Disruption of human limb morphogenesis by a dominant negative mutation in CDMP1
- PMID: 9288098
- DOI: 10.1038/ng0997-58
VSports注册入口 - Disruption of human limb morphogenesis by a dominant negative mutation in CDMP1
VSports在线直播 - Abstract
Chondrodysplasia Grebe type (CGT) is an autosomal recessive disorder characterized by severe limb shortening and dysmorphogenesis. We have identified a causative point mutation in the gene encoding the bone morphogenetic protein (BMP)-like molecule, cartilage-derived morphogenetic protein-1 (CDMP-1). The mutation substitutes a tyrosine for the first of seven highly conserved cysteine residues in the mature active domain of the protein. We demonstrate that the mutation results in a protein that is not secreted and is inactive in vitro. It produces a dominant negative effect by preventing the secretion of other, related BMP family members VSports手机版. We present evidence that this may occur through the formation of heterodimers. The mutation and its proposed mechanism of action provide the first human genetic indication that composite expression patterns of different BMPs dictate limb and digit morphogenesis. .
Publication types (VSports注册入口)
- "VSports" Actions
MeSH terms (VSports)
- "VSports注册入口" Actions
- "V体育2025版" Actions
- "VSports手机版" Actions
- VSports - Actions
- VSports手机版 - Actions
- V体育平台登录 - Actions
- Actions (V体育ios版)
- Actions (V体育官网)
- VSports最新版本 - Actions
- "V体育安卓版" Actions
- V体育安卓版 - Actions
- Actions (VSports最新版本)
- "VSports手机版" Actions
- "V体育ios版" Actions
- V体育2025版 - Actions
- "V体育ios版" Actions
VSports app下载 - Substances
- "V体育2025版" Actions
- Actions (V体育安卓版)
- Actions (VSports在线直播)
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources (V体育ios版)
Molecular Biology Databases
Research Materials
