Journal of Biosciences, ISSN 0250-5991, 9/2018, Volume 43, Issue 4, pp. 707 - 715
Antibiotic resistance in bacteria is a major health concern. Antimicrobial peptides (AMPs) are a class of peptides that are efficient in killing most microbes...
Life Sciences | Biomedicine, general | Life Sciences, general | Microbiology | Zoology | Antimicrobial peptides | human β defensin-3 | pore-forming peptides | Plant Sciences | Cell Biology | peptide–lipid interaction | RESISTANT | HUMAN BETA-DEFENSIN-3 | MEMBRANE | BIOLOGY | peptide-lipid interaction | human beta defensin-3 | beta-Defensins - genetics | Antimicrobial Cationic Peptides - chemistry | Humans | Antimicrobial Cationic Peptides - pharmacology | Bacteria - drug effects | Amino Acid Sequence - genetics | beta-Defensins - chemistry | Microbial Sensitivity Tests | Protein Conformation, beta-Strand | X-Ray Diffraction | Anti-Bacterial Agents - chemistry | beta-Defensins - pharmacology | Anti-Bacterial Agents - pharmacology | Bacteria - pathogenicity | Circular Dichroism | Physiological aspects | Drug resistance in microorganisms | Genetic aspects | Research | Scanning electron microscopy | Membranes | Peptides | Outer membranes | Serine | Tertiary | Amino acids | Confocal microscopy | Electron microscopy | Small angle X ray scattering | Circular dichroism | Mode of action | Disease resistance | X-ray scattering | Antibiotics | Antibiotic resistance | Dichroism | Bacteria | Antibacterial activity | X ray scattering | Control resistance | Curvature | Pore formation
Life Sciences | Biomedicine, general | Life Sciences, general | Microbiology | Zoology | Antimicrobial peptides | human β defensin-3 | pore-forming peptides | Plant Sciences | Cell Biology | peptide–lipid interaction | RESISTANT | HUMAN BETA-DEFENSIN-3 | MEMBRANE | BIOLOGY | peptide-lipid interaction | human beta defensin-3 | beta-Defensins - genetics | Antimicrobial Cationic Peptides - chemistry | Humans | Antimicrobial Cationic Peptides - pharmacology | Bacteria - drug effects | Amino Acid Sequence - genetics | beta-Defensins - chemistry | Microbial Sensitivity Tests | Protein Conformation, beta-Strand | X-Ray Diffraction | Anti-Bacterial Agents - chemistry | beta-Defensins - pharmacology | Anti-Bacterial Agents - pharmacology | Bacteria - pathogenicity | Circular Dichroism | Physiological aspects | Drug resistance in microorganisms | Genetic aspects | Research | Scanning electron microscopy | Membranes | Peptides | Outer membranes | Serine | Tertiary | Amino acids | Confocal microscopy | Electron microscopy | Small angle X ray scattering | Circular dichroism | Mode of action | Disease resistance | X-ray scattering | Antibiotics | Antibiotic resistance | Dichroism | Bacteria | Antibacterial activity | X ray scattering | Control resistance | Curvature | Pore formation
Journal Article
BBA - Biomembranes, ISSN 0005-2736, 2006, Volume 1758, Issue 9, pp. 1499 - 1512
A group of interesting molecules called defensins exhibit multiple functions but have been primarily recognized to possess a broad spectrum of antimicrobial...
Antibacterial peptide | Innate and adaptive immunity | Membrane-disruption | Defensin | Structure | HβD-3 | HUMAN BETA-DEFENSINS | HELICAL ANTIMICROBIAL PEPTIDES | DISULFIDE BONDS | H beta D-3 | SOLID-STATE NMR | MAMMALIAN DEFENSINS | BIOCHEMISTRY & MOLECULAR BIOLOGY | innate and adaptive immunity | LIPID-MEMBRANES | structure | IMMATURE DENDRITIC CELLS | antibacterial peptide | BIOPHYSICS | BACTERICIDAL ACTIVITY | defensin | HOST-DEFENSE | membrane-disruption | INNATE IMMUNITY | Peptides | Proteases | Antibacterial agents | Analysis
Antibacterial peptide | Innate and adaptive immunity | Membrane-disruption | Defensin | Structure | HβD-3 | HUMAN BETA-DEFENSINS | HELICAL ANTIMICROBIAL PEPTIDES | DISULFIDE BONDS | H beta D-3 | SOLID-STATE NMR | MAMMALIAN DEFENSINS | BIOCHEMISTRY & MOLECULAR BIOLOGY | innate and adaptive immunity | LIPID-MEMBRANES | structure | IMMATURE DENDRITIC CELLS | antibacterial peptide | BIOPHYSICS | BACTERICIDAL ACTIVITY | defensin | HOST-DEFENSE | membrane-disruption | INNATE IMMUNITY | Peptides | Proteases | Antibacterial agents | Analysis
Journal Article
JOURNAL OF GENE MEDICINE, ISSN 1099-498X, 03/2009, Volume 11, Issue 3, pp. 220 - 228
Background Infected wounds present a major complication in patients with diabetes. Staphylococcus aureus is the most common single isolate in diabetic wounds....
