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Optics Express
|
September 15, 2015
Dynamics of noise-like pulsing at sub-ns scale in a passively mode-locked fiber laser
H 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 infarction
Jason 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 images
Polina 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 Development
Nádia 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 substrates
Rocio 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 tropism
Kyle D Buchan, Jesus M Duran Ramirez, Jana Gomez, et al.
Annals of Neurology
|
July 1, 1992
L-2-hydroxyglutaric acidemia: a novel inherited neurometabolic disease
P 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 deficiency
G 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 dehydrogenase
S K Wadman, M Duran, F A Beemer, et al.
Page
of 65
Search research articles
Search
Showing results (521-530 of 646) with videos related to
Sort By:
Page
of 65
Optics Express
|
September 15, 2015
Dynamics of noise-like pulsing at sub-ns scale in a passively mode-locked fiber laser
H 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 infarction
Jason 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 images
Polina 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 Development
Nádia 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 substrates
Rocio 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 tropism
Kyle D Buchan, Jesus M Duran Ramirez, Jana Gomez, et al.
Annals of Neurology
|
July 1, 1992
L-2-hydroxyglutaric acidemia: a novel inherited neurometabolic disease
P 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 deficiency
G 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 dehydrogenase
S K Wadman, M Duran, F A Beemer, et al.
Page
of 65