Journal of Pharmacology and Experimental Therapeutics, ISSN 0022-3565, 2006, Volume 319, Issue 3, pp. 998 - 1008
Recent compelling evidence has lead to renewed interest in the role of antibodies and immune complexes in the pathogenesis of several autoimmune disorders,...
RHEUMATOID-ARTHRITIS | GAMMA RECEPTORS | COLLAGEN | BASOPHIL ACTIVATION | ARTHUS REACTION | CELL ACTIVATION | PLATELETS | MAST-CELLS | DEFICIENT | PHARMACOLOGY & PHARMACY | SYK KINASES | Inflammation - pathology | Tetradecanoylphorbol Acetate - pharmacology | Humans | Pyridines - pharmacokinetics | Crystallography | Antigen-Antibody Complex - physiology | Arthritis, Experimental - pathology | Fluorescence Polarization Immunoassay | Oxazines - pharmacokinetics | Receptors, Fc - antagonists & inhibitors | Enzyme Inhibitors - pharmacokinetics | Immunoglobulin G - biosynthesis | Spleen - enzymology | Immunoglobulin G - immunology | Inflammation - drug therapy | Platelet Aggregation - drug effects | Oxazines - pharmacology | Basophils - drug effects | Double-Blind Method | Cells, Cultured | Enzyme Inhibitors - pharmacology | B-Lymphocytes - physiology | Mast Cells - drug effects | Stimulation, Chemical | Blotting, Western | B-Lymphocytes - drug effects | Animals | Signal Transduction - drug effects | Lipopolysaccharides - pharmacology | Macrophages - drug effects | Arthus Reaction - physiopathology | Mice | Mice, Inbred BALB C | Pyridines - pharmacology | Protein-Tyrosine Kinases - antagonists & inhibitors
RHEUMATOID-ARTHRITIS | GAMMA RECEPTORS | COLLAGEN | BASOPHIL ACTIVATION | ARTHUS REACTION | CELL ACTIVATION | PLATELETS | MAST-CELLS | DEFICIENT | PHARMACOLOGY & PHARMACY | SYK KINASES | Inflammation - pathology | Tetradecanoylphorbol Acetate - pharmacology | Humans | Pyridines - pharmacokinetics | Crystallography | Antigen-Antibody Complex - physiology | Arthritis, Experimental - pathology | Fluorescence Polarization Immunoassay | Oxazines - pharmacokinetics | Receptors, Fc - antagonists & inhibitors | Enzyme Inhibitors - pharmacokinetics | Immunoglobulin G - biosynthesis | Spleen - enzymology | Immunoglobulin G - immunology | Inflammation - drug therapy | Platelet Aggregation - drug effects | Oxazines - pharmacology | Basophils - drug effects | Double-Blind Method | Cells, Cultured | Enzyme Inhibitors - pharmacology | B-Lymphocytes - physiology | Mast Cells - drug effects | Stimulation, Chemical | Blotting, Western | B-Lymphocytes - drug effects | Animals | Signal Transduction - drug effects | Lipopolysaccharides - pharmacology | Macrophages - drug effects | Arthus Reaction - physiopathology | Mice | Mice, Inbred BALB C | Pyridines - pharmacology | Protein-Tyrosine Kinases - antagonists & inhibitors
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2011, Volume 128, Issue 4, pp. 800 - 807.e9
Background IL-13 is a key TH 2 cytokine that is implicated in allergic responses. Objective We evaluated the effects of an anti–IL-13–blocking antibody...
