Prevalence of the UGT1A1*6 (c.211G>A) polymorphism and irinotecan toxicity in Iranian populations of different ethnicities

par Shakibi, Reyhaneh, Kamalidehghan, Behnam, Ahmadipour, Fatemeh, Meng, Goh Yong, Houshmand, Massoud
Publié 2015

Gene expression profiling of mitochondrial oxidative phosphorylation (OXPHOS) complex I in Friedreich ataxia (FRDA) patients

par Salehi, Mohammad Hossein, Kamalidehghan, Behnam, Houshmand, Massoud, Goh, Yong Meng, Sadeghizadeh, Majid, Aryani, Omid, Nafissi, Shahriar
Publié 2014

Prevalence of the rs7903146C>T polymorphism in TCF7L2 gene for prediction of type 2 diabetes risk among Iranians of different ethnicities

par Allahdini, Mojgan, Kamalidehghan, Behnam, Akbari, Leila, Azadfar, Parisa, Rahmani, Ali, Ahmadipour, Fatemeh, Goh, Yong Meng, Masserrat, Abbas, Houshmand, Massoud
Publié 2015

Four novel ARSA gene mutations with pathogenic impacts on metachromatic leukodystrophy: a bioinformatics approach to predict pathogenic mutations

par Manshadi, Masoumeh Dehghan, Kamalidehghan, Behnam, Aryani, Omid, Khalili, Elham, Dadgar, Sepideh, Tondar, Mahdi, Ahmadipour, Fatemeh, Goh, Yong Meng, Houshmand, Massoud
Publié 2017

Prevalence of the CYP2D6*10 (C100T), *4 (G1846A), and *14 (G1758A) alleles among Iranians of different ethnicities

par Bagheri, Ali, Kamalidehghan, Behnam, Haghshenas, Maryam, Azadfar, Parisa, Akbari, Leila, Sangtarash, Mohammad Hossein, Vejdandoust, Faramarz, Ahmadipour, Fatemeh, Meng, Goh Yong, Houshmand, Massoud
Publié 2015

Association of nuclear and mitochondrial genes with audiological examinations in Iranian patients with nonaminoglycoside antibiotics-induced hearing loss

par Balali, Maryam, Kamalidehghan, Behnam, Farhadi, Mohammad, Ahmadipour, Fatemeh, Ashkezari, Mahmoud Dehghani, Hemami, Mohsen Rezaei, Arabzadeh, Hossein, Falah, Masoumeh, Goh, Yong Meng, Houshmand, Massoud
Publié 2016