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S W Sauer

Showing results (1-10 of 9) with videos related to

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Journal of Inherited Metabolic Disease|September 20, 2007
Biochemistry and bioenergetics of glutaryl-CoA dehydrogenase deficiencyS W Sauer
Annals of Emergency Medicine|June 1, 2001
Hydroxocobalamin: improved public health readiness for cyanide disastersS W Sauer, M E Keim
Journal of Inherited Metabolic Disease|October 17, 2006
The aetiology of neurological complications of organic acidaemias--a role for the blood-brain barrierS Kölker, S W Sauer, R A H Surtees, et al.
Journal of Inherited Metabolic Disease|October 10, 2009
Long-term exposure of human proximal tubule cells to hydroxycobalamin[c-lactam] as a possible model to study renal disease in methylmalonic aciduriasS W Sauer, S Opp, A Haarmann, et al.
Journal of Inherited Metabolic Disease|April 9, 2008
Pathogenesis of CNS involvement in disorders of amino and organic acid metabolismS Kölker, S W Sauer, G F Hoffmann, et al.
Human Molecular Genetics|October 1, 2015
Molecular and biochemical alterations in tubular epithelial cells of patients with isolated methylmalonic aciduriaT Ruppert, A Schumann, H J Gröne, et al.
Journal of Inherited Metabolic Disease|September 12, 2007
Neurodegeneration and chronic renal failure in methylmalonic aciduria--a pathophysiological approachM A Morath, J G Okun, I B Müller, et al.
FEBS Letters|December 10, 2013
TNF-α mediates mitochondrial uncoupling and enhances ROS-dependent cell migration via NF-κB activation in liver cellsL Kastl, S W Sauer, T Ruppert, et al.
Neurochemistry International|February 17, 2007
Enzymatic and metabolic evidence for a region specific mitochondrial dysfunction in brains of murine succinic semialdehyde dehydrogenase deficiency (Aldh5a1-/- mice)S W Sauer, S Kölker, G F Hoffmann, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Journal of Inherited Metabolic Disease|September 20, 2007
Biochemistry and bioenergetics of glutaryl-CoA dehydrogenase deficiencyS W Sauer
Annals of Emergency Medicine|June 1, 2001
Hydroxocobalamin: improved public health readiness for cyanide disastersS W Sauer, M E Keim
Journal of Inherited Metabolic Disease|October 17, 2006
The aetiology of neurological complications of organic acidaemias--a role for the blood-brain barrierS Kölker, S W Sauer, R A H Surtees, et al.
Journal of Inherited Metabolic Disease|October 10, 2009
Long-term exposure of human proximal tubule cells to hydroxycobalamin[c-lactam] as a possible model to study renal disease in methylmalonic aciduriasS W Sauer, S Opp, A Haarmann, et al.
Journal of Inherited Metabolic Disease|April 9, 2008
Pathogenesis of CNS involvement in disorders of amino and organic acid metabolismS Kölker, S W Sauer, G F Hoffmann, et al.
Human Molecular Genetics|October 1, 2015
Molecular and biochemical alterations in tubular epithelial cells of patients with isolated methylmalonic aciduriaT Ruppert, A Schumann, H J Gröne, et al.
Journal of Inherited Metabolic Disease|September 12, 2007
Neurodegeneration and chronic renal failure in methylmalonic aciduria--a pathophysiological approachM A Morath, J G Okun, I B Müller, et al.
FEBS Letters|December 10, 2013
TNF-α mediates mitochondrial uncoupling and enhances ROS-dependent cell migration via NF-κB activation in liver cellsL Kastl, S W Sauer, T Ruppert, et al.
Neurochemistry International|February 17, 2007
Enzymatic and metabolic evidence for a region specific mitochondrial dysfunction in brains of murine succinic semialdehyde dehydrogenase deficiency (Aldh5a1-/- mice)S W Sauer, S Kölker, G F Hoffmann, et al.
Pageof 1