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Page 1
Recent Advances in CRISPR/Cas9 Delivery Approaches for Therapeutic Gene Editing of Stem Cells.
Stem Cell Rev Rep. 2023 Nov;19(8):2576-2596. doi: 10.1007/s12015-023-10585-3. Epub 2023 Sep 18.
Stem Cell Rev Rep. 2023.
PMID: 37723364
Free PMC article.
Review.
Investigating the association of Lamotrigine and Phenytoin-induced Stevens-Johnson syndrome/Toxic Epidermal Necrolysis with HLA-B*1502 in Iranian population.
Sabourirad S, Mortezaee R, Mojarad M, Eslahi A, Shahrokhi Y, Kiafar B, Jarahi L, Afkhami Ardakani S, Farrokhi S.
Sabourirad S, et al. Among authors: farrokhi s.
Exp Dermatol. 2021 Feb;30(2):284-287. doi: 10.1111/exd.14240. Epub 2020 Dec 4.
Exp Dermatol. 2021.
PMID: 33217035
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Production of Duchenne muscular dystrophy cellular model using CRISPR-Cas9 exon deletion strategy.
Alizadeh F, Abraghan YJ, Farrokhi S, Yousefi Y, Mirahmadi Y, Eslahi A, Mojarrad M.
Alizadeh F, et al. Among authors: farrokhi s.
Mol Cell Biochem. 2023 Jun 8. doi: 10.1007/s11010-023-04759-3. Online ahead of print.
Mol Cell Biochem. 2023.
PMID: 37289342
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TMEM263: a novel candidate gene implicated in human autosomal recessive severe lethal skeletal dysplasia.
Mohajeri MSA, Eslahi A, Khazaii Z, Moradi MR, Pazhoomand R, Farrokhi S, Feizabadi MH, Alizadeh F, Mojarrad M.
Mohajeri MSA, et al. Among authors: farrokhi s.
Hum Genomics. 2021 Jul 8;15(1):42. doi: 10.1186/s40246-021-00343-2.
Hum Genomics. 2021.
PMID: 34238371
Free PMC article.
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