| scholarly article | Q13442814 |
| P50 | author | Timothy W Phares | Q117769739 |
| Stephen A Stohlman | Q117769757 | ||
| Cornelia C. Bergmann | Q55426323 | ||
| P2093 | author name string | Krista D DiSano | |
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| CD27 is acquired by primed B cells at the centroblast stage and promotes germinal center formation | Q45035985 | ||
| Diagnostic significance of intrathecally produced herpes simplex and varizella-zoster virus-specific antibodies in central nervous system infections. | Q45531187 | ||
| Herpes simplex encephalitis: A serological follow-up study. Synthesis of herpes simplex virus immunoglobulin M, A, and G antibodies and development of oligoclonal immunoglobulin G in the central nervous system | Q45792142 | ||
| Sequential infection of glial cells by the murine hepatitis virus JHM strain (MHV-4) leads to a characteristic distribution of demyelination | Q45879088 | ||
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| CNS viral infection diverts homing of antibody-secreting cells from lymphoid organs to the CNS. | Q46275246 | ||
| IFN-gamma is required for viral clearance from central nervous system oligodendroglia | Q46323621 | ||
| Detection of ectopic B-cell follicles with germinal centers in the meninges of patients with secondary progressive multiple sclerosis. | Q47357498 | ||
| Intracerebral expression of CXCL13 and BAFF is accompanied by formation of lymphoid follicle-like structures in the meninges of mice with relapsing experimental autoimmune encephalomyelitis. | Q51027456 | ||
| Cutting edge: the dependence of plasma cells and independence of memory B cells on BAFF and APRIL. | Q51966554 | ||
| Accumulation of class switched IgD-IgM- memory B cells in the cerebrospinal fluid during neuroinflammation. | Q51979636 | ||
| A division-linked mechanism for the rapid generation of Ig-secreting cells from human memory B cells. | Q52008746 | ||
| Generation of memory B cells and plasma cells in vitro. | Q52053106 | ||
| Mouse CD38 is down-regulated on germinal center B cells and mature plasma cells. | Q52196617 | ||
| Plasma cell survival is mediated by synergistic effects of cytokines and adhesion-dependent signals. | Q52950179 | ||
| A BAFF/APRIL-dependent TLR3-stimulated pathway enhances the capacity of rheumatoid synovial fibroblasts to induce AID expression and Ig class-switching in B cells. | Q54356847 | ||
| B cell-activating factor belonging to the TNF family acts through separate receptors to support B cell survival and T cell-independent antibody formation. | Q54707196 | ||
| Single-cell repertoire analysis demonstrates that clonal expansion is a prominent feature of the B cell response in multiple sclerosis cerebrospinal fluid. | Q54759503 | ||
| Antigen-specific interaction between T and B cells | Q59063745 | ||
| Immune processing of proteolipid protein by subsets of antigen-presenting spleen cells | Q67535329 | ||
| B lymphocyte activation: entry into cell cycle is accompanied by decreased expression of IgD but not IgM | Q70983795 | ||
| CXCL13 is the major determinant for B cell recruitment to the CSF during neuroinflammation | Q36161486 | ||
| Macrophages induce differentiation of plasma cells through CXCL10/IP-10 | Q36278025 | ||
| B-cell differentiation in the CNS of patients with multiple sclerosis | Q36281252 | ||
| Coronavirus infection of the central nervous system: host-virus stand-off | Q36369843 | ||
| Chemokine requirements for B cell entry to lymph nodes and Peyer's patches. | Q36371105 | ||
| Early appearance of germinal center-derived memory B cells and plasma cells in blood after primary immunization. | Q36403235 | ||
| The B cell response in multiple sclerosis | Q36474316 | ||
| Regulation of AID, the B-cell genome mutator | Q36557058 | ||
| Recruitment and retention of B cells in the central nervous system in response to alphavirus encephalomyelitis | Q36607157 | ||
| Astrocyte-derived CXCL10 drives accumulation of antibody-secreting cells in the central nervous system during viral encephalomyelitis | Q36667911 | ||
| IL-10-producing regulatory B cells (B10 cells) in autoimmune disease | Q36760499 | ||
| Pathogenicity of antigenic variants of murine coronavirus JHM selected with monoclonal antibodies | Q36863593 | ||
| Interleukin-21 is a critical cytokine for the generation of virus-specific long-lived plasma cells. | Q36978831 | ||
| Finding a way out: lymphocyte egress from lymphoid organs | Q37008187 | ||
| Intrathecal humoral responses are inversely associated with the frequency of simian immunodeficiency virus macrophage-tropic variants in the central nervous system | Q37275046 | ||
| Recapitulation of B cell differentiation in the central nervous system of patients with multiple sclerosis. | Q37285430 | ||
| MHC class II-dependent B cell APC function is required for induction of CNS autoimmunity independent of myelin-specific antibodies | Q37397820 | ||
