• 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

[Genetic factors in the development and progression of malignant melanoma].

作者信息

Rünger T M, Bröcker E B

机构信息

Universitäts-Hautklinik, Würzburg.

出版信息

Hautarzt. 1995 Jun;46(6):394-9. doi: 10.1007/s001050050272.

DOI:10.1007/s001050050272
PMID:7642382
Abstract

Exposure of the skin to ultraviolet irradiation is an important risk factor for the development of malignant melanoma, with UVA possibly playing an important role. Hereditary factors are also relevant. In the dysplastic nevus syndrome a genetic instability has been shown by different methods. In xeroderma pigmentosum the DNA repair defect is thought to be responsible for the high incidence of malignant melanoma. Frequent and non-random changes in certain chromosomes have been demonstrated in melanoma cells. These might contain sequences that control melanoma growth or melanoma suppressor genes. Especially the short arm of chromosome 9 is thought to contain one of these genes. This hypothesis is supported by a genetic linkage analysis in melanoma families and the demonstration of a germ line deletion of the locus 9p21 in a patient with eight primary melanomas. Changes in known tumor suppressor genes and oncogenes have also been reported in melanoma, but no consistent sequence of genetic events is known.

摘要

相似文献

1
[Genetic factors in the development and progression of malignant melanoma].
Hautarzt. 1995 Jun;46(6):394-9. doi: 10.1007/s001050050272.
2
Fluorescence in situ hybridization (FISH) evaluation of chromosomes 6, 7, 9 and 10 throughout human melanocytic tumorigenesis.在人类黑素细胞肿瘤发生过程中对6号、7号、9号和10号染色体进行荧光原位杂交(FISH)评估。
Melanoma Res. 2005 Jun;15(3):155-60. doi: 10.1097/00008390-200506000-00003.
3
[Genetic counseling and DNA testing in patients with increased risks for malignant melanoma].[恶性黑色素瘤风险增加患者的遗传咨询与DNA检测]
Ther Umsch. 2003 Aug;60(8):469-72. doi: 10.1024/0040-5930.60.8.469.
4
Dysplastic nevus syndrome.
Hosp Pract (Off Ed). 1984 Jan;19(1):91-103, 107-8. doi: 10.1080/21548331.1984.11702727.
5
Interphase cytogenetic demonstration of chromosome 9 loss in thick melanomas.
J Cutan Pathol. 1997 Aug;24(7):398-402. doi: 10.1111/j.1600-0560.1997.tb00813.x.
6
Melanoma ex naevo: a study of the associated naevus.痣恶变黑素瘤:相关痣的研究
Melanoma Res. 2003 Apr;13(2):213-7. doi: 10.1097/01.cmr.0000056226.78713.99.
7
Melanocytic nevi and tumor progression: perspectives concerning histomorphology, melanoma risk and molecular genetics.黑素细胞痣与肿瘤进展:关于组织形态学、黑色素瘤风险及分子遗传学的观点
Dermatology. 1993;187(2):86-90. doi: 10.1159/000247212.
8
Human malignant melanoma. A genetic disease?人类恶性黑色素瘤。一种遗传性疾病?
Cancer. 1995 Mar 15;75(6):1228-37. doi: 10.1002/1097-0142(19950315)75:6<1228::aid-cncr2820750604>3.0.co;2-t.
9
Chromosome rearrangements in dysplastic nevus syndrome predisposing to malignant melanoma.发育异常痣综合征中的染色体重排易引发恶性黑色素瘤。
Cancer Genet Cytogenet. 1988 Oct 1;35(1):73-8. doi: 10.1016/0165-4608(88)90124-0.
10
Genomic Characterization of Dysplastic Nevi Unveils Implications for Diagnosis of Melanoma.发育异常痣的基因组特征揭示了对黑色素瘤诊断的意义。
J Invest Dermatol. 2017 Apr;137(4):905-909. doi: 10.1016/j.jid.2016.11.017. Epub 2016 Nov 24.