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2011BMC      Medical
Genomics
Identification of disease-causing genes using microarray data mining and Gene Ontology1
2016Cancer Gene TherapyCirculating microRNA-192 as a diagnostic biomarker in human chronic lymphocytic leukemia2
2014GeneMiR-326 and miR-26a, two potential markers for diagnosis of relapse and remission phases in patient with relapsing-remitting multiple sclerosis3
2011Acta TropicaMolecular characterization of human and animal Echinococcus granulosus isolates in Isfahan, Iran4
2007Journal   of   Drug
Targeting
(Gene delivery to brain cells with apoprotein E derived peptide conjugated to polylysine (apoEdp-PLL5
1996ExperientiaAge-related changes in gene expression in the rat brain revealed by differential display6
2012Acta VirologicaEvaluation of the in vitro antiretroviral potential of some Biginelli-type pyrimidines7
2006Memorias do Instituto
Oswaldo Cruz
Detection of rifampin resistance patterns in Mycobacterium tuberculosis strains isolated in Iran by polymerase chain reaction-single-strand conformation polymorphism and direct sequencing methods8
2012Clinical LaboratoryOccult Hepatitis B Virus (HBV) Infection: a Global Challenge for Medicine9
1999Mechanisms     of A g e i n g        a n d Development Fluorescence in situ hybridization analysis of the fos/jun ratio in the ageing brain10
2011Journal of Research in Medical SciencesFrequency of entamoeba histolytica and entamoeba dispar prevalence among patients with gastrointestinal complaints in Chelgerd city, southwest of Iran11
2011Jundishapur  Journal of MicrobiologyMolecular epidemiology of Echinococcus granulosus strains in domestic herbivores of Lorestan, Iran12
2009Iranian  Journal  of
Immunology
Distribution of HLA-B*27 alleles in patients with ankylosing spondylitis in Iran13
2016Journal  of  Human
Genetics
A novel homozygous mutation in HSF4 causing autosomal recessive congenital cataract14
2016Journal   of   Gene
Medicine
Genetic disruption of the KLF1 gene to overexpress the  -globin gene using the CRISPR/Cas9 system15
2015Clinical       Oral
Investigations
Family-based association analysis between nonsyndromic cleft lip with or without cleft palate and IRF6 polymorphism in an Iranian population16
2014Medical   oncology (Northwood, London,
(England
A miRNA-binding site single nucleotide polymorphism in the 3′-UTR region of the NOD2 gene is associated with colorectal cancer17
2016Archives   of   Oral
Biology
Non-syndromic cleft lip with or without cleft palate in Asian populations: Association analysis on three gene polymorphisms of the folate pathway18
2012J o u r n a l         o f I n f l a m m a t i o n Apoptosis inhibition or inflammation: The role of NAIP protein expression in Hodgkin and non-Hodgkin lymphomas compared to non-neoplastic lymph node19
2011Clinics and Research in  Hepatology  and GastroenterologyHepatitis B virus genotype, HBsAg mutations and co-infection with HCV in occult HBV infection20
2012Asian Pacific Journal of Cancer PreventionAssociation between mismatch repair gene MSH3 codons 1036 and 222 polymorphisms and sporadic prostate cancer in the iranian population21
2017Research        in Pharmaceutical
Sciences
Oligonucleotide aptamers: Potential novel molecules against viral hepatitis22
2016International  Journal of  Molecular  and Cellular MedicineDown syndrome: Current status, challenges and future perspectives23
2015International  Journal of      Preventive
Medicine
Mutation of Kisspeptin 1 Gene in Children with Precocious Puberty in Isfahan City24
2015International  Journal of        Pediatric OtorhinolaryngologyMutation spectrum of autosomal recessive non-syndromic hearing loss in central Iran25
2014GeneInvestigation of sensitivity, specificity and accuracy of Tetra primer ARMS PCR method in comparison with conventional ARMS PCR, based on sequencing technique outcomes in IVS-II-I genotyping of beta thalassemia
patients
26
2010J o u r n a l         o f Dermatology (Incidence rate of mycosis fungoides in Isfahan (Iran27
2008Journal of Research in Medical SciencesEvidence for an association of TP53 codon 72 polymorphism with sporadic colorectal cancer risk in Isfahan28
2016Biotechnology
Letters
Comparison of different methods for erythroid differentiation in the K562 cell line29
2015J o u r n a l         o f Gastrointestinal  and
