Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Sabrine Oueslati"'
Analysis of δ-globin gene alleles in Tunisians: description of three new delta-thalassemia mutations
Autor:
Sana Hammami, Sabrine Oueslati, Malek Dabboussi, Chaima Kasmi, Sondess Hadj-Fredj, Faika Ben Mami, Amina Bibi, Imen Aljane, Yessine Amri, Henda Jamoussi, Rahma Mahjoub, Taieb Messaoud
Publikováno v:
Molecular Biology Reports. 48:5923-5933
Thalassemia is one of the most prevalent worldwide autosomal recessive disorders characterized by a great molecular and clinical expression heterogeneity. Alpha and beta-thalassemia are the main two types observed in case of mutations affecting alpha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::690663f937edb5e8789e174ce38d5c16
https://doi.org/10.1007/s11033-021-06592-7
https://doi.org/10.1007/s11033-021-06592-7
Autor:
Malek Dabboussi, Amina Bibi, Ines Kammoun, E. Haouat, Rahma Mahjoub, Amal Guesmi, Manel Zouaoui, Sabrine Oueslati, Chaima Kassmi
Publikováno v:
Biological research for nursing. 23(4)
Vitamin D (VD) cannot be considered as a true vitamin, but rather as a hormone, which exerts its action via a vitamin D receptor (VDR). Many genes have been shown to be involved in the evolution of diabetes in various populations, such as the vitamin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37da046b9ad889a73095383c520b29db
https://pubmed.ncbi.nlm.nih.gov/33827288
https://pubmed.ncbi.nlm.nih.gov/33827288
Autor:
Sondess Hadj Fredj, Hajer Siala, Sabrine Oueslati, Amina Bibi, Khadija Boussetta, Hajer Aloulou, Sihem Barsaoui, Taieb Messaoud, Lamia Boughamoura
Publikováno v:
Journal of genetics. 95(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a85d1c90f02d1dfad20ed858e1c4da83
https://pubmed.ncbi.nlm.nih.gov/27019450
https://pubmed.ncbi.nlm.nih.gov/27019450
Publikováno v:
Acta physiologica Hungarica. 102(1)
The analysis of some extra- and intragenic markers within or closely linked to the cystic fibrosis transmembrane regulator (CFTR) gene is useful as a molecular method in clinical linkage analysis. Indeed, knowing that the molecular basis of cystic fi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d12807ad787f50c00e1a21301cc838fb
https://pubmed.ncbi.nlm.nih.gov/25481366
https://pubmed.ncbi.nlm.nih.gov/25481366
Autor:
Safa Sahnoun, Amina Bibi, Sondess Hadj Fredj, Taieb Messaoud, K. Boussetta, Monia Boudaya, Sabrine Oueslati, Hajer Siala, Chaima Abdelhafidh Sahli
Publikováno v:
Journal of Genetics. 92:81-83
More than 1800 CFTR (cystic fibrosis transmembrane conductance regulator gene) sequence variations have been identified in the cystic fibrosis (CF) mutation database (http://www.genet.sickkids.on.ca/cftr/). For North African populations, however, the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85a4da5308ceee907a3682a0b46995ab
https://doi.org/10.1007/s12041-013-0208-4
https://doi.org/10.1007/s12041-013-0208-4