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Wyświetlanie 61-80 z 529
Tytuł:
Vitamin K enhances the production of brain sulfatides during remyelination.
Autorzy:
Popescu DC; Department of Biological Sciences, Geauga campus, Kent State University, Burton, Ohio, United States of America.
Huang H; Department of Chemistry and Biology, University of Akron, Akron, Ohio, United States of America.
Singhal NK; Department of Biological Sciences, Kent campus, Kent State University, Kent, Ohio, United States of America.
Shriver L; Department of Chemistry and Biology, University of Akron, Akron, Ohio, United States of America.
McDonough J; Department of Biological Sciences, Kent campus, Kent State University, Kent, Ohio, United States of America.
Clements RJ; Department of Biological Sciences, Kent campus, Kent State University, Kent, Ohio, United States of America.
Freeman EJ; Department of Biological Sciences, Kent campus, Kent State University, Kent, Ohio, United States of America.
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Źródło:
PloS one [PLoS One] 2018 Aug 27; Vol. 13 (8), pp. e0203057. Date of Electronic Publication: 2018 Aug 27 (Print Publication: 2018).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Brain/*drug effects
Encephalomyelitis, Autoimmune, Experimental/*drug therapy
Multiple Sclerosis/*drug therapy
Neuroprotective Agents/*pharmacology
Sulfoglycosphingolipids/*metabolism
Vitamin K/*pharmacology
Animals ; Brain/metabolism ; Brain/pathology ; Cuprizone ; Encephalomyelitis, Autoimmune, Experimental/metabolism ; Encephalomyelitis, Autoimmune, Experimental/pathology ; Galactosylceramides/pharmacology ; Male ; Mice, Inbred C57BL ; Multiple Sclerosis/metabolism ; Multiple Sclerosis/pathology ; Remyelination/drug effects ; Remyelination/physiology ; Swine ; Vitamin D/pharmacology ; Vitamin K/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Invariant natural killer T cells: innate-like T cells with potent immunomodulatory activities.
Autorzy:
Wu L; Department of Microbiology and Immunology, Vanderbilt University School of Medicine, Nashville, TN 37232-2363, USA.
Gabriel CL
Parekh VV
Van Kaer L
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Źródło:
Tissue antigens [Tissue Antigens] 2009 Jun; Vol. 73 (6), pp. 535-45. Date of Electronic Publication: 2009 Apr 08.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Review
MeSH Terms:
Immunity, Innate*
Antigens, CD1d/*immunology
Galactosylceramides/*immunology
Natural Killer T-Cells/*immunology
T-Lymphocyte Subsets/*immunology
Animals ; Antigen-Presenting Cells/immunology ; Antigens, CD1d/metabolism ; Galactosylceramides/metabolism ; Glycolipids/chemistry ; Glycolipids/immunology ; Glycolipids/metabolism ; Humans ; Immunotherapy ; Lymphocyte Activation/immunology ; Mice ; Signal Transduction/immunology
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Identification of distinct human invariant natural killer T-cell response phenotypes to alpha-galactosylceramide.
Autorzy:
Croudace JE; MRC Centre for Immune Regulation, University of Birmingham, Birmingham B15 2TT, UK. />Curbishley SM
Mura M
Willcox CR
Illarionov PA
Besra GS
Adams DH
Lammas DA
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Źródło:
BMC immunology [BMC Immunol] 2008 Dec 03; Vol. 9, pp. 71. Date of Electronic Publication: 2008 Dec 03.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Antigens, CD1d/*immunology
Galactosylceramides/*immunology
Interleukin-4/*immunology
Natural Killer T-Cells/*immunology
Recombinant Proteins/*immunology
Age Factors ; Antigen Presentation/immunology ; Antigens, CD1d/metabolism ; Cell Proliferation ; Cell Separation ; Cells, Cultured ; Flow Cytometry ; Galactosylceramides/metabolism ; Humans ; Immunity, Innate ; Interleukin-4/pharmacology ; Natural Killer T-Cells/cytology ; Natural Killer T-Cells/metabolism ; Recombinant Proteins/pharmacology ; Sex Factors ; Tissue Donors
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Innate Valpha14(+) natural killer T cells mature dendritic cells, leading to strong adaptive immunity.
