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Procédés de Criblage Moléculaire et Cellulaire >> Liste des publications


Amouri M, Masmoudi A, Borgi N, Rebai A et Turki H (2011) Atopic dermatitis in Tunisian schoolchildren. Pan African Medical Journal. 9(1).
Arbi M E, Pigeon P, Rkhis A C, Top S, Rhouma A, Rebai A, Jaouen G et Aifa S (2011) Antimicrobial effect of ferrocenyl diaryl butenes against olive plantlet diseases. Journal of Plant Pathology. 651-657.
Belguith-Maalej S, Rebuffat S A, Charfeddine I, Mnif M, Nadir R F, Abid M, Ghorbel A, Peraldi-Roux S, Ayadi H et Hadj-Kacem H (2011) SLC26A4 expression among autoimmune thyroid tissues. Immunobiology. 216(5): 571-578.
Bensaïd M, Hmani-Aifa M, Hammami B, Tlili A, Hakim B, Charfeddine I, Ayadi H, Ghorbel A, del Castillo I et Masmoudi S (2011) DFNB66 and DFNB67 loci are non allelic and rarely contribute to autosomal recessive nonsyndromic hearing loss. European journal of medical genetics. 54(6): e565-e569.
Bougacha-Elleuch N, Arab S B, Rebai A, Mnif M, Maalej A, Charfi N, Lassouad M B, Jouida J, Abid M et Ayadi H (2011) No major genes in autoimmune thyroid diseases: complex segregation and epidemiological studies in a large Tunisian pedigree. Journal of genetics. 90(2): 333.
Choura M et Rebaï A (2011) Receptor tyrosine kinases: from biology to pathology. Journal of Receptors and Signal Transduction. 31(6): 387-394.
Choura M et Rebaï A (2011) Structural analysis of hubs in human NR-RTK network. Biol Direct. 6: 49.
Daneshpour M S, Rebai A, Houshmand M, Alfadhli S, Zeinali S, Hedayati M, Zarkesh M et Azizi F (2011) 8q24. 3 and 11q25 chromosomal loci association with low HDL‐C in metabolic syndrome. European journal of clinical investigation. 41(10): 1105-1112.
El Arbi M, Pigeon P, Top S, Rhouma A, Aifa S, Rebai A, Vessières A, Plamont M-A et Jaouen G (2011) Evaluation of bactericidal and fungicidal activity of ferrocenyl or phenyl derivatives in the diphenyl butene series. Journal of Organometallic Chemistry. 696(5): 1038-1048.
Fendri-Kriaa N, Boujilbene S, Kammoun F, Mkaouar-Rebai E, Mahmoud A B, Hsairi I, Rebai A, Triki C et Fakhfakh F (2011) A putative disease-associated haplotype within the SCN1A gene in Dravet syndrome. Biochemical and biophysical research communications. 408(4): 654-657.
Fendri‐Kriaa N, Kammoun F, Salem I H, Kifagi C, Mkaouar‐Rebai E, Hsairi I, Rebai A, Triki C et Fakhfakh F (2011) New mutation c. 374C> T and a putative disease‐associated haplotype within SCN1B gene in Tunisian families with febrile seizures. European Journal of Neurology. 18(5): 695-702.
Jemel I, Jellali K, Elloumi J et Aifa S (2011) The offer of chemistry to targeted therapy in cancer. Recent patents on biotechnology. 5(3): 174-182.
Kallel-Bayoudh I, Hassen H B, Khabir A, Boujelbene N, Daoud J, Frikha M, Sallemi-Boudawara T, Aifa S et Rebaï A (2011) Bcl-2 expression and triple negative profile in breast carcinoma. Medical Oncology. 28(1): 55-61.
Khalfallah A, Schrauwen I, Mnejja M, HadjKacem H, Dhouib L, Mosrati M A, Hakim B, Lahmar I, Charfeddine I et Driss N (2011) Association of COL1A1 and TGFB1 polymorphisms with otosclerosis in a Tunisian population. Annals of human genetics. 75(5): 598-604.
Louhichi A, Fourati A et Rebaï A (2011) IGD: a resource for intronless genes in the human genome. Gene. 488(1): 35-40.
Mosrati M A, Hammami B, Rebeh I B, Ayadi L, Dhouib L, Hakim B, Charfeddine I, Mnif J, Ghorbel A et Masmoudi S (2011) A novel dominant mutation in SIX1, affecting a highly conserved residue, result in only auditory defects in humans. European journal of medical genetics. 54(5): e484-e488.
Nair K S, Hmani-Aifa M, Ali Z, Kearney A L, Salem S B, Macalinao D G, Cosma I M, Bouassida W, Hakim B et Benzina Z (2011) Alteration of the serine protease PRSS56 causes angle-closure glaucoma in mice and posterior microphthalmia in humans and mice. Nature genetics. 43(6): 579-584.
Ouechtati F, Merdassi A, Bouyacoub Y, Largueche L, Derouiche K, Ouragini H, Nouira S, Tiab L, Baklouti K et Rebai A (2011) Clinical and genetic investigation of a large Tunisian family with complete achromatopsia: identification of a new nonsense mutation in GNAT2 gene. Journal of human genetics. 56(1): 22-28.
Saïd M B, Ayedi L, Mnejja M, Hakim B, Khalfallah A, Charfeddine I, Khifagi C, Turki K, Ayadi H et BenZina Z (2011) A novel missense mutation in the ESRRB gene causes DFNB35 hearing loss in a Tunisian family. European journal of medical genetics. 54(6): e535-e541.
Salah G B, Kamoun H, Rebai A, Youssef A B, Ayadi H, Belghith-Mahfoudh N, Fourati A, Ayadi H et Fakhfakh F (2011) Sister chromatid exchange (SCE) and high-frequency cells (HFC) in peripheral blood lymphocytes of healthy Tunisian smokers. Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 719(1): 1-6.


