Initiation of Translation of the FMR1 mRNA Occurs Predominantly through 5′-End-Dependent Ribosomal Scanning-Reference-Cited by-同舟云学术

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Initiation of Translation of the FMR1 mRNA Occurs Predominantly through 5′-End-Dependent Ribosomal Scanning

Published:2011-03 Issue:1 Volume:407 Page:21-34
ISSN:0022-2836
Container-title:Journal of Molecular Biology
language:en
Short-container-title:Journal of Molecular Biology

Author:

Ludwig Anna L.,Hershey John W.B.,Hagerman Paul J.

Funder

National Institutes of Health

Roadmap Interdisciplinary Research Consortium

Publisher

Elsevier BV

Subject

Molecular Biology,Structural Biology

Reference83 articles.

1. Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox;Fu;Cell,1991

2. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome;Verkerk;Cell,1991

3. Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome;Oberle;Science,1991

4. Absence of expression of the FMR-1 gene in fragile X syndrome;Pieretti;Cell,1991

5. DNA methylation represses FMR-1 transcription in fragile X syndrome;Sutcliffe;Hum. Mol. Genet.,1992

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3. A native function for RAN translation and CGG repeats in regulating fragile X protein synthesis;Nature Neuroscience;2020-02-17

4. hnRNP Q Regulates Internal Ribosome Entry Site-Mediated fmr1 Translation in Neurons;Molecular and Cellular Biology;2019-02-15

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