Autorzy:
Fujii S; Research Unit for Cellular Immunotherapy, Research Center for Allergy and Immunology (RCAI), RIKEN, Yokohama, Kanagawa, Japan.
Shimizu K
Hemmi H
Steinman RM
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Źródło:
Immunological reviews [Immunol Rev] 2007 Dec; Vol. 220, pp. 183-98.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Review
MeSH Terms:
Dendritic Cells/*immunology
Galactosylceramides/*immunology
Killer Cells, Natural/*immunology
Neoplasms/*prevention & control
T-Lymphocytes/*immunology
Animals ; Cross-Priming ; Galactosylceramides/analysis ; Histocompatibility Antigens Class I/metabolism ; Humans ; Immunity, Cellular ; Interferon-gamma/metabolism ; Mice ; Neoplasms/immunology
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Germline-encoded recognition of diverse glycolipids by natural killer T cells.
Autorzy:
Scott-Browne JP; Department of Immunology, University of Colorado Health Sciences Center and National Jewish Medical and Research Center, Denver, Colorado, 80206, USA.
Matsuda JL
Mallevaey T
White J
Borg NA
McCluskey J
Rossjohn J
Kappler J
Marrack P
Gapin L
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Źródło:
Nature immunology [Nat Immunol] 2007 Oct; Vol. 8 (10), pp. 1105-13. Date of Electronic Publication: 2007 Sep 09.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Galactosylceramides/*immunology
Killer Cells, Natural/*immunology
Receptors, Antigen, T-Cell, alpha-beta/*physiology
Animals ; Antigens, CD1/chemistry ; Antigens, CD1/immunology ; Antigens, CD1d ; Complementarity Determining Regions ; Crystallography ; Galactosylceramides/chemistry ; Immunity, Innate ; Mice ; Mice, Inbred C57BL ; Receptors, Antigen, T-Cell, alpha-beta/chemistry
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Impact of Th1/Th2 cytokine polarity induced by invariant NKT cells on the incidence of pregnancy loss in mice.
Autorzy:
Hoya M; Faculty of Medicine, Department of Obstetrics and Gynecology, The University of Tokyo, Tokyo, Japan.
Nagamatsu T; Faculty of Medicine, Department of Obstetrics and Gynecology, The University of Tokyo, Tokyo, Japan.
Fujii T; Faculty of Medicine, Department of Obstetrics and Gynecology, The University of Tokyo, Tokyo, Japan.
Schust DJ; Department of Obstetrics, Gynecology and Women's Health, University of Missouri, Columbia, MO, USA.
Oda H; Faculty of Medicine, Department of Obstetrics and Gynecology, The University of Tokyo, Tokyo, Japan.
Akiba N; Faculty of Medicine, Department of Obstetrics and Gynecology, The University of Tokyo, Tokyo, Japan.
Iriyama T; Faculty of Medicine, Department of Obstetrics and Gynecology, The University of Tokyo, Tokyo, Japan.
Kawana K; Faculty of Medicine, Department of Obstetrics and Gynecology, The University of Tokyo, Tokyo, Japan.
Osuga Y; Faculty of Medicine, Department of Obstetrics and Gynecology, The University of Tokyo, Tokyo, Japan.
Fujii T; Faculty of Medicine, Department of Obstetrics and Gynecology, The University of Tokyo, Tokyo, Japan.
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Źródło:
American journal of reproductive immunology (New York, N.Y. : 1989) [Am J Reprod Immunol] 2018 Mar; Vol. 79 (3). Date of Electronic Publication: 2018 Jan 24.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Abortion, Spontaneous/*immunology
Natural Killer T-Cells/*immunology
Th1 Cells/*immunology
Th2 Cells/*immunology
Animals ; Antigens, CD1d/metabolism ; Cell Differentiation ; Cell Proliferation ; Cells, Cultured ; Cytokines/metabolism ; Female ; Galactosylceramides/chemistry ; Galactosylceramides/immunology ; Galactosylceramides/metabolism ; Humans ; Male ; Mice ; Mice, Inbred C57BL ; Pregnancy ; Pregnancy Outcome ; Sphingosine/metabolism ; Th1-Th2 Balance
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Glycolipid antigen processing for presentation by CD1d molecules.
