Taylor MRG - Search Results

1

Tachycardia-induced metabolic rewiring as a driver of contractile dysfunction.

Tu C, Caudal A, Liu Y, Gorgodze N, Zhang H, Lam CK, Dai Y, Zhang A, Wnorowski A, Wu MA, Yang H, Abilez OJ, Lyu X, Narayan SM, Mestroni L, Taylor MRG, Recchia FA, Wu JC. Tu C, et al. Among authors: taylor mrg. Nat Biomed Eng. 2024 Apr;8(4):479-494. doi: 10.1038/s41551-023-01134-x. Epub 2023 Nov 27. Nat Biomed Eng. 2024. PMID: 38012305 Free PMC article.

2

[Dilated cardiomyopathy: etiology, clinical criteria for diagnosis and screening of the familial form].

Startari U, Taylor MR, Sinagra G, Di Lenarda A, Mestroni L. Startari U, et al. Ital Heart J Suppl. 2002 Apr;3(4):378-85. Ital Heart J Suppl. 2002. PMID: 12025380 Review. Italian.

3

Familial hypertrophic cardiomyopathy: clinical features, molecular genetics and molecular genetic testing.

Taylor MR, Carniel E, Mestroni L. Taylor MR, et al. Expert Rev Mol Diagn. 2004 Jan;4(1):99-113. doi: 10.1586/14737159.4.1.99. Expert Rev Mol Diagn. 2004. PMID: 14711353 Review.

4

SCN5A mutation associated with dilated cardiomyopathy, conduction disorder, and arrhythmia.

McNair WP, Ku L, Taylor MR, Fain PR, Dao D, Wolfel E, Mestroni L; Familial Cardiomyopathy Registry Research Group. McNair WP, et al. Circulation. 2004 Oct 12;110(15):2163-7. doi: 10.1161/01.CIR.0000144458.58660.BB. Epub 2004 Oct 4. Circulation. 2004. PMID: 15466643

5

Analysis of genetic variations of lamin A/C gene (LMNA) by denaturing high-performance liquid chromatography.

Taylor MR, Robinson ML, Mestroni L. Taylor MR, et al. J Biomol Screen. 2004 Oct;9(7):625-8. doi: 10.1177/1087057104266393. J Biomol Screen. 2004. PMID: 15475483

6

Cardiomyopathy, familial dilated.

Taylor MR, Carniel E, Mestroni L. Taylor MR, et al. Orphanet J Rare Dis. 2006 Jul 13;1:27. doi: 10.1186/1750-1172-1-27. Orphanet J Rare Dis. 2006. PMID: 16839424 Free PMC article. Review.

7

Lamin A/C gene and the heart: how genetics may impact clinical care.

Mestroni L, Taylor MR. Mestroni L, et al. J Am Coll Cardiol. 2008 Oct 7;52(15):1261-2. doi: 10.1016/j.jacc.2008.07.021. J Am Coll Cardiol. 2008. PMID: 18926330 Free PMC article. No abstract available.

8

Heart failure and personalized medicine.

Mestroni L, Merlo M, Taylor MR, Camerini F, Sinagra G. Mestroni L, et al. J Cardiovasc Med (Hagerstown). 2011 Jan;12(1):6-12. doi: 10.2459/JCM.0b013e32833e8b0d. J Cardiovasc Med (Hagerstown). 2011. PMID: 20814312 Review.

9

SCN5A mutations associate with arrhythmic dilated cardiomyopathy and commonly localize to the voltage-sensing mechanism.

McNair WP, Sinagra G, Taylor MR, Di Lenarda A, Ferguson DA, Salcedo EE, Slavov D, Zhu X, Caldwell JH, Mestroni L; Familial Cardiomyopathy Registry Research Group. McNair WP, et al. J Am Coll Cardiol. 2011 May 24;57(21):2160-8. doi: 10.1016/j.jacc.2010.09.084. J Am Coll Cardiol. 2011. PMID: 21596231 Free PMC article.

10

Hearing the noise the challenges of human genome variation in genetic testing.

Mestroni L, Taylor MR. Mestroni L, et al. J Am Coll Cardiol. 2011 Jun 7;57(23):2328-9. doi: 10.1016/j.jacc.2011.02.026. J Am Coll Cardiol. 2011. PMID: 21636033 Free PMC article. No abstract available.

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