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Wyszukujesz frazę ""Murphy KM"" wg kryterium: Autor


Wyświetlanie 1-15 z 15
Tytuł:
Batf3 maintains autoactivation of Irf8 for commitment of a CD8α(+) conventional DC clonogenic progenitor.
Autorzy:
Grajales-Reyes GE; Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.
Iwata A; Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.
Albring J; Department of Medicine A, Hematology and Oncology, University of Muenster, Muenster, Germany.
Wu X; Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.
Tussiwand R; 1] Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA. [2] Department of Biomedicine, University of Basel, Basel, Switzerland.
Kc W; Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.
Kretzer NM; Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.
Briseño CG; Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.
Durai V; Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.
Bagadia P; Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.
Haldar M; Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.
Schönheit J; Max Delbrück Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany.
Rosenbauer F; Institute of Molecular Tumor Biology, University of Münster, Münster, Germany.
Murphy TL; Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.
Murphy KM; 1] Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA. [2] Howard Hughes Medical Institute, Washington University School of Medicine, St. Louis, Missouri, USA.
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Źródło:
Nature immunology [Nat Immunol] 2015 Jul; Vol. 16 (7), pp. 708-17. Date of Electronic Publication: 2015 Jun 08.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Basic-Leucine Zipper Transcription Factors/*immunology
Dendritic Cells/*immunology
Interferon Regulatory Factors/*immunology
Repressor Proteins/*immunology
Stem Cells/*immunology
Animals ; Base Sequence ; Basic-Leucine Zipper Transcription Factors/genetics ; Basic-Leucine Zipper Transcription Factors/metabolism ; Bone Marrow Cells/immunology ; Bone Marrow Cells/metabolism ; CD24 Antigen/immunology ; CD24 Antigen/metabolism ; CD8 Antigens/immunology ; CD8 Antigens/metabolism ; Cells, Cultured ; Clone Cells/immunology ; Clone Cells/metabolism ; Dendritic Cells/metabolism ; Flow Cytometry ; Interferon Regulatory Factors/genetics ; Interferon Regulatory Factors/metabolism ; Mice, 129 Strain ; Mice, Inbred C57BL ; Mice, Knockout ; Mice, Transgenic ; Molecular Sequence Data ; Oligonucleotide Array Sequence Analysis ; Protein Binding ; Receptors, Immunologic/immunology ; Receptors, Immunologic/metabolism ; Repressor Proteins/genetics ; Repressor Proteins/metabolism ; Sequence Homology, Nucleic Acid ; Stem Cells/metabolism ; Transcriptome/genetics ; Transcriptome/immunology
Czasopismo naukowe
Tytuł:
Commensal-dendritic-cell interaction specifies a unique protective skin immune signature.
Autorzy:
Naik S; 1] Immunity at Barrier Sites Initiative, National Institute of Allergy and Infectious Diseases, NIH, Bethesda 20892, USA [2] Mucosal Immunology Section, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, Maryland 20892, USA.
Bouladoux N; 1] Immunity at Barrier Sites Initiative, National Institute of Allergy and Infectious Diseases, NIH, Bethesda 20892, USA [2] Mucosal Immunology Section, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, Maryland 20892, USA.
Linehan JL; 1] Immunity at Barrier Sites Initiative, National Institute of Allergy and Infectious Diseases, NIH, Bethesda 20892, USA [2] Mucosal Immunology Section, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, Maryland 20892, USA.
Han SJ; 1] Immunity at Barrier Sites Initiative, National Institute of Allergy and Infectious Diseases, NIH, Bethesda 20892, USA [2] Mucosal Immunology Section, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, Maryland 20892, USA.
Harrison OJ; 1] Immunity at Barrier Sites Initiative, National Institute of Allergy and Infectious Diseases, NIH, Bethesda 20892, USA [2] Mucosal Immunology Section, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, Maryland 20892, USA.
Wilhelm C; 1] Immunity at Barrier Sites Initiative, National Institute of Allergy and Infectious Diseases, NIH, Bethesda 20892, USA [2] Mucosal Immunology Section, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, Maryland 20892, USA.
Conlan S; Translational and Functional Genomics Branch, National Human Genome Research Institute, Bethesda, Maryland 20892, USA.
Himmelfarb S; 1] Immunity at Barrier Sites Initiative, National Institute of Allergy and Infectious Diseases, NIH, Bethesda 20892, USA [2] Mucosal Immunology Section, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, Maryland 20892, USA.
