2P336 自己集合核酸によるアドレス可能な内破的ナノ構造体(バイオエンジニアリング,第48回日本生物物理学会年会)
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概要
- 論文の詳細を見る
- 日本生物物理学会の論文
- 2010-08-15
著者
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Tahira Tomoko
Division Of Genome Analysis Research Center For Genetic Information Medical Institute Of Bioregulati
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Hayashi Kenshi
Division Of Cardiovascular Medicine Kanazawa University Graduate School Of Medical Science
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Hayashi Kenshi
Division Of Genome Analysis Research Center For Genetic Information Medical Institute Of Bioregulati
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Hayashi Kenshi
Division Of Cardiology Kanazawa University
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Tsutsumi Takanobu
Division of Genome Analysis, Research Center for Genetic Information, Medical Institute of Bioregula
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Okada Takao
Research Institute of Biomolecule Metrology Co., Ltd
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Kanegami Akemi
Research Institute of Biomolecule Metrology Co., Ltd
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Kanegami Akemi
Research Institute Of Biomolecule Metrology Co. Ltd
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Tahira Tomoko
Division Of Genome Analysis Research Center For Genetic Information Medical Institute Of Bioregulati
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Okada Takao
Research Institute Of Biomolecule Metrology Co. Ltd
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Tsutsumi Takanobu
Division Of Genome Analysis Research Center For Genetic Information Medical Institute Of Bioregulati
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Hayashi Kenshi
Division Of Cardiology Ishikawa Prefectural Hospital
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Okada Takao
Research Department R&d Division Taki Chemical Co. Ltd.
関連論文
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- PJ-643 Prediction of Cardiac Events in Patients with Hypertrophic Cardiomyopathy : Usefulness of MIBG Myocardial Scintigraphy(Cardiomyopathy, basic/clinical-7 (M) PJ108,Poster Session (Japanese),The 70th Anniversary Annual Scientific Meeting of the Japane
- PE-067 Late Gadolinium Enhancement Cardiovascular Magnetic Resonance in Hypertrophic Cardiomyopathy Caused by Cardiac Troponinl Gene Mutation(Cardiomyopathy, basic/clinical-3 (M) PE12,Poster Session (English),The 70th Anniversary Annual Scientific Meeting
- OE-284 Usefulness of Late Gadolinium Enhancement Cardiovascular Magnetic Resonance in Patients with Hypertrophic Cardiomyopathy Associated with TNNI3 Gene Mutation(MRI/MRA-1 (I) OE48,Oral Presentation (English),The 70th Anniversary Annual Scientific Meeti
- OE-265 Genotype-Phenotype Variations in Cardiomyopathies Caused by a Cardiac Troponin I Gene Mutation(Cardiomyopathy, basic/clinical-1 (M) OE45,Oral Presentation (English),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Society)
- OE-088 Differences in Diagnostic Value of Various Criteria of Negative T Waves for Hypertrophic Cardiomyopathy in a Genotyped Population(ECG/Body surface potential mapping/Holter-1 (A) OE15,Oral Presentation (English),The 70th Anniversary Annual Scientifi
- FRS-104 Association between Angiotensin II Receptor Gene Polymorphism and Left Ventricular Systolic Dysfunction in Sarcomere Gene Mutation-induced Hypertrophic Cardiomyopathy(Frontier of Cardiomyopathy Research-2 (M) FRS21,Featured Research Session (Engli
- FRS-077 Genetic Analysis of KCR1 Gene in Japanese LQTS Patients(Arrhythmia (basic), The 71st Annual Scientific Meeting of the Japanese Circulation Society)
- PE-279 High Incidence of Sudden Cardiac Death with Conduction Disturbances and Atrial Cardiomyopathy Caused by a Mutation in the STA Gene(Cardiomyopathy, Clinical 3 (M) : PE48)(Poster Session (English))
- PJ-813 Impact of Speckle Tracking Echocardiography on Evaluation of Myocardial Fibrosis in Hypertrophic Cardiomyopathy : Comparison with Study by Cardiovascular Magnetic Resonance(PJ136,Echo/Doppler (Others) 1 (I),Poster Session (Japanese),The 73rd Annual
- PJ-433 Impact of the HERG Channel Activator "Malltoxin" on Type 2 LQTS Related Mutant Channel(PJ073,Arrhythmia, Others (Basic) 1 (A),Poster Session (Japanese),The 73rd Annual Scientific Meeting of The Japanese Circulation Society)
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- 5 Impact of Combined Risk Factors on Reduction of Repolarization Reserve Associated with Drug-induced Abnormal QT Prolongation and Torsade de Pointes(Proarrhythmic Risk of Drugs and Their Evaluation,Symposium 7 (SY-07) (I),The 73rd Annual Scientific Meeti
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- PE-074 Impact of Left Ventricular Systolic Dysfunction on QT Dispersion and Associated Fatal Arrhythmia in Hypertrophic Cardiomyopathy(ECG/Body surface potential mapping/Holter(03)(A),Poster Session(English),The 72nd Annual Scientific Meeting of the Japan
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- 2 Impact of Missense Mutations in Cardiac Ryanodine Receptor Gene as a Cause of Hypertrophic Cardiomyopathy : A New Insight From Ca Handling(Symposium 10 (SY-10) (M) Update in Cardiomyopathy : Novel Approaches ; Novel Targets,Special Program,The 72nd Annu
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- OJ-240 Dilated-Phase Hypertrophic Cardiomyopathy Show More Severe Heart Failure Compared with Idiopathic Dilated Cardiomyopathy in Matched Symptomatic and Echocardiographic Settings(Heart failure, clinical-06, The 71st Annual Scientific Meeting of the Jap
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- OJ-051 Elevation of Plasma Levels of Matrix Metalloproteinase-2 Involves Development of Myocardial Fibrosis in HCM Caused by TNNI3 Gene Mutations(Cardiomyopathy, basic/clinical-2, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
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