Redwood CS - Search Results

1

Familial dilated cardiomyopathy caused by an alpha-tropomyosin mutation: the distinctive natural history of sarcomeric dilated cardiomyopathy.

Lakdawala NK, Dellefave L, Redwood CS, Sparks E, Cirino AL, Depalma S, Colan SD, Funke B, Zimmerman RS, Robinson P, Watkins H, Seidman CE, Seidman JG, McNally EM, Ho CY. Lakdawala NK, et al. Among authors: redwood cs. J Am Coll Cardiol. 2010 Jan 26;55(4):320-9. doi: 10.1016/j.jacc.2009.11.017. J Am Coll Cardiol. 2010. PMID: 20117437 Free PMC article.

2

Effects of two hypertrophic cardiomyopathy mutations in alpha-tropomyosin, Asp175Asn and Glu180Gly, on Ca2+ regulation of thin filament motility.

Bing W, Redwood CS, Purcell IF, Esposito G, Watkins H, Marston SB. Bing W, et al. Among authors: redwood cs. Biochem Biophys Res Commun. 1997 Jul 30;236(3):760-4. doi: 10.1006/bbrc.1997.7045. Biochem Biophys Res Commun. 1997. PMID: 9245729

3

A mutant tropomyosin that causes hypertrophic cardiomyopathy is expressed in vivo and associated with an increased calcium sensitivity.

Bottinelli R, Coviello DA, Redwood CS, Pellegrino MA, Maron BJ, Spirito P, Watkins H, Reggiani C. Bottinelli R, et al. Among authors: redwood cs. Circ Res. 1998 Jan 9-23;82(1):106-15. doi: 10.1161/01.res.82.1.106. Circ Res. 1998. PMID: 9440709

4

Properties of mutant contractile proteins that cause hypertrophic cardiomyopathy.

Redwood CS, Moolman-Smook JC, Watkins H. Redwood CS, et al. Cardiovasc Res. 1999 Oct;44(1):20-36. doi: 10.1016/s0008-6363(99)00213-8. Cardiovasc Res. 1999. PMID: 10615387 Review.

5

Altered regulatory properties of human cardiac troponin I mutants that cause hypertrophic cardiomyopathy.

Elliott K, Watkins H, Redwood CS. Elliott K, et al. Among authors: redwood cs. J Biol Chem. 2000 Jul 21;275(29):22069-74. doi: 10.1074/jbc.M002502200. J Biol Chem. 2000. PMID: 10806205 Free article.

6

Investigation of a truncated cardiac troponin T that causes familial hypertrophic cardiomyopathy: Ca(2+) regulatory properties of reconstituted thin filaments depend on the ratio of mutant to wild-type protein.

Redwood C, Lohmann K, Bing W, Esposito GM, Elliott K, Abdulrazzak H, Knott A, Purcell I, Marston S, Watkins H. Redwood C, et al. Circ Res. 2000 Jun 9;86(11):1146-52. doi: 10.1161/01.res.86.11.1146. Circ Res. 2000. PMID: 10850966

7

Effect of hypertrophic cardiomyopathy mutations in human cardiac muscle alpha -tropomyosin (Asp175Asn and Glu180Gly) on the regulatory properties of human cardiac troponin determined by in vitro motility assay.

Bing W, Knott A, Redwood C, Esposito G, Purcell I, Watkins H, Marston S. Bing W, et al. J Mol Cell Cardiol. 2000 Aug;32(8):1489-98. doi: 10.1006/jmcc.2000.1182. J Mol Cell Cardiol. 2000. PMID: 10900175

8

Mutations in the gamma(2) subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis.

Blair E, Redwood C, Ashrafian H, Oliveira M, Broxholme J, Kerr B, Salmon A, Ostman-Smith I, Watkins H. Blair E, et al. Hum Mol Genet. 2001 May 15;10(11):1215-20. doi: 10.1093/hmg/10.11.1215. Hum Mol Genet. 2001. PMID: 11371514

9

Two mutations in troponin I that cause hypertrophic cardiomyopathy have contrasting effects on cardiac muscle contractility.

Burton D, Abdulrazzak H, Knott A, Elliott K, Redwood C, Watkins H, Marston S, Ashley C. Burton D, et al. Biochem J. 2002 Mar 1;362(Pt 2):443-51. doi: 10.1042/0264-6021:3620443. Biochem J. 2002. PMID: 11853553 Free PMC article.

10

Mutations of the light meromyosin domain of the beta-myosin heavy chain rod in hypertrophic cardiomyopathy.

Blair E, Redwood C, de Jesus Oliveira M, Moolman-Smook JC, Brink P, Corfield VA, Ostman-Smith I, Watkins H. Blair E, et al. Circ Res. 2002 Feb 22;90(3):263-9. doi: 10.1161/hh0302.104532. Circ Res. 2002. PMID: 11861413

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