Published in Exp Cell Res on December 01, 1985
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Molecular cloning and biological characterization of the human excision repair gene ERCC-3. Mol Cell Biol (1990) 1.57
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A third complementation group in xeroderma pigmentosum. Mutat Res (1974) 1.50
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Xeroderma pigmentosum complementation group H falls into complementation group D. Mutat Res (1991) 1.48
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Patients with xeroderma pigmentosum complementation groups C, E and V do not have abnormal sunburn reactions. Br J Dermatol (2013) 1.46
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A seventh complementation group in excision-deficient xeroderma pigmentosum. Mutat Res (1979) 1.45
Cloning and characterization of MN1, a gene from chromosome 22q11, which is disrupted by a balanced translocation in a meningioma. Oncogene (1995) 1.44
Molecular and cellular analysis of the DNA repair defect in a patient in xeroderma pigmentosum complementation group D who has the clinical features of xeroderma pigmentosum and Cockayne syndrome. Am J Hum Genet (1995) 1.44
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The cloned human DNA excision repair gene ERCC-1 fails to correct xeroderma pigmentosum complementation groups A through I. Mutat Res (1989) 1.42
Identification and characterization of XPC-binding domain of hHR23B. Mol Cell Biol (1997) 1.42
Regional assignment of the gene locus for steroid sulfatase. Hum Genet (1980) 1.40
Repair of ultraviolet light damage in a variety of human fibroblast cell strains. Cancer Res (1977) 1.40
Defects in the DNA repair and transcription gene ERCC2 in the cancer-prone disorder xeroderma pigmentosum group D. Cancer Res (1995) 1.37
Mutations in the general transcription factor TFIIH result in beta-thalassaemia in individuals with trichothiodystrophy. Hum Mol Genet (2001) 1.37
Replication pattern of the X chromosomes in three X/autosomal translocations. Cytogenet Cell Genet (1977) 1.37
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Rapid shift in genotype of human mitochondrial DNA in a family with Leber's hereditary optic neuropathy. Biochem Biophys Res Commun (1990) 1.36
Evolution and mutagenesis of the mammalian excision repair gene ERCC-1. Nucleic Acids Res (1988) 1.34
Differences between rodent and human cell lines in the amount of integrated DNA after transfection. Exp Cell Res (1987) 1.34
Two individuals with features of both xeroderma pigmentosum and trichothiodystrophy highlight the complexity of the clinical outcomes of mutations in the XPD gene. Hum Mol Genet (2001) 1.33
Molecular cloning of the human DNA excision repair gene ERCC-6. Mol Cell Biol (1990) 1.32
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Analysis of mutations in the XPD gene in Italian patients with trichothiodystrophy: site of mutation correlates with repair deficiency, but gene dosage appears to determine clinical severity. Am J Hum Genet (1998) 1.32
Tay-Sachs and Sandhoff's disease: intergenic complementation after somatic cell hybridization. Exp Cell Res (1974) 1.32
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Two human homologs of Rad23 are functionally interchangeable in complex formation and stimulation of XPC repair activity. Mol Cell Biol (1997) 1.31
Xeroderma pigmentosum complementation group G associated with Cockayne syndrome. Am J Hum Genet (1993) 1.31