MORISAKI Hiroko | Department of Bioscience and Genetics, National Cerebral and Cardiovascular Center Research Institute

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概要

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著作論文

FRS-091 Impairment of Ubiquitin-Proteasome System Caused by a Missense MYBPC3 Mutation and Associated with Cardiac Dysfunction in Hypertrophic Cardiomyopathy(FRS19,Genetic Abnormalities in Cardiac Hypertrophy and Cardiomyopathy (M),Featured Research Sessi
Genetic Analysis of Young Adult Patients With Aortic Disease Not Fulfilling the Diagnostic Criteria for Marfan Syndrome
2 Significance of Comprehensive Genetic Analysis of Syndromatic and Non-Syndromatic Aortic Aneurysm and Dissection(Recent Progress in Diagnosis and Treatment of Aortic Diseases,Symposium 5 (SY-05) (A),The 73rd Annual Scientific Meeting of The Japanese Cir
PJ-161 Clinical and Genetic Features of Marfan-Like Connective Tissue Disorders(Peripheral circulation/Vascular disease(06)(H),Poster Session(Japanese),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
OJ-084 Ethnic Differences of Phenotypic manifestation of Marfan syndrome(Peripheral circulation/Vascular disease(02)(H),Oral Presentation(Japanese),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
Leptin Gene and Leptin Receptor Gene Polymorphisms Are Associated with Sweet Preference and Obesity
1 Role of the Ubiquitin Proteasome System in the Development of Heart Failure in Hypertrophic Cardiomyopathy(Young Investigator's Award for International Students Finalists Lecture (YIA International),Special Program,The 72nd Annual Scientific Meeting of
Remote Reperfusion Lung Injury is Associated With AMP Deaminase 3 Activation and Attenuated by Inosine Monophosphate
OJ-061 Association analysis between autosomal recessive hypercholesterolemia (ARH) gene and hypercholesterolemia(Lipid Disorders 1 (H) : OJ8)(Oral Presentation (Japanese))
OE-193 Exaggeration of Remote Reperfusion Pulmonary Injury in AMP Deaminase 3 Knockout Mice(Metabolism/Biochemistry/Energetics-1 (H) OE33,Oral Presentation (English),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Society)
Mouse Mef2b Gene: Unique Member of MEF2 Gene Family
Guidelines for Diagnosis and Treatment of Aortic Aneurysm and Aortic Dissection (JCS 2011) : Digest Version

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