Generation of a bile salt export pump deficiency model using patient-specific induced pluripotent stem cell-derived hepatocyte-like cells-Reference-Cited by-同舟云学术

Generation of a bile salt export pump deficiency model using patient-specific induced pluripotent stem cell-derived hepatocyte-like cells

Published:2017-02-02 Issue:1 Volume:7 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Imagawa Kazuo,Takayama Kazuo,Isoyama Shigemi,Tanikawa Ken,Shinkai Masato,Harada Kazuo,Tachibana Masashi,Sakurai Fuminori,Noguchi Emiko,Hirata Kazumasa,Kage Masayoshi,Kawabata Kenji,Sumazaki Ryo,Mizuguchi Hiroyuki

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/srep41806.pdf

Reference39 articles.

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2. Davit-Spraul, A. et al. ATP8B1 and ABCB11 analysis in 62 children with normal gamma-glutamyl transferase progressive familial intrahepatic cholestasis (PFIC): phenotypic differences between PFIC1 and PFIC2 and natural history. Hepatology 51, 1645–1655, doi: 10.1002/hep.23539 (2010).

3. Strautnieks, S. S. et al. A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasis. Nature genetics 20, 233–238, doi: 10.1038/3034 (1998).

4. Hayashi, H., Takada, T., Suzuki, H., Akita, H. & Sugiyama, Y. Two common PFIC2 mutations are associated with the impaired membrane trafficking of BSEP/ABCB11. Hepatology 41, 916–924, doi: 10.1002/hep.20627 (2005).

5. Hayashi, H. et al. AP2 adaptor complex mediates bile salt export pump internalization and modulates its hepatocanalicular expression and transport function. Hepatology 55, 1889–1900, doi: 10.1002/hep.25591 (2012).

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