Imen Chamkha
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- 2024
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Mark
The relationship between mitochondrial respiration, resting metabolic rate and blood cell count in great tits
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- Contribution to journal › Article
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Mark
Correlation of mitochondrial respiration in platelets, peripheral blood mononuclear cells and muscle fibers
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- Contribution to journal › Article
- 2023
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Mark
A whole blood approach improves speed and accuracy when measuring mitochondrial respiration in intact avian blood cells
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- Contribution to journal › Article
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Mark
Plasticity of mitochondrial function safeguards phosphorylating respiration during in vitro simulation of rest-phase hypothermia
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- Contribution to journal › Article
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Mark
Human papillomavirus-associated head and neck squamous cell carcinoma cells rely on glycolysis and display reduced oxidative phosphorylation
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- Contribution to journal › Article
- 2022
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Mark
Towards a treatment for mitochondrial disease : current compounds in clinical development
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- Contribution to journal › Scientific review
- 2021
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Mark
Cell-Permeable Succinate Rescues Mitochondrial Respiration in Cellular Models of Statin Toxicity
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- Contribution to journal › Article
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Mark
Cell‐permeable succinate rescues mitochondrial respiration in cellular models of amiodarone toxicity
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- Contribution to journal › Article
- 2020
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Mark
Cell-permeable succinate prodrugs rescue mitochondrial respiration in cellular models of acute acetaminophen overdose
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- Contribution to journal › Article
- 2018
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Mark
Bioenergetic bypass using cell-permeable succinate, but not methylene blue, attenuates metformin-induced lactate production
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- Contribution to journal › Article
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Mark
Do GSTM1 and GSTT1 polymorphisms influence the risk of developing mitochondrial diseases in a Tunisian population?
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- Contribution to journal › Article
- 2017
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Mark
Co segregation of the m.1555A>G mutation in the MT-RNR1 gene and mutations in MT-ATP6 gene in a family with dilated mitochondrial cardiomyopathy and hearing loss : A whole mitochondrial genome screening
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- Contribution to journal › Article
- 2016
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Mark
Mitochondrial DNA triplication and punctual mutations in patients with mitochondrial neuromuscular disorders
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- Contribution to journal › Article
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Mark
Whole mitochondrial genome analysis in two families with dilated mitochondrial cardiomyopathy : detection of mutations in MT-ND2 and MT-TL1 genes
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- Contribution to journal › Article
- 2014
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Mark
A mitochondrial implication in a Tunisian patient with Friedreich's ataxia-like
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- Contribution to journal › Article
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Mark
A novel MT-CO2 m.8249G>A pathogenic variation and the MT-TW m.5521G>A mutation in patients with mitochondrial myopathy
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- Contribution to journal › Article
- 2013
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Mark
Screening of mitochondrial mutations in Tunisian patients with mitochondrial disorders : an overview study
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- Contribution to journal › Article
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Mark
A novel MT-CO1 m.6498C>A variation associated with the m.7444G>A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes in a patient with hearing impairment, diabetes and congenital visual loss
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- Contribution to journal › Article
- 2012
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Mark
A novel m.12908T>a mutation in the mitochondrial ND5 gene in patient with infantile-onset Pompe disease
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- Contribution to journal › Article
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Mark
Possible association of a novel missense mutation A6375G in the mitochondrial cytochrome C oxidase I gene with asthenospermia in the Tunisian population
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- Contribution to journal › Article
- 2011
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Mark
A Tunisian patient with Pearson syndrome harboring the 4.977kb common deletion associated to two novel large-scale mitochondrial deletions
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- Contribution to journal › Article
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Mark
A novel m.3395A>G missense mutation in the mitochondrial ND1 gene associated with the new tRNA(Ile) m.4316A>G mutation in a patient with hypertrophic cardiomyopathy and profound hearing loss
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- Contribution to journal › Article
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Mark
Molecular-clinical correlation in a family with a novel heteroplasmic Leigh syndrome missense mutation in the mitochondrial cytochrome c oxidase III gene
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- Contribution to journal › Article
- 2010
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Mark
A case of Kearns-Sayre syndrome with two novel deletions (9.768 and 7.253 kb) of the mtDNA associated with the common deletion in blood leukocytes, buccal mucosa and hair follicles
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- Contribution to journal › Article
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Mark
A de novo mutation in the adenosine triphosphatase (ATPase) 8 gene in a patient with mitochondrial disorder
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- Contribution to journal › Article
- 2009
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Mark
Two new mutations in the MT-TW gene leading to the disruption of the secondary structure of the tRNA(Trp) in patients with Leigh syndrome
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- Contribution to journal › Article