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cx3c chemokine receptor 1 (480) 480
index medicus (427) 427
animals (401) 401
humans (336) 336
mice (313) 313
receptors, chemokine - genetics (257) 257
male (253) 253
female (231) 231
receptors, chemokine - metabolism (181) 181
mice, inbred c57bl (173) 173
inflammation (167) 167
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fractalkine (155) 155
expression (131) 131
cx3cr1 (124) 124
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macrophages (109) 109
chemokines (105) 105
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chemokine cx3cl1 (99) 99
article (97) 97
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chemokine (92) 92
analysis (90) 90
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research article (75) 75
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brain (66) 66
immunohistochemistry (66) 66
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cell biology (61) 61
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multidisciplinary sciences (60) 60
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cx3c chemokine receptor 1 - metabolism (57) 57
chemokine receptors (56) 56
medicine (56) 56
chemokine cx3cl1 - genetics (54) 54
cytokines (54) 54
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disease (52) 52
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proteins (51) 51
signal transduction (51) 51
macrophages - metabolism (50) 50
receptors, chemokine - physiology (49) 49
green fluorescent proteins - genetics (48) 48
fractalkine receptor (47) 47
physiological aspects (47) 47
cxcr1 (46) 46
neurons (46) 46
cx3c chemokine receptor 1 - genetics (45) 45
lymphocytes (45) 45
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neurology (44) 44
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science (43) 43
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genetic aspects (39) 39
genotype (39) 39
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rna, messenger - metabolism (38) 38
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chemokines, cx3c - genetics (37) 37
health aspects (36) 36
monocytes - metabolism (36) 36
nervous system (36) 36
case-control studies (35) 35
mice, inbred balb c (35) 35
microglia - drug effects (35) 35
receptor (35) 35
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1. Full Text Decreased CX3CR1 messenger RNA expression is an independent molecular biomarker of early and late mortality in critically ill patients
by Friggeri, Arnaud and Cazalis, Marie-Angélique and Pachot, Alexandre and Cour, Martin and Argaud, Laurent and Allaouchiche, Bernard and Floccard, Bernard and Schmitt, Zoé and Martin, Olivier and Rimmelé, Thomas and Fontaine-Kesteloot, Oriane and Page, Mathieu and Piriou, Vincent and Bohé, Julien and Monneret, Guillaume and Morisset, Stéphane and Textoris, Julien and Vallin, Hélène and Blein, Sophie and Maucort-Boulch, Delphine and Lepape, Alain and Venet, Fabienne and MIP Rea Study Grp and MIP Rea Study Group and for the MIP Rea Study Group
Critical Care, ISSN 1364-8535, 06/2016, Volume 20, Issue 1, p. 204
Background: Chemokine (C-X3-C motif) receptor 1 (CX3CR1) was identified as the most differentially expressed gene between survivors and non-survivors in two... 
Biomarker | Immunosuppression | Prognosis | Transcriptomics | Mortality | CX3CR1 mRNA | Intensive care unit | FRACTALKINE | MULTICENTER | SCORE | MONOCYTES | VALIDATION | FUTURE | DEFINITIONS | SEPTIC SHOCK | SEPSIS-INDUCED IMMUNOSUPPRESSION | THERAPIES | CRITICAL CARE MEDICINE | Prospective Studies | Systemic Inflammatory Response Syndrome - physiopathology | Humans | Middle Aged | Survivors - statistics & numerical data | Real-Time Polymerase Chain Reaction - methods | Critical Illness | RNA, Messenger - analysis | Male | Systemic Inflammatory Response Syndrome - blood | Shock, Septic - blood | Aged, 80 and over | Female | France | Length of Stay | Hospital Mortality | Risk Factors | Biomarkers - analysis | Shock, Septic - complications | Logistic Models | Shock, Septic - physiopathology | Biomarkers - blood | Intensive Care Units - organization & administration | CX3C Chemokine Receptor 1 - analysis | RNA, Messenger - blood | ROC Curve | Aged | Systemic Inflammatory Response Syndrome - complications | CX3C Chemokine Receptor 1 - blood | Cohort Studies | Intensive care units | Services | Usage | Critically ill | Analysis | Research | Gene expression | Biological markers | Health aspects | Life Sciences
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2. High expression of CX3C chemokine receptor 1 (CX3CR1) in human carotid plaques is associated with vulnerability of the lesions
by Masztalewicz, Marta and Nowacki, Przemysław and Szydłowski, Łukasz and Żukowski, Maciej and Gutowski, Piotr
Folia neuropathologica, 2017, Volume 55, Issue 2, p. 174
Introduction: In data based on ex vivo studies and animal models, fractalkine is considered an important mediator in the development and destabilization of... 
