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International Journal of Neonatal Screening
|
April 25, 2022
A New Approach to Objectively Evaluate Inherited Metabolic Diseases for Inclusion on Newborn Screening Programmes
Alberto Burlina, Simon A Jones, Anupam Chakrapani, et al.
Skeletal Muscle
|
January 20, 2012
TNF-α- and tumor-induced skeletal muscle atrophy involves sphingolipid metabolism
Joffrey De Larichaudy, Alessandra Zufferli, Filippo Serra, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 26, 2023
Autosomal dominant Zellweger spectrum disorder caused by de novo variants in PEX14 gene
Hans R Waterham, Janet Koster, Merel S Ebberink, et al.
Plos One
|
May 30, 2008
Early neurodegeneration progresses independently of microglial activation by heparan sulfate in the brain of mucopolysaccharidosis IIIB mice
Jérôme Ausseil, Nathalie Desmaris, Stéphanie Bigou, et al.
Electrophoresis
|
June 6, 2018
Complementarity of electrophoretic, mass spectrometric, and gene sequencing techniques for the diagnosis and characterization of congenital disorders of glycosylation
Arnaud Bruneel, Sophie Cholet, Valérie Drouin-Garraud, et al.
The Journal of Nutrition
|
July 3, 2015
Milk Polar Lipids Affect In Vitro Digestive Lipolysis and Postprandial Lipid Metabolism in Mice
Manon Lecomte, Claire Bourlieu, Emmanuelle Meugnier, et al.
Biochimie
|
November 7, 2015
Creatine biosynthesis and transport in health and disease
Marie Joncquel-Chevalier Curt, Pia-Manuela Voicu, Monique Fontaine, et al.
The Journal of Nutritional Biochemistry
|
January 28, 2019
Acute effects of milk polar lipids on intestinal tight junction expression: towards an impact of sphingomyelin through the regulation of IL-8 secretion?
Marine Milard, Armelle Penhoat, Annie Durand, et al.
Molecular Genetics and Metabolism
|
February 27, 2018
Functional assessment of creatine transporter in control and X-linked SLC6A8-deficient fibroblasts
Marie Joncquel-Chevalier Curt, Marie-Adélaïde Bout, Monique Fontaine, et al.
Plos One
|
July 28, 2017
LC-MS/MS multiplex analysis of lysosphingolipids in plasma and amniotic fluid: A novel tool for the screening of sphingolipidoses and Niemann-Pick type C disease
Magali Pettazzoni, Roseline Froissart, Cécile Pagan, et al.
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of 8
Search research articles
Search
Showing results (31-40 of 74) with videos related to
Sort By:
Page
of 8
International Journal of Neonatal Screening
|
April 25, 2022
A New Approach to Objectively Evaluate Inherited Metabolic Diseases for Inclusion on Newborn Screening Programmes
Alberto Burlina, Simon A Jones, Anupam Chakrapani, et al.
Skeletal Muscle
|
January 20, 2012
TNF-α- and tumor-induced skeletal muscle atrophy involves sphingolipid metabolism
Joffrey De Larichaudy, Alessandra Zufferli, Filippo Serra, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 26, 2023
Autosomal dominant Zellweger spectrum disorder caused by de novo variants in PEX14 gene
Hans R Waterham, Janet Koster, Merel S Ebberink, et al.
Plos One
|
May 30, 2008
Early neurodegeneration progresses independently of microglial activation by heparan sulfate in the brain of mucopolysaccharidosis IIIB mice
Jérôme Ausseil, Nathalie Desmaris, Stéphanie Bigou, et al.
Electrophoresis
|
June 6, 2018
Complementarity of electrophoretic, mass spectrometric, and gene sequencing techniques for the diagnosis and characterization of congenital disorders of glycosylation
Arnaud Bruneel, Sophie Cholet, Valérie Drouin-Garraud, et al.
The Journal of Nutrition
|
July 3, 2015
Milk Polar Lipids Affect In Vitro Digestive Lipolysis and Postprandial Lipid Metabolism in Mice
Manon Lecomte, Claire Bourlieu, Emmanuelle Meugnier, et al.
Biochimie
|
November 7, 2015
Creatine biosynthesis and transport in health and disease
Marie Joncquel-Chevalier Curt, Pia-Manuela Voicu, Monique Fontaine, et al.
The Journal of Nutritional Biochemistry
|
January 28, 2019
Acute effects of milk polar lipids on intestinal tight junction expression: towards an impact of sphingomyelin through the regulation of IL-8 secretion?
Marine Milard, Armelle Penhoat, Annie Durand, et al.
Molecular Genetics and Metabolism
|
February 27, 2018
Functional assessment of creatine transporter in control and X-linked SLC6A8-deficient fibroblasts
Marie Joncquel-Chevalier Curt, Marie-Adélaïde Bout, Monique Fontaine, et al.
Plos One
|
July 28, 2017
LC-MS/MS multiplex analysis of lysosphingolipids in plasma and amniotic fluid: A novel tool for the screening of sphingolipidoses and Niemann-Pick type C disease
Magali Pettazzoni, Roseline Froissart, Cécile Pagan, et al.
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of 8