Works matching AU Mtiraoui, Nabil

Results: 26

Association of matrix metalloproteinase‐2 gene variants with diabetic nephropathy risk.

Published in:

Journal of Gene Medicine, 2023, v. 25, n. 11, p. 1, doi. 10.1002/jgm.3553

By:

Sarray, Sameh;
Lamine, Laila Ben;
Dallel, Meriem;
Ezzidi, Intissar;
Sellami, Nejla;
Turki, Amira;
Moustafa, Amgad Elbaz El‐Agroudy;
Mtiraoui, Nabil

Publication type:

Article

Evaluating the Impact of rs4025935, rs71748309, rs699947, and rs4646994 Genetic Determinants on Polycystic Ovary Syndrome Predisposition—A Case-Control Study.

Published in:

Life (2075-1729), 2025, v. 15, n. 4, p. 558, doi. 10.3390/life15040558

By:

Almotairi, Reema;
Mir, Rashid;
Almasoudi, Kholoud S.;
Husain, Eram;
Mtiraoui, Nabil

Publication type:

Article

Exploring the Association of Biochemical Characterization and Genetic Determinants of TNF-α, CXCR2, and CCR5 Delta 32 Mutation with Predisposition to Polycystic Ovary Syndrome.

Published in:

Life (2075-1729), 2024, v. 14, n. 8, p. 949, doi. 10.3390/life14080949

By:

Almasoudi, Kholoud S.;
Hussain, Eram;
Almotairi, Reema;
Bhat, Tanzeela;
Mtiraoui, Nabil;
Ezzidi, Intissar;
Mir, Rashid

Publication type:

Article

Adiponectin (ADIPOQ) gene variants and haplotypes in Saudi Arabian women with polycystic ovary syndrome (PCOS): a case–control study.

Published in:

Gynecological Endocrinology, 2020, v. 36, n. 1, p. 66, doi. 10.1080/09513590.2019.1632830

By:

Ezzidi, Intissar;
Mtiraoui, Nabil;
Mohmmed Ali, Mohammed Eltigani;
Al Masoudi, Aqeel;
Abu Duhier, Faisel

Publication type:

Article

Identification of specific angiotensin-converting enzyme variants and haplotypes that confer risk and protection against type 2 diabetic nephropathy.

Published in:

Diabetes/Metabolism Research & Reviews, 2009, v. 25, n. 8, p. 717, doi. 10.1002/dmrr.1006

By:

Ezzidi, Intissar;
Mtiraoui, Nabil;
Kacem, Maha;
Chaieb, Molka;
Mahjoub, Touhami;
Almawi, Wassim Y.

Publication type:

Article

Predictive value of interleukin-10 promoter genotypes and haplotypes in determining the susceptibility to nephropathy in type 2 diabetes patients.

Published in:

Diabetes/Metabolism Research & Reviews, 2009, v. 25, n. 1, p. 57, doi. 10.1002/dmrr.892

By:

Mtiraoui, Nabil;
Ezzidi, Intissar;
Kacem, Maha;
Ben Hadj Mohamed, Manel;
Chaieb, Molka;
Haj Jilani, Aoutef Bel;
Mahjoub, Touhami;
Almawi, Wassim Y.

Publication type:

Article

A novel link between KCNQ1 genetic variants and polycystic ovary syndrome susceptibility.

Published in:

Biomedical Reports, 2025, v. 22, n. 6, p. N.PAG, doi. 10.3892/br.2025.1982

By:

Ben Salem, Assila;
Ezzidi, Intissar;
Ben Abdennebi, Hassen;
Mtiraoui, Nabil;
Sarray, Sameh

Publication type:

Article

Interleukin-10–592C/A, –819C/T and –1082A/G promoter variants affect the susceptibility to nephropathy in Tunisian type 2 diabetes (T2DM) patients.

Published in:

Clinical Endocrinology, 2009, v. 70, n. 3, p. 401, doi. 10.1111/j.1365-2265.2008.03337.x

By:

Ezzidi, Intissar;
Mtiraoui, Nabil;
Kacem, Maha;
Mallat, Samir G.;
Mohamed, Manel Ben Hadj;
Chaieb, Molka;
Mahjoub, Touhami;
Almawi, Wassim Y.

Publication type:

Article

Endothelial nitric oxide synthase Glu298Asp, 4b/a, and T-786C polymorphisms in type 2 diabetic retinopathy.

Published in:

Clinical Endocrinology, 2008, v. 68, n. 4, p. 542, doi. 10.1111/j.1365-2265.2007.03089.x

By:

Ezzidi, Intissar;
Mtiraoui, Nabil;
Mohamed, Manel Ben Hadj;
Mahjoub, Touhami;
Kacem, Maha;
Almawi, Wassim Y.

