All Stories

  1. Cardiometabolic disease risk: the joint role of the UCP1, UCP2, UCP3, and FTO gene variants
  2. miR-155-5p Silencing Does Not Alter BTLA Molecule Expression in CLL T Cells: Implications for Targeted Immunotherapy
  3. Effect of HVEM/CD160 Variations on the Clear Cell Renal Carcinoma Risk and Overall Survival
  4. Effect of HVEM/CD160 Variations on the Clear Cell Renal Carcinoma Risk and Overall Survival
  5. BTLA biology in cancer: from bench discoveries to clinical potentials
  6. NGS Sequencing Reveals New UCP1 Gene Variants Potentially Associated with MetS and/or T2DM Risk in the Polish Population—A Preliminary Study
  7. The Variations’ in Genes Encoding TIM-3 and Its Ligand, Galectin-9, Influence on ccRCC Risk and Prognosis
  8. BTLA Expression in CLL: Epigenetic Regulation and Impact on CLL B Cell Proliferation and Ability to IL-4 Production
  9. Editorial: Genetic and Epigenetic Control of Immune Responses
  10. Immune Checkpoint Molecules—Inherited Variations as Markers for Cancer Risk
  11. SNP-SNP Interaction in Genes Encoding PD-1/PD-L1 Axis as a Potential Risk Factor for Clear Cell Renal Cell Carcinoma
  12. Association of Common Variants of TNFSF13 and TNFRSF13B Genes with CLL Risk and Clinical Picture, as Well as Expression of Their Products—APRIL and TACI Molecules
  13. Abnormal Expression of BTLA and CTLA-4 Immune Checkpoint Molecules in Chronic Lymphocytic Leukemia Patients
  14. Polymorphisms of genes encoding cytokines predict the risk of high-grade bladder cancer and outcomes of BCG immunotherapy
  15. sFasL-mediated induction of neutrophil activation in patients with type 2 diabetes mellitus
  16. Polymorphisms in immune-inflammatory response genes and the risk of deficit schizophrenia
  17. Genetic Factors Influencing Outcome After Allogeneic Hematopoietic Stem Cell Transplantation
  18. The mRNA expression levels of uncoupling proteins 1 and 2 in mononuclear cells from patients with metabolic disorders: obesity and type 2 diabetes mellitus
  19. PD-1 gene polymorphic variation is linked with first symptom of disease and severity of relapsing-remitting form of MS
  20. Erratum to: CD28/CTLA-4/ICOS haplotypes confers susceptibility to Graves’ disease and modulates clinical phenotype of disease
  21. Role of UCP1 Gene Variants in Interethnic Differences in the Development of Cardio-Metabolic Diseases
  22. Is the Genetic Background of Co-Stimulatory CD28/CTLA-4 Pathway the Risk Factor for Prostate Cancer?
  23. Intragenic Variations in BTLA Gene Influence mRNA Expression of BTLA Gene in Chronic Lymphocytic Leukemia Patients and Confer Susceptibility to Chronic Lymphocytic Leukemia
  24. CD28/CTLA-4/ICOS haplotypes confers susceptibility to Graves’ disease and modulates clinical phenotype of disease
  25. Association of 3′ nearby gene BTLA polymorphisms with the risk of renal cell carcinoma in the Polish population
  26. Association of variants in BAFF (rs9514828 and rs1041569) and BAFF-R (rs61756766) genes with the risk of chronic lymphocytic leukemia
  27. Polymorphisms in CD28, CTLA-4, CD80 and CD86 genes may influence the risk of multiple sclerosis and its age of onset
  28. CTLA-4andCD28genes' polymorphisms and renal cell carcinoma susceptibility in the Polish population - a prospective study
  29. Polymorphisms in genes of the BAFF/APRIL system may constitute risk factors of B-CLL - a preliminary study on a Polish population
  30. CTLA4 and CD28 Gene Polymorphisms with Respect to Affective Symptom Domain in Schizophrenia
  31. A CT60G>A polymorphism in the CTLA-4 gene of the recipient may confer susceptibility to acute graft versus host disease after allogeneic hematopoietic stem cell transplantation
  32. Pretransplant donor and recipient CTLA-4 mRNA and protein levels as a prognostic marker for aGvHD in allogeneic hematopoietic stem cell transplantation
