xeroderma pigmentosum

  • 着色性干皮病
xeroderma pigmentosumxeroderma pigmentosum

noun

1
a rare genetic condition characterized by an eruption of exposed skin occurring in childhood and photosensitivity with severe sunburn;inherited as a recessive autosomal trait in which DNA repair processes are defective so they are more likely to chromosome breaks and cancers when exposed to ultraviolet light

数据来源:WordNet

  1. Xeroderma pigmentosum - A Report of Three Cases from Two Families

    着色性干皮病:二家系三例报告

  2. Genetic complementation group analysis of xeroderma pigmentosum patients in China

    中国人着色性干皮病遗传互补组分析

  3. Clinical Analysis of 39 Cases with Xeroderma Pigmentosum

    着色性干皮病39例临床分析

  4. Establishment of the fibroblast cell line in the xeroderma pigmentosum patient and a study of its biological characteristics

    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

  5. Xeroderma pigmentosum : immunological studies in the patients

    着色性干皮病患者的免疫学研究

  6. Association between Genetic Polymorphism in Xeroderma Pigmentosum G Gene and Risks of Laryngeal and Hypopharyngeal Carcinomas

    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

  7. Study of AND Repair Enzyme System I. Ultraviolet-Induced H-TdR Unscheduled Incorporations Xeroderma Pigmentosum Lymphocytes

    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

  8. Mild mutations in XPF cause the cancer-prone syndrome xeroderma pigmentosum .

    XPF轻微突变导致致癌倾向综合征着色性干皮病。

  9. Objective To establish skin fibroblast cell strains derived from Chinese xeroderma pigmentosum ( XP ) patients and to analyze the genetic complementation group and distribution .

    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。

  10. BACKGROUND & OBJECTIVE : Xeroderma pigmentosum group C ( XPC ) gene is involved in nucleotide excision repair ( NER ) .

    背景与目的:XPC基因参与核苷酸切除修复,该基因存在单核苷酸多态性(SNP)位点,并可能通过SNP位点碱基的改变影响其修复能力及疾病易感性。

  11. One is Xeroderma Pigmentosum ( XP ) and the other is the Cockayne Syndrome ( OS ) .

    一是着色性干皮病(XP),另一是Cockayne综合征(CS)。

  12. 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 .

    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。

  13. 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 .

    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。

  14. 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 .

    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。