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    Article

    Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy

    Hypertrophic cardiomyopathy (HCM), the most common cause of sudden death in the young, is an autosomal dominant disease characterized by ventricular hypertrophy accompanied by myofibrillar disarrays1. Linkage stu...

    Akinori Kimura, Haruhito Harada, Jeong-Euy Park, Hirofumi Nishi in Nature Genetics (1997)

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    Open Access

    Activation of monocytes, T-lymphocytes and plasma inflammatory markers in angina patients

    Inflammation and activation of immune cells have important roles in the pathogenesis of atherosclerosis. We analyzed the plasma levels of inflammatory markers and the degree of activation of peripheral blood m...

    Won-Ha Lee, Yoon Lee, Jong-Ran Kim, **-A Chu in Experimental & Molecular Medicine (1999)

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    Chapter

    Mutational Profiles and Molecular Etiologies of Hypertrophic Cardiomyopathy and Dilated Cardiomyopathy in Asian Populations

    Idiopathic cardiomyopathy (ICM) had been defined as the cardiac disease of unknown etiology. There are two major clinical phenotypes of ICM; hypertrophic cardiomyopathy (HCM) and dilated cardiomyopathy (DCM). ...

    Akinori Kimura M.D. Ph.D., Manatsu Ito-Satoh in Frontiers in Cardiovascular Health (2003)

  4. Article

    Open Access

    Involvement of tumor necrosis factor receptor superfamily (TNFRSF) members in the pathogenesis of inflammatory diseases

    Current therapies for autoimmune diseases are not cures but merely palliatives, aimed at reducing symptoms. For the most part, these treatments provide nonspecific suppression of the immune system and thus do ...

    Byungsuk Kwon, Byung-Sam Kim, Hong Rae Cho in Experimental & Molecular Medicine (2003)

  5. Article

    Replication of the association between a chromosome 9p21 polymorphism and coronary artery disease in Japanese and Korean populations

    Coronary artery disease (CAD) has become a major health problem in many countries. Recent genome-wide association studies have identified the association between rs1333049 on chromosome 9p21 and susceptibility...

    Kunihiko Hinohara, Toshiaki Nakajima, Megumi Takahashi in Journal of Human Genetics (2008)

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    Article

    Megakaryoblastic leukemia factor-1 gene in the susceptibility to coronary artery disease

    Coronary artery disease (CAD) is based on the atherosclerosis of coronary artery and may manifest with myocardial infarction or angina pectoris. Although it is widely accepted that genetic factors are linked t...

    Kunihiko Hinohara, Toshiaki Nakajima, Michio Yasunami, Shigeru Houda in Human Genetics (2009)

  7. Article

    Open Access

    Efficacy, safety, and tolerability of valsartan/hydrochlorothiazide in Asian patients with essential hypertension

    Previous studies have demonstrated that hypertensive patients need concomitant therapy with one or more drugs from different classes of antihypertensive agents to achieve their blood pressure control targets. ...

    Wen-Ter Lai, Jeong-Euy Park, Neelesh Dongre, Jackson Wang in Advances in Therapy (2011)

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    Article

    Complete versus incomplete revascularization for treatment of multivessel coronary artery disease in the drug-eluting stent era

    Limited data exist regarding the impact of complete revascularization (CR) versus incomplete revascularization (IR) on the long-term outcomes of patients with multivessel coronary artery disease (MVD) who unde...

    Young Bin Song, Sang-Yeub Lee, Joo-Yong Hahn, Seung-Hyuk Choi in Heart and Vessels (2012)

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    Article

    Lipoteichoic acid isolated from Lactobacillus plantarum suppresses LPS-mediated atherosclerotic plaque inflammation

    Chronic inflammation plays an important role in atherogenesis. Experimental studies have demonstrated the accumulation of monocytes/macrophages in atherosclerotic plaques caused by inflammation. Here, we repor...

    Joo Yun Kim, Hangeun Kim, Bong Jun Jung, Na-Ra Kim, Jeong Euy Park in Molecules and Cells (2013)

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    Article

    Genome-based exome sequencing analysis identifies GYG1, DIS3L and DDRGK1 are associated with myocardial infarction in Koreans

    Myocardial infarction (MI) is a complex disease caused by combination of genetic and environmental factors. Although genome-wide association studies (GWAS) identified more than 46 risk loci which are associate...

    Ji-Young Lee, Sanghoon Moon, Yun Kyoung Kim, Sang-Hak Lee in Journal of Genetics (2017)

  11. Article

    Open Access

    Mechanistic insights into the anti-restenotic effects of HSP27 and HO1 modulated by reconstituted HDL on neointimal hyperplasia

    High-density lipoprotein (HDL) therapy has demonstrated beneficial effects in acute stroke and acute myocardial infarction models by reducing infarct size. In this study, we investigated the inhibitory effects...

    Ye Ji Kim, Zinah Hilal Khaleel, Myeongji **, Jo Woon Yi Lee in Scientific Reports (2023)