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Miniature type V-F CRISPR-Cas nucleases enable targeted DNA modification in cells.
Bigelyte G, Young JK, Karvelis T, Budre K, Zedaveinyte R, Djukanovic V, Van Ginkel E, Paulraj S, Gasior S, Jones S, Feigenbutz L, Clair GS, Barone P, Bohn J, Acharya A, Zastrow-Hayes G, Henkel-Heinecke S, Silanskas A, Seidel R, Siksnys V. Bigelyte G, et al. Among authors: jones s. Nat Commun. 2021 Oct 26;12(1):6191. doi: 10.1038/s41467-021-26469-4. Nat Commun. 2021. PMID: 34702830 Free PMC article.
Superior field performance of waxy corn engineered using CRISPR-Cas9.
Gao H, Gadlage MJ, Lafitte HR, Lenderts B, Yang M, Schroder M, Farrell J, Snopek K, Peterson D, Feigenbutz L, Jones S, St Clair G, Rahe M, Sanyour-Doyel N, Peng C, Wang L, Young JK, Beatty M, Dahlke B, Hazebroek J, Greene TW, Cigan AM, Chilcoat ND, Meeley RB. Gao H, et al. Among authors: jones s. Nat Biotechnol. 2020 May;38(5):579-581. doi: 10.1038/s41587-020-0444-0. Epub 2020 Mar 9. Nat Biotechnol. 2020. PMID: 32152597
Complex Trait Loci in Maize Enabled by CRISPR-Cas9 Mediated Gene Insertion.
Gao H, Mutti J, Young JK, Yang M, Schroder M, Lenderts B, Wang L, Peterson D, St Clair G, Jones S, Feigenbutz L, Marsh W, Zeng M, Wagner S, Farrell J, Snopek K, Scelonge C, Sopko X, Sander JD, Betts S, Cigan AM, Chilcoat ND. Gao H, et al. Among authors: jones s. Front Plant Sci. 2020 May 5;11:535. doi: 10.3389/fpls.2020.00535. eCollection 2020. Front Plant Sci. 2020. PMID: 32431725 Free PMC article.
Heritable targeted mutagenesis in maize using a designed endonuclease.
Gao H, Smith J, Yang M, Jones S, Djukanovic V, Nicholson MG, West A, Bidney D, Falco SC, Jantz D, Lyznik LA. Gao H, et al. Among authors: jones s. Plant J. 2010 Jan;61(1):176-87. doi: 10.1111/j.1365-313X.2009.04041.x. Epub 2009 Oct 7. Plant J. 2010. PMID: 19811621 Free article.
The European reference network for metabolic diseases (MetabERN) clinical pathway recommendations for Pompe disease (acid maltase deficiency, glycogen storage disease type II).
Parenti G, Fecarotta S, Alagia M, Attaianese F, Verde A, Tarallo A, Gragnaniello V, Ziagaki A, Guimaraes MJ, Aguiar P, Hahn A, Azevedo O, Donati MA, Kiec-Wilk B, Scarpa M, van der Beek NAME, Del Toro Riera M, Germain DP, Huidekoper H, van den Hout JMP, van der Ploeg AT; and the MetabERN Subnetwork for Lysosomal Disorders. Parenti G, et al. Orphanet J Rare Dis. 2024 Nov 1;19(1):408. doi: 10.1186/s13023-024-03373-w. Orphanet J Rare Dis. 2024. PMID: 39482698 Review.
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