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Wyszukujesz frazę ""Marsh CB"" wg kryterium: Autor


Tytuł:
Molecular Analysis of ZNF71 KRAB in Non-Small-Cell Lung Cancer.
Autorzy:
Ye Q; WVU Cancer Institute, West Virginia University, Morgantown, WV 26506, USA.; Lane Department of Computer Science and Electrical Engineering, West Virginia University, Morgantown, WV 26506, USA.
Mohamed R; WVU Cancer Institute, West Virginia University, Morgantown, WV 26506, USA.
Dakhlallah D; WVU Cancer Institute, West Virginia University, Morgantown, WV 26506, USA.; Department of Microbiology, Immunology & Cell Biology, West Virginia University, Morgantown, WV 26506, USA.; Institute of Global Health and Human Ecology, School of Sciences & Engineering, The American University of Cairo, New Cairo 11835, Egypt.
Gencheva M; Department of Microbiology, Immunology & Cell Biology, West Virginia University, Morgantown, WV 26506, USA.
Hu G; WVU Cancer Institute, West Virginia University, Morgantown, WV 26506, USA.; Department of Microbiology, Immunology & Cell Biology, West Virginia University, Morgantown, WV 26506, USA.
Pearce MC; Cancer Research Laboratory, Department of Environmental and Molecular Toxicology, Oregon State University, Corvallis, OR 97331, USA.
Kolluri SK; Cancer Research Laboratory, Department of Environmental and Molecular Toxicology, Oregon State University, Corvallis, OR 97331, USA.
Marsh CB; Department of Medicine, West Virginia University, Morgantown, WV 26506, USA.
Eubank TD; WVU Cancer Institute, West Virginia University, Morgantown, WV 26506, USA.; Department of Microbiology, Immunology & Cell Biology, West Virginia University, Morgantown, WV 26506, USA.
Ivanov AV; WVU Cancer Institute, West Virginia University, Morgantown, WV 26506, USA.; Department of Biochemistry, West Virginia University, Morgantown, WV 26506, USA.
Guo NL; WVU Cancer Institute, West Virginia University, Morgantown, WV 26506, USA.; Department of Occupational and Environmental Health Sciences, West Virginia University, Morgantown, WV 26506, USA.
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Źródło:
International journal of molecular sciences [Int J Mol Sci] 2021 Apr 04; Vol. 22 (7). Date of Electronic Publication: 2021 Apr 04.
Typ publikacji:
Journal Article
MeSH Terms:
Drug Resistance, Neoplasm*
Gene Expression Regulation, Neoplastic*
Carcinoma, Non-Small-Cell Lung/*metabolism
Kruppel-Like Transcription Factors/*biosynthesis
Lung Neoplasms/*metabolism
Neoplasm Proteins/*biosynthesis
Carcinoma, Non-Small-Cell Lung/genetics ; Carcinoma, Non-Small-Cell Lung/mortality ; Carcinoma, Non-Small-Cell Lung/pathology ; Cell Line, Tumor ; Disease-Free Survival ; Docetaxel/pharmacology ; Female ; Humans ; Kruppel-Like Transcription Factors/genetics ; Lung Neoplasms/genetics ; Lung Neoplasms/mortality ; Lung Neoplasms/pathology ; Male ; Neoplasm Proteins/genetics ; Paclitaxel/pharmacology ; Protein Isoforms/biosynthesis ; Protein Isoforms/genetics ; Survival Rate
Czasopismo naukowe
Tytuł:
Circulating extracellular vesicle content reveals de novo DNA methyltransferase expression as a molecular method to predict septic shock.
Autorzy:
Dakhlallah DA; Department of Microbiology, Immunology and Cell Biology, Robert C. Byrd Health Sciences Center, School of Medicine, West Virginia University, Morgantown, WV, USA.; West Virginia Clinical and Translational Science Institute (WVCTSI), West Virginia University, Morgantown, WV, USA.
Wisler J; Department of Surgery, College of Medicine, Wexner Medical Center, The Ohio State University, Columbus, OH, USA.
