R. El-Khoury

发表

Deletion of the mitochondrial NADH kinase increases mitochondrial DNA stability and life span in the filamentous fungus Podospora anserina

A. Sainsard-Chanet, R. El-Khoury, 2010, Experimental Gerontology.

Expression of the alternative oxidase mitigates beta-amyloid production and toxicity in model systems.

H. Jacobs, P. Rustin, D. Crowther, 2016, Free radical biology & medicine.

Linezolid Toxicity and Mitochondrial Susceptibility: A Novel Neurological Complication in a Lebanese Patient

Ossama K. Abou Hassan, G. Nemer, M. Ahdab-Barmada, 2016, Front. Pharmacol..

Gene deletion and allelic replacement in the filamentous fungus Podospora anserina

A. Boivin, M. Maas, R. Debuchy, 2008, Current Genetics.

Molecular Characteristics of Duchenne Muscular Dystrophy in a Lebanese Cohort

C. Farra, M. Ahdab-Barmada, R. El-Khoury, 2018 .

Traumatic Brain Injury: Oxidative Stress and Novel Anti-Oxidants Such as Mitoquinone and Edaravone

F. Kobeissy, S. Mondello, A. Eid, 2020, Antioxidants.

Alternative Oxidase Expression in the Mouse Enables Bypassing Cytochrome c Oxidase Blockade and Limits Mitochondrial ROS Overproduction

P. Bénit, H. Jacobs, P. Gressens, 2013, PLoS genetics.

Novel pleiotropic BRCA2 pathogenic variants in Lebanese families.

C. Farra, R. El-Khoury, Mirna Hajj, 2019, Cancer genetics.

The NDUFB6 subunit of the mitochondrial respiratory chain complex I is required for electron transfer activity: a proof of principle study on stable and controlled RNA interference in human cell lines.

P. Bénit, P. Rustin, Malgorzata Rak, 2011, Biochemical and biophysical research communications.

Mitochondria are physiologically maintained at close to 50 ̊C

P. Bénit, H. Jacobs, P. Rustin, 2018 .

Mitochondria Are Physiologically Maintained At Close To 50 C

P. Bénit, H. Jacobs, P. Rustin, 2017 .

Cyanide resistant respiration and the alternative oxidase pathway: A journey from plants to mammals.

P. Bénit, H. Jacobs, P. Rustin, 2022, Biochimica et biophysica acta. Bioenergetics.

Divergent Features of Mitochondrial Deficiencies in LGMD2A Associated With Novel Calpain-3 Mutations

M. Ahdab-Barmada, R. Sawaya, R. El-Khoury, 2018, Journal of neuropathology and experimental neurology.

Mitochondria are physiologically maintained at close to 50 °C

P. Bénit, H. Jacobs, P. Rustin, 2017, bioRxiv.

ANT2-defective fibroblasts exhibit normal mitochondrial bioenergetics

P. Rustin, J. Vockley, Malgorzata Rak, 2015, Molecular genetics and metabolism reports.

HIV-1 Tat protein directly induces mitochondrial membrane permeabilization and inactivates cytochrome c oxidase

P. Rustin, C. Péchoux, E. Jacotot, 2012, Cell Death and Disease.

Genetic background influences mitochondrial function: modeling mitochondrial disease for therapeutic development.

P. Bénit, P. Rustin, M. Schiff, 2010, Trends in molecular medicine.

Maintenance and expression of mitochondrial DNA (mtDNA) are essential for the cell and the organism. In humans, several mutations in the adenine nucleotide translocase gene ANT1

A. Sainsard-Chanet, R. El-Khoury, 2009 .

Mitochondria are physiologically maintained at close to

Howard T. Jacobs, Young-Tae Chang, P. Bénit, 2018 .

Engineering the alternative oxidase gene to better understand and counteract mitochondrial defects: state of the art and perspectives

H. Jacobs, P. Rustin, E. Dufour, 2014, British journal of pharmacology.

The Pentose Phosphate Pathway in Cancer: Regulation and Therapeutic Opportunities

N. Darwiche, J. Usta, R. El-Khoury, 2021, Chemotherapy.

Developmental aspects of respiratory chain from fetus to infancy.

P. Bénit, P. Rustin, N. Soussi-Yanicostas, 2011, Seminars in fetal & neonatal medicine.

PGC-1α is Dispensable for Exercise-Induced Mitochondrial Biogenesis in Skeletal Muscle

P. Rustin, Z. Arany, G. Rowe, 2012, PloS one.

Glucose Modulates Respiratory Complex I Activity in Response to Acute Mitochondrial Dysfunction

H. Jacobs, P. Rustin, E. Dufour, 2012, The Journal of Biological Chemistry.

Mitochondrial response to controlled nutrition in health and disease.

P. Bénit, P. Rustin, S. Loublier, 2011, Nutrition reviews.

Mitochondrial cytochrome c oxidase deficiency.

P. Bénit, P. Rustin, Malgorzata Rak, 2016, Clinical science.

Suppression of Mitochondrial DNA Instability of Autosomal Dominant Forms of Progressive External Ophthalmoplegia-Associated ANT1 Mutations in Podospora anserina

A. Sainsard-Chanet, R. El-Khoury, 2009, Genetics.

Running title: adPEO-associated ANT1 mutations and mtDNA maintenance

A. Sainsard-Chanet, R. El-Khoury, 2009 .

Disconnecting mitochondrial content from respiratory chain capacity in PGC-1-deficient skeletal muscle.

P. Rustin, L. Goodyear, M. Hirshman, 2013, Cell reports.

FARS2 Mutations: More Than Two Phenotypes? A Case Report

A. Beydoun, W. Nasreddine, M. Hotait, 2020, Frontiers in Genetics.

Pitfalls in Monitoring Mitochondrial Temperature Using Charged Thermosensitive Fluorophores

P. Bénit, P. Rustin, G. Lenaers, 2020, Chemosensors.

Mitoquinone supplementation alleviates oxidative stress and pathologic outcomes following repetitive mild traumatic brain injury at a chronic time point

Y. Mechref, Kevin K. W. Wang, F. Kobeissy, 2022, Experimental Neurology.

Mouse Studies to Shape Clinical Trials for Mitochondrial Diseases: High Fat Diet in Harlequin Mice

P. Bénit, P. Rustin, M. Schiff, 2011, PloS one.

Fibroblasts-dependent maturation and phenotype exacerbation of dystrophic hiPSC-derived MYOtissues enables muscle strength evaluation for gene therapy screening

D. Israeli, A. Bigot, S. Albini, 2023, bioRxiv.

Expression of the alternative oxidase mitigates beta-amyloid production and toxicity in model systems.

H. Jacobs, P. Rustin, D. Crowther, 2016, Free radical biology & medicine.