DOI year title 2021 A glance at glioblastoma molecular culprits through in-silico analysis 2021 Identification and prediction of common molecular culprits between psoriasis and melanoma via bioinformatical analysis 2021 Thyroid peroxidase in human endometrium and placenta: a potential target for anti-TPO antibodies 2020 Autozygosity‑driven genetic diagnosis in consanguineous families from Italy and the Greater Middle East 2020 A Novel Cadherin 23 Variant for Hereditary Hearing Loss Reveals Additional Support for a DFNB12 Nonsyndromic Phenotype of CDH23 2020 Association of Selenoprotein S Expression and its Variants with Metabolic Syndrome in Subjects with Cardiovascular Disease 2020 Therapeutic plasma exchange may adjust IL‐6 and TGF‐β signals in relapsed MS patients peripheral blood 2020 Altered Expression of Circulating miR-377 and miR-98 in Relapsing-remitting Multiple Sclerosis 2020 A novel carcinogenic PI3Kα mutation suggesting the role of helical domain in transmitting nSH2 regulatory signals to kinase domain 2019 Effect of single nucleotide polymorphisms in SEPS1 and SEPP1 on expression in the protein level in metabolic syndrome in subjects with cardiovascular disease 2019 Further supporting evidence for REEP1 phenotypic and allelic heterogeneity 2019 In silico analysis of synaptonemal complex protein 1 (SYCP1) and acrosin binding protein (ACRBP) antigens to design novel multiepitope peptide cancer vaccine against breast cancer 2019 Production, purification, and in vivo evaluation of a novel multiepitope peptide vaccine consisted of immunodominant epitopes of SYCP1 and ACRBP antigens as a prophylactic melanoma vaccine 2019 Do probiotics, prebiotics and synbiotics affect adiponectin and leptin in adults? A systematic review and meta-analysis of clinical trials 2019 The Effect of Dracocephalum kotschyi Alcoholic Extracton the BCL2 and BAX Expression in SKBR3 Cell Line 2019 Plasmacytoma Variant Translocation 1 with Antisense Locked Nucleic Acid GapmeRs Exerts Tumor-Suppressive Functions in Human Acute Erythroleukemia Cells Through Downregulation of C-MYC Expression 2019 Association of high level of hs-CRP with in-stent restenosis: A case-control study 2019 Clinical Trial: CYP2D6 Related Dose Escalation of Tamoxifen in Breast Cancer Patients With Iranian Ethnic Background Resulted in Increased Concentrations of Tamoxifen and Its Metabolites 2019 Expression Profiles of IGF1, EGF, and FGF2 Genes in Patients With Prostate Cancer in Isfahan Province, Iran 2019 Expression Profiles of miR-93 and miR-330 in Iranian Patients with Chronic Lymphocytic Leukemia 2019 Engineered zinc‐finger nuclease to generate site‐directed modification in the KLF1 gene for fetal hemoglobin induction 2019 Gender identity development in the shadow of socialization: a grounded theory approach 2019 Prevalence of Cystic Fibrosis Trans-membrane Conductance Regulator Gene common mutations in children with cystic fibrosis in Isfahan, Iran 2019 A Comparison Between Full-COLD PCR/HRM and PCR Sequencing for Detection of Mutations in Exon 9 of PIK3CA in Breast Cancer Patients
DOI 10.18502/1 2019 Investigation of the Impact of Foretinib on AURKA and AURKB Expression in T98 Glioblastoma Cell Line 2019 Whole Exome Sequencing Revealed a Novel GJB1 Pathogenic Variant and a Rare BSCL2 Mutation in Two Iranian Large Pedigrees with Multiple Affected Cases of Charcot-Marie-Tooth 2019 A Novel Pathogenic Variant in the CABP2 Gene Causes Severe Nonsyndromic Hearing Loss in a Consanguineous Iranian family 2019 The association between genetic polymorphisms of the interleukin-10, tumor necrosis factor-alpha, and annexin A5 gene loci and restenosis after percutaneous coronary angioplasty and stenting 2019 Distribution of CYP2D6 polymorphism in the Middle Eastern region
2019 Genetic Analysis of MECP2 Gene in Iranian Patients with Rett Syndrome
