المؤلفون: Nathaniel John Himmel, Richard Benton

المصدر: PLoS biology, vol. 20, no. 7, pp. e3001705

مصطلحات موضوعية: Animals, Cell Survival, Drosophila/metabolism, Drosophila Proteins/metabolism, Epithelial Cells/metabolism, Proteostasis, Receptors, Cell Surface/metabolism, Taste/physiology, General Immunology and Microbiology, General Neuroscience, Taste, Drosophila Proteins, Drosophila, Epithelial Cells, Receptors, Cell Surface, General Agricultural and Biological Sciences, General Biochemistry, Genetics and Molecular Biology

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::021c1b1da13046ac6db576bc90ff254b
https://serval.unil.ch/resource/serval:BIB_30CC35FC55DE.P001/REF.pdf

المؤلفون: Foster-Cuevas, Mildred, Westerholt, Tina, Ahmed, Mohamed, Brown, Marion H., Barclay, A. Neil, Voigt, Sebastian

مصطلحات موضوعية: Animals, Viral Proteins/metabolism, Rats, Viral Proteins/chemistry, Protein Binding, Flow Cytometry, Antigens CD/chemistry, Antigens CD/metabolism, Macrophages Peritoneal/metabolism, Muromegalovirus/immunology, Muromegalovirus/metabolism, Receptors Cell Surface/metabolism, 610 Medizin, ddc:610

وصف الملف: application/pdf

Relation: http://edoc.rki.de/oa/articles/rerbCalexvF7/PDF/21DcMAXaLz8E.pdf; http://edoc.rki.de/176904/1343; urn:nbn:de:0257-10027754; http://dx.doi.org/10.25646/1268

الاتاحة: http://edoc.rki.de/oa/articles/rerbCalexvF7/PDF/21DcMAXaLz8E.pdf
http://edoc.rki.de/176904/1343
https://nbn-resolving.org/urn:nbn:de:0257-10027754
https://doi.org/10.1128/JVI.00064-11
https://doi.org/10.25646/1268

المؤلفون: Larsen, P J, Echwald, S M, Sörensen, T I, Borbye Pedersen, O

المصدر: Ugeskrift for Laeger. 168(2):152

المؤلفون: Anonymous

المصدر: Vårdfacket. 29(3):1

المؤلفون: Gregory G. Putzel, David Artis, Jesper B. Moeller, Irina Leonardi, Iliyan D. Iliev, Christine Elise Schøler Jepsen, Ernst-Martin Füchtbauer, Nicholas J. Bessman, Karsten Skjødt, Anders Schlosser, Mark Hammond, Grith Lykke Sørensen, Theresa Thomsen, Uffe Holmskov, Anne-Laure Flamar, Donna L. Farber

المصدر: Moeller, J B, Leonardi, I, Schlosser, A, Flamar, A-L, Bessman, N J, Putzel, G G, Thomsen, T, Hammond, M, Jepsen, C S, Skjødt, K, Füchtbauer, E-M, Farber, D L, Sorensen, G L, Iliev, I D, Holmskov, U & Artis, D 2019, ' Modulation of the fungal mycobiome is regulated by the chitin-binding receptor FIBCD1 ', The Journal of Experimental Medicine, vol. 216, no. 12, pp. 2689-2700 . https://doi.org/10.1084/jem.20182244
The Journal of Experimental Medicine
Moeller, J B, Leonardi, I, Schlosser, A, Flamar, A L, Bessman, N J, Putzel, G G, Thomsen, T, Hammond, M, Jepsen, C S, Skjødt, K, Füchtbauer, E M, Farber, D L, Sorensen, G L, Iliev, I D, Holmskov, U & Artis, D 2019, ' Modulation of the fungal mycobiome is regulated by the chitin-binding receptor FIBCD1 ', The Journal of Experimental Medicine, vol. 216, no. 12, pp. 2689-2700 . https://doi.org/10.1084/jem.20182244

مصطلحات موضوعية: 0301 basic medicine, Gene Expression, Chitin, SUSCEPTIBILITY, chemistry.chemical_compound, Mice, 0302 clinical medicine, Chitin binding, RNA, Ribosomal, 16S, Immunology and Allergy, Intestinal Mucosa, Receptor, Research Articles, Enteritis/etiology, Fungi/physiology, Pattern recognition receptor, Enteritis, PCR, 030220 oncology & carcinogenesis, medicine.symptom, COLITIS, Protein Binding, EXPRESSION, Immunology, INNATE LYMPHOID-CELLS, Inflammation, Mice, Transgenic, Receptors, Cell Surface, IMMUNITY, Biology, Microbiology, Cell wall, 03 medical and health sciences, DYSBIOSIS, Immune system, DNA, Ribosomal Spacer, medicine, Animals, Humans, Receptors, Cell Surface/metabolism, fungi, Fungi, Brief Definitive Report, TRICHURIS-MURIS, medicine.disease, DOMAIN-CONTAINING 1, Gastrointestinal Microbiome, Disease Models, Animal, 030104 developmental biology, chemistry, INFLAMMATORY RESPONSES, Microbial Interactions, Metagenomics, Chitin/metabolism, Dysbiosis, Intestinal Mucosa/metabolism, Mycobiome

