Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Uma Dandekar"'
Autor:
Alejandra Young, Uma Dandekar, Calvin Pan, Avery Sader, Jie J Zheng, Richard A Lewis, Debora B Farber
Publikováno v:
PLoS ONE, Vol 11, Iss 9, p e0162273 (2016)
Ocular albinism type 1 (OA), caused by mutations in the OA1 gene, encodes a G-protein coupled receptor, OA1, localized in melanosomal membranes of the retinal pigment epithelium (RPE). This disorder is characterized by both RPE macro-melanosomes and
Externí odkaz:
https://doaj.org/article/6467a785dc48450a8ddbece4c801fcbf
Autor:
Jie Zheng, Uma Dandekar, Alejandra Young, C. Avery Sader, Calvin Pan, Richard A. Lewis, Debora B. Farber
Publikováno v:
Young, A; Dandekar, U; Pan, C; Sader, A; Zheng, JJ; Lewis, RA; et al.(2016). GNAI3: Another Candidate Gene to Screen in Persons with Ocular Albinism. PLOS ONE, 11(9). doi: 10.1371/journal.pone.0162273. UCLA: Retrieved from: http://www.escholarship.org/uc/item/9hd4r6w4
PloS one, vol 11, iss 9
PLoS ONE, Vol 11, Iss 9, p e0162273 (2016)
PLoS ONE
PloS one, vol 11, iss 9
PLoS ONE, Vol 11, Iss 9, p e0162273 (2016)
PLoS ONE
Ocular albinism type 1 (OA), caused by mutations in the OA1 gene, encodes a G-protein coupled receptor, OA1, localized in melanosomal membranes of the retinal pigment epithelium (RPE). This disorder is characterized by both RPE macro-melanosomes and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58199398a9025a826fb25adfee24df6f
http://www.escholarship.org/uc/item/9hd4r6w4
http://www.escholarship.org/uc/item/9hd4r6w4
Autor:
Ernest P. Noble, Alan M. Steinberg, Julia N. Bailey, Armen K. Goenjian, Uma Dandekar, Devon Schmidt, David P. Walling
Publikováno v:
Journal of affective disorders. 140(3)
To examine the potential contribution of the serotonin hydroxylase (TPH1 and TPH2) genes, and the serotonin transporter promoter polymorphism (5HTTLPR) to the unique and pleiotropic risk of PTSD symptoms and depressive symptoms.Participants included
Autor:
Janet S. Sinsheimer, Mary E. Sehl, Zuo-Feng Zhang, Jeanette C. Papp, Patricia A. Ganz, Uma Dandekar, Shehnaz K. Hussain, Daniel Conn
Publikováno v:
Cancer Prevention Research. 5:A107-A107
Background: Breast cancer aggregates within some families, accounting for about 25% of incident cases. Known genetic variants, such as BRCA1/BRCA2 mutations, account for less than 10% of these familial breast cancer cases, thus, research into additio