Identification and characterization of xpac protein, the gene product of the human XPAC (xeroderma pigmentosum group A complementing) gene.
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference14 articles.
1. Defective Repair Replication of DNA in Xeroderma Pigmentosum
2. The Metabolic Basis of Inherited Disease;Cleaver,1989
3. A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndrome
4. Molecular cloning of a mouse DNA repair gene that complements the defect of group-A xeroderma pigmentosum.
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3. Cyclosporin A inhibits nucleotide excision repair via downregulation of the xeroderma pigmentosum group A and G proteins, which is mediated by calcineurin inhibition;Experimental Dermatology;2011-06-24
4. XPA Gene Mutations Resulting in Subtle Truncation of Protein in Xeroderma Pigmentosum Group A Patients with Mild Skin Symptoms;Journal of Investigative Dermatology;2010-10
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