Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Malihe Alimardani"'
Autor:
Mahsa Farjami, Reza Asadi, Fahimeh Afzal Javan, Malihe Alimardani, Saeed Eslami, Sima Mansoori Derakhshan, Atieh Eslahi, Majid Mojarad
Publikováno v:
Iranian Journal of Basic Medical Sciences, Vol 23, Iss 7, Pp 841-848 (2020)
MYO15A is the third most crucial gene in hereditary sensorineural hearing loss after GJB2 and SLC26A4. In the present study, we reviewed the prevalence of MYO15A mutations in patients with autosomal recessive non-syndromic hearing loss (ARNSHL). In t
Externí odkaz:
https://doaj.org/article/665f9fff3cc149f6b00d08af0fc5219e
Autor:
Mohsen Rajati, Mahsa Farjami, Malihe Alimardani, Mozhgan Fathi, Mohammad Mehdi Ghasemi, Majid Mojarrad, Atieh Eslahi
Publikováno v:
Fetal and pediatric pathology. 40(2)
Hearing loss (HL) is the most common sensory disorder in humans, which affects individuals in both inherited and acquired forms. MYO15A and MYO7A gene mutations have a significant role in the development of deafness. In this study, we assessed the pr
Autor:
Arezoo Gowhari Shabgah, Saeed Aslani, Amirhossein Sahebkar, Malihe Alimardani, Alireza Pasdar, Arash Salmaninejad, Saeed Farajzadeh Valilou
Publikováno v:
Journal of cellular physiology. 234(10)
Over the course of past few years, cancer immunotherapy has been accompanied with promising results. However, preliminary investigations with respect to immunotherapy concentrated mostly on targeting the immune checkpoints, nowadays, emerge as the mo
Autor:
Farjami, Mahsa, Assadi, Reza, Javan, Fahimeh Afzal, Mansoori Derakhshan, Malihe Alimardani Sima, Eslahi, Atieh, Mojarrad, Majid
Publikováno v:
Iranian Journal of Basic Medical Sciences; Jul2020, Vol. 23 Issue 7, p841-848, 8p