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Wyszukujesz frazę ""Chemokine CXCL9"" wg kryterium: Temat


Wyświetlanie 1-17 z 17
Tytuł:
CXCL9, CXCL10, and CXCL11; biomarkers of pulmonary inflammation associated with autoimmunity in patients with collagen vascular diseases-associated interstitial lung disease and interstitial pneumonia with autoimmune features.
Autorzy:
Kameda M; Department of Respiratory Medicine and Allergology, Sapporo Medical University School of Medicine, Sapporo, Hokkaido, Japan.
Otsuka M; Department of Respiratory Medicine, Sapporo-Kosei General Hospital, Sapporo, Hokkaido, Japan.
Chiba H; Department of Respiratory Medicine and Allergology, Sapporo Medical University School of Medicine, Sapporo, Hokkaido, Japan.
Kuronuma K; Department of Respiratory Medicine and Allergology, Sapporo Medical University School of Medicine, Sapporo, Hokkaido, Japan.
Hasegawa T; Sysmex Corporation, Kobe, Japan.
Takahashi H; Department of Rheumatology, Sapporo Medical University School of Medicine, Sapporo, Hokkaido, Japan.
Takahashi H; Department of Respiratory Medicine and Allergology, Sapporo Medical University School of Medicine, Sapporo, Hokkaido, Japan.
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Źródło:
PloS one [PLoS One] 2020 Nov 02; Vol. 15 (11), pp. e0241719. Date of Electronic Publication: 2020 Nov 02 (Print Publication: 2020).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Biomarkers/*blood
Chemokine CXCL10/*blood
Chemokine CXCL11/*blood
Chemokine CXCL9/*blood
Lung Diseases, Interstitial/*diagnosis
Vascular Diseases/*complications
Aged ; Autoimmunity ; Biomarkers/analysis ; Bronchoalveolar Lavage Fluid/chemistry ; Bronchoalveolar Lavage Fluid/cytology ; Bronchoalveolar Lavage Fluid/immunology ; C-Reactive Protein/analysis ; Chemokine CXCL10/analysis ; Chemokine CXCL11/analysis ; Chemokine CXCL9/analysis ; Collagen/metabolism ; Female ; Humans ; Idiopathic Pulmonary Fibrosis/diagnosis ; Lung Diseases, Interstitial/etiology ; Lymphocytes/cytology ; Lymphocytes/metabolism ; Macrophages/cytology ; Macrophages/metabolism ; Male ; Middle Aged ; Retrospective Studies ; Vascular Diseases/pathology ; Vital Capacity
Czasopismo naukowe
Tytuł:
Hepatectomy leads to loss of TRAIL-expressing liver NK cells via downregulation of the CXCL9-CXCR3 axis in mice.
Autorzy:
Yano T; Department of Gastroenterological and Transplant Surgery, Applied Life Sciences, Institute of Biomedical & Health Sciences, Hiroshima University, Hiroshima, Japan.
Ohira M; Department of Gastroenterological and Transplant Surgery, Applied Life Sciences, Institute of Biomedical & Health Sciences, Hiroshima University, Hiroshima, Japan.
Nakano R; Department of Gastroenterological and Transplant Surgery, Applied Life Sciences, Institute of Biomedical & Health Sciences, Hiroshima University, Hiroshima, Japan.
Tanaka Y; Department of Gastroenterological and Transplant Surgery, Applied Life Sciences, Institute of Biomedical & Health Sciences, Hiroshima University, Hiroshima, Japan.
Ohdan H; Department of Gastroenterological and Transplant Surgery, Applied Life Sciences, Institute of Biomedical & Health Sciences, Hiroshima University, Hiroshima, Japan.
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Źródło:
PloS one [PLoS One] 2017 Oct 31; Vol. 12 (10), pp. e0186997. Date of Electronic Publication: 2017 Oct 31 (Print Publication: 2017).
