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DiMauro

Showing results (561-570 of 942) with videos related to

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Gene|May 15, 1988
Sequence of cDNAs encoding subunit Vb of human and bovine cytochrome c oxidaseM Zeviani, S Sakoda, A A Sherbany, et al.
Neurology|April 1, 1991
Biochemical and molecular analysis of cytochrome c oxidase deficiency in Leigh's syndromeA Lombes, H Nakase, H J Tritschler, et al.
Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society|May 17, 2022
Adolescent obesity incurs adult skeletal deficits in murine induced obesity modelSoha Ben Tahar, Julien Garnier, Kerry Eller, et al.
Archives of Neurology|September 12, 2012
MPV17 Mutations Causing Adult-Onset Multisystemic Disorder With Multiple Mitochondrial DNA DeletionsCaterina Garone, Juan Carlos Rubio, Sarah E Calvo, et al.
Scientific Reports|August 8, 2025
Genome-wide identification of selection signatures across altitudinal gradients in dairy sheep breedsSlim Ben Jemaa, Salvatore Mastrangelo, Federica Carta, et al.
Journal of Dairy Science|December 20, 2025
Assessing fertility: Development of a selection index for fertility in Italian Jersey cattlePaola E Milia, Martino Cassandro, Alberto Cesarani, et al.
Muscle & Nerve. Supplement|January 1, 1995
Phenotype-genotype correlations in skeletal muscle of patients with mtDNA deletionsC T Moraes, M Sciacco, E Ricci, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Comparative biochemical studies in fibroblasts from patients with different forms of Leigh syndromeM E Vazquez-Memije, S Shanske, F M Santorelli, et al.
Genomics|March 25, 2008
Glycogen synthase (GYS1) mutation causes a novel skeletal muscle glycogenosisMolly E McCue, Stephanie J Valberg, Michael B Miller, et al.
Journal of Neurochemistry|April 24, 2013
Polyglucosan neurotoxicity caused by glycogen branching enzyme deficiency can be reversed by inhibition of glycogen synthaseOr Kakhlon, Hava Glickstein, Naomi Feinstein, et al.
Pageof 95

Showing results (561-570 of 942) with videos related to

Sort By:
Pageof 95
Gene|May 15, 1988
Sequence of cDNAs encoding subunit Vb of human and bovine cytochrome c oxidaseM Zeviani, S Sakoda, A A Sherbany, et al.
Neurology|April 1, 1991
Biochemical and molecular analysis of cytochrome c oxidase deficiency in Leigh's syndromeA Lombes, H Nakase, H J Tritschler, et al.
Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society|May 17, 2022
Adolescent obesity incurs adult skeletal deficits in murine induced obesity modelSoha Ben Tahar, Julien Garnier, Kerry Eller, et al.
Archives of Neurology|September 12, 2012
MPV17 Mutations Causing Adult-Onset Multisystemic Disorder With Multiple Mitochondrial DNA DeletionsCaterina Garone, Juan Carlos Rubio, Sarah E Calvo, et al.
Scientific Reports|August 8, 2025
Genome-wide identification of selection signatures across altitudinal gradients in dairy sheep breedsSlim Ben Jemaa, Salvatore Mastrangelo, Federica Carta, et al.
Journal of Dairy Science|December 20, 2025
Assessing fertility: Development of a selection index for fertility in Italian Jersey cattlePaola E Milia, Martino Cassandro, Alberto Cesarani, et al.
Muscle & Nerve. Supplement|January 1, 1995
Phenotype-genotype correlations in skeletal muscle of patients with mtDNA deletionsC T Moraes, M Sciacco, E Ricci, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Comparative biochemical studies in fibroblasts from patients with different forms of Leigh syndromeM E Vazquez-Memije, S Shanske, F M Santorelli, et al.
Genomics|March 25, 2008
Glycogen synthase (GYS1) mutation causes a novel skeletal muscle glycogenosisMolly E McCue, Stephanie J Valberg, Michael B Miller, et al.
Journal of Neurochemistry|April 24, 2013
Polyglucosan neurotoxicity caused by glycogen branching enzyme deficiency can be reversed by inhibition of glycogen synthaseOr Kakhlon, Hava Glickstein, Naomi Feinstein, et al.
Pageof 95