Publications by authors named "Mouna Tabebi"

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Role of GDH and PARP inhibitors as novel treatments for SDHB-deficient PPGLs.
Mouna Tabebi, Sallam Abdallah, Ahmed El-Serafi, Peter Söderkvist, Oliver Gimm

Endocr Relat Cancer· October 2025

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Rab7 inhibitor enhances stem cell differentiation into keratinocyte-like cells with anti-inflammatory properties.
Raghad Alghazali, Mouna Tabebi, Moustafa Elmasry, Ahmed El-Serafi

Front Immunol· June 2025

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Modulation of biological activities in adipose derived stem cells by histone deacetylation.
Sallam Abdallah, Mouna Tabebi, Sawsan Qanadilo, Neserin Ali, Jing Wang

Sci Rep· January 2025

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Domain landscapes of somatic NF1 mutations in pheochromocytoma and paraganglioma.
Mouna Tabebi, Fakher Frikha, Massimiliano Volpe, Oliver Gimm, Peter Söderkvist

Gene· July 2023

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Nuclear and mitochondrial DNA alterations in pheochromocytomas and paragangliomas, and their potential treatment.
Mouna Tabebi, Peter Söderkvist, Oliver Gimm

Endocr Relat Cancer· January 2023

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Case report: Two sisters with a germline variant and distinct endocrine neoplasias.
Raphaelle D Vallera, Yanli Ding, Kimmo J Hatanpaa, Justin A Bishop, Sasan Mirfakhraee, Mouna Tabebi

Front Endocrinol (Lausanne)· November 2022

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Novel combined UGT1A1 mutations in Crigler Najjar Syndrome type I.
Nawel Abdellaoui, Balkiss Abdelmoula, Rania Abdelhedi, Najla Kharrat, Mouna Tabebi

J Clin Lab Anal· June 2022

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Loss of SDHB Induces a Metabolic Switch in the hPheo1 Cell Line toward Enhanced OXPHOS.
Mouna Tabebi, Ravi Kumar Dutta, Camilla Skoglund, Peter Söderkvist, Oliver Gimm

Int J Mol Sci· January 2022

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Genetic Alterations in Mitochondrial DNA Are Complementary to Nuclear DNA Mutations in Pheochromocytomas.
Mouna Tabebi, Małgorzata Łysiak, Ravi Kumar Dutta, Sandra Lomazzi, Maria V Turkina

Cancers (Basel)· January 2022

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The first concurrent detection of mitochondrial DNA m.3243A>G mutation, deletion, and depletion in a family with mitochondrial diabetes.
Mouna Tabebi, Wajdi Safi, Rahma Felhi, Olfa Alila Fersi, Leila Keskes

Mol Genet Genomic Med· July 2020

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Potential dysfunctional effects of synonymous variants: Insights from an exhaustive in silico analysis of the ABCB4 gene.
Boudour Khabou, Mouna Tabebi, Olfa Siala-Sahnoun, Emna Mkaouar-Rebai, Ahmed Rebai

Ann Hum Genet· November 2018

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Hypoxia Signaling and Circadian Disruption in and by Pheochromocytoma.
Mouna Tabebi, Peter Söderkvist, Lasse D Jensen

Front Endocrinol (Lausanne)· October 2018

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A novel TBX1 missense mutation in patients with syndromic congenital heart defects.
Amel Jaouadi, Mouna Tabebi, Fatma Abdelhedi, Dorra Abid, Fatma Kamoun

Biochem Biophys Res Commun· May 2018

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First description of a novel mitochondrial mutation in the MT-TI gene associated with multiple mitochondrial DNA deletion and depletion in family with severe dilated mitochondrial cardiomyopathy.
Olfa Alila-Fersi, Mouna Tabebi, Marwa Maalej, Neila Belguith, Leila Keskes

Biochem Biophys Res Commun· March 2018

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Association study of apoptosis gene polymorphisms in mitochondrial diabetes: A potential role in the pathogenicity of MD.
Mouna Tabebi, Bodour Khabou, Hanen Boukadi, Mariam Ben Hamad, Bochra Ben Rhouma

Gene· January 2018

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Oxidative stress and glutathione S-transferase genetic polymorphisms in medical staff professionally exposed to ionizing radiation.
Hajer Doukali, Ghada Ben Salah, Latifa Hamdaoui, Mounira Hajjaji, Mouna Tabebi

Int J Radiat Biol· July 2017

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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, Imen Majdoub, Lamia Gargouri, Emna Mkaouar-Rebai, Mouna Tabebi

Biochem Biophys Res Commun· February 2017

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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, Olfa Alila-Fersi, Afif Ben Mahmoud

J Diabetes Complications· January 2017

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Whole mitochondrial genome analysis in two families with dilated mitochondrial cardiomyopathy: detection of mutations in MT-ND2 and MT-TL1 genes.
Olfa Fersi Alila, Emna Mkaouar Rebai, Mouna Tabebi, Amel Tej, Imen Chamkha

Mitochondrial DNA A DNA Mapp Seq Anal· July 2016

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Mutational screening in patients with profound sensorineural hearing loss and neurodevelopmental delay: Description of a novel m.3861A > C mitochondrial mutation in the MT-ND1 gene.
Marwa Ammar, Mouna Tabebi, Lamia Sfaihi, Olfa Alila-Fersi, Marwa Maalej

Biochem Biophys Res Commun· June 2016

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A de-novo large deletion of 2.8 kb produced in the ABCD1 gene causing adrenoleukodystrophy disease.
Fakhri Kallabi, Ghada Ben Salah, Amel Ben Chehida, Mouna Tabebi, Rahma Felhi

Biochem Cell Biol· June 2016

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Mutational analysis in patients with neuromuscular disorders: Detection of mitochondrial deletion and double mutations in the MT-ATP6 gene.
Rahma Felhi, Emna Mkaouar-Rebai, Lamia Sfaihi-Ben Mansour, Olfa Alila-Fersi, Mouna Tabebi

Biochem Biophys Res Commun· April 2016

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Mitochondrial DNA triplication and punctual mutations in patients with mitochondrial neuromuscular disorders.
Emna Mkaouar-Rebai, Rahma Felhi, Mouna Tabebi, Olfa Alila-Fersi, Imen Chamkha

Biochem Biophys Res Commun· April 2016

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Phenotypic variability in a Tunisian family with X-linked adrenoleukodystrophy caused by the p.Gln316Pro novel mutation.
Fakhri Kallabi, Emna Ellouz, Mouna Tabebi, Ghada Ben Salah, Naziha Kaabechi

Clin Chim Acta· January 2016

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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 severe nephropathy.
Mouna Tabebi, Emna Mkaouar-Rebai, Mouna Mnif, Fakhri Kallabi, Afif Ben Mahmoud

Biochem Biophys Res Commun· April 2015

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