Items where Subject is "QU Biochemistry. Cell Biology and Genetics > QU 300-560 Cell Biology and Genetics"

Article

(2019) Improvement of K562 Cell Line Transduction by FBS Mediated Attachment to the Cell Culture Plate. Biomed Research International. ISSN 2314-6133

(2018) The Role of Efferocytosis in Autoimmune Diseases. Frontiers in Immunology. ISSN 1664-3224

(2019) First cystic fibrosis patient registry annual data report-cystic fibrosis foundation of Iran. Acta Medica Iranica. pp. 33-41. ISSN 00446025 (ISSN)

(2020) Exome-first Approach Identified Novel Homozygous Dedicator of Cytokinesis 8 (DOCK8) Mutations in Three Unrelated Iranian Pedigrees Suspected with Hyper-IgE Syndrome. Iranian Journal of Allergy Asthma and Immunology. pp. 193-199. ISSN 1735-1502

(2020) Upregulation ofMTOR,RPS6KB1, andEIF4EBP1in the whole blood samples of Iranian patients with multiple sclerosis compared to healthy controls. Metabolic Brain Disease. pp. 1309-1316. ISSN 0885-7490

(2019) The prevalence of the genetic polymorphism of GSTM1, GSTT1 AND GSTP1 and its relationship with clinical criteria of multiple sclerosis (Ms) patients in Tehran. Journal of Babol University of Medical Sciences. pp. 157-165. ISSN 15614107 (ISSN)

(2020) Bivariate genome-wide association analyses of the broad depression phenotype combined with major depressive disorder, bipolar disorder or schizophrenia reveal eight novel genetic loci for depression. Molecular Psychiatry. pp. 1420-1429. ISSN 1359-4184

(2018) Hybrid Pharmacophore Design, Molecular Docking, Synthesis, and Biological Evaluation of Novel Aldimine-Type Schiff Base Derivatives as Tubulin Polymerization Inhibitor. Chemistry & Biodiversity. ISSN 1612-1872

(2019) Evaluation of SEPP1 and Selenoprotein S Gene Polymorphisms (rs7579 and rs34713741) in Relation to Colorectal Cancer Susceptibility in Subset of Iranian Population: A Case-control Study. Adv Biomed Res. p. 47. ISSN 2277-9175 (Print) 2277-9175 (Linking)

(2019) High Mobility Group box-1 (HMGB1) Protein As a Biomarker for Acute Cholecystitis. Reports of Biochemistry and Molecular Biology. pp. 204-209. ISSN 2322-3480

(2019) Differentiation of eye field neuroectoderm from human adipose-derived stem cells by using small-molecules and hADSC-conditioned medium. Annals of Anatomy-Anatomischer Anzeiger. pp. 17-26. ISSN 0940-9602

(2020) A case report of sinusoidal diffuse large B-cell lymphoma in a STK4 deficient patient. Medicine. ISSN 0025-7974

(2019) Mutations in GJB2 as Major Causes of Autosomal Recessive Non-Syndromic Hearing Loss: First Report of c.299-300delAT Mutation in Kurdish Population of Iran. Journal of Audiology and Otology. pp. 20-26. ISSN 2384-1621

(2019) Mutation Analysis of GJB2 and GJB6 Genes and Screening of Nine Common DFNB Loci in Iranian Pedigrees with Autosomal Recessive Nonsyndromic Hearing Loss. Indian Journal of Otology. pp. 97-102. ISSN 0971-7749

(2018) Immunology and Genetic of Leishmania infantum: The Role of Endonuclease G in the Apoptosis. Journal of Research in Medical Sciences. ISSN 1735-1995

(2020) TFPI2 and NDRG4 gene promoter methylation analysis in peripheral blood mononuclear cells are novel epigenetic noninvasive biomarkers for colorectal cancer diagnosis. Journal of Gene Medicine. ISSN 1099-498X

