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  1. No Access

    Chapter

    Restriction Fragment Length Polymorphism of HLA-DR7 Alleles and Association with HLA-B Antigens

    Although HLA-DR7 appears to be serologically homo- 2. geneous (1), it may be split according to epitopes recognized by T cells (Dw7, Dwl1) and is normally found in association with either DQw2 or DQw3. This re...

    Elizabeth A. Bidwell, Jeffrey L. Bidwell, Trevor J. Jones in Immunobiology of HLA (1989)

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    Chapter

    Identification of Dw2, Dw12, and “Short” DR2 Splits with Sequential Exon-Specific DRβ, DQβ, and DQα cDNA Probes

    The HLA-DR2 specificity has been divided by alloantisera (DR2 and “short” DR2) and by T cells (Dw2, Dw12, DB9 (LD-5a), FJO, and LD-MN2). The FJO and LD-MN2 splits appear to correlate with the short DR2 serotyp...

    Jeffrey L. Bidwell, Elizabeth A. Bidwell, David A. Savage in Immunobiology of HLA (1989)

  3. Article

    Fanconi anemia in Tunisia: high prevalence of group A and identification of new FANCA mutations

    Fanconi anemia (FA) is a rare autosomal recessive disease characterized by progressive pancytopenia, congenital malformations, and predisposition to acute myeloid leukemia. Fanconi anemia is genetically hetero...

    Chiraz Bouchlaka, Sonia Abdelhak, Ahlem Amouri, Hela Ben Abid in Journal of Human Genetics (2003)

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    Article

    Herpes simplex virus thymidine kinase gene transduction enhances tumor growth rate and cyclooxygenase-2 expression in murine colon cancer cells

    Transduction of tumor cells with herpes simplex virus thymidine kinase (HSV-tk) gene and subsequent treatment with the prodrug ganciclovir (GCV) is the most common system utilized to date for “suicide” gene th...

    Alexander Konson, Tsipi Ben-Kasus, Jamal A Mahajna, Abraham Danon in Cancer Gene Therapy (2004)

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    Article

    Selective gene transfer in vitro to tumor cells via recombinant Newcastle disease virus

    We developed a novel strategy to target recombinant Newcastle disease virus (NDV) to tumor cells for gene therapy. Modifying the virus with a bispecific fusion protein allowed virus receptor-independent tumor ...

    Huijie Bian, Philippe Fournier, Rob Moormann, Ben Peeters in Cancer Gene Therapy (2005)

  6. Article

    A single nucleotide substitution that abolishes the initiator methionine codon of the GLDC gene is prevalent among patients with glycine encephalopathy in Jerusalem

    Glycine encephalopathy (GE) (non-ketotic hyperglycinemia) is an autosomal recessive neurometabolic disease caused by defective activity of the glycine cleavage system. Clinically, patients present usually in t...

    Avihu Boneh, Stanley H. Korman, Kenichi Sato, Junko Kanno in Journal of Human Genetics (2005)

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    Article

    Fragile sites are preferential targets for integrations of MLV vectors in gene therapy

    Following gene therapy of SCID-X1 using murine leukemia virus (MLV) derived vector, two patients developed leukemia owing to an activating vector integration near the LMO2 gene. We found that these integrations r...

    A C Bester, M Schwartz, M Schmidt, A Garrigue, S Hacein-Bey-Abina in Gene Therapy (2006)

  8. Article

    Further evidence of the clinical and genetic heterogeneity of recessive transgressive PPK in the Mediterranean region

    Transgressive palmoplantar keratoderma (PPK) is the phenotypic hallmark of Mal de Meleda (MDM, MIM 24300). It is characterized by erythema and hyperkeratosis that extend to the dorsal face of the hands and fee...

    Cherine Charfeddine, Mourad Mokni, Selma Kassar, Hela Zribi in Journal of Human Genetics (2006)

  9. Article

    Erratum: Fragile sites are preferential targets for integrations of MLV vectors in gene therapy

    Correction to: Gene Therapy (2006) 13, 1057–1059. doi:10.1038/sj.gt.3302752 Since the above publication the authors have noticed an error in the first DNA marker of FRA11E in Supplementary Table 1S. The correc...

