Search Results - "Chen, Suet N"

Myozenin 2 Is a Novel Gene for Human Hypertrophic Cardiomyopathy by Osio, Adriana, Tan, Lily, Chen, Suet N, Lombardi, Raffaella, Nagueh, Sherif F, Shete, Sanjay, Roberts, Robert, Willerson, James T, Marian, Ali J

“…Hypertrophic cardiomyopathy (HCM) is a genetic disorder caused by mutations in sarcomeric proteins (excluding phenocopy). The causal genes in approximately…”
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Antifibrotic Effects of Antioxidant N-Acetylcysteine in a Mouse Model of Human Hypertrophic Cardiomyopathy Mutation by Marian, Ali J., Senthil, Vinitha, Chen, Suet N., Lombardi, Raffaella

“…Antifibrotic Effects of Antioxidant N-Acetylcysteine in a Mouse Model of Human Hypertrophic Cardiomyopathy Mutation Ali J. Marian, Vinitha Senthil, Suet N…”
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Prevention of Cardiac Hypertrophy by Atorvastatin in a Transgenic Rabbit Model of Human Hypertrophic Cardiomyopathy by Senthil, Vinitha, Chen, Suet N, Tsybouleva, Natalie, Halder, Tripti, Nagueh, Sherif F, Willerson, James T, Roberts, Robert, Marian, A J

“…Cardiac hypertrophy, a major determinant of morbidity and mortality in hypertrophic cardiomyopathy (HCM), is considered a secondary phenotype and potentially…”
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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 by Chen, Suet N, Ballantyne, Christie M, Gotto, Jr, Antonio M, Tan, Yanli, Willerson, James T, Marian, Ali J

“…We sought to determine the effects of PCSK9 variants on plasma low-density lipoprotein cholesterol (LDL-C) levels, severity of coronary atherosclerosis, and…”
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A Common PCSK9Haplotype, Encompassing the E670G Coding Single Nucleotide Polymorphism, Is a Novel Genetic Marker for Plasma Low-Density Lipoprotein Cholesterol Levels and Severity of Coronary Atherosclerosis by Chen, Suet N., Ballantyne, Christie M., Gotto, Antonio M., Tan, Yanli, Willerson, James T., Marian, Ali J.

“…We sought to determine the effects of PCSK9variants on plasma low-density lipoprotein cholesterol (LDL-C) levels, severity of coronary atherosclerosis, and…”
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Abstract 20201: Fibro-Adipocyte Progenitors are a Cell Source of Adipocytes in Arrhythmogenic Cardiomyopathy by Lombardi, Raffaella, Chen, Suet N, Ruggiero, Alessandra, Czernuszewicz, Grazyna Z, Gurha, Priyatansh, Chen, Xiaofan, Willerson, James T, Marian, Ali J

“…Abstract only Arrhythmogenic cardiomyopathy (AC) is clinically characterized by arrhythmias, heart failure and sudden death and pathologically by replacement…”
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Candidate genetic analysis of plasma high-density lipoprotein-cholesterol and severity of coronary atherosclerosis by Chen, Suet Nee, Cilingiroglu, Mehmet, Todd, Josh, Lombardi, Raffaella, Willerson, James T, Gotto, Jr, Antonio M, Ballantyne, Christie M, Marian, A J

“…Plasma level of high-density lipoprotein-cholesterol (HDL-C), a heritable trait, is an important determinant of susceptibility to atherosclerosis…”
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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. Commentary by CHEN, Suet N, BALLANTYNE, Christie M, GOTTO, Antonio M, WILLERSON, James T, MARIAN, Ali J, KASTELEIN, John J. P, FOUCHIER, Sigrid W, DEFESCHE, Joep C

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