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1. Full Text CD19 is essential for B cell activation by promoting B cell receptor-antigen microcluster formation in response to membrane-bound ligand
by Depoil, David and Fleire, Sebastian and Treanor, Bebhinn L and Weber, Michele and Harwood, Naomi E and Marchbank, Kevin L and Tybulewicz, Victor L.J and Batista, Facundo D
Nature Immunology, ISSN 1529-2908, 01/2008, Volume 9, Issue 1, pp. 63 - 72
Here we describe the spatiotemporal architecture, at high molecular resolution, of receptors and signaling molecules during the early events of mouse B cell... 
SIGNAL-TRANSDUCTION | IMMUNE-RESPONSE | COMPLEX | TYROSINE PHOSPHORYLATION | DENDRITIC CELLS | LYMPH-NODE | LYMPHOCYTES-B | SYNAPSE FORMATION | MICE | IMMUNOLOGY | T-CELLS | Signal Transduction | Lymphocyte Activation | Receptors, Antigen, B-Cell - metabolism | Antigens, CD19 - physiology | Protein-Tyrosine Kinases - physiology | Animals | B-Lymphocytes - immunology | Lipid Bilayers | Receptors, Complement 3d - physiology | Antigens, CD19 - metabolism | Cell Membrane - metabolism | Mice | In Vitro Techniques | Intracellular Signaling Peptides and Proteins - physiology | Syk Kinase | B-Lymphocytes - metabolism | Microscopy, Fluorescence | Physiological aspects | Cell receptors | Immune response | B cells | Research | Properties
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2. Full Text CD81 gene defect in humans disrupts CD19 complex formation and leads to antibody deficiency
by Zelm, Menno and Smet, Julie and Adams, Brigitte and Mascart, Françoise and Schandené, Liliane and Janssen, Francoise and Ferster, Alina and Kuo, Chiung-Chi and Levy, Shoshana and Dongen, Jacques and Burg, Mirjam
Journal of Clinical Investigation, ISSN 0021-9738, 04/2010, Volume 120, Issue 4, pp. 1265 - 1274
textabstractAntibody deficiencies constitute the largest group of symptomatic primary immunodeficiency diseases. In several patients, mutations in CD19 have... 
MEDICINE, RESEARCH & EXPERIMENTAL | B-LYMPHOCYTES | SIGNAL-TRANSDUCTION COMPLEX | BASE-PAIR SUBSTITUTIONS | COMMON VARIABLE IMMUNODEFICIENCY | IGA NEPHROPATHY | CELL-SURFACE | MUTATIONS | RESIDUAL-DISEASE | INTERNATIONAL-UNION | ANTIGEN | T-Lymphocyte Subsets - immunology | Somatic Hypermutation, Immunoglobulin | Immunologic Deficiency Syndromes - etiology | Antigens, CD19 - analysis | Humans | RNA, Messenger - analysis | Tetraspanin 28 | Antigens, CD19 - physiology | Antigens, CD - genetics | B-Lymphocyte Subsets - immunology | Female | Receptors, Antigen, B-Cell - physiology | Mutation | Child | Interferon-gamma - biosynthesis | Viral antibodies | Care and treatment | Genetic disorders | Antibodies | Development and progression | Genetic aspects | Kidney diseases | T cells
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3. Full Text Impaired function of CD19(+)CD24(hi)CD38(hi) regulatory B cells in patients with pemphigus
by Zhu, HQ and Xu, RC and Chen, YY and Yuan, HJ and Cao, H and Zhao, XQ and Zheng, J and Wang, Y and Pan, M
BRITISH JOURNAL OF DERMATOLOGY, ISSN 0007-0963, 01/2015, Volume 172, Issue 1, pp. 101 - 110
BackgroundPemphigus is an organ-specific autoimmune bullous disease. ObjectivesTo determine the role of regulatory B cells (Bregs) in patients with pemphigus.... 
