Search research articles
Contact Us
Filters
Showing results (41-50 of 223) with videos related to
Page
of 23
Sort By:
The Journal of Biological Chemistry
|
August 10, 2014
Unprenylated RhoA contributes to IL-1β hypersecretion in mevalonate kinase deficiency model through stimulation of Rac1 activity
Robert van der Burgh, Kalliopi Pervolaraki, Marjolein Turkenburg, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
December 25, 2015
Absence of biochemical evidence at an early age delays diagnosis in a patient with a clinically severe peroxisomal biogenesis disorder
Natalia Lüsebrink, Luciana Porto, Hans R Waterham, et al.
Arthritis and Rheumatism
|
June 28, 2006
Manipulation of isoprenoid biosynthesis as a possible therapeutic option in mevalonate kinase deficiency
Marit S Schneiders, Sander M Houten, Marjolein Turkenburg, et al.
Pediatric Neurology
|
May 13, 2009
Mitochondrial trifunctional protein deficiency with recurrent rhabdomyolysis
Oded Scheuerman, Ronald J A Wanders, Hans R Waterham, et al.
Journal of Inherited Metabolic Disease
|
March 5, 2016
The important role of biochemical and functional studies in the diagnostics of peroxisomal disorders
Sacha Ferdinandusse, Merel S Ebberink, Frédéric M Vaz, et al.
JIMD Reports
|
August 13, 2016
The Challenges of a Successful Pregnancy in a Patient with Adult Refsum's Disease due to Phytanoyl-CoA Hydroxylase Deficiency
Karolina M Stepien, Anthony S Wierzbicki, Bwee T Poll-The, et al.
Brain : a Journal of Neurology
|
November 22, 2008
Plasmalogens participate in very-long-chain fatty acid-induced pathology
Pedro Brites, Petra A W Mooyer, Leila El Mrabet, et al.
Frontiers in Cell and Developmental Biology
|
January 28, 2021
Peroxisomal Metabolite and Cofactor Transport in Humans
Serhii Chornyi, Lodewijk IJlst, Carlo W T van Roermund, et al.
Journal of Inherited Metabolic Disease
|
May 22, 2010
The enzymology of mitochondrial fatty acid beta-oxidation and its application to follow-up analysis of positive neonatal screening results
Ronald J A Wanders, Jos P N Ruiter, Lodewijk IJLst, et al.
Blood
|
August 8, 2008
HMG-CoA reductase inhibition induces IL-1beta release through Rac1/PI3K/PKB-dependent caspase-1 activation
Loes M Kuijk, Jeffrey M Beekman, Janet Koster, et al.
Page
of 23
Search research articles
Search
Showing results (41-50 of 223) with videos related to
Sort By:
Page
of 23
The Journal of Biological Chemistry
|
August 10, 2014
Unprenylated RhoA contributes to IL-1β hypersecretion in mevalonate kinase deficiency model through stimulation of Rac1 activity
Robert van der Burgh, Kalliopi Pervolaraki, Marjolein Turkenburg, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
December 25, 2015
Absence of biochemical evidence at an early age delays diagnosis in a patient with a clinically severe peroxisomal biogenesis disorder
Natalia Lüsebrink, Luciana Porto, Hans R Waterham, et al.
Arthritis and Rheumatism
|
June 28, 2006
Manipulation of isoprenoid biosynthesis as a possible therapeutic option in mevalonate kinase deficiency
Marit S Schneiders, Sander M Houten, Marjolein Turkenburg, et al.
Pediatric Neurology
|
May 13, 2009
Mitochondrial trifunctional protein deficiency with recurrent rhabdomyolysis
Oded Scheuerman, Ronald J A Wanders, Hans R Waterham, et al.
Journal of Inherited Metabolic Disease
|
March 5, 2016
The important role of biochemical and functional studies in the diagnostics of peroxisomal disorders
Sacha Ferdinandusse, Merel S Ebberink, Frédéric M Vaz, et al.
JIMD Reports
|
August 13, 2016
The Challenges of a Successful Pregnancy in a Patient with Adult Refsum's Disease due to Phytanoyl-CoA Hydroxylase Deficiency
Karolina M Stepien, Anthony S Wierzbicki, Bwee T Poll-The, et al.
Brain : a Journal of Neurology
|
November 22, 2008
Plasmalogens participate in very-long-chain fatty acid-induced pathology
Pedro Brites, Petra A W Mooyer, Leila El Mrabet, et al.
Frontiers in Cell and Developmental Biology
|
January 28, 2021
Peroxisomal Metabolite and Cofactor Transport in Humans
Serhii Chornyi, Lodewijk IJlst, Carlo W T van Roermund, et al.
Journal of Inherited Metabolic Disease
|
May 22, 2010
The enzymology of mitochondrial fatty acid beta-oxidation and its application to follow-up analysis of positive neonatal screening results
Ronald J A Wanders, Jos P N Ruiter, Lodewijk IJLst, et al.
Blood
|
August 8, 2008
HMG-CoA reductase inhibition induces IL-1beta release through Rac1/PI3K/PKB-dependent caspase-1 activation
Loes M Kuijk, Jeffrey M Beekman, Janet Koster, et al.
Page
of 23