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Feigenbaum

Showing results (681-690 of 761) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 11, 2012
Achieving the "triple aim" for inborn errors of metabolism: a review of challenges to outcomes research and presentation of a new practice-based evidence frameworkBeth K Potter, Pranesh Chakraborty, Jonathan B Kronick, et al.
Sports (Basel, Switzerland)|January 22, 2024
Exposures to Elevated Core Temperatures during Football Training: The Impact on Autonomic Nervous System Recovery and FunctionEric Renaghan, Harrison L Wittels, Luis A Feigenbaum, et al.
Journal of Functional Morphology and Kinesiology|September 27, 2023
Exercise Cardiac Load and Autonomic Nervous System Recovery during In-Season Training: The Impact on Speed Deterioration in American Football AthletesEric Renaghan, Harrison L Wittels, Luis A Feigenbaum, et al.
The Biochemical Journal|November 1, 2008
The selenocysteine tRNA STAF-binding region is essential for adequate selenocysteine tRNA status, selenoprotein expression and early age survival of miceBradley A Carlson, Ulrich Schweizer, Christine Perella, et al.
Pediatric Neurology|June 13, 2009
Rolandic mitochondrial encephalomyelopathy and MT-ND3 mutationsKlaus G E Werner, Chantal F Morel, Adam Kirton, et al.
European Journal of Immunology|September 8, 2009
Accelerated thymic atrophy as a result of elevated homeostatic expression of the genes encoded by the TNF/lymphotoxin cytokine locusDmitry J Liepinsh, Andrei A Kruglov, Arthur R Galimov, et al.
Annals of Neurology|September 3, 2002
Mitochondrial DNA depletion and dGK gene mutationsLeonardo Salviati, Sabrina Sacconi, Michelangelo Mancuso, et al.
Molecular Genetics and Metabolism Reports|March 18, 2021
Arginine to ornithine ratio as a diagnostic marker in patients with positive newborn screening for hyperargininemiaYue Huang, Rajesh Sharma, Annette Feigenbaum, et al.
American Journal of Medical Genetics. Part A|March 8, 2021
Aicardi-Goutières syndrome may present with positive newborn screen for X-linked adrenoleukodystrophyChristina G Tise, Jose Andres Morales, Ariel S Lee, et al.
Blood|October 26, 2010
A novel role for IL-22R1 as a driver of inflammationRam Savan, Adelle P McFarland, Della A Reynolds, et al.
Pageof 77

Showing results (681-690 of 761) with videos related to

Sort By:
Pageof 77
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 11, 2012
Achieving the "triple aim" for inborn errors of metabolism: a review of challenges to outcomes research and presentation of a new practice-based evidence frameworkBeth K Potter, Pranesh Chakraborty, Jonathan B Kronick, et al.
Sports (Basel, Switzerland)|January 22, 2024
Exposures to Elevated Core Temperatures during Football Training: The Impact on Autonomic Nervous System Recovery and FunctionEric Renaghan, Harrison L Wittels, Luis A Feigenbaum, et al.
Journal of Functional Morphology and Kinesiology|September 27, 2023
Exercise Cardiac Load and Autonomic Nervous System Recovery during In-Season Training: The Impact on Speed Deterioration in American Football AthletesEric Renaghan, Harrison L Wittels, Luis A Feigenbaum, et al.
The Biochemical Journal|November 1, 2008
The selenocysteine tRNA STAF-binding region is essential for adequate selenocysteine tRNA status, selenoprotein expression and early age survival of miceBradley A Carlson, Ulrich Schweizer, Christine Perella, et al.
Pediatric Neurology|June 13, 2009
Rolandic mitochondrial encephalomyelopathy and MT-ND3 mutationsKlaus G E Werner, Chantal F Morel, Adam Kirton, et al.
European Journal of Immunology|September 8, 2009
Accelerated thymic atrophy as a result of elevated homeostatic expression of the genes encoded by the TNF/lymphotoxin cytokine locusDmitry J Liepinsh, Andrei A Kruglov, Arthur R Galimov, et al.
Annals of Neurology|September 3, 2002
Mitochondrial DNA depletion and dGK gene mutationsLeonardo Salviati, Sabrina Sacconi, Michelangelo Mancuso, et al.
Molecular Genetics and Metabolism Reports|March 18, 2021
Arginine to ornithine ratio as a diagnostic marker in patients with positive newborn screening for hyperargininemiaYue Huang, Rajesh Sharma, Annette Feigenbaum, et al.
American Journal of Medical Genetics. Part A|March 8, 2021
Aicardi-Goutières syndrome may present with positive newborn screen for X-linked adrenoleukodystrophyChristina G Tise, Jose Andres Morales, Ariel S Lee, et al.
Blood|October 26, 2010
A novel role for IL-22R1 as a driver of inflammationRam Savan, Adelle P McFarland, Della A Reynolds, et al.
Pageof 77