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Human Genetics|February 1, 1996
Cockayne syndrome complementation group B associated with xeroderma pigmentosum phenotypeT Itoh, J E Cleaver, M YamaizumiThe Journal of Investigative Dermatology|January 5, 2000
UVs syndrome: establishment and characterization of fibroblastic cell lines transformed with simian virus 40 DNAT Itoh, M YamaizumiThe Journal of Investigative Dermatology|September 1, 1996
A simple method for diagnosing xeroderma pigmentosum variantT Itoh, T Ono, M YamaizumiThe Journal of Investigative Dermatology|September 1, 1999
A newly identified patient with clinical xeroderma pigmentosum phenotype has a non-sense mutation in the DDB2 gene and incomplete repair in (6-4) photoproductsT Itoh, T Mori, H Ohkubo, et al.American Journal of Human Genetics|June 1, 1995
UVs syndrome, a new general category of photosensitive disorder with defective DNA repair, is distinct from xeroderma pigmentosum variant and rodent complementation group IT Itoh, Y Fujiwara, T Ono, et al.The British Journal of Dermatology|January 1, 1995
A young woman with xeroderma pigmentosum complementation group F and a morphoeic basal cell carcinomaT Itoh, H Watanabe, M Yamaizumi, et al.The Journal of Investigative Dermatology|April 20, 2000
Reinvestigation of the classification of five cell strains of xeroderma pigmentosum group E with reclassification of three of themT Itoh, S Linn, T Ono, et al.The Journal of Biological Chemistry|April 25, 2000
Human damage-specific DNA-binding protein p48. Characterization of XPE mutations and regulation following UV irradiationA F Nichols, T Itoh, J A Graham, et al.The Journal of Investigative Dermatology|December 20, 2000
Xeroderma pigmentosum variant heterozygotes show reduced levels of recovery of replicative DNA synthesis in the presence of caffeine after ultraviolet irradiationT Itoh, S Linn, R Kamide, et al.Pageof 178