Animal models of biliary injury and altered bile acid metabolism.

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Serum and Hepatic Autofluorescence as a Real-Time Diagnostic Tool for Early Cholestasis Assessment Cholangiopathies - Towards a molecular understanding H19 Is Expressed in Hybrid Hepatocyte Nuclear Factor 4α Periportal Hepatocytes but Not Cytokeratin 19 Cholangiocytes in Cholestatic Livers

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P2860

Animal models of biliary injury and altered bile acid metabolism.

Item

http://www.wikidata.org/entity/Q39436033

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

@wuu

2017年学术文章

@zh-cn

2017年学术文章

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2017年学术文章

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2017年學術文章

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name

Animal models of biliary injury and altered bile acid metabolism.

@en

Animal models of biliary injury and altered bile acid metabolism.

@nl

type

Item

label

Animal models of biliary injury and altered bile acid metabolism.

@en

Animal models of biliary injury and altered bile acid metabolism.

@nl

prefLabel

Animal models of biliary injury and altered bile acid metabolism.

@en

Animal models of biliary injury and altered bile acid metabolism.

@nl

P1476

Animal models of biliary injury and altered bile acid metabolism.

@en

P2093

Diego F Calvisi

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Luca Fabris

http://www.w3.org/2001/XMLSchema#string

Mario Strazzabosco

http://www.w3.org/2001/XMLSchema#string

Valeria Mariotti

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P2860

A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasis

The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein

Homozygous disruption of the murine mdr2 P-glycoprotein gene leads to a complete absence of phospholipid from bile and to liver disease

Mutations in PRKCSH cause isolated autosomal dominant polycystic liver disease.

Mutations in the MDR3 gene cause progressive familial intrahepatic cholestasis

Polycystin-1: a master regulator of intersecting cystic pathways

Animal models of chronic liver diseases

Germline mutations in PRKCSH are associated with autosomal dominant polycystic liver disease

The mouse ascending: perspectives for human-disease models

Mutations in SEC63 cause autosomal dominant polycystic liver disease

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1254-1261

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P31

scholarly article

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10.1016/J.BBADIS.2017.06.027

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P433

4 Pt B

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1864

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P577

2017-07-11T00:00:00Z

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28709963

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P932

5764833

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Animal models of biliary injury and altered bile acid metabolism.

about

P2860

P2860

Animal models of biliary injury and altered bile acid metabolism.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P932