The molecular genetics of familial intrahepatic cholestasis - Test2 - elhamkhani - TriplyDB

The molecular genetics of familial intrahepatic cholestasis

The molecular genetics of familial intrahepatic cholestasis

http://www.wikidata.org/entity/Q24670001

about

Helicobacter pylori vaccine development in the post-genomic era: can in silico translate to in vivo.Arsenic exposure through drinking water increases the risk of liver and cardiovascular diseases in the population of West Bengal, India.Hepatic transport systems.Psychiatry, psychotherapy and gastroenterology -- bringing it all together.The role of fecal elastase-1 in detecting exocrine pancreatic disease.Structure based classification for bile salt export pump (BSEP) inhibitors using comparative structural modeling of human BSEP.Obstetric cholestasis with elevated gamma glutamyl transpeptidase: incidence, presentation and treatment.Randomized prospective comparative study of ursodeoxycholic acid and S-adenosyl-L-methionine in the treatment of intrahepatic cholestasis of pregnancy

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P2860

The molecular genetics of familial intrahepatic cholestasis

http://www.wikidata.org/entity/Q24670001

description

2000 nî lūn-bûn

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2000 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2000 թվականի հուլիսին հրատարակված գիտական հոդված

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2000年の論文

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2000年学术文章

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2000年学术文章

@zh-cn

2000年学术文章

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2000年学术文章

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2000年学术文章

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2000年學術文章

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name

The molecular genetics of familial intrahepatic cholestasis

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The molecular genetics of familial intrahepatic cholestasis

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The molecular genetics of familial intrahepatic cholestasis

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type

label

The molecular genetics of familial intrahepatic cholestasis

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The molecular genetics of familial intrahepatic cholestasis

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The molecular genetics of familial intrahepatic cholestasis

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prefLabel

The molecular genetics of familial intrahepatic cholestasis

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The molecular genetics of familial intrahepatic cholestasis

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The molecular genetics of familial intrahepatic cholestasis

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The molecular genetics of familial intrahepatic cholestasis

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M Müller

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P L Jansen

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

Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency

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

Identification of a new inborn error in bile acid synthesis: mutation of the oxysterol 7alpha-hydroxylase gene causes severe neonatal liver disease

Inactivation of the first nucleotide-binding fold of the sulfonylurea receptor, and familial persistent hyperinsulinemic hypoglycemia of infancy

Mutations in the MDR3 gene cause progressive familial intrahepatic cholestasis

A subfamily of P-type ATPases with aminophospholipid transporting activity.

Hepatocanalicular bile salt export pump deficiency in patients with progressive familial intrahepatic cholestasis

Exon-intron organization of the human multidrug-resistance protein 2 (MRP2) gene mutated in Dubin-Johnson syndrome

Mutations in the 70K peroxisomal membrane protein gene in Zellweger syndrome

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