Cardiomyopathy mutations. Medical search. Frequent questions

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Anatomy14

Myocardium Heart Ventricles Heart Septum Myocytes, Cardiac Heart Sarcomeres Endocardium Cell Line Mitral Valve Cells, Cultured Myofibrils Mitochondria, Heart Desmosomes COS Cells

Organisms7

Mice, Transgenic Escherichia coli Mice, Inbred C57BL Saccharomyces cerevisiae Mice, Mutant Strains Mice, Knockout Cricetinae

Diseases46

Cardiomyopathy, Hypertrophic, Familial Cardiomyopathy, Hypertrophic Cardiomyopathy, Dilated Cardiomyopathies Cardiomyopathy, Restrictive Takotsubo Cardiomyopathy Chagas Cardiomyopathy Cardiomyopathy, Alcoholic Arrhythmogenic Right Ventricular Dysplasia Diabetic Cardiomyopathies Myocarditis Ventricular Dysfunction, Left Heart Failure Ventricular Outflow Obstruction Death, Sudden, Cardiac Tachycardia, Ventricular Fibrosis Arrhythmias, Cardiac Disease Models, Animal Endomyocardial Fibrosis Syndrome Hypertrophy, Left Ventricular Myocardial Ischemia Genetic Predisposition to Disease Ventricular Remodeling Heart Diseases Death, Sudden Puerperal Disorders Cardiomegaly Glycogen Storage Disease Type IIb Isolated Noncompaction of the Ventricular Myocardium Pregnancy Complications, Cardiovascular Ventricular Dysfunction Muscular Dystrophy, Duchenne Noonan Syndrome Mitral Valve Insufficiency Muscular Dystrophies Mitochondrial Myopathies Mitochondrial Diseases Disease Progression Genetic Diseases, X-Linked Heart Block Syncope Muscular Diseases Bundle-Branch Block Ventricular Dysfunction, Right

Chemicals and Drugs39

Tropomyosin Cardiac Myosins Troponin T Codon, Nonsense Ventricular Myosins Myosin Heavy Chains Lamin Type A Plakophilins DNA Primers Sarcoglycans Carrier Proteins DNA, Mitochondrial Desmoglein 2 Dystrophin DNA-Binding Proteins Transcription Factors Codon RNA, Messenger Mutant Proteins Desmin Membrane Proteins DNA Adrenergic beta-Antagonists Nuclear Proteins 3-Iodobenzylguanidine Myosins Cardiotonic Agents Bacterial Proteins Muscle Proteins Recombinant Proteins Connectin Troponin I Proto-Oncogene Proteins B-raf LIM Domain Proteins Calcium DNA, Neoplasm Proteins Desmoplakins Desmocollins

Analytical, Diagnostic and Therapeutic Techniques and Equipment49

Pedigree Echocardiography Electrocardiography DNA Mutational Analysis Amino Acid Substitution Polymerase Chain Reaction Genetic Testing Stroke Volume Mutagenesis, Site-Directed Sequence Analysis, DNA Echocardiography, Doppler Disease Models, Animal Chromosome Mapping Heart Transplantation Models, Molecular Cardiac Pacing, Artificial Prognosis Follow-Up Studies Defibrillators, Implantable Magnetic Resonance Imaging, Cine Treatment Outcome Case-Control Studies Heterozygote Detection Cardiac Catheterization Genetic Complementation Test Sequence Alignment Cloning, Molecular Biopsy Models, Genetic Transfection Heart Function Tests Ablation Techniques Predictive Value of Tests Retrospective Studies Catheter Ablation Prospective Studies Mutagenesis, Insertional Reverse Transcriptase Polymerase Chain Reaction Fatal Outcome Blotting, Western Immunohistochemistry Magnetic Resonance Imaging Severity of Illness Index Crosses, Genetic Risk Factors Electrocardiography, Ambulatory Epicardial Mapping Electrophysiologic Techniques, Cardiac Cohort Studies

