The fragile X mental retardation protein FMRP plays a role in the DNA damage response

Autor:	Chao Xu, Zhen Ye, Robert E. Kingston, Chuanbing Bian, Matthew D. Simon, Gangqing Hu, Alexandra Stuetzer, Eric L. Greer, Keji Zhao, Ying Luu, Feizhen Wu, Zhibin Wang, Mika Nakamoto-Kinoshita, Christopher R. Vakoc, Roman Alpatov, William N. Beavers, Ulrich Wagner, Stephen T. Warren, Karim-Jean Armache, Bing Ren, Yahong Guo, Yang Shi, Jinrong Min, Paul T. Morrison, Wolfgang Fischle
Rok vydání:	2012
Předmět:	Genetics congenital hereditary and neonatal diseases and abnormalities Fragile x DNA damage Biology medicine.disease Biochemistry nervous system diseases Fragile X syndrome Intellectual disability medicine Molecular Biology Biotechnology
Zdroj:	The FASEB Journal. 26
ISSN:	1530-6860 0892-6638
DOI:	10.1096/fasebj.26.1_supplement.88.1
Popis:	In humans, loss of the fragile X mental retardation protein, FMRP, leads to the most common inherited form of intellectual disability, the fragile X syndrome. FMRP is predominantly present in the c...
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::7c3db949b4ef533225d0dd20f2bb2462 https://doi.org/10.1096/fasebj.26.1_supplement.88.1 Zobrazit plný text záznamu Plný text