(Q48821834)

English

Subcellular localization of fragile X mental retardation protein with the I304N mutation in the RNA-binding domain in cultured hippocampal neurons.

scientific article published in February 2001

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/11440196

Subcellular localization of fragile X mental retardation protein with the I304N mutation in the RNA-binding domain in cultured hippocampal neurons. (English)

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/11440196

author name string

M Castrén

1

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/11440196

A Haapasalo

2

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/11440196

B A Oostra

3

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/11440196

E Castrén

4

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/11440196

publication date

1 February 2001

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/11440196

Cellular and Molecular Neurobiology

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/11440196

21

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/11440196

1

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/11440196

29-38

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/11440196

https://scigraph.springernature.com/pub.10.1023/a:1007117211490

0 references

Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/11440196

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A nuclear role for the Fragile X mental retardation protein

1 reference

https://pubmed.ncbi.nlm.nih.gov/11440196

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/11440196

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

FMR1 protein: conserved RNP family domains and selective RNA binding

1 reference

https://pubmed.ncbi.nlm.nih.gov/11440196

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Understanding the molecular basis of fragile X syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/11440196

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of neocortex in three males with the fragile X syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/11440196

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal dendritic spines in fragile X knockout mice: maturation and pruning deficits

1 reference

https://pubmed.ncbi.nlm.nih.gov/11440196

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/11440196

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PAK3 mutation in nonsyndromic X-linked mental retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/11440196

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Different targets for the fragile X-related proteins revealed by their distinct nuclear localizations

1 reference

https://pubmed.ncbi.nlm.nih.gov/11440196

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/11440196

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/11440196

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of FMR1 proteins isolated from different tissues

1 reference

https://pubmed.ncbi.nlm.nih.gov/11440196

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

No evidence for disruption of normal patterns of mRNA localization in dendrites or dendritic transport of recently synthesized mRNA in FMR1 knockout mice, a model for human fragile-X mental retardation syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/11440196

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular and cellular genetics of fragile X syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/11440196

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/11440196

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Synaptic synthesis of the Fragile X protein: possible involvement in synapse maturation and elimination

1 reference

https://pubmed.ncbi.nlm.nih.gov/11440196

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/11440196

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/11440196

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/11440196

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/11440196

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in GDI1 are responsible for X-linked non-specific mental retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/11440196

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cognitive and molecular aspects of fragile X.

1 reference

https://pubmed.ncbi.nlm.nih.gov/11440196

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/11440196

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

mRNA localization in neurons: a multipurpose mechanism?

1 reference

https://pubmed.ncbi.nlm.nih.gov/11440196

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/11440196

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/11440196

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/11440196

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of domains affecting intracellular localization of the FMRP protein.

1 reference

https://pubmed.ncbi.nlm.nih.gov/11440196

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sequence-specific RNA binding by a Nova KH domain: implications for paraneoplastic disease and the fragile X syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/11440196

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Adult fragile X syndrome. Clinico-neuropathologic findings.

1 reference

https://pubmed.ncbi.nlm.nih.gov/11440196

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/11440196

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1023/A:1007117211490

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/11440196

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/11440196

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