Gencheva M; Department of Microbiology, Immunology and Cell Biology, Robert C. Byrd Health Sciences Center, School of Medicine, West Virginia University, Morgantown, WV, USA.
Brown CM; Department of Microbiology, Immunology and Cell Biology, Robert C. Byrd Health Sciences Center, School of Medicine, West Virginia University, Morgantown, WV, USA.; West Virginia Clinical and Translational Science Institute (WVCTSI), West Virginia University, Morgantown, WV, USA.; Department of Neuroscience, School of Medicine; Rockefeller Neuroscience Institute, West Virginia University, Morgantown, WV, USA.
Leatherman ER; Department of Statistics, West Virginia University, Morgantown, WV, USA.
Singh K; Department of Surgery, College of Medicine, Wexner Medical Center, The Ohio State University, Columbus, OH, USA.
Brundage K; Department of Microbiology, Immunology and Cell Biology, Robert C. Byrd Health Sciences Center, School of Medicine, West Virginia University, Morgantown, WV, USA.
Karsies T; Department of Critical Care, Nationwide Children's Hospital, Columbus, OH, USA.
Dakhlallah A; Department of Microbiology, Immunology and Cell Biology, Robert C. Byrd Health Sciences Center, School of Medicine, West Virginia University, Morgantown, WV, USA.
Witwer KW; Department of Molecular and Comparative Pathobiology, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Sen CK; Department of Surgery, College of Medicine, Wexner Medical Center, The Ohio State University, Columbus, OH, USA.
Eubank TD; Department of Microbiology, Immunology and Cell Biology, Robert C. Byrd Health Sciences Center, School of Medicine, West Virginia University, Morgantown, WV, USA.; West Virginia Clinical and Translational Science Institute (WVCTSI), West Virginia University, Morgantown, WV, USA.
Marsh CB; Robert C. Byrd Health Sciences Center, School of Medicine, West Virginia University, Morgantown, WV, USA.
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Źródło:
Journal of extracellular vesicles [J Extracell Vesicles] 2019 Sep 28; Vol. 8 (1), pp. 1669881. Date of Electronic Publication: 2019 Sep 28 (Print Publication: 2019).
Typ publikacji:
Journal Article
Czasopismo naukowe
Tytuł:
Involvement of tumor macrophage HIFs in chemotherapy effectiveness: mathematical modeling of oxygen, pH, and glutathione.
Autorzy:
Chen D; Department of Mathematics and Statistics, University of North Carolina at Charlotte, Charlotte, North Carolina, United States of America.
Bobko AA; Division of Pulmonary, Allergy, Critical Care and Sleep Medicine, College of Medicine, The Ohio State University, Columbus, Ohio, United States of America.
Gross AC; Division of Pulmonary, Allergy, Critical Care and Sleep Medicine, College of Medicine, The Ohio State University, Columbus, Ohio, United States of America.
Evans R; Division of Pulmonary, Allergy, Critical Care and Sleep Medicine, College of Medicine, The Ohio State University, Columbus, Ohio, United States of America.
Marsh CB; Division of Pulmonary, Allergy, Critical Care and Sleep Medicine, College of Medicine, The Ohio State University, Columbus, Ohio, United States of America.
Khramtsov VV; Division of Pulmonary, Allergy, Critical Care and Sleep Medicine, College of Medicine, The Ohio State University, Columbus, Ohio, United States of America.
Eubank TD; Division of Pulmonary, Allergy, Critical Care and Sleep Medicine, College of Medicine, The Ohio State University, Columbus, Ohio, United States of America.
Friedman A; Mathematical Biosciences Institute, The Ohio State University, Columbus, Ohio, United States of America; Department of Mathematics, The Ohio State University, Columbus, Ohio, United States of America.
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Źródło:
PloS one [PLoS One] 2014 Oct 08; Vol. 9 (10), pp. e107511. Date of Electronic Publication: 2014 Oct 08 (Print Publication: 2014).
