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Endocrine-Related Cancer|October 11, 2022
Nuclear and mitochondrial DNA alterations in pheochromocytomas and paragangliomas, and their potential treatmentMouna Tabebi, Peter Söderkvist, Oliver GimmFrontiers in Endocrinology|November 3, 2018
Hypoxia Signaling and Circadian Disruption in and by PheochromocytomaMouna Tabebi, Peter Söderkvist, Lasse D JensenCells|January 28, 2026
Integrative Epigenomic and Transcriptomic Profiling Define Malignancy- and Cluster-Specific Signatures in Pheochromocytomas and ParagangliomasMouna Tabebi, Małgorzata Łysiak, Oliver Gimm, et al.Frontiers in Immunology|June 10, 2025
Rab7 inhibitor enhances stem cell differentiation into keratinocyte-like cells with anti-inflammatory propertiesRaghad Alghazali, Mouna Tabebi, Moustafa Elmasry, et al.Gene|April 16, 2023
Domain landscapes of somatic NF1 mutations in pheochromocytoma and paragangliomaMouna Tabebi, Fakher Frikha, Massimiliano Volpe, et al.Endocrine-Related Cancer|September 24, 2025
Role of GDH and PARP inhibitors as novel treatments for SDHB-deficient PPGLsMouna Tabebi, Sallam Abdallah, Ahmed El-Serafi, et al.International Journal of Molecular Sciences|January 11, 2022
Loss of SDHB Induces a Metabolic Switch in the hPheo1 Cell Line toward Enhanced OXPHOSMouna Tabebi, Ravi Kumar Dutta, Camilla Skoglund, et al.Annals of Human Genetics|August 7, 2018
Potential dysfunctional effects of synonymous variants: Insights from an exhaustive in silico analysis of the ABCB4 geneBoudour Khabou, Mouna Tabebi, Olfa Siala-Sahnoun, et al.Journal of Clinical Laboratory Analysis|May 9, 2022
Novel combined UGT1A1 mutations in Crigler Najjar Syndrome type INawel Abdellaoui, Balkiss Abdelmoula, Rania Abdelhedi, et al.Biochemical and Biophysical Research Communications|February 27, 2018
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 cardiomyopathyOlfa Alila-Fersi, Mouna Tabebi, Marwa Maalej, et al.Pageof 3