International Microbiology, ISSN 1139-6709, 2008, Volume 11, Issue 3, pp. 195 - 202
During the Arctic summer, bacteria are active above the permafrost in an environment with sharp temperature and oxygen gradients. The present study addressed...
Active layer | Siberian Arctic | Clone libraries | Bacterial diversity | Nutrient gradients | Tundra | PHYLOGENETIC DIVERSITY | PERMAFROST | active layer | IN-SITU DETECTION | MICROBIOLOGY | FATTY-ACIDS | SP NOV | GRADIENT GEL-ELECTROPHORESIS | bacterial diversity | tundra | GRAM-POSITIVE BACTERIA | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | HIGH ARCTIC WETLANDS | nutrient gradients | clone libraries | TARGETED OLIGONUCLEOTIDE PROBES | 16S RIBOSOMAL-RNA | Bacteroidetes - isolation & purification | DNA, Bacterial - isolation & purification | DNA, Ribosomal - analysis | Gene Library | Soil Microbiology | Molecular Sequence Data | In Situ Hybridization, Fluorescence | Actinobacteria - classification | Ice | Soil - analysis | Bacteroidetes - classification | Bacteria - genetics | Sequence Analysis, DNA | Bacteria - isolation & purification | Arctic Regions | Ecosystem | Actinobacteria - genetics | Cloning, Molecular - methods | Siberia | Bacteria - classification | RNA, Ribosomal, 16S - genetics | DNA, Bacterial - analysis | Actinobacteria - isolation & purification | Bacteroidetes - genetics | bacterial diversity · clone libraries · nutrient gradients · active layer · tundra · Siberian Arctic
Active layer | Siberian Arctic | Clone libraries | Bacterial diversity | Nutrient gradients | Tundra | PHYLOGENETIC DIVERSITY | PERMAFROST | active layer | IN-SITU DETECTION | MICROBIOLOGY | FATTY-ACIDS | SP NOV | GRADIENT GEL-ELECTROPHORESIS | bacterial diversity | tundra | GRAM-POSITIVE BACTERIA | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | HIGH ARCTIC WETLANDS | nutrient gradients | clone libraries | TARGETED OLIGONUCLEOTIDE PROBES | 16S RIBOSOMAL-RNA | Bacteroidetes - isolation & purification | DNA, Bacterial - isolation & purification | DNA, Ribosomal - analysis | Gene Library | Soil Microbiology | Molecular Sequence Data | In Situ Hybridization, Fluorescence | Actinobacteria - classification | Ice | Soil - analysis | Bacteroidetes - classification | Bacteria - genetics | Sequence Analysis, DNA | Bacteria - isolation & purification | Arctic Regions | Ecosystem | Actinobacteria - genetics | Cloning, Molecular - methods | Siberia | Bacteria - classification | RNA, Ribosomal, 16S - genetics | DNA, Bacterial - analysis | Actinobacteria - isolation & purification | Bacteroidetes - genetics | bacterial diversity · clone libraries · nutrient gradients · active layer · tundra · Siberian Arctic
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
Journal of Investigative Dermatology, ISSN 0022-202X, 02/2014, Volume 134, Issue 2, pp. 374 - 380
IL-17C is an important epithelial cell-derived cytokine activating innate immunity by the induction of antimicrobial peptides and cytokines. Here, we...
ATOPIC-DERMATITIS | ACTIVATION | POLYMORPHISMS | CROHNS-DISEASE | IMMUNE-RESPONSES | INNATE | INFECTION | KAPPA-B | SKIN | PSORIATIC-ARTHRITIS | DERMATOLOGY | RNA, Small Interfering - genetics | Staphylococcal Infections - immunology | Humans | Interleukin-17 - immunology | Interleukin-17 - genetics | Nod2 Signaling Adaptor Protein - immunology | Nod2 Signaling Adaptor Protein - genetics | Dermatitis, Atopic - microbiology | Keratinocytes - cytology | Keratinocytes - immunology | Immunity, Innate - immunology | Dermatitis, Atopic - immunology | Gene Expression - immunology | HEK293 Cells | Staphylococcus aureus - immunology | Primary Cell Culture | Promoter Regions, Genetic - immunology | Keratinocytes - microbiology
ATOPIC-DERMATITIS | ACTIVATION | POLYMORPHISMS | CROHNS-DISEASE | IMMUNE-RESPONSES | INNATE | INFECTION | KAPPA-B | SKIN | PSORIATIC-ARTHRITIS | DERMATOLOGY | RNA, Small Interfering - genetics | Staphylococcal Infections - immunology | Humans | Interleukin-17 - immunology | Interleukin-17 - genetics | Nod2 Signaling Adaptor Protein - immunology | Nod2 Signaling Adaptor Protein - genetics | Dermatitis, Atopic - microbiology | Keratinocytes - cytology | Keratinocytes - immunology | Immunity, Innate - immunology | Dermatitis, Atopic - immunology | Gene Expression - immunology | HEK293 Cells | Staphylococcus aureus - immunology | Primary Cell Culture | Promoter Regions, Genetic - immunology | Keratinocytes - microbiology
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 07/2012, Volume 18, Issue 27, pp. 8347 - 8357
Seven derivatives of 1,2‐dicarbadodecaborane (ortho‐carborane, 1,2‐C2B10H12) with a 1,3‐diethyl‐ or 1,3‐diphenyl‐1,3,2‐benzodiazaborolyl group on one cage...