MEDICINE, RESEARCH & EXPERIMENTAL | HUMAN BETA-DEFENSINS | wound healing | gene transfer | HUMAN SKIN | MAST-CELLS | INNATE IMMUNE-RESPONSE | ANTIMICROBIAL PEPTIDES | bacterial infection | IN-VITRO | S. aureus | innate immunity | host defense peptides | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | GENETICS & HEREDITY | HOST-DEFENSE | FOOT ULCERS | STAPHYLOCOCCUS-AUREUS | EXPRESSION
MEDICINE, RESEARCH & EXPERIMENTAL | HUMAN BETA-DEFENSINS | wound healing | gene transfer | HUMAN SKIN | MAST-CELLS | INNATE IMMUNE-RESPONSE | ANTIMICROBIAL PEPTIDES | bacterial infection | IN-VITRO | S. aureus | innate immunity | host defense peptides | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | GENETICS & HEREDITY | HOST-DEFENSE | FOOT ULCERS | STAPHYLOCOCCUS-AUREUS | EXPRESSION
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 12/2014, Volume 111, Issue 52, pp. 18703 - 18708
The pulmonary airways are continuously exposed to bacteria. As a first line of defense against infection, the airway surface liquid (ASL) contains a complex...
Antibacterials | Liquids | Lungs | Antimicrobials | Lung diseases | Luminescence | Cystic fibrosis | Bacteria | Synergism | Cathelicidin | Pseudomonas aeruginosa | Host defense | Staphylococcus aureus | DEFB1 GENE | cathelicidin | MULTIDISCIPLINARY SCIENCES | host defense | BREATH CONDENSATE | IN-VITRO | PEPTIDES | BACTERICIDAL ACTIVITY | ANTIBACTERIAL ACTIVITY | cystic fibrosis | CYSTIC-FIBROSIS PATIENTS | PRECURSOR LIPID II | STAPHYLOCOCCUS-AUREUS | INNATE IMMUNITY | Drug Synergism | beta-Defensins - agonists | Antimicrobial Cationic Peptides - agonists | Anti-Infective Agents - pharmacology | Humans | Pseudomonas aeruginosa - growth & development | Antimicrobial Cationic Peptides - pharmacology | beta-Defensins - pharmacology | Staphylococcus aureus - growth & development | Hydrogen-Ion Concentration | Biological Sciences
Antibacterials | Liquids | Lungs | Antimicrobials | Lung diseases | Luminescence | Cystic fibrosis | Bacteria | Synergism | Cathelicidin | Pseudomonas aeruginosa | Host defense | Staphylococcus aureus | DEFB1 GENE | cathelicidin | MULTIDISCIPLINARY SCIENCES | host defense | BREATH CONDENSATE | IN-VITRO | PEPTIDES | BACTERICIDAL ACTIVITY | ANTIBACTERIAL ACTIVITY | cystic fibrosis | CYSTIC-FIBROSIS PATIENTS | PRECURSOR LIPID II | STAPHYLOCOCCUS-AUREUS | INNATE IMMUNITY | Drug Synergism | beta-Defensins - agonists | Antimicrobial Cationic Peptides - agonists | Anti-Infective Agents - pharmacology | Humans | Pseudomonas aeruginosa - growth & development | Antimicrobial Cationic Peptides - pharmacology | beta-Defensins - pharmacology | Staphylococcus aureus - growth & development | Hydrogen-Ion Concentration | Biological Sciences
Journal Article
PLoS ONE, ISSN 1932-6203, 07/2016, Volume 11, Issue 7, p. e0159700
This study was performed to investigate the effects of genetically modified (GM) milk containing human beta-defensin-3 (HBD3) on mice by a 90-day feeding...