(2019) THE EFFECT OF INHIBITION OF LNCRNA MIR100HG ON THE PROLIFERATION OF HUMAN PROMYELOCYTIC LEUKEMIA CELLS. International Journal of Life Science and Pharma Research. L11-L20. ISSN 2250-0480

(2019) Non-syndromic cleft palate: Association analysis on three gene polymorphisms of the folate pathway in Asian and Italian populations. International Journal of Immunopathology and Pharmacology. p. 5. ISSN 0394-6320

(2020) The identification and stereochemistry analysis of a novel mutation p.(D367Tfs*61) in the CYP1B1 gene: A case report. Journal of Current Ophthalmology. pp. 114-118. ISSN 2452-2325

(2019) Apoptosis-inducing effect of spiroaminopyrimidine analogue in NB4 leukemia cells via down-regulation of BIRC5 expression. Exp Oncol. pp. 312-317. ISSN 1812-9269 (Print) 1812-9269 (Linking)

(2020) Expression and clinicopathological significance of lipin-1 in human breast cancer and its association with p53 tumor suppressor gene. Journal of Cellular Physiology. pp. 5835-5846. ISSN 0021-9541

(2020) Evaluation of long-chain acyl-coenzyme A synthetase 4 (ACSL4) expression in human breast cancer. Research in Pharmaceutical Sciences. pp. 48-56. ISSN 1735-5362

(2020) microRNAs: key modulators of disease-modifying therapies in multiple sclerosis Pancreatic cancer is one of the lethal malignant tumours in the world.In this study, we investigated the CAR T-Cell therapy of pancreatic cancer. International Reviews of Immunology. pp. 264-279. ISSN 0883-0185

(2020) Association of PON1-L55M Genetic Variation and Breast Cancer Risk: A Case-Control Trial. Asian Pac J Cancer Prev. pp. 255-258. ISSN 1513-7368 (Print) 1513-7368

(2020) Association analysis of rs1695 and rs1138272 variations in GSTP1 gene and breast cancer susceptibility. Asian Pac J Cancer Prev. pp. 1167-1172. ISSN 1513-7368 (Print) 1513-7368

(2020) Assessment of the genes and molecular mechanisms of B cells activation through systems biology approaches. Human Antibodies. pp. 83-87. ISSN 10932607 (ISSN)

(2020) Understanding the impact of DIS3 cancer-associated mutations by in silico structure modeling. Gene Reports.

(2020) Clinical display, diagnostics and genetic implication of Novel Coronavirus (COVID-19) epidemic. European Review for Medical and Pharmacological Sciences. pp. 4607-4615. ISSN 1128-3602

(2019) Targeting MCF-7 Cell Line by Listeriolysin O Pore Forming Toxin Fusion with AHNP Targeted Peptide. Adv Biomed Res. p. 33. ISSN 2277-9175 (Print) 2277-9175 (Linking)

(2020) High-resolution melting curve analysis of polymorphisms within CD58, CD226, HLA-G genes and association with multiple sclerosis susceptibility in a subset of Iranian population: a case-control study. Acta Neurologica Belgica. pp. 645-652. ISSN 0300-9009

(2019) Optimization and Comparison of Different Methods and Factors for Efficient Transformation of Brucella abortus RB51strain. Adv Biomed Res. p. 37. ISSN 2277-9175 (Print) 2277-9175 (Linking)

(2020) The effects of fibrin-icariin nanoparticle loaded in poly (lactic-co-glycolic) acid scaffold as a localized delivery system on chondrogenesis of human adipose-derived stem cells. Advanced Biomedical Research. ISSN 2277-9175

(2019) Gene Delivery Using Lipoplexes and Polyplexes: Principles, Limitaions and Solutions. Critical Reviews in Eukaryotic Gene Expression. pp. 29-36. ISSN 1045-4403

(2020) Evaluation of Silencing Effect of miR-133a-5p Mimic on TIM-3 Expression in AML (HL-60) Cell Line. Indian J Clin Biochem. pp. 359-366. ISSN 0970-1915 (Print) 0970-1915 (Linking)

(2020) Anaesthetic Management of a Known Case of Werner Syndrome by Peripheral Nerve Block in the Orthopaedic Surgery of Forearm. Turkish Journal of Anaesthesiology and Reanimation. pp. 251-253.

