405 results on '"Mahjoub, Touhami"'
Search Results
2. Association of MTHFR C677T and A1298C variants with preeclampsia risk and angiogenic imbalance in Tunisian women
3. Interleukin 10 (IL-10) gene variants and haplotypes in Tunisian women with polycystic ovary syndrome (PCOS): a case-control study
4. Preeclampsia is associated with reduced renin, aldosterone, and PlGF levels, and increased sFlt-1/PlGF ratio, and specific angiotensin-converting enzyme Ins-Del gene variants
5. Association of MMP-2 genes variants with diabetic retinopathy in Tunisian population with type 2 diabetes
6. Contribution of -1031T/C and -376G/A tumor necrosis factor alpha polymorphisms and haplotypes to preeclampsia risk in Tunisia (North Africa)
7. Association of matrix metalloproteinase-2 gene polymorphisms with susceptibility to type 2 diabetes: A case control study
8. Increased physical activity is correlated with improved pregnancy outcomes in women with preeclampsia: A retrospective study
9. Relation of rs846910, rs4844880 11β-hydroxysteroid dehydrogenase type 1 (HSD11B1) polymorphisms with the risk of preeclampsia: A case-control study
10. Impact of obesity on the association of active renin and plasma aldosterone concentrations, and aldosterone-to-renin ratio with preeclampsia
11. Association of VEGFA variants with altered VEGF secretion and type 2 diabetes: A case-control study
12. Progesterone Receptor (PGR) Gene Variants Associated with Breast Cancer and Associated Features: a Case-Control Study
13. Association of Genetic Variants in NF-kB with Susceptibility to Breast Cancer: a Case Control Study
14. Vascular endothelial growth factor single nucleotide polymorphisms and haplotypes in pre-eclampsia: A case-control study
15. FGF1 and FGF2 mutations in preeclampsia and related features
16. Placental growth factor and vascular endothelial growth factor serum levels in Tunisian Arab women with suspected preeclampsia
17. IKZF1 genetic variants rs4132601 and rs11978267 and acute lymphoblastic leukemia risk in Tunisian children: a case-control study
18. Thymoquinone induces G2/M cell cycle phase arrest and apoptosis through inhibition of JNK phosphorylation and induction of p53 and p21 expression in HT-1080 fibrosarcoma cells
19. Thymoquinone effects on DMH-induced erythrocyte oxidative stress and haematological alterations during colon cancer promotion in rats
20. Effect of thymoquinone on 1,2-dimethyl-hydrazine-induced oxidative stress during initiation and promotion of colon carcinogenesis
21. Lack of association between genetic polymorphisms within KCNQ1 locus and type 2 diabetes in Tunisian Arabs
22. Single-nucleotide polymorphisms and haplotypes in the adiponectin gene contribute to the genetic risk for type 2 diabetes in Tunisian Arabs
23. miR-146a, miR-196a2, miR-499, and miR-149 linked with susceptibility to acute lymphoblastic leukemia: A case-control study in Tunisia
24. 174G>C interleukin-6 gene polymorphism in Tunisian patients with coronary artery disease
25. Common polymorphisms of calpain-10 and the risk of polycystic ovary syndrome in Tunisian population: a case–control study
26. Polymorphisms of human platelet alloantigens HPA-1 and HPA-2 associated with severe coronary artery disease
27. TNF-α −308G > A and IL-6 −174G > C polymorphisms in Tunisian patients with coronary artery disease
28. Tumor necrosis factor α and lymphotoxin α haplotypes in idiopathic recurrent pregnancy loss
29. Association of Lymphotoxin Alpha Polymorphism with Type 1 Diabetes in a Tunisian Population
30. Factor VII levels, R353Q and -323P0/10 Factor VII variants, and the risk of acute coronary syndrome among Arab-African Tunisians
31. Contribution of coagulation factor VII R353Q, −323P0/10 and HVR4 polymorphisms to coronary artery disease in Tunisians
32. Contribution of JAK2 and STAT3 variants to the genetic susceptibility of recurrent miscarriage among Bahraini and Tunisian Arabs
33. IL-10 modulates fondaparinux inhibition of monocyte-induced thrombin generation
34. Contribution of SELP and PSGL-1 genotypes and haplotypes to the presence of coronary heart disease in Tunisians
35. Association of endothelial nitric oxide synthase Glu298Asp, 4b/a, and −786T>C gene variants with diabetic nephropathy
36. Differential inhibitory effect of fondaparinux on the procoagulant potential of intact monocytes and monocyte-derived microparticles
37. Human platelet alloantigens HPA-1, HPA-2, and HPA-3 polymorphisms associated with extent of severe coronary artery disease
38. Association of three polymorphisms selected from a genome-wide association study with coronary heart disease in the Tunisian population
39. Polymorphisms in Genes Coding for the NK-Cell Receptor NKG2D and its Ligand MICA in Recurrent Miscarriage
40. Association of the IL-10 Receptor A536G (S138G) Loss-of-Function Variant with Recurrent Miscarriage
41. P-selectin gene polymorphisms and risk of coronary heart disease among Tunisians
42. Homocysteine and methylenetetrahydrofolate reductase C677T and A1298C polymorphisms in Tunisian patients with severe coronary artery disease
43. Interaction of angiotensin-converting enzyme and apolipoprotein E gene polymorphisms in ischemic stroke involving large-vessel disease
44. MMP-2 and MMP-9 Polymorphisms and Preeclampsia Risk in Tunisian Arabs: A Case-Control Study
45. Association of Apolipoprotein E Gene Polymorphism With Ischemic Stroke Involving Large-Vessel Disease and Its Relation to Serum Lipid Levels
46. Association of PAI-1 4G/5G and -844G/A Gene Polymorphism and Changes in PAI-1/tPA Levels in Stroke: A Case-Control Study
47. MTHFR C677T and A1298C gene polymorphisms and hyperhomocysteinemia as risk factors of diabetic nephropathy in type 2 diabetes patients
48. Varied Prevalence of Factor V G1691A (Leiden) and Prothrombin G20210A Single Nucleotide Polymorphisms Among Arabs
49. Plasminogen Activator Inhibitor 1 4G/5G and −844G/A Variants in Idiopathic Recurrent Pregnancy Loss
50. Contrasting association of Leptin receptor polymorphisms and haplotypes with polycystic ovary syndrome in Bahraini and Tunisian women: a case–control study
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