M. S. Soltanpour

发表

Study of alloimmunization and autoimmunization in Iranian β-thalassemia major patients

K. Davari, M. Soltanpour, M. S. Soltanpour, 2016, Asian journal of transfusion science.

High Resolution Allotyping of Four Alleles of HLA-DRB1*01 Group in Iranians Using Reverse-SSOPH Assay in Comparison with DNA Sequencing and PCR-SSP

M. Safa, P. Gill, M. Rasaee, 2008 .

The Correlation of Cardiac and Hepatic Hemosiderosis as Measured by T2*MRI Technique with Ferritin Levels and Hemochromatosis Gene Mutations in Iranian Patients with Beta Thalassemia Major.

K. Davari, M. Soltanpour, M. S. Soltanpour, 2018, Oman medical journal.

Frequency of C282Y and H63D Mutations of HFE Gene and Their Correlation with Iron Status in Iranian Beta-Thalassemia Major Patients

K. Kamali, K. Davari, M. Soltanpour, 2017 .

Frequency of C 282 Y and H 63 D Mutations of HFE Gene and Their Correlation with Iron Status in Iranian Beta-Thalassemia Major Patients

K. Kamali, K. Davari, M. Soltanpour, 2017 .

Investigating the methylation status of DACT2 gene and its association with MTHFR C677T polymorphism in patients with colorectal cancer.

A. Jalilvand, M. S. Soltanpour, 2019, Molecular biology research communications.

Prevalence, genotyping and antibiotic resistance of Listeria monocytogenes and Escherichia coli in fresh beef and chicken meats marketed in Zanjan, Iran

Z. Abbasi, H. Hassanzadazar, Majid Aminzare, 2020, Iranian journal of microbiology.

Cardioprotective Effects of Mebudipine in a Rat Model of Doxorubicin-Induced Heart Failure

M. Mahmoudian, H. Ghaznavi, E. Aali, 2020, Iranian journal of medical sciences.

Association study between DNA methylation and genetic variation of APOE gene with the risk of coronary artery disease

H. Ghaznavi, A. Kiani, M. S. Soltanpour, 2018, Molecular biology research communications.

mRNA expression and promoter DNA methylation status of CDKi p21 and p57 genes in ex vivo expanded CD34+ cells following co-culture with mesenchymal stromal cells and growth factors

F. Zaker, A. Kazemi, M. Nikougoftar, 2013, Hematology.

Association Study of the ATP - Binding Cassette Transporter A1 (ABCA1) Rs2230806 Genetic Variation with Lipid Profile and Coronary Artery Disease Risk in an Iranian Population

H. Ghaznavi, E. Aali, M. S. Soltanpour, 2018, Open access Macedonian journal of medical sciences.

Plasma homocysteine levels, methylene tetrahydrofolate reductase A1298C gene polymorphism and risk of retinal vein thrombosis

H. Ghaznavi, S. Samiei, Z. Soheili, 2016, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Association of Methylenetetrahydrofolate Reductase C677T Polymorphism with Hyperhomocysteinemia and Deep Vein Thrombosis in the Iranian Population

H. Ghaznavi, S. Samiei, Z. Soheili, 2015, Vascular specialist international.

Association study of methylenetetrahydrofolate reductase A1298C mutation with cerebral venous thrombosis risk in an Iranian population

M. Soltanpour, Soheili Zahra, Samiei Shahram, 2015, International journal of applied & basic medical research.

Association study of methylenetetrahydrofolate reductase C677T mutation with cerebral venous thrombosis in an Iranian population

H. Ghaznavi, S. Samiei, Z. Soheili, 2015, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

The C-565T Polymorphism (rs2422493) of the ATP-binding Cassette Transporter A1 Gene Contributes to the Development and Severity of Coronary Artery Disease in an Iranian Population.

K. Kamali, H. Ghaznavi, M. Soltanpour, 2018, Oman medical journal.

A preliminary study of the association between the ABCA1 gene promoter DNA methylation and coronary artery disease risk

H. Ghaznavi, M. Soltanpour, Khalil Mahmoodi, 2018, Molecular biology research communications.

Promoter Hypermethylation of Wnt/β-catenin Signaling Pathway Inhibitor WIF-1 Gene and its Association with MTHFR C677T Polymorphism in Patients with Colorectal Cancer

A. Jalilvand, M. S. Soltanpour, 2020, Oman medical journal.

Association of Nitric Oxide Levels and Endothelial Nitric Oxide Synthase G894T Polymorphism with Coronary Artery Disease in the Iranian Population

E. Karami, M. Soltanpour, Khalil Mahmoodi, 2016, Vascular specialist international.

Assessment of the role of plasma nitric oxide levels, T-786C genetic polymorphism, and gene expression levels of endothelial nitric oxide synthase in the development of coronary artery disease

K. Kamali, M. Soltanpour, Khalil Mahmoodi, 2017, Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences.

The Effect of Oxalobacter formigenes Colonization in Patients with Calcium Oxalate Renal Stones in Comparison with Healthy People in Qom: A Case-Control Study

J. Nowroozi, M. Soltanpour, M. Akhavan Sepahi, 2021, Nephro-Urology Monthly.

Development of an Innovative Method by Optimizing qPCR Technique for Isolating and Determining Oxalobacter Formigenes Microbial Load in the Stool of Patients with Urolithiasis.

J. Nowroozi, M. Soltanpour, M. Akhavan Sepahi, 2021, Iranian journal of kidney diseases.

Role of Hyperhomocysteinemia and Methylene Tetrahydrofolate Reductase C677T Polymorphism in Idiopathic Portal Vein Thrombosis

H. Ghaznavi, S. Samiei, Z. Soheili, 2016, Vascular specialist international.

Plasma concentration, genetic variation, and gene expression levels of matrix metalloproteinase 9 in Iranian patients with coronary artery disease

K. Kamali, E. Karami, M. Soltanpour, 2017, Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences.

Evaluation of the Role of -137G/C Single Nucleotide Polymorphism (rs187238) and Gene Expression Levels of the IL-18 in Patients with Coronary Artery Disease.

S. Mahmazi, F. Hoseini, G. Jafari, 2018, Oman medical journal.

Promoter DNA Methylation Frequency and Clinicopathological Role of miR-129-2 Gene in Patients with Chronic Lymphocytic Leukemia

M. Hashemi, M. Mohammadipour, S. Rostami, 2020, Oman medical journal.

Methylenetetrahydrofolate reductase C677T mutation and risk of retinal vein thrombosis

M. Shahjahani, A. Pourfathollah, A. Karimi, 2013, Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences.

Association study between rs2275913 genetic polymorphism and serum levels of IL-17A with risk of coronary artery disease.

H. Ghaznavi, M. Soltanpour, M. S. Soltanpour, 2020, Molecular biology research communications.

Assessment of the role of plasma nitric oxide levels, T-786C genetic polymorphism, and gene expression levels of endothelial nitric oxide synthase in the development of coronary artery disease

K. Kamali, Khalil Mahmoodi, M. S. Soltanpour, 2017, Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences.