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by Murata, K and Mori, M and Ito, H
Journal of the Neurological Sciences, ISSN 0022-510X, 10/2017, Volume 381, pp. 820 - 821
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 12/2013, Volume 22, Issue 24, pp. 4914 - 4928
Phosphorodiamidate morpholino oligomer (PMO)-mediated exon skipping is among the more promising approaches to the treatment of several neuromuscular disorders... 
Cardiotoxins
Journal Article
PLoS ONE, 08/2013, Volume 8, Issue 8
Background Systemic elevations in PAI-1 suppress the fibrinolytic pathway leading to poor collagen remodelling and delayed regeneration of tibialis anterior... 
Cardiotoxins
Journal Article
PloS one, ISSN 1932-6203, 2016, Volume 11, Issue 1, pp. e0147198 - e0147198
Background A longstanding goal in regenerative medicine is to reconstitute functional tissus or organs after injury or disease. Attention has focused on the... 
SKELETAL-MUSCLE | SATELLITE CELL NICHE | STEM-CELLS | ADULT MUSCLE | MACROPHAGES | MYOGENESIS | MULTIDISCIPLINARY SCIENCES | ENDOTHELIAL-CELLS | SELF-RENEWAL | PROLIFERATION | TEMPLATE DNA STRANDS | Barium Compounds - toxicity | Chlorides - toxicity | Muscle, Skeletal - injuries | Cytokines - physiology | Necrosis | Muscle Development | Cold Injury - pathology | Muscle, Skeletal - drug effects | Satellite Cells, Skeletal Muscle - physiology | Freezing - adverse effects | Models, Animal | Myoblasts - physiology | Elapid Venoms - toxicity | Macrophages - physiology | Green Fluorescent Proteins - analysis | Vascular Endothelial Growth Factor Receptor-2 - analysis | Mice, Inbred C57BL | Cobra Cardiotoxin Proteins - toxicity | Mice, Transgenic | Muscle, Skeletal - physiology | Regeneration - physiology | Animals | Fibrosis | Stem Cells - physiology | Mice | Muscle, Skeletal - pathology | Neovascularization, Physiologic | Regeneration - immunology | Cold Injury - physiopathology | Cycles | Barium | Animal models | Transplants & implants | Transgenic | Stem cell transplantation | Confocal microscopy | Infections | Confocal | Epidemiology | Regeneration (physiology) | Cell growth | Histopathology | Rodents | Cell cycle | Gangrene | Basal lamina | Injuries | Immune system | Cytokines | Tissue engineering | Organs | Muscles | Blood vessels | Cell division | Inflammation | Skeletal muscle | Barium chloride | Regeneration | Musculoskeletal system | Microscopy | Experimental design | Stem cells | Infiltration | Chemokines | Index Medicus | Green Fluorescent Proteins | Cobra Cardiotoxin Proteins | Macrophages | Cellular Biology | Vascular Endothelial Growth Factor Receptor-2 | Freezing | Stem Cells | Life Sciences | Cold Injury | Barium Compounds | Chlorides | Myoblasts | Elapid Venoms | Muscle, Skeletal | Satellite Cells, Skeletal Muscle
Journal Article
Nature Medicine, ISSN 1078-8956, 08/2012, Volume 18, Issue 8, pp. 1262 - 1270
Profibrotic cells that develop upon injury generate permanent scar tissue and impair organ recovery, though their origin and fate are unclear. Here we show... 
MEDICINE, RESEARCH & EXPERIMENTAL | PERIPHERAL-NERVES | BIOCHEMISTRY & MOLECULAR BIOLOGY | LIVER FIBROSIS | MESENCHYMAL STEM-CELLS | BETA | CELL BIOLOGY | SKELETAL-MUSCLE | IN-VIVO | MELTRIN ALPHA | SCHWANN-CELLS | NEURAL CREST | EXPRESSION | Ear, External - injuries | Freund's Adjuvant - toxicity | Stromal Cells - pathology | Ear, External - pathology | Muscle, Skeletal - metabolism | Muscle, Skeletal - injuries | Wound Healing | Gene Knockdown Techniques | Parabiosis | Myofibroblasts - metabolism | ADAM12 Protein | Ear, External - metabolism | ADAM Proteins - analysis | Collagen - biosynthesis | Receptor, Platelet-Derived Growth Factor alpha - analysis | Genes, Reporter | Myofibroblasts - pathology | Acute Disease | Dermis - metabolism | Specific Pathogen-Free Organisms | Leg Injuries - metabolism | Stromal Cells - metabolism | ADAM Proteins - deficiency | Cobra Cardiotoxin Proteins - toxicity | Mice, Transgenic | Adipocytes - pathology | Blood Vessels - cytology | Leg Injuries - pathology | Cell Lineage | Animals | Fibrosis | Dermis - pathology | Cicatrix - pathology | Dermis - injuries | Mice | Muscle, Skeletal - pathology | ADAM Proteins - genetics | Crosses, Genetic | Care and treatment | Growth | Stem cells | Genetic aspects | Research | Diagnosis | Gene expression | Cell differentiation | Proteins | Blood vessels | Signal transduction | Cell growth | Injuries | Blood Vessels | Cobra Cardiotoxin Proteins | Dermis | Adipocytes | Cicatrix | Life Sciences | Stromal Cells | Immunology | Leg Injuries | ADAM Proteins | Ear, External | Freund's Adjuvant | Receptor, Platelet-Derived Growth Factor alpha | Collagen | Muscle, Skeletal | Myofibroblasts
Journal Article
Toxicon, ISSN 0041-0101, 06/2015, Volume 99, pp. 23 - 35
The venom proteome of the monocled cobra, , from Thailand, was characterized by RP-HPLC, SDS-PAGE, and MALDI-TOF-TOF analyses, yielding 38 different proteins... 
