Nature Communications, ISSN 2041-1723, 03/2014, Volume 5, Issue 1, p. 3480
Haem oxygenase (HO)-1/carbon monoxide (CO) protects cancer cells from oxidative stress, but the gas-responsive signalling mechanisms remain unknown. Here we...
COLON-CANCER | RAT-LIVER | OXIDATIVE STRESS | CARBON-MONOXIDE | ANTIOXIDANT STATUS | MULTIDISCIPLINARY SCIENCES | CYSTATHIONINE-BETA-SYNTHASE | HYDROGEN-SULFIDE | HEME OXYGENASE-1 | TUMOR-GROWTH | MASS-SPECTROMETRY | Neoplasms - metabolism | Oxidative Stress | Down-Regulation | Humans | Neoplasms - enzymology | Phosphofructokinase-2 - metabolism | Neoplasms - genetics | Phosphofructokinase-2 - genetics | Cell Line, Tumor | Glucose - metabolism | Glycolysis | Heme Oxygenase (Decyclizing) - metabolism | Methylation | Heme Oxygenase (Decyclizing) - genetics | Pentose Phosphate Pathway
COLON-CANCER | RAT-LIVER | OXIDATIVE STRESS | CARBON-MONOXIDE | ANTIOXIDANT STATUS | MULTIDISCIPLINARY SCIENCES | CYSTATHIONINE-BETA-SYNTHASE | HYDROGEN-SULFIDE | HEME OXYGENASE-1 | TUMOR-GROWTH | MASS-SPECTROMETRY | Neoplasms - metabolism | Oxidative Stress | Down-Regulation | Humans | Neoplasms - enzymology | Phosphofructokinase-2 - metabolism | Neoplasms - genetics | Phosphofructokinase-2 - genetics | Cell Line, Tumor | Glucose - metabolism | Glycolysis | Heme Oxygenase (Decyclizing) - metabolism | Methylation | Heme Oxygenase (Decyclizing) - genetics | Pentose Phosphate Pathway
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 1/2012, Volume 109, Issue 4, pp. 1293 - 1298
Enhancement of cerebral blood flow by hypoxia is critical for brain function, but signaling systems underlying its regulation have been unclear. We report a...
Enzymes | Brain | Arterioles | Neurons | Blood vessels | Physiological regulation | Sensors | Brain hypoxia | Vasodilation | Blood flow | Energy metabolism | Neurovascular unit | Gas biology | Gasotransmitter | MULTIDISCIPLINARY SCIENCES | H2S | CYSTATHIONINE BETA-SYNTHASE | DEFICIENT MICE | gas biology | OXYGEN | ENDOGENOUS MODULATOR | HEME | gasotransmitter | NEURAL ACTIVITY | energy metabolism | BRAIN | neurovascular unit | Hydrogen Sulfide - metabolism | Immunohistochemistry | 15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic Acid | Cerebrum - blood supply | DNA Primers - genetics | Cystathionine beta-Synthase - metabolism | Carbon Monoxide - metabolism | Blotting, Western | Microcirculation - physiology | Microscopy, Confocal | Animals | Analysis of Variance | Adenosine Triphosphate - metabolism | Mass Spectrometry | Hypoxia - physiopathology | Mice | Vasodilation - physiology | Heme Oxygenase (Decyclizing) - metabolism | Regional Blood Flow - physiology | Heme Oxygenase (Decyclizing) - genetics | Hydrogen sulfide | Microcirculation | Cerebral circulation | Physiological aspects | Hypoxia | Research | Biological control systems | Biological Sciences
Enzymes | Brain | Arterioles | Neurons | Blood vessels | Physiological regulation | Sensors | Brain hypoxia | Vasodilation | Blood flow | Energy metabolism | Neurovascular unit | Gas biology | Gasotransmitter | MULTIDISCIPLINARY SCIENCES | H2S | CYSTATHIONINE BETA-SYNTHASE | DEFICIENT MICE | gas biology | OXYGEN | ENDOGENOUS MODULATOR | HEME | gasotransmitter | NEURAL ACTIVITY | energy metabolism | BRAIN | neurovascular unit | Hydrogen Sulfide - metabolism | Immunohistochemistry | 15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic Acid | Cerebrum - blood supply | DNA Primers - genetics | Cystathionine beta-Synthase - metabolism | Carbon Monoxide - metabolism | Blotting, Western | Microcirculation - physiology | Microscopy, Confocal | Animals | Analysis of Variance | Adenosine Triphosphate - metabolism | Mass Spectrometry | Hypoxia - physiopathology | Mice | Vasodilation - physiology | Heme Oxygenase (Decyclizing) - metabolism | Regional Blood Flow - physiology | Heme Oxygenase (Decyclizing) - genetics | Hydrogen sulfide | Microcirculation | Cerebral circulation | Physiological aspects | Hypoxia | Research | Biological control systems | Biological Sciences
Journal Article
Nature Communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 1561 - 16
Gold deposition with diagonal angle towards boehmite-based nanostructure creates random arrays of horse-bean-shaped nanostructures named gold-nanofeve (GNF)....
