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Showing results (1141-1150 of 1,983) with videos related to

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Molecular Genetics and Metabolism|September 5, 2002
Structure of human succinic semialdehyde dehydrogenase gene: identification of promoter region and alternatively processed isoformsPaola Blasi, Pietro Pilo Boyl, Mario Ledda, et al.
Journal of Lipid Research|January 1, 1997
Quantitative analysis of plasma acylcarnitines using gas chromatography chemical ionization mass fragmentographyC G Costa, E A Struys, A Bootsma, et al.
Neurology|November 18, 1998
Defective peroxisome biogenesis with a neuromuscular disorder resembling Werdnig-Hoffmann diseaseM R Baumgartner, N M Verhoeven, C Jakobs, et al.
Annals of Neurology|July 23, 2005
Mutations in phenotypically mild D-2-hydroxyglutaric aciduriaEduard A Struys, Stanley H Korman, Gajja S Salomons, et al.
Cardiovascular Drugs and Therapy|September 17, 2020
Metformin Is Associated with Reduced Tissue Factor Procoagulant Activity in Patients with Poorly Controlled DiabetesMarco Witkowski, Julian Friebel, Termeh Tabaraie, et al.
Cellular Signalling|May 14, 2003
Inhibition of Ca(2+) signalling by the sphingosine 1-phosphate receptor S1P(1)Dagmar Meyer zu Heringdorf, Myriam E M Vincent, Matthias Lipinski, et al.
Molecular Genetics and Metabolism|February 4, 2009
Screening for X-linked creatine transporter (SLC6A8) deficiency via simultaneous determination of urinary creatine to creatinine ratio by tandem mass-spectrometrySaadet Mercimek-Mahmutoglu, Adolf Muehl, Gajja S Salomons, et al.
ACS Nano|August 27, 2015
Expression-Enhanced Fluorescent Proteins Based on Enhanced Green Fluorescent Protein for Super-resolution MicroscopySam Duwé, Elke De Zitter, Vincent Gielen, et al.
Gigascience|May 30, 2019
Map and model-moving from observation to prediction in toxicogenomicsAndreas Schüttler, Rolf Altenburger, Madeleine Ammar, et al.
Human Genetics|September 1, 1995
Molecular basis of phenotypic variation in patients with argininemiaT Uchino, S E Snyderman, M Lambert, et al.
Pageof 199

Showing results (1141-1150 of 1,983) with videos related to

Sort By:
Pageof 199
Molecular Genetics and Metabolism|September 5, 2002
Structure of human succinic semialdehyde dehydrogenase gene: identification of promoter region and alternatively processed isoformsPaola Blasi, Pietro Pilo Boyl, Mario Ledda, et al.
Journal of Lipid Research|January 1, 1997
Quantitative analysis of plasma acylcarnitines using gas chromatography chemical ionization mass fragmentographyC G Costa, E A Struys, A Bootsma, et al.
Neurology|November 18, 1998
Defective peroxisome biogenesis with a neuromuscular disorder resembling Werdnig-Hoffmann diseaseM R Baumgartner, N M Verhoeven, C Jakobs, et al.
Annals of Neurology|July 23, 2005
Mutations in phenotypically mild D-2-hydroxyglutaric aciduriaEduard A Struys, Stanley H Korman, Gajja S Salomons, et al.
Cardiovascular Drugs and Therapy|September 17, 2020
Metformin Is Associated with Reduced Tissue Factor Procoagulant Activity in Patients with Poorly Controlled DiabetesMarco Witkowski, Julian Friebel, Termeh Tabaraie, et al.
Cellular Signalling|May 14, 2003
Inhibition of Ca(2+) signalling by the sphingosine 1-phosphate receptor S1P(1)Dagmar Meyer zu Heringdorf, Myriam E M Vincent, Matthias Lipinski, et al.
Molecular Genetics and Metabolism|February 4, 2009
Screening for X-linked creatine transporter (SLC6A8) deficiency via simultaneous determination of urinary creatine to creatinine ratio by tandem mass-spectrometrySaadet Mercimek-Mahmutoglu, Adolf Muehl, Gajja S Salomons, et al.
ACS Nano|August 27, 2015
Expression-Enhanced Fluorescent Proteins Based on Enhanced Green Fluorescent Protein for Super-resolution MicroscopySam Duwé, Elke De Zitter, Vincent Gielen, et al.
Gigascience|May 30, 2019
Map and model-moving from observation to prediction in toxicogenomicsAndreas Schüttler, Rolf Altenburger, Madeleine Ammar, et al.
Human Genetics|September 1, 1995
Molecular basis of phenotypic variation in patients with argininemiaT Uchino, S E Snyderman, M Lambert, et al.
Pageof 199