Liver Diseases
Two different UGT1A1 mutations causing Crigler-Najjar syndrome types I and II in an Iranian family30
2009Cellular ImmunologyEvaluation of ARG protein expression in mature B cell lymphomas compared to non-neoplastic reactive lymph node31
2008NephrologyAngiotensin-converting enzyme gene polymorphism and the progression rate of focal segmental glomerulosclerosis in Iranian children32
2007Multiple SclerosisConjugal multiple sclerosis in Isfahan, Iran: a population-based study33
2016Iranian  Journal  of
Immunology
Th1, Th2 and Th17 cytokine profile in patients with multiple sclerosis following treatment with rapamycin34
2016Research        in Pharmaceutical
Sciences
Exposition of hepatitis B surface antigen (HBsAg) on the surface of HEK293T cell and evaluation of its expression35
2015M  o  l  e  c  u  l  a  r  BiotechnologyA Lentiviral Vector Expressing Desired Gene Only in Transduced Cells: An Approach for Suicide Gene Therapy36
2015GeneHomozygous MAPT R406W mutation causing FTDP phenotype: A unique instance of a unique mutation37
2014Annals of Diagnostic
Pathology
Livin, a novel marker in lymphoma type distinction38
2012Iranian  Journal  of Basic      Medical
Sciences
https://www.ncbi.nlm.nih.gov/pubmed/?term=Simultaneous+detection+of+integrase+and+antibiotic+resistance+genes+within+SXT+constin+in+vibrio+cholerae+O1+El+tor+strains+isolated+from+Iran+using+multiplex-PCR39
2016Journal of Maternal- Fetal  and  Neonatal
Medicine
Detection of paternally inherited fetal point mutations for  -thalassemia in maternal plasma using simple fetal DNA enrichment protocol with or without whole genome amplification: An accuracy assessment40
2016Jundishapur  Journal of MicrobiologyZinc finger nuclease: A new approach to overcome beta-lactam antibiotic resistance41
2015Journal   of   Child
Neurology
Detection of intragenic SMN1 mutations in spinal muscular atrophy patients with a single copy of SMN142
2015International  Journal of        Pediatric OtorhinolaryngologyA new compound heterozygous mutation in GJB2 causes nonsyndromic hearing loss in a consanguineous Iranian family43
2012Pakistan  Journal  of Medical SciencesMutations of Dual Oxidase 2 (DUOX2) Gene among patients with Permanent and Transient Congenital Hypothyroidism44
2007Molecular      and Cellular BiochemistryEffect of hepatocyte growth factor (HGF) on the level of Survivin & XIAP expression in several human cancer cell lines, after treating with DNA damaging agent45
2010International  Journal
of Cardiology
?Can leukocyte telomere length (LTL) be considered as an index in application of neural network in the atherosclerosis risk stratification46
2017Human GeneticsAssociation of AHSG with alopecia and mental retardation (APMR) syndrome47
2017International  Journal of  Molecular  and Cellular MedicineMeDIP real-time qPCR has the potential for noninvasive prenatal screening of fetal trisomy 2148
2016Cell JournalRORA and Autism in Isfahan population: Is there an epigenetic relationship49
2016Iranian  Journal  of Basic      Medical
Sciences
Gamma reactivation using the spongy effect of KLF1-binding site sequence: An approach in gene therapy for beta-thalassemia50
2016Archives of Medical
Research
Novel Multiplex Fluorescent PCR-Based Method for HLA Typing and Preimplantational Genetic Diagnosis of  -Thalassemia51
2015Journal  of  Clinical and     Diagnostic
Research
Prevalence of intestinal parasitic infection among inhabitants and tribes of Chelgerd, Iran, 2008-200952
2014Iranian  Journal  of
Parasitology
(P-glycoprotein A gene expression in glucantime-resistant and sensitive Leishmania major (MRHO/IR/75/ER53
2012Molecular Biology(Introducing a frameshift mutation to the Pol sequence of HIV-1 provirus and evaluation of the immunogenic characteristics of the mutated virions (RINNL4-354
2012Familial CancerTwo novel mutations in hMLH1 gene in Iranian hereditary non-polyposis colorectal cancer patients55
2007Acta CardiologicaEvaluation of TERT mRNA alternative spliced variants in aortic endothelial cells of the rabbit, in the fatty streaks stage of atherosclerosis56
2016Cytogenetic    and Genome   ResearchReciprocal 22q11.2 deletion and duplication in siblings with karyotypically normal parents57
2011African  Journal  of
Biotechnology
