Marian AJ - Search Results

1

Human polymorphism of P-selectin glycoprotein ligand 1 attributable to variable numbers of tandem decameric repeats in the mucinlike region.

Afshar-Kharghan V, Diz-Küçükkaya R, Ludwig EH, Marian AJ, López JA. Afshar-Kharghan V, et al. Among authors: marian aj. Blood. 2001 May 15;97(10):3306-7. doi: 10.1182/blood.v97.10.3306. Blood. 2001. PMID: 11342464 Free article.

2

Detection of a new mutation in the beta-myosin heavy chain gene in an individual with hypertrophic cardiomyopathy.

Marian AJ, Yu QT, Mares A Jr, Hill R, Roberts R, Perryman MB. Marian AJ, et al. J Clin Invest. 1992 Dec;90(6):2156-65. doi: 10.1172/JCI116101. J Clin Invest. 1992. PMID: 1361491 Free PMC article.

3

Apolipoprotein epsilon 4 is not a genetic risk factor for coronary artery disease or restenosis after percutaneous transluminal coronary angioplasty.

Damaraju S, Yu QT, Safavi F, Marian AJ. Damaraju S, et al. Among authors: marian aj. Am J Cardiol. 1995 Jun 1;75(16):1181-3. doi: 10.1016/s0002-9149(99)80756-5. Am J Cardiol. 1995. PMID: 7762511 No abstract available.

4

Angiotensin-converting enzyme polymorphism in hypertrophic cardiomyopathy and sudden cardiac death.

Marian AJ, Yu QT, Workman R, Greve G, Roberts R. Marian AJ, et al. Lancet. 1993 Oct 30;342(8879):1085-6. doi: 10.1016/0140-6736(93)92064-z. Lancet. 1993. PMID: 8105312

5

Localization of a gene responsible for familial dilated cardiomyopathy to chromosome 1q32.

Durand JB, Bachinski LL, Bieling LC, Czernuszewicz GZ, Abchee AB, Yu QT, Tapscott T, Hill R, Ifegwu J, Marian AJ, et al. Durand JB, et al. Among authors: marian aj. Circulation. 1995 Dec 15;92(12):3387-9. doi: 10.1161/01.cir.92.12.3387. Circulation. 1995. PMID: 8521556

6

A variant of human paraoxonase/arylesterase (HUMPONA) gene is a risk factor for coronary artery disease.

Serrato M, Marian AJ. Serrato M, et al. Among authors: marian aj. J Clin Invest. 1995 Dec;96(6):3005-8. doi: 10.1172/JCI118373. J Clin Invest. 1995. PMID: 8675673 Free PMC article.

7

A variant of beta fibrinogen is a genetic risk factor for coronary artery disease and myocardial infarction.

Yu Q, Safavi F, Roberts R, Marian AJ. Yu Q, et al. Among authors: marian aj. J Investig Med. 1996 Apr;44(4):154-9. J Investig Med. 1996. PMID: 8689411

8

A common mutation in methylenetetrahydrofolate reductase gene is not a major risk of coronary artery disease or myocardial infarction.

Brugada R, Marian AJ. Brugada R, et al. Among authors: marian aj. Atherosclerosis. 1997 Jan 3;128(1):107-12. doi: 10.1016/s0021-9150(96)05977-1. Atherosclerosis. 1997. PMID: 9051203

9

Role of candidate modifier genes on the phenotypic expression of hypertrophy in patients with hypertrophic cardiomyopathy.

Brugada R, Kelsey W, Lechin M, Zhao G, Yu QT, Zoghbi W, Quinones M, Elstein E, Omran A, Rakowski H, Wigle D, Liew CC, Sole M, Roberts R, Marian AJ. Brugada R, et al. Among authors: marian aj. J Investig Med. 1997 Dec;45(9):542-51. J Investig Med. 1997. PMID: 9444881

10

Variants of trophic factors and expression of cardiac hypertrophy in patients with hypertrophic cardiomyopathy.

Patel R, Lim DS, Reddy D, Nagueh SF, Lutucuta S, Sole MJ, Zoghbi WA, Quiñones MA, Roberts R, Marian AJ. Patel R, et al. Among authors: marian aj. J Mol Cell Cardiol. 2000 Dec;32(12):2369-77. doi: 10.1006/jmcc.2000.1267. J Mol Cell Cardiol. 2000. PMID: 11113012

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