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MHox and vertebrate skeletogenesis: the long and the short of it.

作者信息

Brickell P M

机构信息

Department of Molecular Pathology, University College London Medical School, UK.

出版信息

Bioessays. 1995 Sep;17(9):750-3. doi: 10.1002/bies.950170903.

Abstract

The development of the vertebrate skeleton is under complex genetic control, and good progress is being made towards identifying the genes responsible. A recent paper contributes to this progress by describing transgenic mice in which the homeobox-containing MHox gene has been disrupted. MHox(-/-) mice have a range of skeletal defects, involving loss or shortening of structures in the skull, face and limb. Puzzling features of the MHox(-/-) mutation, which has similar effects on bones with very different embryological origins and yet spares other bones completely, may hold clues to the mechanisms that shape the skeleton. MHox(-/-) mice, used in conjunction with other skeletal mutants, will be important tools for exploring these mechanisms further.

摘要

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