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Contractile dysfunction irrespective of the mutant protein in human hypertrophic cardiomyopathy with normal systolic function.
van Dijk SJ, Paalberends ER, Najafi A, Michels M, Sadayappan S, Carrier L, Boontje NM, Kuster DW, van Slegtenhorst M, Dooijes D, dos Remedios C, ten Cate FJ, Stienen GJ, van der Velden J. van Dijk SJ, et al. Among authors: van slegtenhorst m, van der velden j. Circ Heart Fail. 2012 Jan;5(1):36-46. doi: 10.1161/CIRCHEARTFAILURE.111.963702. Epub 2011 Dec 16. Circ Heart Fail. 2012. PMID: 22178992 Free article.
Sarcomeric dysfunction in heart failure.
Hamdani N, Kooij V, van Dijk S, Merkus D, Paulus WJ, Remedios CD, Duncker DJ, Stienen GJ, van der Velden J. Hamdani N, et al. Cardiovasc Res. 2008 Mar 1;77(4):649-58. doi: 10.1093/cvr/cvm079. Epub 2007 Nov 30. Cardiovasc Res. 2008. PMID: 18055579 Review.
Myofilament dysfunction in cardiac disease from mice to men.
Hamdani N, de Waard M, Messer AE, Boontje NM, Kooij V, van Dijk S, Versteilen A, Lamberts R, Merkus D, Dos Remedios C, Duncker DJ, Borbely A, Papp Z, Paulus W, Stienen GJ, Marston SB, van der Velden J. Hamdani N, et al. J Muscle Res Cell Motil. 2008;29(6-8):189-201. doi: 10.1007/s10974-008-9160-y. Epub 2009 Jan 13. J Muscle Res Cell Motil. 2008. PMID: 19140019 Review.
Myocardial adaptations in the failing heart: cause or consequence?
van Dijk SJ, Hamdani N, Stienen GJ, van der Velden J. van Dijk SJ, et al. Among authors: van der velden j. J Muscle Res Cell Motil. 2008;29(6-8):159-62. doi: 10.1007/s10974-009-9169-x. Epub 2009 Feb 14. J Muscle Res Cell Motil. 2008. PMID: 19219554 Review.
Cardiac myosin-binding protein C mutations and hypertrophic cardiomyopathy: haploinsufficiency, deranged phosphorylation, and cardiomyocyte dysfunction.
van Dijk SJ, Dooijes D, dos Remedios C, Michels M, Lamers JM, Winegrad S, Schlossarek S, Carrier L, ten Cate FJ, Stienen GJ, van der Velden J. van Dijk SJ, et al. Among authors: van der velden j. Circulation. 2009 Mar 24;119(11):1473-83. doi: 10.1161/CIRCULATIONAHA.108.838672. Epub 2009 Mar 9. Circulation. 2009. PMID: 19273718
The development of familial hypertrophic cardiomyopathy: from mutation to bedside.
Brouwer WP, van Dijk SJ, Stienen GJ, van Rossum AC, van der Velden J, Germans T. Brouwer WP, et al. Among authors: van rossum ac, van dijk sj, van der velden j. Eur J Clin Invest. 2011 May;41(5):568-78. doi: 10.1111/j.1365-2362.2010.02439.x. Epub 2010 Dec 15. Eur J Clin Invest. 2011. PMID: 21158848 Review.
Mutations in MYH7 reduce the force generating capacity of sarcomeres in human familial hypertrophic cardiomyopathy.
Witjas-Paalberends ER, Piroddi N, Stam K, van Dijk SJ, Oliviera VS, Ferrara C, Scellini B, Hazebroek M, ten Cate FJ, van Slegtenhorst M, dos Remedios C, Niessen HW, Tesi C, Stienen GJ, Heymans S, Michels M, Poggesi C, van der Velden J. Witjas-Paalberends ER, et al. Among authors: van dijk sj, van slegtenhorst m, van der velden j. Cardiovasc Res. 2013 Aug 1;99(3):432-41. doi: 10.1093/cvr/cvt119. Epub 2013 May 13. Cardiovasc Res. 2013. PMID: 23674513
The Sydney Heart Bank: improving translational research while eliminating or reducing the use of animal models of human heart disease.
Dos Remedios CG, Lal SP, Li A, McNamara J, Keogh A, Macdonald PS, Cooke R, Ehler E, Knöll R, Marston SB, Stelzer J, Granzier H, Bezzina C, van Dijk S, De Man F, Stienen GJM, Odeberg J, Pontén F, Linke WA, Linke W, van der Velden J. Dos Remedios CG, et al. Biophys Rev. 2017 Aug;9(4):431-441. doi: 10.1007/s12551-017-0305-3. Epub 2017 Aug 14. Biophys Rev. 2017. PMID: 28808947 Free PMC article. Review.
40 results