ANIMALS | DIGESTION | IN-VITRO | FOOD ALLERGENS | SAFETY ASSESSMENT | STABILITY | MULTIDISCIPLINARY SCIENCES | CATTLE | RATS | RISK-ASSESSMENT | MEAT | beta-Defensins - genetics | Animals | Milk - metabolism | Consumer Product Safety | Humans | Food, Genetically Modified - adverse effects | Gastrointestinal Tract - drug effects | Mice | Digestion | Milk - adverse effects | Analysis | Gastrointestinal system | Genetically modified organisms | Physiological aspects | Chemical properties | Research | Health aspects | Milk | Veterinary colleges | Neurosciences | Disease | Laboratories | Microflora | Drug resistance | Veterinary medicine | Immunity | Proteins | E coli | Cattle | Intestine | Bacteria | Physiology | Intestinal microflora | Product safety | Genetic modification | Food | Digestibility | Nutrition | Gene transfer | Health | Gastric emptying | Antimicrobial agents | Gastrointestinal tract | Permeability | Risk analysis | Chemistry | Antibiotics | Breast milk
ANIMALS | DIGESTION | IN-VITRO | FOOD ALLERGENS | SAFETY ASSESSMENT | STABILITY | MULTIDISCIPLINARY SCIENCES | CATTLE | RATS | RISK-ASSESSMENT | MEAT | beta-Defensins - genetics | Animals | Milk - metabolism | Consumer Product Safety | Humans | Food, Genetically Modified - adverse effects | Gastrointestinal Tract - drug effects | Mice | Digestion | Milk - adverse effects | Analysis | Gastrointestinal system | Genetically modified organisms | Physiological aspects | Chemical properties | Research | Health aspects | Milk | Veterinary colleges | Neurosciences | Disease | Laboratories | Microflora | Drug resistance | Veterinary medicine | Immunity | Proteins | E coli | Cattle | Intestine | Bacteria | Physiology | Intestinal microflora | Product safety | Genetic modification | Food | Digestibility | Nutrition | Gene transfer | Health | Gastric emptying | Antimicrobial agents | Gastrointestinal tract | Permeability | Risk analysis | Chemistry | Antibiotics | Breast milk
Journal Article
Journal of Materials Science: Materials in Medicine, ISSN 0957-4530, 2/2015, Volume 26, Issue 2, pp. 1 - 10
Human β-defensin-3 (hBD-3) has been found in synovial fluid and later in periprosthetic tissues in septic joint implant loosening. The aim of the present study...
Biomedical Engineering | Polymer Sciences | Regenerative Medicine/Tissue Engineering | Ceramics, Glass, Composites, Natural Methods | Material Science | Surfaces and Interfaces, Thin Films | Biomaterials | HUMAN BETA-DEFENSINS | DIAGNOSIS | MATERIALS SCIENCE, BIOMATERIALS | EPITHELIAL-CELLS | DENDRITIC CELLS | ENGINEERING, BIOMEDICAL | TOLL-LIKE RECEPTORS | INFECTION | ANTIMICROBIAL PEPTIDES | EXPRESSION | HIP | BIOFILM FORMATION | Heat shock proteins | Analysis | Robots | Resveratrol | Surgical outcomes | Prostheses | Body fluids | Biomedical materials | Joint replacement surgery | Human | Cellular | Fluid dynamics | Loosening | Fluid flow | Staining | Bacteria | Endothelial cells
Biomedical Engineering | Polymer Sciences | Regenerative Medicine/Tissue Engineering | Ceramics, Glass, Composites, Natural Methods | Material Science | Surfaces and Interfaces, Thin Films | Biomaterials | HUMAN BETA-DEFENSINS | DIAGNOSIS | MATERIALS SCIENCE, BIOMATERIALS | EPITHELIAL-CELLS | DENDRITIC CELLS | ENGINEERING, BIOMEDICAL | TOLL-LIKE RECEPTORS | INFECTION | ANTIMICROBIAL PEPTIDES | EXPRESSION | HIP | BIOFILM FORMATION | Heat shock proteins | Analysis | Robots | Resveratrol | Surgical outcomes | Prostheses | Body fluids | Biomedical materials | Joint replacement surgery | Human | Cellular | Fluid dynamics | Loosening | Fluid flow | Staining | Bacteria | Endothelial cells
Journal Article
European Journal of Medicinal Chemistry, ISSN 0223-5234, 02/2015, Volume 91, pp. 91 - 99
Human beta defensin-3 (HβD-3) is a host-defense protein exhibiting antibacterial activity towards both Gram-negative and Gram-positive bacteria. There is...
