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Laura N Bull

Showing results (21-30 of 33) with videos related to

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Gastroenterology|August 10, 2004
Benign recurrent intrahepatic cholestasis type 2 is caused by mutations in ABCB11Saskia W C van Mil, Wendy L van der Woerd, Gerda van der Brugge, et al.
Gastroenterology|March 27, 2021
Deleterious Variants in ABCC12 are Detected in Idiopathic Chronic Cholestasis and Cause Intrahepatic Bile Duct Loss in Model OrganismsDuc-Hung Pham, Ramesh Kudira, Lingfen Xu, et al.
Hepatology (Baltimore, Md.)|June 27, 2006
Atp8b1 deficiency in mice reduces resistance of the canalicular membrane to hydrophobic bile salts and impairs bile salt transportCoen C Paulusma, Annemiek Groen, Cindy Kunne, et al.
Gastroenterology|February 19, 2013
Genetic defects in bile acid conjugation cause fat-soluble vitamin deficiencyKenneth D R Setchell, James E Heubi, Sohela Shah, et al.
Hepatology Communications|May 16, 2018
Outcomes of surgical management of familial intrahepatic cholestasis 1 and bile salt export protein deficienciesLaura N Bull, Ludmila Pawlikowska, Sandra Strautnieks, et al.
Nature Genetics|March 12, 2014
Mutations in TJP2 cause progressive cholestatic liver diseaseMelissa Sambrotta, Sandra Strautnieks, Efterpi Papouli, et al.
Journal of Pediatric Gastroenterology and Nutrition|July 26, 2021
Presentation and Outcomes of Infants With Idiopathic Cholestasis: A Multicenter Prospective StudyPaula M Hertel, Kieran Hawthorne, Sehee Kim, et al.
Hepatology (Baltimore, Md.)|July 28, 2006
Hepatocellular carcinoma in ten children under five years of age with bile salt export pump deficiencyA S Knisely, Sandra S Strautnieks, Yvonne Meier, et al.
Hepatology (Baltimore, Md.)|July 9, 2004
Characterization of mutations in ATP8B1 associated with hereditary cholestasisLeo W J Klomp, Julie C Vargas, Saskia W C van Mil, et al.
Journal of Pediatric Gastroenterology and Nutrition|May 21, 2021
Mutation Analysis and Disease Features at Presentation in a Multi-Center Cohort of Children With Monogenic CholestasisPaula M Hertel, Laura N Bull, Richard J Thompson, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
Gastroenterology|August 10, 2004
Benign recurrent intrahepatic cholestasis type 2 is caused by mutations in ABCB11Saskia W C van Mil, Wendy L van der Woerd, Gerda van der Brugge, et al.
Gastroenterology|March 27, 2021
Deleterious Variants in ABCC12 are Detected in Idiopathic Chronic Cholestasis and Cause Intrahepatic Bile Duct Loss in Model OrganismsDuc-Hung Pham, Ramesh Kudira, Lingfen Xu, et al.
Hepatology (Baltimore, Md.)|June 27, 2006
Atp8b1 deficiency in mice reduces resistance of the canalicular membrane to hydrophobic bile salts and impairs bile salt transportCoen C Paulusma, Annemiek Groen, Cindy Kunne, et al.
Gastroenterology|February 19, 2013
Genetic defects in bile acid conjugation cause fat-soluble vitamin deficiencyKenneth D R Setchell, James E Heubi, Sohela Shah, et al.
Hepatology Communications|May 16, 2018
Outcomes of surgical management of familial intrahepatic cholestasis 1 and bile salt export protein deficienciesLaura N Bull, Ludmila Pawlikowska, Sandra Strautnieks, et al.
Nature Genetics|March 12, 2014
Mutations in TJP2 cause progressive cholestatic liver diseaseMelissa Sambrotta, Sandra Strautnieks, Efterpi Papouli, et al.
Journal of Pediatric Gastroenterology and Nutrition|July 26, 2021
Presentation and Outcomes of Infants With Idiopathic Cholestasis: A Multicenter Prospective StudyPaula M Hertel, Kieran Hawthorne, Sehee Kim, et al.
Hepatology (Baltimore, Md.)|July 28, 2006
Hepatocellular carcinoma in ten children under five years of age with bile salt export pump deficiencyA S Knisely, Sandra S Strautnieks, Yvonne Meier, et al.
Hepatology (Baltimore, Md.)|July 9, 2004
Characterization of mutations in ATP8B1 associated with hereditary cholestasisLeo W J Klomp, Julie C Vargas, Saskia W C van Mil, et al.
Journal of Pediatric Gastroenterology and Nutrition|May 21, 2021
Mutation Analysis and Disease Features at Presentation in a Multi-Center Cohort of Children With Monogenic CholestasisPaula M Hertel, Laura N Bull, Richard J Thompson, et al.
Pageof 4