(2020) Association between polymorphisms in microRNA seed region and warfarin stable dose. Postgraduate Medical Journal. pp. 737-741. ISSN 0032-5473

(2020) Targeting of cholera toxin A (ctxA) gene by zinc finger nuclease: pitfalls of using gene editing tools in prokaryotes. Research in Pharmaceutical Sciences. pp. 182-190. ISSN 1735-5362

(2019) Evaluation of Osteopontin Gene Expression in Endometrium of Diabetic Rat Models Treated with Metformin and Pioglitazone. International Journal of Fertility & Sterility. pp. 293-297. ISSN 2008-076x

(2020) Therapeutic effects of extracellular vesicles from human adipose-derived mesenchymal stem cells on chronic experimental autoimmune encephalomyelitis. Journal of Cellular Physiology. pp. 8779-8790. ISSN 0021-9541

(2020) Mesenchymal Stem Cell-Derived Extracellular Vesicles: A Novel Cell-Free Therapy. Immunological Investigations. pp. 758-780. ISSN 0882-0139

(2020) An A10398G mitochondrial DNA alteration is related to increased risk of breast cancer, and associates with Her2 positive receptor. Mitochondrial DNA Part A. pp. 11-16. ISSN 2470-1394

(2018) A Comprehensive Genetic and Clinical Evaluation of Waardenburg Syndrome Type II in a Set of Iranian Patients. International Journal of Molecular and Cellular Medicine. pp. 23-17. ISSN 2251-9637

(2020) Optimization of interleukin-5 protein expression in BL21 strain of Escherichia coli. Journal of Isfahan Medical School. pp. 694-700. ISSN 10277595 (ISSN)

(2019) Selection and characterization of single-stranded DNA aptamers against interleukin-5. Research in Pharmaceutical Sciences. pp. 515-523. ISSN 1735-5362

(2020) Therapeutic plasma exchange may adjust IL-6 and TGF-beta signals in relapsed MS patients peripheral blood. Journal of Clinical Apheresis. pp. 72-78. ISSN 0733-2459

(2020) Comparison of Expression Levels of miR-29b-3p and miR-326 in T Helper-1 and T Helper-17 Cells Isolated from Responsive and Non-responsive Relapsing-remitting Multiple Sclerosis Patients Treated with Interferon-beta. Iranian Journal of Allergy Asthma and Immunology. pp. 416-425. ISSN 1735-1502

(2020) MicroRNA binding site polymorphism in inflammatory genes associated with colorectal cancer: literature review and bioinformatics analysis. Cancer Gene Therapy. pp. 739-753. ISSN 0929-1903

(2020) Genetic Variation in Cytochrome P450 2R1 and Vitamin D Binding Protein Genes are associated with Vitamin D Deficiency in Adolescents. Int J Vitam Nutr Res. pp. 339-345. ISSN 0300-9831 (Print) 0300-9831 (Linking)

(2020) Exploring the role of circadian clock gene and association with cancer pathophysiology. Chronobiology International. pp. 151-175. ISSN 0742-0528

(2019) CRISPR-Cas9 in genome editing: Its function and medical applications. JOURNAL OF CELLULAR PHYSIOLOGY. ISSN 1097-4652 (Electronic) 0021-9541 (Linking)

(2019) Distribution of CYP2D6 polymorphism in the Middle Eastern region. Journal of Research in Medical Sciences. p. 6. ISSN 1735-1995

(2020) MicroRNAs and target molecules in bladder cancer. Medical Oncology. ISSN 1357-0560