Byrd AL; 1] Immunity at Barrier Sites Initiative, National Institute of Allergy and Infectious Diseases, NIH, Bethesda 20892, USA [2] Mucosal Immunology Section, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, Maryland 20892, USA [3] Translational and Functional Genomics Branch, National Human Genome Research Institute, Bethesda, Maryland 20892, USA.
Deming C; Translational and Functional Genomics Branch, National Human Genome Research Institute, Bethesda, Maryland 20892, USA.
Quinones M; Bioinformatics and Computational Bioscience Branch, National Institute of Allergy and Infectious Diseases, NIH Bethesda, Maryland 20892, USA.
Brenchley JM; 1] Immunity at Barrier Sites Initiative, National Institute of Allergy and Infectious Diseases, NIH, Bethesda 20892, USA [2] Immunopathogenesis Section, Laboratory of Molecular Microbiology, National Institute of Allergy and Infectious Diseases, NIH Bethesda, Maryland 20892, USA.
Kong HH; Dermatology Branch, National Cancer Institute, NIH Bethesda, Maryland 20892, USA.
Tussiwand R; Howard Hughes Medical Institute, Department of Pathology and Immunology, Washington University School of Medicine, St Louis, Missouri 63110, USA.
Murphy KM; Howard Hughes Medical Institute, Department of Pathology and Immunology, Washington University School of Medicine, St Louis, Missouri 63110, USA.
Merad M; Department of Oncological Sciences, Tisch Cancer Institute and Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, New York 10029, USA.
Segre JA; Translational and Functional Genomics Branch, National Human Genome Research Institute, Bethesda, Maryland 20892, USA.
Belkaid Y; 1] Immunity at Barrier Sites Initiative, National Institute of Allergy and Infectious Diseases, NIH, Bethesda 20892, USA [2] Mucosal Immunology Section, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, Maryland 20892, USA.
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Źródło:
Nature [Nature] 2015 Apr 02; Vol. 520 (7545), pp. 104-8. Date of Electronic Publication: 2015 Jan 05.
Typ publikacji:
Journal Article; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't
MeSH Terms:
CD8-Positive T-Lymphocytes/*immunology
Dendritic Cells/*immunology
Skin/*immunology
Skin/*microbiology
Symbiosis/*immunology
Animals ; Antigens, Bacterial/immunology ; CD8-Positive T-Lymphocytes/cytology ; Dendritic Cells/cytology ; Humans ; Immunity, Innate/immunology ; Interleukin-17/immunology ; Langerhans Cells/cytology ; Langerhans Cells/immunology ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Primates ; Skin/cytology ; Staphylococcus epidermidis/immunology
Czasopismo naukowe
Tytuł:
L-Myc expression by dendritic cells is required for optimal T-cell priming.
Autorzy:
KC W; Department of Pathology and Immunology, Washington University School of Medicine, 660 S. Euclid Avenue, St Louis, Missouri 63110, USA.
Satpathy AT; Department of Pathology and Immunology, Washington University School of Medicine, 660 S. Euclid Avenue, St Louis, Missouri 63110, USA.
Rapaport AS; Department of Pathology and Immunology, Washington University School of Medicine, 660 S. Euclid Avenue, St Louis, Missouri 63110, USA.
Briseño CG; Department of Pathology and Immunology, Washington University School of Medicine, 660 S. Euclid Avenue, St Louis, Missouri 63110, USA.
Wu X; Department of Pathology and Immunology, Washington University School of Medicine, 660 S. Euclid Avenue, St Louis, Missouri 63110, USA.
Albring JC; Department of Medicine A, Hematology and Oncology, University of Muenster, 48149 Muenster, Germany.
Russler-Germain EV; Department of Pathology and Immunology, Washington University School of Medicine, 660 S. Euclid Avenue, St Louis, Missouri 63110, USA.
Kretzer NM; Department of Pathology and Immunology, Washington University School of Medicine, 660 S. Euclid Avenue, St Louis, Missouri 63110, USA.
Durai V; Department of Pathology and Immunology, Washington University School of Medicine, 660 S. Euclid Avenue, St Louis, Missouri 63110, USA.
Persaud SP; Department of Pathology and Immunology, Washington University School of Medicine, 660 S. Euclid Avenue, St Louis, Missouri 63110, USA.