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Models, Theoretical*
Basic Helix-Loop-Helix Transcription Factors/*metabolism
Breast Neoplasms/*metabolism
Glutathione/*metabolism
Hypoxia-Inducible Factor 1, alpha Subunit/*metabolism
Macrophages/*metabolism
Oxygen/*metabolism
Animals ; Female ; Hydrogen-Ion Concentration ; Mice
Czasopismo naukowe
Tytuł:
MicroRNA 17-92 cluster mediates ETS1 and ETS2-dependent RAS-oncogenic transformation.
Autorzy:
Kabbout M; Department of Molecular and Cellular Biochemistry, College of Medicine, The Ohio State University, Columbus, Ohio, United States of America; Graduate Program in Molecular Cellular and Developmental Biology, The Ohio State University, Columbus, Ohio, United States of America; Solid Tumor Program, Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio, United States of America.
Dakhlallah D; Graduate Program in Molecular Cellular and Developmental Biology, The Ohio State University, Columbus, Ohio, United States of America; Dorothy M. Davis Heart and Lung Research Institute, The Ohio State University, Columbus, Ohio, United States of America.
Sharma S; Department of Molecular and Cellular Biochemistry, College of Medicine, The Ohio State University, Columbus, Ohio, United States of America; Solid Tumor Program, Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio, United States of America.
Bronisz A; Department of Molecular and Cellular Biochemistry, College of Medicine, The Ohio State University, Columbus, Ohio, United States of America; Solid Tumor Program, Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio, United States of America.
Srinivasan R; Department of Molecular and Cellular Biochemistry, College of Medicine, The Ohio State University, Columbus, Ohio, United States of America; Graduate Program in Molecular Cellular and Developmental Biology, The Ohio State University, Columbus, Ohio, United States of America; Solid Tumor Program, Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio, United States of America.
Piper M; Dorothy M. Davis Heart and Lung Research Institute, The Ohio State University, Columbus, Ohio, United States of America; Division of Pulmonary, Allergy, Critical Care, and Sleep Medicine, Department of Internal Medicine, College of Medicine, The Ohio State University, Columbus, Ohio, United States of America.
Marsh CB; Dorothy M. Davis Heart and Lung Research Institute, The Ohio State University, Columbus, Ohio, United States of America; Division of Pulmonary, Allergy, Critical Care, and Sleep Medicine, Department of Internal Medicine, College of Medicine, The Ohio State University, Columbus, Ohio, United States of America.
Ostrowski MC; Department of Molecular and Cellular Biochemistry, College of Medicine, The Ohio State University, Columbus, Ohio, United States of America; Solid Tumor Program, Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio, United States of America.
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Źródło:
PloS one [PLoS One] 2014 Jun 26; Vol. 9 (6), pp. e100693. Date of Electronic Publication: 2014 Jun 26 (Print Publication: 2014).
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural
MeSH Terms:
Carcinogenesis*
Cell Transformation, Neoplastic*
MicroRNAs/*genetics
MicroRNAs/*metabolism
Oncogene Protein p21(ras)/*metabolism
Proto-Oncogene Protein c-ets-1/*metabolism
Proto-Oncogene Protein c-ets-2/*metabolism
Animals ; Cell Line ; Fibroblasts/metabolism ; Fibroblasts/pathology ; Gene Knockout Techniques ; Humans ; Male ; Mice ; Proto-Oncogene Protein c-ets-1/deficiency ; Proto-Oncogene Protein c-ets-1/genetics ; Proto-Oncogene Protein c-ets-2/deficiency ; Proto-Oncogene Protein c-ets-2/genetics ; Proto-Oncogene Proteins c-myc/metabolism
Czasopismo naukowe
Tytuł:
Macrophage colony-stimulating factor augments Tie2-expressing monocyte differentiation, angiogenic function, and recruitment in a mouse model of breast cancer.
Autorzy:
Forget MA; Department of Internal Medicine, Division of Pulmonary, Allergy, Critical Care, and Sleep Medicine, The Ohio State University, Columbus, Ohio, United States of America; Molecular Cellular and Developmental Biology Program, The Ohio State University, Columbus, Ohio, United States of America.
