Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Brian C. Ray"'
Autor:
Cara Jean Westmark, Shih-Chieh Chuang, Seth A Hays, Mikolaj J Filon, Brian C Ray, Pamela R Westmark, Jay R Gibson, Kimberly M Huber, Robert KS Wong
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 9 (2016)
Amyloid-beta protein precursor (APP) and metabolite levels are altered in fragile X syndrome (FXS) patients and in the mouse model of the disorder, Fmr1KO mice. Normalization of APP levels in Fmr1KO mice (Fmr1KO/APPHET mice) rescues many disease phen
Externí odkaz:
https://doaj.org/article/d4bdf3c5289c432ea68a2eeea7089524
Autor:
Cara J Westmark, Pamela R Westmark, Kenneth J O'Riordan, Brian C Ray, Crystal M Hervey, M Shahriar Salamat, Sara H Abozeid, Kelsey M Stein, Levi A Stodola, Michael Tranfaglia, Corinna Burger, Elizabeth M Berry-Kravis, James S Malter
Publikováno v:
PLoS ONE, Vol 6, Iss 10, p e26549 (2011)
Fragile X syndrome (FXS) is the most common form of inherited intellectual disability and the leading known genetic cause of autism. Fragile X mental retardation protein (FMRP), which is absent or expressed at substantially reduced levels in FXS, bin
Externí odkaz:
https://doaj.org/article/8311371ad7674612900357e2146daa55
Publikováno v:
Current Alzheimer Research. 7:200-206
As the mechanisms underlying neuronal development and degeneration become clarified, a number of common effectors and signaling pathways are becoming apparent. Here we describe the identification of Aβ, long considered a pathologic mediator of Alzhe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a98a6da88bff8e6b14740e188f5cdb3b
https://doi.org/10.2174/156720510791050957
https://doi.org/10.2174/156720510791050957
Autor:
Elizabeth Berry-Kravis, Sara Abozeid, Crystal Hervey, M. Shahriar Salamat, Brian C. Ray, James S. Malter, Corinna Burger, Cara J. Westmark, Pamela R. Westmark, Kenneth J. O’Riordan, Kelsey M. Stein, Levi A. Stodola, Michael Tranfaglia
Publikováno v:
PLoS ONE
PLoS ONE, Vol 6, Iss 10, p e26549 (2011)
PLoS ONE, Vol 6, Iss 10, p e26549 (2011)
Fragile X syndrome (FXS) is the most common form of inherited intellectual disability and the leading known genetic cause of autism. Fragile X mental retardation protein (FMRP), which is absent or expressed at substantially reduced levels in FXS, bin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f564cbdd38f51bad0fe5a437c2949fb0
https://pubmed.ncbi.nlm.nih.gov/22046307
https://pubmed.ncbi.nlm.nih.gov/22046307