RESPONSES | AUTOIMMUNITY | B10 CELLS | HUMANS | MICE | T-CELLS | DERMATOLOGY | B-Lymphocytes, Regulatory - metabolism | Antibodies - metabolism | Humans | Middle Aged | ADP-ribosyl Cyclase 1 - physiology | CD4-Positive T-Lymphocytes - metabolism | Cells, Cultured | Male | Antigens, CD19 - physiology | B-Lymphocytes, Regulatory - immunology | Case-Control Studies | Immunoglobulin M - metabolism | CD24 Antigen - physiology | Desmogleins - immunology | Immunity, Cellular - physiology | Aged, 80 and over | Adult | Female | Interleukin-10 - biosynthesis | Pemphigus - immunology | Aged | Immunoglobulin G - metabolism
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4. Full Text Wiskott-Aldrich Syndrome Interacting Protein Deficiency Uncovers the Role of the Co-receptor CD19 as a Generic Hub for PI3 Kinase Signaling in B Cells
by Keppler, Selina Jessica and Gasparrini, Francesca and Burbage, Marianne and Aggarwal, Shweta and Frederico, Bruno and Geha, Raif S and Way, Michael and Bruckbauer, Andreas and Batista, Facundo D
Immunity, ISSN 1074-7613, 10/2015, Volume 43, Issue 4, pp. 660 - 673
Humans with Wiskott-Aldrich syndrome display a progressive immunological disorder associated with compromised Wiskott-Aldrich Syndrome Interacting Protein... 
ACTIVATION | CYTOSKELETON | ACTIN POLYMERIZATION | TRANSDUCTION | N-WASP | MICE | T-CELL | DIFFERENTIATION | IMMUNOLOGY | ANTIGEN RECEPTOR | WIP | Wiskott-Aldrich syndrome | B cells | T cells | Muscle proteins | Proteins | Antigens | Laboratories | Cytoskeleton | Tumor necrosis factor-TNF | Software | Kinases | Binding sites | Defects
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5. Full Text Immune reconstitution after haploidentical hematopoietic cell transplantation: impact of reduced intensity conditioning and CD3 CD19 depleted grafts
by Federmann, B and Hägele, M and Pfeiffer, M and Wirths, S and Schumm, M and Faul, C and Vogel, W and Handgretinger, R and Kanz, L and Bethge, W.A
Leukemia, ISSN 0887-6924, 01/2011, Volume 25, Issue 1, pp. 121 - 129
Haploidentical hematopoietic cell transplantation (HHCT) using CD34 selected grafts is complicated by slow engraftment and immune reconstitution. Engraftment... 
immune reconstitution | haploidentical hematopoietic cell transplantation | reduced intensity conditioning | CD3/CD19 depletion | PROGENITOR CELLS | REPERTOIRE | STEM-CELLS | BONE-MARROW-TRANSPLANTATION | DONORS | T-CELL | ACUTE-LEUKEMIA | RECOVERY | NK CELLS | ONCOLOGY | HIGH-RISK | HEMATOLOGY | Haplotypes | Hematologic Neoplasms - therapy | Prospective Studies | Receptors, Antigen, T-Cell, alpha-beta - physiology | Humans | Middle Aged | Hematopoietic Stem Cell Transplantation | Male | Antigens, CD19 - physiology | CD3 Complex - physiology | Adult | Female | Receptors, Natural Killer Cell - physiology | T-Lymphocytes - immunology | Aged | Hematologic Neoplasms - immunology | Lymphocyte Transfusion | Transplantation Conditioning | Immune response | Patient outcomes | Leukemia | Transplantation | T cells | Health aspects | Hematopoietic stem cells
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6. Full Text CD38/CD19: A lipid raft-dependent signaling complex in human B cells
by Deaglio, Silvia and Vaisitti, Tiziana and Billington, Richard and Bergui, Luciana and Omede', Paola and Genazzani, Armando A and Malavasi, Fabio
Blood, ISSN 0006-4971, 06/2007, Volume 109, Issue 12, pp. 5390 - 5398
The present work deals with the mechanisms of signal transduction mediated via CD38 in normal and neoplastic human B lymphocytes. The results indicate that... 
MEMBRANE RAFTS | ACTIVATION | ADP-RIBOSYL CYCLASE | HUMAN CD38 | PROTEIN-KINASE | IFN-GAMMA | CHRONIC LYMPHOCYTIC-LEUKEMIA | HEMATOLOGY | ANTIGEN RECEPTOR | HUMAN MONOCYTES | T-CELLS | Cell Line | Signal Transduction | Humans | ADP-ribosyl Cyclase 1 - physiology | Cell Line, Tumor | Protein Binding | Receptors, Cell Surface | Membrane Microdomains - physiology | Antigens, CD19 - physiology | Dimerization | B-Lymphocytes - chemistry | Calcium Signaling
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7. Full Text A c-Myc and surface CD19 signaling amplification loop promotes B cell lymphoma development and progression in mice
by Poe, Jonathan C and Minard-Colin, Veronique and Kountikov, Evgueni I and Haas, Karen M and Tedder, Thomas F
Journal of Immunology, ISSN 0022-1767, 09/2012, Volume 189, Issue 5, pp. 2318 - 2325
Malignant B cells responding to external stimuli are likely to gain a growth advantage in vivo. These cells may therefore maintain surface CD19 expression to... 