DOI: 10.1002/jcla.22586 2018 Evaluation of the utility of peripheral blood vs bone marrow in karyotype and fluorescence in situ hybridization for myelodysplastic syndrome diagnosis 2018 Promising effect of rapamycin on multiple sclerosis 2018 Pregnancy, child bearing and prevention of giving birth to the affected children in patients with primary immunodeficiency disease; a case-series 2018 Effects of selenium supplementation on expression of SEPP1 in mRNA and protein levels in subjects with and without metabolic syndrome suffering from coronary artery disease: Selenegene study a double‐blind randomized controlled trial 2018 An Effective Concentration of 5-Aza-CdR to Induce Cell Death and Apoptosis in Human Pancreatic Cancer Cell Line through Reactivating RASSF1A and Up-Regulation of Bax Genes 2018 Analysis of the expression of mir-34a, mir-199a, mir-30c and mir-19a in peripheral blood CD4+T lymphocytes of relapsing-remitting multiple sclerosis patients 2018 An insertion mutation in HOXC13 underlies pure hair and nail ectodermal dysplasia with lacrimal duct obstruction 2018 GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants 2018 The Relationship Between Breast Cancer and VDR Gene Polymorphisms 2018 A novel homozygous DPH1 mutation causes intellectual disability and unique craniofacial features 2018 A homozygous NOP14 variant is likely to cause recurrent pregnancy loss 2018 OX40 Gene and Serum Protein Expression Profiles in Patients with Parkinson’s Disease 2017 Aberrant expression of PlncRNA-1 and TUG1: potential biomarkers for gastric cancer diagnosis and clinically monitoring cancer progression 2017 Comparison of TaqMan® Assay and PCR-sequencing Method for Analyzing CYP2D10*6 and CYP2D4*6 Alleles: a False Negative Issue 2017 Oligonucleotide aptamers: potential novel molecules against viral hepatitis 2017 Association of expression of selenoprotein P in mRNA and protein levels with metabolic syndrome in subjects with cardiovascular disease: Results of the Selenegene study
DOI 10.1007/s00439-016-1756-5 2017 Association of AHSG with alopecia and mental retardation (APMR) syndrome 2017 Selenium homeostasis and clustering of cardiovascular risk factors: a systematic review 2017 Identification a novel mononucleotide deletion mutation in GAA in pompe disease patients 2017 Evaluation of Energy Balance on Human Telomerase Reverse Transcriptase (hTERT) Alternative Splicing by Semi-quantitative RT-PCR in Human Umbilical Vein Endothelial Cells 2017 Optimal DNA Isolation Method for Detection of Nontuberculous Mycobacteria by Polymerase Chain Reaction 2017 MeDIP Real-Time qPCR has the Potential for Noninvasive Prenatal Screening of Fetal Trisomy 21 2017 RORA and Autism in The Isfahan Population: Is There An Epigenetic Relationship 2017 Lexical Retrieval or Semantic Knowledge Which One Causes Naming Errors in Patients with Mild and Moderate Alzheimer’s Disease 2017 Application of Epstein–Barr Virus for Optimization of Immortalized B-lymphocyte Production as a Positive Control in Genetic Studies 2017 Treatment Outcome of the Drug-resistant Zoonotic Cutaneous Leishmaniasis by Glucantime 2017 Simple and Easy to Perform Preimplantation Genetic Diagnosis for β-thalassemia Major Using Combination of Conventional and Fluorescent Polymerase Chain Reaction 2016 Gamma reactivation using the spongy effect of KLF1-binding site sequence: an approach in gene therapy for beta-thalassemia 2016 Genetic disruption of the KLF1 gene to overexpress the γ‐globin gene using the CRISPR/Cas9 system 2016 Detection of paternally inherited fetal point mutations for β-thalassemia in maternal plasma using simple fetal DNA enrichment protocol with or without whole genome amplification: an accuracy assessment
DOI 10.1007/s10529-016-2101-8 2016 Comparison of different methods for erythroid differentiation in the K562 cell line 2016 Exposition of hepatitis B surface antigen (HBsAg) on the surface of HEK293T cell and evaluation of its expression 2016 Novel Multiplex Fluorescent PCR-Based Method for HLA Typing and Preimplantational Genetic Diagnosis of β-Thalassemia 2016 Peroxiredons: Tryparedoxin Peroxidase from Leishmania major 2016 Induced Pluripotent Stem Cell as a New Source for Cancer Immunotherapy 2016 A novel homozygous mutation in HSF4 causing autosomal recessive congenital cataract 2016 Zinc Finger Nuclease: A New Approach to Overcome Beta-Lactam Antibiotic Resistance 2016 Mutation detection of CYP21A2 gene in nonclassical congenital adrenal hyperplasia patients with premature pubarche 2016 Down Syndrome: Current Status, Challenges and Future Perspectives