وصف الملف: application/octet-stream

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85339131815355f437b5bc445395583b
https://findresearcher.sdu.dk:8443/ws/files/169995901/Open_Access_version

المؤلفون: R'Zik, Samir, Loo, Martine, Beguin, Yves

المصدر: Haematologica, 86 (3), 244-51 (2001)

مصطلحات موضوعية: Animals, Iron Overload/metabolism, Male, Rats, Rats, Wistar, Receptors, Cell Surface/metabolism, Receptors, Transferrin/blood, Reticulocytes/metabolism, Solubility, Human health sciences, Hematology, Sciences de la santé humaine, Hématologie

Relation: urn:issn:0390-6078; urn:issn:1592-8721

URL الوصول: https://orbi.uliege.be/handle/2268/9449

المؤلفون: Marc Hoylaerts, Marleen Lox, Laurens Liesenborghs, Thomas Vanassche, Christophe Vandenbriele, Elizabeth A. V. Jones, Maarten Criel, Peter Verhamme, Katrien Cludts, Soetkin Van kerckhoven, Benedetta Izzi

المصدر: Thrombosis Research, 146, 76-83. Elsevier Science

مصطلحات موضوعية: 0301 basic medicine, Blood Platelets, medicine.medical_specialty, Fibrinogen receptor, Cell Surface/metabolism, Receptors, Cell Surface, Clot retraction, 03 medical and health sciences, chemistry.chemical_compound, Mice, Bleeding time, In vivo, Internal medicine, Receptors, medicine, Animals, Humans, Platelet, Thrombus, Receptors, Cell Surface/metabolism, medicine.diagnostic_test, Chemistry, Thrombosis, Hematology, medicine.disease, 030104 developmental biology, Endocrinology, Dextran, Immunology, Blood Platelets/metabolism, Thrombosis/metabolism, Platelet factor 4

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17807d10dc9577782487e704d1576e8c
https://doi.org/10.1016/j.thromres.2016.08.026

المؤلفون: Christian B. Juul, Sergey N. Fedosov, Christian W. Heegaard, Ebba Nexo

المصدر: Juul, C B, Fedosov, S, Nexø, E & Heegaard, C W 2019, ' Kinetic analysis of transcellular passage of the cobalamin-transcobalamin complex in Caco-2 monolayers ', Molecular Biology of the Cell, vol. 30, no. 4, pp. 467-477 . https://doi.org/10.1091/mbc.E18-09-0571
Molecular Biology of the Cell

مصطلحات موضوعية: Vitamin B 12/metabolism, Receptors, Cell Surface, Biology, Ligands, Cobalamin, 03 medical and health sciences, chemistry.chemical_compound, 0302 clinical medicine, Transcobalamin, Cell surface receptor, Animals, Humans, Transcellular, Cobalt Radioisotopes, Receptor, Receptors, Cell Surface/metabolism, Molecular Biology, 030304 developmental biology, Transcobalamins, 0303 health sciences, Transcobalamins/metabolism, Biological Transport, Articles, Cell Biology, Transport protein, Dissociation constant, Vitamin B 12, Kinetics, chemistry, Transcytosis, Membrane Trafficking, 030220 oncology & carcinogenesis, Biophysics, Cattle, Caco-2 Cells

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0eb2368b39d46c47e7821fcaa60d524
https://pure.au.dk/portal/da/publications/kinetic-analysis-of-transcellular-passage-of-the-cobalamintranscobalamin-complex-in-caco2-monolayers(eee8dcbb-80ad-4c99-846c-1c35fb04936c).html

المؤلفون: Van Der Klaauw, AA, Croizier, S, De Oliveira, E, Stadler, LKJ, Park, S, Kong, Y, Banton, MC, Tandon, P, Hendricks, AE, Keogh, JM, Riley, SE, Papadia, S, Henning, E, Bounds, R, Bochukova, EG, Mistry, V, O'Rahilly, S, Simerly, RB, Interval, Consortium, Uk10K, Minchin, JEN, Barroso, I, Jones, EY, Bouret, SG, Farooqi, IS

