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Procédés de Criblage Moléculaire et Cellulaire >> Liste des publications

2017

Tekari A, May R, Frauchiger D A, Chan S, Benneker L M et Gantenbein B (2017) The BMP2 variant L51P restores the osteogenic differentiation of human mesenchymal stromal cells in the presence of intervertebral disc cells. European cells & materials eCM. 33: 197-210.
Frauchiger D A, Tekari A, Wöltje M, Fortunato G, Benneker L M et Gantenbein B (2017) A review of the application of reinforced hydrogels and silk as biomaterials for intervertebral disc repair. European cells & materials eCM. 34: 271-290.
Belmabrouk S, Kharrat N, Abdelhedi R, Ayed A B, Benmarzoug R et Rebai A (2017) Screening of nucleotide variations in genomic sequences encoding charged protein regions in the human genome. BMC genomics. 18(1): 588.
Ayed R B, Ennouri K, Amar F B, Moreau F, Triki M A et Rebai A (2017) Bayesian and phylogenic approaches for studying relationships among table olive cultivars. Biochemical genetics. 55(4): 300-313.
Ayed R B, Ennouri K, Hlima H B, Smaoui S, Hanana M, Mzid R, Ercişli S et Rebai A (2017) Identification and characterization of single nucleotide polymorphism markers in FADS2 gene associated with olive oil fatty acids composition. Lipids in health and disease. 16(1): 138.
Ben Saad H, Kharrat N, Driss D, Gargouri M, Marrakchi R, Jammoussi K, Magné C, Boudawara T, Ellouz Chaabouni S et Zeghal K M (2017) Effects of vanillin on potassium bromate-induced neurotoxicity in adult mice: impact on behavior, oxidative stress, genes expression, inflammation and fatty acid composition. Archives of physiology and biochemistry. 123(3): 165-174.
Bouhajja H, Kacem F H, Abdelhedi R, Ncir M, Dimitrov J D, Marrakchi R, Jamoussi K, Rebai A, El Feki A et Abid M (2017) Potential Predictive Role of Lipid Peroxidation Markers for Type 2 Diabetes in the Tunisian Population. Canadian journal of diabetes.
Choura M et Rebaï A (2017) Exploring disorder in the human charged biased proteins. Journal of Receptors and Signal Transduction. 37(4): 386-390.
Feki-Sahnoun W, Hamza A, Njah H, Barraj N, Mahfoudi M, Rebai A et Hassen M B (2017) A Bayesian network approach to determine environmental factors controlling Karenia selliformis occurrences and blooms in the Gulf of Gabès, Tunisia. Harmful algae. 63: 119-132.
Feki-Tounsi M, Khlifi R, Louati I, Fourati M, Mhiri M-N, Hamza-Chaffai A et Rebai A (2017) Polymorphisms in XRCC1, ERCC2, and ERCC3 DNA repair genes, CYP1A1 xenobiotic metabolism gene, and tobacco are associated with bladder cancer susceptibility in Tunisian population. Environmental Science and Pollution Research. 24(28): 22476-22484.
Jabeur H, Drira M, Rebai A et Bouaziz M (2017) Putative Markers of Adulteration of Higher-Grade Olive Oil with Less Expensive Pomace Olive Oil Identified by Gas Chromatography Combined with Chemometrics. Journal of agricultural and food chemistry. 65(26): 5375-5383.
Jardak M, Elloumi-Mseddi J, Aifa S et Mnif S (2017) Chemical composition, anti-biofilm activity and potential cytotoxic effect on cancer cells of Rosmarinus officinalis L. essential oil from Tunisia. Lipids in health and disease. 16(1): 190.
Khlifi R, Olmedo P, Gil F, Hammami B, Hamza-Chaffai A et Rebai A (2017) Gene–environment interactions between ERCC2, ERCC3, XRCC1 and cadmium exposure in nasal polyposis disease. Journal of applied genetics. 58(2): 221-229.
Paul A, Drecourt A, Petit F, Deguine D D, Vasnier C, Oufadem M, Masson C, Bonnet C, Masmoudi S et Mosnier I (2017) FDXR Mutations Cause Sensorial Neuropathies and Expand the Spectrum of Mitochondrial Fe-S-Synthesis Diseases. The American Journal of Human Genetics. 101(4): 630-637.
Zghal R Z, Elleuch J, Ali M B, Darriet F, Rebaï A, Chandre F, Jaoua S et Tounsi S (2017) Towards novel Cry toxins with enhanced toxicity/broader: a new chimeric Cry4Ba/Cry1Ac toxin. Applied microbiology and biotechnology. 101(1): 113-122.

