A high incidence of skin cancer characterizes patients with xeroderma pigmentosum (XP). XP patients have hereditary defects in repair mechanisms of ultraviolet light (UV)-in-duced damage to DNA. Progress in elucidating the pathogenesis of cutaneous cancers can be expected by analysis of the biologic defects of cultured cells from XP patients. Such information may also contribute, at least in part, to an understanding of carcinogenesis in general. J Invest Dermatol 92: 289S–292S, 198
This study was performed to elucidate whether xeroderma pigmentosum complementation group A (XPA) ca...
Cells from most patients with xeroderma pigmentosum (XP) can be shown to be defective in repairing u...
textabstractXeroderma pigmentosum (XP) is a rare DNA repair disorder characterized by increased susc...
A high incidence of skin cancer characterizes patients with xeroderma pigmentosum (XP). XP patients ...
Malignant melanomas were found in 15.8% of xeroderma pigmentosum (XP) patients with skin cancer in J...
UV survival, DNA repair and post-UV DNA synthesis were studied in the cells of patients with xeroder...
Xeroderma pigmentosum (XP) occurs with high frequency in Egypt and a continuation of our field studi...
Xeroderma pigmentosum (XP) is a rare, autosomal recessive disorder of DNA repair characterized by su...
Xeroderma pigmentosum (XP) is a rare, autosomal recessive disorder of DNA repair characterized by su...
We report the characterization of a Japanese woman who exhibited many freckles and skin cancers in s...
The subjects are three patients with distinct symptoms of xeroderma pigmentosum (XP) in which the cu...
Inherited molecular defects in nucleotide excision repair genes cause the autosomal recessive condit...
Xeroderma pigmentosum, Cockayne syndrome, the xeroderma pigmentosum-Cockayne syndrome complex, and t...
UV survival, DNA repair and post-UV DNA synthesis were studied in the cells of patients with xeroder...
AbstractXeroderma pigmentosum (XP) type C is a rare autosomal recessive disorder that occurs because...
This study was performed to elucidate whether xeroderma pigmentosum complementation group A (XPA) ca...
Cells from most patients with xeroderma pigmentosum (XP) can be shown to be defective in repairing u...
textabstractXeroderma pigmentosum (XP) is a rare DNA repair disorder characterized by increased susc...
A high incidence of skin cancer characterizes patients with xeroderma pigmentosum (XP). XP patients ...
Malignant melanomas were found in 15.8% of xeroderma pigmentosum (XP) patients with skin cancer in J...
UV survival, DNA repair and post-UV DNA synthesis were studied in the cells of patients with xeroder...
Xeroderma pigmentosum (XP) occurs with high frequency in Egypt and a continuation of our field studi...
Xeroderma pigmentosum (XP) is a rare, autosomal recessive disorder of DNA repair characterized by su...
Xeroderma pigmentosum (XP) is a rare, autosomal recessive disorder of DNA repair characterized by su...
We report the characterization of a Japanese woman who exhibited many freckles and skin cancers in s...
The subjects are three patients with distinct symptoms of xeroderma pigmentosum (XP) in which the cu...
Inherited molecular defects in nucleotide excision repair genes cause the autosomal recessive condit...
Xeroderma pigmentosum, Cockayne syndrome, the xeroderma pigmentosum-Cockayne syndrome complex, and t...
UV survival, DNA repair and post-UV DNA synthesis were studied in the cells of patients with xeroder...
AbstractXeroderma pigmentosum (XP) type C is a rare autosomal recessive disorder that occurs because...
This study was performed to elucidate whether xeroderma pigmentosum complementation group A (XPA) ca...
Cells from most patients with xeroderma pigmentosum (XP) can be shown to be defective in repairing u...
textabstractXeroderma pigmentosum (XP) is a rare DNA repair disorder characterized by increased susc...