CYTOPLASMIC DOMAIN | COMPLEX | PROTEIN STABILITY | TYROSINE KINASE ACTIVATION | HUMAN LYMPHOCYTES-B | CYCLIN D2 | TRANSDUCTION MOLECULE | IMMUNOLOGY | ANTIGEN RECEPTOR | EXPRESSION | TRANSGENIC MICE | Humans | Antigens, CD19 - genetics | Antigens, CD19 - physiology | Lymphoma, B-Cell - genetics | Nucleic Acid Amplification Techniques | Signal Transduction - immunology | Lymphocyte Activation - genetics | Lymphocyte Activation - immunology | Proto-Oncogene Proteins c-myc - biosynthesis | Proto-Oncogene Proteins c-myc - physiology | Lymphoma, B-Cell - immunology | B-Lymphocyte Subsets - immunology | B-Lymphocyte Subsets - pathology | Mice, Inbred C57BL | Mice, Transgenic | Signal Transduction - genetics | Disease Progression | Mice, Knockout | Animals | B-Lymphocyte Subsets - metabolism | Lymphoma, B-Cell - pathology | Survival Analysis | Antigens, CD19 - metabolism | Mice | Proto-Oncogene Proteins c-myc - genetics
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8. Full Text The Tetraspanin CD81 Is Necessary for Partitioning of Coligated CD19/CD21-B Cell Antigen Receptor Complexes into Signaling-Active Lipid Rafts
by Cherukuri, Anu and Shoham, Tsipi and Sohn, Hae Won and Levy, Shoshana and Brooks, Stephen and Carter, Robert and Pierce, Susan K
The Journal of Immunology, ISSN 0022-1767, 01/2004, Volume 172, Issue 1, pp. 370 - 380
Tetraspanins have been hypothesized to facilitate the organization of functional multimolecular membrane complexes. In B cells the tetraspanin CD81 is a... 
B-CELLS | COMPLEMENT | CD81-DEFICIENT MICE | ACQUIRED-IMMUNITY | HUMORAL IMMUNE-RESPONSE | ANTIPROLIFERATIVE ANTIBODY | CROSS-LINKING | EXTRACELLULAR DOMAIN | TRANSDUCTION | IMMUNOLOGY | LYMPHOCYTES | Membrane Microdomains - metabolism | Recombinant Fusion Proteins - physiology | Male | Receptors, Antigen, B-Cell - metabolism | Antigens, CD19 - physiology | Antigens, CD - genetics | Recombinant Fusion Proteins - metabolism | Membrane Microdomains - immunology | Membrane Proteins - deficiency | Signal Transduction - immunology | Membrane Proteins - physiology | Mice, Inbred CBA | B-Lymphocyte Subsets - immunology | Female | Receptors, Antigen, B-Cell - physiology | Tetraspanins | Adjuvants, Immunologic - physiology | Nerve Tissue Proteins - physiology | Membrane Proteins - genetics | Mice, Transgenic | Signal Transduction - genetics | Tetraspanin 28 | Down-Regulation - genetics | Animals | B-Lymphocyte Subsets - metabolism | Down-Regulation - immunology | Antigens, CD - physiology | Ligands | Receptors, Complement 3d - physiology | Antigens, CD19 - metabolism | Mice | Mice, Inbred BALB C | Receptors, Complement 3d - metabolism | Cell Line, Transformed | Membrane Microdomains - genetics
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9. Full Text Wiskott-Aldrich Syndrome Interacting Protein Deficiency Uncovers the Role of the Co-receptor CD19 as a Generic Hub for PI3 Kinase Signaling in B Cells
by Keppler, Selina Jessica and Gasparrini, Francesca and Burbage, Marianne and Aggarwal, Shweta and Frederico, Bruno and Geha, Raif S and Way, Michael and Bruckbauer, Andreas and Batista, Facundo D
Immunity, 10/2015, Volume 43, Issue 4, p. 660
Humans with Wiskott-Aldrich syndrome display a progressive immunological disorder associated with compromised Wiskott-Aldrich Syndrome Interacting Protein... 