(2020) New Variants in the CDH1 Gene in Iranian Families with Hereditary Diffuse Gastric Cancer. Middle East Journal of Cancer. pp. 493-501. ISSN 2008-6709

(2019) A Novel Pathogenic Variant in NAGLU (N-Acetyl-Alpha-Glucosaminidase) gene Identified by Targeted Next-Generation Sequencing Followed by in Silico Analysis. Iranian Journal of Child Neurology. pp. 173-183. ISSN 1735-4668

(2020) Determining the association of thrombophilic gene polymorphisms with recurrent pregnancy loss in Iranian women. Gynecological Endocrinology. pp. 1082-1085. ISSN 0951-3590

(2019) An analysis and survey of interleukin-10 receptor mutation in inflammatory bowel disease (IBD) in the first Iranian IBD cohort. Journal of Laboratory Medicine. pp. 185-189. ISSN 2567-9430

(2020) Association Analysis of Monoamine Oxidase-A Gene Promoter Polymorphism (MAOA uVNTR) for Antisocial Behavior: Absence of the Counting Number Repeats in Central Iran. Archives of Neuroscience. ISSN 2322-3944

(2019) Genetics of Hearing Loss in North Iran Population: An Update of Spectrum and Frequency of GJB2 Mutations. Journal of Audiology and Otology. pp. 175-180. ISSN 2384-1621

(2020) GJB2-related hearing loss in central Iran: Review of the spectrum and frequency of gene mutations. Annals of Human Genetics. pp. 107-113. ISSN 0003-4800

(2019) A Novel Pathogenic Variant in the CABP2 Gene Causes Severe Nonsyndromic Hearing Loss in a Consanguineous Iranian Family. Audiology and Neuro-Otology. pp. 258-263. ISSN 1420-3030

(2019) Screening of 10 DFNB Loci Causing Autosomal Recessive Non-Syndromic Hearing Loss in Two Iranian Populations Negative for GJB2 Mutations. Iranian Journal of Public Health. pp. 1704-1713. ISSN 2251-6085

(2020) The Clinical Effectiveness of Preimplantation Genetic Diagnosis for Chromosomal Translocation Carriers: A Meta-analysis. Global Medical Genetics. pp. 14-21. ISSN 2699-9404

(2020) Identification of a novel HEXB Mutation in an Iranian Family with suspected patient to GM2-gangliosidoses. Clinical Case Reports. pp. 2583-2591. ISSN 2050-0904

(2020) Association of ApaI and TaqI polymorphisms in VDR Gene with Breast Cancer. Asian Pac J Cancer Prev. pp. 2667-2672. ISSN 1513-7368 (Print) 1513-7368

(2018) Inducing indel mutation in the SOX6 gene by zinc finger nuclease for gamma reactivation: An approach towards gene therapy of beta thalassemia. Journal of Cellular Biochemistry. pp. 2512-2519. ISSN 1097-4644 (Electronic) 0730-2312 (Linking)

(2020) In vitro versus in vivo models of kidney fibrosis: Time-course experimental design is crucial to avoid misinterpretations of gene expression data. Journal of Research in Medical Sciences. ISSN 1735-1995

(2020) A pathogenic variant in the transforming growth factor beta I ( TGFBI ) in four Iranian extended families segregating granular corneal dystrophy type II: A literature review. Iranian Journal of Basic Medical Sciences. pp. 1020-1027. ISSN 2008-3866

(2019) Evidence for expression of promoterless GFP cassette: Is GFP an ideal reporter gene in biotechnology science? Research in Pharmaceutical Sciences. pp. 351-358. ISSN 1735-5362

(2020) Influence of Heterologously Expressed azurin from Pseudomonas aeruginosa on the Adhesion and Invasion of Pathogenic Bacteria to the Caco-2 Cell Line. Probiotics and Antimicrobial Proteins. pp. 697-704. ISSN 1867-1306