donor–acceptor systems | luminescence | diazaboroles | charge transfer | carboranes | donor-acceptor systems | CHARGE-TRANSFER EMISSION | CRYSTAL-STRUCTURES | AMORPHOUS MOLECULAR MATERIALS | CHEMICAL-SHIFT CALCULATIONS | CHEMISTRY, MULTIDISCIPLINARY | AGGREGATION-INDUCED EMISSION | PI-ELECTRON SYSTEMS | 2-PHOTON-EXCITED FLUORESCENCE | SET MODEL CHEMISTRY | 3-COORDINATE ORGANOBORON COMPOUNDS | NONLINEAR-OPTICAL-PROPERTIES | Emissions | Low energy | Bands | Cage | Computation | Fluid flow | Fluorescence | Excitation | Orientation
donor–acceptor systems | luminescence | diazaboroles | charge transfer | carboranes | donor-acceptor systems | CHARGE-TRANSFER EMISSION | CRYSTAL-STRUCTURES | AMORPHOUS MOLECULAR MATERIALS | CHEMICAL-SHIFT CALCULATIONS | CHEMISTRY, MULTIDISCIPLINARY | AGGREGATION-INDUCED EMISSION | PI-ELECTRON SYSTEMS | 2-PHOTON-EXCITED FLUORESCENCE | SET MODEL CHEMISTRY | 3-COORDINATE ORGANOBORON COMPOUNDS | NONLINEAR-OPTICAL-PROPERTIES | Emissions | Low energy | Bands | Cage | Computation | Fluid flow | Fluorescence | Excitation | Orientation
Journal Article
5.
Full Text
Electrochemical and spectroelectrochemical studies of C-benzodiazaborolyl-ortho-carboranes
Journal of the Chemical Society. Dalton Transactions, ISSN 1477-9226, 11/2013, Volume 42, Issue 2, pp. 2266 - 2281
Journal Article
Biophysical Journal, ISSN 0006-3495, 07/2015, Volume 109, Issue 1, pp. 26 - 34
We describe a method for quantifying the mechanical properties of cells in suspension with a microfluidic device consisting of a parallel array of micron-sized...
DEFORMABILITY | SMOOTH-MUSCLE | BIOPHYSICS | ACTIN NETWORKS | CYTOSKELETON | MICRORHEOLOGY | BEHAVIOR | FLUCTUATIONS | CHROMATIN DECONDENSATION | CANCER | LIVING CELLS | Microfluidic Analytical Techniques - methods | Models, Theoretical | Rheology | Humans | Microfluidic Analytical Techniques - instrumentation | Lab-On-A-Chip Devices | Glass - chemistry | Equipment Design | Pressure | Cell Nucleus - physiology | Cell Physiological Phenomena - drug effects | Cell Line, Tumor | Cytoskeleton - physiology | Mechanical Phenomena | Microtechnology - instrumentation | Cell Nucleus - drug effects | Cytoskeleton - drug effects | Cell Biophysics
DEFORMABILITY | SMOOTH-MUSCLE | BIOPHYSICS | ACTIN NETWORKS | CYTOSKELETON | MICRORHEOLOGY | BEHAVIOR | FLUCTUATIONS | CHROMATIN DECONDENSATION | CANCER | LIVING CELLS | Microfluidic Analytical Techniques - methods | Models, Theoretical | Rheology | Humans | Microfluidic Analytical Techniques - instrumentation | Lab-On-A-Chip Devices | Glass - chemistry | Equipment Design | Pressure | Cell Nucleus - physiology | Cell Physiological Phenomena - drug effects | Cell Line, Tumor | Cytoskeleton - physiology | Mechanical Phenomena | Microtechnology - instrumentation | Cell Nucleus - drug effects | Cytoskeleton - drug effects | Cell Biophysics
Journal Article
Experimental Dermatology, ISSN 0906-6705, 03/2017, Volume 26, Issue 3, pp. 227 - 233
The ribonuclease RNase 7 is a major skin‐derived human antimicrobial protein expressed in keratinocytes. Here we show that the gram‐negative pathogen...
