The Fragile X mental retardation protein (Q34446600)

2 August 2017

1 reference

title

The Fragile X mental retardation protein (English)

1 reference

2 August 2017

Bardoni B

1 reference

2 August 2017

Schenck A

series ordinal

1 reference

2 August 2017

Mandel JL

series ordinal

1 reference

2 August 2017

publication date

1 October 2001

1 reference

2 August 2017

published in

Brain Research Bulletin

1 reference

2 August 2017

1 reference

2 August 2017

issue

3-4

1 reference

2 August 2017

page(s)

375-382

1 reference

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

2 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

Dissecting FMR1, the protein responsible for fragile X syndrome, in its structural and functional domains

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

Expression of FMR1, FXR1, and FXR2 genes in human prenatal tissues

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

FMR1 Protein: Conserved RNP Family Domains and Selective RNA Binding

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

Human and murine FMR-1: alternative splicing and translational initiation downstream of the CGG-repeat

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

Enhanced expression of the murine FMR1 gene during germ cell proliferation suggests a special function in both the male and the female gonad

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

Enhanced Fmr-1 expression in testis.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

The PROSITE database, its status in 1997.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

Assignment of NUFIP1 (nuclear FMRP interacting protein 1) gene to chromosome 13q14 and assignment of a pseudogene to chromosome 6q12.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

FMR1 gene and fragile X syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

Analysis of domains affecting intracellular localization of the FMRP protein.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

The neuronal RNA binding protein Nova-1 recognizes specific RNA targets in vitro and in vivo

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

The fragile X mental retardation protein is associated with poly(A)+ mRNA in actively translating polyribosomes

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

Highly conserved 3' UTR and expression pattern of FXR1 points to a divergent gene regulation of FXR1 and FMR1

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

Survey of the fragile X syndrome CGG repeat and the short-tandem-repeat and single-nucleotide-polymorphism haplotypes in an African American population

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

Expression of truncated utrophin leads to major functional improvements in dystrophin-deficient muscles of mice

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

Fmr1 knockout mouse has a distinctive strain-specific learning impairment.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

Fine structure of the human FMR1 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

What is associated with the fragile X syndrome?

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

Learning and memory in the FMR1 knockout mouse.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

CRM1 is an export receptor for leucine-rich nuclear export signals

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

Modeling human neurodegenerative diseases in Drosophila: on a wing and a prayer.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

CRM1 is responsible for intracellular transport mediated by the nuclear export signal

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

Transport into and out of the cell nucleus

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

A neurofibromatosis-1-regulated pathway is required for learning in Drosophila

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

Consideration of connective tissue dysfunction in the fragile X syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

The tetranucleotide UCAY directs the specific recognition of RNA by the Nova K-homology 3 domain

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

Novel isoforms of the fragile X related protein FXR1P are expressed during myogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

Alternative splicing in the murine and human FXR1 genes

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

p140Sra-1 (specifically Rac1-associated protein) is a novel specific target for Rac1 small GTPase.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

Neuroanatomy of the fragile X knockout mouse brain studied using in vivo high resolution magnetic resonance imaging

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

Intragenic loss of function mutations demonstrate the primary role of FMR1 in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

Three-dimensional structure and stability of the KH domain: molecular insights into the fragile X syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

Audiogenic seizures susceptibility in transgenic mice with fragile X syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

The nucleolus: an old factory with unexpected capabilities

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

Evidence for a role of CRM1 in signal-mediated nuclear protein export

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

The fragile X syndrome II: preliminary data on growth and development in males

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

(Over)correction of FMR1 deficiency with YAC transgenics: behavioral and physical features

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

A brain-enriched polypyrimidine tract-binding protein antagonizes the ability of Nova to regulate neuron-specific alternative splicing

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

The chicken FMR1 gene is highly conserved with a CCT 5'-untranslated repeat and encodes an RNA-binding protein.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

A modular misexpression screen in Drosophila detecting tissue-specific phenotypes

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

SMART: a web-based tool for the study of genetically mobile domains

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

How proteins enter the nucleus

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

Specific sequences in the fragile X syndrome protein FMR1 and the FXR proteins mediate their binding to 60S ribosomal subunits and the interactions among them

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

Presenilin is required for activity and nuclear access of Notch in Drosophila

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

The fragile X-related proteins FXR1P and FXR2P contain a functional nucleolar-targeting signal equivalent to the HIV-1 regulatory proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

Oligomerization properties of fragile-X mental-retardation protein (FMRP) and the fragile-X-related proteins FXR1P and FXR2P

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

Differential expression of FMR1, FXR1 and FXR2 proteins in human brain and testis

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

Alternative splicing in the fragile X gene FMR1.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

Characterization of dFMR1, a Drosophila melanogaster homolog of the fragile X mental retardation protein

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

Novel point mutation within intron 10 of FMR-1 gene causing fragile X syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

Evidence that processed small dsRNAs may mediate sequence-specific mRNA degradation during RNAi in Drosophila embryos.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900647-5

7 January 2021

10.1016/S0361-9230(01)00647-5

Identifiers

DOI

1 reference

2 August 2017

1 reference