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Showing results (641-650 of 742) with videos related to

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American Journal of Human Genetics|August 2, 2002
Identical mitochondrial DNA deletion in a woman with ocular myopathy and in her son with pearson syndromeSara Shanske, Yingying Tang, Michio Hirano, et al.
Scientific Reports|November 27, 2015
Diverse Roles of Axonemal Dyneins in Drosophila Auditory Neuron Function and Mechanical Amplification in HearingSomdatta Karak, Julie S Jacobs, Maike Kittelmann, et al.
Cell Metabolism|May 13, 2014
NAD(+)-dependent activation of Sirt1 corrects the phenotype in a mouse model of mitochondrial diseaseRaffaele Cerutti, Eija Pirinen, Costanza Lamperti, et al.
Biorxiv : the Preprint Server for Biology|January 16, 2026
Chronic ER Stress Disrupts Mitochondrial-Associated ER Membrane Integrity in Corneal Endothelial CellsStephanie Lee, Stefan Y Kim, H Orhan Akman, et al.
European Journal of Cell Biology|May 31, 2022
Sperm centriole assessment identifies male factor infertility in couples with unexplained infertility - a pilot studyAnkit Jaiswal, Tatiana Baliu-Souza, Katerina Turner, et al.
Foot & Ankle International|August 28, 2020
Consensus on Indications for Isolated Subtalar Joint Fusion and Naviculocuneiform Fusions for Progressive Collapsing Foot DeformityBeat Hintermann, Jonathan T Deland, Cesar de Cesar Netto, et al.
Foot and Ankle Surgery : Official Journal of the European Society of Foot and Ankle Surgeons|February 8, 2018
<sup>☆</sup>Diagnostic and therapeutic injections of the foot and ankle-An overviewCesar de Cesar Netto, Lucas Furtado da Fonseca, Felipe Simeone Nascimento, et al.
The Biochemical Journal|August 25, 2004
Biochemical analysis of respiratory function in cybrid cell lines harbouring mitochondrial DNA mutationsFrancesco Pallotti, Alessandra Baracca, Evelyn Hernandez-Rosa, et al.
Molecular Syndromology|February 6, 2025
A Novel Splice Site Variant in <i>KLHL40</i> Gene in Multiple Affected NEM8 Family Members Who Present Phenotypic VariabilityBeria Sönmez, Mehmet Kocabey, Ayşe İpek Polat, et al.
Neurobiology of Disease|January 22, 2013
Mitochondrial abnormalities in temporal lobe of autistic brainGuomei Tang, Puri Gutierrez Rios, Sheng-Han Kuo, et al.
Pageof 75

Showing results (641-650 of 742) with videos related to

Sort By:
Pageof 75
American Journal of Human Genetics|August 2, 2002
Identical mitochondrial DNA deletion in a woman with ocular myopathy and in her son with pearson syndromeSara Shanske, Yingying Tang, Michio Hirano, et al.
Scientific Reports|November 27, 2015
Diverse Roles of Axonemal Dyneins in Drosophila Auditory Neuron Function and Mechanical Amplification in HearingSomdatta Karak, Julie S Jacobs, Maike Kittelmann, et al.
Cell Metabolism|May 13, 2014
NAD(+)-dependent activation of Sirt1 corrects the phenotype in a mouse model of mitochondrial diseaseRaffaele Cerutti, Eija Pirinen, Costanza Lamperti, et al.
Biorxiv : the Preprint Server for Biology|January 16, 2026
Chronic ER Stress Disrupts Mitochondrial-Associated ER Membrane Integrity in Corneal Endothelial CellsStephanie Lee, Stefan Y Kim, H Orhan Akman, et al.
European Journal of Cell Biology|May 31, 2022
Sperm centriole assessment identifies male factor infertility in couples with unexplained infertility - a pilot studyAnkit Jaiswal, Tatiana Baliu-Souza, Katerina Turner, et al.
Foot & Ankle International|August 28, 2020
Consensus on Indications for Isolated Subtalar Joint Fusion and Naviculocuneiform Fusions for Progressive Collapsing Foot DeformityBeat Hintermann, Jonathan T Deland, Cesar de Cesar Netto, et al.
Foot and Ankle Surgery : Official Journal of the European Society of Foot and Ankle Surgeons|February 8, 2018
<sup>☆</sup>Diagnostic and therapeutic injections of the foot and ankle-An overviewCesar de Cesar Netto, Lucas Furtado da Fonseca, Felipe Simeone Nascimento, et al.
The Biochemical Journal|August 25, 2004
Biochemical analysis of respiratory function in cybrid cell lines harbouring mitochondrial DNA mutationsFrancesco Pallotti, Alessandra Baracca, Evelyn Hernandez-Rosa, et al.
Molecular Syndromology|February 6, 2025
A Novel Splice Site Variant in <i>KLHL40</i> Gene in Multiple Affected NEM8 Family Members Who Present Phenotypic VariabilityBeria Sönmez, Mehmet Kocabey, Ayşe İpek Polat, et al.
Neurobiology of Disease|January 22, 2013
Mitochondrial abnormalities in temporal lobe of autistic brainGuomei Tang, Puri Gutierrez Rios, Sheng-Han Kuo, et al.
Pageof 75