Allergy and Immunology | nasal allergen challenge | anti–IL-13 | Allergic rhinitis | mAb | anti-IL-13 | MEPOLIZUMAB | EFFICACY | SAFETY | EOSINOPHILS | INTERLEUKIN-13 | ANTIBODY | RECEPTOR | IL-13 | IMMUNOLOGY | MUCOSA | ALLERGY | ASTHMA | Double-Blind Method | Interleukin-13 - antagonists & inhibitors | Humans | Middle Aged | Rhinitis, Allergic, Seasonal - drug therapy | Antibodies, Monoclonal - pharmacokinetics | Interleukin-13 - immunology | Male | Fluticasone | Phleum - immunology | Administration, Intranasal | Eosinophils - immunology | Rhinitis, Allergic, Seasonal - immunology | Allergens - administration & dosage | Androstadienes - administration & dosage | Antibodies, Monoclonal - administration & dosage | Rhinitis, Allergic, Seasonal - blood | Adolescent | Adult | Female | Anti-Allergic Agents - administration & dosage | Adrenal Cortex Hormones - administration & dosage | Therapeutic Irrigation | Allergy | Allergens | Universities and colleges | Cytokines | Allergic reaction | Studies | Allergies
Allergy and Immunology | nasal allergen challenge | anti–IL-13 | Allergic rhinitis | mAb | anti-IL-13 | MEPOLIZUMAB | EFFICACY | SAFETY | EOSINOPHILS | INTERLEUKIN-13 | ANTIBODY | RECEPTOR | IL-13 | IMMUNOLOGY | MUCOSA | ALLERGY | ASTHMA | Double-Blind Method | Interleukin-13 - antagonists & inhibitors | Humans | Middle Aged | Rhinitis, Allergic, Seasonal - drug therapy | Antibodies, Monoclonal - pharmacokinetics | Interleukin-13 - immunology | Male | Fluticasone | Phleum - immunology | Administration, Intranasal | Eosinophils - immunology | Rhinitis, Allergic, Seasonal - immunology | Allergens - administration & dosage | Androstadienes - administration & dosage | Antibodies, Monoclonal - administration & dosage | Rhinitis, Allergic, Seasonal - blood | Adolescent | Adult | Female | Anti-Allergic Agents - administration & dosage | Adrenal Cortex Hormones - administration & dosage | Therapeutic Irrigation | Allergy | Allergens | Universities and colleges | Cytokines | Allergic reaction | Studies | Allergies
Journal Article
Cytokine, ISSN 1043-4666, 11/2014, Volume 70, Issue 1, pp. 65 - 65
Journal Article
Cytokine, ISSN 1043-4666, 11/2014, Volume 70, Issue 1, p. 65
The Janus Kinase-Signal Transducer and Activator of Transcription (JAK-STAT) pathway represents a rapid membrane to nucleus signaling system used by cytokines,...
Promoters (Genetics) | Analysis | Genomics | T cells | Methylation | Cell differentiation | Protein binding
Promoters (Genetics) | Analysis | Genomics | T cells | Methylation | Cell differentiation | Protein binding
Journal Article
PLoS ONE, ISSN 1932-6203, 02/2014, Volume 9, Issue 2, p. e90370
Signal transducers and activators of transcription 5(STAT5) are cytokine induced signaling proteins, which regulate key immunological processes, such as...
BREAST-CANCER | HUMAN GENOME | CHROMATIN IMMUNOPRECIPITATION | MULTIDISCIPLINARY SCIENCES | TRANSCRIPTION | RECEPTOR | BINDING-SITES | IDENTIFICATION | EXPRESSION | DNASE HYPERSENSITIVE SITES | SOMATIC MUTATIONS | Luciferases - metabolism | Epigenesis, Genetic | Humans | Molecular Sequence Data | Fos-Related Antigen-2 - genetics | Luciferases - genetics | Janus Kinase 3 - antagonists & inhibitors | STAT5 Transcription Factor - genetics | STAT5 Transcription Factor - metabolism | Fos-Related Antigen-2 - metabolism | Antibodies, Monoclonal, Humanized - pharmacology | Base Sequence | DNA, Intergenic - metabolism | HEK293 Cells | Immunoglobulin G - pharmacology | Transcription, Genetic | Janus Kinase 3 - metabolism | Binding Sites | Genes, Reporter | Signal Transduction | Introns | Lymphocyte Activation | CD4-Positive T-Lymphocytes - cytology | CD4-Positive T-Lymphocytes - metabolism | Gene Expression Regulation | DNA, Intergenic - chemistry | Daclizumab | Histones - genetics | Janus Kinase 3 - genetics | Interleukin-2 - pharmacology | Protein Binding | Histones - metabolism | Primary Cell Culture | Methylation | CD4-Positive T-Lymphocytes - drug effects | Epigenetic inheritance | Chromatin | Cytokines | Genes | DNA binding proteins | Genetic transcription | T cells | Cell differentiation | Fos-related antigen | Transcription factors | Immunoprecipitation | Target recognition | Laboratories | Homeostasis | Lymphocytes T | Genomes | Biology | Activation | Leucine | Kinases | Experiments | Proteins | T-cell receptor | Signal transduction | Reporter gene | Immunology | Fos protein | Interleukin 2 | Fos-related antigen 2 | Lymphocytes | Transcription activation | DNA methylation | Elongation | Transducers | Cloning | Activator protein 1 | Stat5 protein | Gene expression | Immunological tolerance | Leucine zipper proteins | CD4 antigen | Studies | Signaling | Medical prognosis | γ-Interferon | Interferon | Gene mapping | Binding sites | Tumors | Cancer
BREAST-CANCER | HUMAN GENOME | CHROMATIN IMMUNOPRECIPITATION | MULTIDISCIPLINARY SCIENCES | TRANSCRIPTION | RECEPTOR | BINDING-SITES | IDENTIFICATION | EXPRESSION | DNASE HYPERSENSITIVE SITES | SOMATIC MUTATIONS | Luciferases - metabolism | Epigenesis, Genetic | Humans | Molecular Sequence Data | Fos-Related Antigen-2 - genetics | Luciferases - genetics | Janus Kinase 3 - antagonists & inhibitors | STAT5 Transcription Factor - genetics | STAT5 Transcription Factor - metabolism | Fos-Related Antigen-2 - metabolism | Antibodies, Monoclonal, Humanized - pharmacology | Base Sequence | DNA, Intergenic - metabolism | HEK293 Cells | Immunoglobulin G - pharmacology | Transcription, Genetic | Janus Kinase 3 - metabolism | Binding Sites | Genes, Reporter | Signal Transduction | Introns | Lymphocyte Activation | CD4-Positive T-Lymphocytes - cytology | CD4-Positive T-Lymphocytes - metabolism | Gene Expression Regulation | DNA, Intergenic - chemistry | Daclizumab | Histones - genetics | Janus Kinase 3 - genetics | Interleukin-2 - pharmacology | Protein Binding | Histones - metabolism | Primary Cell Culture | Methylation | CD4-Positive T-Lymphocytes - drug effects | Epigenetic inheritance | Chromatin | Cytokines | Genes | DNA binding proteins | Genetic transcription | T cells | Cell differentiation | Fos-related antigen | Transcription factors | Immunoprecipitation | Target recognition | Laboratories | Homeostasis | Lymphocytes T | Genomes | Biology | Activation | Leucine | Kinases | Experiments | Proteins | T-cell receptor | Signal transduction | Reporter gene | Immunology | Fos protein | Interleukin 2 | Fos-related antigen 2 | Lymphocytes | Transcription activation | DNA methylation | Elongation | Transducers | Cloning | Activator protein 1 | Stat5 protein | Gene expression | Immunological tolerance | Leucine zipper proteins | CD4 antigen | Studies | Signaling | Medical prognosis | γ-Interferon | Interferon | Gene mapping | Binding sites | Tumors | Cancer
Journal Article
The Journal of Clinical Pharmacology, ISSN 0091-2700, 02/2017, Volume 57, Issue 2, pp. 194 - 210
The spleen tyrosine kinase (SYK) regulates immune cell activation in response to engagement of a variety of receptors, making it an intriguing target for the...
allergy | immunopharmacology | SYK | PRT062607 | autoimmune | lymphoma | Protein Kinase Inhibitors - pharmacokinetics | Receptors, Antigen, B-Cell - drug effects | Single-Blind Method | Arthritis, Experimental - drug therapy | Humans | Half-Life | Rats | Male | Spleen - drug effects | Pyrimidines - pharmacology | Healthy Volunteers | Cyclohexylamines - pharmacokinetics | Respiratory Burst - drug effects | B-Lymphocytes - drug effects | Basophil Degranulation Test | Animals | Spleen - enzymology | Cyclohexylamines - pharmacology | Pyrimidines - pharmacokinetics | Adult | Dendritic Cells - drug effects | Protein Kinase Inhibitors - pharmacology | Macrophage Activation - drug effects | Protein-Tyrosine Kinases - antagonists & inhibitors | B-CELL DEVELOPMENT | RHEUMATOID-ARTHRITIS | RECEPTOR | NEUTROPHILS | TARGETING BTK | SYK INHIBITOR | SIGNAL-TRANSDUCTION | IN-VIVO | CHRONIC LYMPHOCYTIC-LEUKEMIA | PHARMACOLOGY & PHARMACY | Tyrosine | Care and treatment | Pharmacology | Research | Autoimmune diseases | Pharmacokinetics | Spleen | T cell receptors | Dosing | Antigens | Medical services | Activation | Arthritis | Selectivity | Kinases | Receptors | Inhibition | Immune system | Pharmacodynamics
