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

por Karimi, Ali, Abolhasani, Marziyeh, Hashemzadeh-Chaleshtori, Morteza, Pourgheysari, Batoul
Publicado 2015

Plasma Level Of miR-21 And miR-451 In Primary And Recurrent Breast Cancer Patients

por Motamedi, Maryam, Hashemzadeh Chaleshtori, Morteza, Ghasemi, Sorayya, Mokarian, Fariborz
Publicado 2019

Upregulation of Neuroprogenitor and Neural Markers via Enforced miR-124 and Growth Factor Treatment

por Mehri Ghahfarrokhi, Ameneh, Jami, Mohammad Saeid, Hashemzadeh Chaleshtori, Morteza
Publicado 2020

Clinical Aspects of Microsatellite Instability Testing in Colorectal Cancer

por Zeinalian, Mehrdad, Hashemzadeh-Chaleshtori, Morteza, Salehi, Rasoul, Emami, Mohammad Hassan
Publicado 2018

Genetics of Hearing Loss in North Iran Population: An Update of Spectrum and Frequency of GJB2 Mutations

por Koohiyan, Mahbobeh, Azadegan-Dehkordi, Fatemeh, Koohian, Farideh, Hashemzadeh-Chaleshtori, Morteza
Publicado 2019

Mesenchymal stem cells versus their conditioned medium in the treatment of ischemia/reperfusion injury: Evaluation of efficacy and hepatic specific gene expression in mice

por Khosravi-Farsani, Somayeh, Zaminy, Arash, Kazemi, Sedigheh, Hashemzadeh-Chaleshtori, Morteza
Publicado 2022

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

por Taghizade Mortezaee, Fatemeh, Tabatabaiefar, Mohammad Amin, Hashemzadeh Chaleshtori, Morteza, Miraj, Sepideh
Publicado 2014

Immunohistochemical Analysis of Mismatch Repair Proteins in Iranian Colorectal Cancer Patients at Risk for Lynch Syndrome

por Zeinalian, Mehrdad, Emami, Mohammad Hassan, Naimi, Azar, Salehi, Rasoul, Hashemzadeh-Chaleshtori, Morteza
Publicado 2015

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

por Zeinalian, Mehrdad, Hashemzadeh-Chaleshtori, Morteza, Salehi, Rasoul, Kazemi, Mohammad, Emami, Mohammad Hassan
Publicado 2015

Familial Colorectal Cancer Type X in Central Iran: A New Clinicopathologic Description

por Zeinalian, Mehrdad, Hadian, Mahdi, Hashemzadeh-Chaleshtori, Morteza, Salehi, Rasoul, Emami, Mohammad Hassan
Publicado 2017

Molecular Mechanisms behind Free Radical Scavengers Function against Oxidative Stress

por Ahmadinejad, Fereshteh, Geir Møller, Simon, Hashemzadeh-Chaleshtori, Morteza, Bidkhori, Gholamreza, Jami, Mohammad-Saeid
Publicado 2017

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

por Khatami, Somayeh, Askari, Masomeh, Bahreini, Fatemeh, Hashemzadeh-Chaleshtori, Morteza, Hematian, Saeed, Asgharzade, Samira
Publicado 2020

MicroRNA-183 Family in Inner Ear: Hair Cell Development and Deafness

por Mahmoodian sani, Mohammad Reza, Hashemzadeh-Chaleshtori, Morteza, Saidijam, Massoud, Jami, Mohammad-Saeid, Ghasemi-Dehkordi, Payam
Publicado 2016

Small supernumerary marker chromosomes and their correlation with specific syndromes

por Jafari-Ghahfarokhi, Hamideh, Moradi-Chaleshtori, Maryam, Liehr, Thomas, Hashemzadeh-Chaleshtori, Morteza, Teimori, Hossein, Ghasemi-Dehkordi, Payam
Publicado 2015

Mutation Screening of Exons 7 and 13 of the TMC1 Gene in Autosomal Recessive Non-syndromic Hearing Loss (ARNSHL) in Iran

por Moradipour, Negar, Ghasemi-Dehkordi, Payam, Heibati, Fatemeh, Parchami-Barjui, Shahrbanuo, Abolhasani, Marziyeh, Rashki, Ahmad, Hashemzadeh-Chaleshtori, Morteza
Publicado 2016

rs12480307 and rs6050307 Polymorphisms of VSX1 Gene in Patient with Keratoconusin Southwest Iran Using PCR-RFLP

por KARAMI ESHKAFTAKI, Raziyeh, FARROKHI, Effat, HEYBATI GOJANI, Fatemeh, SALEHI VANANI, Najmeh, KARAMI ESHKAFTAKI, Maryam, MEMARZADEH, Ezzatollah, HASHEMZADEH CHALESHTORI, Morteza
Publicado 2018

Correlation Between Mucosal IL-6 mRNA Expression Level and Virulence Factors of Helicobacter pylori in Iranian Adult Patients With Chronic Gastritis

por Azadegan-Dehkordi, Fatemeh, Bagheri, Nader, Shirzad, Mahsa, Sanei, Mohammad Hossein, Hashemzadeh-Chaleshtori, Morteza, Rafieian-Kopaei, Mahmoud, Tabatabaiefar, Mohammad Amin, Shirzad, Hedayatollah
Publicado 2015

Mutations in GJB2 as Major Causes of Autosomal Recessive Non-Syndromic Hearing Loss: First Report of c.299-300delAT Mutation in Kurdish Population of Iran

por Azadegan-Dehkordi, Fatemeh, Bahrami, Tayyebe, Shirzad, Maryam, Karbasi, Gelareh, Yazdanpanahi, Nasrin, Farrokhi, Effat, Koohiyan, Mahbobeh, Tabatabaiefar, Mohammad Amin, Hashemzadeh-Chaleshtori, Morteza
Publicado 2019

Screening of 10 DFNB Loci Causing Autosomal Recessive Non-Syndromic Hearing Loss in Two Iranian Populations Negative for GJB2 Mutations

por KOOHIYAN, Mahbobeh, REIISI, Somayeh, AZADEGAN-DEHKORDI, Fatemeh, SALEHI, Mansoor, ABTAHI, Hamidreza, HASHEMZADEH-CHALESHTORI, Morteza, NOORI-DALOII, Mohammad Reza, TABATABAIEFAR, Mohammad Amin
Publicado 2019

Investigation of LRTOMT gene (locus DFNB63) mutations in Iranian patients with autosomal recessive non-syndromic hearing loss

por Taghizadeh, Seyyed Hossein, Kazeminezhad, Seyyed Reza, Sefidgar, Seyyed Ali Asghar, Yazdanpanahi, Nasrin, Tabatabaeifar, Mohammad Amin, Yousefi, Ahmad, Lesani, Seyyed Mohammad, Abolhasani, Marziyeh, Hashemzadeh Chaleshtori, Morteza
Publicado 2013