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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 nicotinamide
Srinivasan 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 NEMO
Anne 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 phenotypes
Naif A M Almontashiri, Hsiao-Huei Chen, Ryan J Mailloux, et al.
Nature
|
October 3, 2025
Author Correction: Ribonucleotide incorporation into mitochondrial DNA drives inflammation
Amir Bahat, Dusanka Milenkovic, Eileen Cors, et al.
Nature
|
September 24, 2025
Ribonucleotide incorporation into mitochondrial DNA drives inflammation
Amir 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 failure
Christina 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 isolates
Irena 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 networks
Hilda Delgado de la Herran, Denis Vecellio Reane, Yiming Cheng, et al.
Intensive Care Medicine
|
November 10, 2020
Analgesia and sedation in patients with ARDS
Gerald 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 SCA28
Daniela Di Bella, Federico Lazzaro, Alfredo Brusco, et al.
Page
of 41
Search research articles
Search
Showing results (361-370 of 404) with videos related to
Sort By:
Page
of 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 nicotinamide
Srinivasan 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 NEMO
Anne 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 phenotypes
Naif A M Almontashiri, Hsiao-Huei Chen, Ryan J Mailloux, et al.
Nature
|
October 3, 2025
Author Correction: Ribonucleotide incorporation into mitochondrial DNA drives inflammation
Amir Bahat, Dusanka Milenkovic, Eileen Cors, et al.
Nature
|
September 24, 2025
Ribonucleotide incorporation into mitochondrial DNA drives inflammation
Amir 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 failure
Christina 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 isolates
Irena 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 networks
Hilda Delgado de la Herran, Denis Vecellio Reane, Yiming Cheng, et al.
Intensive Care Medicine
|
November 10, 2020
Analgesia and sedation in patients with ARDS
Gerald 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 SCA28
Daniela Di Bella, Federico Lazzaro, Alfredo Brusco, et al.
Page
of 41