(2020) Global Sequence Analysis and Expression of Azurin Gene in Different Clinical Specimens of Burn Patients with Pseudomonas aeruginosa Infection. Infection and Drug Resistance. pp. 2261-2275. ISSN 1178-6973

(2019) Producing soluble human programmed cell death protein-1: A natural supporter for CD4+t cell cytotoxicity and tumor cells apoptosis. Iranian Journal of Biotechnology. ISSN 17283043 (ISSN)

(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. International Journal of Molecular and Cellular Medicine. pp. 169-178. ISSN 2251-9637

(2019) Detection of Genes Involved in Biofilm Formation in MDR and XDR Acinetobacter baumannii Isolated from Human Clinical Specimens in Isfahan, Iran. Archives of Clinical Infectious Diseases. p. 6. ISSN 2345-2641

(2018) Mesenchymal stem cells: A new platform for targeting suicide genes in cancer. Journal of Cellular Physiology. pp. 3831-3845. ISSN 1097-4652 (Electronic) 0021-9541 (Linking)

(2019) Analysis of time-course microarray data: Comparison of common tools. Genomics. pp. 636-641. ISSN 0888-7543

(2020) Valproic acid restores the down-regulation of SDF-1 following kidney ischemia; experimental validation of a mathematical prediction. Research in Pharmaceutical Sciences. pp. 191-199. ISSN 1735-5362

(2019) Novel Variants and Copy Number Variation in CDH1 Gene in Iranian Patients with Sporadic Diffuse Gastric Cancer. Journal of Gastrointestinal Cancer. pp. 420-427. ISSN 1941-6628

(2020) PBMCs: a new source of diagnostic and prognostic biomarkers. Arch Physiol Biochem. pp. 1-7. ISSN 1381-3455

(2020) Genetically engineered mesenchymal stem cells: targeted delivery of immunomodulatory agents for tumor eradication. Cancer Gene Therapy. pp. 854-868. ISSN 0929-1903

(2019) Single nucleotide polymorphism rs10889677 in miRNAs Let-7e and Let-7f binding site of IL23R gene is a strong colorectal cancer determinant: Report and meta-analysis. Cancer Genetics. pp. 46-53. ISSN 2210-7762

(2020) Connection of miR-185 and miR-320a expression levels with response to interferon-beta in multiple sclerosis patients. Multiple Sclerosis and Related Disorders. ISSN 2211-0348

(2020) Evaluation of the effects of keratin on physical, mechanical and biological properties of poly (3-hydroxybutyrate) electrospun scaffold: Potential application in bone tissue engineering. European Polymer Journal. ISSN 0014-3057

(2020) LNA Inhibitor in microRNA miR-23b as a Potential Anti-proliferative Option in Human Hepatocellular Carcinoma. Journal of Gastrointestinal Cancer. pp. 109-115. ISSN 1941-6628

(2019) LNA Inhibitor in microRNA miR-23b as a Potential Anti-proliferative Option in Human Hepatocellular Carcinoma. J Gastrointest Cancer. ISSN 1941-6636 (Electronic)

(2019) BIRC5 Gene Disruption via CRISPR/Cas9n Platform Suppress Acute Myelocytic Leukemia Progression. Iran Biomed J. ISSN 2008-823X (Electronic) 1028-852X (Linking)

(2019) Knockout Of BIRC5 Gene By CRISPR/Cas9 Induces Apoptosis And Inhibits Cell Proliferation In Leukemic Cell Lines, HL60 And KG1. Blood and Lymphatic Cancer-Targets and Therapy. pp. 53-61. ISSN 1179-9889

(2019) Genetic Analysis of MECP2 Gene in Iranian Patients with Rett Syndrome. Iranian Journal of Child Neurology. pp. 25-34. ISSN 1735-4668

(2020) Bifurcation analysis of a modular model of embryonic kidney development. Biosystems. ISSN 0303-2647