cutaneous innate defense | keratinocytes | epidermal growth factor receptor | antimicrobial peptides | ACTIVATION | DIFFERENTIAL EXPRESSION | CHRONIC WOUNDS | EGFR | DERMATOLOGY | EPITHELIAL-CELLS | IMMUNE-RESPONSES | SKIN | SIGNALING CASCADE | Ribonucleases - genetics | Gene Expression - drug effects | Skin - metabolism | Humans | Receptor, Epidermal Growth Factor - drug effects | Ribonucleases - metabolism | Receptor, Epidermal Growth Factor - metabolism | Organoids | Pseudomonas aeruginosa - metabolism | Hydroxamic Acids - pharmacology | Skin - immunology | Toll-Like Receptor 5 - metabolism | Signal Transduction | Epidermis - drug effects | RNA, Small Interfering - pharmacology | Cells, Cultured | Gene Silencing | Keratinocytes | Antibodies, Neutralizing - pharmacology | Cetuximab - pharmacology | Tyrphostins - pharmacology | ADAM17 Protein - genetics | Epidermis - immunology | Ribonucleases - immunology | Quinazolines - pharmacology | Viral antibodies | Epidermal growth factor | Analysis | Antibodies | Pseudomonas aeruginosa | Skin | Ribonuclease | Gene expression | Enzyme-linked immunosorbent assay | Ribonuclease A | Pathogens | Antimicrobial activity | Stratum corneum | TLR5 protein | Epidermal growth factor receptors | Antimicrobial agents | siRNA | Pattern recognition | Ribonuclease P | Ribonuclease S | Toll-like receptors | Ligands | Ribonuclease 7 | Metalloproteinase
cutaneous innate defense | keratinocytes | epidermal growth factor receptor | antimicrobial peptides | ACTIVATION | DIFFERENTIAL EXPRESSION | CHRONIC WOUNDS | EGFR | DERMATOLOGY | EPITHELIAL-CELLS | IMMUNE-RESPONSES | SKIN | SIGNALING CASCADE | Ribonucleases - genetics | Gene Expression - drug effects | Skin - metabolism | Humans | Receptor, Epidermal Growth Factor - drug effects | Ribonucleases - metabolism | Receptor, Epidermal Growth Factor - metabolism | Organoids | Pseudomonas aeruginosa - metabolism | Hydroxamic Acids - pharmacology | Skin - immunology | Toll-Like Receptor 5 - metabolism | Signal Transduction | Epidermis - drug effects | RNA, Small Interfering - pharmacology | Cells, Cultured | Gene Silencing | Keratinocytes | Antibodies, Neutralizing - pharmacology | Cetuximab - pharmacology | Tyrphostins - pharmacology | ADAM17 Protein - genetics | Epidermis - immunology | Ribonucleases - immunology | Quinazolines - pharmacology | Viral antibodies | Epidermal growth factor | Analysis | Antibodies | Pseudomonas aeruginosa | Skin | Ribonuclease | Gene expression | Enzyme-linked immunosorbent assay | Ribonuclease A | Pathogens | Antimicrobial activity | Stratum corneum | TLR5 protein | Epidermal growth factor receptors | Antimicrobial agents | siRNA | Pattern recognition | Ribonuclease P | Ribonuclease S | Toll-like receptors | Ligands | Ribonuclease 7 | Metalloproteinase
Journal Article
PLoS ONE, ISSN 1932-6203, 03/2013, Volume 8, Issue 3, p. e59531
Human keratinocytes produce several antimicrobial peptides and proteins (AMP) which contribute to the protection of human skin against infection. RNase 7 is a...
