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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 syndrome
Sara 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 Hearing
Somdatta 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 disease
Raffaele 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 Cells
Stephanie 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 study
Ankit 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 Deformity
Beat 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 overview
Cesar 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 mutations
Francesco 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 Variability
Beria Sönmez, Mehmet Kocabey, Ayşe İpek Polat, et al.
Neurobiology of Disease
|
January 22, 2013
Mitochondrial abnormalities in temporal lobe of autistic brain
Guomei Tang, Puri Gutierrez Rios, Sheng-Han Kuo, et al.
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of 75
Search research articles
Search
Showing results (641-650 of 742) with videos related to
Sort By:
Page
of 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 syndrome
Sara 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 Hearing
Somdatta 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 disease
Raffaele 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 Cells
Stephanie 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 study
Ankit 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 Deformity
Beat 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 overview
Cesar 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 mutations
Francesco 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 Variability
Beria Sönmez, Mehmet Kocabey, Ayşe İpek Polat, et al.
Neurobiology of Disease
|
January 22, 2013
Mitochondrial abnormalities in temporal lobe of autistic brain
Guomei Tang, Puri Gutierrez Rios, Sheng-Han Kuo, et al.
Page
of 75