Voorhees JL; Department of Internal Medicine, Division of Pulmonary, Allergy, Critical Care, and Sleep Medicine, The Ohio State University, Columbus, Ohio, United States of America.
Cole SL; Campus Microscopy and Imaging Facility, The Ohio State University, Columbus, Ohio, United States of America.
Dakhlallah D; Department of Internal Medicine, Division of Pulmonary, Allergy, Critical Care, and Sleep Medicine, The Ohio State University, Columbus, Ohio, United States of America.
Patterson IL; Department of Internal Medicine, Division of Pulmonary, Allergy, Critical Care, and Sleep Medicine, The Ohio State University, Columbus, Ohio, United States of America.
Gross AC; Department of Internal Medicine, Division of Pulmonary, Allergy, Critical Care, and Sleep Medicine, The Ohio State University, Columbus, Ohio, United States of America.
Moldovan L; Department of Internal Medicine, Division of Pulmonary, Allergy, Critical Care, and Sleep Medicine, The Ohio State University, Columbus, Ohio, United States of America.
Mo X; The Center for Biostatistics, The Ohio State University, Columbus, Ohio, United States of America.
Evans R; Department of Internal Medicine, Division of Pulmonary, Allergy, Critical Care, and Sleep Medicine, The Ohio State University, Columbus, Ohio, United States of America.
Marsh CB; Department of Internal Medicine, Division of Pulmonary, Allergy, Critical Care, and Sleep Medicine, The Ohio State University, Columbus, Ohio, United States of America; Molecular Cellular and Developmental Biology Program, The Ohio State University, Columbus, Ohio, United States of America; The Ohio State University Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio, United States of America.
Eubank TD; Department of Internal Medicine, Division of Pulmonary, Allergy, Critical Care, and Sleep Medicine, The Ohio State University, Columbus, Ohio, United States of America; The Ohio State University Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio, United States of America.
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Źródło:
PloS one [PLoS One] 2014 Jun 03; Vol. 9 (6), pp. e98623. Date of Electronic Publication: 2014 Jun 03 (Print Publication: 2014).
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Retracted Publication
MeSH Terms:
Breast Neoplasms/*metabolism
Macrophage Colony-Stimulating Factor/*pharmacology
Monocytes/*cytology
Monocytes/*drug effects
Receptor, TIE-2/*metabolism
Animals ; Cell Differentiation/drug effects ; Female ; Human Umbilical Vein Endothelial Cells/cytology ; Human Umbilical Vein Endothelial Cells/drug effects ; Human Umbilical Vein Endothelial Cells/metabolism ; Humans ; Lipopolysaccharide Receptors/metabolism ; Mice ; Monocytes/metabolism
Czasopismo naukowe
Tytuł:
Chronic restraint stress upregulates erythropoiesis through glucocorticoid stimulation.
Autorzy:
Voorhees JL; The Dorothy M. Davis Heart and Lung Research Institute, Division of Pulmonary, Allergy, Critical Care, and Sleep Medicine, The Ohio State University, Columbus, Ohio, United States of America ; Department of Internal Medicine, The Ohio State University, Columbus, Ohio, United States of America.
Powell ND
Moldovan L
Mo X
Eubank TD
Marsh CB
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Źródło:
PloS one [PLoS One] 2013 Oct 18; Vol. 8 (10), pp. e77935. Date of Electronic Publication: 2013 Oct 18 (Print Publication: 2013).
