A case report of congenital myasthenic syndrome caused by a mutation in theCHRNE genein the Iranian population

por FARJAMI, Zahra, KHODAENIA, Negar, EBRAHIMI, Neshat, ZAMANI, Gholamreza, ASHNAEI, Amir Hosein, GALEHDARI, Mohammad, MORADYAR, Mehdi, HOUSHMAND, Massoud
Publicado 2020

Novel Homozygous Pathogenic Mutations of LAMA 2 Gene in Patients with Congen ital Muscular Dystrophy

por KHODAENIA, Negar, FARJAMI, Zahra, ASHNAEI, Amir Hosein, EBRAHIMI, Neshat, CHELVARFOROOSH, Navid, URTIZBEREA, Andoni, RAZMARA, Ehsan, HOUSHMAND, Massoud
Publicado 2021

Construction of a sensitive and specific lead biosensor using a genetically engineered bacterial system with a luciferase gene reporter controlled by pbr and cadA promoters

por Nourmohammadi, Esmail, Hosseinkhani, Saman, Nedaeinia, Reza, Khoshdel-Sarkarizi, Hoda, Nedaeinia, Mozhdeh, Ranjbar, Maryam, Ebrahimi, Neshat, Farjami, Zahra, Nourmohammadi, Mohammad, Mahmoudi, Ali, Goli, Mohammad, Ferns, Gordon A., Sadeghizadeh, Majid
Publicado 2020