CELLS | DIFFERENCE TIME-DOMAIN | IN-VITRO | SERINE | METABOLISM | CARBON-MONOXIDE | GLUTATHIONE | MULTIDISCIPLINARY SCIENCES | CYSTATHIONINE BETA-SYNTHASE | IDENTIFICATION | TAURINE | Gold - chemistry | Neoplasms - metabolism | Taurine - analogs & derivatives | Antioxidants - chemistry | Glutathione - metabolism | Transaminases - genetics | Antioxidants - metabolism | Humans | Liver - metabolism | Metal Nanoparticles - chemistry | Mice, Inbred C57BL | Gold - metabolism | Male | Spectrum Analysis, Raman - methods | Mice, SCID | Liver - chemistry | Animals | Neoplasms - genetics | Transaminases - metabolism | Female | Mice | Taurine - chemistry | Spectrum Analysis, Raman - instrumentation | Taurine - metabolism | Taurine | Quantum chemistry | Liver | Xenotransplantation | Serine | Parenchyma | Glycine | Metabolites | CD44 antigen | Spectrum analysis | Xenografts | Excitation spectra | Glutathione | Gold | Spectroscopy | Cell survival | Vibration | Immunodeficiency | Nanostructure | Raman spectroscopy | Survival | Glycolysis | Boehmite | Cancer | Tumors
CELLS | DIFFERENCE TIME-DOMAIN | IN-VITRO | SERINE | METABOLISM | CARBON-MONOXIDE | GLUTATHIONE | MULTIDISCIPLINARY SCIENCES | CYSTATHIONINE BETA-SYNTHASE | IDENTIFICATION | TAURINE | Gold - chemistry | Neoplasms - metabolism | Taurine - analogs & derivatives | Antioxidants - chemistry | Glutathione - metabolism | Transaminases - genetics | Antioxidants - metabolism | Humans | Liver - metabolism | Metal Nanoparticles - chemistry | Mice, Inbred C57BL | Gold - metabolism | Male | Spectrum Analysis, Raman - methods | Mice, SCID | Liver - chemistry | Animals | Neoplasms - genetics | Transaminases - metabolism | Female | Mice | Taurine - chemistry | Spectrum Analysis, Raman - instrumentation | Taurine - metabolism | Taurine | Quantum chemistry | Liver | Xenotransplantation | Serine | Parenchyma | Glycine | Metabolites | CD44 antigen | Spectrum analysis | Xenografts | Excitation spectra | Glutathione | Gold | Spectroscopy | Cell survival | Vibration | Immunodeficiency | Nanostructure | Raman spectroscopy | Survival | Glycolysis | Boehmite | Cancer | Tumors
Journal Article
Molecular Brain, ISSN 1756-6606, 2012, Volume 5, Issue 1, pp. 35 - 35
Background: Parkinson's disease (PD) is a neurodegenerative disease characterized by selective degeneration of dopaminergic neurons in the substantia nigra...