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Restraint, Physical*
Biomarkers/*metabolism
Erythrocytes/*cytology
Erythroid Precursor Cells/*cytology
Erythropoiesis/*physiology
Glucocorticoids/*metabolism
Stress, Psychological/*physiopathology
Animals ; Blotting, Western ; Cells, Cultured ; Chronic Disease ; Erythrocytes/drug effects ; Erythrocytes/metabolism ; Erythroid Precursor Cells/drug effects ; Erythroid Precursor Cells/metabolism ; Erythropoiesis/drug effects ; Female ; Gene Expression Profiling ; Hormone Antagonists/pharmacology ; Mice ; Mice, Inbred C57BL ; Mifepristone/pharmacology ; Oligonucleotide Array Sequence Analysis ; RNA, Messenger/genetics ; Real-Time Polymerase Chain Reaction ; Receptors, Glucocorticoid/antagonists & inhibitors ; Reverse Transcriptase Polymerase Chain Reaction
Czasopismo naukowe
Tytuł:
Prolonged restraint stress increases IL-6, reduces IL-10, and causes persistent depressive-like behavior that is reversed by recombinant IL-10.
Autorzy:
Voorhees JL; The Dorothy M. Davis Heart and Lung Research Institute, Division of Pulmonary, Allergy, Critical Care, and Sleep Medicine, The Ohio State University, Columbus, Ohio, United States of America.
Tarr AJ
Wohleb ES
Godbout JP
Mo X
Sheridan JF
Eubank TD
Marsh CB
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Źródło:
PloS one [PLoS One] 2013; Vol. 8 (3), pp. e58488. Date of Electronic Publication: 2013 Mar 08.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Depression/*blood
Immobilization/*adverse effects
Interleukin-10/*blood
Interleukin-10/*pharmacology
Interleukin-6/*blood
Stress, Physiological/*drug effects
Animals ; Behavior, Animal ; Depression/etiology ; Mice ; Recombinant Proteins/blood ; Recombinant Proteins/pharmacology ; Time Factors
Czasopismo naukowe
Tytuł:
Thiol-redox antioxidants protect against lung vascular endothelial cytoskeletal alterations caused by pulmonary fibrosis inducer, bleomycin: comparison between classical thiol-protectant, N-acetyl-L-cysteine, and novel thiol antioxidant, N,N'-bis-2-mercaptoethyl isophthalamide.
Autorzy:
Patel RB; Lipid Signaling, Lipidomics, and Vasculotoxicity Laboratory, Division of Pulmonary, Allergy, Critical Care, and Sleep Medicine, Dorothy M. Davis Heart and Lung Research Institute, College of Medicine, The Ohio State University, Columbus, Ohio, USA.
Kotha SR
Sauers LA
Malireddy S
Gurney TO
Gupta NN
Elton TS
Magalang UJ
Marsh CB
Haley BE
Parinandi NL
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Źródło:
Toxicology mechanisms and methods [Toxicol Mech Methods] 2012 Jun; Vol. 22 (5), pp. 383-96.
Typ publikacji:
Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms:
Acetylcysteine/*pharmacology
Actin Cytoskeleton/*drug effects
Antioxidants/*pharmacology
Bleomycin/*pharmacology
Cysteamine/*analogs & derivatives
Endothelium, Vascular/*drug effects
Idiopathic Pulmonary Fibrosis/*prevention & control
Lung/*drug effects
Phthalic Acids/*pharmacology
Sulfhydryl Compounds/*pharmacology
Acetylcysteine/chemistry ; Actin Cytoskeleton/metabolism ; Actin Cytoskeleton/pathology ; Animals ; Antioxidants/chemistry ; Cattle ; Cell Culture Techniques ; Cell Survival/drug effects ; Cells, Cultured ; Cysteamine/chemistry ; Cysteamine/pharmacology ; Endothelial Cells/drug effects ; Endothelial Cells/metabolism ; Endothelial Cells/pathology ; Endothelium, Vascular/metabolism ; Endothelium, Vascular/pathology ; Glutathione/metabolism ; Idiopathic Pulmonary Fibrosis/metabolism ; Idiopathic Pulmonary Fibrosis/pathology ; Lung/blood supply ; Lung/metabolism ; Lung/pathology ; Microscopy, Fluorescence ; Molecular Structure ; Oxidation-Reduction ; Phthalic Acids/chemistry ; Reactive Oxygen Species/metabolism ; Structure-Activity Relationship ; Sulfhydryl Compounds/chemistry
Czasopismo naukowe
Tytuł:
Mesenchymal stem cells for cardiac regeneration: translation to bedside reality.