2016 
Kharrat N, Belmabrouk S, Abdelhedi R, Benmarzoug R, Assidi M, Al Qahtani M H et Rebai A (2016) Screening for clusters of charge in human virus proteomes. BMC genomics. 17(9): 758.
Triki‐Fendri S, Sánchez‐Diz P, Rey‐González D, Alfadhli S, Ayadi I, Ben Marzoug R, Carracedo Á et Rebai A (2016) Genetic structure of the Kuwaiti population revealed by paternal lineages. American Journal of Human Biology. 28(2): 203-212.
Ayadi M, Hanana M, Kharrat N, Merchaoui H, Marzoug R B, Lauvergeat V, Rebaï A et Mzid R (2016) The WRKY transcription factor family in citrus: valuable and useful candidate genes for citrus breeding. Applied biochemistry and biotechnology. 180(3): 516-543.
Ayed R B, Hassen H B, Ennouri K et Rebai A (2016) Genetic markers analyses and bioinformatic approaches to distinguish between olive tree (Olea europaea L.) Cultivars. Interdisciplinary Sciences: Computational Life Sciences. 8(4): 366-373.
Ben Ayed R, Ben Hassen H, Ennouri K, Ben Marzoug R et Rebai A (2016) OGDD (Olive Genetic Diversity Database): a microsatellite markers' genotypes database of worldwide olive trees for cultivar identification and virgin olive oil traceability. Database. 2016.
Ben-Rebeh I, Grati M, Bonnet C, Bouassida W, Hadjamor I, Ayadi H, Ghorbel A, Petit C et Masmoudi S (2016) Genetic analysis of Tunisian families with Usher syndrome type 1: toward improving early molecular diagnosis. Molecular vision. 22: 827.
Ben-Rebeh I, Grati M, Bonnet C, Bouassida W, Hadjamor I, Ayadi H, Ghorbel A, Petit C et Masmoudi S (2016) Genetic analysis of Tunisian families with Usher syndrome type 1: toward improving early molecular diagnosis. Molecular vision. 22: 827.
Bulbul O, Filoglu G, Zorlu T, Altuncul H, Freire-Aradas A, Söchtig J, Ruiz Y, Klintschar M, Triki-Fendri S et Rebai A (2016) Inference of biogeographical ancestry across central regions of Eurasia. International journal of legal medicine. 130(1): 73-79.
Chaabane S, Marzouk S, Akrout R, Hamad M B, Achour Y, Rebai A, Keskes L, Fourati H, Bahloul Z et Maalej A (2016) Genetic determinants of methotrexate toxicity in tunisian patients with rheumatoid arthritis: a study of polymorphisms involved in the MTX metabolic pathway. European journal of drug metabolism and pharmacokinetics. 41(4): 385-393.
Chakroun A, Said M B, Ennouri A, Achour I, Mnif M, Abid M, Ghorbel A, Marshall J D, Naggert J K et Masmoudi S (2016) Long-term clinical follow-up and molecular testing for diagnosis of the first Tunisian family with Alström syndrome. European journal of medical genetics. 59(9): 444-451.
Choura M, Hanin M, Rebaï A et Masmoudi K (2016) From FHB Resistance QTLs to Candidate Genes Identification in Triticum aestivum L. Interdisciplinary Sciences: Computational Life Sciences. 8(4): 352-356.
El Arbi M, Jalléli K, Trigui F, Pigeon P, Görmen M, Top S, Aifa S, Fliss I, Jaouen G et Hammami R (2016) Efficacy of a novel ferrocenyl diaryl butene citrate compound as a biocide for preventing healthcare-associated infections. MedChemComm. 7(5): 948-954.
Grati M h, Yan D, Raval M H, Walsh T, Ma Q, Chakchouk I, Kannan‐Sundhari A, Mittal R, Masmoudi S, Blanton S H et Tekin M (2016) MYO3A Causes Human Dominant Deafness and Interacts with Protocadherin 15‐CD2 Isoform. Human mutation. 37(5): 481-487.
Halim N B, Dorboz I, Kefi R, Kharrat N, Eymard-Pierre E, Nagara M, Romdhane L, Alaya-Bouafif N B, Rebai A et Miladi N (2016) Determination of arylsulfatase A pseudodeficiency allele and haplotype frequency in the Tunisian population. Neurological Sciences. 37(3): 403-409.
Kallabi F, Rebeh I B, Felhi R, Sellami D, Masmoudi S, Keskes L et Kamoun H (2016) Molecular analysis of Libyan families with Allgrove Syndrome: geographic expansion of the ancestral mutation c. 1331+ 1G> A in North Africa. Hormone research in paediatrics. 85(1): 18-21.
Mzid R, Chibani F, Ayed R B, Hanana M, Breidi J, Kabalan R, El-Hajj S, Machlab H, Rebai A et Chalak L (2016) Genetic diversity in barley landraces (Hordeum vulgare L. subsp. vulgare) originated from Crescent Fertile region as detected by seed storage proteins. Journal of genetics. 95(3): 733-739.
Said M B, Grati M h, Ishimoto T, Zou B, Chakchouk I, Ma Q, Yao Q, Hammami B, Yan D et Mittal R (2016) A mutation in SLC22A4 encoding an organic cation transporter expressed in the cochlea strial endothelium causes human recessive non-syndromic hearing loss DFNB60. Human genetics. 135(5): 513-524.
Souiden Y, Mallouli H, Meskhi S, Chaabouni Y, Rebai A, Chéour F et Mahdouani K (2016) MnSOD and GPx1 polymorphism relationship with coronary heart disease risk and severity. Biological research. 49(1): 22.
Yan D, Tekin D, Bademci G, Foster J, Cengiz F B, Kannan-Sundhari A, Guo S, Mittal R, Zou B et Grati M (2016) Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents. Human genetics. 135(8): 953-961.
Zidi I, Kharrat N, Abdelhedi R, Hassine A B, Laaribi A B, Yahia H B, Abdelmoula N B, Abid L, Rebai A et Rizzo R (2016) Nonclassical human leukocyte antigen (HLA-G, HLA-E, and HLA-F) in coronary artery disease. Human immunology. 77(4): 325-329.

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