Craniosynostosis and multiple skeletal anomalies in humans and zebrafish result from a defect in the localized degradation of retinoic acid.
第一作者:
Kathrin,Laue
第一单位:
Institute of Developmental Biology, University of Cologne, D-50674 Cologne, Germany.
作者:
医学主题词
动物(Animals);细胞分化(Cell Differentiation);颅缝(Cranial Sutures);颅缝早闭(Craniosynostoses);细胞色素P450酶系统(Cytochrome P-450 Enzyme System);疾病模型, 动物(Disease Models, Animal);女(雌)性(Female);死胎(Fetal Death);基因表达调控, 发育期(Gene Expression Regulation, Developmental);生长和发育(Growth and Development);人类(Humans);小鼠(Mice);成骨细胞(Osteoblasts);骨生成(Osteogenesis);多态现象, 遗传(Polymorphism, Genetic);妊娠(Pregnancy);序列同源性, 氨基酸(Sequence Homology, Amino Acid);维甲酸(Tretinoin);斑马鱼(Zebrafish);斑马鱼蛋白质类(Zebrafish Proteins)
DOI
10.1016/j.ajhg.2011.09.015
PMID
22019272
发布时间
2021-10-20
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