Lymphopoiesis | Phosphorylation | Germinal Center - immunology | Vaccinia - pathology | Haptens | Antigens, CD19 - physiology | Signal Transduction - immunology | Actins - analysis | Hemocyanins - pharmacology | Chemokines - pharmacology | B-Lymphocytes - ultrastructure | Carrier Proteins - physiology | B-Lymphocytes - enzymology | Cells, Cultured | Chemokines - physiology | Membrane Proteins - immunology | Radiation Chimera | Chemotaxis - drug effects | Germinal Center - pathology | Receptors, Antigen, B-Cell - immunology | B-Lymphocytes - drug effects | Carrier Proteins - genetics | Animals | B-Lymphocytes - immunology | Receptors, Chemokine - physiology | Tetraspanins - analysis | Lymphocyte Activation - drug effects | Antibody Formation | Phosphatidylinositol 3-Kinases - physiology | Vaccinia - immunology | Mice | Protein Processing, Post-Translational | Actin Cytoskeleton - ultrastructure | Plasma Cells - immunology
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10. Full Text Loss of Trex1 in dendritic cells is sufficient to trigger systemic autoimmunity
by Peschke, Katrin and Achleitner, Martin and Frenzel, Kathrin and Gerbaulet, Alexander and Remzi Ada, Servi and Zeller, Nicolas and Lienenklaus, Stefan and Lesche, Mathias and Poulet, Claire and Naumann, Ronald and Dahl, Andreas and Ravens, Ursula and Günther, Claudia and Müller, Werner and Knobeloch, Klaus-Peter and Prinz, Marco and Roers, Axel and Behrendt, Rayk
Journal of Immunology, ISSN 0022-1767, 09/2016, Volume 197, Issue 6, pp. 2157 - 2166
Defects of the intracellular enzyme 39 repair exonuclease 1 (Trex1) cause the rare autoimmune condition Aicardi-Goutie` res syndrome and are associated with... 
RECOMBINATION | AICARDI-GOUTIERES-SYNDROME | ACTIVATION | GENE | DNA EXONUCLEASE TREX1 | DISEASE | CGAS | IMMUNOLOGY | EXPRESSION | GMP-AMP SYNTHASE | I INTERFERON | Autoimmunity | Mice, Inbred C57BL | B-Lymphocytes - physiology | Dendritic Cells - physiology | Antigens, CD19 - physiology | Exodeoxyribonucleases - deficiency | Mice, Knockout | Interferon Type I - biosynthesis | Animals | Phosphoproteins - deficiency | Exodeoxyribonucleases - physiology | Mice | Phosphoproteins - physiology | Brain - immunology | Index Medicus | Abridged Index Medicus
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11. Full Text CD19 Expression Levels Regulate B Lymphocyte Development: Human CD19 Restores Normal Function in Mice Lacking Endogenous CD19
by Sato, Shinichi and Steeber, Douglas A and Jansen, Paul J and Tedder, Thomas F
Journal of Immunology, ISSN 0022-1767, 05/1997, Volume 158, Issue 10, pp. 4662 - 4669
Establishing signal transduction thresholds that regulate B lymphocyte responses to foreign Ags and tolerance to self Ags is critical for humoral immune... 
SIGNAL-TRANSDUCTION MOLECULE | ACTIVATION | COMPLEX | VIABLE MOTHEATEN | BONE-MARROW | MOUSE | DIFFERENTIATION | IMMUNOLOGY | T-CELL DEVELOPMENT | TRANSGENIC MICE | ANTIGEN | Signal Transduction | Lymphocyte Activation | Humans | Antigens, CD19 - physiology | Genetic Complementation Test | Mice, Knockout | Immunoglobulin M - metabolism | Animals | B-Lymphocytes - immunology | Calcium - physiology | Antibody Formation | Mice | Germinal Center - cytology
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12. Full Text Positive Selection from Newly Formed to Marginal Zone B Cells Depends on the Rate of Clonal Production, CD19, and btk
by Martin, Flavius and Kearney, John F
Immunity, ISSN 1074-7613, 01/2000, Volume 12, Issue 1, pp. 39 - 49
Using immunoglobulin heavy chain transgenic mice, we show that B cell clones reaching the long-lived pool are heterogeneous: some are enriched in the... 