Plaque, Atherosclerotic - metabolism | Chemokine CX3CL1 - metabolism | Humans | Middle Aged | Male | Carotid Stenosis - pathology | CX3C Chemokine Receptor 1 - analysis | CX3C Chemokine Receptor 1 - biosynthesis | Carotid Stenosis - metabolism | Aged, 80 and over | Adult | Female | Aged | Plaque, Atherosclerotic - pathology
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3. Full Text Dichotomous Expression of TNF Superfamily Ligands on Antigen-Presenting Cells Controls Post-priming Anti-viral CD4+ T Cell Immunity
by Chang, Yu-Han and Wang, Kuan Chung and Chu, Kuan-Lun and Clouthier, Derek L and Tran, Anh T and Torres Perez, Miguel S and Zhou, Angela C and Abdul-Sater, Ali A and Watts, Tania H
Immunity, ISSN 1074-7613, 11/2017, Volume 47, Issue 5, pp. 943 - 958.e9
T cell antigen-presenting cell (APC) interactions early during chronic viral infection are crucial for determining viral set point and disease outcome, but how... 
type I interferon | monocyte-derived inflammatory APC | viral infection | costimulation | B7 family | lymphocytic choriomeningitis virus | TNF family | influenza A virus | PLASMACYTOID DENDRITIC CELLS | RESPONSES | B-LYMPHOCYTE | HERPESVIRUS ENTRY MEDIATOR | PERSISTENT LCMV INFECTION | CO-STIMULATION | LYMPHOCYTE ATTENUATOR | IMMUNOLOGY | CHRONIC VIRAL-INFECTION | GITR LIGAND | I INTERFERON | Membrane Glycoproteins - analysis | Monocytes - cytology | Dendritic Cells - immunology | Mice, Inbred C57BL | Glucocorticoid-Induced TNFR-Related Protein - analysis | Lymphocytic Choriomeningitis - immunology | Antigen-Presenting Cells - immunology | Tumor Necrosis Factors - analysis | CX3C Chemokine Receptor 1 - analysis | CD4-Positive T-Lymphocytes - immunology | Glucocorticoid-Induced TNFR-Related Protein - physiology | Animals | Female | Mice | CD27 Ligand - analysis | Tumor necrosis factor receptors | CD86 antigen | Chronic infection | Viruses | CX3CR1 protein | Infections | Lymphocytes T | CD70 antigen | Immunity | Accumulation | Lymphocytes | CD25 antigen | Tumor necrosis factor-TNF | Immune system | Antiviral agents | Antigens | Dendritic cells | Priming | CD80 antigen | T cell receptors | CD4 antigen | Monocytes | Ox40L protein | Tumor necrosis factor | Antigen-presenting cells | Ligands | Interferon | Viral infections | Division of labor
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4. Full Text Splitting the "Unsplittable": Dissecting Resident and Infiltrating Macrophages in Experimental Autoimmune Encephalomyelitis
by Koeniger, T and Kuerten, S
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, ISSN 1422-0067, 10/2017, Volume 18, Issue 10
Macrophages predominate the inflammatory landscape within multiple sclerosis (MS) lesions, not only regarding cellularity but also with respect to the diverse... 
monocytes | INFLAMMATORY MONOCYTES | MICROGLIAL ACTIVATION | distinction | BIOCHEMISTRY & MOLECULAR BIOLOGY | EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS | CNS | CHEMISTRY, MULTIDISCIPLINARY | SCAVENGER RECEPTOR CD163 | macrophages | experimental autoimmune encephalomyelitis | FRACTALKINE RECEPTOR | inflammation | HEMATOPOIETIC STEM-CELLS | MONOCYTE-DERIVED MACROPHAGES | PERIVASCULAR MACROPHAGES | PARENCHYMAL MICROGLIA | markers | FATE MAPPING REVEALS | microglia | Inflammation - pathology | Animals | Encephalomyelitis, Autoimmune, Experimental - pathology | Leukocyte Common Antigens - analysis | Macrophages - pathology | Humans | Microglia - pathology | Receptors, CCR2 - analysis | Antigens, Ly - analysis | CX3C Chemokine Receptor 1 - analysis
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5. Full Text Generation of a triple-fluorescent mouse strain allows a dynamic and spatial visualization of different liver phagocytes in vivo
by Nakagaki, Brenda N and Freitas-Lopes, Maria A and Carvalho, Érika and Carvalho-Gontijo, Raquel and Castro-Oliveira, Hortência M and Rezende, Rafael M and Cara, Denise C and Santos, Mônica M and Lopes, Rodrigo Pestana and David, Bruna A and Menezes, Gustavo B
Anais da Academia Brasileira de Ciencias, ISSN 0001-3765, 2019, Volume 91, Issue suppl 1, p. e20170317
Resident and circulating immune cells have been extensively studied due to their almost ubiquitous role in cell biology. Despite their classification under... 