Edelson BT; Department of Pathology and Immunology, Washington University School of Medicine, 660 S. Euclid Avenue, St Louis, Missouri 63110, USA.
Loschko J; Laboratory of Molecular Immunology, Howard Hughes Medical Institute, The Rockefeller University, New York, New York 10065, USA.
Cella M; Department of Pathology and Immunology, Washington University School of Medicine, 660 S. Euclid Avenue, St Louis, Missouri 63110, USA.
Allen PM; Department of Pathology and Immunology, Washington University School of Medicine, 660 S. Euclid Avenue, St Louis, Missouri 63110, USA.
Nussenzweig MC; Laboratory of Molecular Immunology, Howard Hughes Medical Institute, The Rockefeller University, New York, New York 10065, USA.
Colonna M; Department of Pathology and Immunology, Washington University School of Medicine, 660 S. Euclid Avenue, St Louis, Missouri 63110, USA.
Sleckman BP; Department of Pathology and Immunology, Washington University School of Medicine, 660 S. Euclid Avenue, St Louis, Missouri 63110, USA.
Murphy TL; Department of Pathology and Immunology, Washington University School of Medicine, 660 S. Euclid Avenue, St Louis, Missouri 63110, USA.
Murphy KM; 1] Department of Pathology and Immunology, Washington University School of Medicine, 660 S. Euclid Avenue, St Louis, Missouri 63110, USA [2] Howard Hughes Medical Institute, Washington University School of Medicine, 660 S. Euclid Avenue, St Louis, Missouri 63110, USA.
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Źródło:
Nature [Nature] 2014 Mar 13; Vol. 507 (7491), pp. 243-7. Date of Electronic Publication: 2014 Feb 09.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Gene Expression Regulation*
Cross-Priming/*immunology
Dendritic Cells/*immunology
Dendritic Cells/*metabolism
Proto-Oncogene Proteins c-myc/*metabolism
T-Lymphocytes/*immunology
Animals ; Antigens, CD/metabolism ; Cell Division ; Dendritic Cells/cytology ; Female ; Granulocyte-Macrophage Colony-Stimulating Factor/metabolism ; Inflammation/immunology ; Inflammation/metabolism ; Integrin alpha Chains/metabolism ; Interferon Regulatory Factors/metabolism ; Listeria monocytogenes/immunology ; Liver/cytology ; Liver/immunology ; Lung/cytology ; Lung/immunology ; Male ; Mice ; Proto-Oncogene Proteins c-myc/deficiency ; Transcription, Genetic ; Vesiculovirus/immunology
Czasopismo naukowe
Tytuł:
Notch2-dependent classical dendritic cells orchestrate intestinal immunity to attaching-and-effacing bacterial pathogens.
Autorzy:
Satpathy AT; Department of Pathology and Immunology, School of Medicine, Washington University in St. Louis, Missouri, USA.
Briseño CG
Lee JS
Ng D
Manieri NA
Kc W
Wu X
Thomas SR
Lee WL
Turkoz M
McDonald KG
Meredith MM
Song C
Guidos CJ
Newberry RD
Ouyang W
Murphy TL
Stappenbeck TS
Gommerman JL
Nussenzweig MC
Colonna M
Kopan R
Murphy KM
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Źródło:
Nature immunology [Nat Immunol] 2013 Sep; Vol. 14 (9), pp. 937-48. Date of Electronic Publication: 2013 Aug 04.
Typ publikacji:
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:
Citrobacter rodentium/*immunology
Dendritic Cells/*immunology
Dendritic Cells/*metabolism
Intestinal Mucosa/*immunology
Intestinal Mucosa/*metabolism
Receptor, Notch2/*metabolism
Animals ; Antigens, CD/metabolism ; CD11b Antigen/metabolism ; Cell Differentiation/genetics ; Cell Differentiation/immunology ; Dendritic Cells/cytology ; Enterobacteriaceae Infections/immunology ; Enterobacteriaceae Infections/microbiology ; Enterobacteriaceae Infections/mortality ; Host-Pathogen Interactions/genetics ; Host-Pathogen Interactions/immunology ; Interleukin-23/metabolism ; Intestinal Mucosa/microbiology ; Lectins, C-Type/metabolism ; Lymphotoxin beta Receptor/genetics ; Lymphotoxin beta Receptor/metabolism ; Mice ; Mice, Transgenic ; Minor Histocompatibility Antigens ; Receptor, Notch2/deficiency ; Receptors, Cell Surface/metabolism ; Signal Transduction ; Spleen/immunology ; Transcription Factors/genetics ; Transcription Factors/metabolism ; Wound Healing/genetics ; Wound Healing/immunology
Czasopismo naukowe
Tytuł:
Bcl11a controls Flt3 expression in early hematopoietic progenitors and is required for pDC development in vivo.
