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Mechanisms of Ageing and Development
|
May 11, 2010
Yeast as a model to study mitochondrial mechanisms in ageing
Mario 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 subunits
Raquel 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 cerevisiae
Alisha Johnson, Peter Gin, Beth N Marbois, et al.
The FEBS Journal
|
September 30, 2010
Saccharomyces cerevisiae coq10 null mutants are responsive to antimycin A
Cleverson 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 compartments
Fernando Gomes, Flávio Romero Palma, Mario H Barros, et al.
FEMS Yeast Research
|
November 10, 2021
Coq3p relevant residues for protein activity and stability
Janaina 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 health
Tiago 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 Coq10
Michelle C Bradley, Krista Yang, Lucía Fernández-Del-Río, et al.
Redox Biology
|
January 8, 2014
Redox regulation of the proteasome via S-glutathionylation
Marilene 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 mutation
Beatriz Garcia-Diaz, Mario H Barros, Simone Sanna-Cherchi, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 42) with videos related to
Sort By:
Page
of 5
Mechanisms of Ageing and Development
|
May 11, 2010
Yeast as a model to study mitochondrial mechanisms in ageing
Mario 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 subunits
Raquel 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 cerevisiae
Alisha Johnson, Peter Gin, Beth N Marbois, et al.
The FEBS Journal
|
September 30, 2010
Saccharomyces cerevisiae coq10 null mutants are responsive to antimycin A
Cleverson 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 compartments
Fernando Gomes, Flávio Romero Palma, Mario H Barros, et al.
FEMS Yeast Research
|
November 10, 2021
Coq3p relevant residues for protein activity and stability
Janaina 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 health
Tiago 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 Coq10
Michelle C Bradley, Krista Yang, Lucía Fernández-Del-Río, et al.
Redox Biology
|
January 8, 2014
Redox regulation of the proteasome via S-glutathionylation
Marilene 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 mutation
Beatriz Garcia-Diaz, Mario H Barros, Simone Sanna-Cherchi, et al.
Page
of 5