Oxidative stress | Mitochondria | Parkinson's disease | Induced pluripotent stem cells | α-synuclein | Parkin | PROTEIN | DISORDERS | MECHANISMS | DEFICIENT MICE | DOPAMINERGIC-NEURONS | alpha-synuclein | NEUROSCIENCES | FIBROBLASTS | PLURIPOTENT STEM-CELLS | RECESSIVE JUVENILE PARKINSONISM | DISEASE | LEWY BODIES | Neurons - pathology | Humans | Middle Aged | Male | Membrane Potential, Mitochondrial - drug effects | Mitochondria - ultrastructure | Brain - metabolism | Neurons - ultrastructure | Carbonyl Cyanide m-Chlorophenyl Hydrazone - pharmacology | Adult | Female | Neurons - metabolism | Parkinson Disease - metabolism | Lewy Bodies - metabolism | Neurons - drug effects | Lewy Bodies - pathology | Induced Pluripotent Stem Cells - metabolism | Induced Pluripotent Stem Cells - pathology | Parkinson Disease - pathology | Induced Pluripotent Stem Cells - drug effects | Induced Pluripotent Stem Cells - ultrastructure | Mitochondria - metabolism | Mitochondria - drug effects | Mitochondria - pathology | Brain - drug effects | Mitochondrial Turnover - drug effects | Animals | Signal Transduction - drug effects | NF-E2-Related Factor 2 - metabolism | Brain - pathology | Aged | Mice | Oxidative Stress - drug effects | Postmortem Changes | alpha-Synuclein - metabolism | Parkinson’s disease
Oxidative stress | Mitochondria | Parkinson's disease | Induced pluripotent stem cells | α-synuclein | Parkin | PROTEIN | DISORDERS | MECHANISMS | DEFICIENT MICE | DOPAMINERGIC-NEURONS | alpha-synuclein | NEUROSCIENCES | FIBROBLASTS | PLURIPOTENT STEM-CELLS | RECESSIVE JUVENILE PARKINSONISM | DISEASE | LEWY BODIES | Neurons - pathology | Humans | Middle Aged | Male | Membrane Potential, Mitochondrial - drug effects | Mitochondria - ultrastructure | Brain - metabolism | Neurons - ultrastructure | Carbonyl Cyanide m-Chlorophenyl Hydrazone - pharmacology | Adult | Female | Neurons - metabolism | Parkinson Disease - metabolism | Lewy Bodies - metabolism | Neurons - drug effects | Lewy Bodies - pathology | Induced Pluripotent Stem Cells - metabolism | Induced Pluripotent Stem Cells - pathology | Parkinson Disease - pathology | Induced Pluripotent Stem Cells - drug effects | Induced Pluripotent Stem Cells - ultrastructure | Mitochondria - metabolism | Mitochondria - drug effects | Mitochondria - pathology | Brain - drug effects | Mitochondrial Turnover - drug effects | Animals | Signal Transduction - drug effects | NF-E2-Related Factor 2 - metabolism | Brain - pathology | Aged | Mice | Oxidative Stress - drug effects | Postmortem Changes | alpha-Synuclein - metabolism | Parkinson’s disease
Journal Article
ASN Neuro, ISSN 1759-0914, 5/2018, Volume 10, p. 1759091418775562
Oxidative stress plays an important role in the onset and progression of Parkinson disease. Although released dopamine at the synaptic terminal is mostly...