المساهمون: University of Cambridge [UK] (CAM), Addenbrooke's Hospital, Cambridge University NHS Trust, University of Southern California (USC), Université de Lausanne = University of Lausanne (UNIL), University of Oxford, Pathogénèse des Infections vasculaires / Pathogenesis of Vascular Infections, Institut Pasteur [Paris] (IP)-Institut National de la Santé et de la Recherche Médicale (INSERM), Plymouth University, University of Edinburgh, The Wellcome Trust Sanger Institute [Cambridge], University of Colorado [Denver], Queen Mary University of London (QMUL), Vanderbilt University [Nashville], Lille Neurosciences & Cognition - U 1172 (LilNCog), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille), Studies in humans were supported by Wellcome (AAvdK, IB, ISF, 099038/Z/12/Z, 098497/Z/12/Z, WT098051), the Medical Research Council (MRC) (ISF, SOR, MRC_MC_UU_12012/5), the National Institute of Health Research (NIHR), Cambridge Biomedical Research Centre (ISF, IB, SOR), and the Bernard Wolfe Health Neuroscience Endowment (ISF). E.M.d.O. was supported by the Brazilian National Council for Scientific and Technological Development- CNPq (233690/2014-0). J.E.N.M. was supported by a joint University of Edinburgh and British Heart Foundation (BHF) Centre of Research Excellence Fellowship. S.G.B. was supported by the NIH (DK84142, DK102780, and DK118401). Structural analysis was performed by Y.K. and E.Y.J., who are supported by Cancer Research UK and the UK MRC (C375/A17721 and MR/M000141/1 to E.Y.J.) and Wellcome (203141/Z/16/Z, supporting the Wellcome Centre for Human Genetics). Whole-exome sequencing was performed as part of the UK10K consortium (a full list of investigators who contributed to the generation of the data is available from https://www.uk10k.org/). Participants in the INTERVAL randomized controlled trial were recruited with the active collaboration of NHS Blood and Transplant England (https://www.nhsbt.nhs.uk/), which has supported field work and other elements of the trial. DNA extraction and genotyping was co-funded by the NIHR, the NIHR BioResource (https://bioresource.nihr.ac.uk/), and the NIHR Cambridge Biomedical Research Centre (www.cambridgebrc.nihr.org.uk/). The academic coordinating center for INTERVAL was supported by core funding from the NIHR Blood and Transplant Research Unit in Donor Health and Genomics (NIHR BTRU-2014-10024), UK MRC (MR/L003120/1), BHF (RG/13/13/30194), and NIHR Cambridge BRC. A complete list of the investigators and contributors to the INTERVAL trial is provided (Moore et al., 2014)., CCSD, Accord Elsevier, Université de Lausanne (UNIL), University of Oxford [Oxford], Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut Pasteur [Paris], Lille Neurosciences & Cognition - U 1172 (LilNCog (ex-JPARC)), van der Klaauw, Agatha [0000-0001-6971-8828], Stadler, Lukas [0000-0002-7028-4390], Papadia, Sofia [0000-0002-9222-3812], O'Rahilly, Stephen [0000-0003-2199-4449], Barroso, Ines [0000-0001-5800-4520], Farooqi, Ismaa [0000-0001-7609-3504], Apollo - University of Cambridge Repository, INTERVAL, UK10K Consortium

المصدر: Cell
Cell, 2019, 176 (4), pp.729-742.e18. ⟨10.1016/j.cell.2018.12.009⟩
Van Der Klaauw, A A, Croizier, S, Mendes De Oliveira, E, Stadler, L K J, Park, S, Kong, Y, Banton, M C, Tandon, P, Hendricks, A E, Keogh, J M, Riley, S E, Papadia, S, Henning, E, Bounds, R, Bochukova, E G, Mistry, V, O’rahilly, S, Simerly, R B, Minchin, J E N, Barroso, I & Jones, E Y & Bouret, S G & Farooqi, I S 2019, ' Human semaphorin 3 variants link melanocortin circuit development and energy balance ', Cell, vol. 176, no. 4, pp. 729-742 . https://doi.org/10.1016/j.cell.2018.12.009
Cell, Elsevier, 2019, 176 (4), pp.729-742.e18. ⟨10.1016/j.cell.2018.12.009⟩
Cell, vol. 176, no. 4, pp. 729-742.e18

مصطلحات موضوعية: Adult, Leptin, Male, Plexins, obesity, Adolescent, [SDV]Life Sciences [q-bio], Pomc, Nerve Tissue Proteins, Receptors, Cell Surface, Semaphorins, Article, Cell Line, Eating, Mice, Young Adult, Animals, Body Weight, Child, Child, Preschool, Disease Models, Animal, Energy Metabolism/genetics, Female, Genetic Variation/genetics, Homeostasis, Humans, Hypothalamus/metabolism, Leptin/metabolism, Melanocortins/metabolism, Mice, Inbred C57BL, Middle Aged, Nerve Tissue Proteins/metabolism, Neurons/metabolism, Obesity/genetics, Obesity/metabolism, Receptors, Cell Surface/metabolism, Semaphorins/genetics, Semaphorins/metabolism, Zebrafish, AgRP, Neuropilins, Semaphorin 3s, hypothalamus, Neurons, Genetic Variation, Melanocortins, [SDV] Life Sciences [q-bio], nervous system, Energy Metabolism

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80eb92bc3fd4ba670283a473e22557d3
https://hal.science/hal-02375383/file/S0092867418316234.pdf

المؤلفون: Hoveyda, Hamid R, Fraser, Graeme L, Zoute, Ludivine, Dutheuil, Guillaume, Schils, Didier, Brantis, Cyrille, Lapin, Alexey, Parcq, Julien, Guitard, Sandra, Lenoir, François, Bousmaqui, Mohamed El, Rorive, Sarah, Hospied, Sandrine, Blanc, Sébastien, Bernard, Jérôme, Ooms, Frédéric, McNelis, Joanne C, Olefsky, Jerrold M

المصدر: Bioorganic and Medicinal Chemistry, 26 (18), 5169 - 5180 (2018-10-01)