Typ publikacji:
Journal Article
MeSH Terms:
Chemokine CXCL9/*genetics
Hepatectomy/*methods
Killer Cells, Natural/*metabolism
Liver/*metabolism
Receptors, CXCR3/*genetics
TNF-Related Apoptosis-Inducing Ligand/*genetics
Animals ; Chemokine CXCL9/metabolism ; Down-Regulation ; Female ; Flow Cytometry ; Gene Expression ; Male ; Mice, Inbred C57BL ; Mice, Knockout ; Perioperative Period ; Receptors, CXCR3/metabolism ; Reverse Transcriptase Polymerase Chain Reaction ; TNF-Related Apoptosis-Inducing Ligand/metabolism
Czasopismo naukowe
Tytuł:
Serum CXCL9 and CCL17 as biomarkers of declining pulmonary function in chronic bird-related hypersensitivity pneumonitis.
Autorzy:
Nukui Y; Department of Respiratory Medicine, Tokyo Medical and Dental University, Bunkyo-ku, Tokyo, Japan.
Yamana T; Department of Respiratory Medicine, Tokyo Medical and Dental University, Bunkyo-ku, Tokyo, Japan.
Masuo M; Department of Respiratory Medicine, Tokyo Medical and Dental University, Bunkyo-ku, Tokyo, Japan.
Tateishi T; Department of Respiratory Medicine, Tokyo Medical and Dental University, Bunkyo-ku, Tokyo, Japan.
Kishino M; Department of Diagnostic Radiology, Tokyo Medical and Dental University, Bunkyo-ku, Tokyo, Japan.
Tateishi U; Department of Diagnostic Radiology, Tokyo Medical and Dental University, Bunkyo-ku, Tokyo, Japan.
Tomita M; Department of Clinical Research Center, Tokyo Medical and Dental University, Bunkyo-ku, Tokyo, Japan.
Hasegawa T; Sysmex Corporation, Nishi-Ku, Kobe, Japan.
Aritsu T; Sysmex Corporation, Nishi-Ku, Kobe, Japan.
Miyazaki Y; Department of Respiratory Medicine, Tokyo Medical and Dental University, Bunkyo-ku, Tokyo, Japan.
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Źródło:
PloS one [PLoS One] 2019 Aug 01; Vol. 14 (8), pp. e0220462. Date of Electronic Publication: 2019 Aug 01 (Print Publication: 2019).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Allergens*/immunology
Birds*/immunology
Alveolitis, Extrinsic Allergic/*blood
Chemokine CCL17/*blood
Chemokine CXCL9/*blood
Lung/*physiopathology
Adult ; Aged ; Alveolitis, Extrinsic Allergic/diagnosis ; Alveolitis, Extrinsic Allergic/etiology ; Alveolitis, Extrinsic Allergic/physiopathology ; Animals ; Biomarkers/blood ; Bronchoalveolar Lavage Fluid/chemistry ; Bronchoalveolar Lavage Fluid/cytology ; Female ; Humans ; Male ; Middle Aged ; Mucin-1/blood ; Respiratory Function Tests ; Vital Capacity
Czasopismo naukowe
Tytuł:
Extracellular Histones Induce Chemokine Production in Whole Blood Ex Vivo and Leukocyte Recruitment In Vivo.
Autorzy:
Westman J; Department of Clinical Sciences, Division of Infection Medicine, Biomedical Center, Lund, Sweden.
Papareddy P; Department of Clinical Sciences, Division of Infection Medicine, Biomedical Center, Lund, Sweden.
Dahlgren MW; Department of Experimental Medical Science, Adaptive Immunity, Biomedical Center, Lund, Sweden.
Chakrakodi B; Department of Medicine, Center for Infectious Medicine, Karolinska Institutet, Karolinska University Hospital Huddinge, Stockholm, Sweden.
Norrby-Teglund A; Department of Medicine, Center for Infectious Medicine, Karolinska Institutet, Karolinska University Hospital Huddinge, Stockholm, Sweden.
Smeds E; Department of Clinical Sciences, Division of Infection Medicine, Biomedical Center, Lund, Sweden.
Linder A; Department of Clinical Sciences, Division of Infection Medicine, Biomedical Center, Lund, Sweden.
Mörgelin M; Department of Clinical Sciences, Division of Infection Medicine, Biomedical Center, Lund, Sweden.
Johansson-Lindbom B; Department of Experimental Medical Science, Adaptive Immunity, Biomedical Center, Lund, Sweden.
Egesten A; Department of Clinical Sciences, Respiratory Medicine & Allergy, Biomedical Center, Lund, Sweden.
