Genetic defects in hepatocanalicular transport.

Genetic defects in hepatocanalicular transport.

Item
http://www.wikidata.org/entity/Q34081637
New insights in bilirubin metabolism and their clinical implicationsAn essential subfamily of Drs2p-related P-type ATPases is required for protein trafficking between Golgi complex and endosomal/vacuolar systemRequirement for neo1p in retrograde transport from the Golgi complex to the endoplasmic reticulumGenetic cholestasis, causes and consequences for hepatobiliary transport.Biology of a novel organic solute and steroid transporter, OSTalpha-OSTbeta.Nutrition assessment and support in children with end-stage liver disease.Human bile salt export pump promoter is transactivated by the farnesoid X receptor/bile acid receptor.cFLIP-L inhibits p38 MAPK activation: an additional anti-apoptotic mechanism in bile acid-mediated apoptosis.Unexplained cholestasis in adults and adolescents: diagnostic benefit of genetic examination.
P2860

Genetic defects in hepatocanalicular transport.

Item
http://www.wikidata.org/entity/Q34081637
description
2000 nî lūn-bûn
@nan
2000 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Genetic defects in hepatocanalicular transport.
@ast
Genetic defects in hepatocanalicular transport.
@en
Genetic defects in hepatocanalicular transport.
@nl
type
label
Genetic defects in hepatocanalicular transport.
@ast
Genetic defects in hepatocanalicular transport.
@en
Genetic defects in hepatocanalicular transport.
@nl
prefLabel
Genetic defects in hepatocanalicular transport.
@ast
Genetic defects in hepatocanalicular transport.
@en
Genetic defects in hepatocanalicular transport.
@nl
P1433
P1476
P2093
P304
P31
P356
P433
P478
P50
P577
P698
P356
P1433
P1476
Genetic defects in hepatocanalicular transport
@en
P2093
P304
P31
P356
P433
P478
P50
P577
P698