Zobrazeno 1 - 4
of 4
pro vyhledávání: '"J. Chris Lewers"'
Autor:
Kiyoshi Egami, Silaja Yitta, Suhail Kasim, J. Chris Lewers, Rosalinda C. Roberts, Mohamed Lehar, H.A. Jinnah
Publikováno v:
Neurobiology of Disease, Vol 26, Iss 2, Pp 396-407 (2007)
Several rare inherited disorders have provided valuable experiments of nature highlighting specific biological processes of particular importance to the survival or function of midbrain dopamine neurons. In both humans and mice, deficiency of hypoxan
Externí odkaz:
https://doaj.org/article/8ddd82f90ce24391a860402a2830be48
Autor:
Alokes Majumdar, Irène Ceballos-Picot, Mairead Kelly, Kiyoshi Egami, Thomas L. Shirley, Hyder A. Jinnah, J. Chris Lewers, Michael M. Seidman
Publikováno v:
Journal of Neurochemistry. 101:841-853
Mutations in the gene encoding the purine salvage enzyme, hypoxanthine-guanine phosphoribosyltransferase (HPRT) cause Lesch-Nyhan disease, a neurodevelopmental disorder characterized by cognitive, neurological, and behavioral abnormalities. Despite d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::79cf6ba8a851b8213414579eed688421
https://doi.org/10.1111/j.1471-4159.2007.04472.x
https://doi.org/10.1111/j.1471-4159.2007.04472.x
Autor:
Thomas L, Shirley, J Chris, Lewers, Kiyoshi, Egami, Alokes, Majumdar, Mairead, Kelly, Irene, Ceballos-Picot, Michael M, Seidman, H A, Jinnah
Publikováno v:
Journal of neurochemistry. 101(3)
Mutations in the gene encoding the purine salvage enzyme, hypoxanthine-guanine phosphoribosyltransferase (HPRT) cause Lesch-Nyhan disease, a neurodevelopmental disorder characterized by cognitive, neurological, and behavioral abnormalities. Despite d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9985f2923099619a30fb6f8d08f32ec0
https://pubmed.ncbi.nlm.nih.gov/17448149
https://pubmed.ncbi.nlm.nih.gov/17448149
Autor:
Suhail Kasim, Silaja Yitta, Kiyoshi Egami, Rosalinda C. Roberts, Hyder A. Jinnah, J. Chris Lewers, Mohamed Lehar
Publikováno v:
Neurobiology of Disease, Vol 26, Iss 2, Pp 396-407 (2007)
Several rare inherited disorders have provided valuable experiments of nature highlighting specific biological processes of particular importance to the survival or function of midbrain dopamine neurons. In both humans and mice, deficiency of hypoxan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7da33434a0980e43b837b2d021cd4982
https://pubmed.ncbi.nlm.nih.gov/17374562
https://pubmed.ncbi.nlm.nih.gov/17374562