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Holger Prokisch

Showing results (171-180 of 395) with videos related to

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Frontiers in Endocrinology|July 17, 2023
Investigating the role of ASCC1 in the causation of bone fragilityBarbara Voraberger, Johannes A Mayr, Nadja Fratzl-Zelman, et al.
Journal of Hepatology|May 7, 2016
Severe respiratory complex III defect prevents liver adaptation to prolonged fastingLaura S Kremer, Caroline L'hermitte-Stead, Pierre Lesimple, et al.
Nature Communications|December 18, 2025
Single cell spatial transcriptomics integration deciphers the morphological heterogeneity of atherosclerotic carotid arteriesJessica Pauli, Daniel Garger, Fatemeh Peymani, et al.
Annals of Clinical and Translational Neurology|October 1, 2025
The Diverse Neuromuscular Spectrum of VPS13A DiseaseAnne Buchberger, Evamaria Riedel, Marie Hackenberg, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 26, 2022
Mitochondrial diseases mimicking autoimmune diseases of the CNS and good response to steroids initiallyAdela Della Marina, Annikki Bertolini, Andreas Wegener-Panzer, et al.
Plos One|September 7, 2012
Extensive natural variation for cellular hydrogen peroxide release is genetically controlledHoma Attar, Karen Bedard, Eugenia Migliavacca, et al.
European Journal of Neurology|March 10, 2025
Genetic Etiology Influences the Low-Frequency Components of Globus Pallidus Internus Electrophysiology in DystoniaAhmet Kaymak, Luigi M Romito, Fabiana Colucci, et al.
Clinical Epigenetics|October 23, 2020
Smoking-related changes in DNA methylation and gene expression are associated with cardio-metabolic traitsSilvana C E Maas, Michelle M J Mens, Brigitte Kühnel, et al.
Neuron|January 24, 2024
Direct neuronal reprogramming of NDUFS4 patient cells identifies the unfolded protein response as a novel general reprogramming hurdleGiovanna Sonsalla, Ana Belen Malpartida, Therese Riedemann, et al.
Journal of Inherited Metabolic Disease|December 7, 2021
Identification and characterization of novel MPC1 gene variants causing mitochondrial pyruvate carrier deficiencyHuafang Jiang, Ahmad Alahmad, Song Fu, et al.
Pageof 40

Showing results (171-180 of 395) with videos related to

Sort By:
Pageof 40
Frontiers in Endocrinology|July 17, 2023
Investigating the role of ASCC1 in the causation of bone fragilityBarbara Voraberger, Johannes A Mayr, Nadja Fratzl-Zelman, et al.
Journal of Hepatology|May 7, 2016
Severe respiratory complex III defect prevents liver adaptation to prolonged fastingLaura S Kremer, Caroline L'hermitte-Stead, Pierre Lesimple, et al.
Nature Communications|December 18, 2025
Single cell spatial transcriptomics integration deciphers the morphological heterogeneity of atherosclerotic carotid arteriesJessica Pauli, Daniel Garger, Fatemeh Peymani, et al.
Annals of Clinical and Translational Neurology|October 1, 2025
The Diverse Neuromuscular Spectrum of VPS13A DiseaseAnne Buchberger, Evamaria Riedel, Marie Hackenberg, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 26, 2022
Mitochondrial diseases mimicking autoimmune diseases of the CNS and good response to steroids initiallyAdela Della Marina, Annikki Bertolini, Andreas Wegener-Panzer, et al.
Plos One|September 7, 2012
Extensive natural variation for cellular hydrogen peroxide release is genetically controlledHoma Attar, Karen Bedard, Eugenia Migliavacca, et al.
European Journal of Neurology|March 10, 2025
Genetic Etiology Influences the Low-Frequency Components of Globus Pallidus Internus Electrophysiology in DystoniaAhmet Kaymak, Luigi M Romito, Fabiana Colucci, et al.
Clinical Epigenetics|October 23, 2020
Smoking-related changes in DNA methylation and gene expression are associated with cardio-metabolic traitsSilvana C E Maas, Michelle M J Mens, Brigitte Kühnel, et al.
Neuron|January 24, 2024
Direct neuronal reprogramming of NDUFS4 patient cells identifies the unfolded protein response as a novel general reprogramming hurdleGiovanna Sonsalla, Ana Belen Malpartida, Therese Riedemann, et al.
Journal of Inherited Metabolic Disease|December 7, 2021
Identification and characterization of novel MPC1 gene variants causing mitochondrial pyruvate carrier deficiencyHuafang Jiang, Ahmad Alahmad, Song Fu, et al.
Pageof 40