C. Kifagi

Proteomic approaches for discovering biomarkers of diabetic nephropathy.

F. Molina, C. Granier, Laurence Molina, 2010, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

SUMOylation controls the rapid transcriptional reprogramming induced by anthracyclines in Acute Myeloid Leukemias

J. Olsen, C. Andrieu-Soler, L. Vallar, 2022, bioRxiv.

Reversine inhibits Colon Carcinoma Cell Migration by Targeting JNK1

F. Lang, R. Massoumi, Myriam Fezai, 2018, Scientific Reports.

The Identification by Exome Sequencing of Candidate Genes in BRCA-Negative Tunisian Patients at a High Risk of Hereditary Breast/Ovarian Cancer

J. Daoud, R. Mokdad-Gargouri, C. Kifagi, 2022, Genes.

Synergistic Effects of Sanglifehrin-Based Cyclophilin Inhibitor NV651 with Cisplatin in Hepatocellular Carcinoma

R. Massoumi, P. Gallay, E. Elmér, 2022, Cancers.

The ROS/SUMO axis contributes to the response of acute myeloid leukemia cells to chemotherapeutic drugs.

S. Manenti, C. Récher, L. Vallar, 2014, Cell reports.

Preferential Killing of Tetraploid Colon Cancer Cells by Targeting the Mitotic Kinase PLK1.

R. Massoumi, C. Kifagi, Mohamed Jemaà, 2020, Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology.

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.

F. Fakhfakh, C. Kifagi, M. Hachicha, 2011, Biochemical and biophysical research communications.

New mutation c.374C>T and a putative disease‐associated haplotype within SCN1B gene in Tunisian families with febrile seizures

Ahmed Rebai, I. H. Salem, F. Kammoun, 2011, European journal of neurology.

Association of genetic variations in TCF7L2, SLC30A8, HHEX, LOC387761, and EXT2 with Type 2 diabetes mellitus in Tunisia.

C. Granier, C. Kifagi, H. Ayadi, 2011, Genetic testing and molecular biomarkers.

A case of a Tunisian Rett patient with a novel double-mutation of the MECP2 gene.

F. Fakhfakh, C. Kifagi, E. Ellouze, 2011, Biochemical and biophysical research communications.

A novel m.12908T>a mutation in the mitochondrial ND5 gene in patient with infantile-onset Pompe disease.

F. Fakhfakh, C. Kifagi, M. Hachicha, 2012, Biochemical and biophysical research communications.

Identification of novel candidate genes by exome sequencing in Tunisian familial male breast cancer patients

T. Sellami-Boudawara, J. Daoud, R. Mokdad-Gargouri, 2020, Molecular Biology Reports.

DeSUMOylation of chromatin-bound proteins limits the rapid transcriptional reprogramming induced by daunorubicin in acute myeloid leukemias

J. Olsen, C. Andrieu-Soler, L. Vallar, 2023, Nucleic acids research.