Fluorescence | Solid-state NMR | Dye leakage | HβD3 | Antimicrobial peptide | PARDAXIN | CHEMISTRY, MEDICINAL | MECHANISM | BETA-DEFENSINS | PERMEABILIZATION | INDUCTION | IDENTIFICATION | LIPID COMPOSITION | HUMAN-NEUTROPHILS | H beta D3 | EXPRESSION | ANTIBACTERIAL PEPTIDE | Fluoresceins - metabolism | Humans | Cell Membrane Permeability | Fluorescent Dyes - metabolism | Molecular Sequence Data | Structure-Activity Relationship | Cell Membrane - chemistry | Microbial Sensitivity Tests | Salmonella enterica - drug effects | Peptides - chemical synthesis | Biological Transport - drug effects | Cell Membrane - drug effects | Staphylococcus aureus - metabolism | Protein Structure, Tertiary | Amino Acid Sequence | beta-Defensins - chemical synthesis | Protein Structure, Secondary | Membranes, Artificial | Models, Molecular | Salmonella enterica - growth & development | Phosphatidylcholines - chemistry | Salmonella enterica - metabolism | Static Electricity | Erythrocytes - drug effects | Peptides - pharmacology | Anti-Bacterial Agents - chemical synthesis | Phosphatidylglycerols - chemistry | Animals | Erythrocytes - metabolism | beta-Defensins - pharmacology | Sheep | Anti-Bacterial Agents - pharmacology | Staphylococcus aureus - drug effects | Staphylococcus aureus - growth & development | Phosphatidylethanolamines - chemistry | solid state NMR | dye leakage | fluorescence
Fluorescence | Solid-state NMR | Dye leakage | HβD3 | Antimicrobial peptide | PARDAXIN | CHEMISTRY, MEDICINAL | MECHANISM | BETA-DEFENSINS | PERMEABILIZATION | INDUCTION | IDENTIFICATION | LIPID COMPOSITION | HUMAN-NEUTROPHILS | H beta D3 | EXPRESSION | ANTIBACTERIAL PEPTIDE | Fluoresceins - metabolism | Humans | Cell Membrane Permeability | Fluorescent Dyes - metabolism | Molecular Sequence Data | Structure-Activity Relationship | Cell Membrane - chemistry | Microbial Sensitivity Tests | Salmonella enterica - drug effects | Peptides - chemical synthesis | Biological Transport - drug effects | Cell Membrane - drug effects | Staphylococcus aureus - metabolism | Protein Structure, Tertiary | Amino Acid Sequence | beta-Defensins - chemical synthesis | Protein Structure, Secondary | Membranes, Artificial | Models, Molecular | Salmonella enterica - growth & development | Phosphatidylcholines - chemistry | Salmonella enterica - metabolism | Static Electricity | Erythrocytes - drug effects | Peptides - pharmacology | Anti-Bacterial Agents - chemical synthesis | Phosphatidylglycerols - chemistry | Animals | Erythrocytes - metabolism | beta-Defensins - pharmacology | Sheep | Anti-Bacterial Agents - pharmacology | Staphylococcus aureus - drug effects | Staphylococcus aureus - growth & development | Phosphatidylethanolamines - chemistry | solid state NMR | dye leakage | fluorescence
Journal Article
Antimicrobial Agents and Chemotherapy, ISSN 0066-4804, 05/2008, Volume 52, Issue 5, pp. 1876 - 1879
Classifications Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit...
