All Stories

  1. LncRNA SRA1 may play a role in the uterine leiomyoma tumor growth regarding the MED12 mutation pattern
  2. The value of the plasma circulating cell-free DNA concentration and integrity index as a clinical tool for prostate cancer diagnosis: a prospective case–control cohort study in an Iranian population
  3. Expression analysis of CBR3-AS1 and androgen receptor genes in breast cancer
  4. Neuropilin-1 expression is associated with lymph node metastasis in breast cancer tissues
  5. Association analysis of the GABRB3 promoter variant and susceptibility to autism spectrum disorder
  6. Investigation of piwi-interacting RNA pathway genes role in idiopathic non-obstructive azoospermia
  7. The rs4846049 polymorphism in the 3’UTR region of the MTHFR gene increases the migraine susceptibility in an Iranian population
  8. Association study of FOXP3 gene and the risk of 0020 pre-eclampsia
  9. The association between FOXP3 gene variations and autism: True or false positive?
  10. Angiotensin-converting enzyme gene rs4343 polymorphism increases susceptibility to migraine
  11. Association of β-Secretase Functional Polymorphism with Risk of Schizophrenia
  12. SOCS gene family expression profile in the blood of multiple sclerosis patients
  13. The role of parental microRNA alleles in recurrent pregnancy loss: an association study
  14. TTY2 genes deletions as genetic risk factor of male infertility
  15. Single nucleotide polymorphisms in the FOXP3 gene are associated with increased risk of relapsing-remitting multiple sclerosis
  16. Association of SRD5A2 gene mutations with risk of hypospadias in the Iranian population
  17. Comparative expression analysis of hypoxia-inducible factor-alpha and its natural occurring antisense in breast cancer tissues and adjacent noncancerous tissues
  18. RAR-related orphan receptor A (RORA): A new susceptibility gene for multiple sclerosis
  19. Combination of cold atmospheric plasma and iron nanoparticles in breast cancer: gene expression and apoptosis study
  20. Docetaxel-Chitosan nanoparticles for breast cancer treatment: cell viability and gene expression study
  21. TRAIL gene expression analysis in multiple sclerosis patients
  22. Glutamate receptor, metabotropic 7 (GRM7) gene variations and susceptibility to autism: A case-control study
  23. Lactobacilli Differentially Modulate mTOR and Wnt/ β-Catenin Pathways in Different Cancer Cell Lines
  24. The pre-mir-27a variant rs895819 may contribute to type 2 diabetes mellitus susceptibility in an Iranian cohort
  25. MiRNA-Related Polymorphisms in miR-146a andTCF21Are Associated with Increased Susceptibility to Coronary Artery Disease in an Iranian Population
  26. Analysis of the androgen receptor CAG repeats length in Iranian patients with idiopathic non-obstructive azoospermia
  27. Genetic variants and expression study ofFOXP3gene in acute coronary syndrome in Iranian patients
  28. Valproic acid may exerts its cytotoxic effect through rassf1a expression induction in acute myeloid leukemia
  29. A Bioinformatics Approach to the Identification of Variants Associated with Type 1 and Type 2 Diabetes Mellitus that Reside in Functionally Validated miRNAs Binding Sites
  30. MIR17HG Gene Polymorphism and the Risk of Recurrent Spontaneous Abortion
  31. Bioinformatics prioritization of SNPs perturbing microRNA regulation of hematological malignancy-implicated genes
  32. Novel missense mutation in the GALNS gene in an affected patient with severe form of mucopolysaccharidosis type IVA
  33. Expression analysis of four long noncoding RNAs in breast cancer
  34. Aberrant Wnt/β-Catenin Signaling Pathway in Testis of Azoospermic Men​
  35. The study of MED12 gene mutations in uterine leiomyomas from Iranian patients
  36. Regulation of BAX/BCL2 gene expression in breast cancer cells by docetaxel-loaded human serum albumin nanoparticles
  37. RIT2, a susceptibility gene for Parkinson's disease in Iranian population
  38. Myoclonus dystonia syndrome: a novel ε-sarcoglycan gene mutation with variable clinical symptoms
  39. Mutational screening of theNR5A1in azoospermia
  40. The expression analysis of LATS2 gene in de novo AML patients
  41. Prognostic and predictive value of copy number alterations in invasive breast cancer as determined by multiplex ligation-dependent probe amplification
  42. Expression profiling of breast cancer patients treated with tamoxifen: prognostic or predictive significance
  43. Thiamine-responsive megaloblastic anemia syndrome with Ebstein anomaly: a case report
  44. Lack of association between LXRα and LXRβ gene polymorphisms and prevalence of metabolic syndrome: A case–control study of an Iranian population
  45. An Iranian family with azoospermia and premature ovarian insufficiency segregating NR5A1 mutation
  46. Authors response
  47. The prevalence of common CFTR mutations in Iranian infertile men with non-CAVD obstructive azoospermia by using ARMS PCR techniques
  48. A Novel Mutation in the Transactivation-Regulating Domain of the Androgen Receptor in a Patient With Azoospermia
  49. BAK, BAX, and NBK/BIK Proapoptotic Gene Alterations in Iranian Patients with Ataxia Telangiectasia
  50. 7.017 Y chromosome microdeletions in Iranian infertile men
  51. The first study of galactose-1-phosphate uridyl transferase mutations in Iranian galactosemia patients
  52. First Study of CF Mutations in the CFTR Gene of Iranian Patients: Detection of F508, G542X, W1282X, A120T, R117H, and R347H Mutations
  53. Cytogenetic abnormalities in the lymphocytes of a female patient with primary breast carcinoma