allergy | immunopharmacology | SYK | PRT062607 | autoimmune | lymphoma | Protein Kinase Inhibitors - pharmacokinetics | Receptors, Antigen, B-Cell - drug effects | Single-Blind Method | Arthritis, Experimental - drug therapy | Humans | Half-Life | Rats | Male | Spleen - drug effects | Pyrimidines - pharmacology | Healthy Volunteers | Cyclohexylamines - pharmacokinetics | Respiratory Burst - drug effects | B-Lymphocytes - drug effects | Basophil Degranulation Test | Animals | Spleen - enzymology | Cyclohexylamines - pharmacology | Pyrimidines - pharmacokinetics | Adult | Dendritic Cells - drug effects | Protein Kinase Inhibitors - pharmacology | Macrophage Activation - drug effects | Protein-Tyrosine Kinases - antagonists & inhibitors | B-CELL DEVELOPMENT | RHEUMATOID-ARTHRITIS | RECEPTOR | NEUTROPHILS | TARGETING BTK | SYK INHIBITOR | SIGNAL-TRANSDUCTION | IN-VIVO | CHRONIC LYMPHOCYTIC-LEUKEMIA | PHARMACOLOGY & PHARMACY | Tyrosine | Care and treatment | Pharmacology | Research | Autoimmune diseases | Pharmacokinetics | Spleen | T cell receptors | Dosing | Antigens | Medical services | Activation | Arthritis | Selectivity | Kinases | Receptors | Inhibition | Immune system | Pharmacodynamics
Journal Article
PLoS ONE, ISSN 1932-6203, 01/2013, Volume 8, Issue 1, p. e54830
Background: With less than a 5% survival rate pancreatic adenocarcinoma (PDAC) is almost uniformly lethal. In order to make a significant impact on survival of...
INFLAMMATION | MULTIDISCIPLINARY SCIENCES | MAST-CELLS | GENES | STELLATE CELLS | INTRAEPITHELIAL NEOPLASIA | EXPRESSION | CARCINOMA | PROMOTES | TRANSCRIPTOME ANALYSIS | PROGRESSION | Carcinoma in Situ - pathology | Humans | Middle Aged | Pancreatic Neoplasms - pathology | Male | Pancreatic Neoplasms - genetics | Gene Expression Profiling | Disease Progression | Carcinoma in Situ - genetics | Pedigree | Biomarkers, Tumor - metabolism | Adult | Carcinoma - genetics | Biomarkers, Tumor - genetics | Carcinoma - pathology | Neoplasm Staging | Cluster Analysis | Care and treatment | Pancreatic cancer | Genomics | Development and progression | Genetic aspects | Genetic transcription | Health aspects | Adenocarcinoma | Transcription | Genes | Oncology | Genomes | Malignancy | Medical diagnosis | Precursors | Surgery | Lesions | Pancreas | Immune response | Invasiveness | Health risks | Stroma | Histology | Breast cancer | Gene expression | Epithelium | Patients | Survival | Surveillance | Diagnostic systems | Mutation | Cancer
INFLAMMATION | MULTIDISCIPLINARY SCIENCES | MAST-CELLS | GENES | STELLATE CELLS | INTRAEPITHELIAL NEOPLASIA | EXPRESSION | CARCINOMA | PROMOTES | TRANSCRIPTOME ANALYSIS | PROGRESSION | Carcinoma in Situ - pathology | Humans | Middle Aged | Pancreatic Neoplasms - pathology | Male | Pancreatic Neoplasms - genetics | Gene Expression Profiling | Disease Progression | Carcinoma in Situ - genetics | Pedigree | Biomarkers, Tumor - metabolism | Adult | Carcinoma - genetics | Biomarkers, Tumor - genetics | Carcinoma - pathology | Neoplasm Staging | Cluster Analysis | Care and treatment | Pancreatic cancer | Genomics | Development and progression | Genetic aspects | Genetic transcription | Health aspects | Adenocarcinoma | Transcription | Genes | Oncology | Genomes | Malignancy | Medical diagnosis | Precursors | Surgery | Lesions | Pancreas | Immune response | Invasiveness | Health risks | Stroma | Histology | Breast cancer | Gene expression | Epithelium | Patients | Survival | Surveillance | Diagnostic systems | Mutation | Cancer
Journal Article
Drug Design, Development and Therapy, 2017, Volume 11, pp. 123 - 131
This study investigated the effects of ponesimod, a selective S1P1 receptor modulator, on T lymphocyte subsets in 16 healthy subjects. Lymphocyte subset...