glucose | astrocytes | dopamine | glutathione | glutamate | reactive oxygen species | GLUCOSE-UTILIZATION | GLUTAMATE UPTAKE | NEUROSCIENCES | DEFICIENCY | OLIGONUCLEOTIDE MICROARRAY | METABOLISM | NOREPINEPHRINE TRANSPORTER | GENE-EXPRESSION | NEURONS | RAT-BRAIN | Pentose Phosphate Pathway - drug effects | Reactive Oxygen Species | Embryo, Mammalian | Coculture Techniques | Dose-Response Relationship, Drug | NF-E2-Related Factor 2 - genetics | Neurons - drug effects | Dopamine - metabolism | Astrocytes - drug effects | Brain - cytology | Gene Expression Regulation - genetics | Mice, Inbred C57BL | Cells, Cultured | Dopamine - pharmacology | Hydrogen Peroxide - pharmacology | Rats | NF-E2-Related Factor 2 - deficiency | Rats, Sprague-Dawley | Mice, Knockout | Gene Expression Regulation - drug effects | Animals | Lactates - metabolism | Glucose - metabolism | Mice | Oxidative Stress - drug effects | Oxidative stress | Dopamine | Parkinsons disease
glucose | astrocytes | dopamine | glutathione | glutamate | reactive oxygen species | GLUCOSE-UTILIZATION | GLUTAMATE UPTAKE | NEUROSCIENCES | DEFICIENCY | OLIGONUCLEOTIDE MICROARRAY | METABOLISM | NOREPINEPHRINE TRANSPORTER | GENE-EXPRESSION | NEURONS | RAT-BRAIN | Pentose Phosphate Pathway - drug effects | Reactive Oxygen Species | Embryo, Mammalian | Coculture Techniques | Dose-Response Relationship, Drug | NF-E2-Related Factor 2 - genetics | Neurons - drug effects | Dopamine - metabolism | Astrocytes - drug effects | Brain - cytology | Gene Expression Regulation - genetics | Mice, Inbred C57BL | Cells, Cultured | Dopamine - pharmacology | Hydrogen Peroxide - pharmacology | Rats | NF-E2-Related Factor 2 - deficiency | Rats, Sprague-Dawley | Mice, Knockout | Gene Expression Regulation - drug effects | Animals | Lactates - metabolism | Glucose - metabolism | Mice | Oxidative Stress - drug effects | Oxidative stress | Dopamine | Parkinsons disease
Journal Article
Journal of Neuroinflammation, ISSN 1742-2094, 05/2016, Volume 13, Issue 1, p. 99
Background: Toll-like receptor 4 (TLR4) plays a pivotal role in the pathophysiology of stroke-induced inflammation. Both astroglia and microglia express TLR4,...
Ara-C (cytosine β-d-arabinofuranoside hydrochloride) | LME (l-leucine methyl ester) | TLR4 (Toll-like receptor 4) | Astrocyte | ROS (reactive oxygen species) | RNS (reactive nitrogen species) | POSTISCHEMIC INFLAMMATION | OXIDATIVE STRESS | IMMUNOLOGY | LME (L-leucine methyl ester) | NEUROSCIENCES | Ara-C (cytosine beta-D-arabinofuranoside hydrochloride) | REACTIVE OXYGEN | IMMUNE-RESPONSES | CEREBRAL-ARTERY OCCLUSION | TOLL-LIKE RECEPTORS | GENE-EXPRESSION | ISCHEMIC BRAIN-INJURY | ENERGY-METABOLISM | NF-KAPPA-B | Immunohistochemistry | NF-E2-Related Factor 2 - physiology | Microglia - metabolism | Lipopolysaccharides - toxicity | Pentose Phosphate Pathway - physiology | Reactive Oxygen Species - metabolism | Oxidative Stress - physiology | Cells, Cultured | Rats | Kelch-Like ECH-Associated Protein 1 - metabolism | Reverse Transcriptase Polymerase Chain Reaction | Rats, Sprague-Dawley | Blotting, Western | Stroke - metabolism | Animals | Spectrometry, Mass, Electrospray Ionization | Signal Transduction - physiology | In Vitro Techniques | Nitric Oxide - metabolism | Astrocytes - metabolism | Disease Models, Animal | Stroke (Disease) | Complications and side effects | Physiology, Pathological | Analysis | Influence | Inflammation | Research | Risk factors | Lipopolysaccharides
