Results 41 to 50 of about 4,897 (187)

Impact of decitabine on immunohistochemistry expression of the putative tumor suppressor genes FHIT, WWOX, FUS1 and PTEN in clinical tumor samples. [PDF]

open access: yes, 2014
BackgroundSince tumor suppressor gene function may be lost through hypermethylation, we assessed whether the demethylating agent decitabine could increase tumor suppressor gene expression clinically.
Aldaz, Marcelo   +8 more
core   +3 more sources

WWOX tumor suppressor gene.

open access: yesHistology and histopathology, 2008
Loss of heterozygosity and chromosomal rearrangement of the WWOX gene, which is located at 16q23.3-24.1, have been detected in ovarian, breast, hepatocellular, and prostate carcinomas and in other neoplasias. This gene, which spans the common chromosomal fragile site 16D, contains 9 exons and encodes a 46 kDa WWOX protein that contains 414 amino acids.
Yang, Jilong, Zhang, Wei
openaire   +3 more sources

Characterization of WWOX expression and function in canine mast cell tumors and malignant mast cell lines

open access: yesBMC Veterinary Research, 2020
Background The WW domain-containing oxidoreductase (WWOX) tumor suppressor gene is frequently lost in a variety of solid and hematopoietic malignancies in humans. Dysregulation of WWOX has been implicated as playing a key role in tumor cell survival, DNA
Rebecca Makii   +7 more
doaj   +1 more source

A multi-exon deletion within WWOX is associated with a 46,XY disorder of sex development [PDF]

open access: yes, 2011
Disorders of sex development (DSD) are congenital conditions where chromosomal, gonad or genital development is atypical. In a significant proportion of 46,XY DSD cases it is not possible to identify a causative mutation, making genetic counseling ...
AJ Notini   +32 more
core   +1 more source

Generation and characterization of mice carrying a conditional allele of the Wwox tumor suppressor gene.

open access: yesPLoS ONE, 2009
WWOX, the gene that spans the second most common human chromosomal fragile site, FRA16D, is inactivated in multiple human cancers and behaves as a suppressor of tumor growth.
John H Ludes-Meyers   +5 more
doaj   +1 more source

The cancer gene WWOX behaves as an inhibitor of SMAD3 transcriptional activity via direct binding [PDF]

open access: yes, 2013
Background: The WW domain containing protein WWOX has been postulated to behave as a tumor suppressor in breast and other cancers. Expression of this protein is lost in over 70% of ER negative tumors.
Abba, Martín Carlos   +6 more
core   +3 more sources

Novel principles of gamma-retroviral insertional transcription activation in murine leukemia virus-induced end-stage tumors [PDF]

open access: yes, 2014
BACKGROUND: Insertional mutagenesis screens of retrovirus-induced mouse tumors have proven valuable in human cancer research and for understanding adverse effects of retroviral-based gene therapies.
Finn Pedersen   +3 more
core   +6 more sources

Associations between TUBB-WWOX SNPs, their haplotypes, gene-gene, and gene-environment interactions and dyslipidemia

open access: yesAging, 2021
In this study, we investigated associations between single nucleotide polymorphisms (SNPs) in the tubulin beta class I (TUBB) and WW domain-containing oxidoreductase (WWOX) genes, gene-gene interactions, and gene-environment interactions and dyslipidemia in the Chinese Maonan ethnic group. Four SNPs (rs3132584, rs3130685, rs2222896, and rs2548861) were
Liu, Chun-Xiao   +6 more
openaire   +2 more sources

Genome-wide association analysis identifies six new loci associated with forced vital capacity [PDF]

open access: yes, 2014
Forced vital capacity (FVC), a spirometric measure of pulmonary function, reflects lung volume and is used to diagnose and monitor lung diseases. We performed genome-wide association study meta-analysis of FVC in 52,253 individuals from 26 studies and ...
A Bill Musk   +216 more
core   +8 more sources

Loss of Wwox Perturbs Neuronal Migration and Impairs Early Cortical Development

open access: yesFrontiers in Neuroscience, 2020
Mutations in the WWOX gene cause a broad range of ultra-rare neurodevelopmental and brain degenerative disorders, associated with a high likelihood of premature death in animal models as well as in humans.
Michele Iacomino   +31 more
doaj   +1 more source

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