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

por ASGHARZADE, Samira, REIISI, Somayeh, TABATABAIEFAR, Mohammad Amin, CHALESHTORI, Morteza HASHEMZADEH
Publicado 2017

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...

por Reiisi, Somayeh, Tabatabaiefar, Mohammad Amin, Sanati, Mohammad Hosein, Chaleshtori, Morteza Hashemzadeh
Publicado 2016

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

por Mehri-Ghahfarrokhi, Ameneh, Pourteymourfard-Tabrizi, Zahra, Farrokhi, Effat, Chaleshtori, Morteza Hashemzadeh, Jami, Mohammad-Saeid
Publicado 2019

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

por Sarmadi, Akram, Mohammadi, Aliasgar, Tabatabaei, Fatemeh, Nouri, Zahra, Chaleshtori, Morteza Hashemzadeh, Tabatabaiefar, Mohammad Amin
Publicado 2020

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

por Jouneghani, Alizamen Salehifard, Chaleshtori, Morteza Hashemzadeh, Khoshdel, Abolfazl, Kheiri, Soleiman, Farrokhi, Effat, Khalafian, Pooran, Aliyari, Zahra
Publicado 2017

Compound Heterozygosity for Two Novel SLC26A4 Mutations in a Large Iranian Pedigree with Pendred Syndrome

por Yazdanpanahi, Nasrin, Tabatabaiefar, Mohammad Amin, Farrokhi, Effat, Abdian, Narges, Bagheri, Nader, Shahbazi, Shirin, Noormohammadi, Zahra, Chaleshtori, Morteza Hashemzadeh
Publicado 2013

Mutation analysis of VSX1 and SOD1 in Iranian patients with keratoconus

por Saee-Rad, Samira, Hashemi, Hassan, Miraftab, Mohammad, Noori-Daloii, Mohammad Reza, Chaleshtori, Morteza Hashemzadeh, Raoofian, Reza, Jafari, Fatemeh, Greene, Wayne, Fakhraie, Ghasem, Rezvan, Farhad, Heidari, Mansour
Publicado 2011