P50-HL54313/HL/NHLBI NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
1999	1
2000	1
2001	1
2004	4
2005	1
2006	1
2024	0

1

Marian AJ, Nambi V. Marian AJ, et al. Expert Rev Mol Diagn. 2004 Nov;4(6):805-20. doi: 10.1586/14737159.4.6.805. Expert Rev Mol Diagn. 2004. PMID: 15525223 Review.

2

Effects of PPARalpha, gamma and delta haplotypes on plasma levels of lipids, severity and progression of coronary atherosclerosis and response to statin therapy in the lipoprotein coronary atherosclerosis study.

Chen S, Tsybouleva N, Ballantyne CM, Gotto AM Jr, Marian AJ. Chen S, et al. Pharmacogenetics. 2004 Jan;14(1):61-71. doi: 10.1097/00008571-200401000-00007. Pharmacogenetics. 2004. PMID: 15128052

3

Molecular cloning, expression analysis, and chromosome mapping of WDR6, a novel human WD-repeat gene.

Li D, Burch P, Gonzalez O, Kashork CD, Shaffer LG, Bachinski LL, Roberts R. Li D, et al. Biochem Biophys Res Commun. 2000 Jul 21;274(1):117-23. doi: 10.1006/bbrc.2000.3012. Biochem Biophys Res Commun. 2000. PMID: 10903905

4

Desmin mutation responsible for idiopathic dilated cardiomyopathy.

Li D, Tapscoft T, Gonzalez O, Burch PE, Quiñones MA, Zoghbi WA, Hill R, Bachinski LL, Mann DL, Roberts R. Li D, et al. Circulation. 1999 Aug 3;100(5):461-4. doi: 10.1161/01.cir.100.5.461. Circulation. 1999. PMID: 10430757

5

Antifibrotic effects of antioxidant N-acetylcysteine in a mouse model of human hypertrophic cardiomyopathy mutation.

Marian AJ, Senthil V, Chen SN, Lombardi R. Marian AJ, et al. J Am Coll Cardiol. 2006 Feb 21;47(4):827-34. doi: 10.1016/j.jacc.2005.10.041. Epub 2006 Jan 26. J Am Coll Cardiol. 2006. PMID: 16487852 Free PMC article.

6

A common PCSK9 haplotype, encompassing the E670G coding single nucleotide polymorphism, is a novel genetic marker for plasma low-density lipoprotein cholesterol levels and severity of coronary atherosclerosis.

Chen SN, Ballantyne CM, Gotto AM Jr, Tan Y, Willerson JT, Marian AJ. Chen SN, et al. J Am Coll Cardiol. 2005 May 17;45(10):1611-9. doi: 10.1016/j.jacc.2005.01.051. Epub 2005 Apr 21. J Am Coll Cardiol. 2005. PMID: 15893176 Free PMC article. Clinical Trial.

7

Induction and reversal of cardiac phenotype of human hypertrophic cardiomyopathy mutation cardiac troponin T-Q92 in switch on-switch off bigenic mice.

Lutucuta S, Tsybouleva N, Ishiyama M, Defreitas G, Wei L, Carabello B, Marian AJ. Lutucuta S, et al. J Am Coll Cardiol. 2004 Dec 7;44(11):2221-30. doi: 10.1016/j.jacc.2004.09.005. J Am Coll Cardiol. 2004. PMID: 15582321 Free PMC article.

8

Genomic organization and isoform-specific tissue expression of human NAPOR (CUGBP2) as a candidate gene for familial arrhythmogenic right ventricular dysplasia.

Li D, Bachinski LL, Roberts R. Li D, et al. Genomics. 2001 Jun 15;74(3):396-401. doi: 10.1006/geno.2001.6558. Genomics. 2001. PMID: 11414768

9

Evolution of expression of cardiac phenotypes over a 4-year period in the beta-myosin heavy chain-Q403 transgenic rabbit model of human hypertrophic cardiomyopathy.

Nagueh SF, Chen S, Patel R, Tsybouleva N, Lutucuta S, Kopelen HA, Zoghbi WA, Quiñones MA, Roberts R, Marian AJ. Nagueh SF, et al. J Mol Cell Cardiol. 2004 May;36(5):663-73. doi: 10.1016/j.yjmcc.2004.02.010. J Mol Cell Cardiol. 2004. PMID: 15135661 Free PMC article.

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