Search Results - Houshmand, Massoud
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Gene expression profiling of mitochondrial oxidative phosphorylation (OXPHOS) complex I in Friedreich ataxia (FRDA) patients by Salehi, Mohammad Hossein, Kamalidehghan, Behnam, Houshmand, Massoud, Goh, Yong Meng, Sadeghizadeh, Majid, Aryani, Omid, Nafissi, Shahriar
Published 2014Get full text
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Prevalence of the rs7903146C>T polymorphism in TCF7L2 gene for prediction of type 2 diabetes risk among Iranians of different ethnicities by Allahdini, Mojgan, Kamalidehghan, Behnam, Akbari, Leila, Azadfar, Parisa, Rahmani, Ali, Ahmadipour, Fatemeh, Goh, Yong Meng, Masserrat, Abbas, Houshmand, Massoud
Published 2015Get full text
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Four novel ARSA gene mutations with pathogenic impacts on metachromatic leukodystrophy: a bioinformatics approach to predict pathogenic mutations by Manshadi, Masoumeh Dehghan, Kamalidehghan, Behnam, Aryani, Omid, Khalili, Elham, Dadgar, Sepideh, Tondar, Mahdi, Ahmadipour, Fatemeh, Goh, Yong Meng, Houshmand, Massoud
Published 2017Get full text
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Prevalence of the CYP2D6*10 (C100T), *4 (G1846A), and *14 (G1758A) alleles among Iranians of different ethnicities by Bagheri, Ali, Kamalidehghan, Behnam, Haghshenas, Maryam, Azadfar, Parisa, Akbari, Leila, Sangtarash, Mohammad Hossein, Vejdandoust, Faramarz, Ahmadipour, Fatemeh, Meng, Goh Yong, Houshmand, Massoud
Published 2015Get full text
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Association of nuclear and mitochondrial genes with audiological examinations in Iranian patients with nonaminoglycoside antibiotics-induced hearing loss by Balali, Maryam, Kamalidehghan, Behnam, Farhadi, Mohammad, Ahmadipour, Fatemeh, Ashkezari, Mahmoud Dehghani, Hemami, Mohsen Rezaei, Arabzadeh, Hossein, Falah, Masoumeh, Goh, Yong Meng, Houshmand, Massoud
Published 2016Get full text
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