All Stories

  1. Hematopoietic Stem Cell Transplantation as Treatment for Patients with DOCK8 Deficiency
  2. Underlying molecular genetic defects of the Dystrophic Epidermolysis Bullosa Diseases in Hail, Saudi Arabia and literature review
  3. Loss of NHEJ1 Protein Due to a Novel Splice Site Mutation in a Family Presenting with Combined Immunodeficiency, Microcephaly, and Growth Retardation and Literature Review
  4. Metabolic syndrome, dyslipidemia and regulation of lipoprotein metabolism
  5. Novel mutation in DOCK8-HIES with severe phenotype and successful transplantation
  6. Hematopoietic stem cell transplantation corrects WIP deficiency
  7. Inhibition of RORγT Skews TCRα Gene Rearrangement and Limits T Cell Repertoire Diversity
  8. Unbiased targeted next-generation sequencing molecular approach for primary immunodeficiency diseases
  9. TSH overcomes Braf V600E -induced senescence to promote tumor progression via downregulation of p53 expression in papillary thyroid cancer
  10. Comprehensive gene panels provide advantages over clinical exome sequencing for Mendelian diseases
  11. Hematopoietic stem cell transplant for hyper-IgM syndrome due to CD40L defects: A single-center experience
  12. DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options - a Review of 136 Patients
  13. Specification of Vδ and Vα Usage byTcra/TcrdLocus V Gene Segment Promoters
  14. Grave aortic aneurysmal dilatation in DOCK8 deficiency
  15. Clinical, Immunological, and Molecular Characterization of Hyper-IgM Syndrome Due to CD40 Deficiency in Eleven Patients
  16. In DOCK8 deficiency donor cell engraftment post–genoidentical hematopoietic stem cell transplantation is possible without conditioning
  17. C5 Complement Deficiency in a Saudi Family, Molecular Characterization of Mutation and Literature Review
  18. The Inducible Tissue-Specific Expression of the Human IL-3/GM-CSF Locus Is Controlled by a Complex Array of Developmentally Regulated Enhancers
  19. Clinical, Immunological and Molecular Characterization of DOCK8 and DOCK8-like Deficient Patients: Single Center Experience of Twenty Five Patients
  20. Successful outcome in two patients with CD40 deficiency treated with allogeneic HCST
  21. Hematopoietic SCT in children with Griscelli syndrome: a single-center experience
  22. Multiple Constraints at the Level of TCR  Rearrangement Impact V 14i NKT Cell Development
  23. Role for rearranged variable gene segments in directing secondary T cell receptor α recombination
  24. Regulation of TCR δ and α repertoires by local and long-distance control of variable gene segment chromatin structure
  25. Regulation of T cell receptor α gene assembly by a complex hierarchy of germline Jα promoters
  26. Enforcing order within a complex locus: current perspectives on the control of V(D)J recombination at the murine T-cell receptor alpha/delta locus
  27. The Human IL-3 Locus Is Regulated Cooperatively by Two NFAT-Dependent Enhancers That Have Distinct Tissue-Specific Activities
  28. Regulation of the TCRα repertoire by the survival window of CD4+CD8+ thymocytes
  29. Reconstitution of T Cell-Specific Transcription Directed by Composite NFAT/Oct Elements
  30. Molecular, antibiogram and serological typing of Staphylococcus aureus isolates recovered from Al-Makased hospital in East Jerusalem
  31. Safety and immunogenicity of a tetravalent group B streptococcal polysaccharide vaccine in healthy adults
  32. A simple, quantitative, reproducible avidin-biotin ELISA for the evaluation of group B Streptococcus type-specific antibodies in humans
  33. Effect of conjugation methodology, carrier protein, and adjuvants on the immune response to Staphylococcus aureus capsular polysaccharides