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Sven W Sauer

Showing results (11-20 of 26) with videos related to

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Biochimica Et Biophysica Acta|January 7, 2015
Multifactorial modulation of susceptibility to l-lysine in an animal model of glutaric aciduria type ISven W Sauer, Silvana Opp, Shoko Komatsuzaki, et al.
Journal of Inherited Metabolic Disease|September 13, 2014
Understanding cerebral L-lysine metabolism: the role of L-pipecolate metabolism in Gcdh-deficient mice as a model for glutaric aciduria type IRoland Posset, Silvana Opp, Eduard A Struys, et al.
Biochimica Et Biophysica Acta|March 23, 2010
Glutaric aciduria type I and methylmalonic aciduria: simulation of cerebral import and export of accumulating neurotoxic dicarboxylic acids in in vitro models of the blood-brain barrier and the choroid plexusSven W Sauer, Silvana Opp, Anne Mahringer, et al.
The Journal of Biological Chemistry|April 21, 2005
Bioenergetics in glutaryl-coenzyme A dehydrogenase deficiency: a role for glutaryl-coenzyme ASven W Sauer, Jürgen G Okun, Marina A Schwab, et al.
Plos One|April 18, 2019
QDPR homologues in Danio rerio regulate melanin synthesis, early gliogenesis, and glutamine homeostasisMaximilian Breuer, Luca Guglielmi, Matthias Zielonka, et al.
Cell Reports|November 22, 2012
T cell activation is driven by an ADP-dependent glucokinase linking enhanced glycolysis with mitochondrial reactive oxygen species generationMarcin M Kamiński, Sven W Sauer, Marian Kamiński, et al.
Iucrj|July 23, 2020
Crystal structure and interaction studies of human DHTKD1 provide insight into a mitochondrial megacomplex in lysine catabolismGustavo A Bezerra, William R Foster, Henry J Bailey, et al.
Biochimica Et Biophysica Acta|March 20, 2008
Transport and distribution of 3-hydroxyglutaric acid before and during induced encephalopathic crises in a mouse model of glutaric aciduria type 1Britta Keyser, Markus Glatzel, Franziska Stellmer, et al.
American Journal of Human Genetics|November 13, 2012
DHTKD1 mutations cause 2-aminoadipic and 2-oxoadipic aciduriaKatharina Danhauser, Sven W Sauer, Tobias B Haack, et al.
Journal of Neurochemistry|April 1, 2006
Intracerebral accumulation of glutaric and 3-hydroxyglutaric acids secondary to limited flux across the blood-brain barrier constitute a biochemical risk factor for neurodegeneration in glutaryl-CoA dehydrogenase deficiencySven W Sauer, Jürgen G Okun, Gert Fricker, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
Biochimica Et Biophysica Acta|January 7, 2015
Multifactorial modulation of susceptibility to l-lysine in an animal model of glutaric aciduria type ISven W Sauer, Silvana Opp, Shoko Komatsuzaki, et al.
Journal of Inherited Metabolic Disease|September 13, 2014
Understanding cerebral L-lysine metabolism: the role of L-pipecolate metabolism in Gcdh-deficient mice as a model for glutaric aciduria type IRoland Posset, Silvana Opp, Eduard A Struys, et al.
Biochimica Et Biophysica Acta|March 23, 2010
Glutaric aciduria type I and methylmalonic aciduria: simulation of cerebral import and export of accumulating neurotoxic dicarboxylic acids in in vitro models of the blood-brain barrier and the choroid plexusSven W Sauer, Silvana Opp, Anne Mahringer, et al.
The Journal of Biological Chemistry|April 21, 2005
Bioenergetics in glutaryl-coenzyme A dehydrogenase deficiency: a role for glutaryl-coenzyme ASven W Sauer, Jürgen G Okun, Marina A Schwab, et al.
Plos One|April 18, 2019
QDPR homologues in Danio rerio regulate melanin synthesis, early gliogenesis, and glutamine homeostasisMaximilian Breuer, Luca Guglielmi, Matthias Zielonka, et al.
Cell Reports|November 22, 2012
T cell activation is driven by an ADP-dependent glucokinase linking enhanced glycolysis with mitochondrial reactive oxygen species generationMarcin M Kamiński, Sven W Sauer, Marian Kamiński, et al.
Iucrj|July 23, 2020
Crystal structure and interaction studies of human DHTKD1 provide insight into a mitochondrial megacomplex in lysine catabolismGustavo A Bezerra, William R Foster, Henry J Bailey, et al.
Biochimica Et Biophysica Acta|March 20, 2008
Transport and distribution of 3-hydroxyglutaric acid before and during induced encephalopathic crises in a mouse model of glutaric aciduria type 1Britta Keyser, Markus Glatzel, Franziska Stellmer, et al.
American Journal of Human Genetics|November 13, 2012
DHTKD1 mutations cause 2-aminoadipic and 2-oxoadipic aciduriaKatharina Danhauser, Sven W Sauer, Tobias B Haack, et al.
Journal of Neurochemistry|April 1, 2006
Intracerebral accumulation of glutaric and 3-hydroxyglutaric acids secondary to limited flux across the blood-brain barrier constitute a biochemical risk factor for neurodegeneration in glutaryl-CoA dehydrogenase deficiencySven W Sauer, Jürgen G Okun, Gert Fricker, et al.
Pageof 3