Publication type:

Article

Renin-angiotensin-aldosterone system genotypes and haplotypes affect the susceptibility to nephropathy in type 2 diabetes patients.

Published in:

2011

By:

Mtiraoui, Nabil;
Ezzidi, Intissar;
Turki, Amira;
Chaieb, Molka;
Mahjoub, Touhami;
Almawi, Wassim Y

Publication type:

Journal Article

Renin–angiotensin–aldosterone system genotypes and haplotypes affect the susceptibility to nephropathy in type 2 diabetes patients.

Published in:

Journal of the Renin-Angiotensin-Aldosterone System, 2011, v. 12, n. 4, p. 572, doi. 10.1177/1470320310396542

By:

Mtiraoui, Nabil;
Ezzidi, Intissar;
Turki, Amira;
Chaieb, Molka;
Mahjoub, Touhami;
Almawi, Wassim Y

Publication type:

Article

Impact of variants on type-2 diabetes risk genes identified through genomewide association studies in polycystic ovary syndrome: a case-control study.

Published in:

Journal of Genetics, 2018, v. 97, n. 5, p. 1213, doi. 10.1007/s12041-018-1031-8

By:

Ezzidi, Intissar;
Mtiraoui, Nabil;
Mohmmed Ali, Mohammed Eltigani;
Al Masoudi, Aqeel;
Abu Duhier, Faisel

Publication type:

Article

Human Alu Insertion Polymorphisms in North African Populations.

Published in:

Human Biology, 2011, v. 83, n. 5, p. 611, doi. 10.3378/027.083.0503

By:

CHERNI, LOTFI;
FRIGI, SABEH;
ENNAFAA, HAJER;
MTIRAOUI, NABIL;
MAHJOUB, TOUHAMI;
BENAMMAR-ELGAAIED, AMEL

Publication type:

Article

Lack of Consistent Association Between Endothelial Nitric Oxide Synthase Gene Polymorphisms, Homocysteine Levels and Recurrent Pregnancy Loss in Tunisian Women.

Published in:

American Journal of Reproductive Immunology, 2008, v. 59, n. 2, p. 139, doi. 10.1111/j.1600-0897.2007.00551.x

By:

Zammiti, Walid;
Mtiraoui, Nabil;
Mahjoub, Touhami

Publication type:

Article

Biochemical Characterization and Molecular Determination of Estrogen Receptor-α (ESR1 PvuII-rs2234693 T>C) and MiRNA-146a (rs2910164 C>G) Polymorphic Gene Variations and Their Association with the Risk of Polycystic Ovary Syndrome.

Published in:

International Journal of Environmental Research & Public Health, 2022, v. 19, n. 5, p. 3114, doi. 10.3390/ijerph19053114

By:

Mir, Rashid;
Tayeb, Faris J.;
Barnawi, Jameel;
Jalal, Mohammed M.;
Saeedi, Nizar H.;
Hamadi, Abdullah;
Altayar, Malik A.;
Alshammari, Sanad E.;
Mtiraoui, Nabil;
Ali, Mohammed Eltigani;
Duhier, Faisel M. Abu;
Ullah, Mohammad Fahad

Publication type:

Article

Interleukin 10 (IL-10) gene variants and haplotypes in Tunisian women with polycystic ovary syndrome (PCOS): a case-control study.

Published in:

Molecular Biology Reports, 2023, v. 50, n. 10, p. 8089, doi. 10.1007/s11033-023-08706-9

By:

Ben Salem, Assila;
Ezzidi, Intissar;
Ben Abdennebi, Hassen;
Mahjoub, Touhami;
Sarray, Sameh;
Mtiraoui, Nabil

Publication type:

Article

Common polymorphisms of calpain-10 and the risk of polycystic ovary syndrome in Tunisian population: a case-control study.

Published in:

Molecular Biology Reports, 2014, v. 41, n. 10, p. 6569, doi. 10.1007/s11033-014-3540-8

By:

Ben Salem, Assila;
Attaoua, Redha;
Mtiraoui, Nabil;
Belkahla, Sana;
Ezzidi, Intissar;
Ajina, Mounir;
Souissi, Moncef;
Poucheret, Patrick;
Vintila, Madalina;
Grigorescu, Florin;
Mahjoub, Touhami

Publication type:

Article

Molecular determination of progesterone receptor's PROGINS allele (Alu insertion) and its association with the predisposition and susceptibility to polycystic ovary syndrome (PCOS).

Published in:

Mammalian Genome, 2022, v. 33, n. 3, p. 508, doi. 10.1007/s00335-021-09941-w

By:

Mir, Rashid;
Altayar, Malik A.;
Hamadi, Abdullah;
Tayeb, Faris J.;
Saeedi, Nizar H.;
Jalal, Mohammed M.;
Barnawi, Jameel;
Alshammari, Sanad E.;
Mtiraoui, Nabil;
Ali, Mohammed Eltigani M.;
Abuduhier, Faisel M.;
Ullah, Mohammad Fahad

Publication type:

Article

Clinical Implications of Krüpple-like Transcription Factor KLF-14 and Certain Micro-RNA (miR-27a, miR-196a2, miR-423) Gene Variations as a Risk Factor in the Genetic Predisposition to PCOS.

