DOI

year

title

https://doi.org/10.1016/j.genrep.2021.101048

2021

A glance at glioblastoma molecular culprits through in-silico analysis

https://doi.org/10.1016/j.genrep.2021.101143

2021

Identification and prediction of common molecular culprits between psoriasis and melanoma via bioinformatical analysis

https://doi.org/10.1007/s10238-020-00663-y

2021

Thyroid peroxidase in human endometrium and placenta: a potential target for anti-TPO antibodies

https://doi.org/10.1007/s00439-020-02187-7

2020

Autozygosity‑driven genetic diagnosis in consanguineous families from Italy and the Greater Middle East

https://doi.org/10.1159/000506500

2020

A Novel Cadherin 23 Variant for Hereditary Hearing Loss Reveals Additional Support for a DFNB12 Nonsyndromic Phenotype of CDH23

https://doi.org/10.1016/j.arcmed.2020.05.005

2020

Association of Selenoprotein S Expression and its Variants with Metabolic Syndrome in Subjects with Cardiovascular Disease

https://doi.org/10.1002/jca.21755

2020

Therapeutic plasma exchange may adjust IL‐6 and TGF‐β signals in relapsed MS patients peripheral blood

https://doi.org/10.18502/ijml.v7i1.2464

2020

Altered Expression of Circulating miR-377 and miR-98 in Relapsing-remitting Multiple Sclerosis

https://doi.org/10.1016/j.lfs.2020.118759

2020

A novel carcinogenic PI3Kα mutation suggesting the role of helical domain in transmitting nSH2 regulatory signals to kinase domain

https://doi.org/10.1007/s11033-019-05000-5

2019

Effect of single nucleotide polymorphisms in SEPS1 and SEPP1 on expression in the protein level in metabolic syndrome in subjects with cardiovascular disease

https://doi.org/10.1212/NXG.0000000000000379

2019

Further supporting evidence for REEP1 phenotypic and allelic heterogeneity

https://doi.org/10.1007/s10989-018-9780-z

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

https://doi.org/10.1016/j.intimp.2019.105872

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

https://doi.org/10.1016/j.clnu.2018.09.033

2019

Do probiotics, prebiotics and synbiotics affect adiponectin and leptin in adults? A systematic review and meta-analysis of clinical trials

https://doi.org/10.32598/rmm.7.3.15

2019

The Effect of Dracocephalum kotschyi Alcoholic Extract

on the BCL2 and BAX Expression in SKBR3 Cell Line

https://doi.org/10.1089/cbr.2018.2510

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

https://doi.org/10.1016/j.carrev.2018.08.015

2019

Association of high level of hs-CRP with in-stent restenosis: A case-control study

https://doi.org/10.3389/fphar.2019.00530

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

http://dx.doi.org/https://doi.org/10.32598/rmm.7.2.39

2019

Expression Profiles of IGF1, EGF, and FGF2 Genes in Patients With Prostate Cancer in Isfahan Province, Iran

http://dx.doi.org/10.18502/ijml.v6i2.1027

2019

Expression Profiles of miR-93 and miR-330 in Iranian Patients with Chronic Lymphocytic Leukemia

https://doi.org/10.1002/jcb.28130

2019

Engineered zinc‐finger nuclease to generate site‐directed modification in the KLF1 gene for fetal hemoglobin induction

https://doi.org/10.1007/s00737-018-0888-0

2019

Gender identity development in the shadow of socialization: a grounded theory approach

https://dx.doi.org/10.22038/ijp.2018.36309.3168

2019

Prevalence of Cystic Fibrosis Trans-membrane Conductance Regulator Gene common mutations in children with cystic fibrosis in Isfahan, Iran

https://doi.org/10.1007/s12010-018-2859-3

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

https://dx.doi.org/10.22088%2FIJMCM.BUMS.8.3.169

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

https://doi.org/10.1159/000502251

2019

A Novel Pathogenic Variant in the CABP2 Gene Causes Severe Nonsyndromic Hearing Loss in a Consanguineous Iranian family

https://dx.doi.org/10.4103%2Fjrms.JRMS_293_18

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

https://dx.doi.org/10.4103%2Fjrms.JRMS_1076_18

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

https://doi.org/10.1016/j.msard.2018.08.009

2018

Promising effect of rapamycin on multiple sclerosis

https://doi.org/10.1186/s12884-018-1927-6

2018

Pregnancy, child bearing and prevention of giving birth to the affected children in patients with primary immunodeficiency disease; a case-series

https://doi.org/10.1002/jcb.26844

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

http://www.ncbi.nlm.nih.gov/pmc/articles/pmc6123548/

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

https://doi.org/10.1016/j.gene.2018.03.035

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

https://doi.org/10.1111/bjd.16276

2018

An insertion mutation in HOXC13 underlies pure hair and nail ectodermal dysplasia with lacrimal duct obstruction

https://doi.org/10.1016/j.ijporl.2018.01.012

2018

GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants

https://doi.org/10.19187/abc.20185126-31

2018

The Relationship Between Breast Cancer and VDR Gene Polymorphisms

https://doi.org/10.1038/s10038-017-0404-9

2018

A novel homozygous DPH1 mutation causes intellectual disability and unique craniofacial features

