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M Duran

Showing results (581-590 of 646) with videos related to

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Human Molecular Genetics|July 13, 1999
Identification and characterization of three novel missense mutations in mevalonate kinase cDNA causing mevalonic aciduria, a disorder of isoprene biosynthesisS M Houten, G J Romeijn, J Koster, et al.
The EMBO Journal|November 27, 2012
Sphingomyelin organization is required for vesicle biogenesis at the Golgi complexJuan M Duran, Felix Campelo, Josse van Galen, et al.
The Journal of Trauma and Acute Care Surgery|August 1, 2012
Still making the case against prehospital intubation: a rat hemorrhagic shock modelSharven Taghavi, Jason M Duran, Senthil Jayarajan, et al.
American Journal of Human Genetics|July 31, 1998
Smith-Lemli-Opitz syndrome is caused by mutations in the 7-dehydrocholesterol reductase geneH R Waterham, F A Wijburg, R C Hennekam, et al.
Journal of Inherited Metabolic Disease|January 1, 1985
Dihydropyrimidine dehydrogenase deficiency leading to thymine-uraciluria. An inborn error of pyrimidine metabolismS K Wadman, R Berger, M Duran, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 31, 1984
Dihydropyrimidine dehydrogenase deficiency leading to thymine-uraciluria. An inborn error of pyrimidine metabolismR Berger, S A Stoker-de Vries, S K Wadman, et al.
Journal of Inherited Metabolic Disease|July 15, 2000
Mevalonic aciduria in 12 unrelated patients with hyperimmunoglobulinaemia D and periodic fever syndromeB T Poll-The, J Frenkel, S M Houten, et al.
Frontiers in Plant Science|November 30, 2018
Laboratory Microprobe X-Ray Fluorescence in Plant Science: Emerging Applications and Case StudiesEduardo S Rodrigues, Marcos H F Gomes, Nádia M Duran, et al.
Journal of Inherited Metabolic Disease|September 16, 2003
High activity of fatty acid oxidation enzymes in human placenta: implications for fetal-maternal diseaseN A Oey, M E J den Boer, J P N Ruiter, et al.
Journal of Inherited Metabolic Disease|November 5, 1997
L-2-Hydroxyglutaric aciduria: normal L-2-hydroxyglutarate dehydrogenase activity in liver from two new patientsR J Wanders, L Vilarinho, H P Hartung, et al.
Pageof 65

Showing results (581-590 of 646) with videos related to

Sort By:
Pageof 65
Human Molecular Genetics|July 13, 1999
Identification and characterization of three novel missense mutations in mevalonate kinase cDNA causing mevalonic aciduria, a disorder of isoprene biosynthesisS M Houten, G J Romeijn, J Koster, et al.
The EMBO Journal|November 27, 2012
Sphingomyelin organization is required for vesicle biogenesis at the Golgi complexJuan M Duran, Felix Campelo, Josse van Galen, et al.
The Journal of Trauma and Acute Care Surgery|August 1, 2012
Still making the case against prehospital intubation: a rat hemorrhagic shock modelSharven Taghavi, Jason M Duran, Senthil Jayarajan, et al.
American Journal of Human Genetics|July 31, 1998
Smith-Lemli-Opitz syndrome is caused by mutations in the 7-dehydrocholesterol reductase geneH R Waterham, F A Wijburg, R C Hennekam, et al.
Journal of Inherited Metabolic Disease|January 1, 1985
Dihydropyrimidine dehydrogenase deficiency leading to thymine-uraciluria. An inborn error of pyrimidine metabolismS K Wadman, R Berger, M Duran, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 31, 1984
Dihydropyrimidine dehydrogenase deficiency leading to thymine-uraciluria. An inborn error of pyrimidine metabolismR Berger, S A Stoker-de Vries, S K Wadman, et al.
Journal of Inherited Metabolic Disease|July 15, 2000
Mevalonic aciduria in 12 unrelated patients with hyperimmunoglobulinaemia D and periodic fever syndromeB T Poll-The, J Frenkel, S M Houten, et al.
Frontiers in Plant Science|November 30, 2018
Laboratory Microprobe X-Ray Fluorescence in Plant Science: Emerging Applications and Case StudiesEduardo S Rodrigues, Marcos H F Gomes, Nádia M Duran, et al.
Journal of Inherited Metabolic Disease|September 16, 2003
High activity of fatty acid oxidation enzymes in human placenta: implications for fetal-maternal diseaseN A Oey, M E J den Boer, J P N Ruiter, et al.
Journal of Inherited Metabolic Disease|November 5, 1997
L-2-Hydroxyglutaric aciduria: normal L-2-hydroxyglutarate dehydrogenase activity in liver from two new patientsR J Wanders, L Vilarinho, H P Hartung, et al.
Pageof 65