๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Analysis of FMRP, the protein deficient in fragile X syndrome

โœ Scribed by Small, Kersten ;Warren, Stephen T.

Book ID
112147023
Publisher
John Wiley and Sons
Year
1995
Tongue
English
Weight
637 KB
Volume
1
Category
Article
ISSN
1080-4013

No coin nor oath required. For personal study only.

๐Ÿ“œ SIMILAR VOLUMES

Molecular phenotype of Fragile X syndrom
Molecular phenotype of Fragile X syndrome: FMRP, FXRPs, and protein targets
โœ Walter E. Kaufmann; Sonia Cohen; Hong-Tao Sun; George Ho ๐Ÿ“‚ Article ๐Ÿ“… 2002 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 596 KB

Fragile X syndrome (FraX) is one of the most prevalent genetic causes of mental retardation. FraX is associated with an unstable expansion of a polymorphism within the 5' untranslated region of the FMR1 gene. The main consequence of this mutation is a reduction in the levels of the gene product (FMR

Developmental expression of FMRP in the
Developmental expression of FMRP in the astrocyte lineage: Implications for fragile X syndrome
โœ Laura K. K. Pacey; Laurie C. Doering ๐Ÿ“‚ Article ๐Ÿ“… 2007 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 643 KB

## Abstract One of the most common causes of mental retardation in humans, Fragile X syndrome, results from the absence of FMRP, the protein product of the FMR1 gene. In the nervous system, expression of FMRP has been thought to be confined mainly to neurons as little research has examined FMRP exp