Ara-C (cytosine β-d-arabinofuranoside hydrochloride) | LME (l-leucine methyl ester) | TLR4 (Toll-like receptor 4) | Astrocyte | ROS (reactive oxygen species) | RNS (reactive nitrogen species) | POSTISCHEMIC INFLAMMATION | OXIDATIVE STRESS | IMMUNOLOGY | LME (L-leucine methyl ester) | NEUROSCIENCES | Ara-C (cytosine beta-D-arabinofuranoside hydrochloride) | REACTIVE OXYGEN | IMMUNE-RESPONSES | CEREBRAL-ARTERY OCCLUSION | TOLL-LIKE RECEPTORS | GENE-EXPRESSION | ISCHEMIC BRAIN-INJURY | ENERGY-METABOLISM | NF-KAPPA-B | Immunohistochemistry | NF-E2-Related Factor 2 - physiology | Microglia - metabolism | Lipopolysaccharides - toxicity | Pentose Phosphate Pathway - physiology | Reactive Oxygen Species - metabolism | Oxidative Stress - physiology | Cells, Cultured | Rats | Kelch-Like ECH-Associated Protein 1 - metabolism | Reverse Transcriptase Polymerase Chain Reaction | Rats, Sprague-Dawley | Blotting, Western | Stroke - metabolism | Animals | Spectrometry, Mass, Electrospray Ionization | Signal Transduction - physiology | In Vitro Techniques | Nitric Oxide - metabolism | Astrocytes - metabolism | Disease Models, Animal | Stroke (Disease) | Complications and side effects | Physiology, Pathological | Analysis | Influence | Inflammation | Research | Risk factors | Lipopolysaccharides
Journal Article
Clinical Chemistry, ISSN 0009-9147, 10/2018, Volume 64, Issue 10, pp. 1463 - 1473
BACKGROUND: Although circulating exosomes in blood play crucial roles in cancer development and progression, difficulties in quantifying exosomes hamper their...
CELLS | EXTRACELLULAR VESICLES | MARKERS | MEDICAL LABORATORY TECHNOLOGY | PROTEINS | CANCER | MODULATION | BEADS | Cell culture | Flow cytometry | CD9 antigen | Ovarian carcinoma | Surface antigens | Colorectal cancer | Antibodies | CD147 antigen | Exosomes | Ovarian cancer | Proteins | Carcinoembryonic antigen | Epidermal growth factor | Optical properties | Labeling | Growth factors | Enzyme-linked immunosorbent assay | Antigens | Immunoglobulins | CD63 antigen | Cloning | Breast cancer | Roles | Patients | ErbB-2 protein | Disk drives | Blood circulation | Linearity | MicroRNAs | Methods | Counting | Cancer
CELLS | EXTRACELLULAR VESICLES | MARKERS | MEDICAL LABORATORY TECHNOLOGY | PROTEINS | CANCER | MODULATION | BEADS | Cell culture | Flow cytometry | CD9 antigen | Ovarian carcinoma | Surface antigens | Colorectal cancer | Antibodies | CD147 antigen | Exosomes | Ovarian cancer | Proteins | Carcinoembryonic antigen | Epidermal growth factor | Optical properties | Labeling | Growth factors | Enzyme-linked immunosorbent assay | Antigens | Immunoglobulins | CD63 antigen | Cloning | Breast cancer | Roles | Patients | ErbB-2 protein | Disk drives | Blood circulation | Linearity | MicroRNAs | Methods | Counting | Cancer
Journal Article
Cell Stem Cell, ISSN 1934-5909, 01/2013, Volume 12, Issue 1, pp. 127 - 137
Heart disease remains a major cause of death despite advances in medical technology. Heart-regenerative therapy that uses pluripotent stem cells (PSCs) is a...