B-1 CELLS | RESPONSES | ACTIVATION | MOUSE | LYMPHOCYTES-B | GENE-EXPRESSION | IMMUNOGLOBULIN | IMMUNOLOGY | TRANSGENIC MICE | SELF-TOLERANCE | DELETION | Protein-Tyrosine Kinases - metabolism | Antigens, CD19 - genetics | Receptors, Antigen, B-Cell - metabolism | Antigens, CD19 - physiology | Protein-Tyrosine Kinases - physiology | Hematopoietic Stem Cells - immunology | Bone Marrow Cells - immunology | Mice, Inbred CBA | Cell Differentiation | Clone Cells | B-Lymphocytes - cytology | Bone Marrow Cells - cytology | Mice, Inbred C57BL | Cells, Cultured | Immunophenotyping | Mice, Transgenic | Spleen - cytology | Animals | B-Lymphocytes - immunology | Immunoglobulin Idiotypes | Receptors, IgE - metabolism | Hematopoietic Stem Cells - cytology | Antigens, CD19 - metabolism | Mice | Mice, Inbred BALB C | Receptors, Complement 3d - metabolism
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13. Full Text The Physiologic Role of CD19 Cytoplasmic Tyrosines
by Wang, Yue and Brooks, Stephen R and Li, Xiaoli and Anzelon, Amy N and Rickert, Robert C and Carter, Robert H
Immunity, ISSN 1074-7613, 2002, Volume 17, Issue 4, pp. 501 - 514
The physiologic role of eight CD19 tyrosines was examined in CD19-knockout mice expressing transgenic CD19 constructs. CD19 Y482 and Y513 were essential for... 
IMMUNE-RESPONSE | B1B CELLS | SIGNAL-TRANSDUCTION MOLECULE | ACTIVATION | CELL-DEVELOPMENT | MARGINAL ZONE | PHOSPHATIDYLINOSITOL 3-KINASE | B-LYMPHOCYTE RESPONSES | IMMUNOLOGY | PHOSPHOINOSITIDE 3-KINASE | ANTIGEN | Autoimmunity | B-Lymphocytes - cytology | Immunization | Phosphorylation | Mutagenesis, Site-Directed | Antigens, CD19 - chemistry | Germinal Center - immunology | Humans | Mice, Transgenic | Antigens, CD19 - genetics | Antigens, CD19 - physiology | Mice, Knockout | Animals | B-Lymphocytes - immunology | Cell Cycle | Cytoplasm - immunology | Antibody Formation | Cell Differentiation | Mice | Germinal Center - cytology | Tyrosine - chemistry | Proteins | Flow cytometry | Research & development--R&D | Rodents | Cell cycle | Kinases | Binding sites | Immune system
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14. Full Text Inhibitory Role of CD19 in the Progression of Experimental Autoimmune Encephalomyelitis by Regulating Cytokine Response
by Matsushita, Takashi and Fujimoto, Manabu and Hasegawa, Minoru and Komura, Kazuhiro and Takehara, Kazuhiko and Tedder, Thomas F and Sato, Shinichi
The American Journal of Pathology, ISSN 0002-9440, 2006, Volume 168, Issue 3, pp. 812 - 821
Experimental autoimmune encephalomyelitis (EAE) is an inflammatory demyelinating disease of the central nerve system that is considered a T helper type 1... 
B-CELLS | MYELIN OLIGODENDROCYTE GLYCOPROTEIN | SIGNAL-TRANSDUCTION MOLECULE | MULTIPLE-SCLEROSIS | CELL-DEFICIENT MICE | EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS | INTERFERON-GAMMA GENE | CENTRAL-NERVOUS-SYSTEM | PATHOLOGY | TIGHT-SKIN MOUSE | CD8(+) T-CELLS | Antibodies - metabolism | Encephalomyelitis, Autoimmune, Experimental - immunology | Antigens, CD19 - genetics | Th2 Cells - immunology | Adoptive Transfer | Interferon-gamma - metabolism | Antigens, CD19 - physiology | Th1 Cells - immunology | Immunoglobulins - metabolism | Mice, Mutant Strains | Spinal Cord - pathology | Interleukin-10 - metabolism | Encephalomyelitis, Autoimmune, Experimental - genetics | Encephalomyelitis, Autoimmune, Experimental - pathology | Cytokines - metabolism | Myelin-Oligodendrocyte Glycoprotein | Disease Progression | Spinal Cord - immunology | Myelin-Associated Glycoprotein - immunology | Animals | B-Lymphocytes - immunology | Myelin Proteins | Mice | CD8-Positive T-Lymphocytes - immunology | B-Lymphocytes - transplantation | Original Research Paper
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