INVASIVE BACTERIAL-INFECTION | HYPER-IGE SYNDROME | ATOPIC-DERMATITIS | HUMAN SKIN | MULTIDISCIPLINARY SCIENCES | MECHANISMS | ANTIMICROBIAL PEPTIDES | PROTEINS | IMMUNE DEFENSE | PSORIASIS | PROTECTS | S100 Calcium Binding Protein A7 | Gene Expression Regulation, Enzymologic - drug effects | Ribonucleases - genetics | beta-Defensins - genetics | Staphylococcus aureus - physiology | Humans | Interleukin-17 - pharmacology | Ribonucleases - metabolism | Dose-Response Relationship, Drug | Drug Synergism | S100 Proteins - genetics | Keratinocytes - drug effects | Keratinocytes - metabolism | Staphylococcus aureus - drug effects | Keratinocytes - microbiology | Interferon-gamma - pharmacology | STAT3 Transcription Factor - metabolism | Ribonuclease A | Antimicrobial activity | Immune response | Bacterial infections | Psoriasis | Cytokines | Peptides | Dermatology | Stat3 protein | Keratinocytes | Staphylococcus infections | Antimicrobial agents | siRNA | Tumor necrosis factor-α | Gene expression | Dermatitis | Antiinfectives and antibacterials | Proteins | S100 protein | γ-Interferon | Antimicrobial peptides | Skin | Ribonuclease 7 | Immune system
INVASIVE BACTERIAL-INFECTION | HYPER-IGE SYNDROME | ATOPIC-DERMATITIS | HUMAN SKIN | MULTIDISCIPLINARY SCIENCES | MECHANISMS | ANTIMICROBIAL PEPTIDES | PROTEINS | IMMUNE DEFENSE | PSORIASIS | PROTECTS | S100 Calcium Binding Protein A7 | Gene Expression Regulation, Enzymologic - drug effects | Ribonucleases - genetics | beta-Defensins - genetics | Staphylococcus aureus - physiology | Humans | Interleukin-17 - pharmacology | Ribonucleases - metabolism | Dose-Response Relationship, Drug | Drug Synergism | S100 Proteins - genetics | Keratinocytes - drug effects | Keratinocytes - metabolism | Staphylococcus aureus - drug effects | Keratinocytes - microbiology | Interferon-gamma - pharmacology | STAT3 Transcription Factor - metabolism | Ribonuclease A | Antimicrobial activity | Immune response | Bacterial infections | Psoriasis | Cytokines | Peptides | Dermatology | Stat3 protein | Keratinocytes | Staphylococcus infections | Antimicrobial agents | siRNA | Tumor necrosis factor-α | Gene expression | Dermatitis | Antiinfectives and antibacterials | Proteins | S100 protein | γ-Interferon | Antimicrobial peptides | Skin | Ribonuclease 7 | Immune system
Journal Article
PLOS ONE, ISSN 1932-6203, 04/2019, Volume 14, Issue 4, p. e0215316
Glaucoma drainage devices are used in surgical glaucoma therapy. Success of controlling the intraocular pressure is limited due to fibrous implant...
FIBROSIS | BIOCOMPATIBILITY | MULTIDISCIPLINARY SCIENCES | AQUEOUS-HUMOR | VALVE | DRAINAGE DEVICES | INTRAOCULAR-PRESSURE | OUTCOMES | DEEP SCLERECTOMY | DIFFERENT BIOMATERIALS | CLINICAL-EXPERIENCE | Glaucoma | Trabeculectomy | Rabbits | Lasers in surgery | Physiological aspects | Diagnosis | Comparative analysis | Transplants & implants | Drainage control | Drainage facilities | Adhesion tests | Flow characteristics | Macrophages | Veterinary medicine | Eye | Design | Biomedical materials | Obstructions | Lymphocytes | Surgery | Prototypes | Cell adhesion | Outflow | Biocompatibility | Statistical analysis | Aqueous humour | Mechanical properties | Inflammation | Humour | Pressure | Low level | Drainage | Fibrin | Fibrosis | Intraocular pressure
FIBROSIS | BIOCOMPATIBILITY | MULTIDISCIPLINARY SCIENCES | AQUEOUS-HUMOR | VALVE | DRAINAGE DEVICES | INTRAOCULAR-PRESSURE | OUTCOMES | DEEP SCLERECTOMY | DIFFERENT BIOMATERIALS | CLINICAL-EXPERIENCE | Glaucoma | Trabeculectomy | Rabbits | Lasers in surgery | Physiological aspects | Diagnosis | Comparative analysis | Transplants & implants | Drainage control | Drainage facilities | Adhesion tests | Flow characteristics | Macrophages | Veterinary medicine | Eye | Design | Biomedical materials | Obstructions | Lymphocytes | Surgery | Prototypes | Cell adhesion | Outflow | Biocompatibility | Statistical analysis | Aqueous humour | Mechanical properties | Inflammation | Humour | Pressure | Low level | Drainage | Fibrin | Fibrosis | Intraocular pressure
Journal Article
PloS one, ISSN 1932-6203, 2016, Volume 11, Issue 1, p. e0147118
Staphylococcus (S.) aureus is an important pathogen causing various infections including those of the skin. Keratinocytes are able to sense invading S. aureus...