Multiple dose | CD45RA/CCR7 | S1P | receptor | Ponesimod | Lymphocyte subsets | Clearing | Lymphocyte receptors | CC chemokine receptors | CD8 antigen | CCR7 protein | CD45RA antigen | Effector cells | Cytotoxicity | Lymphocytes T | CD3 antigen | CD4 antigen | Homing | Lymphocytes B | Lymphocytes | Cell number | Natural killer cells | Cell migration | Flow cytometry | Multiple sclerosis | Memory cells | Immunoglobulins | Variance analysis | Cell adhesion & migration | Ethics | Immunology | Drug dosages
Multiple dose | CD45RA/CCR7 | S1P | receptor | Ponesimod | Lymphocyte subsets | Clearing | Lymphocyte receptors | CC chemokine receptors | CD8 antigen | CCR7 protein | CD45RA antigen | Effector cells | Cytotoxicity | Lymphocytes T | CD3 antigen | CD4 antigen | Homing | Lymphocytes B | Lymphocytes | Cell number | Natural killer cells | Cell migration | Flow cytometry | Multiple sclerosis | Memory cells | Immunoglobulins | Variance analysis | Cell adhesion & migration | Ethics | Immunology | Drug dosages
Journal Article
Microchimica Acta, ISSN 0026-3672, 06/2017, Volume 184, Issue 6, pp. 1773 - 1780
Three peptides (each containing 13-18 amino acids) were synthesized and used as templates for molecular imprinting and epitope recognition of the Regenerating...
Cyclic voltammetry | Hexacyanoferrate | Epitope recognition | PDAC | MIP | Peptide imprinted polymer | AFM | ESCA | CHEMISTRY, ANALYTICAL | RECOGNITION | POTENTIOSTAT | SENSORS | QUANTUM DOTS | TEMPLATES | NANOPARTICLES | POLY(ETHYLENE-CO-VINYL ALCOHOL) | SURFACE | Adenocarcinoma | Peptides | Analysis | Pancreatic cancer | Amino acids | Electric properties | Antigenic determinants | Urine | Proteins | Gold | Imprinted polymers | Biomarkers | Chemical synthesis | Molecular imprinting
Cyclic voltammetry | Hexacyanoferrate | Epitope recognition | PDAC | MIP | Peptide imprinted polymer | AFM | ESCA | CHEMISTRY, ANALYTICAL | RECOGNITION | POTENTIOSTAT | SENSORS | QUANTUM DOTS | TEMPLATES | NANOPARTICLES | POLY(ETHYLENE-CO-VINYL ALCOHOL) | SURFACE | Adenocarcinoma | Peptides | Analysis | Pancreatic cancer | Amino acids | Electric properties | Antigenic determinants | Urine | Proteins | Gold | Imprinted polymers | Biomarkers | Chemical synthesis | Molecular imprinting
Journal Article
British Journal of Clinical Pharmacology, ISSN 0306-5251, 12/2015, Volume 80, Issue 6, pp. 1324 - 1336
Aims The aim of the present study was to investigate whether selective antagonism of the cysteine‐X‐cysteine chemokine receptor‐2 (CXCR2) receptor has any...
