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Mario H Barros

Showing results (31-40 of 42) with videos related to

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Mechanisms of Ageing and Development|May 11, 2010
Yeast as a model to study mitochondrial mechanisms in ageingMario H Barros, Fernanda M da Cunha, Graciele A Oliveira, et al.
Cell Biology International|November 22, 2017
Mitochondrial ribosome bL34 mutants present diminished translation of cytochrome c oxidase subunitsRaquel Fonseca Guedes-Monteiro, José Ribamar Ferreira-Junior, Lucas Bleicher, et al.
The Journal of Biological Chemistry|July 20, 2005
COQ9, a new gene required for the biosynthesis of coenzyme Q in Saccharomyces cerevisiaeAlisha Johnson, Peter Gin, Beth N Marbois, et al.
The FEBS Journal|September 30, 2010
Saccharomyces cerevisiae coq10 null mutants are responsive to antimycin ACleverson Busso, Erich B Tahara, Renata Ogusucu, et al.
The Journal of Biological Chemistry|August 20, 2017
Proteolytic cleavage by the inner membrane peptidase (IMP) complex or Oct1 peptidase controls the localization of the yeast peroxiredoxin Prx1 to distinct mitochondrial compartmentsFernando Gomes, Flávio Romero Palma, Mario H Barros, et al.
FEMS Yeast Research|November 10, 2021
Coq3p relevant residues for protein activity and stabilityJanaina A Paulela, Fernando Gomes, Vittoria de Lima Camandona, et al.
Antioxidants & Redox Signaling|December 19, 2012
Mitochondria as a source of reactive oxygen and nitrogen species: from molecular mechanisms to human healthTiago R Figueira, Mario H Barros, Anamaria A Camargo, et al.
The Journal of Biological Chemistry|March 25, 2020
<i>COQ11</i> deletion mitigates respiratory deficiency caused by mutations in the gene encoding the coenzyme Q chaperone protein Coq10Michelle C Bradley, Krista Yang, Lucía Fernández-Del-Río, et al.
Redox Biology|January 8, 2014
Redox regulation of the proteasome via S-glutathionylationMarilene Demasi, Luis E S Netto, Gustavo M Silva, et al.
American Journal of Human Genetics|October 2, 2012
Infantile encephaloneuromyopathy and defective mitochondrial translation are due to a homozygous RMND1 mutationBeatriz Garcia-Diaz, Mario H Barros, Simone Sanna-Cherchi, et al.
Pageof 5

Showing results (31-40 of 42) with videos related to

Sort By:
Pageof 5
Mechanisms of Ageing and Development|May 11, 2010
Yeast as a model to study mitochondrial mechanisms in ageingMario H Barros, Fernanda M da Cunha, Graciele A Oliveira, et al.
Cell Biology International|November 22, 2017
Mitochondrial ribosome bL34 mutants present diminished translation of cytochrome c oxidase subunitsRaquel Fonseca Guedes-Monteiro, José Ribamar Ferreira-Junior, Lucas Bleicher, et al.
The Journal of Biological Chemistry|July 20, 2005
COQ9, a new gene required for the biosynthesis of coenzyme Q in Saccharomyces cerevisiaeAlisha Johnson, Peter Gin, Beth N Marbois, et al.
The FEBS Journal|September 30, 2010
Saccharomyces cerevisiae coq10 null mutants are responsive to antimycin ACleverson Busso, Erich B Tahara, Renata Ogusucu, et al.
The Journal of Biological Chemistry|August 20, 2017
Proteolytic cleavage by the inner membrane peptidase (IMP) complex or Oct1 peptidase controls the localization of the yeast peroxiredoxin Prx1 to distinct mitochondrial compartmentsFernando Gomes, Flávio Romero Palma, Mario H Barros, et al.
FEMS Yeast Research|November 10, 2021
Coq3p relevant residues for protein activity and stabilityJanaina A Paulela, Fernando Gomes, Vittoria de Lima Camandona, et al.
Antioxidants & Redox Signaling|December 19, 2012
Mitochondria as a source of reactive oxygen and nitrogen species: from molecular mechanisms to human healthTiago R Figueira, Mario H Barros, Anamaria A Camargo, et al.
The Journal of Biological Chemistry|March 25, 2020
<i>COQ11</i> deletion mitigates respiratory deficiency caused by mutations in the gene encoding the coenzyme Q chaperone protein Coq10Michelle C Bradley, Krista Yang, Lucía Fernández-Del-Río, et al.
Redox Biology|January 8, 2014
Redox regulation of the proteasome via S-glutathionylationMarilene Demasi, Luis E S Netto, Gustavo M Silva, et al.
American Journal of Human Genetics|October 2, 2012
Infantile encephaloneuromyopathy and defective mitochondrial translation are due to a homozygous RMND1 mutationBeatriz Garcia-Diaz, Mario H Barros, Simone Sanna-Cherchi, et al.
Pageof 5