المؤلفون: François Trottein, Adam P Uldrich, Thierry Mallevaey, Christophe Paget, Paul J Neeson, Dale I. Godfrey, Geoffrey R. Hill, N. A. Gherardin, Paul A. Beavis, David Dombrowicz, Delphine Staumont-Sallé, Maya Hassane, Denis A. Mogilenko, N. K. Escalante, Mark J. Smyth, Fernando Souza-Fonseca-Guimaraes, Melvyn T. Chow, Helene Duret, David Ritchie, Gabrielle T. Belz

المساهمون: Derudas, Marie-Hélène, Centre d’Infection et d’Immunité de Lille - INSERM U 1019 - UMR 9017 - UMR 8204 (CIIL), Institut Pasteur de Lille, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille)-Centre National de la Recherche Scientifique (CNRS), Cancer immunology program, Peter MacCallum Cancer Center, Sir Peter MacCallum Department of Oncology and Department of Pathology, University of Melbourne, Department of Microbiology and Immunology, QIMR Berghofer Medical Research Institute, Récepteurs nucléaires, maladies cardiovasculaires et diabète - U 1011 (RNMCD), Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille), European Genomic Institute of Diabetes (EGID), Service de dermatologie, Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille), Department of Immunology, University of Toronto, Department of Bone Marrow Transplantation, Royal Brisbane Hospital, Division of Molecular Immunology, The Walter and Eliza Hall Institute of Medical Research (WEHI), School of Medicine, University of Queensland [Brisbane], his work was supported by an NHMRC Program Grant (454569 and 1013367). CP was supported by a postdoctoral fellowship from the US Department of Defense (W81XWH‐11‐1‐0585) and INSERM. MJS and FSFG were supported by a National Health and Medical Research Council of Australia (NHMRC) Australia Fellowship and Program Grant (1013367). MTC was supported by a Cancer Research Institute PhD scholarship. GTB was supported by an ARC Future Fellowship. FT was supported by CNRS. PN was supported by a National Health and Medical Research Council of Australia (NHMRC) Program Grant (1013367). DIG was supported by an NHMRC Senior Principal Research Fellowship (1020770). NAG was supported by a Leukaemia Foundation of Australia postgraduate scholarship. TM is supported by research grants from the Canadian Institutes of Health Research and the Crohn and Colitis Foundation of Canada, as well as a Tier 2 Canada Research Chair. NKE is a recipient of a Vanier Canada Graduate Scholarship. DAM, DS‐S and DD were supported by the Agence Nationale de la Recherche (ANR‐10‐LABX‐46) and the ‘Fondation de France’., We thank Josette Fontaine, Shin‐Foong Ngiow, Deborah Knight, Sébastien Fleury, Julien Wartelle and Kim Steegh for technical assistance. We thank Qerime Mundrea, Ben Venville, Jessica May, Joanne Sutton and Liam Town for maintaining and caring for the mice. We also thank the Peter MacCallum flow cytometry core facility for technical assistance., Institut Européen de Génomique du Diabète - European Genomic Institute for Diabetes - FR 3508 (EGID), Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille-Centre National de la Recherche Scientifique (CNRS), Centre National de la Recherche Scientifique (CNRS)-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille)-Université de Lille-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut Pasteur de Lille, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP), Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)-Université de Lille-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille)-Institut National de la Santé et de la Recherche Médicale (INSERM)

المصدر: Immunology and Cell Biology
Immunology and Cell Biology, 2015, 93 (2), pp.198-212. ⟨10.1038/icb.2014.94⟩
Immunology and Cell Biology, Nature Publishing Group, 2015, 93 (2), pp.198-212. ⟨10.1038/icb.2014.94⟩

مصطلحات موضوعية: Male, CD3 Complex, Inflammasomes, T-Lymphocytes, Interleukin-1beta, MESH: Amino Acid Sequence, MESH: Interleukin-1beta/metabolism, Interleukin-23, MESH: Lung/drug effects, MESH: Skin/immunology, MESH: Lung/immunology, MESH: CD3 Complex/chemistry, MESH: Lymphocyte Subsets/immunology, Immunology and Allergy, Homeostasis, MESH: Animals, IL-2 receptor, MESH: Homeostasis/drug effects, Lung, MESH: Immunity, Skin, MESH: Interleukin-23, Orphan receptor, education.field_of_study, Imiquimod, biology, MESH: Nuclear Receptor Subfamily 1, Group F, Member 3/metabolism, Interleukin-17, Receptors, Antigen, T-Cell, gamma-delta, MESH: T-Lymphocytes/immunology, Nuclear Receptor Subfamily 1, Group F, Member 3, MESH: CD3 Complex/metabolism, 3. Good health, MESH: NLR Family, Pyrin Domain-Containing 3 Protein, medicine.anatomical_structure, Phenotype, MESH: Aminoquinolines/pharmacology, MESH: Carrier Proteins/metabolism, Aminoquinolines, [SDV.IMM]Life Sciences [q-bio]/Immunology, MESH: Interleukin-17/biosynthesis, [SDV.IMM] Life Sciences [q-bio]/Immunology, MESH: Skin/drug effects, CD3, T cell, MESH: T-Lymphocytes/drug effects, Immunology, Population, Molecular Sequence Data, MESH: Germ Cells/drug effects, MESH: Imiquimod, MESH: Phenotype, Immune system, Antigen, MESH: Mice, Inbred C57BL, NLR Family, Pyrin Domain-Containing 3 Protein, MESH: Inflammasomes/drug effects, medicine, Animals, Amino Acid Sequence, education, MESH: Molecular Sequence Data, Innate immune system, MESH: Inflammasomes/metabolism, Immunity, Cell Biology, MESH: Lymphocyte Subsets/drug effects, MESH: Male, Lymphocyte Subsets, Mice, Inbred C57BL, Germ Cells, MESH: Receptors, Antigen, T-Cell, gamma-delta/metabolism, biology.protein, Carrier Proteins