مصطلحات موضوعية: FFA2 agonist, Fsp(3), GPCR, GPR43 agonist, LLE, OGTT, FFA2R protein, human, Receptors, Cell Surface, Thiazoles, Animals, Diabetes Mellitus, Experimental/drug therapy, Dose-Response Relationship, Drug, Humans, Mice, Mice, Knockout, Molecular Structure, Rats, Receptors, Cell Surface/agonists, Receptors, Cell Surface/deficiency, Receptors, Cell Surface/metabolism, Structure-Activity Relationship, Thiazoles/chemistry, Thiazoles/pharmacology, Disease Models, Animal, Drug Discovery, Diabetes Mellitus, Experimental, Biochemistry, Molecular Medicine, Molecular Biology, Pharmaceutical Science, Clinical Biochemistry, Organic Chemistry, Physical, chemical, mathematical & earth Sciences, Chemistry, Physique, chimie, mathématiques & sciences de la terre, Chimie

Relation: https://api.elsevier.com/content/article/PII:S096808961830110X?httpAccept=text/xml; urn:issn:0968-0896; urn:issn:1464-3391

URL الوصول: https://orbi.uliege.be/handle/2268/320297

المؤلفون: Albert E. Jergens, Cameron J. Nowell, Lina Maria Martinez Lopez, Wayne G. Kimpton, Caroline S Mansfield, Andrew Stent, Karin Allenspach, Julien R.S. Dandrieux, Simon M. Firestone

المصدر: Innate Immunity
Dandrieux, J R, Martinez Lopez, L M, Stent, A, Jergens, A, Allenspach, K, Nowell, C J, Firestone, S M, Kimpton, W & Mansfield, C S 2018, ' Changes in duodenal CD163-positive cells in dogs with chronic enteropathy after successful treatment ', Innate Immunity, vol. 24, no. 7, pp. 400-410 . https://doi.org/10.1177/1753425918799865

مصطلحات موضوعية: 0301 basic medicine, Male, Antigens, CD/metabolism, Macrophages/immunology, Leukocyte L1 Antigen Complex/metabolism, Biomarkers/metabolism, Inflammatory bowel disease, Gastroenterology, Canine, 0403 veterinary science, Pathogenesis, Enteropathy, Cell Differentiation, 04 agricultural and veterinary sciences, Immunohistochemistry, Infectious Diseases, medicine.anatomical_structure, Antigens, Differentiation, Myelomonocytic/metabolism, Female, medicine.medical_specialty, 040301 veterinary sciences, Duodenum, Immunology, Antigens, Differentiation, Myelomonocytic, Receptors, Cell Surface, macrophage, Microbiology, Duodenum/immunology, 03 medical and health sciences, Dogs, Antigen, Antigens, CD, inflammatory bowel disease, Internal medicine, Inflammatory Bowel Diseases/drug therapy, medicine, Animals, Humans, Receptors, Cell Surface/metabolism, Molecular Biology, Retrospective Studies, business.industry, Macrophages, Cell Biology, Original Articles, medicine.disease, Inflammatory Bowel Diseases, chronic enteropathy, Disease Models, Animal, 030104 developmental biology, CD163, Calprotectin, business, Leukocyte L1 Antigen Complex, Biomarkers

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97bbebd05acc0035ca6fa6a50e277887
https://pubmed.ncbi.nlm.nih.gov/30223681

المؤلفون: Jon Dobson, Carlos Rinaldi

Resource Type: eBook.

الموضوعات: Receptors, Cell Surface--metabolism, Magnetite Nanoparticles, Signal Transduction--physiology, Theranostic Nanomedicine--methods

Categories: MEDICAL / Biotechnology, TECHNOLOGY & ENGINEERING / Materials Science / General, TECHNOLOGY & ENGINEERING / Biomedical

المؤلفون: Wenbin Wang, Nathanael S. Gray, Adam J. Pearson, William Vermi, Zhengui Xia, Katherine G. Finegan, Jinhua Wang, Ilaria Russo, Silvia Lonardi, Cathy Tournier, Qiuping Xu, Brian A. Telfer, Emanuele Giurisato

المصدر: Proceedings of the National Academy of Sciences of the United States of America
Giurisato, E, Xu, Q, Lonardi, S, Telfer, B, Russo, I, Pearson, A, Finegan, K, Wang, W, Wang, J, Gray, N S, Vermi, W, Xia, Z & Tournier, C 2018, ' Myeloid ERK5 deficiency suppresses tumor growth by blocking protumor macrophage polarization via STAT3 inhibition ', Proceedings of the National Academy of Sciences, vol. 115, no. 12, pp. E2801-E2810 . https://doi.org/10.1073/pnas.1707929115

