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Troponin phosphorylation and regulatory function in human heart muscle: dephosphorylation of Ser23/24 on troponin I could account for the contractile defect in end-stage heart failure.
Messer AE, Jacques AM, Marston SB. Messer AE, et al. J Mol Cell Cardiol. 2007 Jan;42(1):247-59. doi: 10.1016/j.yjmcc.2006.08.017. Epub 2006 Nov 1. J Mol Cell Cardiol. 2007. PMID: 17081561
Temperature-sensitive sarcomeric protein post-translational modifications revealed by top-down proteomics.
Cai W, Hite ZL, Lyu B, Wu Z, Lin Z, Gregorich ZR, Messer AE, McIlwain SJ, Marston SB, Kohmoto T, Ge Y. Cai W, et al. Among authors: messer ae. J Mol Cell Cardiol. 2018 Sep;122:11-22. doi: 10.1016/j.yjmcc.2018.07.247. Epub 2018 Jul 23. J Mol Cell Cardiol. 2018. PMID: 30048711 Free PMC article.
Investigation of changes in skeletal muscle alpha-actin expression in normal and pathological human and mouse hearts.
Copeland O, Nowak KJ, Laing NG, Ravenscroft G, Messer AE, Bayliss CR, Marston SB. Copeland O, et al. J Muscle Res Cell Motil. 2010 Sep;31(3):207-14. doi: 10.1007/s10974-010-9224-7. Epub 2010 Aug 13. J Muscle Res Cell Motil. 2010. PMID: 20706863
Z-band alternatively spliced PDZ motif protein (ZASP) is the major O-linked β-N-acetylglucosamine-substituted protein in human heart myofibrils.
Leung MC, Hitchen PG, Ward DG, Messer AE, Marston SB. Leung MC, et al. J Biol Chem. 2013 Feb 15;288(7):4891-8. doi: 10.1074/jbc.M112.410316. Epub 2012 Dec 27. J Biol Chem. 2013. PMID: 23271734 Free PMC article.
Familial dilated cardiomyopathy mutations uncouple troponin I phosphorylation from changes in myofibrillar Ca²⁺ sensitivity.
Memo M, Leung MC, Ward DG, dos Remedios C, Morimoto S, Zhang L, Ravenscroft G, McNamara E, Nowak KJ, Marston SB, Messer AE. Memo M, et al. Cardiovasc Res. 2013 Jul 1;99(1):65-73. doi: 10.1093/cvr/cvt071. Epub 2013 Mar 27. Cardiovasc Res. 2013. PMID: 23539503
Abnormal contractility in human heart myofibrils from patients with dilated cardiomyopathy due to mutations in TTN and contractile protein genes.
Vikhorev PG, Smoktunowicz N, Munster AB, Copeland O, Kostin S, Montgiraud C, Messer AE, Toliat MR, Li A, Dos Remedios CG, Lal S, Blair CA, Campbell KS, Guglin M, Richter M, Knöll R, Marston SB. Vikhorev PG, et al. Among authors: messer ae. Sci Rep. 2017 Nov 1;7(1):14829. doi: 10.1038/s41598-017-13675-8. Sci Rep. 2017. PMID: 29093449 Free PMC article.
Mutations in troponin T associated with Hypertrophic Cardiomyopathy increase Ca(2+)-sensitivity and suppress the modulation of Ca(2+)-sensitivity by troponin I phosphorylation.
Messer AE, Bayliss CR, El-Mezgueldi M, Redwood CS, Ward DG, Leung MC, Papadaki M, Dos Remedios C, Marston SB. Messer AE, et al. Arch Biochem Biophys. 2016 Jul 1;601:113-20. doi: 10.1016/ Epub 2016 Mar 29. Arch Biochem Biophys. 2016. PMID: 27036851 Free PMC article.
Uncoupling of myofilament Ca2+ sensitivity from troponin I phosphorylation by mutations can be reversed by epigallocatechin-3-gallate.
Papadaki M, Vikhorev PG, Marston SB, Messer AE. Papadaki M, et al. Among authors: messer ae. Cardiovasc Res. 2015 Oct 1;108(1):99-110. doi: 10.1093/cvr/cvv181. Epub 2015 Jun 24. Cardiovasc Res. 2015. PMID: 26109583 Free PMC article.
The dilated cardiomyopathy-causing mutation ACTC E361G in cardiac muscle myofibrils specifically abolishes modulation of Ca(2+) regulation by phosphorylation of troponin I.
Vikhorev PG, Song W, Wilkinson R, Copeland O, Messer AE, Ferenczi MA, Marston SB. Vikhorev PG, et al. Biophys J. 2014 Nov 18;107(10):2369-80. doi: 10.1016/j.bpj.2014.10.024. Biophys J. 2014. PMID: 25418306 Free PMC article.
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