Forced usage of positively charged amino acids in immunoglobulin CDR-H3 impairs B cell development and antibody production.
about
The pre-B cell receptor; selecting for or against autoreactivityPrimary immunoglobulin repertoire development: time and space matterSpecific Recognition of a Single-Stranded RNA Sequence by a Synthetic Antibody FragmentPorcine reproductive and respiratory syndrome (PRRS): an immune dysregulatory pandemic.Exposure to the Epstein-Barr Viral Antigen Latent Membrane Protein 1 Induces Myelin-Reactive Antibodies In VivoThe promise and challenge of high-throughput sequencing of the antibody repertoire.Clonal Progression during the T Cell-Dependent B Cell Antibody Response Depends on the Immunoglobulin DH Gene Segment Repertoire.The Antibody Germline/Maturation Hypothesis, Elicitation of Broadly Neutralizing Antibodies Against HIV-1 and Cord Blood IgM RepertoiresThe pre-B cell receptor checkpoint.Antibody repertoires in humanized NOD-scid-IL2Rγ(null) mice and human B cells reveals human-like diversification and tolerance checkpoints in the mouseHuman peripheral blood antibodies with long HCDR3s are established primarily at original recombination using a limited subset of germline genes.Receptor editing in lymphocyte development and central tolerance.Violation of an evolutionarily conserved immunoglobulin diversity gene sequence preference promotes production of dsDNA-specific IgG antibodies.Absence of N addition facilitates B cell development, but impairs immune responses.Limiting CDR-H3 diversity abrogates the antibody response to the bacterial polysaccharide α 1→3 dextran.Partial versus productive immunoglobulin heavy locus rearrangements in chronic lymphocytic leukemia: implications for B-cell receptor stereotypyHeterosubtypic immunity to influenza A virus infection requires a properly diversified antibody repertoireGeneration and analyses of human synthetic antibody libraries and their application for protein microarrays.The role of evolutionarily conserved germ-line DH sequence in B-1 cell development and natural antibody production.Molecular characterization of the early B cell response to pulmonary Cryptococcus neoformans infection.HIV-1 gp140 epitope recognition is influenced by immunoglobulin DH gene segment sequence.Global analysis of B cell selection using an immunoglobulin light chain-mediated model of autoreactivityThe link between antibodies to OxLDL and natural protection against pneumococci depends on D(H) gene conservation.Recirculating bone marrow B cells in C57BL/6 mice are more tolerant of highly hydrophobic and highly charged CDR-H3s than those in BALB/c mice.Immunoglobulin class switching appears to be regulated by B-cell antigen receptor-specific T-cell action.Immunogenetic characteristics of immunoglobulin E in allergic disease.The Global Self-Reactivity Profile of the Natural Antibody Repertoire Is Largely Independent of Germline DH Sequence.Preferential use of DH reading frame 2 alters B cell development and antigen-specific antibody productionRegulation of repertoire development through genetic control of DH reading frame preferenceA hypothesis accounting for the paradoxical expression of the D gene segment in the BCR and the TCR.Differences in the composition of the human antibody repertoire by B cell subsets in the blood.VpreB serves as an invariant surrogate antigen for selecting immunoglobulin antigen-binding sites.Genetic control of DH reading frame and its effect on B-cell development and antigen-specifc antibody production.The Autoimmune Risk Variant PTPN22 C1858T Alters B Cell Tolerance at Discrete Checkpoints and Differentially Shapes the Naive Repertoire.Temporal stability and molecular persistence of the bone marrow plasma cell antibody repertoire.Significant Differences in Physicochemical Properties of Human Immunoglobulin Kappa and Lambda CDR3 Regions.The peritoneal cavity B-2 antibody repertoire appears to reflect many of the same selective pressures that shape the B-1a and B-1b repertoires.The CDR-H3 repertoire from TdT-deficient adult bone marrow is a close, but not exact, homologue of the CDR-H3 repertoire from perinatal liver.Immunoglobulin analysis tool: a novel tool for the analysis of human and mouse heavy and light chain transcripts.DH and JH usage in murine fetal liver mirrors that of human fetal liver
P2860
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P2860
Forced usage of positively charged amino acids in immunoglobulin CDR-H3 impairs B cell development and antibody production.
description
2006 nî lūn-bûn
@nan
2006 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Forced usage of positively cha ...... pment and antibody production.
@ast
Forced usage of positively cha ...... pment and antibody production.
@en
type
label
Forced usage of positively cha ...... pment and antibody production.
@ast
Forced usage of positively cha ...... pment and antibody production.
@en
prefLabel
Forced usage of positively cha ...... pment and antibody production.
@ast
Forced usage of positively cha ...... pment and antibody production.
@en
P2093
P2860
P50
P356
P1476
Forced usage of positively cha ...... pment and antibody production.
@en
P2093
Cosima Zemlin
G Larry Gartland
Harry W Schroeder
Ivaylo I Ivanov
Jukka Pelkonen
Kohtaro Fujihashi
Lars Nitschke
Robert L Schelonka
Ryoki Kobayashi
P2860
P304
P356
10.1084/JEM.20052217
P407
P577
2006-06-05T00:00:00Z