مصطلحات موضوعية: 0301 basic medicine, MAPK/ERK pathway, Medical Sciences, medicine.medical_treatment, Antigens, CD/metabolism, Inbred C57BL, ERK5, MAPK, STAT3, macrophages, tumors, Transgenic, STAT3, Mice, Mitogen-Activated Protein Kinase 7/genetics, Cancer immunotherapy, Neoplasms, Receptors, Macrophage, Phosphorylation, Multidisciplinary, biology, Manchester Cancer Research Centre, Cell Polarity, Biological Sciences, CD, ERK5, Manchester Institute for Collaborative Research on Ageing, PNAS Plus, Macrophages, MAPK, Tumors, Animals, Antigens, CD, Antigens, Differentiation, Myelomonocytic, Humans, Mice, Inbred C57BL, Mice, Transgenic, Mitogen-Activated Protein Kinase 7, Receptors, Cell Surface, STAT3 Transcription Factor, Tyrosine, Xenograft Model Antitumor Assays, Differentiation, Cell Surface, Antigens, Differentiation, Myelomonocytic/metabolism, Tyrosine/metabolism, Neoplasms/metabolism, ResearchInstitutes_Networks_Beacons/MICRA, STAT3 Transcription Factor/genetics, Macrophage polarization, Proinflammatory cytokine, QH301, 03 medical and health sciences, Macrophages/metabolism, medicine, Antigens, Protein kinase A, Receptors, Cell Surface/metabolism, QH, ResearchInstitutes_Networks_Beacons/mcrc, Myelomonocytic, 030104 developmental biology, biology.protein, Cancer research, STAT protein

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::063d62af4140b663639014d420c46470
http://hdl.handle.net/11379/537884

المؤلفون: Roth, Ronelle, Chiapello, Marco, Montero, Héctor, Gehrig, Peter, Grossmann, Jonas, O’Holleran, Kevin, Hartken, Denise, Walters, Fergus, Yang, Shu-Yi, Hillmer, Stefan, Schumacher, Karin, Bowden, Sarah, Craze, Melanie, Wallington, Emma J., Miyao, Akio, Sawers, Ruairidh, Martinoia, Enrico, Paszkowski, Uta

المساهمون: University of Zurich, Roth, Ronelle, Roth, Ronelle [0000-0001-5566-8954], Chiapello, Marco [0000-0001-7768-3047], Montero, Héctor [0000-0001-8590-6394], Bowden, Sarah [0000-0001-5105-076X], Wallington, Emma J [0000-0003-3715-7901], Miyao, Akio [0000-0002-2822-2866], Paszkowski, Uta [0000-0002-7279-7632], Apollo - University of Cambridge Repository

المصدر: Nature Communications, 9 (1)
Nature communications, vol. 9, no. 1, pp. 4677
Nature Communications, Vol 9, Iss 1, Pp 1-12 (2018)
Nature Communications

مصطلحات موضوعية: Proteome, Science, 610 Medicine & health, 10071 Functional Genomics Center Zurich, 1600 General Chemistry, Receptors, Cell Surface, Laser Capture Microdissection, Protein Serine-Threonine Kinases, Zea mays, Article, stomatognathic system, 1300 General Biochemistry, Genetics and Molecular Biology, Mycorrhizae, parasitic diseases, lcsh:Science, Promoter Regions, Genetic, Symbiosis, Plant Proteins, Membranes, Membrane Proteins/metabolism, Mutation/genetics, Mycorrhizae/metabolism, Mycorrhizae/ultrastructure, Oryza/enzymology, Oryza/microbiology, Oryza/ultrastructure, Plant Proteins/metabolism, Promoter Regions, Genetic/genetics, Protein-Serine-Threonine Kinases/metabolism, Proteome/metabolism, Receptors, Cell Surface/metabolism, Transcriptome/genetics, Zea mays/metabolism, Zea mays/microbiology, fungi, food and beverages, Membrane Proteins, Oryza, 3100 General Physics and Astronomy, Mutation, 570 Life sciences, biology, lcsh:Q, Transcriptome

وصف الملف: application/application/pdf; application/pdf; s41467-018-06865-z.pdf - application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c764082fb099f71a3ec448f522bb4b7b

المؤلفون: Helga D. Manthey, Martin Busch, Christian Weber, Alma Zernecke, Jaroslav Pelisek, Ela Karshovska, Miriam Koch, Stefanie Barnsteiner, Rory R. Koenen, Hans-Henning Eckstein, Clément Cochain, Sweena M. Chaudhari

المصدر: Thrombosis and Haemostasis, 110(6), 1267-77. Georg Thieme Verlag

مصطلحات موضوعية: 0301 basic medicine, Chemokine, T-Lymphocytes, C-C chemokine receptor type 6, Macrophages/immunology, 030204 cardiovascular system & hematology, Inbred C57BL, Monocytes, Chemokine receptor, Mice, 0302 clinical medicine, Cell Movement, Inflammation/genetics, Receptors, Receptors, LDL/genetics, Cells, Cultured, Mice, Knockout, Cultured, biology, hemic and immune systems, Hematology, medicine.anatomical_structure, Disease Susceptibility, medicine.symptom, Atherosclerosis/immunology, Receptors, CCR6, Endothelium, Cell Adhesion/genetics, Cells, Knockout, Receptors, CCR6/genetics, Cell Surface/metabolism, LDL/genetics, Receptors, Cell Surface, Inflammation, chemical and pharmacologic phenomena, Diet, High-Fat, 03 medical and health sciences, Immune system, Cell Adhesion, medicine, Cell Movement/genetics, Animals, Receptors, Cell Surface/metabolism, Animal, Macrophages, Monocyte, Monocytes/immunology, T-Lymphocytes/immunology, Atherosclerosis, Diet, Mice, Inbred C57BL, CCL20, Disease Models, Animal, High-Fat, 030104 developmental biology, Receptors, LDL, Immunology, Disease Models, biology.protein, CCR6/genetics

