Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
Iranian Journal of Basic Medical Sciences|April 18, 2022
G-CSF augments the neuroprotective effect of conditioned medium of dental pulp stem cells against hypoxic neural injury in SH-SY5Y cellsFarahnaz Ahmadi, Zahra Salmasi, Majid Mojarad, et al.
Molecular Biotechnology|October 21, 2024
Assessment the Efficacy of the CRISPR System for Inducing Mutations in the AIMP2 Gene to Create a Cell Line Model of HLD17 DiseaseShima Farrokhi, Atieh Eslahi, Farzaneh Alizadeh, et al.
Heliyon|December 6, 2024
An extensive in silico analysis of missense mutations of the human AIMP2 geneShima Farrokhi, Atieh Eslahi, Farzaneh Alizadeh, et al.
Biochemistry and Biophysics Reports|February 27, 2026
Enhancement of prime editing by recruiting engineered or evolved components and implementing novel strategiesMobina Arabi, Farzaneh Alizadeh, Yasamin Yousefi, et al.
Fetal and Pediatric Pathology|January 31, 2020
Investigation of MYO15A and MYO7A Mutations in Iranian Patients with Nonsyndromic Hearing LossMahsa Farjami, Mozhgan Fathi, Mohammad Mehdi Ghasemi, et al.
Molecular and Cellular Biochemistry|June 8, 2023
Production of Duchenne muscular dystrophy cellular model using CRISPR-Cas9 exon deletion strategyFarzaneh Alizadeh, Yousef Jafari Abraghan, Shima Farrokhi, et al.
Journal of Pediatric Gastroenterology and Nutrition|May 23, 2020
NR1H4-related Progressive Familial Intrahepatic Cholestasis 5: Further Evidence for Rapidly Progressive Liver FailureRyan W Himes, Majid Mojarrad, Atieh Eslahi, et al.
Gene|March 13, 2023
New advancements in CRISPR based gene therapy of Duchenne muscular dystrophyAtieh Eslahi, Farzaneh Alizadeh, Amir Avan, et al.
Iranian Journal of Basic Medical Sciences|August 11, 2020
The worldwide frequency of MYO15A gene mutations in patients with non-syndromic hearing loss: A meta-analysisMahsa Farjami, Reza Assadi, Fahimeh Afzal Javan, et al.
Pageof 3