(Q29616495)

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=11719188

30 April 2017

1 reference

Brown V

1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=11719188

30 April 2017

Jin P

2

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30 April 2017

Ceman S

3

1 reference

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30 April 2017

Darnell JC

4

1 reference

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30 April 2017

O'Donnell WT

5

1 reference

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30 April 2017

Tenenbaum SA

6

1 reference

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30 April 2017

Jin X

7

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=11719188

30 April 2017

Feng Y

8

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=11719188

30 April 2017

Wilkinson KD

9

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=11719188

30 April 2017

Keene JD

10

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=11719188

30 April 2017

Darnell RB

11

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=11719188

30 April 2017

Warren ST

12

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=11719188

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=11719188

30 April 2017

language of work or name

1 reference

30 April 2017

publication date

16 November 2001

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=11719188

30 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=11719188

30 April 2017

volume

107

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=11719188

30 April 2017

issue

4

1 reference

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30 April 2017

page(s)

477-87

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=11719188

Drosophila UNC-13 is essential for synaptic transmission

30 April 2017

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The cerebellum-specific Munc13 isoform Munc13-3 regulates cerebellar synaptic transmission and motor learning in mice

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7 January 2021

A novel RNA-binding nuclear protein that interacts with the fragile X mental retardation (FMR1) protein

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7 January 2021

FMRP involvement in formation of synapses among cultured hippocampal neurons.

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Purified recombinant Fmrp exhibits selective RNA binding as an intrinsic property of the fragile X mental retardation protein

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7 January 2021

Intrinsic neuronal determinants that promotes axonal sprouting and elongation

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Isolation of an FMRP-associated messenger ribonucleoprotein particle and identification of nucleolin and the fragile X-related proteins as components of the complex

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7 January 2021

Identification of mouse YB1/p50 as a component of the FMRP-associated mRNP particle

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7 January 2021

Fragile X mental retardation protein targets G quartet mRNAs important for neuronal function

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A point mutation in the FMR-1 gene associated with fragile X mental retardation

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The fragile X mental retardation protein is a ribonucleoprotein containing both nuclear localization and nuclear export signals

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Neuronal abnormalities in microtubule-associated protein 1B mutant mice

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Cluster analysis and display of genome-wide expression patterns

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7 January 2021

FMRP associates with polyribosomes as an mRNP, and the I304N mutation of severe fragile X syndrome abolishes this association

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7 January 2021

Fragile X mental retardation protein: nucleocytoplasmic shuttling and association with somatodendritic ribosomes

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7 January 2021

Shared and unique roles of CAP23 and GAP43 in actin regulation, neurite outgrowth, and anatomical plasticity

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7 January 2021

Analysis of neocortex in three males with the fragile X syndrome

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7 January 2021

Distinct regional distribution in the brain of messenger RNAs for the two isoforms of synaphin associated with the docking/fusion complex

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7 January 2021

Turning on ARF: the Sec7 family of guanine-nucleotide-exchange factors

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7 January 2021

Understanding the molecular basis of fragile X syndrome

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7 January 2021

Ribonucleoprotein infrastructure regulating the flow of genetic information between the genome and the proteome

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7 January 2021

The fragile X mental retardation protein is associated with ribosomes

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7 January 2021

Evidence that fragile X mental retardation protein is a negative regulator of translation

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7 January 2021

The fragile X mental retardation protein inhibits translation via interacting with mRNA

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7 January 2021

Controlling small guanine-nucleotide-exchange factor function through cytoplasmic RNA intramers

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7 January 2021

Neuritin: a gene induced by neural activity and neurotrophins that promotes neuritogenesis

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7 January 2021

Direct interaction between the ARF-specific guanine nucleotide exchange factor msec7-1 and presynaptic Munc13-1.

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7 January 2021

Abnormal development of dendritic spines in FMR1 knock-out mice

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7 January 2021

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

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7 January 2021

Human GluR6 kainate receptor (GRIK2): molecular cloning, expression, polymorphism, and chromosomal assignment

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7 January 2021

A common RNA recognition motif identified within a defined U1 RNA binding domain of the 70K U1 snRNP protein

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7 January 2021

DAP-1, a novel protein that interacts with the guanylate kinase-like domains of hDLG and PSD-95

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7 January 2021

A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P

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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

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

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7 January 2021

RNAs that interact with the fragile X syndrome RNA binding protein FMRP.

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DNA methylation represses FMR-1 transcription in fragile X syndrome

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Identifying mRNA subsets in messenger ribonucleoprotein complexes by using cDNA arrays

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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

Fragile X mental retardation protein is translated near synapses in response to neurotransmitter activation

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7 January 2021