Autorzy:
Prigozy TI; Division of Developmental Immunology, La Jolla Institute for Allergy and Immunology, 10355 Science Center Drive, San Diego, CA 92121, USA.
Naidenko O
Qasba P
Elewaut D
Brossay L
Khurana A
Natori T
Koezuka Y
Kulkarni A
Kronenberg M
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Źródło:
Science (New York, N.Y.) [Science] 2001 Jan 26; Vol. 291 (5504), pp. 664-7.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
MeSH Terms:
Antigen Presentation*
Macrolides*
Antigens, CD1/*immunology
Galactosylceramides/*immunology
Galactosylceramides/*metabolism
T-Lymphocytes/*immunology
alpha-Galactosidase/*metabolism
Amino Acid Motifs ; Animals ; Anti-Bacterial Agents/pharmacology ; Antigen-Presenting Cells/immunology ; Antigens, CD1/chemistry ; Antigens, CD1/metabolism ; Antigens, CD1d ; Carbohydrate Conformation ; Cytokines/biosynthesis ; Epitopes/immunology ; Galactosylceramides/chemistry ; Lysosomes/enzymology ; Mice ; Mice, Inbred C57BL ; Protein Transport ; Receptors, Antigen, T-Cell/immunology ; Transfection ; Tumor Cells, Cultured
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
alpha-Galactosylceramide therapy for autoimmune diseases: prospects and obstacles.
Autorzy:
Van Kaer L; Department of Microbiology and Immunology, Vanderbilt University School of Medicine, 1161 21st Avenue South, Nashville, Tennessee 37232, USA.
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Źródło:
Nature reviews. Immunology [Nat Rev Immunol] 2005 Jan; Vol. 5 (1), pp. 31-42.
Typ publikacji:
Journal Article; Research Support, U.S. Gov't, P.H.S.; Review
MeSH Terms:
Autoimmune Diseases/*drug therapy
Autoimmunity/*drug effects
Galactosylceramides/*pharmacology
Immunologic Factors/*pharmacology
Animals ; Autoimmune Diseases/immunology ; Autoimmunity/immunology ; Galactosylceramides/therapeutic use ; Humans ; Killer Cells, Natural/drug effects ; Killer Cells, Natural/immunology ; T-Lymphocyte Subsets/drug effects ; T-Lymphocyte Subsets/immunology
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Horse-Derived Ceramide Accentuates Glucosylceramide Synthase and Ceramide Synthase 3 by Activating PPARβ/δ and/or PPARγ to Stimulate Ceramide Synthesis.
Autorzy:
Igarashi, Tami
Yanagi, Hiroki
Yagi, Masayuki
Ichihashi, Masamitsu
Imokawa, Genji
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Temat:
CERAMIDES
LIPID analysis
GENE expression
GALACTOSYLCERAMIDES
ATOPIC dermatitis
THYMIC stromal lymphopoietin
Źródło:
Biomedicines; Feb2023, Vol. 11 Issue 2, p548, 23p
Czasopismo naukowe
Szczegóły
Tytuł:
Guillain-Barré Syndrome: A Variant Consisting of Facial Diplegia and Paresthesia with Left Facial Hemiplegia Associated with Antibodies to Galactocerebroside and Phosphatidic Acid.
Autorzy:
Nishiguchi S; Department of General Internal Medicine, Shonan Kamakura General Hospital, Kamakura, Kanagawa, Japan.
Branch J; Department of General Internal Medicine, Shonan Kamakura General Hospital, Kamakura, Kanagawa, Japan.
Tsuchiya T; Department of General Internal Medicine, Shonan Kamakura General Hospital, Kamakura, Kanagawa, Japan.
Ito R; Department of General Internal Medicine, Shonan Kamakura General Hospital, Kamakura, Kanagawa, Japan.
Kawada J; Department of Neurology, Shonan Kamakura General Hospital, Kamakura, Kanagawa, Japan.
