Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Prawien Raghoe"'
Autor:
Cathy E. Bakker, Yolanda De Diego Otero, Ben A. Oostra, Rob Willemsen, Lies-Anne Severijnen, Prawien Raghoe, André T. Hoogeveen
Publikováno v:
Gene Funct. Dis., 1, 28-37
The absence of the FMR1 (fragile X mental retardation gene 1) gene product, protein FMRP (fragile X mental retardation protein) is causing the fragile X syndrome. FMRP, together with two homologues, called FXR1P and FXR2P, belongs to a small family o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d765766c467c5f9c31547a70634aad69
https://doi.org/10.1002/1438-826x(200005)1:1<28::aid-gnfd28>3.0.co
https://doi.org/10.1002/1438-826x(200005)1:1<28::aid-gnfd28>3.0.co
Autor:
Yolanda De Diego Otero, Prawien Raghoe, Carola Bontekoe, Rob Willemsen, Cathy E. Bakker, Tanya Luteijn, Ben A. Oostra, André T. Hoogeveen
Publikováno v:
Experimental Cell Research, 258, 162-170. Elsevier Inc.
Fragile X syndrome is caused by the absence of expression of the FMR1 gene. Both FXR1 and FXR2 are autosomal gene homologues of FMR1. The products of the three genes are belonging to a family of RNA-binding proteins, called FMRP, FXR1P, and FXR2P, re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85221f2ec2a1eec3eb428990d98ac03c
https://doi.org/10.1006/excr.2000.4932
https://doi.org/10.1006/excr.2000.4932