The E-T (elephant-tadpole) paradox necessitates the concept of a unit of B-cell function: the protection.
about
Lower Affinity T Cells are Critical Components and Active Participants of the Immune ResponseImmunoglobulin heavy chain diversity in Pteropid bats: evidence for a diverse and highly specific antigen binding repertoireThe use of phage display in the study of receptors and their ligands.Estimating the diversity, completeness, and cross-reactivity of the T cell repertoire.Analysis of patterns of DNA sequence variation in flanking and coding regions of murine germ-line immunoglobulin heavy-chain variable genes: evolutionary implications.Away with words: commentary on the Atlan-Cohen essay 'Immune information, self-organization and meaning'.An in depth analysis of the concept of "polyspecificity" assumed to characterize TCR/BCR recognitionRevisiting thymic positive selection and the mature T cell repertoire for antigen.Studies on CD4 T cell immunity using somatic transgene immunization.Early high-affinity neutralizing anti-viral IgG responses without further overall improvements of affinity.Splitting the difference: the germline-somatic mutation debate on generating antibody diversity.In vivo role of B lymphocytes in somatic transgene immunization.How many TCR clonotypes does a body maintain?Most alpha/beta T cell receptor diversity is due to terminal deoxynucleotidyl transferaseWhen three is not a crowd: a Crossregulation model of the dynamics and repertoire selection of regulatory CD4+ T cells.A rationalized set of default postulates that permit a coherent description of the immune system amenable to computer modeling.A hypothesis accounting for the paradoxical expression of the D gene segment in the BCR and the TCR.Quantifying the development of the peripheral naive CD4+ T-cell pool in humansOn the critique by Colin Anderson of 'A reply to Dembic: on an end to the beginning of mis-understanding the immune response'.Antigen receptor 'capacity' and the sensitivity of self-tolerance.A critique of the Cohn-Langman protection theory.Diversity 1990.A stepwise model of polyreactivity of the T cell antigen-receptor (TCR): its impact on the self-nonself discrimination and on related observations (receptor editing, anergy, dual receptor cells).Learning from a contemporary history of immunology.Giving Context to Non-self-marker Theories of Immune Responsiveness.The immune system: a weapon of mass destruction invented by evolution to even the odds during the war of the DNAsA computerized model for the self-non-self discrimination at the level of the T(h) (Th genesis). I. The origin of 'primer' effector T(h) cells.The history of ecoimmunology and its integration with disease ecology.On being the right size: antibody repertoire formation in the mouse and human.Analysis of Paris meeting redefining the "self" of the immune system.Recombination signature of germline immunoglobulin variable genes.Activation-threshold tuning in an affinity model for the T-cell repertoire.An antigen valence theory to explain the evolution and organization of the humoral immune response.Functional diversity of natural IgM.
P2860
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P2860
The E-T (elephant-tadpole) paradox necessitates the concept of a unit of B-cell function: the protection.
description
1987 nî lūn-bûn
@nan
1987年の論文
@ja
1987年学术文章
@wuu
1987年学术文章
@zh-cn
1987年学术文章
@zh-hans
1987年学术文章
@zh-my
1987年学术文章
@zh-sg
1987年學術文章
@yue
1987年學術文章
@zh
1987年學術文章
@zh-hant
name
The E-T (elephant-tadpole) par ...... cell function: the protection.
@en
type
label
The E-T (elephant-tadpole) par ...... cell function: the protection.
@en
prefLabel
The E-T (elephant-tadpole) par ...... cell function: the protection.
@en
P1433
P1476
The E-T (elephant-tadpole) par ...... cell function: the protection.
@en
P2093
P304
P356
10.1016/0161-5890(87)90050-2
P577
1987-07-01T00:00:00Z