Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies in a consanguineous Iranian family is associated with a homozygous start loss variant in the...

por Gholizadeh, Mehdi Agha, Mohammadi-Sarband, Mina, Fardanesh, Fatemeh, Garshasbi, Masoud
Publicado 2022

Identification of hub genes associated with RNAi-induced silencing of XIAP through targeted proteomics approach in MCF7 cells

por Gholizadeh, Mehdi Agha, Shamsabadi, Fatemeh T., Yamchi, Ahad, Golalipour, Masoud, Jhingan, Gagan Deep, Shahbazi, Majid
Publicado 2020