  33. The function of a novel immunophenotype candidate molecule PD-1 in chronic lymphocytic leukemia
  34. Sex differences in TGFB-β signaling with respect to age of onset and cognitive functioning in schizophrenia
  35. Common variation at 12q24.13 (OAS3) influences chronic lymphocytic leukemia risk
  36. Interleukin-6: the missing element of the neurocognitive deterioration in schizophrenia? The focus on genetic underpinnings, cognitive impairment and clinical manifestation
  37. Gene Polymorphisms of Novel Immunotolerant Molecule BTLA: Distribution of Alleles, Genotypes and Haplotypes in Polish Caucasian Population
  38. Associations between genes for killer immunoglobulin-like receptors and their ligands in patients with epithelial ovarian cancer
  39. Patients with the most advanced rheumatoid arthritis remain with Th1 systemic defects after TNF inhibitors treatment despite clinical improvement
  40. Genetic variants in transforming growth factor-β gene (TGFB1) affect susceptibility to schizophrenia
  41. The role of genetic variations of immune system regulatory molecules CD28 and CTLA-4 in schizophrenia
  42. rs2072135, a low-penetrance variant for chronic lymphocytic leukaemia?
  43. 16thIHIW: Population Global Distribution of Killer Immunoglobulin-like Receptor (KIR) and Ligands
  44. The Role of Polymorphisms in Co-Signalling Molecules’ Genes in Susceptibility to B-Cell Chronic Lymphocytic Leukaemia
  45. CTLA-4, CD28, and ICOS gene polymorphism associations with non-small-cell lung cancer
  46. Variations in Suppressor Molecule CTLA-4 Gene Are Related to Susceptibility to Multiple Myeloma in a Polish Population
  47. KIR/HLA gene combinations influence susceptibility to B-cell chronic lymphocytic leukemia and the clinical course of disease
  48. Common genetic variation at 15q25.2 impacts on chronic lymphocytic leukaemia risk
  49. ICOS gene polymorphisms in B-cell chronic lymphocytic leukemia in the Polish population
  50. Influence of CTLA-4/CD28/ICOS gene polymorphisms on the susceptibility to cervical squamous cell carcinoma and stage of differentiation in the Polish population
  51. Soluble CTLA-4 receptor an immunological marker of Graves' disease and severity of ophthalmopathy is associated with CTLA-4 Jo31 and CT60 gene polymorphisms
  52. TheCTLA-4gene polymorphisms are associated with CTLA-4 protein expression levels in multiple sclerosis patients and with susceptibility to disease
  53. Association studies of CTLA-4, CD28, and ICOS gene polymorphisms with B-cell chronic lymphocytic leukemia in the Polish population
  54. Cytotoxic T-Lymphocyte Associated Antigen 4 Gene Polymorphisms and Autoimmune Thyroid Disease: A Meta-Analysis
  55. IL-6 Is Present in Sera of Bone Marrow-transplanted Patients in Aplastic Period and High Levels of IL-6 during Acute Graft-versus-Host Disease Are Associated with Severe Gut Symptomsa
  56. Interleukin-6- and Interleukin-4-related Proteins (C-reactive Protein and IgE) Are Prognostic Factors of Asbestos-related Cancera
  57. 2'-Deoxy-2'-fluoro- -D-arabinonucleic acid (2'F-ANA) modified oligonucleotides (ON) effect highly efficient, and persistent, gene silencing
  58. IL-6 and IL-10 Promoter Gene Polymorphisms of Patients and Donors of Allogeneic Sibling Hematopoietic Stem Cell Transplants Associate With the Risk of Acute Graft-Versus-Host Disease
  59. IL-6 and IL-10 promoter gene polymorphisms do not associate with the susceptibility for multiple myeloma
  60. Lack of IFN-gamma 2/2 homozygous genotype independently of recipient age and intensity of conditioning regimen influences the risk of aGVHD manifestation after HLA-matched sibling haematopoietic stem cell transplantation
  61. HLA typing for donor-recipient matching in unrelated donor hematopotetic stem cell transplantation