Výsledky vyhledávání - "Fatma, Midani"

Association of BglII Polymorphism in ITGA2 and (894G/T and −786T/C) Polymorphisms in eNOS Gene With Stroke Susceptibility in Tunisian Patients α2 Gene Polymorphism in α2β1 Integrin and eNOS Gene Variants and Stroke

Autor: Sondess Hadj Fredj, Hayet Soualmia, Fayçal Hentati, T. Messaoud, Akrem Jalel, Fatma Midani

Publikováno v: Biological Research For Nursing. 23:408-417

Background: This study investigated the association of BglII polymorphism in α2β1 integrin gene ( ITGA2) and eNOS (894G/T and –786T/C) polymorphisms with ischemic stroke (IS) in Tunisian patients. Methods: The study comprised 210 patients with IS

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::86cb5747df251edafea617a45873c407
https://doi.org/10.1177/1099800420977685

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Contribution of the ACE (rs1799752) and CYP11B2 (rs1799998) Gene Polymorphisms to Atrial Fibrillation in the Tunisian Population

Autor: Hayet Soualmia, Ameni Kallele, Moncef Feki, Sana Ouali, Neila Ben Romdhane, Mohamed Sami Mourali, Fatma Midani, Ilhem Gouissem, Meryem Bouchemi

Publikováno v: Biological research for nursing. 24(1)

Background: This study investigated the association of angiotensin–converting enzyme (ACE I/D) and aldosterone synthase (CYP11B2-344C/T) gene polymorphisms in the renin–angiotensin–aldosterone system (RAAS) with atrial fibrillation (AF) in the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdd7f088421be1bc4d2f60047195698f
https://pubmed.ncbi.nlm.nih.gov/34227426

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The Role of Genetic Variants (rs869109213 and rs2070744) Of theeNOSGene andBglII in the α2Subunit of the α2β1Integrin Gene in Diabetic Retinopathy in a Tunisian Population

Autor: Zohra Ben Amor, Moncef Feki, Mohamed Ali El Afrit, Fatma Midani, Amani Kallel, Hayet Soualmia

Publikováno v: Seminars in Ophthalmology. 34:365-374

Purpose: In this study, we investigated the association of two polymorphisms (rs869109213 and rs2070744) in the eNOS gene and one polymorphism BglII in the α2β1 integrin gene (ITGA2) with the risk ...

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::43131d0d1e9d34d306736589811577f0
https://doi.org/10.1080/08820538.2019.1632354

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Association of

Autor: Akrem, Jalel, Fatma, Midani, Sondess Hadj, Fredj, Taieb, Messaoud, Fayçal, Hentati, Hayet, Soualmia

Publikováno v: Biological research for nursing. 23(3)

This study investigated the association ofThe study comprised 210 patients with IS and 208 controls. The genotypes of theThe genotype distribution of theThis study suggests that the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::df3448376a2f90e12aac012724fbc4d8
https://pubmed.ncbi.nlm.nih.gov/33297767

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Impaired nitric oxide production in patients with primary open-angle glaucoma

Autor: Meryem, Bouchemi, Hayet, Soualmia, Fatma, Midani, Mohamed Ali, El Afrit, Monia, El Asmi, Moncef, Feki

Publikováno v: La Tunisie medicale. 98(2)

Glaucoma is an optic neuropathy induced by many factors. Vascular dysfunction is involved in the mechanism underlying glaucoma.To determine the involvement of nitric oxide (NO), which is implicated in the regulation of ocular blood flow, in primary o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::921a2603df2f249346baa36d21f6cc69
https://pubmed.ncbi.nlm.nih.gov/32395804

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Association of MTHFR C677T, MTHFR A1298C, and MTRR A66G Polymorphisms with Neural Tube Defects in Tunisian Parents

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

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The A445C Variant in Apelin Receptor and Diabetic Retinopathy in Tunisian Patients

Autor: Zohra Ben-Amor, Fatma Midani, Mehdi Ben Lassoued, Taieb Messoud, Sondess Hadj-Fradj, Monia Gharbi, Hayet Soualmia, Nedra Saadi

Publikováno v: Clinical laboratory. 63(2)

BACKGROUND Apelin and apelin receptor (APLN/APLNR) are involved in the retinal neovascularization of diabetic retinopathy (DR). METHODS This study investigated the impact of the APLNR A445C variant on the risk of DR in a sample of the Tunisian popula

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::243b4af777423bfe1e4e965d94924d38
https://pubmed.ncbi.nlm.nih.gov/28182349

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Alpha Adducin G460T Variant is a Risk Factor for Hypertension in Tunisian Population

Autor: Riadh Jemaa, Moncef Feki, Amani Kallel, Neziha Kaabachi, Fatma Midani, Ben Romdhane A, Hayet Soualmia

Publikováno v: Clinical laboratory. 62(5)

BACKGROUND Adducin is a membrane cytoskeletal protein, consisting of three subunits: α, β, and γ subunits encoded by three different genes (ADD1, ADD2, ADD3). A specific mutation G460T of the α-adducin gene (ADD1) is associated with high renal tu

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f64df2a08bc47b9dd980cf5835861d0
https://pubmed.ncbi.nlm.nih.gov/27349000

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