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Photochemical activation of TRPA1 channels in neurons and animals.
Kokel D, Cheung CY, Mills R, Coutinho-Budd J, Huang L, Setola V, Sprague J, Jin S, Jin YN, Huang XP, Bruni G, Woolf CJ, Roth BL, Hamblin MR, Zylka MJ, Milan DJ, Peterson RT. Kokel D, et al. Among authors: mills r. Nat Chem Biol. 2013 Apr;9(4):257-63. doi: 10.1038/nchembio.1183. Epub 2013 Feb 10. Nat Chem Biol. 2013. PMID: 23396078 Free PMC article.
Overexpression of KCNN3 results in sudden cardiac death.
Mahida S, Mills RW, Tucker NR, Simonson B, Macri V, Lemoine MD, Das S, Milan DJ, Ellinor PT. Mahida S, et al. Among authors: mills rw. Cardiovasc Res. 2014 Feb 1;101(2):326-34. doi: 10.1093/cvr/cvt269. Epub 2013 Dec 1. Cardiovasc Res. 2014. PMID: 24296650 Free PMC article.
Bioengineering Human Myocardium on Native Extracellular Matrix.
Guyette JP, Charest JM, Mills RW, Jank BJ, Moser PT, Gilpin SE, Gershlak JR, Okamoto T, Gonzalez G, Milan DJ, Gaudette GR, Ott HC. Guyette JP, et al. Among authors: mills rw. Circ Res. 2016 Jan 8;118(1):56-72. doi: 10.1161/CIRCRESAHA.115.306874. Epub 2015 Oct 26. Circ Res. 2016. PMID: 26503464 Free PMC article.
Discovery and validation of sub-threshold genome-wide association study loci using epigenomic signatures.
Wang X, Tucker NR, Rizki G, Mills R, Krijger PH, de Wit E, Subramanian V, Bartell E, Nguyen XX, Ye J, Leyton-Mange J, Dolmatova EV, van der Harst P, de Laat W, Ellinor PT, Newton-Cheh C, Milan DJ, Kellis M, Boyer LA. Wang X, et al. Among authors: mills r. Elife. 2016 May 10;5:e10557. doi: 10.7554/eLife.10557. Elife. 2016. PMID: 27162171 Free PMC article.
Diminished PRRX1 Expression Is Associated With Increased Risk of Atrial Fibrillation and Shortening of the Cardiac Action Potential.
Tucker NR, Dolmatova EV, Lin H, Cooper RR, Ye J, Hucker WJ, Jameson HS, Parsons VA, Weng LC, Mills RW, Sinner MF, Imakaev M, Leyton-Mange J, Vlahakes G, Benjamin EJ, Lunetta KL, Lubitz SA, Mirny L, Milan DJ, Ellinor PT. Tucker NR, et al. Among authors: mills rw. Circ Cardiovasc Genet. 2017 Oct;10(5):e001902. doi: 10.1161/CIRCGENETICS.117.001902. Circ Cardiovasc Genet. 2017. PMID: 28974514 Free PMC article.
Novel Mutation in FLNC (Filamin C) Causes Familial Restrictive Cardiomyopathy.
Tucker NR, McLellan MA, Hu D, Ye J, Parsons VA, Mills RW, Clauss S, Dolmatova E, Shea MA, Milan DJ, Scott NS, Lindsay M, Lubitz SA, Domian IJ, Stone JR, Lin H, Ellinor PT. Tucker NR, et al. Among authors: mills rw. Circ Cardiovasc Genet. 2017 Dec;10(6):e001780. doi: 10.1161/CIRCGENETICS.117.001780. Circ Cardiovasc Genet. 2017. PMID: 29212899 Free PMC article.
1,482 results