(Q33899309)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10782066%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

review article

1 reference

title

Fragile X syndrome at the turn of the century (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10782066%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10782066%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

author name string

R Willemsen

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10782066%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

B A Oostra

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10782066%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

publication date

1 May 2000

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10782066%20AND%20SRC:MED&resulttype=core&format=json

Trends in Molecular Medicine

6 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10782066%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

volume

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10782066%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10782066%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

page(s)

193-198

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10782066%20AND%20SRC:MED&resulttype=core&format=json

The fragile X syndrome and other fragile site disorders

6 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2800%2901674-9

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%2FS1357-4310%2800%2901674-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2800%2901674-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2800%2901674-9

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%2FS1357-4310%2800%2901674-9

7 January 2021

The fragile X mental retardation protein is associated with ribosomes

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2800%2901674-9

7 January 2021

FMR1 protein: conserved RNP family domains and selective RNA binding

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2800%2901674-9

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%2FS1357-4310%2800%2901674-9

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%2FS1357-4310%2800%2901674-9

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%2FS1357-4310%2800%2901674-9

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%2FS1357-4310%2800%2901674-9

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%2FS1357-4310%2800%2901674-9

7 January 2021

FMRP is associated to the ribosomes via RNA.

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2800%2901674-9

7 January 2021

Association of FMRP with ribosomal precursor particles in the nucleolus

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2800%2901674-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2800%2901674-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2800%2901674-9

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%2FS1357-4310%2800%2901674-9

7 January 2021

Transgenic mouse model for the fragile X syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2800%2901674-9

7 January 2021

Mildly impaired water maze performance in male Fmr1 knockout mice.

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2800%2901674-9

7 January 2021

Long-term potentiation in the hippocampus of fragile X knockout mice

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2800%2901674-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2800%2901674-9

7 January 2021

Analysis of neocortex in three males with the fragile X syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2800%2901674-9

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%2FS1357-4310%2800%2901674-9

7 January 2021

Audiogenic seizures susceptibility in transgenic mice with fragile X syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2800%2901674-9

7 January 2021

Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardation

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2800%2901674-9

7 January 2021

Rapid antibody test for fragile X syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2800%2901674-9

7 January 2021

Noninvasive test for fragile X syndrome, using hair root analysis

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2800%2901674-9

7 January 2021

Molecular basis of genetic instability of triplet repeats

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2800%2901674-9

7 January 2021

Stability of the human fragile X (CGG)(n) triplet repeat array in Saccharomyces cerevisiae deficient in aspects of DNA metabolism

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2800%2901674-9

7 January 2021

The full mutation in the FMR-1 gene of male fragile X patients is absent in their sperm.

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2800%2901674-9

7 January 2021

Postmortem examination of two fragile X brothers with an FMR1 full mutation.

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2800%2901674-9

7 January 2021

Characterization of the full fragile X syndrome mutation in fetal gametes.

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2800%2901674-9

7 January 2021

Introduction of aFMR1 transgene in the fragile X knockout mouse

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2800%2901674-9

7 January 2021

Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells.

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2800%2901674-9

7 January 2021

Nuclease sensitivity of permeabilized cells confirms altered chromatin formation at the fragile X locus

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2800%2901674-9

7 January 2021

In vitro reactivation of the FMR1 gene involved in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2800%2901674-9

7 January 2021

Synergistic effect of histone hyperacetylation and DNA demethylation in the reactivation of the FMR1 gene.

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2800%2901674-9

7 January 2021

Synergy of demethylation and histone deacetylase inhibition in the re-expression of genes silenced in cancer

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2800%2901674-9

7 January 2021

In vivo protein transduction: delivery of a biologically active protein into the mouse

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2800%2901674-9

7 January 2021

10.1016/S1357-4310(00)01674-9

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10782066%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

1 reference