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Źródło:
The American journal of case reports [Am J Case Rep] 2017 Oct 02; Vol. 18, pp. 1048-1052. Date of Electronic Publication: 2017 Oct 02.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Antibodies/*blood
Facial Paralysis/*etiology
Galactosylceramides/*immunology
Guillain-Barre Syndrome/*diagnosis
Paresthesia/*etiology
Phosphatidic Acids/*immunology
Humans ; Immunoglobulin G/blood ; Male ; Middle Aged ; Respiratory Tract Infections
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Skewed Invariant Natural Killer T (iNKT) Cells, Impaired iNKT:B Cell Help and Decreased SAP Expression in Blood Lymphocytes from Patients with Common Variable Immunodeficiency.
Autorzy:
Erazo-Borrás LV; Grupo de Inmunodeficiencias Primarias, Facultad de Medicina, Universidad de Antioquia, Medellín, Colombia.
Álvarez-Álvarez JA; Grupo de Inmunodeficiencias Primarias, Facultad de Medicina, Universidad de Antioquia, Medellín, Colombia.
Perez-Romero CA; Grupo de Inmunodeficiencias Primarias, Facultad de Medicina, Universidad de Antioquia, Medellín, Colombia.
Orrego-Arango JC; Grupo de Inmunodeficiencias Primarias, Facultad de Medicina, Universidad de Antioquia, Medellín, Colombia.
Franco-Restrepo JL; Grupo de Inmunodeficiencias Primarias, Facultad de Medicina, Universidad de Antioquia, Medellín, Colombia.
Trujillo-Vargas CM; Grupo de Inmunodeficiencias Primarias, Facultad de Medicina, Universidad de Antioquia, Medellín, Colombia.
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Źródło:
Scandinavian journal of immunology [Scand J Immunol] 2017 Sep; Vol. 86 (3), pp. 171-178.
Typ publikacji:
Journal Article
MeSH Terms:
Cell Communication*
B-Lymphocytes/*immunology
Common Variable Immunodeficiency/*immunology
Natural Killer T-Cells/*immunology
Saposins/*metabolism
Adolescent ; Adult ; CD4 Antigens/metabolism ; CD8 Antigens/metabolism ; Cell Proliferation ; Cells, Cultured ; Coculture Techniques ; Female ; Galactosylceramides/immunology ; Humans ; Immunoglobulins/metabolism ; Immunologic Memory ; Lymphocyte Activation ; Male ; Middle Aged ; Receptors, CCR5/metabolism ; Receptors, CXCR3/metabolism ; Tumor Necrosis Factor-alpha/metabolism ; Young Adult
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
In vivo activation of invariant natural killer T cells induces systemic and local alterations in T-cell subsets prior to preterm birth.
Autorzy:
Gomez-Lopez N; Perinatology Research Branch, NICHD/NIH/DHHS, Bethesda, MD, and Detroit, MI, USA.; Department of Obstetrics & Gynecology, Wayne State University, School of Medicine, Detroit, MI, USA.; Department of Immunology & Microbiology, Wayne State University School of Medicine, Detroit, MI, USA.
Romero R; Perinatology Research Branch, NICHD/NIH/DHHS, Bethesda, MD, and Detroit, MI, USA.; Department of Obstetrics & Gynecology, University of Michigan, Ann Arbor, MI, USA.; Department of Epidemiology & Biostatistics, Michigan State University, East Lansing, MI, USA.; Center for Molecular Medicine & Genetics, Wayne State University, Detroit, MI, USA.
Arenas-Hernandez M; Perinatology Research Branch, NICHD/NIH/DHHS, Bethesda, MD, and Detroit, MI, USA.; Department of Obstetrics & Gynecology, Wayne State University, School of Medicine, Detroit, MI, USA.; Department of Molecular Biomedicine, CINVESTAV, Mexico City, Mexico.
Schwenkel G; Perinatology Research Branch, NICHD/NIH/DHHS, Bethesda, MD, and Detroit, MI, USA.; Department of Obstetrics & Gynecology, Wayne State University, School of Medicine, Detroit, MI, USA.
