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Cell Biochemistry and Function|September 28, 2022
The phospholipid flippase ATP8B1 is required for lysosomal fusion in macrophagesValentina E Gómez-Mellado, Kam S Ho-Mok, Vincent A van der Mark, et al.Molecular Therapy. Advances|May 15, 2026
Rapid multiplex liver gene-editing in mice using adeno-associated virus 8 or lipid nanoparticlesDandan Wu, Isabelle Bolt, Dagmar W Tolenaars, et al.Journal of Hepatology|April 3, 2019
Liver-directed gene therapy results in long-term correction of progressive familial intrahepatic cholestasis type 3 in miceSem J Aronson, Robert S Bakker, Xiaoxia Shi, et al.Antioxidants (Basel, Switzerland)|December 24, 2021
Long-Term Effects of Biliverdin Reductase a Deficiency in <i>Ugt1</i><sup>-/-</sup> Mice: Impact on Redox Status and MetabolismGiulia Bortolussi, Xiaoxia Shi, Lysbeth Ten Bloemendaal, et al.Plos One|April 5, 2019
The P4-ATPase ATP9A is a novel determinant of exosome releaseJyoti Naik, Chi M Hau, Lysbeth Ten Bloemendaal, et al.Hepatology (Baltimore, Md.)|May 29, 2019
Blocking Sodium-Taurocholate Cotransporting Polypeptide Stimulates Biliary Cholesterol and Phospholipid Secretion in MiceReinout L P Roscam Abbing, Davor Slijepcevic, Joanne M Donkers, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|November 25, 2020
Collagen release by human hepatic stellate cells requires vitamin C and is efficiently blocked by hydroxylase inhibitionNatalia Smith-Cortinez, Raphael R Fagundes, Valentina Gomez, et al.Cellular and Molecular Life Sciences : CMLS|September 16, 2016
Phospholipid flippases attenuate LPS-induced TLR4 signaling by mediating endocytic retrieval of Toll-like receptor 4Vincent A van der Mark, Mohammed Ghiboub, Casper Marsman, et al.Gastroenterology|August 9, 2011
Complementary functions of the flippase ATP8B1 and the floppase ABCB4 in maintaining canalicular membrane integrityAnnemiek Groen, Marta Rodriguez Romero, Cindy Kunne, et al.Hepatology (Baltimore, Md.)|May 29, 2014
Sodium taurocholate cotransporting polypeptide (SLC10A1) deficiency: conjugated hypercholanemia without a clear clinical phenotypeFrédéric M Vaz, Coen C Paulusma, Hidde Huidekoper, et al.Pageof 6