HEARTS | LACTATE | MUSCLE | DIFFERENTIATION | FETAL | CELL & TISSUE ENGINEERING | CELL BIOLOGY | Mice | Animals | Pluripotent Stem Cells - cytology | Myocytes, Cardiac - cytology | Cell Culture Techniques - methods | Humans
HEARTS | LACTATE | MUSCLE | DIFFERENTIATION | FETAL | CELL & TISSUE ENGINEERING | CELL BIOLOGY | Mice | Animals | Pluripotent Stem Cells - cytology | Myocytes, Cardiac - cytology | Cell Culture Techniques - methods | Humans
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 9/2015, Volume 112, Issue 37, pp. 11642 - 11647
Loss of prolyl hydroxylase 2 (PHD2) activates the hypoxia-inducible factor-dependent hypoxic response, including anaerobic glycolysis, which causes large...
Hyperlactatemia | Sepsis | PHD inhibitor | Hypoxic response | Gluconeogenesis | hyperlactatemia | MYOCARDIAL-INFARCTION | HIF | MULTIDISCIPLINARY SCIENCES | MOUSE | HYPOXIA | gluconeogenesis | FAMILY | INACTIVATION | hypoxic response | METABOLISM | LACTATE | DISEASE | SEPTIC SHOCK | sepsis | Liver - metabolism | Mice, Inbred C57BL | Blood Gas Analysis | Genotype | Male | Hepatocytes - metabolism | Oxygen - metabolism | Hypoxia - metabolism | Mice, Knockout | Animals | Lactates - metabolism | Hypoxia-Inducible Factor 1, alpha Subunit - metabolism | Hypoxia-Inducible Factor-Proline Dioxygenases - metabolism | Sepsis - metabolism | Acidosis, Lactic - metabolism | Mice | Blood Glucose - metabolism | Physical Conditioning, Animal | Physiological aspects | Hydroxylases | Acidosis | Health aspects | Liver | Biological Sciences
Hyperlactatemia | Sepsis | PHD inhibitor | Hypoxic response | Gluconeogenesis | hyperlactatemia | MYOCARDIAL-INFARCTION | HIF | MULTIDISCIPLINARY SCIENCES | MOUSE | HYPOXIA | gluconeogenesis | FAMILY | INACTIVATION | hypoxic response | METABOLISM | LACTATE | DISEASE | SEPTIC SHOCK | sepsis | Liver - metabolism | Mice, Inbred C57BL | Blood Gas Analysis | Genotype | Male | Hepatocytes - metabolism | Oxygen - metabolism | Hypoxia - metabolism | Mice, Knockout | Animals | Lactates - metabolism | Hypoxia-Inducible Factor 1, alpha Subunit - metabolism | Hypoxia-Inducible Factor-Proline Dioxygenases - metabolism | Sepsis - metabolism | Acidosis, Lactic - metabolism | Mice | Blood Glucose - metabolism | Physical Conditioning, Animal | Physiological aspects | Hydroxylases | Acidosis | Health aspects | Liver | Biological Sciences
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 12035 - 13
The energy metabolism of the failing heart is characterized by reduced fatty acid (FA) oxidation and an increase in glucose utilization. However, little is...
MULTIDISCIPLINARY SCIENCES | DISEASE | GROWTH | CARDIAC DYSFUNCTION | MECHANISMS | ANAPLEROSIS | ABSORPTION | EXPRESSION | DEFICIENCY | CARDIOMYOCYTE-SPECIFIC ABLATION | CYCLE | Heart failure | Tricarboxylic acid cycle | Energy metabolism | Contractility | CD36 antigen | Metabolism | Pressure | Fatty acids | Muscle contraction | Glucose metabolism | Clonal deletion | Fibrosis | Glycolysis | Aorta | Oxidation | Heart diseases | Hypertrophy
MULTIDISCIPLINARY SCIENCES | DISEASE | GROWTH | CARDIAC DYSFUNCTION | MECHANISMS | ANAPLEROSIS | ABSORPTION | EXPRESSION | DEFICIENCY | CARDIOMYOCYTE-SPECIFIC ABLATION | CYCLE | Heart failure | Tricarboxylic acid cycle | Energy metabolism | Contractility | CD36 antigen | Metabolism | Pressure | Fatty acids | Muscle contraction | Glucose metabolism | Clonal deletion | Fibrosis | Glycolysis | Aorta | Oxidation | Heart diseases | Hypertrophy
Journal Article
Frontiers in Microbiology, ISSN 1664-302X, 11/2018, Volume 9, p. 2902
Coenzyme A (CoA) is an essential cofactor for numerous cellular reactions in all living organisms. In the protozoan parasite Entamoeba histolytica, CoA is...
