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Cederbaum

Showing results (771-780 of 783) with videos related to

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Molecular Genetics and Metabolism|June 29, 2013
Expanding research to provide an evidence base for nutritional interventions for the management of inborn errors of metabolismKathryn M Camp, Michele A Lloyd-Puryear, Lynne Yao, et al.
American Journal of Respiratory Cell and Molecular Biology|May 15, 2012
Protein kinase C-α and arginase I mediate pneumolysin-induced pulmonary endothelial hyperpermeabilityRudolf Lucas, Guang Yang, Boris A Gorshkov, et al.
Plos One|May 8, 2012
Spiroindolines identify the vesicular acetylcholine transporter as a novel target for insecticide actionAnn Sluder, Sheetal Shah, Jérôme Cassayre, et al.
Molecular Genetics and Metabolism|March 2, 2010
Establishing a consortium for the study of rare diseases: The Urea Cycle Disorders ConsortiumJennifer Seminara, Mendel Tuchman, Lauren Krivitzky, et al.
The Journal of Chemical Physics|November 17, 2019
Electron spectroscopic study of nanoplasma formation triggered by intense soft x-ray pulsesAkinobu Niozu, Naomichi Yokono, Toshiyuki Nishiyama, et al.
Brain Communications|March 10, 2023
Characterization of spastic paraplegia in a family with a novel <i>PSEN1</i> mutationJohn M Ringman, Naghmeh Dorrani, Sara Gutiérrez Fernández, et al.
Molecular Genetics and Metabolism|August 23, 2015
Self-reported treatment-associated symptoms among patients with urea cycle disorders participating in glycerol phenylbutyrate clinical trialsSandesh C S Nagamani, George A Diaz, William Rhead, et al.
Physical Review Letters|August 8, 2009
Photo- and auger-electron recoil induced dynamics of interatomic Coulombic decayK Kreidi, Ph V Demekhin, T Jahnke, et al.
Molecular Genetics and Metabolism|September 11, 2012
Urinary phenylacetylglutamine as dosing biomarker for patients with urea cycle disordersM Mokhtarani, G A Diaz, W Rhead, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 16, 2014
Blood ammonia and glutamine as predictors of hyperammonemic crises in patients with urea cycle disorderBrendan Lee, George A Diaz, William Rhead, et al.
Pageof 79

Showing results (771-780 of 783) with videos related to

Sort By:
Pageof 79
Molecular Genetics and Metabolism|June 29, 2013
Expanding research to provide an evidence base for nutritional interventions for the management of inborn errors of metabolismKathryn M Camp, Michele A Lloyd-Puryear, Lynne Yao, et al.
American Journal of Respiratory Cell and Molecular Biology|May 15, 2012
Protein kinase C-α and arginase I mediate pneumolysin-induced pulmonary endothelial hyperpermeabilityRudolf Lucas, Guang Yang, Boris A Gorshkov, et al.
Plos One|May 8, 2012
Spiroindolines identify the vesicular acetylcholine transporter as a novel target for insecticide actionAnn Sluder, Sheetal Shah, Jérôme Cassayre, et al.
Molecular Genetics and Metabolism|March 2, 2010
Establishing a consortium for the study of rare diseases: The Urea Cycle Disorders ConsortiumJennifer Seminara, Mendel Tuchman, Lauren Krivitzky, et al.
The Journal of Chemical Physics|November 17, 2019
Electron spectroscopic study of nanoplasma formation triggered by intense soft x-ray pulsesAkinobu Niozu, Naomichi Yokono, Toshiyuki Nishiyama, et al.
Brain Communications|March 10, 2023
Characterization of spastic paraplegia in a family with a novel <i>PSEN1</i> mutationJohn M Ringman, Naghmeh Dorrani, Sara Gutiérrez Fernández, et al.
Molecular Genetics and Metabolism|August 23, 2015
Self-reported treatment-associated symptoms among patients with urea cycle disorders participating in glycerol phenylbutyrate clinical trialsSandesh C S Nagamani, George A Diaz, William Rhead, et al.
Physical Review Letters|August 8, 2009
Photo- and auger-electron recoil induced dynamics of interatomic Coulombic decayK Kreidi, Ph V Demekhin, T Jahnke, et al.
Molecular Genetics and Metabolism|September 11, 2012
Urinary phenylacetylglutamine as dosing biomarker for patients with urea cycle disordersM Mokhtarani, G A Diaz, W Rhead, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 16, 2014
Blood ammonia and glutamine as predictors of hyperammonemic crises in patients with urea cycle disorderBrendan Lee, George A Diaz, William Rhead, et al.
Pageof 79