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骨质疏松症基因鉴定的分子遗传学研究

Molecular genetic studies of gene identification for osteoporosis.

作者信息

Guo Yan, Yang Tie-Lin, Pan Feng, Xu Xiang-Hong, Dong Shan-Shan, Deng Hong-Wen

机构信息

a The Key Laboratory of Biomedical Information Engineering of Ministry of Education and Institute of Molecular Genetics, School of Life Science and Technology, Xi'an Jiaotong University, Xi'an 710049, PR China.

b The Key Laboratory of Biomedical Information Engineering of Ministry of Education and Institute of Molecular Genetics, School of Life Science and Technology, Xi'an Jiaotong University, Xi'an 710049, PR China and Departments of Orthopedic Surgery and Basic Medical Sciences, University of Missouri - Kansas City, Kansas City, MO 64108, USA.

出版信息

Expert Rev Endocrinol Metab. 2008 Mar;3(2):223-267. doi: 10.1586/17446651.3.2.223.

Abstract

This review comprehensively summarizes the most important and representative molecular genetics studies of gene identification for osteoporosis published up to the end of September 2007. It is intended to constitute a sequential update of our previously published reviews covering the available data up to the end of 2004. Evidence from candidate gene-association studies, genome-wide linkage and association studies, as well as functional genomic studies (including gene-expression microarray and proteomics) on osteogenesis and osteoporosis, are reviewed separately. Studies of transgenic and knockout mice models relevant to osteoporosis are summarized. The major results of all studies are tabulated for comparison and ease of reference. Comments are made on the most notable findings and representative studies for their potential influence and implications on our present understanding of genetics of osteoporosis. The format adopted by this review should be ideal for accommodating future new advances and studies.

摘要

本综述全面总结了截至2007年9月底发表的关于骨质疏松症基因鉴定的最重要且具代表性的分子遗传学研究。它旨在对我们之前发表的涵盖截至2004年底可用数据的综述进行连续更新。分别对候选基因关联研究、全基因组连锁和关联研究以及关于骨生成和骨质疏松症的功能基因组学研究(包括基因表达微阵列和蛋白质组学)的证据进行了综述。总结了与骨质疏松症相关的转基因和基因敲除小鼠模型的研究。列出了所有研究的主要结果以供比较和方便参考。对最显著的发现和代表性研究进行了评论,阐述了它们对我们目前对骨质疏松症遗传学理解的潜在影响和意义。本综述采用的格式应非常适合纳入未来的新进展和研究。

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