Autorzy:
Wu X; Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, United States of America.
Satpathy AT
Kc W
Liu P
Murphy TL
Murphy KM
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Źródło:
PloS one [PLoS One] 2013 May 31; Vol. 8 (5), pp. e64800. Date of Electronic Publication: 2013 May 31 (Print Publication: 2013).
Typ publikacji:
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:
Gene Expression Regulation*/drug effects
Carrier Proteins/*genetics
Dendritic Cells/*metabolism
Hematopoietic Stem Cells/*metabolism
Nuclear Proteins/*genetics
fms-Like Tyrosine Kinase 3/*genetics
Animals ; Carrier Proteins/metabolism ; Cell Differentiation ; Cell Lineage/drug effects ; Cell Lineage/genetics ; DNA-Binding Proteins ; Dendritic Cells/cytology ; Dendritic Cells/drug effects ; Granulocyte-Macrophage Colony-Stimulating Factor/metabolism ; Granulocyte-Macrophage Colony-Stimulating Factor/pharmacology ; Hematopoietic Stem Cells/cytology ; Hematopoietic Stem Cells/drug effects ; Immunophenotyping ; Lymphoid Progenitor Cells/cytology ; Lymphoid Progenitor Cells/drug effects ; Lymphoid Progenitor Cells/metabolism ; Membrane Proteins/metabolism ; Membrane Proteins/pharmacology ; Mice ; Mice, Knockout ; Nuclear Proteins/metabolism ; Receptors, Interleukin-7/genetics ; Receptors, Interleukin-7/metabolism ; Repressor Proteins ; fms-Like Tyrosine Kinase 3/metabolism
Czasopismo naukowe
Tytuł:
Re(de)fining the dendritic cell lineage.
Autorzy:
Satpathy AT; Department of Pathology and Immunology, Washington University in St. Louis, School of Medicine, St. Louis, Missouri, USA.
Wu X
Albring JC
Murphy KM
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Źródło:
Nature immunology [Nat Immunol] 2012 Dec; Vol. 13 (12), pp. 1145-54. Date of Electronic Publication: 2012 Nov 16.
Typ publikacji:
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.; Review
MeSH Terms:
Cell Differentiation*
Cell Lineage*
Dendritic Cells/*immunology
Bone Marrow Cells/cytology ; Bone Marrow Cells/immunology ; Cytokines/metabolism ; Dendritic Cells/cytology ; Dendritic Cells/metabolism ; Humans ; Macrophages/immunology ; Monocytes/immunology ; Stem Cells/cytology ; Stem Cells/metabolism ; Transcription Factors/metabolism
Czasopismo naukowe
Tytuł:
Compensatory dendritic cell development mediated by BATF-IRF interactions.
Autorzy:
Tussiwand R; Department of Pathology and Immunology, Washington University School of Medicine, 660 South Euclid Avenue, St Louis, Missouri 63110, USA.
Lee WL
Murphy TL
Mashayekhi M
KC W
Albring JC
Satpathy AT
Rotondo JA
Edelson BT
Kretzer NM
Wu X
Weiss LA
Glasmacher E
Li P
Liao W
Behnke M
Lam SS
Aurthur CT
Leonard WJ
Singh H
Stallings CL
Sibley LD
Schreiber RD
Murphy KM
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Źródło:
Nature [Nature] 2012 Oct 25; Vol. 490 (7421), pp. 502-7. Date of Electronic Publication: 2012 Sep 19.