Herwald H; Department of Clinical Sciences, Division of Infection Medicine, Biomedical Center, Lund, Sweden.
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Źródło:
PLoS pathogens [PLoS Pathog] 2015 Dec 08; Vol. 11 (12), pp. e1005319. Date of Electronic Publication: 2015 Dec 08 (Print Publication: 2015).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chemokine CXCL10/*biosynthesis
Chemokine CXCL9/*biosynthesis
Chemotaxis, Leukocyte/*immunology
Histones/*immunology
Leukocytes/*immunology
Animals ; Chemokine CXCL10/immunology ; Chemokine CXCL9/immunology ; Chemokines/biosynthesis ; Enzyme-Linked Immunosorbent Assay ; Female ; Humans ; Leukocytes/metabolism ; Male ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Mice, Knockout ; Microscopy, Immunoelectron ; Monocytes/immunology ; Surface Plasmon Resonance
Czasopismo naukowe
Tytuł:
Left Ventricular Dysfunction and CXCR3 Ligands in Hypertension: From Animal Experiments to a Population-Based Pilot Study.
Autorzy:
Altara R; Department of Pharmacology and Toxicology, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, The Netherlands.
Gu YM; Studies Coordinating Centre, Research Unit Hypertension and Cardiovascular Epidemiology, KU Leuven Department of Cardiovascular Sciences, University of Leuven, Leuven, Belgium.
Struijker-Boudier HA; Department of Pharmacology and Toxicology, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, The Netherlands.
Thijs L; Studies Coordinating Centre, Research Unit Hypertension and Cardiovascular Epidemiology, KU Leuven Department of Cardiovascular Sciences, University of Leuven, Leuven, Belgium.
Staessen JA; Studies Coordinating Centre, Research Unit Hypertension and Cardiovascular Epidemiology, KU Leuven Department of Cardiovascular Sciences, University of Leuven, Leuven, Belgium; VitaK Research and Development, Maastricht University, Maastricht, The Netherlands.
Blankesteijn WM; Department of Pharmacology and Toxicology, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, The Netherlands.
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Źródło:
PloS one [PLoS One] 2015 Oct 27; Vol. 10 (10), pp. e0141394. Date of Electronic Publication: 2015 Oct 27 (Print Publication: 2015).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chemokine CXCL10/*blood
Chemokine CXCL11/*blood
Chemokine CXCL9/*blood
Hypertension/*blood
Ventricular Dysfunction, Left/*blood
Animals ; Blood Pressure ; Chemokine CXCL9/genetics ; Female ; Humans ; Hypertension/genetics ; Hypertension/physiopathology ; Inflammation/blood ; Inflammation/genetics ; Inflammation/physiopathology ; Ligands ; Male ; Mice ; Natriuretic Peptide, Brain/blood ; Peptide Fragments/blood ; Receptors, CXCR3/blood ; Receptors, CXCR3/genetics ; Ventricular Dysfunction, Left/genetics ; Ventricular Dysfunction, Left/physiopathology
Czasopismo naukowe
Tytuł:
Effect of JAK Inhibitors on Release of CXCL9, CXCL10 and CXCL11 from Human Airway Epithelial Cells.
Autorzy:
Fenwick PS; Airway Disease, National Heart and Lung Institute, Imperial College London, London, United Kingdom.
Macedo P; Airway Disease, National Heart and Lung Institute, Imperial College London, London, United Kingdom.
Kilty IC; Pfizer Inc, Cambridge, Massachusetts, United States of America.
Barnes PJ; Airway Disease, National Heart and Lung Institute, Imperial College London, London, United Kingdom.
Donnelly LE; Airway Disease, National Heart and Lung Institute, Imperial College London, London, United Kingdom.