INTERLEUKIN-1-ALPHA SECRETION | ACTIVATION | ADAM17 | PRECURSOR | HUMAN BETA-DEFENSIN-2 | MULTIDISCIPLINARY SCIENCES | IL-1-BETA | KAPPA-B | SKIN | RNASE 7 | EXPRESSION | ADAM17 Protein | RNA, Small Interfering - genetics | ErbB Receptors - antagonists & inhibitors | ADAM Proteins - physiology | Staphylococcus aureus - physiology | Humans | Cells, Cultured | Gene Expression Regulation | Interleukin-1alpha - metabolism | Interleukin-1beta - genetics | Protein Precursors - metabolism | ErbB Receptors - physiology | Inflammasomes - physiology | RNA Interference | Interleukin-1beta - metabolism | Keratinocytes - metabolism | CARD Signaling Adaptor Proteins | Interleukin-1alpha - biosynthesis | Interleukin-1alpha - genetics | Interleukin-1beta - biosynthesis | Protein Processing, Post-Translational | Caspase 1 - physiology | Cytoskeletal Proteins - physiology | Keratinocytes - microbiology | Shedding | Peptides | Blocking antibodies | Infections | Interleukin 1 receptors | Inactivation | Caspase-1 | Proteins | Epidermal growth factor | Rodents | Interleukin 1 | Antimicrobial peptides | Bacteria | Deactivation | Cytokines | Epidermal growth factor receptors | Dermatology | Secretion | Keratinocytes | Caspase | Staphylococcus infections | Antimicrobial agents | siRNA | Gene expression | Speck | Skin | Cancer | Apoptosis
INTERLEUKIN-1-ALPHA SECRETION | ACTIVATION | ADAM17 | PRECURSOR | HUMAN BETA-DEFENSIN-2 | MULTIDISCIPLINARY SCIENCES | IL-1-BETA | KAPPA-B | SKIN | RNASE 7 | EXPRESSION | ADAM17 Protein | RNA, Small Interfering - genetics | ErbB Receptors - antagonists & inhibitors | ADAM Proteins - physiology | Staphylococcus aureus - physiology | Humans | Cells, Cultured | Gene Expression Regulation | Interleukin-1alpha - metabolism | Interleukin-1beta - genetics | Protein Precursors - metabolism | ErbB Receptors - physiology | Inflammasomes - physiology | RNA Interference | Interleukin-1beta - metabolism | Keratinocytes - metabolism | CARD Signaling Adaptor Proteins | Interleukin-1alpha - biosynthesis | Interleukin-1alpha - genetics | Interleukin-1beta - biosynthesis | Protein Processing, Post-Translational | Caspase 1 - physiology | Cytoskeletal Proteins - physiology | Keratinocytes - microbiology | Shedding | Peptides | Blocking antibodies | Infections | Interleukin 1 receptors | Inactivation | Caspase-1 | Proteins | Epidermal growth factor | Rodents | Interleukin 1 | Antimicrobial peptides | Bacteria | Deactivation | Cytokines | Epidermal growth factor receptors | Dermatology | Secretion | Keratinocytes | Caspase | Staphylococcus infections | Antimicrobial agents | siRNA | Gene expression | Speck | Skin | Cancer | Apoptosis
Journal Article
The Journal of Allergy and Clinical Immunology, ISSN 0091-6749, 2006, Volume 117, Issue 2, pp. 418 - 425
IL-31 is a newly discovered T-cell cytokine that, when overexpressed in mice, results in pruritus and skin dermatitis resembling human atopic dermatitis (AD)....
