Targeting senescent cholangiocytes and activated fibroblasts with B-cell lymphoma-extra large inhibitors ameliorates fibrosis in multidrug resistance 2 gene knockout (Mdr2<sup>-/-</sup> ) mice.
作者:
主题词
动物(Animals);苯并噻唑类(Benzothiazoles);胆管(Bile Ducts);活组织检查, 针吸(Biopsy, Needle);细胞增殖(Cell Proliferation);细胞存活(Cell Survival);细胞, 培养的(Cells, Cultured);胆管炎, 硬化性(Cholangitis, Sclerosing);疾病模型, 动物(Disease Models, Animal);抗药性, 多药(Drug Resistance, Multiple);成纤维细胞(Fibroblasts);免疫组织化学(Immunohistochemistry);异喹啉类(Isoquinolines);小鼠(Mice);小鼠, 近交BALB C(Mice, Inbred BALB C);小鼠, 基因敲除(Mice, Knockout);分子靶向治疗(Molecular Targeted Therapy);血小板源性生长因子(Platelet-Derived Growth Factor);随机分配(Random Allocation);参考值(Reference Values)
DOI
10.1002/hep.29464
PMID
28802066
发布时间
2019-01-07
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Hepatology (Baltimore, Md.)
247-259页
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