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Laura N Bull

Showing results (11-20 of 33) with videos related to

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World Journal of Clinical Cases|May 28, 2021
Progressive familial intrahepatic cholestasis - farnesoid X receptor deficiency due to <i>NR1H4</i> mutation: A case reportPiotr Czubkowski, Richard J Thompson, Irena Jankowska, et al.
BMC Gastroenterology|October 22, 2008
Bile composition in Alagille Syndrome and PFIC patients having Partial External Biliary DiversionKaran M Emerick, Marc S Elias, Hector Melin-Aldana, et al.
Plos One|October 3, 2013
CCBE1 mutation in two siblings, one manifesting lymphedema-cholestasis syndrome, and the other, fetal hydropsSohela Shah, Laura K Conlin, Luis Gomez, et al.
Hepatology Communications|October 22, 2021
Liver Disease and Risk of Hepatocellular Carcinoma in Children With Mutations in TALDO1Tassos Grammatikopoulos, Nedim Hadzic, Pierre Foskett, et al.
Human Molecular Genetics|February 21, 2004
A mouse genetic model for familial cholestasis caused by ATP8B1 mutations reveals perturbed bile salt homeostasis but no impairment in bile secretionLudmila Pawlikowska, Annemiek Groen, Elaine F Eppens, et al.
Plos One|February 4, 2010
Strain background modifies phenotypes in the ATP8B1-deficient mouseSohela Shah, Ukina R Sanford, Julie C Vargas, et al.
Gastroenterology|February 28, 2004
Progressive familial intrahepatic cholestasis, type 1, is associated with decreased farnesoid X receptor activityFrank Chen, M Ananthanarayanan, Sukru Emre, et al.
Hepatology (Baltimore, Md.)|March 2, 2016
ATP11C targets basolateral bile salt transporter proteins in mouse central hepatocytesDirk R de Waart, Jyoti Naik, Karina S Utsunomiya, et al.
Plos One|July 1, 2015
Intrahepatic Cholestasis of Pregnancy (ICP) in U.S. Latinas and Chileans: Clinical features, Ancestry Analysis, and Admixture MappingLaura N Bull, Donglei Hu, Sohela Shah, et al.
Nature Genetics|April 22, 2003
Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAATVictoria E H Carlton, Baruch Z Harris, Erik G Puffenberger, et al.
Pageof 4

Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 4
World Journal of Clinical Cases|May 28, 2021
Progressive familial intrahepatic cholestasis - farnesoid X receptor deficiency due to <i>NR1H4</i> mutation: A case reportPiotr Czubkowski, Richard J Thompson, Irena Jankowska, et al.
BMC Gastroenterology|October 22, 2008
Bile composition in Alagille Syndrome and PFIC patients having Partial External Biliary DiversionKaran M Emerick, Marc S Elias, Hector Melin-Aldana, et al.
Plos One|October 3, 2013
CCBE1 mutation in two siblings, one manifesting lymphedema-cholestasis syndrome, and the other, fetal hydropsSohela Shah, Laura K Conlin, Luis Gomez, et al.
Hepatology Communications|October 22, 2021
Liver Disease and Risk of Hepatocellular Carcinoma in Children With Mutations in TALDO1Tassos Grammatikopoulos, Nedim Hadzic, Pierre Foskett, et al.
Human Molecular Genetics|February 21, 2004
A mouse genetic model for familial cholestasis caused by ATP8B1 mutations reveals perturbed bile salt homeostasis but no impairment in bile secretionLudmila Pawlikowska, Annemiek Groen, Elaine F Eppens, et al.
Plos One|February 4, 2010
Strain background modifies phenotypes in the ATP8B1-deficient mouseSohela Shah, Ukina R Sanford, Julie C Vargas, et al.
Gastroenterology|February 28, 2004
Progressive familial intrahepatic cholestasis, type 1, is associated with decreased farnesoid X receptor activityFrank Chen, M Ananthanarayanan, Sukru Emre, et al.
Hepatology (Baltimore, Md.)|March 2, 2016
ATP11C targets basolateral bile salt transporter proteins in mouse central hepatocytesDirk R de Waart, Jyoti Naik, Karina S Utsunomiya, et al.
Plos One|July 1, 2015
Intrahepatic Cholestasis of Pregnancy (ICP) in U.S. Latinas and Chileans: Clinical features, Ancestry Analysis, and Admixture MappingLaura N Bull, Donglei Hu, Sohela Shah, et al.
Nature Genetics|April 22, 2003
Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAATVictoria E H Carlton, Baruch Z Harris, Erik G Puffenberger, et al.
Pageof 4