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Human OPRM1 and murine Oprm1 promoter driven viral constructs for genetic access to μ-opioidergic cell types.
Salimando GJ, Tremblay S, Kimmey BA, Li J, Rogers SA, Wojick JA, McCall NM, Wooldridge LM, Rodrigues A, Borner T, Gardiner KL, Jayakar SS, Singeç I, Woolf CJ, Hayes MR, De Jonghe BC, Bennett FC, Bennett ML, Blendy JA, Platt ML, Creasy KT, Renthal WR, Ramakrishnan C, Deisseroth K, Corder G. Salimando GJ, et al. Among authors: gardiner kl. Nat Commun. 2023 Sep 13;14(1):5632. doi: 10.1038/s41467-023-41407-2. Nat Commun. 2023. PMID: 37704594 Free PMC article.
Neural signatures of natural behaviour in socializing macaques.
Testard C, Tremblay S, Parodi F, DiTullio RW, Acevedo-Ithier A, Gardiner KL, Kording K, Platt ML. Testard C, et al. Among authors: gardiner kl. Nature. 2024 Apr;628(8007):381-390. doi: 10.1038/s41586-024-07178-6. Epub 2024 Mar 13. Nature. 2024. PMID: 38480888
Hypercholesterolemia exacerbates in-stent restenosis in rabbits: Studies of the mitigating effect of stent surface modification with a CD47-derived peptide.
Fishbein I, Inamdar VV, Alferiev IS, Bratinov G, Zviman MM, Yekhilevsky A, Nagaswami C, Gardiner KL, Levy RJ, Stachelek SJ. Fishbein I, et al. Among authors: gardiner kl. Atherosclerosis. 2024 Mar;390:117432. doi: 10.1016/j.atherosclerosis.2023.117432. Epub 2023 Dec 24. Atherosclerosis. 2024. PMID: 38241977
Application of simultaneous selective pressures slows adaptation.
Merlo LMF, Sprouffske K, Howard TC, Gardiner KL, Caulin AF, Blum SM, Evans P, Bedalov A, Sniegowski PD, Maley CC. Merlo LMF, et al. Among authors: gardiner kl. Evol Appl. 2020 Aug 15;13(7):1615-1625. doi: 10.1111/eva.13062. eCollection 2020 Aug. Evol Appl. 2020. PMID: 32952608 Free PMC article.
Long-Term Structural Outcomes of Late-Stage RPE65 Gene Therapy.
Gardiner KL, Cideciyan AV, Swider M, Dufour VL, Sumaroka A, Komáromy AM, Hauswirth WW, Iwabe S, Jacobson SG, Beltran WA, Aguirre GD. Gardiner KL, et al. Mol Ther. 2020 Jan 8;28(1):266-278. doi: 10.1016/j.ymthe.2019.08.013. Epub 2019 Sep 3. Mol Ther. 2020. PMID: 31604676 Free PMC article.
Overlap of abnormal photoreceptor development and progressive degeneration in Leber congenital amaurosis caused by NPHP5 mutation.
Downs LM, Scott EM, Cideciyan AV, Iwabe S, Dufour V, Gardiner KL, Genini S, Marinho LF, Sumaroka A, Kosyk MS, Swider M, Aguirre GK, Jacobson SG, Beltran WA, Aguirre GD. Downs LM, et al. Among authors: gardiner kl. Hum Mol Genet. 2016 Oct 1;25(19):4211-4226. doi: 10.1093/hmg/ddw254. Epub 2016 Aug 9. Hum Mol Genet. 2016. PMID: 27506978 Free PMC article.
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