(2020) C1QTNF4gene p.His198Gln mutation is correlated with early-onset systemic lupus erythematosus in Iranian patients. International Journal of Rheumatic Diseases. pp. 1594-1598. ISSN 1756-1841

(2020) Autozygosity-driven genetic diagnosis in consanguineous families from Italy and the Greater Middle East. Human Genetics. pp. 1429-1441. ISSN 0340-6717

(2019) A pathogenic variant in SLC26A4 is associated with Pendred syndrome in a consanguineous Iranian family. Int J Audiol. pp. 1-7. ISSN 1708-8186 (Electronic) 1499-2027 (Linking)

(2020) MiR-196: emerging of a new potential therapeutic target and biomarker in colorectal cancer. Molecular Biology Reports. pp. 9913-9920. ISSN 0301-4851

(2020) Differential Expression Profile of miR-27b, miR-29a, and miR-155 in Chronic Lymphocytic Leukemia and Breast Cancer Patients. Molecular Therapy-Oncolytics. pp. 230-237. ISSN 2372-7705

(2020) Bioinformatics prediction and experimental validation of a novel microRNA: hsa-miR-B43 within human CDH4 gene with a potential metastasis-related function in breast cancer. Journal of Cellular Biochemistry. pp. 1307-1316. ISSN 0730-2312

(2020) The Association between Cyclin D1 (CCND1) rs9344 AA Genotype and Increased Risk of Colorectal Cancer in An Iranian Population. Middle East Journal of Cancer. pp. 360-364. ISSN 2008-6709

(2020) Systems biology approaches toward autosomal dominant polycystic kidney disease (ADPKD). Clinical and Translational Medicine. ISSN 2001-1326

(2020) The challenging nature of primary T lymphocytes for transfection: Effect of protamine sulfate on the transfection efficiency of chemical transfection reagents. Research in Pharmaceutical Sciences. pp. 437-446. ISSN 1735-5362

(2019) MDA-7/interleukin 24 (IL-24) in tumor gene therapy: application of tumor penetrating/homing peptides for improvement of the effects. Expert Opinion on Biological Therapy. pp. 211-223. ISSN 1471-2598

(2020) Gene delivery by PeI-nanocomplex into breast and colorectal tumor cell lines, the impacts of N/P ratio, size and type of the cell. Fabad Journal of Pharmaceutical Sciences. pp. 19-27. ISSN 13004182 (ISSN)

(2020) The Evaluation of tLyP-1-Bound Mda-7/IL-24 Killing Activity on a Liver Tumor Cell Line. Cancer Biother Radiopharm. ISSN 1084-9785

(2018) Co-Transplantation of Human Neurotrophic Factor Secreting Cells and Adipose-Derived Stem Cells in Rat Model of Multiple Sclerosis. Cell Journal. pp. 46-52. ISSN 2228-5806 (Print) 2228-5806 (Linking)

(2018) Semaphorin-3A as An Immune Modulator Is Suppressed by MicroRNA-145-5p. Cell Journal. pp. 113-119. ISSN 2228-5806 (Print) 2228-5806 (Linking)

(2019) Blockage of HOTAIR Reduced Cell Proliferation in Human Ovarian Cancer Cells Through Upregulation of AKT2. Indian Journal of Gynecologic Oncology. p. 6. ISSN 2363-8397

(2020) Degradation of HOX Transcript Antisense RNA Provoked Apoptosis and Necrosis in Human Ovarian Cancer Cells. Indian Journal of Gynecologic Oncology. ISSN 2363-8397

(2019) Next-generation sequencing reveals a novel pathological mutation in the TMC1 gene causing autosomal recessive non-syndromic hearing loss in an Iranian kindred. Int J Pediatr Otorhinolaryngol. pp. 99-105. ISSN 1872-8464 (Electronic) 0165-5876 (Linking)

