Varaico: Literature-Extracted Genetic Variants

Gene:WWOX
Variant:p.P282A
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WWOX

NM_016373.4:p.P282A

Associated Papers

Genetic and Functional Evidence Links Germline Biallelic Inactivating Variants in WWOX to Histological Mixed-Type Thyroid Cancer.

Zhang X et al.

Advanced Science (weinheim, Baden-wurttemberg, Germany), 2026

WWOX somatic ablation in skeletal muscles alters glucose metabolism.

Abu-Remaileh M et al.

Molecular Metabolism, 2019

30755385 (PubMed )
Supplement: mmc1.pdf

Association of WWOX rs9926344 polymorphism with poor prognosis of hepatocellular carcinoma.

Chen W et al.

Journal of Cancer, 2018

Relationship of genetic variant distributions of WW domain-containing oxidoreductase gene with uterine cervical cancer.

Lin YH et al.

International Journal of Medical Sciences, 2018

A Comprehensive Meta-analysis of Case-Control Association Studies to Evaluate Polymorphisms Associated with the Risk of Differentiated Thyroid Carcinoma.

Figlioli G et al.

Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology, 2016

Identification of cancer predisposition variants in apparently healthy individuals using a next-generation sequencing-based family genomics approach.

Karageorgos I et al.

Human Genomics, 2015

26092435 (PubMed )
Supplement: 40246_2015_34_MOESM1_ESM.xlsx › FamilyA

Epigenetic and genetic alterations affect the WWOX gene in head and neck squamous cell carcinoma.

Ekizoglu S et al.

Plos One, 2015

Genetic alterations of the WWOX gene in breast cancer.

Ekizoglu S et al.

Medical Oncology (northwood, London, England), 2012

Evidences that the polymorphism Pro-282-Ala within the tumor suppressor gene WWOX is a new risk factor for differentiated thyroid carcinoma.

Cancemi L et al.

International Journal of Cancer, 2011

WWOX gene may contribute to progression of non-small-cell lung cancer (NSCLC).

Baykara O et al.

Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine, 2010

Genome-wide analysis to predict protein sequence variations that change phosphorylation sites or their corresponding kinases.

Ryu GM et al.

Nucleic Acids Research, 2009

19139070 (PubMed )
Supplement: gkn1008_nar-01723-s-2008-File009.xls › TypeIII

Identification of homozygous deletions at chromosome 16q23 in aflatoxin B1 exposed hepatocellular carcinoma.

Yakicier MC et al.

Oncogene, 2001

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."