Monocled cobra | Naja kaouthia | Snake venom: proteomics | Toxicity | Immunity | Human IgG response | BITE | ANTIVENOM DEVELOPMENT | PHAGE DISPLAY | PHOSPHOLIPASE A | ELAPIDAE | SINGLE-DOMAIN ANTIBODIES | SKELETAL-MUSCLE | EVOLUTION | PURIFICATION | PHARMACOLOGY & PHARMACY | THAI COBRA | TOXICOLOGY | Elapid Venoms - chemistry | Immunoglobulin G - isolation & purification | Reptilian Proteins - chemistry | Peptide Fragments - toxicity | Humans | Molecular Sequence Data | Snake Bites - metabolism | Cobra Cardiotoxin Proteins - chemistry | Cobra Cardiotoxin Proteins - antagonists & inhibitors | Thailand | Snake Bites - immunology | Cobra Neurotoxin Proteins - antagonists & inhibitors | Peptide Mapping | Immunoglobulin G - analysis | Snake Bites - blood | Cobra Cardiotoxin Proteins - isolation & purification | Elapidae - immunology | Phospholipases A2 - chemistry | Elapid Venoms - toxicity | Amino Acid Sequence | Antivenins - analysis | Enzyme-Linked Immunosorbent Assay | Cobra Neurotoxin Proteins - isolation & purification | Peptide Fragments - isolation & purification | Cobra Neurotoxin Proteins - toxicity | Cobra Cardiotoxin Proteins - toxicity | Elapid Venoms - antagonists & inhibitors | Lethal Dose 50 | Phospholipases A2 - toxicity | Reptilian Proteins - isolation & purification | Cobra Neurotoxin Proteins - chemistry | Peptide Fragments - chemistry | Animals | Peptide Fragments - antagonists & inhibitors | Elapidae - metabolism | Proteomics | Mice | Reptilian Proteins - toxicity | Reptilian Proteins - antagonists & inhibitors | Phospholipases A2 - isolation & purification | Oxidases | Cysteine | Analysis | Immunoglobulin G | Venom | Nerve growth factor | Investigations | Enzyme-linked immunosorbent assay | Nucleotidases | Index Medicus | Human | Proteins | Adenosines | Nucleosides | Toxins | Snakes | ELISA
Journal Article
ChemBioChem, ISSN 1439-4227, 08/2012, Volume 13, Issue 12, pp. 1805 - 1812
Insulin secretion from pancreatic β‐cells is a complex process, involving the integration and interaction of multiple external and internal stimuli, in which... 
peptides | structure–function relationships | insulin | cardiotoxin‐I | ion channels | Ion channels | Peptides | Insulin | Cardiotoxin-I | Structure-function relationships | CHEMISTRY, MEDICINAL | BIOCHEMISTRY & MOLECULAR BIOLOGY | cardiotoxin-I | COBRA VENOM CARDIOTOXIN | TOXINS | SKELETAL-MUSCLE | GLUCAGON-LIKE PEPTIDE-1 | structure-function relationships | ION-CHANNEL | PANCREATIC BETA-CELLS | TITYUS-SERRULATUS | SECRETION | TAIWAN COBRA | K+ CHANNEL | Elapid Venoms - chemistry | Hemolysis - drug effects | Humans | Cobra Cardiotoxin Proteins - pharmacology | Molecular Sequence Data | Cobra Cardiotoxin Proteins - chemistry | Insulin-Secreting Cells - metabolism | Insulin-Secreting Cells - cytology | Insulin Secretion | Cobra Cardiotoxin Proteins - isolation & purification | Amino Acid Sequence | Cell Line | Cell Survival | Tissue Culture Techniques | Aorta - drug effects | Elapidae - physiology | Models, Molecular | Rats | Complex Mixtures - chemistry | Glucose - pharmacology | Hypoglycemic Agents - chemistry | Erythrocytes - drug effects | Hypoglycemic Agents - pharmacology | L-Lactate Dehydrogenase | Hypoglycemic Agents - isolation & purification | Insulin - metabolism | Animals | Insulin-Secreting Cells - drug effects | Chemical Fractionation | Glucose - metabolism | Pancreatic beta cells | Metabolites | Venom | Glucose | Dextrose | Index Medicus | Life Sciences | Biomolecules | Biochemistry, Molecular Biology
Journal Article
Protein Expression and Purification, ISSN 1046-5928, 02/2017, Volume 130, pp. 13 - 20
Journal Article
Toxins, ISSN 2072-6651, 01/2019, Volume 11, Issue 1, p. 52
Native disulfide formation is crucial to the process of disulfide-rich protein folding in vitro. As such, analysis of the disulfide bonds can be used to track... 
Cardiotoxin | Disulfide bond analysis | Folding isomer | Mass spectrometry | PEPTIDES | COBRA CARDIOTOXIN | folding isomer | STABILITY | FOOD SCIENCE & TECHNOLOGY | VENOM CARDIOTOXIN | TOXINS | disulfide bond analysis | mass spectrometry | TOXICOLOGY | PROTEINS | cardiotoxin
Journal Article