St Louis D; Perinatology Research Branch, NICHD/NIH/DHHS, Bethesda, MD, and Detroit, MI, USA.; Department of Obstetrics & Gynecology, Wayne State University, School of Medicine, Detroit, MI, USA.
Hassan SS; Perinatology Research Branch, NICHD/NIH/DHHS, Bethesda, MD, and Detroit, MI, USA.; Department of Obstetrics & Gynecology, Wayne State University, School of Medicine, Detroit, MI, USA.
Mial TN; Perinatology Research Branch, NICHD/NIH/DHHS, Bethesda, MD, and Detroit, MI, USA.; Department of Obstetrics & Gynecology, Wayne State University, School of Medicine, Detroit, MI, USA.
Pokaż więcej
Źródło:
Clinical and experimental immunology [Clin Exp Immunol] 2017 Aug; Vol. 189 (2), pp. 211-225. Date of Electronic Publication: 2017 May 10.
Typ publikacji:
Journal Article
MeSH Terms:
Natural Killer T-Cells/*immunology
PPAR gamma/*agonists
Premature Birth/*prevention & control
T-Lymphocyte Subsets/*immunology
Thiazolidinediones/*administration & dosage
Animals ; Cytokines/immunology ; Female ; Flow Cytometry ; Galactosylceramides ; Immunophenotyping ; Lymphocyte Activation/drug effects ; Mice ; Mice, Inbred C57BL ; Natural Killer T-Cells/drug effects ; Pregnancy ; Premature Birth/chemically induced ; Premature Birth/immunology ; Rosiglitazone
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Suppression of murine tumour growth through CD8 dendritic cells by sequential administration of α-galactosylceramide in vivo.
Autorzy:
Kogo H; Department of Microbiology and Immunology, Nippon Medical School, Tokyo, Japan.; Department of Gastrointestinal and Hepato-Biliary-Pancreatic Surgery, Nippon Medical School, Tokyo, Japan.
Shimizu M; Department of Microbiology and Immunology, Nippon Medical School, Tokyo, Japan.
Negishi Y; Department of Microbiology and Immunology, Nippon Medical School, Tokyo, Japan.
Uchida E; Department of Gastrointestinal and Hepato-Biliary-Pancreatic Surgery, Nippon Medical School, Tokyo, Japan.
Takahashi H; Department of Microbiology and Immunology, Nippon Medical School, Tokyo, Japan.
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Źródło:
Immunology [Immunology] 2017 Jul; Vol. 151 (3), pp. 324-339. Date of Electronic Publication: 2017 Apr 18.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Carcinoma, Hepatocellular/*therapy
Dendritic Cells/*drug effects
Galactosylceramides/*administration & dosage
Immunologic Factors/*administration & dosage
Immunotherapy/*methods
Liver Neoplasms/*therapy
Lymphocyte Activation/*drug effects
Lymphocytes, Tumor-Infiltrating/*drug effects
T-Lymphocytes, Cytotoxic/*drug effects
Tumor Burden/*drug effects
Animals ; Carcinoma, Hepatocellular/genetics ; Carcinoma, Hepatocellular/immunology ; Carcinoma, Hepatocellular/pathology ; Cell Communication/drug effects ; Cell Line, Tumor ; Cross-Priming/drug effects ; Dendritic Cells/immunology ; Female ; Genotype ; Immunotherapy, Adoptive ; Liver Neoplasms/genetics ; Liver Neoplasms/immunology ; Liver Neoplasms/pathology ; Lymphocytes, Tumor-Infiltrating/immunology ; Lymphocytes, Tumor-Infiltrating/transplantation ; Mice, Inbred C57BL ; Mice, Knockout ; Natural Killer T-Cells/drug effects ; Natural Killer T-Cells/immunology ; Phenotype ; T-Lymphocytes, Cytotoxic/immunology ; T-Lymphocytes, Cytotoxic/transplantation ; Time Factors ; Tumor Microenvironment
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Dendritic cells combined with tumor cells and α-galactosylceramide induce a potent, therapeutic and NK-cell dependent antitumor immunity in B cell lymphoma.
