FGF9 on the move

被引：4

作者：

Spicer, Douglas ^{[1
]}

机构：

[1] Ctr Mol Med, Maine Med Ctr Res Inst, Scarborough, ME 04074 USA

来源：

NATURE GENETICS | 2009年 / 41卷 / 03期

关键词：

HEPARAN-SULFATE; MUTATIONS; DYSPLASIA; BINDING;

D O I：

10.1038/ng0309-272

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

FGF receptors have been implicated in a number of syndromes that involve skeletal disorders. A new study in mice has identified a spontaneous mutation in Fgf9 with reduced activity but increased diffusion through tissues, resulting in a gain-of-function phenotype comparable to those due to activating mutations in genes encoding FGF receptors.

引用

页码：272 / 273

页数：2

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