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Life Sciences|August 28, 2017
Specific immune responses in mice following subchronic exposure to acetamipridSoumaya Marzouki, Ines Bini Dhouib, Chaouki Benabdessalem, et al.Frontiers in Immunology|September 17, 2021
Case Report: FOXP3 Mutation in a Patient Presenting With ALPSAfef Rais, Najla Mekki, Faten Fedhila, et al.Frontiers in Immunology|January 8, 2025
PGM3 insufficiency: a glycosylation disorder causing a notable T cell defectLinlin Yang, Barbara Zerbato, Alex Pessina, et al.Clinical and Molecular Allergy : CMA|April 25, 2012
Oral HPV infection and MHC class II deficiency (A study of two cases with atypical outcome)Naouel Guirat-Dhouib, Yemen Baccar, Imène Ben Mustapha, et al.Immunogenetics|October 16, 2013
A 1,100-year-old founder effect mutation in IL12B gene is responsible for Mendelian susceptibility to mycobacterial disease in Tunisian patientsImen Ben-Mustapha, Meriem Ben-Ali, Najla Mekki, et al.Tropical Medicine and Infectious Disease|March 27, 2024
A Longitudinal Study in Tunisia to Assess the Anti-RBD IgG and IgA Responses Induced by Three Different COVID-19 Vaccine PlatformsWafa Ben Hamouda, Mariem Hanachi, Sonia Ben Hamouda, et al.Cytokine|April 24, 2018
Impaired TGF-β signaling in patients with active systemic lupus erythematosus is associated with an overexpression of IL-22Raja Rekik, Monia Smiti Khanfir, Thara Larbi, et al.Tuberculosis (Edinburgh, Scotland)|October 31, 2020
Performance of GeneXpert ultra in the diagnosis of Tuberculous Cervical lymphadenitis in formalin fixed paraffin embedded tissuesEmna Romdhane, Amira Arfaoui, Chaouki Benabdessalem, et al.Molecular Immunology|October 8, 2016
Activation induced cytidine deaminase mutant (AID-His130Pro) from Hyper IgM 2 patient retained mutagenic activity on SHM artificial substrateHanen Ouadani, Imen Ben-Mustapha, Meriem Ben-Ali, et al.Molecular Immunology|July 14, 2017
A founder mutation underlies a severe form of phosphoglutamase 3 (PGM3) deficiency in Tunisian patientsLeila Ben-Khemis, Najla Mekki, Imen Ben-Mustapha, et al.Pageof 9