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M Duran

Showing results (521-530 of 646) with videos related to

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Optics Express|September 15, 2015
Dynamics of noise-like pulsing at sub-ns scale in a passively mode-locked fiber laserH Santiago-Hernandez, O Pottiez, M Duran-Sanchez, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
Familial hypoketotic hypoglycaemia associated with peripheral neuropathy, pigmentary retinopathy and C6-C14 hydroxydicarboxylic aciduria. A new defect in fatty acid oxidation?B T Poll-The, J P Bonnefont, H Ogier, et al.
Clinical and Translational Science|October 17, 2012
A characterization and targeting of the infarct border zone in a swine model of myocardial infarctionJason M Duran, Sharven Taghavi, Remus M Berretta, et al.
Scientific Reports|March 24, 2016
Nuquantus: Machine learning software for the characterization and quantification of cell nuclei in complex immunofluorescent tissue imagesPolina Gross, Nicolas Honnorat, Erdem Varol, et al.
Journal of Agricultural and Food Chemistry|August 18, 2017
X-ray Spectroscopy Uncovering the Effects of Cu Based Nanoparticle Concentration and Structure on Phaseolus vulgaris Germination and Seedling DevelopmentNádia M Duran, Susilaine M Savassa, Rafael Giovanini de Lima, et al.
Applied Microbiology and Biotechnology|March 4, 2014
The role of Aspergillus flavus veA in the production of extracellular proteins during growth on starch substratesRocio M Duran, Scott Gregersen, Timothy D Smith, et al.
Biorxiv : the Preprint Server for Biology|April 10, 2026
Carbapenem-resistant <i>Klebsiella pneumoniae</i> lineage CG307 displays urinary tract tropismKyle D Buchan, Jesus M Duran Ramirez, Jana Gomez, et al.
Annals of Neurology|July 1, 1992
L-2-hydroxyglutaric acidemia: a novel inherited neurometabolic diseaseP G Barth, G F Hoffmann, J Jaeken, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Early signs and course of disease of glutaryl-CoA dehydrogenase deficiencyG F Hoffmann, H J Böhles, A Burlina, et al.
Journal of Inherited Metabolic Disease|January 1, 1983
Absence of hepatic molybdenum cofactor: an inborn error of metabolism leading to a combined deficiency of sulphite oxidase and xanthine dehydrogenaseS K Wadman, M Duran, F A Beemer, et al.
Pageof 65

Showing results (521-530 of 646) with videos related to

Sort By:
Pageof 65
Optics Express|September 15, 2015
Dynamics of noise-like pulsing at sub-ns scale in a passively mode-locked fiber laserH Santiago-Hernandez, O Pottiez, M Duran-Sanchez, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
Familial hypoketotic hypoglycaemia associated with peripheral neuropathy, pigmentary retinopathy and C6-C14 hydroxydicarboxylic aciduria. A new defect in fatty acid oxidation?B T Poll-The, J P Bonnefont, H Ogier, et al.
Clinical and Translational Science|October 17, 2012
A characterization and targeting of the infarct border zone in a swine model of myocardial infarctionJason M Duran, Sharven Taghavi, Remus M Berretta, et al.
Scientific Reports|March 24, 2016
Nuquantus: Machine learning software for the characterization and quantification of cell nuclei in complex immunofluorescent tissue imagesPolina Gross, Nicolas Honnorat, Erdem Varol, et al.
Journal of Agricultural and Food Chemistry|August 18, 2017
X-ray Spectroscopy Uncovering the Effects of Cu Based Nanoparticle Concentration and Structure on Phaseolus vulgaris Germination and Seedling DevelopmentNádia M Duran, Susilaine M Savassa, Rafael Giovanini de Lima, et al.
Applied Microbiology and Biotechnology|March 4, 2014
The role of Aspergillus flavus veA in the production of extracellular proteins during growth on starch substratesRocio M Duran, Scott Gregersen, Timothy D Smith, et al.
Biorxiv : the Preprint Server for Biology|April 10, 2026
Carbapenem-resistant <i>Klebsiella pneumoniae</i> lineage CG307 displays urinary tract tropismKyle D Buchan, Jesus M Duran Ramirez, Jana Gomez, et al.
Annals of Neurology|July 1, 1992
L-2-hydroxyglutaric acidemia: a novel inherited neurometabolic diseaseP G Barth, G F Hoffmann, J Jaeken, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Early signs and course of disease of glutaryl-CoA dehydrogenase deficiencyG F Hoffmann, H J Böhles, A Burlina, et al.
Journal of Inherited Metabolic Disease|January 1, 1983
Absence of hepatic molybdenum cofactor: an inborn error of metabolism leading to a combined deficiency of sulphite oxidase and xanthine dehydrogenaseS K Wadman, M Duran, F A Beemer, et al.
Pageof 65