INVASIVE BACTERIAL-INFECTION | RESISTANT | BETA-DEFENSIN EXPRESSION | PEPTIDES | KERATINOCYTES | MICROBIOLOGY | PHARMACOLOGY & PHARMACY | STAPHYLOCOCCUS-AUREUS | SKIN | INDUCTION | IDENTIFICATION | PROTECTS | Amino Acid Sequence | beta-Defensins - genetics | Gene Expression - drug effects | Anti-Infective Agents - pharmacology | Humans | RNA, Messenger - genetics | Cells, Cultured | Molecular Sequence Data | Keratinocytes - cytology | RNA, Messenger - metabolism | Reverse Transcriptase Polymerase Chain Reaction | Microbial Sensitivity Tests | Sequence Homology, Amino Acid | Animals | Candida albicans - drug effects | Keratinocytes - drug effects | Keratinocytes - metabolism | beta-Defensins - pharmacology | Mice | Staphylococcus aureus - drug effects | Interferon-gamma - pharmacology | Transforming Growth Factor alpha - pharmacology | Susceptibility
INVASIVE BACTERIAL-INFECTION | RESISTANT | BETA-DEFENSIN EXPRESSION | PEPTIDES | KERATINOCYTES | MICROBIOLOGY | PHARMACOLOGY & PHARMACY | STAPHYLOCOCCUS-AUREUS | SKIN | INDUCTION | IDENTIFICATION | PROTECTS | Amino Acid Sequence | beta-Defensins - genetics | Gene Expression - drug effects | Anti-Infective Agents - pharmacology | Humans | RNA, Messenger - genetics | Cells, Cultured | Molecular Sequence Data | Keratinocytes - cytology | RNA, Messenger - metabolism | Reverse Transcriptase Polymerase Chain Reaction | Microbial Sensitivity Tests | Sequence Homology, Amino Acid | Animals | Candida albicans - drug effects | Keratinocytes - drug effects | Keratinocytes - metabolism | beta-Defensins - pharmacology | Mice | Staphylococcus aureus - drug effects | Interferon-gamma - pharmacology | Transforming Growth Factor alpha - pharmacology | Susceptibility
Journal Article
Food and Chemical Toxicology, ISSN 0278-6915, 02/2017, Volume 100, pp. 34 - 41
In recent years, transgenic technology has been widely applied in many fields. There is concern about the safety of genetically modified (GM) products with the...
triglyceride | total bilirubin | Genetically modified milk | ALP | HBD3 | alanine aminotransferase | ALT | GLO | globulin | hematoxylin-eosin | total cholesterol | 90-Day feeding study | OECD | total protein | Organization for Economic Co-operation and Development | AIN93G diet | alkaline phosphatase | BUN | w/w | WHO | Food and Agriculture Organization | AST | World Health Organization | CAC | human beta-defensin-3 | T-CHOL | weight/weight | aspartate aminotransferase | Codex Alimentarius Commission | Growth purified diet for rodents recommended by the American Institute of Nutrition | Safety assessment | genetically modified | FAO | TBIL | ALB | albumin | urea nitrogen | SPRAGUE-DAWLEY RATS | METABOLIC SYNDROME | FOOD SCIENCE & TECHNOLOGY | MAIZE GRAIN | DISEASE | COWS | MASTITIS | TOXICOLOGY | HEALTH | EXPRESSION | MAMMARY-GLAND | RICE | Milk - chemistry | Risk Assessment | Animals, Genetically Modified | Consumer Product Safety | Humans | Body Weight - drug effects | Rats | Male | Rats, Sprague-Dawley | Organ Size - drug effects | Animals | Diet | Cattle | Food, Genetically Modified - toxicity | beta-Defensins - pharmacology | Female | Drug resistance in microorganisms | Safety and security measures | Agricultural biotechnology | Genetically modified organisms | Dairy cattle | Animal genetic engineering | Histochemistry | Index Medicus
triglyceride | total bilirubin | Genetically modified milk | ALP | HBD3 | alanine aminotransferase | ALT | GLO | globulin | hematoxylin-eosin | total cholesterol | 90-Day feeding study | OECD | total protein | Organization for Economic Co-operation and Development | AIN93G diet | alkaline phosphatase | BUN | w/w | WHO | Food and Agriculture Organization | AST | World Health Organization | CAC | human beta-defensin-3 | T-CHOL | weight/weight | aspartate aminotransferase | Codex Alimentarius Commission | Growth purified diet for rodents recommended by the American Institute of Nutrition | Safety assessment | genetically modified | FAO | TBIL | ALB | albumin | urea nitrogen | SPRAGUE-DAWLEY RATS | METABOLIC SYNDROME | FOOD SCIENCE & TECHNOLOGY | MAIZE GRAIN | DISEASE | COWS | MASTITIS | TOXICOLOGY | HEALTH | EXPRESSION | MAMMARY-GLAND | RICE | Milk - chemistry | Risk Assessment | Animals, Genetically Modified | Consumer Product Safety | Humans | Body Weight - drug effects | Rats | Male | Rats, Sprague-Dawley | Organ Size - drug effects | Animals | Diet | Cattle | Food, Genetically Modified - toxicity | beta-Defensins - pharmacology | Female | Drug resistance in microorganisms | Safety and security measures | Agricultural biotechnology | Genetically modified organisms | Dairy cattle | Animal genetic engineering | Histochemistry | Index Medicus
Journal Article
Mediators of Inflammation, ISSN 0962-9351, 2017, Volume 2017, pp. 1 - 8
Platelet-released growth factors (PRGF) and its related clinically used formulations (e.g., Vivostat Platelet-Rich Fibrin (PRF (R))) contain a variety of...
