Reinvestigation of the Classification of Five Cell Strains of Xeroderma Pigmentosum Group E with Reclassification of Three of Them

This publication has 28 references indexed in Scilit:

• A new UV-sensitive syndrome not belonging to any complementation groups of xeroderma pigmentosum or Cockayne syndrome: siblings showing biochemical characteristics of Cockayne syndrome without typical clinical manifestations
  Published by Elsevier ,2002
• A Newly Identified Patient with Clinical Xeroderma Pigmentosum Phenotype has a Non-Sense Mutation in the DDB2 Gene and Incomplete Repair in (6-4) Photoproducts
  Journal of Investigative Dermatology, 1999
• DDB, a Putative DNA Repair Protein, Can Function as a Transcriptional Partner of E2F1
  Molecular and Cellular Biology, 1998
• A Simple Method for Diagnosing Xeroderma Pigmentosum Variant
  Journal of Investigative Dermatology, 1996
• Cockayne syndrome complementation group B associated with xeroderma pigmentosum phenotype
  Human Genetics, 1996
• Chromosomal Localization and cDNA Cloning of the Genes (DDB1 and DDB2) for the p127 and p48 Subunits of a Human Damage-Specific DNA Binding Protein
  Genomics, 1995
• Xeroderma Pigmentosum Group E Cells Lack a Nuclear Factor That Binds to Damaged DNA
  Science, 1988
• Assignment of 2 patients with xeroderma pigmentosum to complementation group E
  Mutation Research/DNA Repair Reports, 1985
• Different inherited levels of DNA repair replication in xeroderma pigmentosum cell strains after exposure to ultraviolet irradiation
  Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 1970
• Xeroderma Pigmentosum
  Published by American Medical Association (AMA) ,1969