FRACTALKINE | intravital microscopy | phagocytes | MACROPHAGES | MULTIDISCIPLINARY SCIENCES | hepatology | MONOCYTES | RECEPTOR | fluorescent markers | gastroenterology | CX3CL1 | MICROGLIA | liver immunology | immunology | BRAIN | Liver - metabolism | Mice, Inbred C57BL | Fluorescence | Mice, Transgenic | CD11c Antigen - analysis | Phagocytes - metabolism | Receptors, CCR2 - analysis | CX3C Chemokine Receptor 1 - analysis | Microscopy, Confocal | Animals | Flow Cytometry | Liver - cytology | Mice | Phagocytes - cytology
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6. Influence of aspirin on the CX3CL1/CX3CR1 signaling pathway in acute pulmonary embolism
by Zhang, Zhirong and Yang, Weiji and Ying, Rongbiao and Shi, Ying and Jiang, Huifang and Cai, Danli and Kuang, Jing and Yang, Ruhui and Wang, Lingcong
International journal of molecular medicine, 06/2017, Volume 39, Issue 6, p. 1580
The present study aimed to explore the influence of aspirin on the CX3CL1/CX3CR1 signaling pathway in acute pulmonary embolism (APE) in rats. Our previous... 
CX3C Chemokine Receptor 1 - immunology | Acute Disease | Chemokine CX3CL1 - analysis | NF-kappa B - immunology | Male | Rats, Sprague-Dawley | CX3C Chemokine Receptor 1 - analysis | Pulmonary Embolism - pathology | Animals | Pulmonary Embolism - immunology | Signal Transduction - drug effects | Anti-Inflammatory Agents, Non-Steroidal - therapeutic use | Chemokine CX3CL1 - immunology | Pulmonary Embolism - drug therapy | Aspirin - therapeutic use | NF-kappa B - analysis
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7. Full Text T cells in IgA nephropathy: role in pathogenesis, clinical significance and potential therapeutic target
by Ruszkowski, Jakub and Lisowska, Katarzyna A and Pindel, Małgorzata and Heleniak, Zbigniew and Dębska-Ślizień, Alicja and Witkowski, Jacek M
Clinical and Experimental Nephrology, ISSN 1342-1751, 2018, Volume 23, Issue 3, pp. 291 - 303
BackgroundImmunoglobulin A nephropathy (IgAN), the most frequent cause of primary glomerulonephritis worldwide, is an autoimmune disease with complex... 
Glomerulonephritis | T lymphocytes | IgA nephropathy | DOSE CYCLOPHOSPHAMIDE | GAMMA | GENE G-1082A POLYMORPHISM | O-GLYCOSYLATION | ANTITHYMOCYTE GLOBULIN | PERIPHERAL-BLOOD | IMMUNOGLOBULIN-A NEPHROPATHY | TRANSPLANT RECIPIENTS | INDUCTION THERAPY | UROLOGY & NEPHROLOGY | TH17 CELLS | T-Lymphocytes - physiology | Humans | Immunoglobulin A - immunology | Immunosuppressive Agents - therapeutic use | Glomerulonephritis, IGA - immunology | Glomerulonephritis, IGA - etiology | T-Lymphocyte Subsets - physiology | Adrenal Cortex Hormones - therapeutic use | Autoantibodies - biosynthesis | Glomerulonephritis, IGA - drug therapy | CX3C Chemokine Receptor 1 - analysis | Autoimmunity | Epigenetic inheritance | Medical colleges | Kidney diseases | T cells | Immunoglobulin A | Health aspects | Drugs | Subpopulations | Phenotypes | Autoantibodies | Hematuria | Pathogenesis | Therapeutic applications | Helper cells | Clinical trials | Lymphocytes T | Drug delivery | Drug development | Immunosuppressive agents | Interleukins | Lymphocytes | Galactose | Proteinuria | Review
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8. Full Text Proinflammatory Role of Monocyte-Derived CX3CR1 int Macrophages in Helicobacter hepaticus-Induced Colitis
by Bain, Calum C and Oliphant, Christopher J and Thomson, Carolyn A and Kullberg, Marika C and Mowat, Allan M
Infection and immunity, 02/2018, Volume 86, Issue 2
Cells of the monocyte/macrophage lineage play important roles in the pathogenesis of inflammatory bowel diseases, but they are also present in the normal... 
