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Thomas Langer

Showing results (361-370 of 404) with videos related to

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Biochemical and Biophysical Research Communications|July 20, 2017
Crystal structures of monkey and mouse nicotinamide N-methyltransferase (NNMT) bound with end product, 1-methyl nicotinamideSrinivasan Swaminathan, Swarnakumari Birudukota, Manish Kumar Thakur, et al.
Molecular Cell|March 5, 2013
The E3 ligase parkin maintains mitochondrial integrity by increasing linear ubiquitination of NEMOAnne Kathrin Müller-Rischart, Anna Pilsl, Patrick Beaudette, et al.
Cell Reports|April 29, 2014
SPG7 variant escapes phosphorylation-regulated processing by AFG3L2, elevates mitochondrial ROS, and is associated with multiple clinical phenotypesNaif A M Almontashiri, Hsiao-Huei Chen, Ryan J Mailloux, et al.
Nature|October 3, 2025
Author Correction: Ribonucleotide incorporation into mitochondrial DNA drives inflammationAmir Bahat, Dusanka Milenkovic, Eileen Cors, et al.
Nature|September 24, 2025
Ribonucleotide incorporation into mitochondrial DNA drives inflammationAmir Bahat, Dusanka Milenkovic, Eileen Cors, et al.
EMBO Molecular Medicine|February 4, 2015
Inhibition of insulin/IGF-1 receptor signaling protects from mitochondria-mediated kidney failureChristina Ising, Sybille Koehler, Sebastian Brähler, et al.
Biotechnology for Biofuels|August 16, 2016
Unraveling the microbiome of a thermophilic biogas plant by metagenome and metatranscriptome analysis complemented by characterization of bacterial and archaeal isolatesIrena Maus, Daniela E Koeck, Katharina G Cibis, et al.
The EMBO Journal|September 11, 2024
Systematic mapping of mitochondrial calcium uniporter channel (MCUC)-mediated calcium signaling networksHilda Delgado de la Herran, Denis Vecellio Reane, Yiming Cheng, et al.
Intensive Care Medicine|November 10, 2020
Analgesia and sedation in patients with ARDSGerald Chanques, Jean-Michel Constantin, John W Devlin, et al.
Nature Genetics|March 9, 2010
Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28Daniela Di Bella, Federico Lazzaro, Alfredo Brusco, et al.
Pageof 41

Showing results (361-370 of 404) with videos related to

Sort By:
Pageof 41
Biochemical and Biophysical Research Communications|July 20, 2017
Crystal structures of monkey and mouse nicotinamide N-methyltransferase (NNMT) bound with end product, 1-methyl nicotinamideSrinivasan Swaminathan, Swarnakumari Birudukota, Manish Kumar Thakur, et al.
Molecular Cell|March 5, 2013
The E3 ligase parkin maintains mitochondrial integrity by increasing linear ubiquitination of NEMOAnne Kathrin Müller-Rischart, Anna Pilsl, Patrick Beaudette, et al.
Cell Reports|April 29, 2014
SPG7 variant escapes phosphorylation-regulated processing by AFG3L2, elevates mitochondrial ROS, and is associated with multiple clinical phenotypesNaif A M Almontashiri, Hsiao-Huei Chen, Ryan J Mailloux, et al.
Nature|October 3, 2025
Author Correction: Ribonucleotide incorporation into mitochondrial DNA drives inflammationAmir Bahat, Dusanka Milenkovic, Eileen Cors, et al.
Nature|September 24, 2025
Ribonucleotide incorporation into mitochondrial DNA drives inflammationAmir Bahat, Dusanka Milenkovic, Eileen Cors, et al.
EMBO Molecular Medicine|February 4, 2015
Inhibition of insulin/IGF-1 receptor signaling protects from mitochondria-mediated kidney failureChristina Ising, Sybille Koehler, Sebastian Brähler, et al.
Biotechnology for Biofuels|August 16, 2016
Unraveling the microbiome of a thermophilic biogas plant by metagenome and metatranscriptome analysis complemented by characterization of bacterial and archaeal isolatesIrena Maus, Daniela E Koeck, Katharina G Cibis, et al.
The EMBO Journal|September 11, 2024
Systematic mapping of mitochondrial calcium uniporter channel (MCUC)-mediated calcium signaling networksHilda Delgado de la Herran, Denis Vecellio Reane, Yiming Cheng, et al.
Intensive Care Medicine|November 10, 2020
Analgesia and sedation in patients with ARDSGerald Chanques, Jean-Michel Constantin, John W Devlin, et al.
Nature Genetics|March 9, 2010
Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28Daniela Di Bella, Federico Lazzaro, Alfredo Brusco, et al.
Pageof 41