IN-VITRO | HUMAN SKIN | QUANTIFICATION | STAPHYLOCOCCUS-AUREUS | INDUCTION | DIFFERENTIATION | IMMUNOLOGY | IDENTIFICATION | BETA-DEFENSIN 3 | EXPRESSION | RICH PLASMA | CELL BIOLOGY | Platelet-derived growth factor | Peptides | Keratinocytes | Physiological research | Research | Gene expression | Health aspects | Cell culture | Antimicrobial activity | HBD-3 gene | Cell adhesion & migration | Lysates | Ultrasonic imaging | Epidermal growth factor | Immunology | Antimicrobial peptides | Growth factors | Wound healing | Cytokines | Epidermal growth factor receptors | Antimicrobial agents | Wounding | Fibrin | Hospitals | Biofilms | Skin | Diabetes | Platelets | Chemokines
IN-VITRO | HUMAN SKIN | QUANTIFICATION | STAPHYLOCOCCUS-AUREUS | INDUCTION | DIFFERENTIATION | IMMUNOLOGY | IDENTIFICATION | BETA-DEFENSIN 3 | EXPRESSION | RICH PLASMA | CELL BIOLOGY | Platelet-derived growth factor | Peptides | Keratinocytes | Physiological research | Research | Gene expression | Health aspects | Cell culture | Antimicrobial activity | HBD-3 gene | Cell adhesion & migration | Lysates | Ultrasonic imaging | Epidermal growth factor | Immunology | Antimicrobial peptides | Growth factors | Wound healing | Cytokines | Epidermal growth factor receptors | Antimicrobial agents | Wounding | Fibrin | Hospitals | Biofilms | Skin | Diabetes | Platelets | Chemokines
Journal Article
PLoS ONE, ISSN 1932-6203, 04/2014, Volume 9, Issue 4, p. e93941
Human keratinocytes are able to express various antimicrobial peptides (AMP) to protect the skin from exaggerated microbial colonization and infection....
DEFENSE | PATTERN-RECOGNITION RECEPTOR | MULTIDISCIPLINARY SCIENCES | DECTIN-2 | ANTIMICROBIAL PEPTIDES | SKIN | DERMATOPHYTES | Ribonucleases - genetics | beta-Defensins - genetics | ErbB Receptors - metabolism | Humans | Epidermal Growth Factor - metabolism | Interleukin-17 - pharmacology | Immunity, Innate | Keratinocytes - immunology | Trichophyton - physiology | Gene Expression Regulation - drug effects | Keratinocytes - drug effects | Keratinocytes - metabolism | Trichophyton - growth & development | Keratinocytes - microbiology | Interferon-gamma - pharmacology | Infectious skin diseases | Care and treatment | Epidermal growth factor | Analysis | Ribonuclease | Diagnosis | Gene expression | Health aspects | Risk factors | Ribonuclease A | Peptides | Blocking antibodies | Infections | Mycelia | Microorganisms | Ribonuclease T | Antimicrobial peptides | Inhibition | Cytokines | Epidermal growth factor receptors | Dermatology | Secretion | Germination | Keratinocytes | Antimicrobial agents | Pattern recognition | Defensins | γ-Interferon | Skin | Interferon | Ribonuclease 7 | Colonization | Conidia
DEFENSE | PATTERN-RECOGNITION RECEPTOR | MULTIDISCIPLINARY SCIENCES | DECTIN-2 | ANTIMICROBIAL PEPTIDES | SKIN | DERMATOPHYTES | Ribonucleases - genetics | beta-Defensins - genetics | ErbB Receptors - metabolism | Humans | Epidermal Growth Factor - metabolism | Interleukin-17 - pharmacology | Immunity, Innate | Keratinocytes - immunology | Trichophyton - physiology | Gene Expression Regulation - drug effects | Keratinocytes - drug effects | Keratinocytes - metabolism | Trichophyton - growth & development | Keratinocytes - microbiology | Interferon-gamma - pharmacology | Infectious skin diseases | Care and treatment | Epidermal growth factor | Analysis | Ribonuclease | Diagnosis | Gene expression | Health aspects | Risk factors | Ribonuclease A | Peptides | Blocking antibodies | Infections | Mycelia | Microorganisms | Ribonuclease T | Antimicrobial peptides | Inhibition | Cytokines | Epidermal growth factor receptors | Dermatology | Secretion | Germination | Keratinocytes | Antimicrobial agents | Pattern recognition | Defensins | γ-Interferon | Skin | Interferon | Ribonuclease 7 | Colonization | Conidia
Journal Article
Langmuir, ISSN 0743-7463, 02/2016, Volume 32, Issue 7, pp. 1782 - 1790
Human β-defensin-3 (hBD3) is an endogenous antimicrobial peptide that exhibits broad-spectrum antibacterial activity without eukaryotic cytotoxicity. In this...
