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فیلتر نتایج
Somayeh Reiisi
Journal Paper
Mitochondrial gene mutation screening in hearing loss patients, Hormozgan, Iran
Authors:
Fatemeh Taji
،
Sousan Keshavarz
،
Kourosh Ashrafi
،
Effat Farrokhi
،
Mojtaba Saeedi Morghmaleki
،
Azam Hoseinipor
،
Morteza Hashemzadeh Chaleshtori
،
Golandam Banitalebi Dehkordi
،
Marziyeh Abolhasani
،
Azam Asghari
،
Mostafa Montazer Zohori
،
Fatemeh Azadegha
Year 1390
Publish place:
Hormozgan Medical Journal Issue 1، Vol 15
Pages:
7
| Language: English
View And Download
Journal Paper
Mitochondrial gene mutation screening in hearing loss patients, Hormozgan, Iran
Authors:
Fatemeh Taji
،
Sousan Keshavarz
،
Kourosh Ashrafi
،
Effat Farrokhi
،
Mojtaba Saeedi Morghmaleki
،
Azam Hoseinipor
،
Morteza Hashemzadeh Chaleshtori
،
Golandam Banitalebi Dehkordi
،
Marziyeh Abolhasani
،
Azam Asghari
،
Mostafa Montazer Zohori
،
Fatemeh Azadegha
Year 1390
Publish place:
Hormozgan Medical Journal Issue 1، Vol 15
Pages:
7
| Language: English
View And Download
Journal Paper
Evaluation of the effect of Chrysin and Caffeic acid phenethyl ester on eIF۴E expression in AGS cell line
Authors:
Marziyeh Abolhasani
،
Morteza Hashemzadeh-Chaleshtori
،
Abbas Doosti
،
Nematolah Amini Sarteshnizi
،
Mostafa Gholami-Arjenaki
،
Hossein Teimori
Year 1393
Publish place:
Journal of Herbmed Pharmacology Issue 2، Vol 3
Pages:
5
| Language: English
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Journal Paper
Population Data on D۷S۲۴۲۵ Marker in Five Ethnic Groups of the Iranian Population: A Highly Informative Marker for Molecular Diagnosis of ARNSHL
Authors:
Marjan Mojtabavi Naeini
،
Sadeq Vallian Boroujeni
،
Morteza Hashemzadeh Chaleshtori
Year 1393
Publish place:
Journal of Kerman University of Medical Sciences Issue 6، Vol 21
Pages:
11
| Language: English
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Journal Paper
A Study of Cytogenetic Stability of Induced Pluripotent Stem Cells Using Karyotyping and Comet Assay Techniques
Authors:
Payam Ghasemi-Dehkordi
،
Mehdi Allahbakhshian-Farsani
،
Narges Abdian
،
Hamideh Jafari-Ghahfarokhi
،
Javad Saffari-Chaleshtori
،
Marzieh Sadeghiani
،
Amin Mirzaeian
،
Morteza Hashemzadeh-Chaleshtori
Year 1394
Publish place:
Journal of Kerman University of Medical Sciences Issue 4، Vol 22
Pages:
15
| Language: English
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Journal Paper
Screening of DFNB۳ in Iranian families with autosomal recessive non-syndromic hearing loss reveals a novel pathogenic mutation in the MyTh۴ domain of the MYO۱۵A gene in a linked family
Authors:
Somayeh Reiisi
،
Mohammad Amin Tabatabaiefar
،
Mohammad Hosein Sanati
،
Morteza Hashemzadeh Chaleshtori
Year 1395
Publish place:
Iranian Journal of Basic Medical Sciences Issue 7، Vol 19
Pages:
7
| Language: English
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