Autorzy:
Elnakish MT; Department of Physiology and Cell Biology, The Dorothy M. Davis Heart & Lung Research Institute, The Ohio State University, Columbus, OH 43210, USA.
Hassan F
Dakhlallah D
Marsh CB
Alhaider IA
Khan M
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Źródło:
Stem cells international [Stem Cells Int] 2012; Vol. 2012, pp. 646038. Date of Electronic Publication: 2012 Jun 07.
Typ publikacji:
Journal Article
Czasopismo naukowe
Tytuł:
Reprogramming of the tumour microenvironment by stromal PTEN-regulated miR-320.
Autorzy:
Bronisz A; Tumor Microenvironment Program, Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio 43210, USA.
Godlewski J
Wallace JA
Merchant AS
Nowicki MO
Mathsyaraja H
Srinivasan R
Trimboli AJ
Martin CK
Li F
Yu L
Fernandez SA
Pécot T
Rosol TJ
Cory S
Hallett M
Park M
Piper MG
Marsh CB
Yee LD
Jimenez RE
Nuovo G
Lawler SE
Chiocca EA
Leone G
Ostrowski MC
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Źródło:
Nature cell biology [Nat Cell Biol] 2011 Dec 18; Vol. 14 (2), pp. 159-67. Date of Electronic Publication: 2011 Dec 18.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Gene Expression Profiling*
Gene Expression Regulation, Neoplastic*
MicroRNAs/*genetics
PTEN Phosphohydrolase/*genetics
Tumor Microenvironment/*genetics
Animals ; Blotting, Western ; Breast Neoplasms/genetics ; Breast Neoplasms/metabolism ; Breast Neoplasms/pathology ; COS Cells ; Cell Line, Tumor ; Chlorocebus aethiops ; Female ; Fibroblasts/metabolism ; Humans ; Kaplan-Meier Estimate ; Mammary Neoplasms, Experimental/genetics ; Mammary Neoplasms, Experimental/metabolism ; Mammary Neoplasms, Experimental/pathology ; Mice ; Mice, Knockout ; MicroRNAs/metabolism ; Oligonucleotide Array Sequence Analysis ; PTEN Phosphohydrolase/metabolism ; Proto-Oncogene Protein c-ets-2/genetics ; Proto-Oncogene Protein c-ets-2/metabolism ; RNA Interference ; Reverse Transcriptase Polymerase Chain Reaction ; Stromal Cells/metabolism
Czasopismo naukowe
Tytuł:
Thrombospondin-1 contributes to mortality in murine sepsis through effects on innate immunity.
Autorzy:
McMaken S; Division of Pulmonary, Allergy, Critical Care, and Sleep Medicine, Department of Internal Medicine, The Dorothy M. Davis Heart and Lung Research Institute, Ohio State University, Columbus, Ohio, United States of America.
Exline MC
Mehta P
Piper M
Wang Y
Fischer SN
Newland CA
Schrader CA
Balser SR
Sarkar A
Baran CP
Marsh CB
Cook CH
Phillips GS
Ali NA
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Źródło:
PloS one [PLoS One] 2011 May 09; Vol. 6 (5), pp. e19654. Date of Electronic Publication: 2011 May 09.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Immunity, Innate/*immunology
Sepsis/*immunology
Sepsis/*pathology
Thrombospondin 1/*metabolism
Animals ; Bacterial Load/immunology ; Cecum/microbiology ; Cecum/pathology ; Cell Count ; Cytokines/blood ; Cytoprotection ; Disease Models, Animal ; Humans ; Inflammation Mediators/metabolism ; Ligation ; Macrophages/cytology ; Mice ; Peritoneal Lavage ; Peritoneum/microbiology ; Peritoneum/pathology ; Phagocytosis ; Punctures ; Sepsis/blood ; Sepsis/microbiology ; Survival Analysis ; Thrombospondin 1/deficiency ; Wound Healing
Czasopismo naukowe
Tytuł:
An in silico modeling approach to understanding the dynamics of sarcoidosis.
