Somatic evolution of variable region structures during an immune response.
about
The structural basis of repertoire shift in an immune response to phosphocholineCytologic assessment of nuclear and cytoplasmic O-linked N-acetylglucosamine distribution by using anti-streptococcal monoclonal antibodiesImmunoglobulin heavy chain gene expression in peripheral blood B lymphocytes.Identification of mutant monoclonal antibodies with increased antigen bindingMolecular cloning of the primary IgH repertoire: a quantitative analysis of VH gene usage in adult miceStructural correlates of high antibody affinity: three engineered amino acid substitutions can increase the affinity of an anti-p-azophenylarsonate antibody 200-foldProtein evolution on partially correlated landscapes.Silent development of memory progenitor B cellsSomatic hypermutation as a generator of antinuclear antibodies in a murine model of systemic autoimmunity.Analysis of autoantibodies to recombinant La (SS-B) peptides in systemic lupus erythematosus and primary Sjogren's syndrome.Protein evolution on rugged landscapes.Kinetic and affinity limits on antibodies produced during immune responses.Retention of an idiotypic determinant in a human B-cell lymphoma undergoing immunoglobulin variable-region mutationSelf-tolerance checkpoints in CD4 T cells specific for a peptide derived from the B cell antigen receptor.Aborted germinal center reactions and B cell memory by follicular T cells specific for a B cell receptor V region peptide.Different epitope structures select distinct mutant forms of an antibody variable region for expression during the immune response.A model for the evolution of the mammalian t-cell receptor α/δ and μ loci based on evidence from the duckbill Platypus.Clonal analysis of a human antibody response. II. Sequences of the VH genes of human IgM, IgG, and IgA to rabies virus reveal preferential utilization of VHIII segments and somatic hypermutationAnti-DNA antibodies from autoimmune mice arise by clonal expansion and somatic mutation.Spontaneous loss and alteration of antigen receptor expression in mature CD4+ T cells.Parallel evolution of antibody variable regions by somatic processes: consecutive shared somatic alterations in VH genes expressed by independently generated hybridomas apparently acquired by point mutation and selection rather than by gene conversiA single germline VH gene segment of normal A/J mice encodes autoantibodies characteristic of systemic lupus erythematosusIdiotype variant cell populations in patients with B cell lymphoma.Single germline VH and V kappa genes encode predominating antibody variable regions elicited in strain A mice by immunization with p-azophenylarsonate.Influence of the macromolecular form of a B cell epitope on the expression of antibody variable and constant region structure.Boundaries of somatic mutation in rearranged immunoglobulin genes: 5' boundary is near the promoter, and 3' boundary is approximately 1 kb from V(D)J gene.Mutational hot spots in Ig V region genes of human follicular lymphomasT cell receptor gene usage in the response to lambda repressor cI protein. An apparent bias in the usage of a V alpha gene elementMacrophages phagocytose thymic lymphocytes with productively rearranged T cell receptor alpha and beta genes.Relationship of variable region genes expressed by a human B cell lymphoma secreting pathologic anti-Pr2 erythrocyte autoantibodies.Early onset of somatic mutation in immunoglobulin VH genes during the primary immune responseEvolution of antibody structure during the immune response. The differentiative potential of a single B lymphocyte.Molecular analysis of original antigenic sin. I. Clonal selection, somatic mutation, and isotype switching during a memory B cell responseSomatically mutated forms of a major anti-p-azophenylarsonate antibody variable region with drastically reduced affinity for p-azophenylarsonate. By-products of an antigen-driven immune response?Protective and nonprotective monoclonal antibodies to Cryptococcus neoformans originating from one B cellTracing the development of single memory-lineage B cells in a highly defined immune response.Very low affinity B cells form germinal centers, become memory B cells, and participate in secondary immune responses when higher affinity competition is reducedAntigen-driven clonal proliferation of B cells within the target tissue of an autoimmune disease. The salivary glands of patients with Sjögren's syndromeCrystal structure of the antigen-binding fragment of the murine anti-arsonate monoclonal antibody 36-71 at 2.9-A resolution.The biologic significance of human natural autoimmune responses: relationship to the germline, early immune and malignant B cell variable gene repertoire.
