着色性干皮病
- 名xeroderma pigmentosum
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着色性干皮病:二家系三例报告
Xeroderma pigmentosum - A Report of Three Cases from Two Families
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着色性干皮病39例临床分析
Clinical Analysis of 39 Cases with Xeroderma Pigmentosum
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DNA修复酶系统的研究&Ⅰ.紫外线诱发~3H-TdR在着色性干皮病淋巴细胞中的非合成期掺入
Study of AND Repair Enzyme System I. Ultraviolet-Induced H-TdR Unscheduled Incorporations Xeroderma Pigmentosum Lymphocytes
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着色性干皮病G组基因多态性与喉癌和喉咽癌风险的相关性
Association between Genetic Polymorphism in Xeroderma Pigmentosum G Gene and Risks of Laryngeal and Hypopharyngeal Carcinomas
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一是着色性干皮病(XP),另一是Cockayne综合征(CS)。
One is Xeroderma Pigmentosum ( XP ) and the other is the Cockayne Syndrome ( OS ) .
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目的研究DNA修复基因着色性干皮病G组基因(XPG)Asp1104His多态性与喉癌和喉咽癌风险的相关性。
Objective To study the association between polymorphism of DNA repair gene xeroderma pigmentosum G ( XPG ) Asp1104His and the risks of developing laryngeal and hypopharyngeal carcinomas .
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目的建立中国人着色性干皮病(xerodermapigmentosum,XP)患者成纤维细胞株,分析其遗传互补组及分布。
Objective To establish skin fibroblast cell strains derived from Chinese xeroderma pigmentosum ( XP ) patients and to analyze the genetic complementation group and distribution .
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XPF轻微突变导致致癌倾向综合征着色性干皮病。
Mild mutations in XPF cause the cancer-prone syndrome xeroderma pigmentosum .
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报告了1984~1992年宁夏地区6家系13例着色性干皮病(XP)患者的临床及两家系4例患者长达8年的随访情况。
Clinical data of 13 cases of xeroderma pigmentosum ( XP ) in 6 families collected in Ningxia region from 1984 to 1992 are presented . Among them , 4 patients from 2 families were followed up for 8 years .
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中国人着色性干皮病遗传互补组分析
Genetic complementation group analysis of xeroderma pigmentosum patients in China
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着色性干皮病患者的免疫学研究
Xeroderma pigmentosum : immunological studies in the patients
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着色性干皮病皮肤成纤维细胞系(XP4SH)的建立及其生物学特性
Establishment of the fibroblast cell line in the xeroderma pigmentosum patient and a study of its biological characteristics
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本文分析了国内1955~1986年文献报道的27个家族45例着色性干皮病。
Fourty fiue cases with xeroderma pigmentosum in 27 families reported by literatures in China from 1955 to 1985 . The age of patients at onset of the disease range from 3 months to 20 years .