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a087bd2b0aecfab3cd059fae174b81a
https://doi.org/10.1160/th13-01-0017

المؤلفون: Doortje W. Dekens, Petrus J.W. Naudé, Yannick Vermeiren, Sebastiaan Engelborghs, Debby Van Dam, Ulrich L. M. Eisel, Richard C. Oude Voshaar, Peter Paul De Deyn

المساهمون: Clinical sciences, Neurology, Eisel lab, Interdisciplinary Centre Psychopathology and Emotion regulation (ICPE), Clinical Cognitive Neuropsychiatry Research Program (CCNP), Molecular Neuroscience and Ageing Research (MOLAR)

المصدر: Journal of Alzheimer's disease
Journal of Alzheimer's Disease
Journal of alzheimers disease, 55(2), 763-776. IOS Press
Journal of Alzheimer's Disease, 55, 2, pp. 763-776
Journal of Alzheimer's Disease, 55, 763-776
Journal of Alzheimer's Disease, 55(2), 763-776
Journal of Alzheimer's Disease 55 (2017) 2

مصطلحات موضوعية: Male, 0301 basic medicine, MILD COGNITIVE IMPAIRMENT, hippocampus, LATE-LIFE DEPRESSION, Hippocampus, INFLAMMATORY MARKERS, PREFRONTAL CORTEX, Lipocalin, 24p3R, Lipocalin-2/blood, 0302 clinical medicine, NGAL, Prefrontal cortex, Depression (differential diagnoses), Medicine(all), AMYLOID BETA-PEPTIDE, Depression, General Neuroscience, Brain, General Medicine, Alzheimer's disease, Late life depression, Low Density Lipoprotein Receptor-Related Protein-2, Psychiatry and Mental health, Clinical Psychology, medicine.anatomical_structure, Depression/complications, depression, lipocalin 2, Female, medicine.symptom, APOLIPOPROTEIN J, Psychology, Alzheimer’s disease, Research Article, medicine.medical_specialty, Alzheimer Disease/complications, Central nervous system, Enzyme-Linked Immunosorbent Assay, Receptors, Cell Surface, Inflammation, VASCULAR-DEMENTIA, 03 medical and health sciences, CEREBROSPINAL-FLUID, Lipocalin-2, Alzheimer Disease, Internal medicine, medicine, Brain/metabolism, Humans, Receptors, Cell Surface/metabolism, Vascular dementia, Biology, Psychiatric Status Rating Scales, Analysis of Variance, Low Density Lipoprotein Receptor-Related Protein-2/metabolism, Other Research Radboud Institute for Health Sciences [Radboudumc 0], CENTRAL-NERVOUS-SYSTEM, MAJOR DEPRESSION, medicine.disease, 030104 developmental biology, Endocrinology, inflammation, Human medicine, Geriatrics and Gerontology, megalin, 030217 neurology & neurosurgery

وصف الملف: pdf; application/pdf; application/octet-stream; text/html

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::763ceaf2c82c4d906611873528ff9bb2
https://hdl.handle.net/10067/1358620151162165141

المؤلفون: Léger, Psylvia, Tetard, Marilou, Youness, Berthe, Cordes, Nicole, Rouxel, Ronan N, Flamand, Marie, Lozach, Pierre-Yves

المساهمون: Heidelberg University Hospital [Heidelberg], Institut Armand Frappier (INRS-IAF), Institut National de la Recherche Scientifique [Québec] (INRS)-Réseau International des Instituts Pasteur (RIIP), Unité de recherche Virologie et Immunologie Moléculaires (VIM), Institut National de la Recherche Agronomique (INRA), Virologie Structurale, Institut Pasteur [Paris]-Centre National de la Recherche Scientifique (CNRS), Funded by - CellNetworks Research Group - Natural Sciences and Engineering Research Council of Canada. Grant Number: 419538-2012 - Banting Research Foundation, Unité de recherche Virologie et Immunologie Moléculaires (VIM (UR 0892)), Virologie Structurale - Structural Virology, Centre National de la Recherche Scientifique (CNRS)-Institut Pasteur [Paris], Institut Pasteur [Paris] (IP)-Centre National de la Recherche Scientifique (CNRS)

المصدر: Traffic
Traffic, Wiley, 2016, 17 (6), pp.639-56. ⟨10.1111/tra.12393 ⟩
Traffic, Wiley, 2016, 17 (6), pp.639-56. ⟨10.1111/tra.12393⟩
Traffic, 2016, 17 (6), pp.639-56. ⟨10.1111/tra.12393⟩