phagocytosis | CXCR2 antagonist | oxidative burst | asthma | neutrophil recruitment | COPD | CHEMOKINE RECEPTOR CXCR2 | SEVERE ASTHMA | NADPH-OXIDASE | SPUTUM NEUTROPHILS | HEALTHY-SUBJECTS | AIRWAY INFLAMMATION | INTERLEUKIN-8 RECEPTORS | OBSTRUCTIVE PULMONARY-DISEASE | PHAGOCYTIC FUNCTION | PHARMACOLOGY & PHARMACY | CYSTIC-FIBROSIS | Phagocytosis - drug effects | Double-Blind Method | Immunity, Innate - drug effects | Humans | Middle Aged | Neutrophils - drug effects | Inflammation Mediators - blood | Neutrophils - immunology | Pyrimidines - pharmacology | Receptors, Interleukin-8B - antagonists & inhibitors | Sulfonamides - pharmacology | Respiratory Burst - drug effects | Cross-Over Studies | Granulocyte Colony-Stimulating Factor - pharmacology | Exercise | Adolescent | Pyrimidines - adverse effects | Sulfonamides - adverse effects | Adult | Leukocyte Count | Cysteine | Lung diseases, Obstructive | Superoxide | Escherichia coli | Clinical Trials
phagocytosis | CXCR2 antagonist | oxidative burst | asthma | neutrophil recruitment | COPD | CHEMOKINE RECEPTOR CXCR2 | SEVERE ASTHMA | NADPH-OXIDASE | SPUTUM NEUTROPHILS | HEALTHY-SUBJECTS | AIRWAY INFLAMMATION | INTERLEUKIN-8 RECEPTORS | OBSTRUCTIVE PULMONARY-DISEASE | PHAGOCYTIC FUNCTION | PHARMACOLOGY & PHARMACY | CYSTIC-FIBROSIS | Phagocytosis - drug effects | Double-Blind Method | Immunity, Innate - drug effects | Humans | Middle Aged | Neutrophils - drug effects | Inflammation Mediators - blood | Neutrophils - immunology | Pyrimidines - pharmacology | Receptors, Interleukin-8B - antagonists & inhibitors | Sulfonamides - pharmacology | Respiratory Burst - drug effects | Cross-Over Studies | Granulocyte Colony-Stimulating Factor - pharmacology | Exercise | Adolescent | Pyrimidines - adverse effects | Sulfonamides - adverse effects | Adult | Leukocyte Count | Cysteine | Lung diseases, Obstructive | Superoxide | Escherichia coli | Clinical Trials
Journal Article
British Journal of Clinical Pharmacology, ISSN 0306-5251, 12/2015, Volume 80, Issue 6, pp. 1324 - 1336
Journal Article
Nature Medicine, ISSN 1078-8956, 10/2003, Volume 9, Issue 10, pp. 1275 - 1280
Although the underlying mechanisms are not well understood, it is generally believed that antigen recognition by T cells in the absence of costimulation may...
MEDICINE, RESEARCH & EXPERIMENTAL | ANIMAL TRANSPLANT MODEL | TOLERANCE | BIOCHEMISTRY & MOLECULAR BIOLOGY | CD40 LIGAND | MONOCLONAL-ANTIBODY | DEFICIENT MICE | CUTTING EDGE | CELL BIOLOGY | RENAL-ALLOGRAFT REJECTION | NONOBESE DIABETIC MICE | DIABETOGENIC AUTOIMMUNITY | FUSION PROTEIN | Graft Survival - immunology | Immune System - physiology | Antibodies - metabolism | Immunoglobulin Fc Fragments - metabolism | Lymphocyte Activation | Mice, Inbred C57BL | Lymph Nodes - metabolism | Sirolimus - metabolism | Lymph Nodes - cytology | CD40 Ligand - immunology | Transplantation, Homologous | Complement System Proteins - metabolism | Immunosuppression | Animals | CD40 Antigens - metabolism | Immunoglobulin Fc Fragments - immunology | T-Lymphocytes - metabolism | Antibodies - immunology | Female | T-Lymphocytes - immunology | Mice | Mice, Inbred BALB C | CD40 Antigens - immunology
MEDICINE, RESEARCH & EXPERIMENTAL | ANIMAL TRANSPLANT MODEL | TOLERANCE | BIOCHEMISTRY & MOLECULAR BIOLOGY | CD40 LIGAND | MONOCLONAL-ANTIBODY | DEFICIENT MICE | CUTTING EDGE | CELL BIOLOGY | RENAL-ALLOGRAFT REJECTION | NONOBESE DIABETIC MICE | DIABETOGENIC AUTOIMMUNITY | FUSION PROTEIN | Graft Survival - immunology | Immune System - physiology | Antibodies - metabolism | Immunoglobulin Fc Fragments - metabolism | Lymphocyte Activation | Mice, Inbred C57BL | Lymph Nodes - metabolism | Sirolimus - metabolism | Lymph Nodes - cytology | CD40 Ligand - immunology | Transplantation, Homologous | Complement System Proteins - metabolism | Immunosuppression | Animals | CD40 Antigens - metabolism | Immunoglobulin Fc Fragments - immunology | T-Lymphocytes - metabolism | Antibodies - immunology | Female | T-Lymphocytes - immunology | Mice | Mice, Inbred BALB C | CD40 Antigens - immunology
Journal Article
Separation and Purification Technology, ISSN 1383-5866, 02/2018, Volume 192, pp. 213 - 219
Seven peptides (13–18 amino acids) were synthesized and used as templates for imprinting and recognition of Regenerating Protein 1 (REG1). Peptide-imprinted...
