Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Imen, Mahjoubi"'
Autor:
Mehdi Ben Lassoued, Raja Marrakchi, Kaouther Nasri, Souhail Omar, Soumeya Siala Gaigi, Nadia Ben Jemaa, Mohamed Kacem Ben Fradj, Imen Mahjoubi, Moncef Feki, Riadh Jemaa, Safa Ben Wafi, Mariem Aloui, Fatma Midani, Mariem Soussi, Miryam Boulares, Amani Kallel, Abir Baara, Meriam Ben Halima
Publikováno v:
Pathobiology : journal of immunopathology, molecular and cellular biology. 86(4)
Objective: This study aims to investigate the association of 5,10-methylenetetrahydrofolate reductase (MTHFR C677T and A1298C) and methionine synthase reductase (MTRR A66G) gene polymorphisms with neural tube defects (NTDs) in a Tunisian population.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3ecf344de65027132175425bd31b36f
https://pubmed.ncbi.nlm.nih.gov/31238314
https://pubmed.ncbi.nlm.nih.gov/31238314
Autor:
Imen, Mahjoubi, Amani, Kallel, Mohamed Hédi, Sbaï, Bochra, Ftouhi, Meriam, Ben Halima, Zeineb, Jemaa, Moncef, Feki, Hedia, Slimane, Riadh, Jemaa, Naziha, Kaabachi
Publikováno v:
The Indian Journal of Medical Research
Background & objectives: The impact of several environmental and genetic factors on diabetes is well documented. Though the association between the vitamin D receptor (VDR) gene polymorphisms and type 2 diabetes mellitus (T2DM) has been analyzed in d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::144255f1df14d16a605ba82cf5bc754f
https://pubmed.ncbi.nlm.nih.gov/27834325
https://pubmed.ncbi.nlm.nih.gov/27834325
Autor:
M.S. Mourali, Mohamed Hédi Sbaï, Zeineb Jemaa, S. Ben Wafi, M. Ben Halima, Imen Mahjoubi, Neziha Kaabachi, Riadh Jemaa, Amani Kallel, Abir Baara, Meriem Soussi
Publikováno v:
Archives of Cardiovascular Diseases Supplements. 9:98
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3033ab49fdcf238c92f9322addd4c48d
https://doi.org/10.1016/s1878-6480(17)30293-8
https://doi.org/10.1016/s1878-6480(17)30293-8
Autor:
Bochra Ftouhi, Imen Mahjoubi, Hedia Slimane, Riadh Jemaa, Amani Kallel, Chaker Sleimi, Naziha Kaabachi, Zeineb Jemaa, Moncef Feki
Publikováno v:
Diabetesmetabolic syndrome. 9(4)
Background and aims Peroxisome proliferator-activated receptor-γ co-activator-1α (PGC-1α) is a transcriptional co-activator involved in adaptive thermogenesis, skeletal muscle metabolism, fatty acid oxidation, and gluconeogenesis. Several studies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5942b5b7a19c26baa8cb3bac441c5366
https://pubmed.ncbi.nlm.nih.gov/25470625
https://pubmed.ncbi.nlm.nih.gov/25470625
Autor:
Imen Mahjoubi, Moncef Feki, Amani Kallel, Bochra Ftouhi, Naziha Kaabachi, Riadh Jemaa, Hedia Slimane, Zeineb Jemaa
Publikováno v:
Diabetes research and clinical practice. 102(2)
Aims Tumor necrosis factor α (TNFα) plays a key role in orchestrating the complex events involved in inflammation and immunity. Accordingly, TNF α has been implicated in a wide range of autoimmune and infectious diseases, but also in conditions su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edb5728c23488f31d3e3c9f96e2d346c
https://pubmed.ncbi.nlm.nih.gov/24139907
https://pubmed.ncbi.nlm.nih.gov/24139907
Autor:
Bochra Ftouhi, Naziha Kaabachi, Riadh Jemaa, Amani Kallel, Zeineb Jemaa, Imen Mahjoubi, Meriam Ben Halima, Moncef Feki, Hedia Slimane, Mohamed Hédi Sbaï
Publikováno v:
Indian Journal of Medical Research, Vol 144, Iss 1, Pp 46-51 (2016)
Background & objectives: The impact of several environmental and genetic factors on diabetes is well documented. Though the association between the vitamin D receptor (VDR) gene polymorphisms and type 2 diabetes mellitus (T2DM) has been analyzed in d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d318c75a9d5aba76f2e58d24e97a711b
https://doi.org/10.4103/0971-5916.193282
https://doi.org/10.4103/0971-5916.193282
Autor:
Imen Darragi, Arij Ben Chaabene, Yossra Said, Leila Chaouch, Salem Abbes, Abderraouf Ghanem, Imen Mahjoubi, Imen Moumni
Publikováno v:
Annales de Biologie Clinique
Annales de Biologie Clinique, John Libbey Eurotext, 2012, 70 (6), pp.702-6. ⟨10.1684/abc.2012.0743⟩
Annales de Biologie Clinique, John Libbey Eurotext, 2012, 70 (6), pp.702-6. ⟨10.1684/abc.2012.0743⟩
International audience; Bilirubin is conjugated with glucoronic acid in the liver by UDP-glucuronosyltransferase 1A1 (UGT1A1). Polymorphisms at the promoter region or exon1 of UGT1A1 gene result in unconjugated hyperbilirubinemia and could be at the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27861b1ec57a07ff20734b45be4f6fe0
https://pubmed.ncbi.nlm.nih.gov/23207817
https://pubmed.ncbi.nlm.nih.gov/23207817