Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway-Reference-Cited by-同舟云学术

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Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway

Published:2004-01-04 Issue:2 Volume:7 Page:113-117
ISSN:1097-6256
Container-title:Nature Neuroscience
language:en
Short-container-title:Nat Neurosci

Author:

Jin Peng,Zarnescu Daniela C,Ceman Stephanie,Nakamoto Mika,Mowrey Julie,Jongens Thomas A,Nelson David L,Moses Kevin,Warren Stephen T

Publisher

Springer Science and Business Media LLC

Subject

General Neuroscience

Link

http://www.nature.com/articles/nn1174.pdf

Reference39 articles.

1. O'Donnell, W.T. & Warren, S.T. A decade of molecular studies of fragile X syndrome. Annu. Rev. Neurosci. 25, 315–338 (2002).

2. Siomi, M.C. et al. FXR1, an autosomal homolog of the fragile X mental retardation gene. Embo J. 14, 2401–2408 (1995).

3. Zhang, Y. et al. The fragile X mental retardation syndrome protein interacts with novel homologs FXR1 and FXR2. Embo J. 14, 5358–5366 (1995).

4. Li, Z. et al. The fragile X mental retardation protein inhibits translation via interacting with mRNA. Nucleic Acids Res. 29, 2276–2283 (2001).

5. Laggerbauer, B., Ostareck, D., Keidel, E.M., Ostareck-Lederer, A. & Fischer, U. Evidence that fragile X mental retardation protein is a negative regulator of translation. Hum. Mol. Genet. 10, 329–338 (2001).

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