着色性干皮病

zhuó sè xìnɡ ɡān pí bìnɡ
  • xeroderma pigmentosum
着色性干皮病着色性干皮病
  1. 着色性干皮病:二家系三例报告

    Xeroderma pigmentosum - A Report of Three Cases from Two Families

  2. 着色性干皮病39例临床分析

    Clinical Analysis of 39 Cases with Xeroderma Pigmentosum

  3. 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

  4. 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

  5. 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 ) .

  6. 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 .

  7. 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 .

  8. 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 .

  9. 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 .

  10. 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

  11. 着色性干皮病患者的免疫学研究

    Xeroderma pigmentosum : immunological studies in the patients

  12. 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

  13. 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 .