Typ publikacji:
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:
Basic-Leucine Zipper Transcription Factors/*metabolism
Dendritic Cells/*cytology
Dendritic Cells/*metabolism
Interferon Regulatory Factors/*metabolism
Animals ; Antigen Presentation ; Antigens, CD/metabolism ; Basic-Leucine Zipper Transcription Factors/chemistry ; Basic-Leucine Zipper Transcription Factors/deficiency ; Basic-Leucine Zipper Transcription Factors/genetics ; CD4-Positive T-Lymphocytes/cytology ; CD4-Positive T-Lymphocytes/immunology ; CD8 Antigens/immunology ; CD8 Antigens/metabolism ; CTLA-4 Antigen/metabolism ; Cell Differentiation ; Cell Line, Tumor ; Cell Lineage ; Dendritic Cells/immunology ; Female ; Fibrosarcoma/immunology ; Fibrosarcoma/metabolism ; Fibrosarcoma/pathology ; Gene Expression Regulation ; Integrin alpha Chains/metabolism ; Interferon Regulatory Factors/deficiency ; Interferon Regulatory Factors/genetics ; Interleukin-10/metabolism ; Interleukin-12/immunology ; Interleukin-12/metabolism ; Leucine Zippers ; Male ; Mice ; Mice, Inbred C57BL ; Neoplasm Transplantation ; Oncogene Protein p65(gag-jun)/metabolism ; Protein Binding ; Protein Structure, Tertiary ; Repressor Proteins/deficiency ; Repressor Proteins/genetics ; T-Lymphocytes, Helper-Inducer/cytology ; T-Lymphocytes, Helper-Inducer/immunology ; T-Lymphocytes, Helper-Inducer/metabolism ; Toxoplasma/immunology
Czasopismo naukowe
Tytuł:
Batf3-dependent CD11b(low/-) peripheral dendritic cells are GM-CSF-independent and are not required for Th cell priming after subcutaneous immunization.
Autorzy:
Edelson BT; Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, United States of America.
Bradstreet TR
KC W
Hildner K
Herzog JW
Sim J
Russell JH
Murphy TL
Unanue ER
Murphy KM
Pokaż więcej
Źródło:
PloS one [PLoS One] 2011; Vol. 6 (10), pp. e25660. Date of Electronic Publication: 2011 Oct 17.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Immunization*
Basic-Leucine Zipper Transcription Factors/*metabolism
CD11b Antigen/*metabolism
Cross-Priming/*drug effects
Dendritic Cells/*immunology
Granulocyte-Macrophage Colony-Stimulating Factor/*pharmacology
Repressor Proteins/*metabolism
T-Lymphocytes, Helper-Inducer/*immunology
Animals ; Antigens, CD/metabolism ; Antigens, Surface/metabolism ; CD8 Antigens/metabolism ; Cytokine Receptor Common beta Subunit/deficiency ; Dendritic Cells/drug effects ; Dermis/immunology ; Dermis/pathology ; Disease Susceptibility ; Encephalomyelitis, Autoimmune, Experimental/immunology ; Encephalomyelitis, Autoimmune, Experimental/pathology ; Integrin alpha Chains/metabolism ; Lectins, C-Type/metabolism ; Lymph Nodes/drug effects ; Lymph Nodes/immunology ; Mannose-Binding Lectins/metabolism ; Mice ; Mice, Inbred C57BL ; Myelin Proteins/immunology ; Myelin-Oligodendrocyte Glycoprotein ; Signal Transduction/drug effects ; Spleen/drug effects ; Spleen/immunology ; Subcutaneous Tissue/drug effects ; Subcutaneous Tissue/immunology ; T-Lymphocytes, Helper-Inducer/drug effects
Czasopismo naukowe
Tytuł:
Dendritic cell regulation of TH1-TH2 development.
Autorzy:
Moser M; Département de Biologie Moleculaire, Université Libre de Bruxelles, Rue des Prof. Jeener et Brochet 12, 6041 Gosselies, Belgium.
Murphy KM
Pokaż więcej
Źródło:
Nature immunology [Nat Immunol] 2000 Sep; Vol. 1 (3), pp. 199-205.
Typ publikacji:
Journal Article; Review
MeSH Terms:
Dendritic Cells/*immunology
Th1 Cells/*immunology
Th2 Cells/*immunology
Animals ; DNA-Binding Proteins/immunology ; Dendritic Cells/metabolism ; Humans ; Interleukin-12/biosynthesis ; Interleukin-12/immunology ; STAT4 Transcription Factor ; Th1 Cells/cytology ; Th2 Cells/cytology ; Trans-Activators/immunology
Czasopismo naukowe
    Wyświetlanie 1-15 z 15

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