303 results on '"Ayadi, Hammadi"'
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2. Affinity kinetics of leptin-reactive immunoglobulins are associated with plasma leptin and markers of obesity and diabetes
3. Segregation of S292F TPO gene mutation in three large Tunisian families with thyroid dyshormonogenesis: evidence of a founder effect
4. IL-1β and TSH disturb thyroid epithelium integrity in autoimmune thyroid diseases
5. Segregation of a new mutation in SLC26A4 and p.E47X mutation in GJB2 within a consanguineous Tunisian family affected with Pendred syndrome
6. Analysis of the variability of human normal urine by 2D-GE reveals a “public” and a “private” proteome
7. DFNB66 and DFNB67 loci are non allelic and rarely contribute to autosomal recessive nonsyndromic hearing loss
8. A novel missense mutation in the ESRRB gene causes DFNB35 hearing loss in a Tunisian family
9. SLC26A4 expression among autoimmune thyroid tissues
10. Analysis of two Arab families reveals additional support for a DFNB2 nonsyndromic phenotype of MYO7A
11. A Novel Autosomal Recessive Non-Syndromic Deafness Locus, DFNB66 , Maps to Chromosome 6p21.2-22.3 in a Large Tunisian Consanguineous Family
12. Genetic association between AZF region polymorphism and Klinefelter syndrome
13. An interethnic variability and a functional prediction of DNA repair gene polymorphisms: the example of XRCC3 (p.Thr241>Met) and XPD (p.Lys751>Gln) in a healthy Tunisian population
14. No major genes in autoimmune thyroid diseases: complex segregation and epidemiological studies in a large Tunisian pedigree
15. A potential role of TNFR gene polymorphisms in autoimmune thyroid diseases in the Tunisian population
16. Thyroglobulin polymorphisms in Tunisian patients with autoimmune thyroid diseases (AITD)
17. DNase1 exon2 analysis in Tunisian patients with rheumatoid arthritis, systemic lupus erythematosus and Sjögren syndrome and healthy subjects
18. A genome-wide linkage scan in Tunisian families identifies a novel locus for non-syndromic posterior microphthalmia to chromosome 2q37.1
19. Lack of Association of VDR Gene Polymorphisms with Thyroid Autoimmune Disorders: Familial and Case/Control Studies
20. Allelic structure and distribution of 103 STR loci in a Southern Tunisian population
21. New FKRP mutations causing congenital muscular dystrophy associated with mental retardation and central nervous system abnormalities. Identification of a founder mutation in Tunisian families
22. Hashimoto's Disease
23. Association of intronic repetition of SLC26A4 gene with Hashimoto thyroiditis disease
24. Evaluation of CTLA-4, CD28 and CD86 Genes Polymorphisms in Acute Renal Allograft Rejection among Tunisian Patients
25. Cloning and expression of functional single-chain Fv antibodies directed against NIa and coat proteins of potato virus Y
26. Association of COL1A1 and TGFB1 Polymorphisms with Otosclerosis in a Tunisian Population
27. Proteomic approaches for discovering biomarkers of diabetic nephropathy
28. Genetic variants in RELN are associated with otosclerosis in a non-European population from Tunisia
29. Renal α-smooth muscle actin: A new prognostic factor for lupus nephritis
30. TMC1 but Not TMC2 Is Responsible for Autosomal Recessive Nonsyndromic Hearing Impairment in Tunisian Families
31. Gene and protein markers of diabetic nephropathy
32. Erratum to: Segregation of S292F TPO gene mutation in three large Tunisian families with thyroid dyshormonogenesis: evidence of a founder effect
33. The genetics of autoimmune thyroid disease
34. Androgen receptor gene CAG repeats length in fertile and infertile Tunisian men
35. Evolution of the rabbit immunoglobulin κ chain genes
36. The A/T mutation in exon 2 of the DNASE1 gene is not present in Tunisian patients with systemic lupus erythematosus or in healthy subjects
37. PDS Is a New Susceptibility Gene to Autoimmune Thyroid Diseases: Association and Linkage Study
38. Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin
39. HLA class I and II polymorphisms in a large multiplex family with autoimmune thyroid diseases
40. Determination of the frequency of connexin26 mutations in inherited sensorineural deafness and carrier rates in the Tunisian population using DGGE
41. Mutations of GJB2 in three geographic isolates from northern Tunisia: evidence for genetic heterogeneity within isolates
42. Potential role of liver enzyme levels as predictive markers of glucose metabolism disorders in a Tunisian population
43. CTLA-4 Gene Polymorphisms in Tunisian Patients with Graves' Disease
44. Lack of linkage and association between autoimmune thyroid diseases and the CTLA-4 gene in a large tunisian family
45. Down-expression of P2RX2, KCNQ5, ERBB3 and SOCS3 through DNA hypermethylation in elderly women with presbycusis
46. SLC26A4 Variations Among Graves’ Hyper-Functioning Thyroid Gland
47. Molecular modelling: a tool for understanding the cytoplasm-nucleus-nucleolus shuttling of the ceramide kinase-like protein
48. Down-expression of <italic>P2RX2</italic>, <italic>KCNQ5</italic>, <italic>ERBB3</italic> and <italic>SOCS3</italic> through DNA hypermethylation in elderly women with presbycusis.
49. <italic>Retracted</italic>: Genotyping of Tunisian azoospermic men with Sertoli cell‐only and maturation arrest.
50. A 20year history of clinical and genetic study of thyroid autoimmunity in a Tunisian multigenerational family: Evidence for gene interaction
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