    A C Bester, M Schwartz, M Schmidt, A Garrigue, S Hacein-Bey-Abina in Gene Therapy (2007)

  10. Article

    Contribution of the BRCA1 and BRCA2 mutations to breast cancer in Tunisia

    Hereditary breast cancer accounts for 3–8% of all breast cancers, with mutations in the BRCA1 and BRCA2 genes responsible for up to 30% of these. To investigate the prevalence of BRCA1 and BRCA2 gene mutations...

    Wafa Troudi, N. Uhrhammer, C. Sibille, C. Dahan, W. Mahfoudh in Journal of Human Genetics (2007)

  11. Article

    Association of the serotonin transporter gene, neuroticism and smoking behaviours

    Cigarette consumption and smoking cessation are influenced in part by genes. Personality traits have also been implicated in the aetiology of smoking. Neuroticism, a personality trait with a heritable componen...

    Colin O’Gara, Jo Knight, John Stapleton, Jason Luty, Ben Neale in Journal of Human Genetics (2008)

  12. No Access

    Article

    Antiangiogenic systemic gene therapy combined with doxorubicin administration induced caspase 8 and 9-mediated apoptosis in endothelial cells and an anti-metastasis effect

    Ad-PPE-Fas-c is an adenovector that expresses Fas-c under the control of the modified pre-proendothelin-1 (PPE-1) promoter. Fas-c is a chimeric death receptor containing the extracellular portion of tumour nec...

    M Peled, A Shaish, S Greenberger, A Katav, I Hodish, D Ben-Shushan in Cancer Gene Therapy (2008)

  13. Article

    Erratum: Selective oncolytic effect of an attenuated Newcastle disease virus (NDV-HUJ) in lung tumors

    Cancer Gene Therapy (2008) 15, 795–807; doi:10.1038/cgt.2008.31 The authors have noticed a spelling error in the author line. The correct author is shown below. E Eliahoo The authors would like to apologize fo...

    B Yaacov, E Elihaoo, I lazar, M Ben-Shlomo, I Greenbaum, A Panet in Cancer Gene Therapy (2008)

  14. No Access

    Article

    Selective oncolytic effect of an attenuated Newcastle disease virus (NDV-HUJ) in lung tumors

    Newcastle disease virus (NDV), an avian paramyxovirus, has a potential oncolytic effect that may be of significance in the treatment of a variety of cancer diseases. An attenuated lentogenic isolate of NDV (HU...

    B Yaacov, E Elihaoo, I lazar, M Ben-Shlomo, I Greenbaum, A Panet in Cancer Gene Therapy (2008)

  15. Chapter

    Nucleic Acids-Based Therapeutics in the Battle Against Pathogenic Viruses

    For almost three decades, researchers have studied the possibility to use nucleic acids as antiviral therapeutics. In theory, compounds such as antisense oligonucleotides, ribozymes, DNAzymes, and aptamers can...

    Joost Haasnoot, Ben Berkhout in Antiviral Strategies (2009)

  16. No Access

    Article

    Consanguinity, endogamy, and genetic disorders in Tunisia

    Nizar Ben Halim, Nissaf Ben Alaya Bouafif, Lilia Romdhane in Journal of Community Genetics (2013)

  17. Article

    Open Access

    Flowing through the CRISPR-CAScade: Will genome editing boost cell therapies?

    Recent years have seen great advancements in genome editing technologies, allowing for efficient and specific targeting of DNA sequences into the genome. In parallel, advancements in stem cell research, and es...

    Uri Ben-David in Molecular and Cellular Therapies (2013)

  18. Article

    Open Access

    Mutation spectrum of Joubert syndrome and related disorders among Arabs

    Joubert syndrome (JS) is a rare autosomal recessive (AR), neurological condition characterized by dysgenesis of the cerebellar vermis with the radiological hallmark of molar tooth sign, oculomotor apraxia, rec...

    Salma Ben-Salem, Aisha M Al-Shamsi, Joseph G Gleeson in Human Genome Variation (2014)

  19. No Access

    Book

  20. No Access

    Chapter

    Gene Therapy Strategies to Block HIV-1 Replication by RNA Interference

    The cellular mechanism of RNA interference (RNAi) plays an antiviral role in many organisms and can be used for the development of therapeutic strategies against viral pathogens. Persistent infections like the...

    Elena Herrera-Carrillo Ph.D. in Gene Therapy for HIV and Chronic Infections (2015)

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