Autorzy:
Escribà-Garcia L; Hematology Service, Hospital de la Santa Creu i Sant Pau, Mas Casanovas 90, 08041, Barcelona, Spain.; Laboratory of Experimental Hematology-IIB, Institut Recerca Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
Alvarez-Fernández C; Hematology Service, Hospital de la Santa Creu i Sant Pau, Mas Casanovas 90, 08041, Barcelona, Spain.; Laboratory of Experimental Hematology-IIB, Institut Recerca Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
Tellez-Gabriel M; Hematology Service, Hospital de la Santa Creu i Sant Pau, Mas Casanovas 90, 08041, Barcelona, Spain.; Laboratory of Experimental Hematology-IIB, Institut Recerca Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
Sierra J; Hematology Service, Hospital de la Santa Creu i Sant Pau, Mas Casanovas 90, 08041, Barcelona, Spain.; Autonomous University, Barcelona, Spain.
Briones J; Hematology Service, Hospital de la Santa Creu i Sant Pau, Mas Casanovas 90, 08041, Barcelona, Spain. .; Laboratory of Experimental Hematology-IIB, Institut Recerca Hospital de la Santa Creu i Sant Pau, Barcelona, Spain. .; Autonomous University, Barcelona, Spain. .
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Źródło:
Journal of translational medicine [J Transl Med] 2017 May 26; Vol. 15 (1), pp. 115. Date of Electronic Publication: 2017 May 26.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Dendritic Cells/*immunology
Galactosylceramides/*pharmacology
Killer Cells, Natural/*immunology
Lymphoma, B-Cell/*immunology
Animals ; Antigens, CD1d/metabolism ; Antineoplastic Agents/pharmacology ; Cancer Vaccines/pharmacology ; Cell Line, Tumor ; Coculture Techniques ; Cytokines/metabolism ; Dendritic Cells/cytology ; Disease Models, Animal ; Female ; Flow Cytometry ; Immunotherapy ; Mice ; Mice, Inbred BALB C ; Phenotype
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
α- Galactosylceramide suppresses murine eosinophil production through interferon-γ-dependent induction of NO synthase and CD95.
Autorzy:
Gaspar ‐ Elsas, Maria Ignez
Queto, Túlio
Masid ‐ de ‐ Brito, Daniela
Vieira, Bruno Marques
Luca, Bianca
Cunha, Fernando Queiroz
Xavier ‐ Elsas, Pedro
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Źródło:
British Journal of Pharmacology. Jul2015, Vol. 172 Issue 13, p3313-3325. 13p. 1 Chart, 7 Graphs.
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Tailored design of NKT-stimulatory glycolipids for polarization of immune responses.
Autorzy:
Hung JT; Institute of Stem Cell & Translational Cancer Research, Chang Gung Memorial Hospital at Linkou and Chang Gung University, No. 5, Fu-Shin St., Kuei Shang, Taoyuan, 333, Taiwan.
Huang JR; Institute of Stem Cell & Translational Cancer Research, Chang Gung Memorial Hospital at Linkou and Chang Gung University, No. 5, Fu-Shin St., Kuei Shang, Taoyuan, 333, Taiwan.
Yu AL; Institute of Stem Cell & Translational Cancer Research, Chang Gung Memorial Hospital at Linkou and Chang Gung University, No. 5, Fu-Shin St., Kuei Shang, Taoyuan, 333, Taiwan. .; Department of Pediatrics, University of California in San Diego, San Diego, CA, USA. .
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Źródło:
Journal of biomedical science [J Biomed Sci] 2017 Mar 23; Vol. 24 (1), pp. 22. Date of Electronic Publication: 2017 Mar 23.
Typ publikacji:
Journal Article; Review
MeSH Terms:
Immunity, Cellular*
Galactosylceramides/*immunology
Lymphocyte Activation/*immunology
Natural Killer T-Cells/*immunology
Animals ; Humans ; Mice
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
The role of natural killer T cells in a mouse model with spontaneous bile duct inflammation.