Metabolome | Gene silencing | Coenzyme A | Entamoeba histolytica | Drug development | TARGET | PURINE | CRYSTAL-STRUCTURE | gene silencing | drug development | MICROBIOLOGY | IDENTIFICATION | DISCOVERY | coenzyme A | NUCLEOSIDE | ERYTHROCYTES | PLASMODIUM-FALCIPARUM | SEQUENCE ALIGNMENT | METRONIDAZOLE | metabolome
Metabolome | Gene silencing | Coenzyme A | Entamoeba histolytica | Drug development | TARGET | PURINE | CRYSTAL-STRUCTURE | gene silencing | drug development | MICROBIOLOGY | IDENTIFICATION | DISCOVERY | coenzyme A | NUCLEOSIDE | ERYTHROCYTES | PLASMODIUM-FALCIPARUM | SEQUENCE ALIGNMENT | METRONIDAZOLE | metabolome
Journal Article
Scientific Reports, ISSN 2045-2322, 01/2017, Volume 7, Issue 1, p. 39752
Histone acetylation has been linked to cardiac hypertrophy and heart failure. However, the pathological implications of changes in histone methylation and the...
CARVEDILOL | METHYLATION | MULTIDISCIPLINARY SCIENCES | CARDIAC-HYPERTROPHY | GENE-EXPRESSION | HDAC INHIBITION | GENECODIS | DEACETYLASES | DILATED CARDIOMYOPATHY | IDENTIFICATION | ENRICHMENT ANALYSIS | RNA, Small Interfering - genetics | Prognosis | Humans | Cardiomegaly - drug therapy | Rats | Male | Nuclear Proteins - metabolism | Piperazines - therapeutic use | Transcription Factors - genetics | Rats, Sprague-Dawley | Heart Failure - drug therapy | Transcription Factors - metabolism | Histone-Lysine N-Methyltransferase - antagonists & inhibitors | Animals | Cardiomegaly - diagnosis | Cardiomegaly - chemically induced | Heart Failure - diagnosis | Acetylation | Diet Therapy | Nuclear Proteins - genetics | Chronic Disease | Sodium Chloride - metabolism | Heart Failure - chemically induced | Heart failure | Gene silencing | Mitochondria | Lysine | Medical prognosis | Rodents | Histone methyltransferase | Methylation | Heart diseases | Hypertrophy
CARVEDILOL | METHYLATION | MULTIDISCIPLINARY SCIENCES | CARDIAC-HYPERTROPHY | GENE-EXPRESSION | HDAC INHIBITION | GENECODIS | DEACETYLASES | DILATED CARDIOMYOPATHY | IDENTIFICATION | ENRICHMENT ANALYSIS | RNA, Small Interfering - genetics | Prognosis | Humans | Cardiomegaly - drug therapy | Rats | Male | Nuclear Proteins - metabolism | Piperazines - therapeutic use | Transcription Factors - genetics | Rats, Sprague-Dawley | Heart Failure - drug therapy | Transcription Factors - metabolism | Histone-Lysine N-Methyltransferase - antagonists & inhibitors | Animals | Cardiomegaly - diagnosis | Cardiomegaly - chemically induced | Heart Failure - diagnosis | Acetylation | Diet Therapy | Nuclear Proteins - genetics | Chronic Disease | Sodium Chloride - metabolism | Heart Failure - chemically induced | Heart failure | Gene silencing | Mitochondria | Lysine | Medical prognosis | Rodents | Histone methyltransferase | Methylation | Heart diseases | Hypertrophy
Journal Article