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Nandaki Keshavan

Showing results (1-10 of 14) with videos related to

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Essays in Biochemistry|July 8, 2018
Natural history of mitochondrial disorders: a systematic reviewNandaki Keshavan, Shamima Rahman
Molecular Genetics and Metabolism|July 30, 2024
Natural history of deoxyguanosine kinase deficiencyNandaki Keshavan, Shamima Rahman
Journal of Inherited Metabolic Disease|January 15, 2024
Mission possible: Gene therapy for inherited metabolic diseasesJulien Baruteau, Nandaki Keshavan, Charles P Venditti
Journal of Inherited Metabolic Disease|January 3, 2024
Gene therapy for mitochondrial disordersNandaki Keshavan, Michal Minczuk, Carlo Viscomi, et al.
Annals of Neurology|September 25, 2024
Interferon Stimulated Gene Expression Is a Biomarker for Primary Mitochondrial DiseaseNandaki Keshavan, Lana Mhaldien, Kimberly Gilmour, et al.
Journal of Inherited Metabolic Disease|July 4, 2020
Moving towards clinical trials for mitochondrial diseasesRobert D S Pitceathly, Nandaki Keshavan, Joyeeta Rahman, et al.
Development (Cambridge, England)|January 23, 2014
A nutrient-sensitive restriction point is active during retinal progenitor cell differentiationNicola K Love, Nandaki Keshavan, Rebecca Lewis, et al.
JIMD Reports|March 14, 2022
Clinical status, biochemical profile and management of a single cohort of patients with arginase deficiencyNandaki Keshavan, Michelle Wood, Lucy M Alderson, et al.
Molecular Therapy. Methods & Clinical Development|February 3, 2025
Gene therapy prevents hepatic mitochondrial dysfunction in murine deoxyguanosine kinase deficiencyNandaki Keshavan, Miriam Greenwood, Helen Prunty, et al.
Journal of Medical Genetics|November 28, 2019
Cardiac valve involvement in <i>ADAR</i>-related type I interferonopathyYanick Crow, Nandaki Keshavan, Jacques Patrick Barbet, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Essays in Biochemistry|July 8, 2018
Natural history of mitochondrial disorders: a systematic reviewNandaki Keshavan, Shamima Rahman
Molecular Genetics and Metabolism|July 30, 2024
Natural history of deoxyguanosine kinase deficiencyNandaki Keshavan, Shamima Rahman
Journal of Inherited Metabolic Disease|January 15, 2024
Mission possible: Gene therapy for inherited metabolic diseasesJulien Baruteau, Nandaki Keshavan, Charles P Venditti
Journal of Inherited Metabolic Disease|January 3, 2024
Gene therapy for mitochondrial disordersNandaki Keshavan, Michal Minczuk, Carlo Viscomi, et al.
Annals of Neurology|September 25, 2024
Interferon Stimulated Gene Expression Is a Biomarker for Primary Mitochondrial DiseaseNandaki Keshavan, Lana Mhaldien, Kimberly Gilmour, et al.
Journal of Inherited Metabolic Disease|July 4, 2020
Moving towards clinical trials for mitochondrial diseasesRobert D S Pitceathly, Nandaki Keshavan, Joyeeta Rahman, et al.
Development (Cambridge, England)|January 23, 2014
A nutrient-sensitive restriction point is active during retinal progenitor cell differentiationNicola K Love, Nandaki Keshavan, Rebecca Lewis, et al.
JIMD Reports|March 14, 2022
Clinical status, biochemical profile and management of a single cohort of patients with arginase deficiencyNandaki Keshavan, Michelle Wood, Lucy M Alderson, et al.
Molecular Therapy. Methods & Clinical Development|February 3, 2025
Gene therapy prevents hepatic mitochondrial dysfunction in murine deoxyguanosine kinase deficiencyNandaki Keshavan, Miriam Greenwood, Helen Prunty, et al.
Journal of Medical Genetics|November 28, 2019
Cardiac valve involvement in <i>ADAR</i>-related type I interferonopathyYanick Crow, Nandaki Keshavan, Jacques Patrick Barbet, et al.
Pageof 2