Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Ryuichiro Murakami
Pressure Overload-Induced Cardiomyopathy in Heterozygous Carrier Mice of Carnitine Transporter Gene Mutation
Hypertension
Internal Medicine
The Effects of Endothelial Nitric Oxide Synthase Gene Polymorphisms on Endothelial Function and Metabolic Risk Factors in Healthy Subjects: The Significance of Plasma Adiponectin Levels
European Journal of Endocrinology
Medicine
Endocrinology
Metabolism
Diabetes
Related publications
CXCR4 Gene Transfer Prevents Pressure Overload Induced Heart Failure
Journal of Molecular and Cellular Cardiology
Cardiovascular Medicine
Molecular Biology
Cardiology
Haploinsufficiency of MYBPC3 Exacerbates the Development of Hypertrophic Cardiomyopathy in Heterozygous Mice
Journal of Molecular and Cellular Cardiology
Cardiovascular Medicine
Molecular Biology
Cardiology
Diet-Induced Atherosclerosis in Mice Heterozygous and Homozygous for Apolipoprotein E Gene Disruption.
Journal of Clinical Investigation
Medicine
Norepinephrine Transporter Heterozygous Knockout Mice Exhibit Altered Transport and Behavior
Genes, Brain and Behavior
Neurology
Genetics
Behavioral Neuroscience
Mild Dopa-Responsive Dystonia in Heterozygous Tyrosine Hydroxylase Mutation Carrier: Evidence of Symptomatic Enzyme Deficiency?
Parkinsonism and Related Disorders
Gerontology
Geriatrics
Neurology
Analyzing Gene Expression Profiles With Preliminary Validations in Cardiac Hypertrophy Induced by Pressure-Overload
Canadian Journal of Physiology and Pharmacology
Medicine
Physiology
Pharmacology
Antimony-Induced Cardiomyopathy in Guinea-Pig and Protection by L-Carnitine
British Journal of Pharmacology
Pharmacology
Loop-Tail Phenotype in Heterozygous Mice and Neural Tube Defects in Homozygous Mice Result From a Nonsense Mutation in the Vangl2 Gene
Genetics and Molecular Research
Medicine
Genetics
Molecular Biology
Neonatal Cardiomyopathy in Mice Homozygous for the Arg403Gln Mutation in the Α Cardiac Myosin Heavy Chain Gene
Journal of Clinical Investigation
Medicine