HUMAN BETA-DEFENSINS | HIGH-THROUGHPUT | MATERIALS SCIENCE, MULTIDISCIPLINARY | CHEMISTRY, PHYSICAL | CHEMISTRY, MULTIDISCIPLINARY | PEPTIDE | BUILDER | DYNAMICS | SURFACE | FORCE-FIELD | SIMULATIONS | CHARMM | LIPIDS | Amino Acid Sequence | Drug Resistance, Multiple - drug effects | Humans | Bacteria - drug effects | Molecular Sequence Data | Molecular Dynamics Simulation | beta-Defensins - chemistry | Cell Membrane - chemistry | Thermodynamics | Adsorption | Bacteria - cytology | Drug Design | beta-Defensins - pharmacology | Protein Conformation | Cell Membrane - drug effects | Index Medicus
HUMAN BETA-DEFENSINS | HIGH-THROUGHPUT | MATERIALS SCIENCE, MULTIDISCIPLINARY | CHEMISTRY, PHYSICAL | CHEMISTRY, MULTIDISCIPLINARY | PEPTIDE | BUILDER | DYNAMICS | SURFACE | FORCE-FIELD | SIMULATIONS | CHARMM | LIPIDS | Amino Acid Sequence | Drug Resistance, Multiple - drug effects | Humans | Bacteria - drug effects | Molecular Sequence Data | Molecular Dynamics Simulation | beta-Defensins - chemistry | Cell Membrane - chemistry | Thermodynamics | Adsorption | Bacteria - cytology | Drug Design | beta-Defensins - pharmacology | Protein Conformation | Cell Membrane - drug effects | Index Medicus
Journal Article
13.
Full Text
Thrombocytes are effectors of the innate immune system releasing human beta defensin-3
Injury, ISSN 0020-1383, 2010, Volume 42, Issue 7, pp. 682 - 686
Abstract Background Thrombocyte concentrate i.e. platelet-rich plasma (PRP) has become a popular adjunct for many surgical procedures. It is believed to...
Orthopedics | Antimicrobial peptide (AMP) | Platelet-rich plasma (PRP) | Pseudarthrosis | Fracture healing | SURGERY | MANAGEMENT | REGENERATION | ANTIMICROBIAL PEPTIDES | GEL | OPEN FRACTURES | IN-VITRO | EMERGENCY MEDICINE | HUMAN BETA-DEFENSIN-3 | SHAFT FRACTURES | GROWTH-FACTORS | ORTHOPEDICS | EXPRESSION | CRITICAL CARE MEDICINE | Immunohistochemistry | Blood Platelets - immunology | Gram-Negative Bacteria | Humans | Platelet-Rich Plasma - physiology | Gram-Negative Bacterial Infections - immunology | Gram-Negative Bacterial Infections - therapy | Fractures, Open - therapy | Wounds and Injuries - therapy | Blood Platelets - metabolism | Orthopedic Procedures | Fracture Healing - physiology | beta-Defensins - metabolism | Cross infection | Fractures | Nosocomial infections | Universities and colleges | Peptides | Health aspects | Antimicrobial agents
Orthopedics | Antimicrobial peptide (AMP) | Platelet-rich plasma (PRP) | Pseudarthrosis | Fracture healing | SURGERY | MANAGEMENT | REGENERATION | ANTIMICROBIAL PEPTIDES | GEL | OPEN FRACTURES | IN-VITRO | EMERGENCY MEDICINE | HUMAN BETA-DEFENSIN-3 | SHAFT FRACTURES | GROWTH-FACTORS | ORTHOPEDICS | EXPRESSION | CRITICAL CARE MEDICINE | Immunohistochemistry | Blood Platelets - immunology | Gram-Negative Bacteria | Humans | Platelet-Rich Plasma - physiology | Gram-Negative Bacterial Infections - immunology | Gram-Negative Bacterial Infections - therapy | Fractures, Open - therapy | Wounds and Injuries - therapy | Blood Platelets - metabolism | Orthopedic Procedures | Fracture Healing - physiology | beta-Defensins - metabolism | Cross infection | Fractures | Nosocomial infections | Universities and colleges | Peptides | Health aspects | Antimicrobial agents
Journal Article
Journal of Molecular Medicine, ISSN 0946-2716, 12/2017, Volume 95, Issue 12, pp. 1315 - 1325
Human beta-defensin-3 (HBD3), which is secreted from cells in the skin, salivary gland, and bone marrow, exhibits antimicrobial and immunomodulatory...
