These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

323 related articles for article (PubMed ID: 9500542)

  • 21. Benign recurrent intrahepatic cholestasis.
    Luketic VA; Shiffman ML
    Clin Liver Dis; 2004 Feb; 8(1):133-49, vii. PubMed ID: 15062197
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Progressive familial intrahepatic cholestasis type 1 and extrahepatic features: no catch-up of stature growth, exacerbation of diarrhea, and appearance of liver steatosis after liver transplantation.
    Lykavieris P; van Mil S; Cresteil D; Fabre M; Hadchouel M; Klomp L; Bernard O; Jacquemin E
    J Hepatol; 2003 Sep; 39(3):447-52. PubMed ID: 12927934
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Benign recurrent intrahepatic cholestasis type-II--a rare cause of direct hyperbilirubinemia exacerbations with hepatic fibrosis].
    Mizrahi M; Lalazar G; Horwich Y; Adar T; Safadi R
    Harefuah; 2008 May; 147(5):381-3, 480. PubMed ID: 18770956
    [TBL] [Abstract][Full Text] [Related]  

  • 24. New Insights in Genetic Cholestasis: From Molecular Mechanisms to Clinical Implications.
    Sticova E; Jirsa M; Pawłowska J
    Can J Gastroenterol Hepatol; 2018; 2018():2313675. PubMed ID: 30148122
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Cholestatic liver diseases: slow progress in understanding and treating slowly progressive disorders.
    Vleggaar FP; Van Ooteghem NA; Van Buuren HR; Van Berge Henegouwen GP
    Scand J Gastroenterol Suppl; 2000; (232):86-92. PubMed ID: 11232499
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Mapping of a locus for progressive familial intrahepatic cholestasis (Byler disease) to 18q21-q22, the benign recurrent intrahepatic cholestasis region.
    Carlton VE; Knisely AS; Freimer NB
    Hum Mol Genet; 1995 Jun; 4(6):1049-53. PubMed ID: 7655458
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Novel splice-site mutation in ATP8B1 results in atypical progressive familial intrahepatic cholestasis type 1.
    Copeland E; Renault N; Renault M; Dyack S; Bulman DE; Bedard K; Otley A; Magee F; Acott P; Greer WL
    J Gastroenterol Hepatol; 2013 Mar; 28(3):560-4. PubMed ID: 23033845
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Genetic and morphological findings in progressive familial intrahepatic cholestasis (Byler disease [PFIC-1] and Byler syndrome): evidence for heterogeneity.
    Bull LN; Carlton VE; Stricker NL; Baharloo S; DeYoung JA; Freimer NB; Magid MS; Kahn E; Markowitz J; DiCarlo FJ; McLoughlin L; Boyle JT; Dahms BB; Faught PR; Fitzgerald JF; Piccoli DA; Witzleben CL; O'Connell NC; Setchell KD; Agostini RM; Kocoshis SA; Reyes J; Knisely AS
    Hepatology; 1997 Jul; 26(1):155-64. PubMed ID: 9214465
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Genome screening by searching for shared segments: mapping a gene for benign recurrent intrahepatic cholestasis.
    Houwen RH; Baharloo S; Blankenship K; Raeymaekers P; Juyn J; Sandkuijl LA; Freimer NB
    Nat Genet; 1994 Dec; 8(4):380-6. PubMed ID: 7894490
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Characterization of the P5 subfamily of P-type transport ATPases in mice.
    Schultheis PJ; Hagen TT; O'Toole KK; Tachibana A; Burke CR; McGill DL; Okunade GW; Shull GE
    Biochem Biophys Res Commun; 2004 Oct; 323(3):731-8. PubMed ID: 15381061
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Effects of bezafibrate on dyslipidemia with cholestasis in children with familial intrahepatic cholestasis-1 deficiency manifesting progressive familial intrahepatic cholestasis.
    Nagasaka H; Yorifuji T; Hirano K; Ota A; Toyama-Nakagawa Y; Takatani T; Tsukahara H; Kobayashi K; Takayanagi M; Inomata Y; Uemoto S; Miida T
    Metabolism; 2009 Jan; 58(1):48-54. PubMed ID: 19059530
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A flippase-independent function of ATP8B1, the protein affected in familial intrahepatic cholestasis type 1, is required for apical protein expression and microvillus formation in polarized epithelial cells.
    Verhulst PM; van der Velden LM; Oorschot V; van Faassen EE; Klumperman J; Houwen RH; Pomorski TG; Holthuis JC; Klomp LW
    Hepatology; 2010 Jun; 51(6):2049-60. PubMed ID: 20512993
    [TBL] [Abstract][Full Text] [Related]  

  • 33. ATP8B1 and ATP11C: Two Lipid Flippases Important for Hepatocyte Function.
    Naik J; de Waart DR; Utsunomiya K; Duijst S; Mok KH; Oude Elferink RP; Bosma PJ; Paulusma CC
    Dig Dis; 2015; 33(3):314-8. PubMed ID: 26045263
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Autosomal dominant benign recurrent intrahepatic cholestasis (BRIC) unlinked to 18q21 and 2q24.
    Floreani A; Molaro M; Mottes M; Sangalli A; Baragiotta A; Roda A; Naccarato R; Clementi M
    Am J Med Genet; 2000 Dec; 95(5):450-3. PubMed ID: 11146465
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A mouse genetic model for familial cholestasis caused by ATP8B1 mutations reveals perturbed bile salt homeostasis but no impairment in bile secretion.
    Pawlikowska L; Groen A; Eppens EF; Kunne C; Ottenhoff R; Looije N; Knisely AS; Killeen NP; Bull LN; Elferink RP; Freimer NB
    Hum Mol Genet; 2004 Apr; 13(8):881-92. PubMed ID: 14976163
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Genetic cholestasis].
    Ciocca M; Alvarez F
    Arch Argent Pediatr; 2009 Aug; 107(4):340-6. PubMed ID: 19753442
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Altered hepatobiliary gene expressions in PFIC1: ATP8B1 gene defect is associated with CFTR downregulation.
    Demeilliers C; Jacquemin E; Barbu V; Mergey M; Paye F; Fouassier L; Chignard N; Housset C; Lomri NE
    Hepatology; 2006 May; 43(5):1125-34. PubMed ID: 16628629
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The type 4 subfamily of P-type ATPases, putative aminophospholipid translocases with a role in human disease.
    Paulusma CC; Oude Elferink RP
    Biochim Biophys Acta; 2005 Jun; 1741(1-2):11-24. PubMed ID: 15919184
    [TBL] [Abstract][Full Text] [Related]  

  • 39. ATP8B1 mutations in British cases with intrahepatic cholestasis of pregnancy.
    Müllenbach R; Bennett A; Tetlow N; Patel N; Hamilton G; Cheng F; Chambers J; Howard R; Taylor-Robinson SD; Williamson C
    Gut; 2005 Jun; 54(6):829-34. PubMed ID: 15888793
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Differential effects of progressive familial intrahepatic cholestasis type 1 and benign recurrent intrahepatic cholestasis type 1 mutations on canalicular localization of ATP8B1.
    Folmer DE; van der Mark VA; Ho-Mok KS; Oude Elferink RP; Paulusma CC
    Hepatology; 2009 Nov; 50(5):1597-605. PubMed ID: 19731236
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 17.