| P50 | author | Simon N. Waddington | Q37835224 |
| | Neil J. Sebire | Q38549176 |
| | Jemima J Burden | Q41786684 |
| | Blerida Banushi | Q55755081 |
| | Anne-Marie Lyne | Q58879615 |
| | Paul Gissen | Q60647294 |
| P2093 | author name string | Peter Clayton | |
| | Alex Virasami | |
| | A S Knisely | |
| | Frédéric P Lemaigre | |
| | Anna Straatman-Iwanowska | |
| | Kevin Mills | |
| | Holly Smith | |
| | Dipok Kumar Dhar | |
| | Coen C Paulusma | |
| | Francesca Mazzacuva | |
| | Rebeca Fiadeiro | |
| | Joanna Hanley | |
| | Steven Howe | |
| P2860 | cites work | Mutations in VIPAR cause an arthrogryposis, renal dysfunction and cholestasis syndrome phenotype with defects in epithelial polarization | Q24301355 |
| | Overexpression of ABCG5 and ABCG8 promotes biliary cholesterol secretion and reduces fractional absorption of dietary cholesterol | Q24306058 |
| | Rab11a and myosin Vb are required for bile canalicular formation in WIF-B9 cells | Q24536054 |
| | Par1b induces asymmetric inheritance of plasma membrane domains via LGN-dependent mitotic spindle orientation in proliferating hepatocytes | Q27316277 |
| | Gene Expression Omnibus: NCBI gene expression and hybridization array data repository | Q27860523 |
| | Drug- and estrogen-induced cholestasis through inhibition of the hepatocellular bile salt export pump (Bsep) of rat liver | Q28143360 |
| | Mutational spectrum of beta-catenin, AXIN1, and AXIN2 in hepatocellular carcinomas and hepatoblastomas | Q28213290 |
| | Regulation of post-Golgi LH3 trafficking is essential for collagen homeostasis | Q28314912 |
| | VPS33B regulates protein sorting into and maturation of α-granule progenitor organelles in mouse megakaryocytes | Q28504778 |
| | The sister of P-glycoprotein represents the canalicular bile salt export pump of mammalian liver | Q28571688 |
| | Differential induction of gamma-glutamyl transpeptidase in primary cultures of rat and mouse hepatocytes parallels induction during hepatocarcinogenesis | Q30472397 |
| | Cell adhesion, polarity, and epithelia in the dawn of metazoans. | Q33340425 |
| | Mutations in TJP2 cause progressive cholestatic liver disease | Q33770688 |
| | Liver-specific β-catenin knockout mice have bile canalicular abnormalities, bile secretory defect, and intrahepatic cholestasis | Q34164068 |
| | Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT. | Q34191705 |
| | Hepatobiliary disposition of 3alpha,6alpha,7alpha,12alpha-tetrahydroxy-cholanoyl taurine: a substrate for multiple canalicular transporters | Q34211135 |
| | Rab GTPase-Myo5B complexes control membrane recycling and epithelial polarization. | Q34582966 |
| | Structural and functional hepatocyte polarity and liver disease | Q36090717 |
| | Abcb11 deficiency induces cholestasis coupled to impaired β-fatty acid oxidation in mice | Q36098104 |
| | Morphologic findings in progressive familial intrahepatic cholestasis 2 (PFIC2): correlation with genetic and immunohistochemical studies | Q36154600 |
| | deep-orange and carnation define distinct stages in late endosomal biogenesis in Drosophila melanogaster | Q36323472 |
| | The apical conjugate efflux pump ABCC2 (MRP2). | Q36539096 |
| | Systemic errors in quantitative polymerase chain reaction titration of self-complementary adeno-associated viral vectors and improved alternative methods | Q36807045 |
| | Hepatocyte polarity | Q36972087 |
| | Associations among genotype, clinical phenotype, and intracellular localization of trafficking proteins in ARC syndrome. | Q37101681 |
| | Identification of novel bile acids as biomarkers for the early diagnosis of Niemann-Pick C disease | Q37384927 |
| | MYO5B and bile salt export pump contribute to cholestatic liver disorder in microvillous inclusion disease | Q39283295 |
| | Class III P-glycoproteins mediate the formation of lipoprotein X in the mouse | Q39813339 |
| | Identification of regions required for apical membrane localization of human multidrug resistance protein 2. | Q39996188 |
| | Formation of lipoprotein-X. Its relationship to bile compounds | Q40983043 |
| | Rab11a is required for apical protein localisation in the intestine. | Q41665284 |
| | A direct role for the Sec1/Munc18-family protein Vps33 as a template for SNARE assembly | Q42288650 |
| | Hepatic transport mechanisms of cholyl-L-lysyl-fluorescein | Q43101004 |
| | Paediatric hepatocellular carcinoma due to somatic CTNNB1 and NFE2L2 mutations in the setting of inherited bi-allelic ABCB11 mutations | Q43586888 |
| | Hepatocyte-specific expression of Cre recombinase | Q43604415 |
| | Increased iNOS activity is essential for hepatic epithelial tight junction dysfunction in endotoxemic mice | Q44567711 |
| | Severe cholestasis induced by cholic acid feeding in knockout mice of sister of P-glycoprotein | Q44675039 |
| | A lethal familial syndrome associating arthrogryposis multiplex congenita, renal dysfunction, and a cholestatic and pigmentary liver disease | Q45039586 |
| | Purification of recombinant adeno-associated virus type 8 vectors by ion exchange chromatography generates clinical grade vector stock | Q45585678 |
| | Factors influencing in vivo transduction by recombinant adeno-associated viral vectors expressing the human factor IX cDNA. | Q45875077 |
| | Claudin-1 gene mutations in neonatal sclerosing cholangitis associated with ichthyosis: a tight junction disease | Q55671093 |
| | Clinical and molecular genetic features of ARC syndrome | Q64446137 |
| | Regulation of transporter expression in mouse liver, kidney, and intestine during extrahepatic cholestasis | Q79400125 |
| P433 | issue | 5 | |
| P304 | page(s) | 1001-1011 | |
| P577 | publication date | 2017-01-09 | |
| P1433 | published in | Journal of Hepatology | Q15724402 |
| P1476 | title | Vps33b is crucial for structural and functional hepatocyte polarity | |
| P478 | volume | 66 | |