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Źródło:
PloS one [PLoS One] 2015 Jun 19; Vol. 10 (6), pp. e0128757. Date of Electronic Publication: 2015 Jun 19 (Print Publication: 2015).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chemokine CXCL10/*metabolism
Chemokine CXCL11/*metabolism
Chemokine CXCL9/*metabolism
Epithelial Cells/*drug effects
Epithelial Cells/*metabolism
Protein Kinase Inhibitors/*pharmacology
Respiratory Mucosa/*metabolism
Aged ; Cell Line ; Chemokine CXCL10/genetics ; Chemokine CXCL11/genetics ; Chemokine CXCL9/genetics ; Female ; Gene Expression Regulation/drug effects ; Humans ; Inhibitory Concentration 50 ; Janus Kinases/antagonists & inhibitors ; Male ; Middle Aged ; Receptors, CXCR3/metabolism ; STAT1 Transcription Factor/metabolism ; Transcription, Genetic
Czasopismo naukowe
Tytuł:
CXCL9 associated with sustained virological response in chronic hepatitis B patients receiving peginterferon alfa-2a therapy: a pilot study.
Autorzy:
Lee IC; Division of Gastroenterology, Department of Medicine, Taipei Veterans General Hospital, Taipei, Taiwan ; Institute of Clinical Medicine, National Yang-Ming University School of Medicine, Taipei, Taiwan ; Department of Medicine, National Yang-Ming University Hospital, I-Lan, Taiwan.
Huang YH
Su CW
Wang YJ
Huo TI
Lee KC
Lin HC
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Źródło:
PloS one [PLoS One] 2013 Oct 04; Vol. 8 (10), pp. e76798. Date of Electronic Publication: 2013 Oct 04 (Print Publication: 2013).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Hepatitis B virus*/genetics
Hepatitis B virus*/immunology
Chemokine CXCL9/*metabolism
Hepatitis B, Chronic/*metabolism
Hepatitis B, Chronic/*virology
Adult ; Alanine Transaminase/blood ; Alanine Transaminase/metabolism ; Antiviral Agents/therapeutic use ; Chemokine CXCL9/blood ; Cytokines/blood ; Cytokines/metabolism ; Female ; Genotype ; Hepatitis B e Antigens/immunology ; Hepatitis B, Chronic/drug therapy ; Humans ; Interferon-alpha/therapeutic use ; Male ; Middle Aged ; Pilot Projects ; Polyethylene Glycols/therapeutic use ; Prognosis ; Recombinant Proteins/therapeutic use ; Time Factors ; Treatment Outcome ; Viral Load
Czasopismo naukowe
Tytuł:
Myocardial chemokine expression and intensity of myocarditis in Chagas cardiomyopathy are controlled by polymorphisms in CXCL9 and CXCL10.
Autorzy:
Nogueira LG; Laboratory of Immunology, Heart Institute (InCor), School of Medicine, University of São Paulo, São Paulo, Brazil.
Santos RH
Ianni BM
Fiorelli AI
Mairena EC
Benvenuti LA
Frade A
Donadi E
Dias F
Saba B
Wang HT
Fragata A
Sampaio M
Hirata MH
Buck P
Mady C
Bocchi EA
Stolf NA
Kalil J
Cunha-Neto E
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Źródło:
PLoS neglected tropical diseases [PLoS Negl Trop Dis] 2012; Vol. 6 (10), pp. e1867. Date of Electronic Publication: 2012 Oct 25.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Polymorphism, Genetic*
Chagas Cardiomyopathy/*genetics
Chagas Cardiomyopathy/*pathology
Chemokine CXCL10/*biosynthesis
Chemokine CXCL9/*biosynthesis
Trypanosoma cruzi/*pathogenicity
Adolescent ; Adult ; Chemokine CXCL10/genetics ; Chemokine CXCL9/genetics ; Disease Resistance ; Female ; Gene Expression Profiling ; Humans ; Male ; Middle Aged ; Young Adult
Czasopismo naukowe
Tytuł:
MIG and the regulatory cytokines IL-10 and TGF-β1 correlate with malaria vaccine immunogenicity and efficacy.
Autorzy:
Dunachie SJ; Centre for Clinical Vaccinology and Tropical Medicine, The Jenner Institute, University of Oxford, Oxford, United Kingdom. />Berthoud T
Keating SM
Hill AV
Fletcher HA
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Źródło:
PloS one [PLoS One] 2010 Sep 03; Vol. 5 (9), pp. e12557. Date of Electronic Publication: 2010 Sep 03.