Belguith-Maalej S, Hadj-Kacem H, Rebuffat S A, Mnif-Feki M, Nguyen B, Abid M, Gross R, Ayadi H et Peraldi-Roux S (2009) Absence of anti-pendrin auto-antibodies in the sera of Tunisian patients with autoimmune thyroid diseases. Clinical laboratory. 56(7-8): 335-343.
Hakim I R, Kammoun N G, Makhloufi E et Rebaï A (2009) Discovery and potential of SNP markers in characterization of Tunisian olive germplasm. Diversity. 2(1): 17-27.
Ben H M, Cornelis F, Mbarek H, Chabchoub G, Marzouk S, Bahloul Z, Rebai A, Fakhfakh F, Ayadi H et Petit-Teixeira E (2010) Signal transducer and activator of transcription and the risk of rheumatoid arthritis and thyroid autoimmune disorders. Clinical and experimental rheumatology. 29(2): 269-274.
AlFadhli S, AlKharrat N et AlRebai A (2010) Genome scan meta-analysis in systemic lupus erythematosus strong linkage with loci 6p22. 3-p21. 1 and 2q31. 1-34. J Med Genet Genomics. 2: 001-009.
AlFadhli S, AlTamimy B, Kharrat N, AlSaeid K, Haider M Z et Rebai A (2010) Molecular analysis of HumDN1 VNTR polymorphism of the human deoxyribonuclease I in systemic lupus erythematosus. International journal of immunogenetics. 37(1): 5-8.
Ben Rebeh I, Morinière M, Ayadi L, Benzina Z, Charfedine I, Feki J, Ayadi H, Ghorbel A, Baklouti F et Masmoudi S (2010) Reinforcement of a minor alternative splicing event in MYO7A due to a missense mutation results in a mild form of retinopathy and deafness.
Bouchaala L, Masmoudi A, Gargouri F et Rebai A (2010) Improving algorithms for structure learning in Bayesian Networks using a new implicit score. Expert Systems with Applications. 37(7): 5470-5475.
Choura M, Frikha F, Kharrat N, Aifa S et Rebaï A (2010) Investigating the function of three non-synonymous SNPs in EGFR gene: structural modelling and association with breast cancer. The protein journal. 29(1): 50-54.
Choura M et Rebaï A (2010) Application of computational approaches to study signalling networks of nuclear and Tyrosine kinase receptors. Biology direct. 5(1): 58.
Fendri-Kriaa N, Louhichi N, Mkaouar-Rebai E, Chabchoub G, Kammoun F, Salem I H, Rebai A, Triki C et Fakhfakh F (2010) The first genome-wide scan in a Tunisian family with generalized epilepsy with febrile seizure plus (GEFS+). Journal of child neurology.
Hadj-Kacem H, Kallel R, Belguith-Maalej S, Mnif M, Charfeddine I, Ghorbel A, Abid M, Ayadi H et Masmoudi S (2010) SLC26A4 variations among Graves' hyper-functioning thyroid gland. Disease markers. 29(2): 63-69.
Kallel I, Kharrat N, Al-fadhly S, Rebai M, Khabir A, Boudawara T S et Rebaï A (2010) HER2 polymorphisms and breast cancer in Tunisian women. Genetic testing and molecular biomarkers. 14(1): 29-35.
Khalfallah A, Schrauwen I, Mnaja M, Fransen E, Lahmar I, Ealy M, Dhouib L, Ayadi H, Charfedine I et Driss N (2010) Genetic variants in RELN are associated with otosclerosis in a non‐European population from Tunisia. Annals of human genetics. 74(5): 399-405.
Masmoudi Y, Chabchoub H, Hanafi S et Rebaï A (2010) A mathematical programming based procedure for breast cancer classification. Journal of Mathematical Modelling and Algorithms. 9(3): 247-255.
Rebeh I B, Yoshimi N, Hadj‐Kacem H, Yanohco S, Hammami B, Mnif M, Araki M, Ghorbel A, Ayadi H et Masmoudi S (2010) Two missense mutations in SLC26A4 gene: a molecular and functional study. Clinical genetics. 78(1): 74-80.
Saïd M B, Hmani-Aifa M, Amar I, Baig S M, Mustapha M, Delmaghani S, Tlili A, Ghorbel A, Ayadi H et Van Camp G (2010) High frequency of the p. R34X mutation in the TMC1 gene associated with nonsyndromic hearing loss is due to founder effects. Genetic testing and molecular biomarkers. 14(3): 307-311.
Siala O, Rebai A, Baklouti F et Fakhfakh F (2010) Subtle discrepancies of SF2/ASF ESE sequence motif among human tissues: A computational approach. Computational biology and chemistry. 34(3): 203-209.
Triki-Fendri S, Alfadhli S, Ayadi I, Kharrat N, Ayadi H et Rebai A (2010) Genetic structure of Kuwaiti population revealed by Y-STR diversity. Annals of human biology. 37(6): 827-835.

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