Yolanda Cámara Selected Research

Combined Oxidative Phosphorylation Deficiency 1

1/2022

Dysfunctional mitochondrial translation and combined oxidative phosphorylation deficiency in a mouse model of hepatoencephalopathy due to Gfm1 mutations.

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Yolanda Cámara Research Topics

Disease

7	Mitochondrial Diseases (Mitochondrial Disease) 01/2022 - 05/2014
4	Muscular Diseases (Myopathy) 01/2020 - 04/2013
1	Combined Oxidative Phosphorylation Deficiency 1 01/2022
1	Obesity 01/2019
1	Type 2 Diabetes Mellitus (MODY) 01/2019
1	Cardiomegaly (Heart Hypertrophy) 01/2018
1	Hypertrophy 01/2018
1	Respiratory Insufficiency (Respiratory Failure) 01/2018
1	Genomic Instability 01/2016
1	Sarcopenia 12/2013
1	Ophthalmoplegia (External Ophthalmoplegia) 04/2013
1	Proteinuria 04/2013
1	Focal Segmental Glomerulosclerosis (Glomerulosclerosis, Focal) 04/2013
1	Leigh Disease (Leigh's Disease) 01/2012
1	Neurodegenerative Diseases (Neurodegenerative Disease) 01/2012
1	Cytochrome-c Oxidase Deficiency 01/2012

Drug/Important Bio-Agent (IBA)

7	Mitochondrial DNA (mtDNA)IBA 06/2021 - 05/2014
2	DeoxyuridineIBA 01/2016 - 05/2014
2	ThymidineIBA 01/2016 - 05/2014
1	EnzymesIBA 01/2022
1	Peptide Elongation Factors (Elongation Factor)IBA 01/2022
1	polyacrylamideIBA 01/2022
1	Growth Differentiation Factor 15IBA 01/2020
1	Biomarkers (Surrogate Marker)IBA 01/2020
1	Glucose (Dextrose)FDA LinkGeneric 01/2019
1	Reactive Oxygen Species (Oxygen Radicals)IBA 01/2018
1	humaninIBA 01/2018
1	endonuclease GIBA 01/2018
1	triphosphoric acid (triphosphate)IBA 01/2016
1	DNA (Deoxyribonucleic Acid)IBA 01/2016
1	thymidine kinase 2IBA 06/2015
1	MyostatinIBA 12/2013
1	Asn Transfer RNAIBA 04/2013
1	Electron Transport Complex IV (Cytochrome c Oxidase)IBA 04/2013
1	Proteins (Proteins, Gene)FDA Link 01/2012
1	Leucine (L-Leucine)FDA Link 01/2012