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Cellular and Molecular Life Sciences : CMLS
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January 17, 2022
Mice harboring the FXN I151F pathological point mutation present decreased frataxin levels, a Friedreich ataxia-like phenotype, and mitochondrial alterations
Marta Medina-Carbonero, Arabela Sanz-Alcázar, Elena Britti, et al.
Microbiology (Reading, England)
|
November 3, 2007
Chronological and replicative life-span extension in Saccharomyces cerevisiae by increased dosage of alcohol dehydrogenase 1
Gemma Reverter-Branchat, Elisa Cabiscol, Jordi Tamarit, et al.
Redox Biology
|
September 7, 2024
Deciphering the ferroptosis pathways in dorsal root ganglia of Friedreich ataxia models. The role of LKB1/AMPK, KEAP1, and GSK3β in the impairment of the NRF2 response
Arabela Sanz-Alcázar, Marta Portillo-Carrasquer, Fabien Delaspre, et al.
The Journal of Biological Chemistry
|
July 26, 2002
Structure-function analysis of yeast Grx5 monothiol glutaredoxin defines essential amino acids for the function of the protein
Gemma Bellí, Julio Polaina, Jordi Tamarit, et al.
Cellular and Molecular Life Sciences : CMLS
|
December 21, 2023
Mitochondrial impairment, decreased sirtuin activity and protein acetylation in dorsal root ganglia in Friedreich Ataxia models
Arabela Sanz-Alcázar, Elena Britti, Fabien Delaspre, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 28, 2002
DnaK dependence of mutant ethanol oxidoreductases evolved for aerobic function and protective role of the chaperone against protein oxidative damage in Escherichia coli
Pedro Echave, M Angel Esparza-Cerón, Elisa Cabiscol, et al.
Archives of Biochemistry and Biophysics
|
April 26, 2011
Sir2 is induced by oxidative stress in a yeast model of Huntington disease and its activation reduces protein aggregation
M Alba Sorolla, Clara Nierga, M José Rodríguez-Colman, et al.
Free Radical Biology & Medicine
|
July 20, 2010
Protein oxidation in Huntington disease affects energy production and vitamin B6 metabolism
Ma Alba Sorolla, Ma José Rodríguez-Colman, Jordi Tamarit, et al.
The Biochemical Journal
|
December 11, 2020
Calcitriol increases frataxin levels and restores mitochondrial function in cell models of Friedreich Ataxia
Elena Britti, Fabien Delaspre, A Sanz-Alcázar, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie
|
January 24, 2026
Targeting frataxin deficiency in DRG neurons and fibroblasts: omaveloxolone restores metabolic and iron balance to reduce ferroptosis
Marta Portillo-Carrasquer, Arabela Sanz-Alcázar, Begoña Sánchez-López, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 44) with videos related to
Sort By:
Page
of 5
Cellular and Molecular Life Sciences : CMLS
|
January 17, 2022
Mice harboring the FXN I151F pathological point mutation present decreased frataxin levels, a Friedreich ataxia-like phenotype, and mitochondrial alterations
Marta Medina-Carbonero, Arabela Sanz-Alcázar, Elena Britti, et al.
Microbiology (Reading, England)
|
November 3, 2007
Chronological and replicative life-span extension in Saccharomyces cerevisiae by increased dosage of alcohol dehydrogenase 1
Gemma Reverter-Branchat, Elisa Cabiscol, Jordi Tamarit, et al.
Redox Biology
|
September 7, 2024
Deciphering the ferroptosis pathways in dorsal root ganglia of Friedreich ataxia models. The role of LKB1/AMPK, KEAP1, and GSK3β in the impairment of the NRF2 response
Arabela Sanz-Alcázar, Marta Portillo-Carrasquer, Fabien Delaspre, et al.
The Journal of Biological Chemistry
|
July 26, 2002
Structure-function analysis of yeast Grx5 monothiol glutaredoxin defines essential amino acids for the function of the protein
Gemma Bellí, Julio Polaina, Jordi Tamarit, et al.
Cellular and Molecular Life Sciences : CMLS
|
December 21, 2023
Mitochondrial impairment, decreased sirtuin activity and protein acetylation in dorsal root ganglia in Friedreich Ataxia models
Arabela Sanz-Alcázar, Elena Britti, Fabien Delaspre, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 28, 2002
DnaK dependence of mutant ethanol oxidoreductases evolved for aerobic function and protective role of the chaperone against protein oxidative damage in Escherichia coli
Pedro Echave, M Angel Esparza-Cerón, Elisa Cabiscol, et al.
Archives of Biochemistry and Biophysics
|
April 26, 2011
Sir2 is induced by oxidative stress in a yeast model of Huntington disease and its activation reduces protein aggregation
M Alba Sorolla, Clara Nierga, M José Rodríguez-Colman, et al.
Free Radical Biology & Medicine
|
July 20, 2010
Protein oxidation in Huntington disease affects energy production and vitamin B6 metabolism
Ma Alba Sorolla, Ma José Rodríguez-Colman, Jordi Tamarit, et al.
The Biochemical Journal
|
December 11, 2020
Calcitriol increases frataxin levels and restores mitochondrial function in cell models of Friedreich Ataxia
Elena Britti, Fabien Delaspre, A Sanz-Alcázar, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie
|
January 24, 2026
Targeting frataxin deficiency in DRG neurons and fibroblasts: omaveloxolone restores metabolic and iron balance to reduce ferroptosis
Marta Portillo-Carrasquer, Arabela Sanz-Alcázar, Begoña Sánchez-López, et al.
Page
of 5