Macrophages - chemistry | Cytokines - metabolism | Colon - pathology | Mice, Inbred C57BL | Colitis - pathology | Helicobacter Infections - pathology | CX3C Chemokine Receptor 1 - analysis | Animals | Helicobacter hepaticus - pathogenicity | Female | Granulocytes - immunology | Macrophages - immunology | Disease Models, Animal
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9. Full Text Upregulation of CC chemokine ligand 18 and downregulation of CX3C chemokine receptor 1 expression in human T-cell leukemia virus type 1-associated lymph node lesions: Results of chemokine and chemokine receptor DNA chip analysis
by Shimizu, Kei and Karube, Kennosuke and Arakawa, Fumiko and Nomura, Yuko and Komatani, Hideki and Yamamoto, Kouhei and Yoshida, Shiro and Aoki, Ryosuke and Sugita, Yasuo and Takeshita, Morishige and Ohshima, Koichi
Cancer Science, ISSN 1347-9032, 12/2007, Volume 98, Issue 12, pp. 1875 - 1880
Adult T-cell leukemia/lymphoma (ATLL) is a human malignancy associated with human T-cell leukemia virus type 1 (HTLV-1). The pathological features of the lymph... 
ONCOLOGY | PROGNOSIS | VIRUS TYPE-I | T-CELL LEUKEMIA | GENE-EXPRESSION | HISTOLOGIC FEATURES | LEUKEMIA/LYMPHOMA | CARCINOMA | ATLL | LYMPHOCYTES | Immunohistochemistry | Up-Regulation | Lymph Nodes - pathology | Oligonucleotide Array Sequence Analysis | Leukemia-Lymphoma, Adult T-Cell - genetics | Down-Regulation | Humans | RNA, Messenger - genetics | Gene Expression Regulation, Neoplastic | Leukemia-Lymphoma, Adult T-Cell - physiopathology | Lymph Nodes - virology | Leukemia-Lymphoma, Adult T-Cell - pathology | Reverse Transcriptase Polymerase Chain Reaction | HTLV-I Infections - pathology | Chemokines, CC - genetics | RNA, Neoplasm - genetics | HTLV-I Infections - physiopathology | Human T-lymphotropic virus 1 - pathogenicity | Receptors, Chemokine - genetics | CX3C Chemokine Receptor 1 | DNA microarrays | Cytokines | Analysis | DNA | Physiological aspects | Genetic aspects | T cells | Gene expression | Cancer
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10. Full Text Chemokine–Chemokine Receptor CCL2–CCR2 and CX3CL1–CX3CR1 Axis May Play a Role in the Aggravated Inflammation in Primary Biliary Cirrhosis
by Sasaki, Motoko and Miyakoshi, Masami and Sato, Yasunori and Nakanuma, Yasuni
Digestive Diseases and Sciences, ISSN 0163-2116, 2/2014, Volume 59, Issue 2, pp. 358 - 364
Senescent cells can alter local tissue environments by secretion of various senescence-associated secretory phenotypes (SASP), such as cytokines and... 
