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Stephan Zierz

Showing results (91-100 of 123) with videos related to

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Metabolites|November 24, 2022
Normal Thermostability of p.Ser113Leu and p.Arg631Cys Variants of Mitochondrial Carnitine Palmitoyltransferase II (CPT II) in Human Muscle HomogenatePushpa Raj Joshi, Maria Gräfin Zu Stolberg-Stolberg, Leila Motlagh Scholle, et al.
Biomolecules|July 30, 2020
The Effect of Resveratrol on Mitochondrial Function in Myoblasts of Patients with the Common m.3243A>G MutationLeila Motlagh Scholle, Helena Schieffers, Samiya Al-Robaiy, et al.
Brain : a Journal of Neurology|May 20, 2005
Mitochondrial changes in skeletal muscle in amyotrophic lateral sclerosis and other neurogenic atrophiesAnna Krasnianski, Marcus Deschauer, Stephan Neudecker, et al.
Neuromuscular Disorders : NMD|December 3, 2014
A novel m.7539C>T point mutation in the mt-tRNA(Asp) gene associated with multisystemic mitochondrial diseaseDiana Lehmann, Kathrin Schubert, Pushpa R Joshi, et al.
Molecular Genetics and Metabolism|June 18, 2003
A splice junction mutation in muscle carnitine palmitoyltransferase II deficiencyMarcus Deschauer, Zofia M A Chrzanowska-Lightowlers, Eckhard Biekmann, et al.
Neurology. Genetics|November 9, 2016
Peripheral neuropathy in patients with CPEO associated with single and multiple mtDNA deletionsDiana Lehmann, Malte E Kornhuber, Carolina Clajus, et al.
Plos One|December 19, 2013
Sialylation and muscle performance: sialic acid is a marker of muscle ageingFrank Hanisch, Wenke Weidemann, Mona Großmann, et al.
Frontiers in Immunology|September 21, 2023
Skeletal muscle fibers produce B-cell stimulatory factors in chronic myositisPer-Ole Carstens, Luisa M Müllar, Arne Wrede, et al.
Bioscience Reports|November 7, 2002
Mitochondrial dysfunction in sepsis: evidence from bacteraemic baboons and endotoxaemic rabbitsFrank Norbert Gellerich, Sonata Trumbeckaite, Jens Rüdiger Opalka, et al.
Molecular Biology Reports|May 16, 2019
Myositis in Lewis rats induced by the superantigen Staphylococcal enterotoxin AAlexander Emmer, Abimbola Abobarin-Adeagbo, Andreas Posa, et al.
Pageof 13

Showing results (91-100 of 123) with videos related to

Sort By:
Pageof 13
Metabolites|November 24, 2022
Normal Thermostability of p.Ser113Leu and p.Arg631Cys Variants of Mitochondrial Carnitine Palmitoyltransferase II (CPT II) in Human Muscle HomogenatePushpa Raj Joshi, Maria Gräfin Zu Stolberg-Stolberg, Leila Motlagh Scholle, et al.
Biomolecules|July 30, 2020
The Effect of Resveratrol on Mitochondrial Function in Myoblasts of Patients with the Common m.3243A>G MutationLeila Motlagh Scholle, Helena Schieffers, Samiya Al-Robaiy, et al.
Brain : a Journal of Neurology|May 20, 2005
Mitochondrial changes in skeletal muscle in amyotrophic lateral sclerosis and other neurogenic atrophiesAnna Krasnianski, Marcus Deschauer, Stephan Neudecker, et al.
Neuromuscular Disorders : NMD|December 3, 2014
A novel m.7539C>T point mutation in the mt-tRNA(Asp) gene associated with multisystemic mitochondrial diseaseDiana Lehmann, Kathrin Schubert, Pushpa R Joshi, et al.
Molecular Genetics and Metabolism|June 18, 2003
A splice junction mutation in muscle carnitine palmitoyltransferase II deficiencyMarcus Deschauer, Zofia M A Chrzanowska-Lightowlers, Eckhard Biekmann, et al.
Neurology. Genetics|November 9, 2016
Peripheral neuropathy in patients with CPEO associated with single and multiple mtDNA deletionsDiana Lehmann, Malte E Kornhuber, Carolina Clajus, et al.
Plos One|December 19, 2013
Sialylation and muscle performance: sialic acid is a marker of muscle ageingFrank Hanisch, Wenke Weidemann, Mona Großmann, et al.
Frontiers in Immunology|September 21, 2023
Skeletal muscle fibers produce B-cell stimulatory factors in chronic myositisPer-Ole Carstens, Luisa M Müllar, Arne Wrede, et al.
Bioscience Reports|November 7, 2002
Mitochondrial dysfunction in sepsis: evidence from bacteraemic baboons and endotoxaemic rabbitsFrank Norbert Gellerich, Sonata Trumbeckaite, Jens Rüdiger Opalka, et al.
Molecular Biology Reports|May 16, 2019
Myositis in Lewis rats induced by the superantigen Staphylococcal enterotoxin AAlexander Emmer, Abimbola Abobarin-Adeagbo, Andreas Posa, et al.
Pageof 13