4.2 Article

Molecular genetics of familial renal cell carcinoma syndromes

期刊

CLINICS IN LABORATORY MEDICINE
卷 25, 期 2, 页码 259-+

出版社

W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1016/j.cll.2005.01.003

关键词

-

向作者/读者索取更多资源

Renal cell carcinoma (RCC) represents a group of clinically and genetically diverse diseases. Familial RCC syndromes, although rare, provide an invaluable model to study the molecular mechanisms of renal carcinogenesis. Many oncogenes, and tumor suppressor genes have been identified as responsible for several forms of familial RCC syndromes. Understanding of the molecular pathways of these genes will have significant impact on the diagnosis and treatment of familial and sporadic RCCs.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.2
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据