(Q22010778)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10556305%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10556305%20AND%20SRC:MED&resulttype=core&format=json

Nuclear FMR1 interacting protein 1

1 November 2019

main subject

1 reference

GOA release 2020-03-11

RNA processing

1 reference

Nuclear FMR1 interacting protein 1

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

3

J L Mandel

J L

Mandel

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10556305%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

1

B Bardoni

B

Bardoni

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10556305%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

2

A Schenck

A

Schenck

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10556305%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

language of work or name

English

0 references

publication date

1 December 1999

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10556305%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

published in

Human Molecular Genetics

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10556305%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

volume

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10556305%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

page(s)

2557-2566

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10556305%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

issue

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10556305%20AND%20SRC:MED&resulttype=core&format=json

Analysis of domains affecting intracellular localization of the FMRP protein.

1 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2557

7 January 2021

A single protocol to detect transcripts of various types and expression levels in neural tissue and cultured cells: in situ hybridization using digoxigenin-labelled cRNA probes

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2557

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/10.1093%2FHMG%2F8.13.2557

7 January 2021

Mammalian Ras interacts directly with the serine/threonine kinase Raf

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2557

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/10.1093%2FHMG%2F8.13.2557

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/10.1093%2FHMG%2F8.13.2557

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/10.1093%2FHMG%2F8.13.2557

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/10.1093%2FHMG%2F8.13.2557

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/10.1093%2FHMG%2F8.13.2557

7 January 2021

Localization of nascent RNA and CREB binding protein with the PML-containing nuclear body.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2557

7 January 2021

Interactions between the human RNA polymerase II subunits

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2557

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/10.1093%2FHMG%2F8.13.2557

7 January 2021

DNA methylation represses FMR-1 transcription in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2557

7 January 2021

Alternative splicing in the fragile X gene FMR1.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2557

7 January 2021

Fine structure of the human FMR1 gene

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2557

7 January 2021

Characterization of FMR1 proteins isolated from different tissues

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2557

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2557

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/10.1093%2FHMG%2F8.13.2557

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2557

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/10.1093%2FHMG%2F8.13.2557

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2557

7 January 2021

A cellular model that recapitulates major pathogenic steps of Huntington's disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2557

7 January 2021

The RNA-binding properties of SMN: deletion analysis of the zebrafish orthologue defines domains conserved in evolution.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2557

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2557

7 January 2021

Improved method for high efficiency transformation of intact yeast cells

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2557

7 January 2021

A new version of the two-hybrid assay for detection of protein-protein interactions

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2557

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2557

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2557

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/10.1093%2FHMG%2F8.13.2557

7 January 2021