• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

A young woman with xeroderma pigmentosum complementation group F and a morphoeic basal cell carcinoma.

作者信息

Itoh T, Watanabe H, Yamaizumi M, Ono T

机构信息

Department of Dermatology, Kumamoto University School of Medicine, Japan.

出版信息

Br J Dermatol. 1995 Jan;132(1):122-7. doi: 10.1111/j.1365-2133.1995.tb08637.x.

DOI:10.1111/j.1365-2133.1995.tb08637.x
PMID:7756123
Abstract

We report an 18-year-old Japanese woman who had mild photosensitivity and a facial tumour, which was shown to be a morphoeic basal cell carcinoma. Although a line of fibroblasts derived from the patient, Kps6 cells, were slightly more sensitive to UV irradiation than normal cells, their level of unscheduled DNA synthesis was about 20% that of normal cells, and recovery of RNA synthesis after UV irradiation was moderately depressed. Complementation tests, carried out by cell fusion or by microinjection of plasmids harbouring xeroderma pigmentosum (XP) genes, indicated that the patient had XP group F. To our knowledge, this is the youngest XP group F patient with a malignant tumour reported to date.

摘要

相似文献

1
A young woman with xeroderma pigmentosum complementation group F and a morphoeic basal cell carcinoma.
Br J Dermatol. 1995 Jan;132(1):122-7. doi: 10.1111/j.1365-2133.1995.tb08637.x.
2
Xeroderma pigmentosum patients belonging to complementation group F and efficient liquid-holding recovery of ultraviolet damage.属于互补组F的着色性干皮病患者及紫外线损伤的高效液体保持恢复
Photodermatol Photoimmunol Photomed. 1991 Aug;8(4):146-50.
3
Report of three sisters with XP-E, a rare xeroderma pigmentosum complementation group.三名患有XP-E(一种罕见的着色性干皮病互补组)的姐妹的报告。
Photodermatol. 1984 Oct;1(5):232-6.
4
Late onset of skin cancers in 2 xeroderma pigmentosum group F siblings and a review of 30 Japanese xeroderma pigmentosum patients in groups D, E and F.2例着色性干皮病F组同胞患皮肤癌的迟发情况及对30例D、E和F组日本着色性干皮病患者的综述
Photodermatol. 1989 Apr;6(2):89-95.
5
Xeroderma pigmentosum variant associated with multiple cancers.与多种癌症相关的着色性干皮病变异型
Photodermatol Photoimmunol Photomed. 1999 Jun-Aug;15(3-4):127-32. doi: 10.1111/j.1600-0781.1999.tb00072.x.
6
A new UV-sensitive syndrome not belonging to any complementation groups of xeroderma pigmentosum or Cockayne syndrome: siblings showing biochemical characteristics of Cockayne syndrome without typical clinical manifestations.一种不属于着色性干皮病或科凯恩综合征任何互补组的新型紫外线敏感综合征:同胞表现出科凯恩综合征的生化特征但无典型临床表现。
Mutat Res. 1994 May;314(3):233-48. doi: 10.1016/0921-8777(94)90068-x.
7
A novel mutation in the XPA gene associated with unusually mild clinical features in a patient who developed a spindle cell melanoma.一名患梭形细胞黑色素瘤的患者中,XPA基因出现一种新突变,该突变与异常轻微的临床特征相关。
Br J Dermatol. 2006 Jul;155(1):81-8. doi: 10.1111/j.1365-2133.2006.07272.x.
8
Xeroderma pigmentosum group D patient bearing lentigo maligna without neurological symptoms.患有恶性雀斑且无神经症状的着色性干皮病D组患者。
Dermatologica. 1990;181(2):129-33. doi: 10.1159/000247901.
9
UVs syndrome, a new general category of photosensitive disorder with defective DNA repair, is distinct from xeroderma pigmentosum variant and rodent complementation group I.UVs综合征是一种新的具有DNA修复缺陷的光敏性疾病类别,与着色性干皮病变异型和啮齿动物互补组I不同。
Am J Hum Genet. 1995 Jun;56(6):1267-76.
10
[Xeroderma pigmentosum. What may be expected from biological studies?].
Ann Dermatol Venereol. 1994;121(5):434-9.

引用本文的文献

1
Clinical and Molecular Features of Morpheaform Basal Cell Carcinoma: A Systematic Review.Morpheaform 基底细胞癌的临床和分子特征:系统评价。
Curr Oncol. 2023 Nov 13;30(11):9906-9928. doi: 10.3390/curroncol30110720.