Typ publikacji:
Clinical Trial; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Gene Expression Regulation*
Chemokine CXCL9/*immunology
Interleukin-10/*immunology
Malaria Vaccines/*immunology
Malaria, Falciparum/*immunology
Transforming Growth Factor beta1/*immunology
Antibodies, Protozoan/immunology ; Chemokine CXCL9/genetics ; Humans ; Interferon-gamma/genetics ; Interferon-gamma/immunology ; Interleukin-10/genetics ; Malaria Vaccines/administration & dosage ; Malaria, Falciparum/parasitology ; Malaria, Falciparum/prevention & control ; Plasmodium falciparum/immunology ; Protozoan Proteins/administration & dosage ; Protozoan Proteins/immunology ; Transforming Growth Factor beta1/genetics
Czasopismo naukowe
Tytuł:
Chemokine Transfer by Liver Sinusoidal Endothelial Cells Contributes to the Recruitment of CD4+ T Cells into the Murine Liver.
Autorzy:
Neumann K; Department of Medicine I for Gastroenterology, Infectious Diseases and Rheumatology, Campus Benjamin Franklin, Charité-Universitätsmedizin Berlin, Berlin, Germany; Research Center Immunosciences, Charité-Universitätsmedizin, Berlin, Germany; Department of Cellular Immunology, Clinic for Rheumatology and Clinical Immunology, Charité-Universitätsmedizin, Berlin, Germany.
Erben U; Department of Medicine I for Gastroenterology, Infectious Diseases and Rheumatology, Campus Benjamin Franklin, Charité-Universitätsmedizin Berlin, Berlin, Germany; Research Center Immunosciences, Charité-Universitätsmedizin, Berlin, Germany.
Kruse N; Department of Medicine I for Gastroenterology, Infectious Diseases and Rheumatology, Campus Benjamin Franklin, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Wechsung K; Department of Medicine I for Gastroenterology, Infectious Diseases and Rheumatology, Campus Benjamin Franklin, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Schumann M; Department of Medicine I for Gastroenterology, Infectious Diseases and Rheumatology, Campus Benjamin Franklin, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Klugewitz K; Department of Medicine I for Gastroenterology, Infectious Diseases and Rheumatology, Campus Benjamin Franklin, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Scheffold A; Department of Cellular Immunology, Clinic for Rheumatology and Clinical Immunology, Charité-Universitätsmedizin, Berlin, Germany; German Rheumatism Research Centre Berlin, an Institute of the Leibniz-Association, Berlin, Germany.
Kühl AA; Department of Medicine I for Gastroenterology, Infectious Diseases and Rheumatology, Campus Benjamin Franklin, Charité-Universitätsmedizin Berlin, Berlin, Germany; Research Center Immunosciences, Charité-Universitätsmedizin, Berlin, Germany.
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Źródło:
PloS one [PLoS One] 2015 Jun 08; Vol. 10 (6), pp. e0123867. Date of Electronic Publication: 2015 Jun 08 (Print Publication: 2015).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chemokine CXCL10/*metabolism
Chemokine CXCL12/*metabolism
Chemokine CXCL9/*metabolism
Endothelial Cells/*metabolism
Liver/*pathology
Animals ; CD4-Positive T-Lymphocytes/immunology ; Caveolae/drug effects ; Caveolae/metabolism ; Chlorpromazine/pharmacology ; Clathrin/metabolism ; Clathrin-Coated Vesicles/drug effects ; Clathrin-Coated Vesicles/metabolism ; Endocytosis/drug effects ; Endosomes/drug effects ; Endosomes/metabolism ; Endothelial Cells/drug effects ; Hepatitis/immunology ; Hepatitis/pathology ; Homeostasis/drug effects ; Inflammation/pathology ; Inflammation Mediators/metabolism ; Liver/drug effects ; Liver/immunology ; Lysosomes/drug effects ; Lysosomes/metabolism ; Mice, Inbred C57BL
Czasopismo naukowe
Tytuł:
CXCL9 contributes to antimicrobial protection of the gut during citrobacter rodentium infection independent of chemokine-receptor signaling.
Autorzy:
Reid-Yu SA; Michael G. DeGroote Institute for Infectious Disease Research, Hamilton, Ontario, Canada; Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Ontario, Canada.
Tuinema BR; Michael G. DeGroote Institute for Infectious Disease Research, Hamilton, Ontario, Canada; Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Ontario, Canada.
