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Wyświetlanie 1-20 z 84
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
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
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
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
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
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
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
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
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
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
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
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
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
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
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
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
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
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
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
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
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
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
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
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Human alveolar macrophages display marked hypo-responsiveness to IFN-γ in both proteomic and gene expression analysis.
Autorzy:
Thiel, Bonnie A. (AUTHOR)
Lundberg, Kathleen C. (AUTHOR)
Schlatzer, Daniela (AUTHOR)
Jarvela, Jessica (AUTHOR)
Li, Qing (AUTHOR)
Shaw, Rachel (AUTHOR)
Reba, Scott M. (AUTHOR)
Fletcher, Shane (AUTHOR)
Beckloff, Sara E. (AUTHOR)
Chance, Mark R. (AUTHOR)
Boom, W. Henry (AUTHOR)
Silver, Richard F. (AUTHOR)
Bebek, Gurkan (AUTHOR)
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Źródło:
PLoS ONE. 2/1/2024, Vol. 19 Issue 2, p1-14. 14p.
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
CXCR2 signaling might have a tumor-suppressive role in patients with cholangiocarcinoma.
Autorzy:
Yamamoto, Yurie (AUTHOR)
Sugimoto, Atsushi (AUTHOR)
Maruo, Koji (AUTHOR)
Tsujio, Gen (AUTHOR)
Sera, Tomohiro (AUTHOR)
Kushiyama, Shuhei (AUTHOR)
Nishimura, Sadaaki (AUTHOR)
Kuroda, Kenji (AUTHOR)
Togano, Shingo (AUTHOR)
Eguchi, Shinpei (AUTHOR)
Tanaka, Ryota (AUTHOR)
Kimura, Kenjiro (AUTHOR)
Amano, Ryosuke (AUTHOR)
Ohira, Masaichi (AUTHOR)
Yashiro, Masakazu (AUTHOR)
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Źródło:
PLoS ONE. 4/4/2022, Vol. 17 Issue 4, p1-10. 10p.
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Wyświetlanie 1-20 z 84

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