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Increasing the Targeting Scope of CRISPR Base Editing System Beyond NGG.
CRISPR J. 2022 Apr;5(2):187-202. doi: 10.1089/crispr.2021.0109. Epub 2022 Mar 2.
CRISPR J. 2022.
PMID: 35238621
Review.
CRISPR/Cas9 Editing: Sparking Discussion on Safety in Light of the Need for New Therapeutics.
Carlaw TM, Zhang LH, Ross CJD.
Carlaw TM, et al.
Hum Gene Ther. 2020 Aug;31(15-16):794-807. doi: 10.1089/hum.2020.111. Epub 2020 Jul 24.
Hum Gene Ther. 2020.
PMID: 32586150
Review.
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Systemic delivery of proteins using novel peptides via the sublingual route.
Wu J, Jones N, Hohenwarter L, Zhao F, Chan V, Tan Z, Carlaw T, Morin T, Li J, Kaur T, Andrew LJ, Ross CJD, Hedtrich S, Li SD.
Wu J, et al. Among authors: carlaw t.
J Control Release. 2024 Apr;368:290-302. doi: 10.1016/j.jconrel.2024.02.042. Epub 2024 Mar 4.
J Control Release. 2024.
PMID: 38423473
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A luciferase reporter mouse model to optimize in vivo gene editing validated by lipid nanoparticle delivery of adenine base editors.
Yu SY, Carlaw T, Thomson T, Birkenshaw A, Basha G, Kurek D, Huang C, Kulkarni J, Zhang LH, Ross CJD.
Yu SY, et al. Among authors: carlaw t.
Mol Ther. 2023 Apr 5;31(4):1159-1166. doi: 10.1016/j.ymthe.2023.02.009. Epub 2023 Feb 15.
Mol Ther. 2023.
PMID: 36793209
Free PMC article.
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