Peptide imprinting | Electrochemical sensing | Extraction | Regenerating protein | ENGINEERING, CHEMICAL | NANOPARTICLES | SERUM-ALBUMIN | URINE | ELECTROCHEMICAL SENSORS | BINDING | QUANTUM DOTS | Proteins | Usage | Pancreatic cancer | Escherichia coli | Antigenic determinants
Peptide imprinting | Electrochemical sensing | Extraction | Regenerating protein | ENGINEERING, CHEMICAL | NANOPARTICLES | SERUM-ALBUMIN | URINE | ELECTROCHEMICAL SENSORS | BINDING | QUANTUM DOTS | Proteins | Usage | Pancreatic cancer | Escherichia coli | Antigenic determinants
Journal Article
Drug Design, Development and Therapy, ISSN 1177-8881, 01/2017, Volume 11, p. 123
This study investigated the effects of ponesimod, a selective S1Pj receptor modulator, on T lymphocyte subsets in 16 healthy subjects. Lymphocyte subset...
Pharmacology, Experimental | Lymphocytes | Sphingosine | Physiological aspects | Research | Health aspects | Immunopharmacology | Immunosuppressive agents
Pharmacology, Experimental | Lymphocytes | Sphingosine | Physiological aspects | Research | Health aspects | Immunopharmacology | Immunosuppressive agents
Journal Article
Drug Design, Development and Therapy, ISSN 1177-8881, 12/2016, Volume 11, pp. 123 - 131
Journal Article
Drug design, development and therapy, 2017, Volume 11, p. 123
This study investigated the effects of ponesimod, a selective S1P receptor modulator, on T lymphocyte subsets in 16 healthy subjects. Lymphocyte subset...
Administration, Oral | Lymphocyte Subsets - drug effects | Humans | Thiazoles - administration & dosage | Healthy Volunteers | Dose-Response Relationship, Drug | B-Lymphocytes - drug effects | Lymphocyte Subsets - metabolism | Flow Cytometry | T-Lymphocytes - metabolism | T-Lymphocytes - drug effects | Thiazoles - pharmacology | Receptors, Lysosphingolipid - metabolism | B-Lymphocytes - metabolism
Administration, Oral | Lymphocyte Subsets - drug effects | Humans | Thiazoles - administration & dosage | Healthy Volunteers | Dose-Response Relationship, Drug | B-Lymphocytes - drug effects | Lymphocyte Subsets - metabolism | Flow Cytometry | T-Lymphocytes - metabolism | T-Lymphocytes - drug effects | Thiazoles - pharmacology | Receptors, Lysosphingolipid - metabolism | B-Lymphocytes - metabolism
Journal Article
Clinical Therapeutics, ISSN 0149-2918, 2008, Volume 30, Issue 1, pp. 131 - 142
Abstract Background: Several studies have suggested that a significant proportion of the toxicity profile of the an-tifolate methotrexate can be attributed to...
Internal Medicine | Medical Education | Psoriasis | Methotrexate | Autoimmune diseases | rheumatoid arthritis | CH-1504 | autoimmune diseases | psoriasis | RATS | methotrexate | PHARMACOLOGY & PHARMACY | Drug Eruptions - etiology | Folic Acid Antagonists - administration & dosage | Double-Blind Method | Humans | Aminopterin - pharmacokinetics | Male | Aminopterin - adverse effects | Aminopterin - administration & dosage | Dose-Response Relationship, Drug | Adult | Molecular Structure | Aminopterin - analogs & derivatives | Folic Acid Antagonists - adverse effects | Folic Acid Antagonists - pharmacokinetics | Index Medicus
Internal Medicine | Medical Education | Psoriasis | Methotrexate | Autoimmune diseases | rheumatoid arthritis | CH-1504 | autoimmune diseases | psoriasis | RATS | methotrexate | PHARMACOLOGY & PHARMACY | Drug Eruptions - etiology | Folic Acid Antagonists - administration & dosage | Double-Blind Method | Humans | Aminopterin - pharmacokinetics | Male | Aminopterin - adverse effects | Aminopterin - administration & dosage | Dose-Response Relationship, Drug | Adult | Molecular Structure | Aminopterin - analogs & derivatives | Folic Acid Antagonists - adverse effects | Folic Acid Antagonists - pharmacokinetics | Index Medicus
Journal Article