Zobrazeno 1 - 4
of 4
pro vyhledávání: '"M T, Abrams"'
Autor:
C A, Omer, Z, Chen, R E, Diehl, M W, Conner, H Y, Chen, M E, Trumbauer, S, Gopal-Truter, G, Seeburger, H, Bhimnathwala, M T, Abrams, J P, Davide, M S, Ellis, J B, Gibbs, I, Greenberg, K S, Koblan, A M, Kral, D, Liu, R B, Lobell, P J, Miller, S D, Mosser, T J, O'Neill, E, Rands, M D, Schaber, E T, Senderak, A, Oliff, N E, Kohl
Publikováno v:
Cancer research. 60(10)
For Ras oncoproteins to transform mammalian cells, they must be posttranslationally modified with a farnesyl group in a reaction catalyzed by the enzyme farnesyl:protein transferase (FPTase). Inhibitors of FPTase have therefore been developed as pote
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2912ec44ca2d1ecb77982ce053c4c10a
https://pubmed.ncbi.nlm.nih.gov/10825141
https://pubmed.ncbi.nlm.nih.gov/10825141
Publikováno v:
American journal of medical genetics. 83(4)
The study of the neurobehavioral consequences of mutations of FMR1, the gene responsible for fragile X syndrome (FraX), has been based largely on correlations between mutation patterns and cognitive profile. Following the characterization of FMRP, th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e9d33ce8cd19fb5b2119a2df6acb1f03
https://pubmed.ncbi.nlm.nih.gov/10208163
https://pubmed.ncbi.nlm.nih.gov/10208163
Autor:
M T, Abrams, W E, Kaufmann, F, Rousseau, B A, Oostra, B, Wolozin, C V, Taylor, N, Lishaa, M L, Morel, A, Hoogeveen, A L, Reiss
Publikováno v:
American journal of medical genetics. 82(1)
The fragile X mental retardation 1 gene (FMR1) mutation is strongly correlated with specific and marked neurobehavioral and neuroanatomical abnormalities. The protein product, FMRP, is highly expressed in neurons of the normal mammalian brain, and ab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::31051dda42d938b0e5a6c72039017e34
https://pubmed.ncbi.nlm.nih.gov/9916838
https://pubmed.ncbi.nlm.nih.gov/9916838
Autor:
M T, Abrams, K F, Doheny, M M, Mazzocco, S J, Knight, T L, Baumgardner, L S, Freund, K E, Davies, A L, Reiss
Publikováno v:
American journal of medical genetics. 74(1)
Standardized cognitive, behavioral, and neuroanatomical data are presented on 2 unrelated boys with the FRAXE (FMR2) GCC expansion mutation. In the context of normal IQ, both boys had a history of developmental delay, including significant problems w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e505abf524f1584ca79be8c69ff348dd
https://pubmed.ncbi.nlm.nih.gov/9034011
https://pubmed.ncbi.nlm.nih.gov/9034011