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Journal of Applied Physiology, ISSN 8750-7587, 01/2013, Volume 114, Issue 1, pp. 131 - 147
We have previously reported chronic low-intensity interval exercise training attenuates fibrosis, impaired cardiac mitochondrial function, and coronary... 
Diastolic heart failure | Exercise | Coronary flow | Fibrosis | MVO | Speckle tracking | Hypertrophic signaling | Protein Kinases - genetics | Connectin | Heart - physiology | Natriuretic Peptide, Brain - metabolism | Ventricular Function, Left - genetics | Heart Failure - physiopathology | Extracellular Matrix - metabolism | Male | Oxygen Consumption - physiology | Tissue Inhibitor of Metalloproteinases - genetics | Hypertrophy, Left Ventricular - genetics | Swine | Myocardium - metabolism | Ventricular Remodeling - genetics | Sarcomeres - physiology | Proto-Oncogene Proteins c-akt - metabolism | Natriuretic Peptide, Brain - genetics | Fibrosis - physiopathology | Matrix Metalloproteinase 2 - metabolism | Sarcomeres - metabolism | Diastole - genetics | Heart Failure - genetics | Heart Failure - metabolism | Arterial Pressure - physiology | Diastole - physiology | Muscle Proteins - genetics | Matrix Metalloproteinase 2 - genetics | MAP Kinase Kinase 4 - genetics | Hypertrophy, Left Ventricular - physiopathology | Regional Blood Flow - physiology | Protein Kinases - metabolism | Regional Blood Flow - genetics | Myocardial Contraction - physiology | Collagen Type III - metabolism | Fibrosis - metabolism | Oxygen - metabolism | Proto-Oncogene Proteins c-akt - genetics | Extracellular Matrix - genetics | Myocardial Contraction - genetics | Arterial Pressure - genetics | MAP Kinase Kinase 4 - metabolism | Sarcomeres - genetics | Muscle Proteins - metabolism | Ventricular Function, Left - physiology | Citrate (si)-Synthase - metabolism | Heart Failure - rehabilitation | Fibrosis - genetics | Hypertrophy, Left Ventricular - metabolism | RNA, Messenger - genetics | Collagen Type III - genetics | Ventricular Remodeling - physiology | Physical Conditioning, Animal - physiology | Tissue Inhibitor of Metalloproteinases - metabolism | Animals | Oxygen Consumption - genetics | Citrate (si)-Synthase - genetics | speckle tracking | coronary flow | hypertrophic signaling | exercise | fibrosis | diastolic heart failure | MV̇o2
Journal Article
Forensic Science International, ISSN 0379-0738, 12/2018, Volume 293, pp. 70 - 76
Cases of sudden cardiac death (SCD) in young and apparently healthy individuals represent a devastating event in affected families. Hereditary arrhythmia... 
Genetics | Massive parallel sequencing | Sudden cardiac death | Arrhythmia syndromes | Sudden death | BRUGADA SYNDROME | VARIANTS | MEDICINE, LEGAL | UNEXPLAINED DEATH | EUROPEAN-SOCIETY | HYPERTROPHIC CARDIOMYOPATHY | RECOMMENDATIONS | MOLECULAR AUTOPSY | CARDIAC DEATH | EPIDEMIOLOGY | CHANNELOPATHIES | Cardiac Myosins - genetics | Humans | Connectin - genetics | Myosin Heavy Chains - genetics | Infant | Male | Death, Sudden, Cardiac - etiology | Sequence Analysis, DNA | Genetic Variation | Young Adult | Cardiomyopathies - genetics | Channelopathies - genetics | Calcium Channels, L-Type - genetics | Dystrophin - genetics | Hypertrophy, Left Ventricular - pathology | Ankyrins - genetics | Forensic Genetics | Adult | Female | High-Throughput Nucleotide Sequencing | alpha Catenin - genetics | Microfilament Proteins - genetics | Arrhythmia | Demographic aspects | Cardiac arrest | Causes of | Youth | Genetic aspects | Teenagers | Health aspects | Death of | Heart | Cardiac arrhythmia | Cardiomyopathy | Epilepsy | Genes | Cardiovascular disease | Family medical history | Genetic screening | Gene sequencing | Analgesics | Autopsy | Genetic analysis | Deoxyribonucleic acid--DNA | Genetic disorders | Forensic science | Legal medicine | Mortality | Preventive medicine | Disease prevention | Studies | Pathology | Sleep | Genetic counseling | Death
Journal Article
Journal of Neurology, Neurosurgery and Psychiatry, ISSN 0022-3050, 2014, Volume 85, Issue 3, pp. 345 - 353
Journal Article
Journal of Cell Biology, ISSN 0021-9525, 09/2012, Volume 198, Issue 5, pp. 833 - 846
Striated muscle fibers are characterized by their tightly organized cytoplasm. Here, we show that the Drosophila melanogaster KASH proteins Klarsicht (Klar)... 
