The supposed tumor suppressor gene WWOX is mutated in an early lethal microcephaly syndrome with epilepsy, growth retardation and retinal degeneration-Reference-Cited by-同舟云学术

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

Published:2014-01-23 Issue:1 Volume:9 Page:
ISSN:1750-1172
Container-title:Orphanet Journal of Rare Diseases
language:en
Short-container-title:Orphanet J Rare Dis

Author:

Abdel-Salam Ghada,Thoenes Michaela,Afifi Hanan H,Körber Friederike,Swan Daniel,Bolz Hanno Jörn

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Genetics (clinical),General Medicine

Link

https://link.springer.com/content/pdf/10.1186/1750-1172-9-12.pdf

Reference22 articles.

1. Dayan S, O’Keefe LV, Choo A, Richards RI: Common chromosomal fragile site FRA16D tumor suppressor WWOX gene expression and metabolic reprograming in cells. Genes Chromosomes Cancer. 2013, 52: 823-831. 10.1002/gcc.22078.

2. Del Mare S, Salah Z, Aqeilan RI: WWOX: its genomics, partners, and functions. J Cell Biochem. 2009, 108: 737-745. 10.1002/jcb.22298.

3. Ferguson BW, Gao X, Kil H, Lee J, Benavides F, Abba MC, Aldaz CM: Conditional Wwox deletion in mouse mammary gland by means of two Cre recombinase approaches. PLoS One. 2012, 7: e36618-10.1371/journal.pone.0036618.

4. Ludes-Meyers JH, Kil H, Parker-Thornburg J, Kusewitt DF, Bedford MT, Aldaz CM: Generation and characterization of mice carrying a conditional allele of the Wwox tumor suppressor gene. PLoS One. 2009, 4: e7775-10.1371/journal.pone.0007775.

5. Chen ST, Chuang JI, Cheng CL, Hsu LJ, Chang NS: Light-induced retinal damage involves tyrosine 33 phosphorylation, mitochondrial and nuclear translocation of WW domain-containing oxidoreductase in vivo. Neuroscience. 2005, 130: 397-407. 10.1016/j.neuroscience.2004.07.054.

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