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 Extracton 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 |
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|
|
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 |
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