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Results 1 - 10 of 14 for Xeroderma pigmentosum group A
  1. ... cross-complementing rodent repair deficiency, complementation group 3 (xeroderma pigmentosum group B complementing) GTF2H RAD25 TFIIH 89 kDa subunit ... transcription factor complex helicase XPB subunit TFIIH p89 xeroderma pigmentosum group B-complementing protein ... complementation group B ...
  2. ... TFIIH p80 TTD xeroderma pigmentosum complementary group D xeroderma pigmentosum group D-complementing protein Tests of ERCC2 PubMed ERCC ... abstract available. Citation on PubMed Lehmann AR. The xeroderma pigmentosum group D (XPD) gene: one gene, two functions, three ...
  3. ... Registry: ERCC1-Related Xeroderma Pigmentosum Genetic Testing Registry: Xeroderma pigmentosum group B Genetic Testing Registry: Xeroderma pigmentosum Genetic Testing ...
  4. ... do not. More About This Health Condition RAD4 Xeroderma pigmentosum group C-complementing protein xeroderma pigmentosum, complementation group C XP3 XPC_HUMAN XPCC Tests of XPC ...
  5. ... Jones CJ, Wood RD. Preferential binding of the xeroderma pigmentosum group A complementing protein to damaged DNA. Biochemistry. 1993 ...
  6. ... disorder with defective DNA repair, is distinct from xeroderma pigmentosum variant and rodent complementation group I. Am J Hum Genet. 1995 Jun;56( ...
  7. The POLH gene provides instructions for making a protein called DNA polymerase eta. DNA polymerases are a group of enzymes that "read" sequences of DNA and ...
  8. ... of DNA repair deficiency disorders in western Europe: Xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy. DNA Repair (Amst). 2008 ...
  9. ... of genetic syndromes affecting the skin such as xeroderma pigmentosum. Additionally, individuals who have previously had melanoma are ...
  10. ... Schiffmann R, Brooks BP, Tamura D, DiGiovanna JJ. Xeroderma pigmentosum, trichothiodystrophy and Cockayne syndrome: a complex genotype-phenotype ...
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