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XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP E

Known as: XERODERMA PIGMENTOSUM V, XP5, XP, GROUP E 
An autosomal recessive genetic disorder caused by mutations in the DDB2 gene. This disease exhibits the mildest degree of sun sensitivity of all… 
National Institutes of Health

Related topics

Related topics

7 relations
Basal cell carcinomaCutaneous MelanomaDDB2 geneIntegumentary system

Broader (1)

Xeroderma Pigmentosum

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
Tumor and Stem Cell Biology DDB 2 Suppresses Epithelial-to-Mesenchymal Transition in Colon Cancer
Colon cancer is one of the deadliest cancers worldwide because of its metastasis to other essential organs. Metastasis of colon… 
2006
2006
Charakterizace proteinů xeroderma pigmentosum v globálním mechanismu opravy lézí vyvolaných v DNA protinádorově účinnými komplexy platiny
V parci je popsano zavedeni polyakrylamidove gelove elektroforezy s pentafluorooktanovou kyselinou (PFO-PAGE), ktera umožňuje… 
2002
2002
CROSSLINKED UHMWPE IN TOTAL KNEES : CLEAN VERSUS ABRASIVE CONDITIONS
  • 2002
  • Corpus ID: 29493873
INTRODUCTION Crosslinked ultra high molecular weight polyethylene (XPE) of various formulations is currently being used… 
1984
1984
Report of three sisters with XP-E, a rare xeroderma pigmentosum complementation group.
Three sisters with a rare complementation group of classical xeroderma pigmentosum (XP-E) are presented. The patients developed… 
1968
1968
Structure and composition of Xanthomonas pruni bacteriophage.
This communication deals with the detailed morphology, buoyant density, and chemical composition of Xanthomonas pruni phage XP5…