Phenomena and Processes62

Mutation Point Mutation Mutation, Missense Frameshift Mutation Germ-Line Mutation Heterozygote Ventricular Function, Left Exons Base Sequence Mutation Rate Amino Acid Substitution Phenotype Genotype Polymorphism, Single-Stranded Conformational Alleles Myocardial Contraction Homozygote Codon, Nonsense Amino Acid Sequence Stroke Volume Genes, Recessive Peripartum Period Genes, Dominant Mutagenesis Sequence Deletion Protein Structure, Tertiary Genetic Predisposition to Disease Genetic Linkage Gene Deletion Ventricular Remodeling Hemodynamics Penetrance Diastole Time Factors Suppression, Genetic Binding Sites Sequence Homology, Amino Acid Codon Consanguinity Founder Effect Protein Binding Systole Polymorphism, Genetic Signal Transduction Exome Genes, p53 Transfection Gene Frequency Plasmids Gene Expression Transcription, Genetic Genetic Variation Gene Expression Regulation Promoter Regions, Genetic Mutagenesis, Insertional Introns Genes, Lethal Protein Conformation Genetic Heterogeneity Genes, BRCA1 Kinetics Microsatellite Repeats

Disciplines and Occupations1

Immunohistochemistry

Information Science4

Base Sequence Molecular Sequence Data Amino Acid Sequence Fatal Outcome

Named Groups1

Infant, Newborn

Health Care13

Genetic Testing Follow-Up Studies Treatment Outcome Case-Control Studies Family Health Age of Onset Predictive Value of Tests Retrospective Studies Prospective Studies Fatal Outcome Severity of Illness Index Risk Factors Cohort Studies

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Phenomena and Processes Disciplines and Occupations Information Science Named Groups Health Care

Cardiomyopathy, Hypertrophic, Familial Cardiomyopathy, Hypertrophic Tropomyosin Cardiomyopathy, Dilated Cardiac Myosins Troponin T Mutation Cardiomyopathies Point Mutation Mutation, Missense Cardiomyopathy, Restrictive Takotsubo Cardiomyopathy Chagas Cardiomyopathy Frameshift Mutation Pedigree Myocardium Cardiomyopathy, Alcoholic Germ-Line Mutation Echocardiography Arrhythmogenic Right Ventricular Dysplasia Electrocardiography Diabetic Cardiomyopathies Heterozygote DNA Mutational Analysis Ventricular Function, Left Exons Myocarditis Heart Ventricles Ventricular Dysfunction, Left Base Sequence Mutation Rate Amino Acid Substitution Heart Septum Heart Failure Polymerase Chain Reaction Molecular Sequence Data Phenotype Genotype Polymorphism, Single-Stranded Conformational Alleles Myocytes, Cardiac Myocardial Contraction Ventricular Outflow Obstruction Homozygote Genetic Testing Heart Codon, Nonsense Death, Sudden, Cardiac Amino Acid Sequence Stroke Volume Mutagenesis, Site-Directed Sequence Analysis, DNA Ventricular Myosins Myosin Heavy Chains Genes, Recessive Peripartum Period Sarcomeres Genes, Dominant Mice, Transgenic Tachycardia, Ventricular Lamin Type A Echocardiography, Doppler Mutagenesis Fibrosis Sequence Deletion Arrhythmias, Cardiac Plakophilins Disease Models, Animal Endomyocardial Fibrosis Syndrome Hypertrophy, Left Ventricular Myocardial Ischemia Endocardium DNA Primers Protein Structure, Tertiary Chromosome Mapping Heart Transplantation Genetic Predisposition to Disease Genetic Linkage Sarcoglycans Gene Deletion Ventricular Remodeling Carrier Proteins Models, Molecular Hemodynamics Penetrance Cardiac Pacing, Artificial Diastole Cell Line Time Factors DNA, Mitochondrial Prognosis Heart Diseases Follow-Up Studies Desmoglein 2 Death, Sudden Puerperal Disorders Escherichia coli Suppression, Genetic Cardiomegaly

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