The fragile site WWOX gene and the developing brain (Q38270425)

From Wikidata

Jump to navigation Jump to search

scientific article

edit

Language	Label	Description	Also known as
English	The fragile site WWOX gene and the developing brain	scientific article

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PMC publication ID

4935222

retrieved

1 September 2017

review article

1 reference

stated in

Europe PubMed Central

title

The fragile site WWOX gene and the developing brain (English)

1 reference

stated in

Europe PubMed Central

PMC publication ID

4935222

retrieved

1 September 2017

author name string

Brahim Tabarki

series ordinal

1

1 reference

stated in

Europe PubMed Central

PMC publication ID

4935222

retrieved

1 September 2017

Fuad Al Mutairi

series ordinal

2

1 reference

stated in

Europe PubMed Central

PMC publication ID

4935222

retrieved

1 September 2017

Amal Al Hashem

series ordinal

3

1 reference

stated in

Europe PubMed Central

PMC publication ID

4935222

retrieved

1 September 2017

publication date

21 November 2014

1 reference

stated in

Europe PubMed Central

PMC publication ID

4935222

retrieved

1 September 2017

published in

Experimental Biology and Medicine

1 reference

stated in

Europe PubMed Central

PMC publication ID

4935222

retrieved

1 September 2017

volume

240

1 reference

stated in

Europe PubMed Central

PMC publication ID

4935222

retrieved

1 September 2017

issue

3

1 reference

stated in

Europe PubMed Central

PMC publication ID

4935222

retrieved

1 September 2017

page(s)

400-402

1 reference

stated in

Europe PubMed Central

PMC publication ID

4935222

retrieved

1 September 2017

cites work

WWOX at the crossroads of cancer, metabolic syndrome related traits and CNS pathologies.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935222

retrieved

6 September 2017

Characterizing WW domain interactions of tumor suppressor WWOX reveals its association with multiprotein networks

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935222

retrieved

6 September 2017

Common Chromosomal Fragile Site Gene WWOX in Metabolic Disorders and Tumors

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935222

retrieved

6 September 2017

WW domain-containing oxidoreductase's role in myriad cancers: clinical significance and future implications

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935222

retrieved

6 September 2017

The supposed tumor suppressor gene WWOX is mutated in an early lethal microcephaly syndrome with epilepsy, growth retardation and retinal degeneration

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935222

retrieved

6 September 2017

The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935222

retrieved

6 September 2017

WW domain-containing oxidoreductase promotes neuronal differentiation via negative regulation of glycogen synthase kinase 3β.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935222

retrieved

6 September 2017

Signaling from membrane receptors to tumor suppressor WW domain-containing oxidoreductase

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935222

retrieved

6 September 2017

WWOX in biological control and tumorigenesis

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935222

retrieved

6 September 2017

WWOX protein expression in normal human tissues.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935222

retrieved

6 September 2017

Expression of WW domain-containing oxidoreductase WOX1 in the developing murine nervous system

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935222

retrieved

6 September 2017

Hyaluronidase induction of a WW domain-containing oxidoreductase that enhances tumor necrosis factor cytotoxicity

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935222

retrieved

6 September 2017

WWOX, a novel WW domain-containing protein mapping to human chromosome 16q23.3-24.1, a region frequently affected in breast cancer

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935222

retrieved

6 September 2017

WWOX-mediated apoptosis in A549 cells mainly involves the mitochondrial pathway

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935222

retrieved

6 September 2017

MPP+-induced neuronal death in rats involves tyrosine 33 phosphorylation of WW domain-containing oxidoreductase WOX1.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935222

retrieved

14 September 2017

A spontaneous mutation of the Wwox gene and audiogenic seizures in rats with lethal dwarfism and epilepsy.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4935222

retrieved

23 June 2018

Gene mapping and expression analysis of 16q loss of heterozygosity identifies WWOX and CYLD as being important in determining clinical outcome in multiple myeloma

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1177%2F1535370214561952

retrieved

21 January 2018

Identifiers

DOI

10.1177/1535370214561952

1 reference

stated in

Europe PubMed Central

PMC publication ID

4935222

retrieved

1 September 2017

PMC publication ID

4935222

1 reference

stated in

Europe PubMed Central

PMC publication ID

4935222

retrieved

1 September 2017

PubMed publication ID

25416187

1 reference

stated in

Europe PubMed Central

PMC publication ID

4935222

retrieved

1 September 2017

ResearchGate publication ID

268789985

0 references

 

Sitelinks

Wikipedia(0 entries)

edit

Wikibooks(0 entries)

edit

Wikinews(0 entries)

edit

Wikiquote(0 entries)

edit

Wikisource(0 entries)

edit

Wikiversity(0 entries)

edit

Wikivoyage(0 entries)

edit

Wiktionary(0 entries)

edit

Multilingual sites(0 entries)

edit

Retrieved from "https://www.wikidata.org/w/index.php?title=Q38270425&oldid=1751651733"