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Hepatology (Baltimore, Md.)
|
July 24, 2020
Pharmacological Premature Termination Codon Readthrough of ABCB11 in Bile Salt Export Pump Deficiency: An In Vitro Study
Rachida Amzal, Alice Thébaut, Martine Lapalus, et al.
Liver International : Official Journal of the International Association for the Study of the Liver
|
September 16, 2005
Increase in liver antioxidant enzyme activities in non-alcoholic fatty liver disease
Gabriel Perlemuter, Anne Davit-Spraul, Claudine Cosson, et al.
Liver International : Official Journal of the International Association for the Study of the Liver
|
May 21, 2020
Functional rescue of an ABCB11 mutant by ivacaftor: A new targeted pharmacotherapy approach in bile salt export pump deficiency
Elodie Mareux, Martine Lapalus, Rachida Amzal, et al.
Hepatology (Baltimore, Md.)
|
December 31, 2013
MYO5B and bile salt export pump contribute to cholestatic liver disorder in microvillous inclusion disease
Muriel Girard, Florence Lacaille, Virginie Verkarre, et al.
Molecular Genetics and Metabolism
|
December 14, 2020
Adenosine kinase deficiency: Three new cases and diagnostic value of hypermethioninemia
Pierre-Hadrien Becker, Zeynep Demir, Yael Mozer Glassberg, et al.
Gut
|
February 7, 2019
TGR5-dependent hepatoprotection through the regulation of biliary epithelium barrier function
Grégory Merlen, Nicolas Kahale, Jose Ursic-Bedoya, et al.
JHEP Reports : Innovation in Hepatology
|
September 13, 2023
Outcomes of 38 patients with PFIC3: Impact of genotype and of response to ursodeoxycholic acid therapy
Emmanuel Gonzales, Antoine Gardin, Marion Almes, et al.
Orphanet Journal of Rare Diseases
|
December 7, 2023
∆<sup>4</sup>-3-oxo-5β-reductase deficiency: favorable outcome in 16 patients treated with cholic acid
Antoine Gardin, Mathias Ruiz, Jan Beime, et al.
Clinical Chemistry
|
December 6, 2021
Galaxy Is a Suitable Bioinformatics Platform for the Molecular Diagnosis of Human Genetic Disorders Using High-Throughput Sequencing Data Analysis: Five Years of Experience in a Clinical Laboratory
Kenneth Chappell, Bruno Francou, Christophe Habib, et al.
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of 3
Search research articles
Search
Showing results (21-30 of 29) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 29 results.
Hepatology (Baltimore, Md.)
|
July 24, 2020
Pharmacological Premature Termination Codon Readthrough of ABCB11 in Bile Salt Export Pump Deficiency: An In Vitro Study
Rachida Amzal, Alice Thébaut, Martine Lapalus, et al.
Liver International : Official Journal of the International Association for the Study of the Liver
|
September 16, 2005
Increase in liver antioxidant enzyme activities in non-alcoholic fatty liver disease
Gabriel Perlemuter, Anne Davit-Spraul, Claudine Cosson, et al.
Liver International : Official Journal of the International Association for the Study of the Liver
|
May 21, 2020
Functional rescue of an ABCB11 mutant by ivacaftor: A new targeted pharmacotherapy approach in bile salt export pump deficiency
Elodie Mareux, Martine Lapalus, Rachida Amzal, et al.
Hepatology (Baltimore, Md.)
|
December 31, 2013
MYO5B and bile salt export pump contribute to cholestatic liver disorder in microvillous inclusion disease
Muriel Girard, Florence Lacaille, Virginie Verkarre, et al.
Molecular Genetics and Metabolism
|
December 14, 2020
Adenosine kinase deficiency: Three new cases and diagnostic value of hypermethioninemia
Pierre-Hadrien Becker, Zeynep Demir, Yael Mozer Glassberg, et al.
Gut
|
February 7, 2019
TGR5-dependent hepatoprotection through the regulation of biliary epithelium barrier function
Grégory Merlen, Nicolas Kahale, Jose Ursic-Bedoya, et al.
JHEP Reports : Innovation in Hepatology
|
September 13, 2023
Outcomes of 38 patients with PFIC3: Impact of genotype and of response to ursodeoxycholic acid therapy
Emmanuel Gonzales, Antoine Gardin, Marion Almes, et al.
Orphanet Journal of Rare Diseases
|
December 7, 2023
∆<sup>4</sup>-3-oxo-5β-reductase deficiency: favorable outcome in 16 patients treated with cholic acid
Antoine Gardin, Mathias Ruiz, Jan Beime, et al.
Clinical Chemistry
|
December 6, 2021
Galaxy Is a Suitable Bioinformatics Platform for the Molecular Diagnosis of Human Genetic Disorders Using High-Throughput Sequencing Data Analysis: Five Years of Experience in a Clinical Laboratory
Kenneth Chappell, Bruno Francou, Christophe Habib, et al.
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of 3