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C Jakobs

Showing results (131-140 of 417) with videos related to

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Clinica Chimica Acta; International Journal of Clinical Chemistry|August 31, 1993
Bile acid metabolism in three patients with mevalonic aciduria due to mevalonate kinase deficiencyK M Gibson, F Stellaard, G F Hoffmann, et al.
Experimental Eye Research|October 7, 2022
Microglia depletion exacerbates retinal ganglion cell loss in a mouse model of glaucomaZizhu Tan, Yinjie Guo, Maleeka Shrestha, et al.
Biochimica Et Biophysica Acta|June 20, 1998
Pristanic acid beta-oxidation in peroxisomal disorders: studies in cultured human fibroblastsN M Verhoeven, D S Schor, C R Roe, et al.
Biochimica Et Biophysica Acta|December 31, 1997
Phytanic acid alpha-oxidation in peroxisomal disorders: studies in cultured human fibroblastsN M Verhoeven, D S Schor, C R Roe, et al.
Pediatric Research|July 1, 1996
Relative kinetics of phenylalanine and leucine in low birth weight infants during nutrient administrationL van Toledo-Eppinga, S C Kalhan, W Kulik, et al.
Annals of Clinical Biochemistry|March 1, 1994
Heterogeneity in di/trihydroxycholestanoic acidaemiaH J ten Brink, R J Wanders, E Christensen, et al.
The Journal of Pediatrics|September 1, 1992
Familial hypotonia of childhood caused by isolated 3-methylcrotonyl-coenzyme A carboxylase deficiencyO N Elpeleg, S Havkin, V Barash, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
4-Hydroxybutyric aciduria: a new inborn error of metabolism. I. Clinical reviewD Rating, F Hanefeld, H Siemes, et al.
Annals of Neurology|July 14, 2000
Pipecolic acid elevation in plasma and cerebrospinal fluid of two patients with pyridoxine-dependent epilepsyB Plecko, S Stöckler-Ipsiroglu, E Paschke, et al.
Biochimica Et Biophysica Acta|September 14, 1999
Identification of amino acids responsible for the oxygen sensitivity of ferredoxins from Anabaena variabilis using site-directed mutagenesisB B Singh, I Curdt, C Jakobs, et al.
Pageof 42

Showing results (131-140 of 417) with videos related to

Sort By:
Pageof 42
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 31, 1993
Bile acid metabolism in three patients with mevalonic aciduria due to mevalonate kinase deficiencyK M Gibson, F Stellaard, G F Hoffmann, et al.
Experimental Eye Research|October 7, 2022
Microglia depletion exacerbates retinal ganglion cell loss in a mouse model of glaucomaZizhu Tan, Yinjie Guo, Maleeka Shrestha, et al.
Biochimica Et Biophysica Acta|June 20, 1998
Pristanic acid beta-oxidation in peroxisomal disorders: studies in cultured human fibroblastsN M Verhoeven, D S Schor, C R Roe, et al.
Biochimica Et Biophysica Acta|December 31, 1997
Phytanic acid alpha-oxidation in peroxisomal disorders: studies in cultured human fibroblastsN M Verhoeven, D S Schor, C R Roe, et al.
Pediatric Research|July 1, 1996
Relative kinetics of phenylalanine and leucine in low birth weight infants during nutrient administrationL van Toledo-Eppinga, S C Kalhan, W Kulik, et al.
Annals of Clinical Biochemistry|March 1, 1994
Heterogeneity in di/trihydroxycholestanoic acidaemiaH J ten Brink, R J Wanders, E Christensen, et al.
The Journal of Pediatrics|September 1, 1992
Familial hypotonia of childhood caused by isolated 3-methylcrotonyl-coenzyme A carboxylase deficiencyO N Elpeleg, S Havkin, V Barash, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
4-Hydroxybutyric aciduria: a new inborn error of metabolism. I. Clinical reviewD Rating, F Hanefeld, H Siemes, et al.
Annals of Neurology|July 14, 2000
Pipecolic acid elevation in plasma and cerebrospinal fluid of two patients with pyridoxine-dependent epilepsyB Plecko, S Stöckler-Ipsiroglu, E Paschke, et al.
Biochimica Et Biophysica Acta|September 14, 1999
Identification of amino acids responsible for the oxygen sensitivity of ferredoxins from Anabaena variabilis using site-directed mutagenesisB B Singh, I Curdt, C Jakobs, et al.
Pageof 42