(2019) Immunization using male germ cells and gametes as rich sources of cancer/testis antigens for inhibition of 4T1 breast tumors' growth and metastasis in BALB/c mice. International Immunopharmacology. p. 6. ISSN 1567-5769

(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. International Journal of Peptide Research and Therapeutics. pp. 1343-1359. ISSN 1573-3149

(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. International Immunopharmacology. p. 8. ISSN 1567-5769

(2019) Application of Hanging Drop Culture for Retinal Precursor-Like Cells Differentiation of Human Adipose-Derived Stem Cells Using Small Molecules. Journal of Molecular Neuroscience. pp. 597-607. ISSN 0895-8696

(2019) Knockdown of Long Noncoding RNA 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. Cancer Biotherapy and Radiopharmaceuticals. pp. 371-379. ISSN 1084-9785

(2020) Gut Microbiota and Host Gene Mutations in Colorectal Cancer Patients and Controls of Iranian and Finnish Origin. Anticancer Research. pp. 1325-1334. ISSN 0250-7005

(2020) Molecular genetic study in a cohort of Iranian families suspected to maturity-onset diabetes of the young, reveals a recurrent mutation and a high-risk variant in the CEL gene. Advanced Biomedical Research. ISSN 2277-9175

(2020) A novel pathogenic variant in the LRTOMT gene causes autosomal recessive non-syndromic hearing loss in an Iranian family. Bmc Medical Genetics.

(2020) Whole exome sequencing identifies novel compound heterozygous pathogenic variants in the MYO15A gene leading to autosomal recessive non-syndromic hearing loss. Molecular Biology Reports. pp. 5355-5364. ISSN 0301-4851

(2020) Single-Strand DNA-Like Oligonucleotide Aptamer Against Proprotein Convertase Subtilisin/Kexin 9 Using CE-SELEX: PCSK9 Targeting Selection. Cardiovascular Drugs and Therapy. pp. 475-485. ISSN 0920-3206

(2019) Profiling of 17 Y-STR loci in Mazandaran and Gilan provinces of Iran. Turkish Journal of Medical Sciences. pp. 1277-1286. ISSN 1300-0144

(2020) Genetic polymorphisms of Y-chromosome short tandem repeats (Y-STRs) in a male population from Golestan province, Iran. Molecular Biology Research Communications. pp. 11-16. ISSN 2322-181X

(2019) Motor neuron diseases caused by a novel VRK1 variant - A genotype/phenotype study. Annals of Clinical and Translational Neurology. pp. 2197-2204. ISSN 2328-9503

(2020) Can the Decreased Expression of Human Leukocyte Antigen Class Ⅰ and Ⅱ by Spermatozoa Lead to Recurrent Spontaneous Abortion? Iran J Pathol. pp. 19-22. ISSN 1735-5303 (Print) 1735-5303

(2019) Genetic mutations and immunological features of severe combined immunodeficiency patients in Iran. Immunology Letters. pp. 70-78. ISSN 0165-2478

(2019) Negative Regulation of Semaphorin-3A Expression in Peripheral Blood Mononuclear Cells Using MicroRNA-497-5p. Iranian Journal of Medical Sciences. pp. 325-333. ISSN 0253-0716

(2020) Meta-Analysis on the Association of C-Reactive Protein Polymorphisms with Metabolic Syndrome. Global Medical Genetics. pp. 8-13. ISSN 2699-9404

(2020) Epigenetic changes in FOXO3 and CHEK2 genes and their correlation with clinicopathological findings in myelodysplastic syndromes. Hematol Oncol Stem Cell Ther. pp. 214-219. ISSN 1658-3876 (Print)

(2020) Retraction Note: Blockage of miR-92a-3p with locked nucleic acid induces apoptosis and prevents cell proliferation in human acute megakaryoblastic leukemia. Cancer Gene Ther. p. 113. ISSN 0929-1903