MIGRATION | DOMAIN PROTEINS | TRANSPORT | SPECTRIN SUPERFAMILY | ENVELOPE | DREIFUSS MUSCULAR-DYSTROPHY | ACTIN CYTOSKELETON | KLARSICHT | NUCLEAR-MEMBRANE PROTEIN | DROSOPHILA EYE | CELL BIOLOGY | Connectin | Locomotion - genetics | Nuclear Envelope - physiology | Organelles - physiology | Endoplasmic Reticulum - metabolism | Myofibrils - genetics | Muscle Fibers, Skeletal - metabolism | Drosophila Proteins - metabolism | Cell Nucleus - physiology | Actomyosin - genetics | Organelles - genetics | Microtubules - metabolism | Cell Nucleus - metabolism | Mitochondria - genetics | Membrane Transport Proteins - genetics | Muscle Proteins - metabolism | Membrane Transport Proteins - metabolism | Microfilament Proteins - metabolism | Microfilament Proteins - genetics | Muscle Fibers, Skeletal - physiology | Nuclear Envelope - genetics | Endoplasmic Reticulum - genetics | Endoplasmic Reticulum - physiology | Mitochondria - metabolism | Mutation - genetics | Actomyosin - metabolism | Muscle Proteins - genetics | Nuclear Envelope - metabolism | Animals | Cell Nucleus - genetics | Microtubules - genetics | Myofibrils - metabolism | Drosophila Proteins - genetics | Locomotion - physiology | Mitochondria - physiology | Drosophila melanogaster | Organelles - metabolism | Proteins | Physiological aspects | Muscles | Cell organelles | Drosophila
Journal Article
Journal Article
Journal Article
Journal Article
Journal of Translational Medicine, ISSN 1479-5876, 08/2018, Volume 16, Issue 1, pp. 241 - 9
Background: Cardiomyopathies are the most common clinical and genetic heterogeneity cardiac diseases, and genetic contribution in particular plays a major role... 
Inherited cardiomyopathy | Mutation | Next generation sequencing | TTN | MEDICINE, RESEARCH & EXPERIMENTAL | HYPERTROPHIC CARDIOMYOPATHY | GENOMICS | DILATED CARDIOMYOPATHY | MUTATIONS | ASSOCIATION | TRANSPLANTATION | Cardiomyopathy, Dilated - genetics | Adenine Nucleotide Translocator 1 - genetics | Cardiomyopathy, Hypertrophic - genetics | Genetic Predisposition to Disease | Cardiac Myosins - genetics | Humans | Connectin - genetics | Myosin Heavy Chains - genetics | Male | Arrhythmogenic Right Ventricular Dysplasia - genetics | Young Adult | Cardiomyopathies - genetics | Carrier Proteins - genetics | Cardiomyopathies - physiopathology | Phenotype | Ventricular Dysfunction, Left - genetics | Cardiomyopathy, Restrictive - genetics | Adult | Female | Polymorphism, Single Nucleotide | High-Throughput Nucleotide Sequencing - methods | Usage | Gene mutations | Cardiomyopathy | Genetic aspects | Research | Nucleotide sequencing | Diagnosis | Heart diseases | DNA sequencing | Heart | Connectin | Transplants & implants | Disease | Genes | Genomics | Medical services | Genomes | Family medical history | Data bases | Eutrophication | Gene sequencing | Integrated circuits | Design | Heterogeneity | Databases | Cardiology | Deoxyribonucleic acid--DNA | Custom designed | Patients | Coronary artery disease | Cost control | Genetic counseling | Dilated cardiomyopathy | Point mutation | Informed consent | Ventricle
Journal Article
Journal Article