Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Malek Nefzi"'
Autor:
Pascale Fanen, K. Boussetta, Sondess Hadj Fredj, Rym Dabboubi, R. Othmani, Malek Nefzi, Imen Wahabi, Taieb Messaoud
Publikováno v:
Journal of Asthma. 59:1-11
This study aims to describe the molecular variability in theWe used direct sequencing for the genotyping of theThe molecular study revealed 26 variants including 24 intronic variations and 2 exonic variations (T138N and S186N) with respective frequen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e8fb72ffe240e7f8208f0188b29ced2
https://doi.org/10.1080/02770903.2020.1827419
https://doi.org/10.1080/02770903.2020.1827419
Autor:
F. Khalsi, Malek Nefzi, Khedija Bousetta, Hajer Siala, Sondess Hadj Fredj, Imen Wahabi, Rym Dabboubi, Taieb Messaoud
Publikováno v:
Allergologia et Immunopathologia. 47:159-165
Introduction and Objectives Asthma is a complex genetic disorder. Several genes have been found associated with asthma. The cystic fibrosis transmembrane conductance regulator (CFTR) gene is one of them. The aim of this study was to perform a compara
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d310d45b25dcf574bb68bc18f4b14d31
https://doi.org/10.1016/j.aller.2018.06.007
https://doi.org/10.1016/j.aller.2018.06.007
Autor:
Sondess Hadj Fredj, Malek Nefzi, Neji Tebib, K. Boussetta, S. Hamouda, Taieb Messaoud, Rym Dabboubi
Publikováno v:
Annales de biologie clinique. 79(1)
BACKGROUND & OBJECTIVES Cystic fibrosis (CF) is caused by mutations in the gene encoding the CF transmembrane regulator (CFTR) protein, a chloride channel located in the epithelial cell membrane. Over than 2,000 CFTR mutations have been identified, w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1dc16d437eac2ee9386ffbbadb70b944
https://pubmed.ncbi.nlm.nih.gov/33589413
https://pubmed.ncbi.nlm.nih.gov/33589413
Autor:
Neji Tebib, Malek Nefzi, Sihem Barsaoui, Hajer Siala, S. Hadj Fredj, K. Boussetta, Taieb Messaoud
Publikováno v:
Pathologie Biologie. 63:169-174
Purpose Determining the frequency of M470V polymorphism in cystic fibrosis and healthy cohort in Tunisia to establish the contribution of M470V polymorphism in cystic fibrosis variable presentation and course. Additionally, studying the origin of cys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdb8731c2a4943b2249a855cb82ddd71
https://doi.org/10.1016/j.patbio.2015.07.004
https://doi.org/10.1016/j.patbio.2015.07.004