https://doi.org/10.1038/s10038-018-0410-6

2018

A homozygous NOP14 variant is likely to cause recurrent pregnancy loss

https://dx.doi.org/10.22074%2Fcellj.2018.5038

2018

OX40 Gene and Serum Protein Expression Profiles in Patients with Parkinson’s Disease

https://doi.org/10.2217/bmm-2017-0090

2017

Aberrant expression of PlncRNA-1 and TUG1: potential biomarkers for gastric cancer diagnosis and clinically monitoring cancer progression

http://dx.doi.org/10.21859/mci-supp-22

2017

Comparison of TaqMan® Assay and PCR-sequencing Method for Analyzing CYP2D10*6 and CYP2D4*6 Alleles: a False Negative Issue

https://dx.doi.org/10.4103%2F1735-5362.202447

2017

Oligonucleotide aptamers: potential novel molecules against viral hepatitis

https://doi.org/10.1002/jgm.2945

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

https://dx.doi.org/10.23750%2Fabm.v%25vi%25i.5701

2017

Selenium homeostasis and clustering of cardiovascular risk factors: a systematic review

https://dx.doi.org/10.4103%2Fjrms.JRMS_874_16

2017

Identification a novel mononucleotide deletion mutation in GAA in pompe disease patients

https://dx.doi.org/10.4103%2F2277-9175.204591

2017

Evaluation of Energy Balance on Human Telomerase Reverse Transcriptase (hTERT) Alternative Splicing by Semi-quantitative RT-PCR in Human Umbilical Vein Endothelial Cells

https://dx.doi.org/10.4103%2F2277-9175.217216

2017

Optimal DNA Isolation Method for Detection of Nontuberculous Mycobacteria by Polymerase Chain Reaction

https://www.ncbi.nlm.nih.gov/pubmed/28868265

2017

MeDIP Real-Time qPCR has the Potential for Noninvasive Prenatal Screening of Fetal Trisomy 21

https://dx.doi.org/10.22074%2Fcellj.2016.4720

2017

RORA and Autism in The Isfahan Population: Is There An Epigenetic Relationship

https://doi.org/10.1159/000484137

2017

Lexical Retrieval or Semantic Knowledge Which One Causes Naming Errors in Patients with Mild and Moderate Alzheimer’s Disease

https://dx.doi.org/10.4103%2F2277-9175.210659

2017

Application of Epstein–Barr Virus for Optimization of Immortalized B-lymphocyte Production as a Positive Control in Genetic Studies

https://dx.doi.org/10.4103%2F2277-9175.201329

2017

Treatment Outcome of the Drug-resistant Zoonotic Cutaneous Leishmaniasis by Glucantime

https://dx.doi.org/10.4103%2F2277-9175.201682

2017

Simple and Easy to Perform Preimplantation Genetic Diagnosis for β-thalassemia Major Using Combination of Conventional and Fluorescent Polymerase Chain Reaction

   

http://www.ncbi.nlm.nih.gov/pmc/articles/pmc5110654/

2016

Gamma reactivation using the spongy effect of KLF1-binding site sequence: an approach in gene therapy for beta-thalassemia

https://doi.org/10.1002/jgm.2928

2016

Genetic disruption of the KLF1 gene to overexpress the γ‐globin gene using the CRISPR/Cas9 system

https://doi.org/10.3109/14767058.2015.1095883

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

https://dx.doi.org/10.4103%2F1735-5362.192485

2016

Exposition of hepatitis B surface antigen (HBsAg) on the surface of HEK293T cell and evaluation of its expression

https://doi.org/10.1016/j.arcmed.2016.07.006

2016

Novel Multiplex Fluorescent PCR-Based Method for HLA Typing and Preimplantational Genetic Diagnosis of β-Thalassemia

https://doi.org/10.2174/2468424407666170130165135

2016

Peroxiredons: Tryparedoxin Peroxidase from Leishmania major

http://dx.doi.org/10.1155/2016/3451807

2016

Induced Pluripotent Stem Cell as a New Source for Cancer Immunotherapy

http://dx.doi.org/10.1038/jhg.2015.127

2016

A novel homozygous mutation in HSF4 causing autosomal recessive congenital cataract

https://dx.doi.org/10.5812%2Fjjm.29384

2016

Zinc Finger Nuclease: A New Approach to Overcome Beta-Lactam Antibiotic Resistance

https://dx.doi.org/10.4103%2F2277-9175.178794

2016

Mutation detection of CYP21A2 gene in nonclassical congenital adrenal hyperplasia patients with premature pubarche

https://www.ncbi.nlm.nih.gov/pubmed/27942498

2016

Down Syndrome: Current Status, Challenges and Future Perspectives

   
   
 

Medical Genetics Center of Genome,Mohtasham Kashani St, Esfahan, Iran

   reseach@cmgrc.ir

  genome.res.cent@gmail.com

03136259017

 

مشاوره ژنتیک و جوابدهی