Intermittent PTH (1-34) injection rescues the retarded skeletal development and postnatal lethality of mice mimicking human achondroplasia and thanatophoric dysplasia.
第一作者:
Yangli,Xie
第一单位:
State Key Laboratory of Trauma, Burns and Combined Injury, Center of Bone Metabolism and Repair, Institute of Surgery Research, Daping Hospital, Third Military Medical University, Chongqing 400042, China.
作者:
医学主题词
软骨发育不全(Achondroplasia);动物(Animals);体重(Body Weight);骨密度(Bone Density);骨密度保护剂(Bone Density Conservation Agents);骨发育(Bone Development);骨疾病, 代谢性(Bone Diseases, Metabolic);骨和骨组织(Bone and Bones);细胞分化(Cell Differentiation);细胞增殖(Cell Proliferation);细胞, 培养的(Cells, Cultured);软骨细胞(Chondrocytes);药物评价, 临床前(Drug Evaluation, Preclinical);基因表达(Gene Expression);基因表达调控(Gene Expression Regulation);人类(Humans);肢芽(Limb Buds);小鼠(Mice);小鼠, 转基因(Mice, Transgenic);突变, 误义(Mutation, Missense);甲状旁腺激素相关蛋白质(Parathyroid Hormone-Related Protein);放射摄影术(Radiography);受体, 成纤维细胞生长因子, 3型(Receptor, Fibroblast Growth Factor, Type 3);甲状旁腺激素肽(1-34)(Teriparatide);致死性发育不良(Thanatophoric Dysplasia);组织培养技术(Tissue Culture Techniques)
DOI
10.1093/hmg/dds181
PMID
22634226
发布时间
2016-11-25
- 浏览38
Human molecular genetics
3941-55页
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