Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: Fibrosis and ABCB4[original query] |
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ABCB4 heterozygous gene mutations associated with fibrosing cholestatic liver disease in adults. Gastroenterology 2008 Jul 135 (1): 131-41. Ziol Marianne, Barbu Véronique, Rosmorduc Olivier, Frassati-Biaggi Annonciade, Barget Nathalie, Hermelin Brigitte, Scheffer Georges L, Bennouna Selma, Trinchet Jean-Claude, Beaugrand Michel, Ganne-Carrié Nathal |
An MBL2 haplotype and ABCB4 variants modulate the risk of liver disease in cystic fibrosis patients: a multicentre study. Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver 2009 Nov 41 (11): 817-22. Tomaiuolo R, Degiorgio D, Coviello D A, Baccarelli A, Elce A, Raia V, Motta V, Seia M, Castaldo G, Colombo |
Increased frequency of double and triple heterozygous gene variants in children with intrahepatic cholestasis. Hepatology research : the official journal of the Japan Society of Hepatology 2015 Jun . Goldschmidt Monique L, Mourya Reena, Connor Jessica, Dexheimer Phillip, Karns Rebekah, Miethke Alexander, Sheridan Rachel, Zhang Kejian, Bezerra Jorge |
ABCB4 Gene Aberrations in Human Liver Disease: An Evolving Spectrum. Seminars in liver disease 2018 10 38 (4): 299-307. Reichert Matthias Christian, Lammert Fra |
Genetic variant c.711A>T in the hepatobiliary phospholipid transporter ABCB4 is associated with significant liver fibrosis. Journal of physiology and pharmacology : an official journal of the Polish Physiological Society 2020 9 71 (3): . Smyk W, Weber S N, Hall R, Gruenhage F, Lammert F, Krawczyk |
Common ABCB4 and ABCB11 Genotypes Are Associated with Idiopathic Chronic Cholestasis in Adults. Digestive diseases (Basel, Switzerland) 2021 8 40 (4): 489-496. Jüngst Christoph, Justinger Christina, Fischer Janett, Berg Thomas, Lammert Fra |
A common variant in the hepatobiliary phospholipid transporter ABCB4 modulates liver injury in PBC but not in PSC: prospective analysis in 867 patients. Orphanet journal of rare diseases 2022 11 17 (1): 419. Kruk Beata, Milkiewicz Malgorzata, Raszeja-Wyszomirska Joanna, Milkiewicz Piotr, Krawczyk Marc |
Influence of the Bile Acid Transporter Genes ABCB4, ABCB8, and ABCB11 and the Farnesoid X Receptor on the Response to Ursodeoxycholic Acid in Patients with Nonalcoholic Steatohepatitis. Journal of personalized medicine 2023 7 13 (7): . Henriette Kreimeyer, Katharina Vogt, Tobias Götze, Jan Best, Oliver Götze, Jochen Weigt, Alisan Kahraman, Mustafa Özçürümez, Julia Kälsch, Wing-Kin Syn, Svenja Sydor, Ali Canbay, Paul Man |
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