HRPT2, a tumor suppressor gene for hyperparathyroidism-jaw tumor syndrome

被引：21

作者：

Wang, PF

Tan, MH

Zhang, C

Morreau, H

Teh, BT

机构：

[1] Van Andel Res Inst, Canc Genet Lab, Grand Rapids, MI 49503 USA

[2] Alexandra Hosp, Dept Med, Singapore, Singapore

[3] Leiden Univ, Med Ctr, Dept Pathol, Leiden, Netherlands

来源：

HORMONE AND METABOLIC RESEARCH | 2005年 / 37卷 / 06期

关键词：

hyperparathyroidism-jaw tumor syndrome; HRPT2; parafibromin; parathyroid carcinoma;

D O I：

10.1055/s-2005-870150

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Hyperparathyroidism-jaw tumor (HPT-JT) syndrome is a familial multi-tumor syndrome resulting from inactivating mutations in the HRPT2 tumor suppressor gene, which encodes a protein product named parafibromin. Here, we will review recent advances in genetic and protein studies on parafibromin, and examine its biological functions.

引用

页码：380 / 383

页数：4

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