Human Genetics | Bone resorption | Biomedicine | Internal Medicine | Molecular Medicine | Human beta-defensin-3 | Osteoclast | Podosome belt formation | MEDICINE, RESEARCH & EXPERIMENTAL | ACTIVATION | PROTEIN | DEFENSINS | ANTIMICROBIAL PEPTIDES | INDUCTION | ORGANIZATION | GENETICS & HEREDITY | LIPOPOLYSACCHARIDE | MICE | EXPRESSION | INNATE IMMUNITY | Aggregatibacter - chemistry | Osteoclasts - pathology | Mice, Inbred C57BL | NFATC Transcription Factors - metabolism | Bone Resorption - drug therapy | Proto-Oncogene Proteins c-fos - metabolism | Down-Regulation - drug effects | Osteoclasts - metabolism | beta-Defensins - chemistry | Lipopolysaccharides | Peptides - pharmacology | Podosomes - metabolism | RANK Ligand - pharmacology | Animals | Cell Differentiation - drug effects | Bone Resorption - pathology | Osteoclasts - drug effects | Peptides - therapeutic use | Podosomes - drug effects | Physiological aspects | Genetic aspects | Research | Osteoclasts (Biology) | Surgical implants | Antimicrobial activity | Destruction | Peptides | Amino acids | Antiinfectives and antibacterials | Bone growth | Biomedical materials | Antimicrobial peptides | Bone marrow | Cofilin | Biocompatibility | Inhibition | TRANCE protein | Bone loss | Immunomodulation | Implantation | Salivary gland | Antimicrobial agents | Pharmacology | Chemical compounds | Osteoclastogenesis | Acids | Vinculin | Osteoclasts | Skin | Bone | Disruption | Differentiation | Pits
Human Genetics | Bone resorption | Biomedicine | Internal Medicine | Molecular Medicine | Human beta-defensin-3 | Osteoclast | Podosome belt formation | MEDICINE, RESEARCH & EXPERIMENTAL | ACTIVATION | PROTEIN | DEFENSINS | ANTIMICROBIAL PEPTIDES | INDUCTION | ORGANIZATION | GENETICS & HEREDITY | LIPOPOLYSACCHARIDE | MICE | EXPRESSION | INNATE IMMUNITY | Aggregatibacter - chemistry | Osteoclasts - pathology | Mice, Inbred C57BL | NFATC Transcription Factors - metabolism | Bone Resorption - drug therapy | Proto-Oncogene Proteins c-fos - metabolism | Down-Regulation - drug effects | Osteoclasts - metabolism | beta-Defensins - chemistry | Lipopolysaccharides | Peptides - pharmacology | Podosomes - metabolism | RANK Ligand - pharmacology | Animals | Cell Differentiation - drug effects | Bone Resorption - pathology | Osteoclasts - drug effects | Peptides - therapeutic use | Podosomes - drug effects | Physiological aspects | Genetic aspects | Research | Osteoclasts (Biology) | Surgical implants | Antimicrobial activity | Destruction | Peptides | Amino acids | Antiinfectives and antibacterials | Bone growth | Biomedical materials | Antimicrobial peptides | Bone marrow | Cofilin | Biocompatibility | Inhibition | TRANCE protein | Bone loss | Immunomodulation | Implantation | Salivary gland | Antimicrobial agents | Pharmacology | Chemical compounds | Osteoclastogenesis | Acids | Vinculin | Osteoclasts | Skin | Bone | Disruption | Differentiation | Pits
Journal Article