(2019) Retraction Note to: Inhibition of microRNA miR-92a induces apoptosis and inhibits cell proliferation in human acute promyelocytic leukemia through modulation of p63 expression. Mol Biol Rep. p. 5667. ISSN 1573-4978 (Electronic) 0301-4851 (Linking)

(2020) Phenotypic and Genotypic Characteristics of Clostridium difficile Isolates in Patients with Type 2 Diabetes in Iran. Infection and Drug Resistance. pp. 683-690. ISSN 1178-6973

(2019) Clinical and molecular assessment of 13 Iranian families with Wolfram syndrome. Endocrine. pp. 185-191. ISSN 1355-008X

(2020) Clinical and genetic analysis of two wolfram syndrome families with high occurrence of wolfram syndrome and diabetes type II: a case report. Bmc Medical Genetics.

(2019) A Patient with Trisomy 4p and Monosomy 10q. Arch Iran Med. pp. 414-417. ISSN 1735-3947 (Electronic) 1029-2977 (Linking)

(2019) The First Report of a Patient with Trisomy 4p and Monosomy 10q. Archives of Iranian Medicine. pp. 414-417. ISSN 1029-2977

(2020) Therapeutic Effects of Garlic on Hepatic Steatosis in Nonalcoholic Fatty Liver Disease Patients: A Randomized Clinical Trial. Diabetes Metabolic Syndrome and Obesity-Targets and Therapy. pp. 2389-2397. ISSN 1178-7007

(2018) A homozygous NOP14 variant is likely to cause recurrent pregnancy loss. Journal of Human Genetics. pp. 425-430. ISSN 1434-5161

(2018) A Novel Pathologic Variant in OTOF in an Iranian Family Segregating Hereditary Hearing Loss. Otolaryngology-Head and Neck Surgery. pp. 1084-1092. ISSN 0194-5998

(2019) A novel pathogenic variant in the MARVELD2 gene causes autosomal recessive non-syndromic hearing loss in an Iranian family. Genomics. pp. 840-848. ISSN 0888-7543

(2020) miR-504 expression level is increased in multiple sclerosis patients responder to interferon-beta. Journal of Neuroimmunology. ISSN 0165-5728

(2020) The anti-tumor activity of exopolysaccharides from Pseudomonas strains against HT-29 colorectal cancer cell line. International Journal of Biological Macromolecules. pp. 1072-1076. ISSN 0141-8130

(2020) Chondrogenic activity of two herbal products; pomegranate fruit extract and avocado/soybean unsaponifiable. Research in Pharmaceutical Sciences. pp. 358-366. ISSN 1735-5362

(2020) Evaluation of Muc1 Gene Expression at The Time of implantation in Diabetic Rat Models Treated with Insulin, Metformin and Pioglitazone in The Normal Cycle and Ovulation Induction Cycle. International Journal of Fertility & Sterility. pp. 218-222. ISSN 2008-076X

(2020) Evaluation of vascular endothelial growth factor A and leukemia inhibitory factor expressions at the time of implantation in diabetic rats following treatment with Metformin and Pioglitazone. International Journal of Reproductive Biomedicine. pp. 713-722. ISSN 2476-4108

(2019) Identification and Clinical Implications of a Novel MYO15A Variant in a Consanguineous Iranian Family by Targeted Exome Sequencing. Audiology and Neuro-Otology. pp. 25-31. ISSN 1420-3030

(2018) Modulatory Effects of Dexrazoxane Against Genotoxicity and Lipid Peroxidation Induced by Idarubicin in HepG2 Cells. International Journal of Cancer Management. ISSN 2538-4422

Book Section

(2019) Epigenetics and Common Non Communicable Disease. In: Primordial Prevention of Non Communicable Disease. Advances in Experimental Medicine and Biology, 1121 . Springer International Publishing Ag, Cham, pp. 7-20. ISBN 978-3-030-10616-4; 978-3-030-10615-7