Different Types of the Coagulation Disorders in Hamadan and A Comparison of the ABO & Rh Blood Group Distribution in the Patients and the Control Group

by Hamid Pour-Jafari, Morteza Hashemzadeh Chaleshtori
Published 2003-12-01

Correlation of Endothelial Nitric Oxide Synthase Gene Polymorphism (GG, TT and GT Genotype) with Proteinuria and Retinopathy in Type 2 Diabetic Patients

by Ali Momeni, Morteza Hashemzadeh Chaleshtori, Saeed Saadatmand, Soleiman Kheiri
Published 2016-02-01

A preliminary study of inherited thrombophilic risk factors in different clinical manifestations of venous thromboembolism in central Iran

by Ali Karimi, Marziyeh Abolhasani, Morteza Hashemzadeh-Chaleshtori, Batoul Pourgheysari
Published 2015-01-01

Screening of Myo7A Mutations in Iranian Patients with Autosomal Recessive Hearing Loss from West of Iran

by Samira ASGHARZADE, Somayeh REIISI, Mohammad Amin TABATABAIEFAR, Morteza HASHEMZADEH CHALESHTORI
Published 2017-01-01

Clinical Aspects of Microsatellite Instability Testing in Colorectal Cancer

by Mehrdad Zeinalian, Morteza Hashemzadeh-Chaleshtori, Rasoul Salehi, Mohammad Hassan Emami
Published 2018-01-01

Lack of Association between ESR1 and CYP1A1 Gene Polymorphisms and Susceptibility to Uterine Leiomyoma in Female Patients of Iranian Descent

by Fatemeh Taghizade Mortezaee, Mohammad Amin Tabatabaiefar, Morteza Hashemzadeh Chaleshtori, Sepideh Miraj
Published 2014-06-01

Screening of DFNB3 in Iranian families with autosomal recessive non-syndromic hearing loss reveals a novel pathogenic mutation in the MyTh4 domain of the MYO15A gene in a linked fa...

by Somayeh Reiisi, Mohammad Amin Tabatabaiefar, Mohammad Hosein Sanati, Morteza Hashemzadeh Chaleshtori
Published 2016-07-01

Familial Colorectal CancerType X in Central Iran: A New Clinicopathologic Description

by Mehrdad Zeinalian, Mahdi Hadian, Morteza Hashemzadeh-Chaleshtori, Rasoul Salehi, Mohammad Hassan Emami
Published 2016-10-01

Tumor microsatellite instability and clinicopathologic features in Iranian colorectal cancer patients at risk for Lynch syndrome

by Mehrdad Zeinalian, Morteza Hashemzadeh-Chaleshtori, Rasoul Salehi, Mohammad Kazemi, Mohammad Hassan Emami
Published 2015-01-01

بررسی جهش‌های ژن LRTOMT (لوکوس 63DFNB) در بیماران مبتلا به ناشنوایی غیر سندرمیک مغلوب استان هرمزگان با استفاده از روش‌های PCR-SSCP، PCR-HA و توالی‌یابی DNA...

by Shahrbanoo Parchami-Barjui, Somayeh Reiisi, Fatemeh Rezaiean, Fatemeh Heybati, Morteza Hashemzadeh-Chaleshtori
Published 2014-10-01

Association of Hypoxia-inducible factor α subunits with TSGA10 transcripts in HeLa, MCF7 and MDA-MB231- cell lines

by Parya Rahmani Rad, Maryam Beigom Mobasheri, Morteza Hashemzadeh-Chaleshtori, Mohammad Hossein Modarressi
Published 2018-01-01

Molecular Mechanisms behind Free Radical Scavengers Function against Oxidative Stress

by Fereshteh Ahmadinejad, Simon Geir Møller, Morteza Hashemzadeh-Chaleshtori, Gholamreza Bidkhori, Mohammad-Saeid Jami
Published 2017-07-01

Investigation of Mutations in Exons 15 and 18 of MYBPC3 Gene in Hypertrophic Cardiomyopathy Patients

by Behnaz Sadat Abedi, Seyedeh Zohreh kiyani, Morteza Hashemzadeh Chaleshtori, Shahrbanoo Parchami, Abbas Doosti
Published 2015-08-01

Novel MYO15A variants are associated with hearing loss in the two Iranian pedigrees

by Somayeh Khatami, Masomeh Askari, Fatemeh Bahreini, Morteza Hashemzadeh-Chaleshtori, Saeed Hematian, Samira Asgharzade
Published 2020-11-01

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

by Akram Sarmadi, Aliasgar Mohammadi, Fatemeh Tabatabaei, Zahra Nouri, Morteza Hashemzadeh Chaleshtori, Mohammad Amin Tabatabaiefar
Published 2020-01-01

تجزیه و تحلیل پیوستگی ژنتیکی لوکوس‌های DFNB40 و DFNB48 در خانواده‌هایی با ناشنوایی غیر سندرمی مغلوب اتوزومی از استان‌های غربی کشور...

by Azam Pourahmadiyan, Mohammad Amin Tabatabaiefar, Somayeh Reiisi, Paria Alipour, Najmeh Fattahi, Morteza Hashemzadeh-Chaleshtori
Published 2016-05-01

Increased levels of miR-124 in human dental pulp stem cells alter the expression of neural markers

by Ameneh Mehri-Ghahfarrokhi, Zahra Pourteymourfard-Tabrizi, Effat Farrokhi, Morteza Hashemzadeh Chaleshtori, Mohammad-Saeid Jami
Published 2019-12-01

A Simple, Rapid, and Efficient Method for Isolating Mesenchymal Stem Cells from the Entire Umbilical Cord

by Mehdi Banitalebi Dehkordi, Zahra Madjd, Morteza Hashemzadeh Chaleshtori, Reza Meshkani, Laleh Nikfarjam, Abdol-Mohammad Kajbafzadeh
Published 2016-07-01

Evaluation of response to hepatitis B vaccine in iranian 6–18-year-old students

by Alizamen Salehifard Jouneghani, Morteza Hashemzadeh Chaleshtori, Abolfazl Khoshdel, Soleiman Kheiri, Effat Farrokhi, Pooran Khalafian, Zahra Aliyari
Published 2017-01-01

Association of estrogen receptor α-351 and -397 polymorphisms with uterine leiomyoma in Chaharmahal & Bakhtiari women

by Fatemeh Taghizade Mortezaee, Sepideh Miraj, Golandam Bani Talebi, Morteza Hashemzadeh Chaleshtori, Faramarz Sedgh Azar, Maryam Haj Hashemi
Published 2013-09-01