Biochemistry, general | Chemokine | CX3CR1 | Primary biliary cirrhosis | Medicine & Public Health | Hepatology | Gastroenterology | Cellular senescence | Oncology | Senescence-associated secretory phenotype | Transplant Surgery | CCR2 | SMALL BILE-DUCTS | FRACTALKINE | RECRUITMENT | P21(WAF1/CIP1) | LIVER-DISEASE | REPLICATIVE SENESCENCE | EPITHELIAL-CELLS | CHOLANGITIS | GASTROENTEROLOGY & HEPATOLOGY | EXPRESSION | Immunohistochemistry | Chemokine CX3CL1 - analysis | Humans | Receptors, Chemokine - analysis | Hepatitis - pathology | Epithelial Cells - pathology | Liver Cirrhosis, Biliary - pathology | Receptors, CCR2 - analysis | Case-Control Studies | Liver Cirrhosis, Biliary - immunology | Inflammation Mediators - analysis | Cellular Senescence | Epithelial Cells - immunology | Hepatitis - immunology | CX3C Chemokine Receptor 1 | Bile Ducts - immunology | Bile Ducts - pathology | Chemokine CCL2 - analysis | Virus diseases | Hepatitis | Biliary cirrhosis | Inflammation | Dendritic cells | T cells
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11. Full Text Interactions of Chemokines and Chemokine Receptors Mediate the Migration of Mesenchymal Stem Cells to the Impaired Site in the Brain After Hypoglossal Nerve Injury
by Ji, Jun Feng and He, Bei Ping and Dheen, S. Thameem and Tay, Samuel Sam Wah
STEM CELLS, ISSN 1066-5099, 05/2004, Volume 22, Issue 3, pp. 415 - 427
Mesenchymal stem cells (MSCs), cultured ex vivo, recently were shown to be able to migrate into sites of brain injuries when transplanted systemically or... 
Transplantation | Hypoglossal nerve | Lateral ventricle | Chemokines | Chemokine receptors | Mesenchymal stem cells | lateral ventricle | chemokine receptors | G-PROTEINS | FACTOR-I | chemokines | CELL & TISSUE ENGINEERING | CELL BIOLOGY | MESSENGER-RNAS | ONCOLOGY | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | mesenchymal stem cells | THERAPEUTIC BENEFIT | transplantation | ADULT BONE-MARROW | hypoglossal nerve | GROWTH-FACTOR PRODUCTION | RAT-BRAIN | HEMATOLOGY | NONHEMATOPOIETIC TISSUES | CEREBRAL-ISCHEMIA | MARROW STROMAL CELLS | Chemokine CXCL12 | Rats, Wistar | Receptors, Chemokine - metabolism | Cells, Cultured | Mesenchymal Stromal Cells - metabolism | Rats | Membrane Proteins - pharmacology | Hypoglossal Nerve - metabolism | Cell Movement - physiology | Hypoglossal Nerve Injuries | Receptors, CXCR4 - metabolism | Cell Movement - drug effects | Chemokine CX3CL1 | Chemokines, CX3C - pharmacology | Mesenchymal Stromal Cells - cytology | Animals | Hypoglossal Nerve - cytology | Brain - pathology | Chemokines, CXC - pharmacology | GTP-Binding Proteins - metabolism
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12. Full Text CX3CL1/CX3CR1 and CCL2/CCR2 chemokine/chemokine receptor complex in patients with AMD
by Falk, Mads Krüger and Singh, Amardeep and Faber, Carsten and Nissen, Mogens Holst and Hviid, Thomas and Sørensen, Torben Lykke
PLoS ONE, ISSN 1932-6203, 12/2014, Volume 9, Issue 12, p. e112473
Purpose: The chemokine receptors CX3CR1 and CCR2 have been implicated in the development of age-related macular degeneration (AMD). The evidence is mainly... 
PATHOGENESIS | RETINAL MICROGLIA | MULTIDISCIPLINARY SCIENCES | MONOCYTES | MACULAR DEGENERATION | ANIMAL-MODEL | CHEMOKINE | ACCUMULATION | EXPRESSION | T-CELLS | SUBRETINAL MICROGLIA | CD8-Positive T-Lymphocytes - pathology | Chemokine CX3CL1 - analysis | Humans | Receptors, Chemokine - analysis | Male | Chemokine CCL2 - blood | Macular Degeneration - blood | Receptors, CCR2 - analysis | Macular Degeneration - diagnosis | Chemokine CX3CL1 - blood | Aged, 80 and over | Female | Aged | CX3C Chemokine Receptor 1 | Chemokine CCL2 - analysis | Macular Degeneration - pathology | Diabetic retinopathy | Cell culture | CC chemokine receptors | Flow cytometry | Health sciences | Animal models | Pathogenesis | CD8 antigen | CX3CR1 protein | Alcohol | Lymphocytes T | Macular degeneration | Receptors | Immunology | CCR2 protein | Lymphocytes | Age | Medical imaging | Phlebotomy | Imaging techniques | Inflammation | Patients | Chemokine receptors | White blood cells | Studies | Cytometry | Hospitals | Photoreceptors | Plasma levels | Chemokines | Monocyte chemoattractant protein 1
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13. Full Text Control of microglial neurotoxicity by the fractalkine receptor
by Pioro, Erik P and Littman, Dan R and Ransohoff, Richard M and Huang, DeRen and Kostenko, Volodymyr and Cardona, Sandra M and Sasse, Margaret E and Dutta, RanJan and Cardona, Astrid E and Cook, Donald N and Dijkstra, Ineke M and Jung, Steffen and Kidd, Grahame and Dombrowski, Stephen and Lee, Jar-Chi and Lira, Sergio A
Nature Neuroscience, ISSN 1097-6256, 07/2006, Volume 9, Issue 7, pp. 917 - 924
Microglia, the resident inflammatory cells of the CNS, are the only CNS cells that express the fractalkine receptor ( CX3CR1). Using three different in vivo... 