Autorzy:
Schrumpf E; Norwegian PSC Research Center, Division of Surgery, Inflammatory Diseases and Transplantation Oslo University Hospital, Rikshospitalet, Oslo, Norway.; K.G. Jebsen Inflammation Research Centre, Institute of Clinical Medicine, University of Oslo, Oslo, Norway.; Research Institute of Internal Medicine, Division of Surgery, Inflammatory Diseases and Transplantation Oslo University Hospital, Rikshospitalet, Oslo, Norway.
Jiang X; Norwegian PSC Research Center, Division of Surgery, Inflammatory Diseases and Transplantation Oslo University Hospital, Rikshospitalet, Oslo, Norway.; K.G. Jebsen Inflammation Research Centre, Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
Zeissig S; Department of Medicine 1, University Medical Center Dresden Technical University Dresden, Dresden, Germany.; Center for Regenerative Therapies (CRTD), Technical University Dresden, Dresden, Germany.
Pollheimer MJ; Division of Gastroenterology and Hepatology, Department of Internal Medicine, Research Unit for Experimental and Molecular Hepatology, Graz, Austria.; Institute of Pathology, Medical University of Graz, Graz, Austria.
Anmarkrud JA; Norwegian PSC Research Center, Division of Surgery, Inflammatory Diseases and Transplantation Oslo University Hospital, Rikshospitalet, Oslo, Norway.
Tan C; Norwegian PSC Research Center, Division of Surgery, Inflammatory Diseases and Transplantation Oslo University Hospital, Rikshospitalet, Oslo, Norway.; K.G. Jebsen Inflammation Research Centre, Institute of Clinical Medicine, University of Oslo, Oslo, Norway.; Research Institute of Internal Medicine, Division of Surgery, Inflammatory Diseases and Transplantation Oslo University Hospital, Rikshospitalet, Oslo, Norway.
Exley MA; Manchester Collaborative Centre for Inflammation Research (MCCIR), Faculty of Medical & Human Sciences, University of Manchester, Manchester, United Kingdom.; Division of Gastroenterology, Hepatology and Endoscopy, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Karlsen TH; Norwegian PSC Research Center, Division of Surgery, Inflammatory Diseases and Transplantation Oslo University Hospital, Rikshospitalet, Oslo, Norway.; K.G. Jebsen Inflammation Research Centre, Institute of Clinical Medicine, University of Oslo, Oslo, Norway.; Research Institute of Internal Medicine, Division of Surgery, Inflammatory Diseases and Transplantation Oslo University Hospital, Rikshospitalet, Oslo, Norway.; Section of Gastroenterology, Division of Surgery, Inflammatory Diseases and Transplantation, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
Blumberg RS; Division of Gastroenterology, Hepatology and Endoscopy, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Melum E; Norwegian PSC Research Center, Division of Surgery, Inflammatory Diseases and Transplantation Oslo University Hospital, Rikshospitalet, Oslo, Norway .; K.G. Jebsen Inflammation Research Centre, Institute of Clinical Medicine, University of Oslo, Oslo, Norway.; Research Institute of Internal Medicine, Division of Surgery, Inflammatory Diseases and Transplantation Oslo University Hospital, Rikshospitalet, Oslo, Norway.; Section of Gastroenterology, Division of Surgery, Inflammatory Diseases and Transplantation, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
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Źródło:
Physiological reports [Physiol Rep] 2017 Feb; Vol. 5 (4).
Typ publikacji:
Journal Article
MeSH Terms:
Antigens, CD1d/*genetics
Bile Duct Diseases/*immunology
Inflammation/*immunology
Natural Killer T-Cells/*immunology
Animals ; Antigens, CD1d/immunology ; Bile Duct Diseases/metabolism ; Bile Duct Diseases/pathology ; Disease Models, Animal ; Galactosylceramides/pharmacology ; Inflammation/metabolism ; Inflammation/pathology ; Liver/immunology ; Liver/metabolism ; Liver/pathology ; Mice ; Mice, Knockout ; Natural Killer T-Cells/drug effects ; Natural Killer T-Cells/metabolism ; Spleen/immunology ; Spleen/metabolism ; Spleen/pathology ; Thymus Gland/immunology ; Thymus Gland/metabolism ; Thymus Gland/pathology
Czasopismo naukowe
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Wyświetlanie 61-80 z 529

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