Published in:

Journal of Personalized Medicine, 2022, v. 12, n. 4, p. 586, doi. 10.3390/jpm12040586

By:

Mir, Rashid;
Saeedi, Nizar H.;
Jalal, Mohammed M.;
Altayar, Malik A.;
Barnawi, Jameel;
Hamadi, Abdullah;
Tayeb, Faris J.;
Alshammari, Sanad E.;
Mtiraoui, Nabil;
M. Ali, Mohammed Eltigani;
Abuduhier, Faisel M.;
Ullah, Mohammad Fahad

Publication type:

Article

Varied Prevalence of Factor V G1691A (Leiden) and Prothrombin G20210A Single Nucleotide Polymorphisms Among Arabs.

Published in:

Journal of Thrombosis & Thrombolysis, 2005, v. 20, n. 3, p. 163, doi. 10.1007/s11239-005-3550-4

By:

Almawi, Wassim;
Keleshian, Sose;
Borgi, Lobna;
Fawaz, Naglaa;
Abboud, Nisreen;
Mtiraoui, Nabil;
Mahjoub, Touhami

Publication type:

Article

Distinct association of factor V‐Leiden and prothrombin G20210A mutations with deep venous thrombosis in Tunisia and Lebanon.

Published in:

American Journal of Hematology, 2006, v. 81, n. 8, p. 641, doi. 10.1002/ajh.20582

By:

Lobna Bouaziz‐Borgi;
Wassim Y. Almawi;
Nabil Mtiraoui;
Brahim Nsiri;
Sose H. Keleshian;
Raghid Kreidy;
Bessem Louzir;
Nathalie Hezard;
Touhami Mahjoub

Publication type:

Article

Association between adverse pregnancy outcomes and maternal factor V G1691A (Leiden) and prothrombin G20210A genotypes in women with a history of recurrent idiopathic miscarriages.

Published in:

American Journal of Hematology, 2005, v. 80, n. 1, p. 12, doi. 10.1002/ajh.20419

By:

Touhami Mahjoub;
Nabil Mtiraoui;
Hala Tamim;
Sondes Hizem;
Ramzi R. Finan;
Brahim Nsiri;
Wassim Y. Almawi

Publication type:

Article

Reduction in coagulation factor VII plasma levels by R353Q but not the -323P0/10 promoter polymorphism in healthy Tunisians.

Published in:

American Journal of Hematology, 2005, v. 79, n. 1, p. 11, doi. 10.1002/ajh.20328

By:

Nabil Mtiraoui;
Nesrine Aboud;
Hatem Bouraoui;
Sondes Haizem;
Jean Christophe Gris;
Marc Busson;
Hala Tamim;
Wassim Y. Almawi;
Touhami Mahjoub

Publication type:

Article

Polymorphisms in Genes Coding for the NK-Cell Receptor NKG2D and its Ligand MICA in Recurrent Miscarriage.

Published in:

American Journal of Reproductive Immunology, 2014, v. 72, n. 6, p. 577, doi. 10.1111/aji.12314

By:

Hizem, Sondes;
Mtiraoui, Nabil;
Massaoudi, Safia;
Fortier, Catherine;
Boukouaci, Wahid;
Kahina, Amokrane;
Charron, Dominique;
Mahjoub, Touhami;
Tamouza, Ryad

Publication type:

Article

Common polymorphisms of calpain-10 and the risk of Type 2 Diabetes in a Tunisian Arab population: a case-control study.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 75, doi. 10.1186/1471-2350-11-75

By:

Ezzidi, Intissar;
Turki, Amira;
Messaoudi, Safia;
Chaieb, Molka;
Kacem, Maha;
Al-Khateeb, Ghada M.;
Mahjoub, Touhami;
Almawi, Wassim Y.;
Mtiraoui, Nabil

Publication type:

Article

Contribution of type 2 diabetes associated loci in the Arabic population from Tunisia: a case-control study.

Published in:

BMC Medical Genetics, 2009, v. 10, p. 1, doi. 10.1186/1471-2350-10-33

By:

Ezzidi, Intissar;
Mtiraoui, Nabil;
Cauchi, Stéphane;
Vaillant, Emmanuel;
Dechaume, Aurélie;
Chaieb, Molka;
Kacem, Maha;
Almawi, Wassim Y.;
Froguel, Philippe;
Mahjoub, Touhami;
Vaxillaire, Martine

Publication type:

Article