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Chromosome 9 Short Arm Deletions in Malignant Diseases

 

作者: EinhornStefan,   HeymanMats,  

 

期刊: Leukemia&Lymphoma  (Taylor Available online 1993)
卷期: Volume 11, issue 3-4  

页码: 191-196

 

ISSN:1042-8194

 

年代: 1993

 

DOI:10.3109/10428199309086995

 

出版商: Taylor&Francis

 

关键词: Chromosome 9;interferon;tumor suppressor genes

 

数据来源: Taylor

 

摘要:

Deletions of 9p21-22, that frequently include theα-,β-andω-IFN gene cluster, are common in malignant diseases such as acute lymphocytic leukemia, malignant melanoma and malignant glioma. There is also evidence to support the role of a gene(s) on chromosome 9p21 in predisposition for familial malignant melanoma.Although initial studies implicated that the IFN genes could serve as tumor suppressor genes, there is now data, mainly based on estimations of minimum region of overlap for the deletions, indicating that the relevant tumor suppressor gene is located centromeric of theα-,β-,ω-IFN gene cluster.

 

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