Mouna Tabebi

Loss of SDHB Induces a Metabolic Switch in the hPheo1 Cell Line toward Enhanced OXPHOS

Mouna Tabebi, Ravi Kumar Dutta, Camilla Skoglund et al. · International Journal of Molecular Sciences · 2022 · 25 citations · Full text

Sdhb Gene Expression, Lipid Peroxidation, Pathology +23

A novel mutation MT-COIII m.9267G>C and MT-COI m.5913G>A mutation in mitochondrial genes in a Tunisian family with maternally inherited diabetes and deafness (MIDD) associated with sever nephropathy

Mouna Tabebi, Emna Mkaouar‐Rebai, Mouna Mnif et al. · Biochemical and Biophysical Research Communications · 2015 · 23 citations

Mendelian Disorder, Mitochondrial Function, Genetic Disorder +14

Oxidative stress and glutathione S-transferase genetic polymorphisms in medical staff professionally exposed to ionizing radiation

Hajer Doukali, Ghada Ben Salah, Latifa Hamdaoui et al. · International Journal of Radiation Biology · 2017 · 21 citations

Whole mitochondrial genome screening of a family with maternally inherited diabetes and deafness (MIDD) associated with retinopathy: A putative haplotype associated to MIDD and a novel MT-CO2 m.8241T>G mutation

Mouna Tabebi, Nadia Charfi, Fakhri Kallabi et al. · Journal of Diabetes and its Complications · 2016 · 18 citations

Mendelian Disorder, Ophthalmology, Genetic Disorder +10

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

Olfa Alila‐Fersi, Imen Chamkha, I. Majdoub et al. · Biochemical and Biophysical Research Communications · 2017 · 15 citations

Molecular Physiology, Mendelian Disorder, Mitochondrial Function +10