Small CN; Michael G. DeGroote Institute for Infectious Disease Research, Hamilton, Ontario, Canada; Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Ontario, Canada.
Xing L; Michael G. DeGroote Institute for Infectious Disease Research, Hamilton, Ontario, Canada; Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Ontario, Canada.
Coombes BK; Michael G. DeGroote Institute for Infectious Disease Research, Hamilton, Ontario, Canada; Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Ontario, Canada; Farncombe Family Digestive Health Research Institute, Hamilton, Ontario, Canada.
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Źródło:
PLoS pathogens [PLoS Pathog] 2015 Feb 02; Vol. 11 (2), pp. e1004648. Date of Electronic Publication: 2015 Feb 02 (Print Publication: 2015).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chemokine CXCL9/*immunology
Enterobacteriaceae Infections/*immunology
Intestinal Mucosa/*immunology
Signal Transduction/*immunology
Animals ; Chemokines/immunology ; Citrobacter rodentium/immunology ; Enzyme-Linked Immunosorbent Assay ; Mice ; Mice, Inbred C57BL ; Mice, Knockout
Czasopismo naukowe
Tytuł:
Knock-down of CD44 regulates endothelial cell differentiation via NFκB-mediated chemokine production.
Autorzy:
Olofsson B; Ludwig Institute for Cancer Research, Science for Life Laboratory, Uppsala University, Biomedical Center, Uppsala, Sweden.
Porsch H; Ludwig Institute for Cancer Research, Science for Life Laboratory, Uppsala University, Biomedical Center, Uppsala, Sweden.
Heldin P; Ludwig Institute for Cancer Research, Science for Life Laboratory, Uppsala University, Biomedical Center, Uppsala, Sweden.
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Źródło:
PloS one [PLoS One] 2014 Mar 10; Vol. 9 (3), pp. e90921. Date of Electronic Publication: 2014 Mar 10 (Print Publication: 2014).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Cell Differentiation*
Gene Knockdown Techniques*
Chemokine CXCL12/*metabolism
Chemokine CXCL9/*metabolism
Endothelial Cells/*cytology
Endothelial Cells/*metabolism
Hyaluronan Receptors/*metabolism
NF-kappa B/*metabolism
Cell Adhesion ; Cell Adhesion Molecules/metabolism ; Cell Line, Tumor ; Extracellular Signal-Regulated MAP Kinases/metabolism ; GPI-Linked Proteins/metabolism ; Gene Expression Regulation ; Gene Silencing ; Humans ; Hyaluronic Acid/metabolism ; Hyaluronoglucosaminidase/metabolism ; Male ; Membrane Fusion ; Microvessels/cytology ; Neovascularization, Physiologic ; Protein Transport ; Receptors, Chemokine/metabolism ; Signal Transduction ; Telomerase/metabolism ; Vacuoles/metabolism
Czasopismo naukowe
Tytuł:
Serum CXCL9 levels are associated with tumor progression and treatment outcome in patients with nasopharyngeal carcinoma.
Autorzy:
Hsin LJ; Department of Otolaryngology-Head & Neck Surgery, Chang Gung Memorial Hospital at Lin-Kou, Tao-Yuan, Taiwan.
Kao HK
Chen IH
Tsang NM
Hsu CL
Liu SC
Chang YS
Chang KP
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Źródło:
PloS one [PLoS One] 2013 Nov 21; Vol. 8 (11), pp. e80052. Date of Electronic Publication: 2013 Nov 21 (Print Publication: 2013).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chemokine CXCL9/*blood
Nasopharyngeal Neoplasms/*blood
Adult ; Case-Control Studies ; DNA, Viral/blood ; Disease Progression ; Enzyme-Linked Immunosorbent Assay ; Female ; Herpesvirus 4, Human/isolation & purification ; Humans ; Male ; Middle Aged ; Nasopharyngeal Neoplasms/pathology ; Nasopharyngeal Neoplasms/therapy ; Real-Time Polymerase Chain Reaction ; Treatment Outcome ; Viral Load
Czasopismo naukowe
Tytuł:
CSF CXCL10, CXCL9, and neopterin as candidate prognostic biomarkers for HTLV-1-associated myelopathy/tropical spastic paraparesis.