Nitric oxide level and von willebrand factor (vWF) secretion are not candidate markers of endothelial cell dysfunction in adenosine triphosphate (ATP) depleted endothelial cells58
2019Journal  of  cellular
biochemistry
Engineered zinc-finger nuclease to generate site-directed modification in the KLF1 gene for fetal hemoglobin induction59
2018International  journal of     hematology- oncology  and  stem
cell research
Association between (GT)n Repeats in Heme Oxygenase-1 Gene Promoter and 3-Year Survival of Patients with Acute Leukemia: a Controlled, Cross-Sectional Study60
2018The British journal of
dermatology
An insertion mutation in HOXC13 underlies pure hair and nail ectodermal dysplasia with lacrimal duct obstruction61
2013Journal of community
genetics
Two decades of pre-marital screening for beta-thalassemia in central Iran62
2018Iranian  journal  of
public health
Autism and Probable Prerequisites: Severe and Scheduled Prenatal Stresses at Spotlight63
2019Cardiovascular revascularization medicine : including m o l e c u l a r 
interventions
Association of high level of Hs-CRP with in-stent restenosis: A case-control study64
2018Multiple sclerosis and related disordersPromising effect of rapamycin on multiple sclerosis65
2019Applied biochemistry and biotechnologyA Comparison Between Full-COLD PCR/HRM and PCR Sequencing for Detection of Mutations in Exon 9 of PIK3CA in Breast Cancer Patients66
2017BMC pregnancy and
childbirth
.Pregnancy, child bearing and prevention of giving birth to the affected children in patients with primary immunodeficiency disease; a case-series67
2018Journal  of  Cellular
Biochemistry
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
68
2018Journal  of  clinical laboratory analysisEvaluation of the utility of peripheral blood vs bone marrow in karyotype and fluorescence in situ hybridization for myelodysplastic syndrome diagnosis69
2018CELL JOURNALOX40 Gene and Serum Protein Expression Profiles in Patients with Parkinson’s Disease70
2018GeneAnalysis of the expression of mir-34a, mir-199a, mir-30c and mir-19a in peripheral blood CD4+T lymphocytes of relapsing-remitting multiple sclerosis patients71
2018International  journal of        pediatric otorhinolaryngologyGJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants72
2018BiomedicinesGJA4/Connexin 37 Mutations Correlate with Secondary Lymphedema Following Surgery in Breast Cancer Patients73
2018Journal  of  human
genetics
A homozygous NOP14 variant is likely to cause recurrent pregnancy loss74
2018Journal  of  human
genetics
A novel homozygous DPH1 mutation causes intellectual disability and unique craniofacial features75
2017Biomarkers      in
medicine
.Aberrant expression of PlncRNA-1 and TUG1: potential biomarkers for gastric cancer diagnosis and clinically monitoring cancer progression76
2017Journal of research in medical sciences : the official  journal  of Isfahan University of Medical SciencesIdentification a novel mononucleotide deletion mutation in in pompe disease patients77
2017Advanced biomedical
research
Application of Epstein-Barr Virus for Optimization of Immortalized B-lymphocyte Production as a Positive Control in Genetic Studies78
2017Advanced biomedical
research
Evaluation of Energy Balance on Human Telomerase Reverse Transcriptase (hTERT) Alternative Splicing by Semi-quantitative RT-PCR in Human Umbilical Vein Endothelial Cells79
2017Advanced biomedical
research
Simple and Easy to Perform Preimplantation Genetic Diagnosis for  -thalassemia Major Using Combination of Conventional and Fluorescent Polymerase Chain Reaction80
2017Advanced biomedical
research
Treatment Outcome of the Drug-resistant Zoonotic Cutaneous Leishmaniasis by Glucantime81
2016Advanced biomedical
research
Prevalence of 22q11.2 microdeletion syndrome in Iranian patients with cleft palate82
2016Journal of research in medical sciences : the official  journal  of Isfahan University of Medical SciencesGenomic rearrangement screening of the from seventy Iranian high-risk breast cancer families83
2016Cell journalRORA and Autism in The Isfahan Population: Is There An Epigenetic Relationship84
2016Advanced biomedical
research
Expression of microRNA-370 in human breast cancer compare with normal samples85
2016Advanced biomedical
research
In vivo/In vitro immune responses to L. major isolates from patients with no clinical response to Glucantime86