Items where Author is "Arefian, E."

Jamalkhah, M. and Asaadi, Y. and Azangou-Khyavy, M. and Khanali, J. and Soleimani, M. and Kiani, J. and Arefian, E. (2021) MSC-derived exosomes carrying a cocktail of exogenous interfering RNAs an unprecedented therapy in era of COVID-19 outbreak. Journal of Translational Medicine, 19 (1).

Honardoost, M. and Keramati, F. and Arefian, E. and Mohammadi Yeganeh, S. and Soleimani, M. (2019) Network of three specific microRNAs influence type 2 diabetes through inducing insulin resistance in muscle cell lines. Journal of Cellular Biochemistry, 120 (2). pp. 1532-1538.

Nejati, A. and Shahmahmoodi, S. and Arefian, E. and Shoja, Z. and Marashi, S.-M. and Tabatabaie, H. and Mollaei-Kandelous, Y. and Soleimani, M. and Nategh, R. (2016) Efficient inhibition of human immunodeficiency virus replication using novel modified microRNA-30a targeting 3'-untranslated region transcripts. Experimental and Therapeutic Medicine, 11 (5). pp. 1833-1838.

Jaberi, E. and Rohani, M. and Shahidi, G.A. and Nafissi, S. and Arefian, E. and Soleimani, M. and Rasooli, P. and Ahmadieh, H. and Daftarian, N. and KaramiNejadRanjbar, M. and Klotzle, B. and Fan, J.-B. and Turk, C. and Steemers, F. and Elahi, E. (2016) Identification of mutation in GTPBP2 in patients of a family with neurodegeneration accompanied by iron deposition in the brain. Neurobiology of Aging, 38. 216.e11-216.e18.

Jaberi, E. and Rohani, M. and Shahidi, G.A. and Nafissi, S. and Arefian, E. and Soleimani, M. and Moghadam, A. and Arzenani, M.K. and Keramatian, F. and Klotzle, B. and Fan, J.-B. and Turk, C. and Steemers, F. and Elahi, E. (2016) Mutation in ADORA1 identified as likely cause of early-onset parkinsonism and cognitive dysfunction. Movement Disorders, 31 (7). pp. 1004-1011.

Jaberi, E. and Rohani, M. and Shahidi, G.A. and Nafissi, S. and Arefian, E. and Soleimani, M. and Rasooli, P. and Ahmadieh, H. and Daftarian, N. and KaramiNejadRanjbar, M. and Klotzle, B. and Fan, J.-B. and Turk, C. and Steemers, F. and Elahi, E. (2015) Identification of mutation in GTPBP2 in patients of a family with neurodegeneration accompanied by iron deposition in the brain. Neurobiology of Aging, 38. 216.e11-216.e18.

Aghaee-Bakhtiari, S.H. and Arefian, E. and Naderi, M. and Noorbakhsh, F. and Nodouzi, V. and Asgari, M. and Fard-Esfahani, P. and Mahdian, R. and Soleimani, M. (2015) MAPK and JAK/STAT pathways targeted by miR-23a and miR-23b in prostate cancer: computational and in vitro approaches. Tumor Biology, 36 (6). pp. 4203-4212.