换一批A dominant mutation etiologic for human tricho-dento-osseous syndrome impairs the ability of DLX3 to downregulate ΔNp63α.
第一作者：
Antonella,Di Costanzo
第一单位：
Department of Structural and Molecular Biology, University of Naples, Naples, Italy.
作者：
医学主题词
畸形, 多发性(Abnormalities, Multiple);细胞周期蛋白质类(Cell Cycle Proteins);细胞分化(Cell Differentiation);细胞系(Cell Line);细胞, 培养的(Cells, Cultured);颅面骨畸形(Craniofacial Abnormalities);牙釉质发育不全(Dental Enamel Hypoplasia);减量调节(Down-Regulation);外胚层发育不良症(Ectodermal Dysplasia);女(雌)性(Female);基因, 显性(Genes, Dominant);毛发疾病(Hair Diseases);同源盒结构域蛋白质类(Homeodomain Proteins);人类(Humans);序列缺失(Sequence Deletion);皮肤(Skin);转录因子(Transcription Factors);肿瘤抑制蛋白质类(Tumor Suppressor Proteins)
DOI
10.1002/jcp.22553
PMID
21520071
发布时间
2015-11-19
- 浏览20
相似文献
- 中文期刊
- 外文期刊
- 学位论文
- 会议论文