Autorzy:
Aguda BD; Neuro-Oncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland, United States of America.
Marsh CB
Thacker M
Crouser ED
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Źródło:
PloS one [PLoS One] 2011; Vol. 6 (5), pp. e19544. Date of Electronic Publication: 2011 May 27.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Computer Simulation*
Models, Immunological*
Sarcoidosis/*immunology
Antibodies/pharmacology ; Antibodies/therapeutic use ; Antigens/immunology ; Cell Communication/drug effects ; Drug Therapy, Combination ; Granuloma/immunology ; Granuloma/pathology ; Humans ; Interferon-gamma/immunology ; Interleukin-2/immunology ; Lymphocyte Activation/drug effects ; Lymphocyte Activation/immunology ; Phenotype ; Sarcoidosis/drug therapy ; Sarcoidosis/pathology ; T-Lymphocytes, Regulatory/drug effects ; T-Lymphocytes, Regulatory/immunology ; Th1 Cells/drug effects ; Th1 Cells/immunology ; Tumor Necrosis Factor-alpha/immunology
Czasopismo naukowe
Tytuł:
M-CSF induces monocyte survival by activating NF-κB p65 phosphorylation at Ser276 via protein kinase C.
Autorzy:
Wang Y; Department of Internal Medicine, The Ohio State University, Columbus, Ohio, USA.
Mo X
Piper MG
Wang H
Parinandi NL
Guttridge D
Marsh CB
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Źródło:
PloS one [PLoS One] 2011; Vol. 6 (12), pp. e28081. Date of Electronic Publication: 2011 Dec 22.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural
MeSH Terms:
Cell Survival/*physiology
Macrophage Colony-Stimulating Factor/*physiology
Monocytes/*cytology
Protein Kinase C/*metabolism
Serine/*metabolism
Transcription Factor RelA/*metabolism
Animals ; Cell Line ; Electrophoretic Mobility Shift Assay ; Indoles/pharmacology ; Mice ; Phosphorylation ; Protein Kinase C/antagonists & inhibitors ; Protein Kinase Inhibitors/pharmacology ; Real-Time Polymerase Chain Reaction ; Transcription Factor RelA/chemistry
Czasopismo naukowe
Tytuł:
MiR-155 induction by F. novicida but not the virulent F. tularensis results in SHIP down-regulation and enhanced pro-inflammatory cytokine response.
Autorzy:
Cremer TJ; Molecular, Cellular, and Developmental Biology Program, The Ohio State University, Columbus, Ohio, United States of America.
Ravneberg DH
Clay CD
Piper-Hunter MG
Marsh CB
Elton TS
Gunn JS
Amer A
Kanneganti TD
Schlesinger LS
Butchar JP
Tridandapani S
Pokaż więcej
Źródło:
PloS one [PLoS One] 2009 Dec 30; Vol. 4 (12), pp. e8508. Date of Electronic Publication: 2009 Dec 30.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Cytokines/*immunology
Francisella/*physiology
Francisella tularensis/*pathogenicity
Inflammation Mediators/*immunology
MicroRNAs/*genetics
Phosphoric Monoester Hydrolases/*genetics
Animals ; Base Sequence ; Caspase 1/metabolism ; Cell Line ; Cytokines/biosynthesis ; Down-Regulation/genetics ; Endocytosis ; Enzyme Activation ; Francisella/cytology ; Gram-Negative Bacterial Infections/enzymology ; Gram-Negative Bacterial Infections/genetics ; Humans ; Inflammation Mediators/metabolism ; Inositol Polyphosphate 5-Phosphatases ; Mice ; MicroRNAs/metabolism ; Microbial Viability ; Models, Biological ; Molecular Sequence Data ; Phosphoric Monoester Hydrolases/metabolism ; Signal Transduction ; Toll-Like Receptors ; Virulence/genetics
Czasopismo naukowe

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