The fragile X mental retardation protein is associated with ribosomes (Q42818787)

7 November 2017

title

The fragile X mental retardation protein is associated with ribosomes (English)

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7 November 2017

Khandjian EW

1

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7 November 2017

Corbin F

series ordinal

2

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7 November 2017

Woerly S

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3

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7 November 2017

Rousseau F

series ordinal

4

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7 November 2017

language of work or name

English

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publication date

1 January 1996

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7 November 2017

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7 November 2017

volume

12

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7 November 2017

issue

1

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7 November 2017

page(s)

91-93

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Regulation of translation in eukaryotic systems

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cites work

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Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

21 January 2018

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7 January 2021

Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n

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7 January 2021

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

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7 January 2021

Absence of expression of the FMR-1 gene in fragile X syndrome

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7 January 2021

DNA methylation represses FMR-1 transcription in fragile X syndrome

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7 January 2021

The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation

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7 January 2021

Characterization and localization of the FMR-1 gene product associated with fragile X syndrome

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7 January 2021

A heterogeneous set of FMR1 proteins is widely distributed in mouse tissues and is modulated in cell culture

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7 January 2021

Characterization of FMR1 proteins isolated from different tissues

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7 January 2021

FMR1 Protein: Conserved RNP Family Domains and Selective RNA Binding

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7 January 2021

The protein product of the fragile X gene, FMR1, has characteristics of an RNA-binding protein

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7 January 2021

Essential role for KH domains in RNA binding: impaired RNA binding by a mutation in the KH domain of FMR1 that causes fragile X syndrome

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7 January 2021

Oncogenic activation of the human trk proto-oncogene by recombination with the ribosomal large subunit protein L7a

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7 January 2021

Dissociation of mammalian polyribosomes into subunits by puromycin

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7 January 2021

Monoclonal antibodies to nucleic acid-containing cellular constituents: probes for molecular biology and autoimmune disease

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7 January 2021

Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndrome

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7 January 2021

Nucleus basalis magnocellularis and hippocampus are the major sites of FMR-1 expression in the human fetal brain

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7 January 2021

Tissue-specific expression of a FMR1/beta-galactosidase fusion gene in transgenic mice.

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7 January 2021

Alternative splicing of exon 14 determines nuclear or cytoplasmic localisation of fmr1 protein isoforms

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7 January 2021

Eukaryotic protein synthesis

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7 January 2021

Fmr1 knockout mice: A model to study fragile X mental retardation

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7 January 2021

Turnover of protein in the nervous system

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7 January 2021

Central nervous system function in systemic lupus erythematosus

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7 January 2021

Separation of multiple phosphorylated forms of 40 S ribosomal protein S6 by two-dimensional polyacrylamide gel electrophoresis

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7 January 2021

Identifiers

DOI

10.1038/NG0196-91

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Dimensions Publication ID

7 November 2017

1052009945

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