Intrahepatic cholestasis of pregnancy: the severe form is associated with common variants of the hepatobiliary phospholipid transporter ABCB4 gene.
about
Low phospholipid associated cholelithiasis: association with mutation in the MDR3/ABCB4 gene.Bile acid metabolism and signalingAtypical causes of cholestasisBile acid signaling in metabolic disease and drug therapyIntrahepatic Cholestasis of Pregnancy (ICP) in U.S. Latinas and Chileans: Clinical features, Ancestry Analysis, and Admixture MappingXenobiotic, bile acid, and cholesterol transporters: function and regulation.Inhibition of Na+-taurocholate Co-transporting polypeptide-mediated bile acid transport by cholestatic sulfated progesterone metabolites.First description of ABCB4 gene deletions in familial low phospholipid-associated cholelithiasis and oral contraceptives-induced cholestasis.Molecular pathogenesis of intrahepatic cholestasis of pregnancy.The molecular genetics of intrahepatic cholestasis of pregnancy.Intrahepatic cholestasis of pregnancy-current achievements and unsolved problemsA comprehensive analysis of common genetic variation around six candidate loci for intrahepatic cholestasis of pregnancy.The Multiple Facets of ABCB4 (MDR3) DeficiencyMultidrug resistance protein 3 R652G may reduce susceptibility to idiopathic infant cholestasisRole of the bile salt export pump, BSEP, in acquired forms of cholestasis.Genetic variations of bile salt transporters as predisposing factors for drug-induced cholestasis, intrahepatic cholestasis of pregnancy and therapeutic response of viral hepatitis.An update on genetic analysis of cholestatic liver diseases: digging deeper.Effect of drug transporter pharmacogenetics on cholestasis.Management of intrahepatic cholestasis of pregnancy.Immunology of hepatic diseases during pregnancy.An expanded role for heterozygous mutations of ABCB4, ABCB11, ATP8B1, ABCC2 and TJP2 in intrahepatic cholestasis of pregnancy.Analysis of mutations of MDR3 exons 9 and 23 in infants with parenteral nutrition-associated cholestasis.Analysis of gene mutations in children with cholestasis of undefined etiology.Genotype-phenotype relationships in the low-phospholipid-associated cholelithiasis syndrome: a study of 156 consecutive patients.Intrahepatic cholestasis of pregnancy and associated hepatobiliary disease: a population-based cohort study.Genetic profiling of children with advanced cholestatic liver disease.Bone marrow transplantation demonstrates medullar origin of CD34+ fibrocytes and ameliorates hepatic fibrosis in Abcb4-/- mice.Phenotypic spectrum and diagnostic pitfalls of ABCB4 deficiency depending on age of onset.
P2860
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P2860
Intrahepatic cholestasis of pregnancy: the severe form is associated with common variants of the hepatobiliary phospholipid transporter ABCB4 gene.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
2006年论文
@zh
2006年论文
@zh-cn
name
Intrahepatic cholestasis of pr ...... olipid transporter ABCB4 gene.
@ast
Intrahepatic cholestasis of pr ...... olipid transporter ABCB4 gene.
@en
type
label
Intrahepatic cholestasis of pr ...... olipid transporter ABCB4 gene.
@ast
Intrahepatic cholestasis of pr ...... olipid transporter ABCB4 gene.
@en
prefLabel
Intrahepatic cholestasis of pr ...... olipid transporter ABCB4 gene.
@ast
Intrahepatic cholestasis of pr ...... olipid transporter ABCB4 gene.
@en
P2093
P2860
P356
P1433
P1476
Intrahepatic cholestasis of pr ...... olipid transporter ABCB4 gene.
@en
P2093
H E Wasmuth
H Keppeler
H-U Marschall
L-A Mattsson
P2860
P304
P356
10.1136/GUT.2006.092742
P407
P577
2006-08-04T00:00:00Z