IN-VIVO | NEURONS | CENTRAL-NERVOUS-SYSTEM | MICE | MECHANISMS | AMYOTROPHIC-LATERAL-SCLEROSIS | TARGETED DELETION | EXPRESSION | NEUROSCIENCES | BRAIN | CHEMOKINE FRACTALKINE | Neurotoxicity Syndromes - genetics | Lipopolysaccharides - administration & dosage | Motor Neuron Disease - metabolism | Flow Cytometry | Microglia - physiology | Motor Neuron Disease - genetics | Neurotoxicity Syndromes - pathology | Parkinson Disease - metabolism | Cell Death - drug effects | Neurons - drug effects | Disease Models, Animal | Calcium-Binding Proteins - metabolism | Green Fluorescent Proteins - metabolism | Parkinson Disease - pathology | Cytokines - metabolism | Microglia - drug effects | Mice, Inbred C57BL | Cells, Cultured | Mice, Transgenic | Parkinson Disease - genetics | Motor Neuron Disease - pathology | Receptors, Chemokine - deficiency | Immunohistochemistry - methods | Nerve Tissue Proteins - metabolism | Neurotoxicity Syndromes - etiology | Animals | Receptors, Chemokine - physiology | Analysis of Variance | Central Nervous System - cytology | Microfilament Proteins | Neurotoxicity Syndromes - metabolism | Mice | CX3C Chemokine Receptor 1 | Physiological aspects | Cellular signal transduction | Parkinson's disease | Research | Risk factors | Neurotoxic agents
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14. Full Text Synaptic Pruning by Microglia Is Necessary for Normal Brain Development
by Rosa C. Paolicelli and Giulia Bolasco and Francesca Pagani and Laura Maggi and Maria Scianni and Patrizia Panzanelli and Maurizio Giustetto and Tiago Alves Ferreira and Eva Guiducci and Laura Dumas and Davide Ragozzino and Cornelius T. Gross
Science, ISSN 0036-8075, 9/2011, Volume 333, Issue 6048, pp. 1456 - 1458
Microglia are highly motile phagocytic cells that infiltrate and take up residence in the developing brain, where they are thought to provide a surveillance... 
Brain | Knockout mice | Neurons | REPORTS | Materials | Pruning | Delay lines | Immatures | Behavioral neuroscience | Synapses | Microglia | PARENCHYMA | CELLS | FRACTALKINE RECEPTOR | MULTIDISCIPLINARY SCIENCES | IN-VIVO | ELIMINATION | RAT HIPPOCAMPUS | DEATH | TARGETED DELETION | FATE | REVEALS | Disks Large Homolog 4 Protein | Synaptosomal-Associated Protein 25 - analysis | Chemokine CX3CL1 - metabolism | Brain - growth & development | Brain - physiology | Membrane Proteins - analysis | Microglia - physiology | Excitatory Postsynaptic Potentials | Pyramidal Cells - physiology | Guanylate Kinases - analysis | Receptors, Cytokine - metabolism | Receptors, Chemokine - genetics | Hippocampus - growth & development | Receptors, Cytokine - genetics | Signal Transduction | Synapses - physiology | Receptors, Chemokine - metabolism | Dendritic Spines - physiology | Receptors, HIV - genetics | Long-Term Synaptic Depression | Mice, Knockout | Patch-Clamp Techniques | Animals | Receptors, HIV - metabolism | Miniature Postsynaptic Potentials | Neuronal Plasticity | Mice | Hippocampus - physiology | CX3C Chemokine Receptor 1 | Dendritic Spines - ultrastructure | Neural transmission | Genetic aspects | Growth | Cellular biology | Developmental biology | Rodents | Neurological disorders
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