P2860
Q27624954-8E5F0FD4-17CE-48FA-B6B0-6E74FEC2B0B1Q28329475-20043F72-0067-4C99-8468-FEC5CAAA31D3Q31131763-CE8425F9-31A7-4EC3-BE7E-2542F29B8707Q33564356-DAF0E628-1F97-4B6A-9DE1-DD75EE4D8569Q33572492-40732130-2557-4D8E-AE57-E2159B78DC05Q33646218-58EB04C0-4ADD-48BB-A70C-76BD4F811B2BQ33860729-4667DBC3-B00C-4A04-A694-FCAA5253E500Q33959225-AE7FB197-0FC3-4527-A1F9-28B40A3027B9Q34161517-70D5D13B-CDC8-4B4A-8A75-4120994D3F6EQ34241668-2E143F6B-DEBE-4DB7-BD2A-C3482078C9ADQ34296709-D70995EC-CB73-4F65-A64D-1A70C5F7A97BQ34598643-0EFB8DF8-D24D-435F-8E0C-A74F8F3D1737Q34641348-0B6DF138-288D-4CD2-AA69-5049FDBF6E22Q35071223-A8552321-E584-4D65-B525-BB3642F66422Q35097270-FE799CA1-22C8-4484-9C2D-7CA17185A1B0Q36229997-4B0E8984-955D-4779-95C5-4755528A75E0Q36278222-21836FE9-C07B-464B-8C82-0F7D6986B02EQ36341119-016AB9D1-D1AB-4E52-BBBF-D22B1E912ACAQ36350233-F85021A4-8910-48C8-9D67-42CF72868DB2Q36351344-90845299-D080-4DA2-83D7-08BB71EE623EQ36352059-99A5FA70-47B6-4C77-B0EE-7611818FC684Q36352279-017FCDF6-075E-4991-911F-66AFEBA6023EQ36353115-6AB8EBD8-2DF4-4824-A0BB-C8882393F41CQ36353768-23EDC060-B2BE-4760-8802-28BBA1073EB1Q36353883-89332A55-ED93-4658-B9FB-9F78EE4C3CCBQ36354162-FC91B99A-62F3-4C31-B6C5-21F5C5F913CFQ36355166-0E1DE005-3F3D-49AF-9A67-051B0E76EE0FQ36355341-4A9CA532-2187-46A5-9799-7352E53AAFA7Q36355765-660F22FF-B382-41E2-A34C-7D3FF1914655Q36356325-AC46E84F-5B39-453A-95A4-35074A9CEB35Q36356525-0923A911-8851-467A-8B94-A04E05B82BE2Q36356890-C3681EE3-3CE2-4C1E-8C2E-7325C3A70CA7Q36356910-542A306A-E5E8-4423-BE5D-E9404EBF8514Q36357474-2294D2CC-1D4A-46C4-97F2-8130D1E8C5DEQ36364342-49EF6E44-C094-4D63-A89B-78B4A23CFF76Q36366754-97E68022-6762-4A88-BB58-D66AAF6BC16AQ36370154-7A0B3CB5-2319-4D11-A73D-A284959D739CQ37384819-83C8F72C-EA14-402F-B2F3-FB1DEF90ED59Q37666230-5A002F6F-9A23-47D1-AC54-3294C86D687BQ37837361-213B2C75-AE5A-4661-BC4C-78B171803F4D
P2860
Somatic evolution of variable region structures during an immune response.
description
1986 nî lūn-bûn
@nan
1986年の論文
@ja
1986年論文
@yue
1986年論文
@zh-hant
1986年論文
@zh-hk
1986年論文
@zh-mo
1986年論文
@zh-tw
1986年论文
@wuu
1986年论文
@zh
1986年论文
@zh-cn
name
Somatic evolution of variable region structures during an immune response.
@ast
Somatic evolution of variable region structures during an immune response.
@en
type
label
Somatic evolution of variable region structures during an immune response.
@ast
Somatic evolution of variable region structures during an immune response.
@en
prefLabel
Somatic evolution of variable region structures during an immune response.
@ast
Somatic evolution of variable region structures during an immune response.
@en
P2093
P2860
P356
P1476
Somatic evolution of variable region structures during an immune response.
@en
P2093
P2860
P304
P356
10.1073/PNAS.83.6.1847
P407
P577
1986-03-01T00:00:00Z