pruritus | macrophages | Atopic dermatitis | IL-31 receptor A | keratinocytes | IL-31 | skin-homing T cells | Skin-homing T cells | Keratinocytes | Pruritus | Macrophages | MACROPHAGE-DERIVED CHEMOKINE | atopic dermatitis | IMMUNOLOGY | ACTIVATION-REGULATED CHEMOKINE | THYMUS | ALLERGY | CYTOKINE RECEPTOR | TARC | ALLERGIC DISEASES | EXPRESSION | Membrane Glycoproteins - analysis | Psoriasis - immunology | Antigens, Neoplasm | Lymphocyte Activation | Humans | Middle Aged | Male | Receptors, Interleukin | Receptors, Lymphocyte Homing - metabolism | Dermatitis, Atopic - physiopathology | Antigens, Differentiation, T-Lymphocyte | Interleukins - metabolism | Interleukins - genetics | Psoriasis - physiopathology | Dermatitis, Atopic - immunology | Adult | Female | T-Lymphocytes - immunology | Skin - immunology | Immunohistochemistry | Autoimmunity | Antigens | T cells | Proteins | Human subjects | Flow cytometry | Cytokines | Psoriasis | Disease | Pathogenesis | Lymphocytes | Rodents | T cell receptors | Chemokines
pruritus | macrophages | Atopic dermatitis | IL-31 receptor A | keratinocytes | IL-31 | skin-homing T cells | Skin-homing T cells | Keratinocytes | Pruritus | Macrophages | MACROPHAGE-DERIVED CHEMOKINE | atopic dermatitis | IMMUNOLOGY | ACTIVATION-REGULATED CHEMOKINE | THYMUS | ALLERGY | CYTOKINE RECEPTOR | TARC | ALLERGIC DISEASES | EXPRESSION | Membrane Glycoproteins - analysis | Psoriasis - immunology | Antigens, Neoplasm | Lymphocyte Activation | Humans | Middle Aged | Male | Receptors, Interleukin | Receptors, Lymphocyte Homing - metabolism | Dermatitis, Atopic - physiopathology | Antigens, Differentiation, T-Lymphocyte | Interleukins - metabolism | Interleukins - genetics | Psoriasis - physiopathology | Dermatitis, Atopic - immunology | Adult | Female | T-Lymphocytes - immunology | Skin - immunology | Immunohistochemistry | Autoimmunity | Antigens | T cells | Proteins | Human subjects | Flow cytometry | Cytokines | Psoriasis | Disease | Pathogenesis | Lymphocytes | Rodents | T cell receptors | Chemokines
Journal Article
Experimental Dermatology, ISSN 0906-6705, 03/2017, Volume 26, Issue 3, pp. 227 - 233
Journal Article
Nature, ISSN 0028-0836, 01/2007, Volume 445, Issue 7124, pp. 206 - 209
Touch and mechanical pain are first detected at our largest sensory surface, the skin. The cell bodies of sensory neurons that detect such stimuli are located...
LOCALIZATION | PAIN | RAT | MULTIDISCIPLINARY SCIENCES | RECEPTOR NEURONS | SENSING ION CHANNELS | MEMBRANE-PROTEIN | MECHANOSENSATION | C-ELEGANS | MECHANORECEPTOR | SENSORY NEURONS | Protein Structure, Tertiary | Acid Sensing Ion Channels | Membrane Proteins - genetics | Nerve Tissue Proteins - deficiency | Rats | Male | Electric Conductivity | Ganglia, Spinal - cytology | Mutation - genetics | Nerve Tissue Proteins - genetics | Nerve Tissue Proteins - metabolism | Membrane Proteins - deficiency | Nerve Tissue Proteins - chemistry | Animals | Membrane Proteins - chemistry | Sodium Channels - metabolism | Female | Membrane Proteins - metabolism | Mice | Touch - physiology | Mechanoreceptors - metabolism | Afferent Pathways | Ganglia, Spinal - metabolism | Proteins | Neurology | Pain | Touch | Sensory perception | Rodents
LOCALIZATION | PAIN | RAT | MULTIDISCIPLINARY SCIENCES | RECEPTOR NEURONS | SENSING ION CHANNELS | MEMBRANE-PROTEIN | MECHANOSENSATION | C-ELEGANS | MECHANORECEPTOR | SENSORY NEURONS | Protein Structure, Tertiary | Acid Sensing Ion Channels | Membrane Proteins - genetics | Nerve Tissue Proteins - deficiency | Rats | Male | Electric Conductivity | Ganglia, Spinal - cytology | Mutation - genetics | Nerve Tissue Proteins - genetics | Nerve Tissue Proteins - metabolism | Membrane Proteins - deficiency | Nerve Tissue Proteins - chemistry | Animals | Membrane Proteins - chemistry | Sodium Channels - metabolism | Female | Membrane Proteins - metabolism | Mice | Touch - physiology | Mechanoreceptors - metabolism | Afferent Pathways | Ganglia, Spinal - metabolism | Proteins | Neurology | Pain | Touch | Sensory perception | Rodents
Journal Article