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Molecular Genetics and Metabolism
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June 29, 2013
Expanding research to provide an evidence base for nutritional interventions for the management of inborn errors of metabolism
Kathryn 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 hyperpermeability
Rudolf 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 action
Ann 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 Consortium
Jennifer 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 pulses
Akinobu 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> mutation
John 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 trials
Sandesh 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 decay
K 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 disorders
M 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 disorder
Brendan Lee, George A Diaz, William Rhead, et al.
Page
of 79
Search research articles
Search
Showing results (771-780 of 783) with videos related to
Sort By:
Page
of 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 metabolism
Kathryn 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 hyperpermeability
Rudolf 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 action
Ann 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 Consortium
Jennifer 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 pulses
Akinobu 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> mutation
John 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 trials
Sandesh 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 decay
K 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 disorders
M 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 disorder
Brendan Lee, George A Diaz, William Rhead, et al.
Page
of 79