Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Omoye Akhile"'
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 4, Iss C, Pp 92-98 (2015)
Smith Lemli Opitz syndrome (SLOS) is an inherited malformation and mental retardation metabolic disorder with no cure. Mutations in the last enzyme of the cholesterol biosynthetic pathway, 7-dehydrocholesterol reductase (DHCR7), lead to cholesterol i
Externí odkaz:
https://doaj.org/article/50925a798f5747f4b73dd9a1cb1d8f47
Autor:
Feng Yang, James Pickel, Daniel Akuma, Randy Xun, Jingshan Chen, Peixiong Yuan, Francesco Papaleo, Gregory V. Carr, Omoye Akhile, Paul Glineburg, James C. Barrow, Grace Y Zhang, Audrey Bebensee, Qingjun Tian, Ming Ren, Jing Du, Daniel R. Weinberger
Publikováno v:
Molecular psychiatry
Overexpression in humans of KCNH2-3.1, which encodes a primate-specific and brain-selective isoform of the human ether-a-go-go-related (hERG) potassium channel, is associated with impaired cognition, inefficient neural processing, and schizophrenia.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::730da1274bd7d64324ff37dab82004e1
https://doi.org/10.1038/mp.2015.219
https://doi.org/10.1038/mp.2015.219
Publikováno v:
Neuropsychopharmacology; Dec2012 Supplement, Vol. 38, pS79-S197, 119p