مصطلحات موضوعية: binding, MESH: Liver/virology, MESH: Cell Adhesion Molecules/metabolism, MESH: Virus Internalization, Receptors, Cell Surface, bunyavirus, MESH: Endothelial Cells/metabolism, DC-SIGN, virus receptor, L-SIGN, MESH: Phlebovirus/pathogenicity, MESH: Endothelial Cells/virology, Humans, endocytosis, MESH: Protein Binding, Lectins, C-Type, C-type lectins, CD209L, phlebovirus, MESH: Receptors, Cell Surface/genetics, MESH: Humans, MESH: Phlebovirus/physiology, MESH: Lectins, C-Type/genetics, Endothelial Cells, Uukuniemi virus, endocytic motif, Virus Internalization, MESH: Liver/cytology, CD209, Rift Valley fever virus, DC-SIGNR, Liver, uptake, MESH: Endocytosis, MESH: HeLa Cells, [SDV.MP.VIR]Life Sciences [q-bio]/Microbiology and Parasitology/Virology, MESH: Receptors, Cell Surface/metabolism, MESH: Cell Adhesion Molecules/genetics, Cell Adhesion Molecules, MESH: Lectins, C-Type/metabolism, HeLa Cells, Protein Binding

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::855ecf8d3ad357eb2892ccef090f8a46
https://hal-riip.archives-ouvertes.fr/pasteur-01351418/document

المؤلفون: Nathalie C Girardin, Maud Frieden, Nicolas Demaurex, Wolfgang F. Graier, Roland Malli, Hélène Jousset

المصدر: Cell Calcium, Vol. 43, No 1 (2008) pp. 83-94

مصطلحات موضوعية: Calcium Channel Blockers/pharmacology, Histamine/pharmacology, Agonist, Calcium/metabolism, SERCA, Calcium Channels/metabolism, Physiology, medicine.drug_class, Cell Respiration, Mitochondria/drug effects/metabolism, Receptors, Cell Surface, Stimulation, Endoplasmic Reticulum, Article, chemistry.chemical_compound, Lanthanum, Cell Respiration/drug effects, medicine, Extracellular, Humans, Calcium Signaling, ddc:612, Receptor, Endoplasmic Reticulum/metabolism, Molecular Biology, Cells, Cultured, Imidazoles/pharmacology, Receptors Cell Surface/metabolism, Chemistry, Biological Transport/drug effects, Endoplasmic reticulum, Imidazoles, Endothelial Cells, Biological Transport, Depolarization, Cell Biology, Calcium Channel Blockers, Mitochondria, Cell biology, Endothelial Cells/drug effects/metabolism, Calcium, Calcium Channels, Cells Cultured, Lanthanum/pharmacology, Histamine

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a95f287a6e57a87779620807b28bbe8
https://doi.org/10.1016/j.ceca.2007.04.006

المؤلفون: Carine Duval, Johan Auwerx, Christophe Dardenne, Jean Loup Lemesre, Alexis Valentin, Hélène Authier, Bernard Pipy, Etienne Meunier, David Olagnier, Lise Lefèvre, Olivier Neyrolles, Geanncarlo Lugo-Villarino, Agnès Coste, José Bernad

المساهمون: Infections Parasitaires : Transmission, Physiopathologie et Thérapeutiques (IP-TPT), Service de Santé des Armées-Assistance Publique - Hôpitaux de Marseille (APHM)-Aix Marseille Université (AMU)-Institut de Recherche pour le Développement (IRD), Institut de pharmacologie et de biologie structurale (IPBS), Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Centre National de la Recherche Scientifique (CNRS), Focal Area Infection Biology, Biozentrum, University of Basel (Unibas), Division of Infectious Diseases, University of South Florida (USF), Université Paris Descartes - Faculté de Médecine (UPD5 Médecine), Université Paris Descartes - Paris 5 (UPD5), Departament de Bioquímica i Biologia Molecular, Universitat de Barcelona (UB), Pharmacochimie et Biologie pour le Développement (PHARMA-DEV), Institut de Recherche pour le Développement (IRD)-Institut de Chimie de Toulouse (ICT-FR 2599), Institut National Polytechnique (Toulouse) (Toulouse INP), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Centre National de la Recherche Scientifique (CNRS)-Institut National Polytechnique (Toulouse) (Toulouse INP), Université Fédérale Toulouse Midi-Pyrénées-Centre National de la Recherche Scientifique (CNRS), Laboratoire de la Signalisation et de la Différenciation des Macrophages, Institution Louis Bugnard, Institut de génétique et biologie moléculaire et cellulaire (IGBMC), Université Louis Pasteur - Strasbourg I-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut de Chimie de Toulouse (ICT-FR 2599), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Institut de Chimie du CNRS (INC)-Institut National Polytechnique (Toulouse) (Toulouse INP), Université Fédérale Toulouse Midi-Pyrénées-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD)-Institut de Chimie du CNRS (INC)-Institut de Recherche pour le Développement (IRD), Centre National de la Recherche Scientifique (CNRS)-Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées, Institut de Recherche pour le Développement (IRD)-Aix Marseille Université (AMU)-Assistance Publique - Hôpitaux de Marseille (APHM)-Service de Santé des Armées, Institut de Recherche pour le Développement (IRD)-Institut de Chimie de Toulouse (ICT), Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Université de Toulouse (UT)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Institut National Polytechnique (Toulouse) (Toulouse INP), Université de Toulouse (UT)-Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT), Université de Toulouse (UT)-Université de Toulouse (UT)-Centre National de la Recherche Scientifique (CNRS)

