Items where Author is "Abolhasani, Marziyeh."

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Number of items: 10.

Article

Moradipour, Negar. and Ghasemi-Dehkordi, Payam. and Heibati, Fatemeh. and Parchami Barjui, Shahrbanoo. and Abolhasani, Marziyeh. and Rashki, Ahmad. and Hashemzadeh-Chaleshtori, Morteza. (2016) Mutation screening of exons 7 and 13 of the TMC1 gene in autosomal recessive non-syndromic hearing loss (ARNSHL) in Iran. Iranian Red Crescent Medical Journal, 18 (2).

Ghasemi-Dehkordi, Payam. and Allahbakhshian-Farsani, Mehdi. and Abdian, Narges. and Mirzaeian, Amin. and Saffari-Chaleshtori, Javad. and Heybati, Fatemeh. and Mardani, Gashtasb. and Karimi-Taghanaki, Alireza. and Doosti, Abbas. and Jami, Mohammad-Saeid. and Abolhasani, Marziyeh. and Hashemzadeh-Chaleshtori, Morteza. (2015) Comparison between the cultures of human induced pluripotent stem cells (hiPSCs) on feeder- and serum-free system (Matrigel matrix), MEF and HDF feeder cell lines. JOURNAL OF CELL COMMUNICATION AND SIGNALING, 9 (3). pp. 233-246.

Karimi, Ali. and Abolhasani, Marziyeh. and Hashemzadeh-Chaleshtori, Morteza. and Pourgheysari, Batoul. (2015) A preliminary study of inherited thrombophilic risk factors in different clinical manifestations of venous thromboembolism in central Iran. INDIAN JOURNAL OF MEDICAL RESEARCH, 142. pp. 46-52.

Abolhasani, Marziyeh. and Hashemzadeh-Chaleshtori, Morteza. and Doosti, Abbas. and Amini Sarteshnizi, Neamatollah. and Gholami-Arjenaki, Mostafa. and Teimori, Hossein. (2014) Evaluation of the effect of Chrysin and Caffeic acid phenethyl ester on eIF4E expression in AGS cell line. Journal of HerbMed Pharmacology, 3.

Rezaeian, Fatemeh. and Tabatabaiefar, Mohammad Amin. and Heybati, Fatemeh. and Reiisi, Somayeh. and Parchami Barjui, Shahrbanoo. and Abolhasani, Marziyeh. and Amiri, Beheshteh. and Salehi Chaleshtori, Ahmad Reza. and Hashemzadeh-Chaleshtori, Morteza. (2014) Genetic linkage analysis of DFNB93 locus in a group of families with autosomal recessive non-syndromic hearing loss in Chahar Mahal & Bakhtiari and Kohkiluyeh & Boyer Ahmad provinces of Iran. Journal of Shahrekord Uuniversity of Medical Sciences, 16.

Kooshavar, Daniz. and Tabatabaiefar, Mohammad Amin. and Farrokhi, Effat. and Abolhasani, Marziyeh. and Noori-Daloii, Mohammad Reza. and Hashemzadeh-Chaleshtori, Morteza. (2013) Digenic inheritance in autosomal recessive non-syndromic hearing loss cases carrying GJB2 heterozygote mutations: Assessment of GJB4, GJA1, and GJC3. INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 77 (2). pp. 189-193.

Taghizadeh, Seyyed Hossein. and Kazeminezhad, Seyyed Reza and Sefidgar, Seyyed Ali and Yazdanpanahi, Nasrin. and Tabatabaeifar, Mohammad Amin. and Yousefi, Ahmad. and Lesani, Seyyed Mohammad. and Abolhasani, Marziyeh. and Hashemzadeh-Chaleshtori, Morteza. (2013) Investigation of LRTOMT gene (locus DFNB63) mutations in Iranian patients with autosomal recessive non-syndromic hearing loss. International journal of molecular and cellular medicine, 2 (1). pp. 41-5. ISSN 2251-9637

Heydari, Soraya. and Khaledifar, Arsalan. and Pourahmad-Jaktaji, Razieh. and Hashemzadeh-Chaleshtori, Morteza. and Heydari, Somayeh. and Bagheri, Nader. and Reisi, Somayeh and Abolhasani, Marziyeh. (2013) Investigation of mutations in exons 19-23 MYH7 gene in hypertrophic cardiomyopathy patients using PCR-SSCP/HA technique in Chaharmahal va Bakhtiari province. Journal of Shahrekord Uuniversity of Medical Sciences, 15.

Moazeni-Bistgani, Mohammad. and Taghipoor, Simin. and Abolhasani, Marziyeh. and Hashemzadeh-Chaleshtori, Morteza. and Zarean, Elham. and Yousofi Darani, Hossein. (2013) Molecular characterization of the human and sheep hydatid cyst strains in Chaharmahal va Bakhtiari province of Iran using restriction fragment length plolymorphism (PCR RFLP). Cell biology, 2 (2).

Taherzadeh Ghahfarrokhi, Maryam. and Farrokhi, Effat. and Shirmardi, Seyed Abolfath. and Safari Chaleshtori, Javad. and Asadi, Somayeh. and Ghatreh Samani, Keihan. and Abolhasani, Marziyeh. and Haji Hoseini, Reza. and Hashemzadeh-Chaleshtori, Morteza. and Parvin, Neda. and Raeisi, Marziye. and Mobini, Gholam Reza. and Banitalebi, Golandam. and Azadegan-Dehkordi, Fatemeh. and Reiisi, Somayeh. (2010) DFNB59 gene mutations screening in non syndromic deaf subjects in Chaharmahal va Bakhtiari province. Journal of Shahrekord Uuniversity of Medical Sciences, 11.

This list was generated on Thu Jun 21 01:04:04 2018 IRDT.