Activation of Trpv4 reduces the hyperproliferative phenotype of cystic cholangiocytes from an animal model of ARPKD.
第一作者:
Sergio A,Gradilone
第一单位:
Miles and Shirley Fiterman Center for Digestive Diseases, Division of Gastroenterology and Hepatology, Mayo Clinic College of Medicine, Rochester, Minnesota, USA.
作者:
主题词
动物(Animals);胆管(Bile Ducts);钙(Calcium);细胞增殖(Cell Proliferation);疾病模型, 动物(Disease Models, Animal);细胞外信号调节MAP激酶类(Extracellular Signal-Regulated MAP Kinases);人类(Humans);亮氨酸(Leucine);表型(Phenotype);佛波醇酯类(Phorbol Esters);多囊肾, 常染色体隐性(Polycystic Kidney, Autosomal Recessive);原癌基因蛋白质B-raf(Proto-Oncogene Proteins B-raf);原癌基因蛋白质c-akt(Proto-Oncogene Proteins c-akt);大鼠(Rats);大鼠, Sprague-Dawley(Rats, Sprague-Dawley);信号传导(Signal Transduction);磺胺类(Sulfonamides);TRPV阳离子通道(TRPV Cation Channels)
DOI
10.1053/j.gastro.2010.04.010
PMID
20399209
发布时间
2021-10-20
- 浏览14

Gastroenterology
304-14.e2页
相似文献
- 中文期刊
- 外文期刊
- 学位论文
- 会议论文