Blair E - Search Results

1

Identification and functional characterization of cardiac troponin I as a novel disease gene in autosomal dominant dilated cardiomyopathy.

Carballo S, Robinson P, Otway R, Fatkin D, Jongbloed JD, de Jonge N, Blair E, van Tintelen JP, Redwood C, Watkins H. Carballo S, et al. Among authors: blair e. Circ Res. 2009 Aug 14;105(4):375-82. doi: 10.1161/CIRCRESAHA.109.196055. Epub 2009 Jul 9. Circ Res. 2009. PMID: 19590045

2

The inheritance of hypertrophic cardiomyopathy.

Burch M, Blair E. Burch M, et al. Among authors: blair e. Pediatr Cardiol. 1999 Sep-Oct;20(5):313-6. doi: 10.1007/s002469900475. Pediatr Cardiol. 1999. PMID: 10441682 Review.

3

Dilated cardiomyopathy and the desmin gene.

Mayosi B, Blair E, Watkins H. Mayosi B, et al. Among authors: blair e. Circulation. 2000 Sep 26;102(13):E100-1. doi: 10.1161/01.cir.102.13.e100. Circulation. 2000. PMID: 11004158 No abstract available.

4

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

5

Mutations in cis can confound genotype-phenotype correlations in hypertrophic cardiomyopathy.

Blair E, Price SJ, Baty CJ, Ostman-Smith I, Watkins H. Blair E, et al. J Med Genet. 2001 Jun;38(6):385-8. doi: 10.1136/jmg.38.6.385. J Med Genet. 2001. PMID: 11424919 Free PMC article. No abstract available.

6

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

7

Hypertrophic cardiomyopathy:a paradigm for myocardial energy depletion.

Ashrafian H, Redwood C, Blair E, Watkins H. Ashrafian H, et al. Among authors: blair e. Trends Genet. 2003 May;19(5):263-8. doi: 10.1016/S0168-9525(03)00081-7. Trends Genet. 2003. PMID: 12711218 Review.

8

Hypertrophic cardiomyopathy due to sarcomeric gene mutations is characterized by impaired energy metabolism irrespective of the degree of hypertrophy.

Crilley JG, Boehm EA, Blair E, Rajagopalan B, Blamire AM, Styles P, McKenna WJ, Ostman-Smith I, Clarke K, Watkins H. Crilley JG, et al. Among authors: blair e. J Am Coll Cardiol. 2003 May 21;41(10):1776-82. doi: 10.1016/s0735-1097(02)03009-7. J Am Coll Cardiol. 2003. PMID: 12767664 Free article.

9

Ascertainment strategies and genotype:phenotype correlations in hypertrophic cardiomyopathy.

Blair E, Redwood C, Watkins H. Blair E, et al. Circulation. 2003 Jul 29;108(4):e24-5; author reply e24-5. doi: 10.1161/01.CIR.0000081440.49766.A6. Circulation. 2003. PMID: 12885737 No abstract available.

10

Mutation analysis of AMP-activated protein kinase subunits in inherited cardiomyopathies: implications for kinase function and disease pathogenesis.

Oliveira SM, Ehtisham J, Redwood CS, Ostman-Smith I, Blair EM, Watkins H. Oliveira SM, et al. J Mol Cell Cardiol. 2003 Oct;35(10):1251-5. doi: 10.1016/s0022-2828(03)00237-2. J Mol Cell Cardiol. 2003. PMID: 14519435

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