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Gholizad-Kolveiri, S. and Hooman, N. and Alizadeh, R. and Hoseini, R. and Otukesh, H. and Talebi, S. and Akouchekian, M. (2020) Whole exome sequencing revealed a novel homozygous variant in the DGKE catalytic domain: A case report of familial hemolytic uremic syndrome. BMC Medical Genetics, 21 (1).
Beiranvandi, F. and Akouchekian, M. and Javadi, G.R. and Darvish, H. (2020) The association of CNTNAP2 rs2710102 and ENGRAILED-2 rs1861972 genes polymorphism and autism in Iranian population. Meta Gene, 24.
Abghari, F.Z. and Moradi, Y. and Akouchekian, M. (2019) PTEN gene mutations in patients with macrocephaly and classic autism: A systematic review. Medical Journal of the Islamic Republic of Iran, 33 (1). pp. 52-59.
Akouchekian, M. and Hakim Shooshtari, M. and Heidary, H. and Zahedi Abghari, F. and Moeinian, P. (2019) The causative variants of amyloidosis in the autism. International Journal of Neuroscience, 129 (1). pp. 10-15.
Mehrgou, A. and Akouchekian, M. (2017) Therapeutic impacts of microRNAs in breast cancer by their roles in regulating processes involved in this disease. Journal of Research in Medical Sciences, 22 (12).
Akouchekian, M. and Hemati, S. and Jafari, D. and Jalilian, N. and Manshadi, M.D. (2016) Does PTEN gene mutation play any role in Li-Fraumeni syndrome? Medical Journal of the Islamic Republic of Iran, 30 (1).
Mehrgou, A. and Akouchekian, M. (2016) The importance of BRCA1 and BRCA2 genes mutations in breast cancer development. Medical Journal of the Islamic Republic of Iran, 30 (1).
Akouchekian, M. and Hemati, S. and Kachoei, Z.A. (2015) Analysis of PTEN in two BRCA1 and BRCA2 wild-type familial breast cancer patients. Journal of Research in Medical Sciences, 20 (6). pp. 629-630.
Akouchekian, M. and Houshmand, M. and Akbari, M.H.H. and Kamalidehghand, B. and Dehghane, M. (2011) Analysis of mitochondrial ND1 gene in human colorectal cancer. Journal of Research in Medical Sciences, 16 (1). pp. 50-55.