| Role of CD25(+) CD4(+) T cells in acute and persistent coronavirus infection of the central nervous system | Q37532418 | ||
| B cells promote induction of experimental autoimmune encephalomyelitis by facilitating reactivation of T cells in the central nervous system | Q37601825 | ||
| B cells mediate chronic allograft rejection independently of antibody production | Q37602189 | ||
| Finding the right niche: B-cell migration in the early phases of T-dependent antibody responses | Q37761265 | ||
| Control systems and decision making for antibody production. | Q37774242 | ||
| An inverse correlation of HTLV-I viral load in CSF and intrathecal synthesis of HTLV-I antibodies in TSP/HAM. | Q39370476 | ||
| Experimental intracerebral vaccination protects mouse from a neurotropic virus by attracting antibody secreting cells to the CNS. | Q39529876 | ||
| In Semliki Forest virus encephalitis, antibody rapidly clears infectious virus and is required to eliminate viral material from the brain, but is not required to generate lesions of demyelination | Q39939080 | ||
| TACI, unlike BAFF-R, is solely activated by oligomeric BAFF and APRIL to support survival of activated B cells and plasmablasts | Q40066472 | ||
| A proliferation-inducing ligand (APRIL) is expressed by astrocytes and is increased in multiple sclerosis | Q40185060 | ||
| The nervous system as ectopic germinal center: CXCL13 and IgG in lyme neuroborreliosis | Q40414775 | ||
| The relationship between measles virus-specific antibodies and oligoclonal IgG in the cerebrospinal fluid from patients with subacute sclerosing panencephalitis and multiple sclerosis | Q40480580 | ||
| Surface immunoglobulins of lipopolysaccharide-stimulated spleen cells The behaviour of IgM, IgD and IgG | Q40647416 | ||
| IL-1R signaling within the central nervous system regulates CXCL12 expression at the blood-brain barrier and disease severity during experimental autoimmune encephalomyelitis | Q41480082 | ||
| The role of antibody in recovery from alphavirus encephalitis | Q41672969 | ||
| Inverted immunodominance and impaired cytolytic function of CD8+ T cells during viral persistence in the central nervous system. | Q41689082 | ||
| Specific B lymphocytes efficiently pick up, process and present antigen to T cells | Q41916848 | ||
| Detection of virus specific IgG subclasses in Japanese encephalitis patients | Q42985097 | ||
| Virus-specific antibody-producing cells in blood and cerebrospinal fluid in acute Japanese encephalitis | Q42991711 | ||
| TACI is required for efficient plasma cell differentiation in response to T-independent type 2 antigens | Q43596939 | ||
| Regional differences in blood-brain barrier permeability changes and inflammation in the apathogenic clearance of virus from the central nervous system | Q43684853 | ||
| Mechanisms of central nervous system viral persistence: the critical role of antibody and B cells. | Q43985466 | ||
| Analysis of oligoclonal antibody bands against individual HIV structural proteins in the CSF of patients infected with HIV. | Q44076429 | ||
| Specific TLR ligands regulate APRIL secretion by dendritic cells in a PKR-dependent manner | Q44885882 | ||
| Antibody reactivity to individual structural proteins of measles virus in the CSF of SSPE and MS patients | Q44913049 | ||
| P433 | issue | 16 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Coronaviridae | Q1134583 |
| P304 | page(s) | 8853-8867 | |
| P577 | publication date | 2014-05-28 | |
| P1433 | published in | Journal of Virology | Q1251128 |
| P1476 | title | Progression from IgD+ IgM+ to isotype-switched B cells is site specific during coronavirus-induced encephalomyelitis | |
| P478 | volume | 88 |
| Q40530656 | Activated GL7+ B cells are maintained within the inflamed CNS in the absence of follicle formation during viral encephalomyelitis. |
| Q40204989 | An optimized method for enumerating CNS derived memory B cells during viral-induced inflammation. |
| Q36788638 | CXCL13 promotes isotype-switched B cell accumulation to the central nervous system during viral encephalomyelitis |
| Q92712543 | Central Nervous System Inflammatory Aggregates in the Theiler's Virus Model of Progressive Multiple Sclerosis |
| Q37270693 | Differential Regulation of Self-reactive CD4+ T Cells in Cervical Lymph Nodes and Central Nervous System during Viral Encephalomyelitis |
| Q58546206 | Dynamics of Virus-Specific Memory B Cells and Plasmablasts following CNS Viral Infection |
| Q36584434 | Interleukin-10 is a critical regulator of white matter lesion containment following viral induced demyelination |
| Q41933450 | Protective Humoral Immunity in the CNS Requires Peripheral CD19-Dependent Germinal Center Formation Following Coronavirus Encephalomyelitis. |
| Q98879302 | Why do SARS-CoV-2 NSPs rush to the ER? |
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