318 related articles for article (PubMed ID: 34942279)
41. Linkage between a new splicing site mutation in the MDR3 alias ABCB4 gene and intrahepatic cholestasis of pregnancy.
Schneider G; Paus TC; Kullak-Ublick GA; Meier PJ; Wienker TF; Lang T; van de Vondel P; Sauerbruch T; Reichel C
Hepatology; 2007 Jan; 45(1):150-8. PubMed ID: 17187437
[TBL] [Abstract][Full Text] [Related]
42. Genetic cholestasis, causes and consequences for hepatobiliary transport.
Jansen PL; Sturm E
Liver Int; 2003 Oct; 23(5):315-22. PubMed ID: 14708891
[TBL] [Abstract][Full Text] [Related]
43. A study of exons 14, 15, and 24 of the ABCB11 gene in Egyptian children with normal GGT cholestasis.
Selim N; Omair H; El-Karaksy H; Fathy M; Mahmoud E; Baroudy S; Fathy M; Yassin N
Arab J Gastroenterol; 2022 Feb; 23(1):15-19. PubMed ID: 35153175
[TBL] [Abstract][Full Text] [Related]
44. Variants in ABCB4 (MDR3) across the spectrum of cholestatic liver diseases in adults.
Stättermayer AF; Halilbasic E; Wrba F; Ferenci P; Trauner M
J Hepatol; 2020 Sep; 73(3):651-663. PubMed ID: 32376413
[TBL] [Abstract][Full Text] [Related]
45. ABCB4 and ABCB11 mutations in intrahepatic cholestasis of pregnancy in an Italian population.
Anzivino C; Odoardi MR; Meschiari E; Baldelli E; Facchinetti F; Neri I; Ruggiero G; Zampino R; Bertolotti M; Loria P; Carulli L
Dig Liver Dis; 2013 Mar; 45(3):226-32. PubMed ID: 23022423
[TBL] [Abstract][Full Text] [Related]
46. Jaundice revisited: recent advances in the diagnosis and treatment of inherited cholestatic liver diseases.
Chen HL; Wu SH; Hsu SH; Liou BY; Chen HL; Chang MH
J Biomed Sci; 2018 Oct; 25(1):75. PubMed ID: 30367658
[TBL] [Abstract][Full Text] [Related]
47. Molecular basis of intrahepatic cholestasis.
Carlton VE; Pawlikowska L; Bull LN
Ann Med; 2004; 36(8):606-17. PubMed ID: 15768832
[TBL] [Abstract][Full Text] [Related]
48. Benign recurrent intrahepatic cholestasis type 2 is caused by mutations in ABCB11.
van Mil SW; van der Woerd WL; van der Brugge G; Sturm E; Jansen PL; Bull LN; van den Berg IE; Berger R; Houwen RH; Klomp LW
Gastroenterology; 2004 Aug; 127(2):379-84. PubMed ID: 15300568
[TBL] [Abstract][Full Text] [Related]
49. [Liver disease associated with hereditary defects of hepatobiliary transporters].
Wendum D
Ann Pathol; 2010 Dec; 30(6):426-31. PubMed ID: 21167428
[TBL] [Abstract][Full Text] [Related]
50. Comprehensive bile acid profiling in hereditary intrahepatic cholestasis: Genetic and clinical correlations.
Liu T; Wang RX; Han J; Hao CZ; Qiu YL; Yan YY; Li LT; Wang NL; Gong JY; Lu Y; Zhang MH; Xie XB; Yang JC; You YJ; Li JQ; Knisely AS; Borchers CH; Ling V; Wang JS
Liver Int; 2018 Sep; 38(9):1676-1685. PubMed ID: 29412511
[TBL] [Abstract][Full Text] [Related]
51. [Recurrent intrahepatic cholestasis of pregnancy and chain-like choledocholithiasis in a female patient with stop codon in the ABDC4-gene of the hepatobiliary phospholipid transporter].
Muehlenberg K; Wiedmann K; Keppeler H; Sauerbruch T; Lammert F
Z Gastroenterol; 2008 Jan; 46(1):48-53. PubMed ID: 18188816
[TBL] [Abstract][Full Text] [Related]
52. Characterization of ATP8B1 gene mutations and a hot-linked mutation found in Chinese children with progressive intrahepatic cholestasis and low GGT.
Liu LY; Wang XH; Wang ZL; Zhu QR; Wang JS
J Pediatr Gastroenterol Nutr; 2010 Feb; 50(2):179-83. PubMed ID: 20038848
[TBL] [Abstract][Full Text] [Related]
53. Progressive familial intrahepatic cholestasis. Genetic basis and treatment.
Jacquemin E
Clin Liver Dis; 2000 Nov; 4(4):753-63. PubMed ID: 11232355
[TBL] [Abstract][Full Text] [Related]
54. Hepatocanalicular bile salt export pump deficiency in patients with progressive familial intrahepatic cholestasis.
Jansen PL; Strautnieks SS; Jacquemin E; Hadchouel M; Sokal EM; Hooiveld GJ; Koning JH; De Jager-Krikken A; Kuipers F; Stellaard F; Bijleveld CM; Gouw A; Van Goor H; Thompson RJ; Müller M
Gastroenterology; 1999 Dec; 117(6):1370-9. PubMed ID: 10579978
[TBL] [Abstract][Full Text] [Related]
55. The spectrum of Progressive Familial Intrahepatic Cholestasis diseases: Update on pathophysiology and emerging treatments.
Felzen A; Verkade HJ
Eur J Med Genet; 2021 Nov; 64(11):104317. PubMed ID: 34478903
[TBL] [Abstract][Full Text] [Related]
56. Ductopenia and cirrhosis in a 32-year-old woman with progressive familial intrahepatic cholestasis type 3: A case report and review of the literature.
Tan YW; Ji HL; Lu ZH; Ge GH; Sun L; Zhou XB; Sheng JH; Gong YH
World J Gastroenterol; 2018 Nov; 24(41):4716-4720. PubMed ID: 30416319
[TBL] [Abstract][Full Text] [Related]
57. Reduced hepatic expression of farnesoid X receptor in hereditary cholestasis associated to mutation in ATP8B1.
Alvarez L; Jara P; Sánchez-Sabaté E; Hierro L; Larrauri J; Díaz MC; Camarena C; De la Vega A; Frauca E; López-Collazo E; Lapunzina P
Hum Mol Genet; 2004 Oct; 13(20):2451-60. PubMed ID: 15317749
[TBL] [Abstract][Full Text] [Related]
58. Update on progressive familial intrahepatic cholestasis.
Alissa FT; Jaffe R; Shneider BL
J Pediatr Gastroenterol Nutr; 2008 Mar; 46(3):241-52. PubMed ID: 18376240
[TBL] [Abstract][Full Text] [Related]
59. A Rare BSEP Mutation Associated with a Mild Form of Progressive Familial Intrahepatic Cholestasis Type 2.
Waisbourd-Zinman O; Surrey LF; Schwartz AE; Russo PA; Wen J
Ann Hepatol; 2017; 16(3):465-468. PubMed ID: 28425419
[TBL] [Abstract][Full Text] [Related]
60. Hepatic cytochrome P450 deficiency in mouse models for intrahepatic cholestasis predispose to bile salt-induced cholestasis.
Kunne C; de Graaff M; Duijst S; de Waart DR; Oude Elferink RP; Paulusma CC
Lab Invest; 2014 Oct; 94(10):1103-13. PubMed ID: 25068656
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]