Cholestatic liver disease in children - Wikidata - awgldk - TriplyDB

Cholestatic liver disease in children

Cholestatic liver disease in children

http://www.wikidata.org/entity/Q24598006

about

p53-mediated biliary defects caused by knockdown of cirh1a, the zebrafish homolog of the gene responsible for North American Indian Childhood Cirrhosis Gene expression profiling of extrahepatic ducts in children with biliary atresia.A case of lipoid congenital adrenal hyperplasia presenting with cholestasis.A novel keratin18 promoter that drives reporter gene expression in the intrahepatic and extrahepatic biliary system allows isolation of cell-type specific transcripts from zebrafish liver.Improved outcome of biliary atresia with postoperative high-dose steroid.Interleukin-8: A critical chemokine in biliary atresia.Changes in epigenetic regulation of CD4+ T lymphocytesin biliary atresia.Cirrhosis in children and adolescents: An overview.Jaundice revisited: recent advances in the diagnosis and treatment of inherited cholestatic liver diseases

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P2860

Cholestatic liver disease in children

http://www.wikidata.org/entity/Q24598006

description

2010 nî lūn-bûn

@nan

2010 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի փետրվարին հրատարակված գիտական հոդված

@hy

2010年の論文

@ja

2010年論文

@yue

2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

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2010年論文

@zh-tw

2010年论文

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name

Cholestatic liver disease in children

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Cholestatic liver disease in children

@en

Cholestatic liver disease in children

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type

label

Cholestatic liver disease in children

@ast

Cholestatic liver disease in children

@en

Cholestatic liver disease in children

@nl

prefLabel

Cholestatic liver disease in children

@ast

Cholestatic liver disease in children

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Cholestatic liver disease in children

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Current gastroenterology reports

P1476

Cholestatic liver disease in children

@en

P2093

Jorge A Bezerra

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

Jorge L Santos

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

Monique Choquette

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

P2860

Differential effects of progressive familial intrahepatic cholestasis type 1 and benign recurrent intrahepatic cholestasis type 1 mutations on canalicular localization of ATP8B1

Mutations in the MDR3 gene cause progressive familial intrahepatic cholestasis

Maternal microchimerism in the livers of patients with biliary atresia

Hepatocellular carcinoma in ten children under five years of age with bile salt export pump deficiency

High-dose immunoglobulin during pregnancy for recurrent neonatal haemochromatosis

Missense mutations and single nucleotide polymorphisms in ABCB11 impair bile salt export pump processing and function or disrupt pre-messenger RNA splicing

Sox17 regulates organ lineage segregation of ventral foregut progenitor cells

Reversal of left-right asymmetry: a situs inversus mutation.

CFC1 gene involvement in biliary atresia with polysplenia syndrome.

Hepatocyte-specific ablation of Foxa2 alters bile acid homeostasis and results in endoplasmic reticulum stress.

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s11894-009-0081-8

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30-9

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scholarly article

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10.1007/S11894-009-0081-8

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1

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2010-02-01T00:00:00Z

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1000607931

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2882095

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