Autorzy:
Sato T; Department of Rare Diseases Research, Institute of Medical Science, St. Marianna University School of Medicine, Kawasaki, Kanagawa, Japan.
Coler-Reilly A
Utsunomiya A
Araya N
Yagishita N
Ando H
Yamauchi J
Inoue E
Ueno T
Hasegawa Y
Nishioka K
Nakajima T
Jacobson S
Izumo S
Yamano Y
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Źródło:
PLoS neglected tropical diseases [PLoS Negl Trop Dis] 2013 Oct 10; Vol. 7 (10), pp. e2479. Date of Electronic Publication: 2013 Oct 10 (Print Publication: 2013).
Typ publikacji:
Evaluation Study; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Biomarkers/*cerebrospinal fluid
Chemokine CXCL10/*cerebrospinal fluid
Chemokine CXCL9/*cerebrospinal fluid
HTLV-I Infections/*diagnosis
Neopterin/*cerebrospinal fluid
Adult ; Aged ; Disease Progression ; Female ; Humans ; Male ; Middle Aged ; Prognosis ; ROC Curve ; Retrospective Studies ; Young Adult
Czasopismo naukowe
Tytuł:
Gene profile of chemokines on hepatic stellate cells of schistosome-infected mice and antifibrotic roles of CXCL9/10 on liver non-parenchymal cells.
Autorzy:
Liang YJ; Department of Pathogen Biology, Key Laboratory of Pathogen Biology of Jiangsu Province, Nanjing Medical University, Nanjing, Jiangsu, China.
Luo J
Lu Q
Zhou Y
Wu HW
Zheng D
Ren YY
Sun KY
Wang Y
Zhang ZS
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Źródło:
PloS one [PLoS One] 2012; Vol. 7 (8), pp. e42490. Date of Electronic Publication: 2012 Aug 08.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Gene Expression Regulation*
Chemokine CXCL10/*metabolism
Chemokine CXCL9/*metabolism
Chemokines/*biosynthesis
Hepatic Stellate Cells/*metabolism
Liver/*metabolism
Schistosoma japonicum/*immunology
Schistosomiasis/*metabolism
Animals ; Chemokine CXCL11/metabolism ; Chemokines/metabolism ; Female ; Gene Expression Profiling ; Genome ; Humans ; Mice ; Mice, Inbred BALB C ; Platelet Factor 4/metabolism ; Praziquantel/pharmacology ; Schistosoma japonicum/metabolism
Czasopismo naukowe
Tytuł:
Interferon-inducible CXC chemokines directly contribute to host defense against inhalational anthrax in a murine model of infection.
Autorzy:
Crawford MA; Department of Medicine, University of Virginia, Charlottesville, VA, USA.
Burdick MD
Glomski IJ
Boyer AE
Barr JR
Mehrad B
Strieter RM
Hughes MA
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Źródło:
PLoS pathogens [PLoS Pathog] 2010 Nov 18; Vol. 6 (11), pp. e1001199. Date of Electronic Publication: 2010 Nov 18.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Disease Models, Animal*
Anthrax/*immunology
Bacillus anthracis/*drug effects
Chemokine CXCL10/*immunology
Chemokine CXCL11/*immunology
Chemokine CXCL9/*immunology
Interferons/*pharmacology
Administration, Inhalation ; Animals ; Anthrax/microbiology ; Antiviral Agents/pharmacology ; Bacillus anthracis/pathogenicity ; Female ; Luminescence ; Lung/immunology ; Lung/metabolism ; Lung/microbiology ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Spores, Bacterial/immunology
Czasopismo naukowe
Tytuł:
ESAT6-induced IFNgamma and CXCL9 can differentiate severity of tuberculosis.
Autorzy:
Hasan Z; Department of Pathology and Microbiology, The Aga Khan University, Karachi, Pakistan. />Jamil B
Ashraf M
Islam M
Yusuf MS
Khan JA
Hussain R
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Źródło:
PloS one [PLoS One] 2009; Vol. 4 (4), pp. e5158. Date of Electronic Publication: 2009 Apr 02.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Antigens, Bacterial/*physiology
Bacterial Proteins/*physiology
Chemokine CXCL9/*physiology
Interferon-gamma/*physiology
Humans
Czasopismo naukowe
    Wyświetlanie 1-17 z 17

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