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Anuradha Karunanidhi

Showing results (1-10 of 25) with videos related to

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Molecular Genetics and Metabolism|March 14, 2013
Molecular and cellular pathology of very-long-chain acyl-CoA dehydrogenase deficiencyManuel Schiff, Al-Walid Mohsen, Anuradha Karunanidhi, et al.
Journal of Inherited Metabolic Disease|January 25, 2022
Medium branched chain fatty acids improve the profile of tricarboxylic acid cycle intermediates in mitochondrial fatty acid β-oxidation deficient cells: A comparative studyAnuradha Karunanidhi, Clinton Van't Land, Dhivyaa Rajasundaram, et al.
Molecular Genetics and Metabolism|September 3, 2023
Heptanoic and medium branched-chain fatty acids as anaplerotic treatment for medium chain acyl-CoA dehydrogenase deficiencyAnuradha Karunanidhi, Shakuntala Basu, Xue-Jun Zhao, et al.
Cells|September 9, 2022
Treatment of VLCAD-Deficient Patient Fibroblasts with Peroxisome Proliferator-Activated Receptor δ Agonist Improves Cellular BioenergeticsOlivia M D'Annibale, Yu Leng Phua, Clinton Van't Land, et al.
Molecular Genetics and Metabolism|May 21, 2024
A multiomics approach reveals evidence for phenylbutyrate as a potential treatment for combined D,L-2- hydroxyglutaric aciduriaYu Leng Phua, Olivia M D'Annibale, Anuradha Karunanidhi, et al.
Biorxiv : the Preprint Server for Biology|February 13, 2023
A multiomics approach to understanding pathology of Combined D,L-2- Hydroxyglutaric Aciduria and phenylbutyrate as potential treatmentYu Leng Phua, Olivia M D'Annibale, Anuradha Karunanidhi, et al.
Journal of Tissue Engineering|February 26, 2011
Preclinical Toxicology Studies of Recombinant Human Platelet-Derived Growth Factor-BB Either Alone or in Combination with Beta-Tricalcium Phosphate and Type I CollagenConan S Young, Gino Bradica, Charlie E Hart, et al.
Plos One|December 10, 2020
ACAD10 protein expression and Neurobehavioral assessment of Acad10-deficient miceKaitlyn Bloom, Anuradha Karunanidhi, Kimimasa Tobita, et al.
Molecular Genetics and Metabolism|September 18, 2021
Characterization of variants of uncertain significance in isovaleryl-CoA dehydrogenase identified through newborn screening: An approach for faster analysisOlivia M D'Annibale, Erik A Koppes, Ahmad N Alodaib, et al.
Molecular Genetics and Metabolism|March 11, 2020
Clinical, biochemical, mitochondrial, and metabolomic aspects of methylmalonate semialdehyde dehydrogenase deficiency: Report of a fifth caseSteven F Dobrowolski, Ahmad Alodaib, Anuradha Karunanidhi, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
Molecular Genetics and Metabolism|March 14, 2013
Molecular and cellular pathology of very-long-chain acyl-CoA dehydrogenase deficiencyManuel Schiff, Al-Walid Mohsen, Anuradha Karunanidhi, et al.
Journal of Inherited Metabolic Disease|January 25, 2022
Medium branched chain fatty acids improve the profile of tricarboxylic acid cycle intermediates in mitochondrial fatty acid β-oxidation deficient cells: A comparative studyAnuradha Karunanidhi, Clinton Van't Land, Dhivyaa Rajasundaram, et al.
Molecular Genetics and Metabolism|September 3, 2023
Heptanoic and medium branched-chain fatty acids as anaplerotic treatment for medium chain acyl-CoA dehydrogenase deficiencyAnuradha Karunanidhi, Shakuntala Basu, Xue-Jun Zhao, et al.
Cells|September 9, 2022
Treatment of VLCAD-Deficient Patient Fibroblasts with Peroxisome Proliferator-Activated Receptor δ Agonist Improves Cellular BioenergeticsOlivia M D'Annibale, Yu Leng Phua, Clinton Van't Land, et al.
Molecular Genetics and Metabolism|May 21, 2024
A multiomics approach reveals evidence for phenylbutyrate as a potential treatment for combined D,L-2- hydroxyglutaric aciduriaYu Leng Phua, Olivia M D'Annibale, Anuradha Karunanidhi, et al.
Biorxiv : the Preprint Server for Biology|February 13, 2023
A multiomics approach to understanding pathology of Combined D,L-2- Hydroxyglutaric Aciduria and phenylbutyrate as potential treatmentYu Leng Phua, Olivia M D'Annibale, Anuradha Karunanidhi, et al.
Journal of Tissue Engineering|February 26, 2011
Preclinical Toxicology Studies of Recombinant Human Platelet-Derived Growth Factor-BB Either Alone or in Combination with Beta-Tricalcium Phosphate and Type I CollagenConan S Young, Gino Bradica, Charlie E Hart, et al.
Plos One|December 10, 2020
ACAD10 protein expression and Neurobehavioral assessment of Acad10-deficient miceKaitlyn Bloom, Anuradha Karunanidhi, Kimimasa Tobita, et al.
Molecular Genetics and Metabolism|September 18, 2021
Characterization of variants of uncertain significance in isovaleryl-CoA dehydrogenase identified through newborn screening: An approach for faster analysisOlivia M D'Annibale, Erik A Koppes, Ahmad N Alodaib, et al.
Molecular Genetics and Metabolism|March 11, 2020
Clinical, biochemical, mitochondrial, and metabolomic aspects of methylmalonate semialdehyde dehydrogenase deficiency: Report of a fifth caseSteven F Dobrowolski, Ahmad Alodaib, Anuradha Karunanidhi, et al.
Pageof 3