ff5
Autor:
Syed H Jafri, Arash Mollaeian, Mahran Shoukier, Rahat Hussain, Syed Mojiz Hasan, Hazem Edmond El-Osta, Bindu Akkanti, Faisal Ali, Jessica T. Williams
Publikováno v:
Clinical Medicine Insights. Oncology
Clinical Medicine Insights: Oncology, Vol 13 (2019)
Clinical Medicine Insights: Oncology, Vol 13 (2019)
Background: Lung cancer is the leading cause of cancer-related mortality and is strongly linked with smoking. We sought to determine whether major stressful life events (e.g. divorce) are also a risk factor for developing lung cancers. Methods: We pe
Autor:
Bindu Akkanti, Shailesh Advani, Faisal Ali, Arash Mollaeian, Syed Mojiz Hasan, Jessica T. Williams, Rahat Hussain, Hazem Edmond El-Osta, Syed H Jafri
Publikováno v:
Journal of Clinical Oncology. 35:1575-1575
1575 Background: Lung cancer is the leading cause of cancer-related mortality linked with smoking, though only 6-18% of heavy smokers die of lung cancer. We hypothesized that major stressful life events are a risk factor for developing lung cancer. M
Autor:
Jessica T. Williams, Kaylie D. Webb, David G. Birch, Stephen P. Daiger, Sara J. Bowne, Abigail T. Fahim, Lori S. Sullivan, Dianna K. Wheaton
Publikováno v:
Retinal Degenerative Diseases ISBN: 9781461406303
Mutations in retinitis pigmentosa GTPase regulator (RPGR) account for over 70% of X-linked retinitis pigmentosa (XlRP), characterized by retinal degeneration and eventual blindness. RPGR mutations demonstrate extreme phenotypic heterogeneity, even wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24b8126e776ba55c1552a45858faf8e0
https://europepmc.org/articles/PMC4114075/
https://europepmc.org/articles/PMC4114075/
Autor:
E. Lightsey, Jessica T. Williams
Publikováno v:
AIAA Guidance, Navigation and Control Conference and Exhibit.
Autor:
Sara J. Bowne, Stephen P. Daiger, Kaylie D. Webb, Lori S. Sullivan, Jessica T. Williams, David G. Birch, Abigail T. Fahim, Dianna K. Wheaton
Publikováno v:
PLoS ONE, Vol 6, Iss 8, p e23021 (2011)
PLoS ONE
PLoS ONE
Mutations in RPGR account for over 70% of X-linked retinitis pigmentosa (XlRP), characterized by retinal degeneration and eventual blindness. The clinical consequences of RPGR mutations are highly varied, even among individuals with the same mutation