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b35bf10d50efbdf73d623901fa7b5233
https://pubmed.ncbi.nlm.nih.gov/25385067

المؤلفون: Edgar Meinl, Jean Luc Bodmer, Helmut Fickenscher, Michael Schröter, Marcus E. Peter, Kim Burns, Jürg Tschopp, Frank Neipel, Carsten Scaffidi, Chantal Mattmann, Kay Hofmann, Pascal Schneider, Peter H. Krammer, Margot Thome

المصدر: Nature, vol. 386, no. 6624, pp. 517-521

مصطلحات موضوعية: Fas-Associated Death Domain Protein, viruses, Molecular Sequence Data, Apoptosis, Virus Replication, Caspase 8, Receptors, Tumor Necrosis Factor, Cell Line, Herpesvirus 2, Saimiriine, TNF-Related Apoptosis-Inducing Ligand, Mice, Viral Proteins, Gammaherpesvirinae, Animals, Humans, Amino Acid Sequence, fas Receptor, FADD, Receptors, Tumor Necrosis Factor, Member 25, Adaptor Proteins, Signal Transducing, Membrane Glycoproteins, Antigens, CD95/metabolism, Apoptosis Regulatory Proteins, Carrier Proteins/metabolism, Caspase 9, Caspases, Cell Transformation, Viral, Cysteine Endopeptidases/metabolism, Gammaherpesvirinae/genetics, Gammaherpesvirinae/physiology, Herpesvirus 2, Saimiriine/physiology, Membrane Glycoproteins/metabolism, Receptors, Tumor Necrosis Factor/metabolism, Sequence Homology, Amino Acid, Signal Transduction, Tumor Necrosis Factor-alpha/metabolism, Viral Proteins/physiology, Multidisciplinary, biology, Tumor Necrosis Factor-alpha, Fas receptor, Cell biology, Cysteine Endopeptidases, Viral replication, Lytic cycle, biology.protein, Death effector domain, Signal transduction, Carrier Proteins

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c9fcd891ba8ab7bd9978078d41b7440
https://doi.org/10.1038/386517a0

المؤلفون: G. J. Cooper, R. A. Fenton, A. Howorth, Rosaria Meccariello, I. D. Morris, Craig P. Smith

المصدر: Scopus-Elsevier
Fenton, R A, Howorth, A, Cooper, G J, Meccariello, R, Morris, I D & Smith, C P 2000, ' Molecular characterization of a novel UT-A urea transporter isoform (UT-A5) in testis ', American journal of physiology. Cell physiology, vol. 279, no. 5, pp. C1425-31 . https://doi.org/10.1152/ajpcell.2000.279.5.C1425

مصطلحات موضوعية: Male, Gene isoform, DNA, Complementary, Physiology, Urea transporter, Molecular Sequence Data, RNA, Messenger/metabolism, Carrier Proteins/metabolism, Mice, Inbred Strains, Permeability, Mice, Testis, Gene expression, Animals, Tissue Distribution, Amino Acid Sequence, RNA, Messenger, Kidney Medulla, Amino Acid Sequence/genetics, Water/metabolism, Membrane Glycoproteins, Base Sequence, Sequence Homology, Amino Acid, biology, Membrane Glycoproteins/metabolism, Gene Amplification, Membrane Transport Proteins, Water, DNA, Complementary/genetics, Transporter, Cell Biology, Membrane transport, Base Sequence/genetics, Blotting, Northern, SLC14A2, Transmembrane protein, Rats, Membrane protein, Biochemistry, Testis/metabolism, biology.protein, Carrier Proteins, Kidney Medulla/metabolism

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f63e3f0e494322097dd280b7dbcee82
http://www.scopus.com/inward/record.url?eid=2-s2.0-0033725142&partnerID=MN8TOARS