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Publications by Sergio Goncalves

The Variability of the Harlequin Mouse Phenotype Resembles That of Human Mitochondrial-Complex I-Deficiency Syndromes

PLoS ONE
Multidisciplinary
2008English

Impaired Nuclear Nrf2 Translocation Undermines the Oxidative Stress Response in Friedreich Ataxia

PLoS ONE
Multidisciplinary
2009English

Related publications

Cell-Permeable Succinate Prodrugs Bypass Mitochondrial Complex I Deficiency

Nature Communications
AstronomyGeneticsMolecular BiologyBiochemistryChemistryPhysics
2016English

Molecular Diagnosis in Mitochondrial Complex I Deficiency Using Exome Sequencing

Journal of Medical Genetics
Genetics
2012English

Image Gallery: A Case of Harlequin and Horner Syndromes

British Journal of Dermatology
DermatologyMedicine
2019English

The Cortical Thickness Phenotype of Individuals With DISC1 Translocation Resembles Schizophrenia

Journal of Clinical Investigation
Medicine
2015English

The Mutant Human ND4 Subunit of Complex I Induces Optic Neuropathy in the Mouse

Investigative Ophthalmology and Visual Science
Molecular NeuroscienceOphthalmologySensory SystemsCellular
2007English

Chemomechanical Coupling of Mitochondrial Complex I

Biophysical Journal
Biophysics
2019English

NDUFB8 Mutations Cause Mitochondrial Complex I Deficiency in Individuals With Leigh-Like Encephalomyopathy

American Journal of Human Genetics
Genetics
2018English

Modulation of Lupus Phenotype by Adiponectin Deficiency in Autoimmune Mouse Models

Journal of Clinical Immunology
AllergyImmunology
2010English

Loss of Human Arylamine N-Acetyltransferase I Regulates Mitochondrial Function by Inhibition of the Pyruvate Dehydrogenase Complex

International Journal of Biochemistry and Cell Biology
BiochemistryCell Biology
2019English

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