المصدر: Immunity
Immunity, Elsevier, 2013, 38 (5), pp.1038-1049. ⟨10.1016/j.immuni.2013.04.010⟩
Lefèvre, L, Lugo-Villarino, G, Meunier, E, Valentin, A, Olagnier, D, Authier, H, Duval, C, Dardenne, C, Bernad, J, Lemesre, J L, Auwerx, J, Neyrolles, O, Pipy, B & Coste, A 2013, ' The C-type lectin receptors dectin-1, MR, and SIGNR3 contribute both positively and negatively to the macrophage response to Leishmania infantum ' Immunity, vol. 38, no. 5, pp. 1038-49 . https://doi.org/10.1016/j.immuni.2013.04.010
Immunity, 2013, 38 (5), pp.1038-1049. ⟨10.1016/j.immuni.2013.04.010⟩

مصطلحات موضوعية: MESH: Signal Transduction, MESH: Mannose-Binding Lectins / metabolism, [SDV]Life Sciences [q-bio], Interleukin-1beta, MESH: Leishmaniasis, Visceral / immunology, Antigens, CD/metabolism, Macrophages/immunology, MESH: Mice, Knockout, MESH: Antigens, CD / metabolism, MESH: Protein-Tyrosine Kinases / metabolism, Caspase 1/metabolism, Mice, 0302 clinical medicine, MESH: Leishmania infantum / immunology, MESH: Caspase 1 / metabolism, C-type lectin, MESH: RNA, Small Interfering, MESH: Interleukin-1beta / antagonists & inhibitors, Macrophage, Immunology and Allergy, MESH: Animals, MESH: Leishmaniasis, Visceral / parasitology, MESH: Receptors, Cell Surface / metabolism, Leishmania infantum, RNA, Small Interfering, Receptor, MESH: NADPH Oxidases / metabolism, Cells, Cultured, ComputingMilieux_MISCELLANEOUS, Mice, Knockout, 0303 health sciences, Arachidonic Acid, biology, Effector, Caspase 1, Intracellular Signaling Peptides and Proteins, Protein-Tyrosine Kinases, MESH: Macrophages / immunology, 3. Good health, Cell biology, MESH: Leukotriene B4 / antagonists & inhibitors, Infectious Diseases, Intracellular Signaling Peptides and Proteins/metabolism, NADPH Oxidases/metabolism, Leishmaniasis, Visceral, [SDV.IMM]Life Sciences [q-bio]/Immunology, RNA Interference, Signal transduction, Interleukin-1beta/antagonists & inhibitors, Mannose receptor, Mannose Receptor, Signal Transduction, MESH: Cells, Cultured, MESH: Reactive Oxygen Species / metabolism, Immunology, MESH: RNA Interference, Receptors, Cell Surface, Leukotriene B4, Arachidonic Acid/metabolism, MESH: Syk Kinase, 03 medical and health sciences, Antigens, CD, Reactive Oxygen Species/metabolism, MESH: Mice, Inbred C57BL, parasitic diseases, MESH: Arachidonic Acid / metabolism, Animals, Humans, Syk Kinase, Lectins, C-Type, Lectins, C-Type/immunology, MESH: Interleukin-1beta / metabolism, Receptors, Cell Surface/metabolism, Mannose-Binding Lectins/metabolism, MESH: Mice, 030304 developmental biology, MESH: Humans, Leishmania infantum/immunology, Macrophages, NADPH Oxidases, biology.organism_classification, Leishmania, MESH: Mannose Receptor, Leishmaniasis, Visceral/immunology, Protein-Tyrosine Kinases/metabolism, MESH: Lectins, C-Type / metabolism, Mice, Inbred C57BL, MESH: Lectins, C-Type / immunology, Mannose-Binding Lectins, Leukotriene B4/antagonists & inhibitors, Reactive Oxygen Species, MESH: Intracellular Signaling Peptides and Proteins / metabolism, 030215 immunology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6effd582598ceebe3d4eb3a68796326c
https://hal.archives-ouvertes.fr/hal-02348593

المؤلفون: Antoine Hadengue, Jean-Louis Frossard, François Mach, Catherine M. Pastor, Marc Chanson, Brenda R. Kwak, Jérôme Pugin

المصدر: Critical Care Medicine, Vol. 32, No 8 (2004) pp. 1759-63

مصطلحات موضوعية: Lung Diseases, Lipopolysaccharides, Pathology, medicine.medical_specialty, Pancreatic disease, Receptors, Cell Surface, Lung injury, Critical Care and Intensive Care Medicine, Lung Diseases/chemically induced/etiology/metabolism, Mice, Amylases/blood/secretion, Intensive care, medicine, Animals, Receptors, Cell Surface/metabolism, Pancreas, Ceruletide, ddc:616, Membrane Glycoproteins, ddc:618, business.industry, Toll-Like Receptors, Membrane Glycoproteins/metabolism, medicine.disease, Pancreatitis/chemically induced/complications/metabolism, Caerulein, Toll-Like Receptor 4, Disease Models, Animal, medicine.anatomical_structure, Pancreatitis, Amylases, Acute Disease, TLR4, Pancreas/enzymology, Acute pancreatitis, lipids (amino acids, peptides, and proteins), business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::601f532d8b4334614ac6e5af77bf7ac0
https://doi.org/10.1097/01.ccm.0000133020.47243.8e