| scholarly article | Q13442814 |
| P2093 | author name string | Melvin Cohn | |
| P2860 | cites work | Nothing in Biology Makes Sense except in the Light of Evolution | Q22064567 |
| The Tritope Model for restrictive recognition of antigen by T-cells II. Implications for ontogeny, evolution and physiology | Q28756528 | ||
| The standard model of T-cell receptor function: a critical reassessment | Q33650391 | ||
| An in depth analysis of the concept of "polyspecificity" assumed to characterize TCR/BCR recognition | Q33944138 | ||
| Monovalent ligation of the B cell receptor induces receptor activation but fails to promote antigen presentation. | Q34480372 | ||
| Haplotype exclusion: the solution to a problem in natural selection | Q34772057 | ||
| Tritope model of restrictive recognition by the TCR. | Q35077151 | ||
| Some thoughts on the response to antigens that are effector T-helper independent ('thymus independence') | Q35167130 | ||
| Forced usage of positively charged amino acids in immunoglobulin CDR-H3 impairs B cell development and antibody production | Q35540125 | ||
| The evolutionary and structural 'logic' of antigen receptor diversity | Q35937393 | ||
| Degeneracy, mimicry and crossreactivity in immune recognition | Q35988442 | ||
| The Tritope Model for restrictive recognition of antigen by T-cells I. What assumptions about structure are needed to explain function? | Q36160213 | ||
| What are the commonalities governing the behavior of humoral immune recognitive repertoires? | Q36247965 | ||
| On a regulatory gene controlling the expression of the murine lambda1 light chain | Q36342047 | ||
| On a key postulate of T-cell receptor restrictive function: the V-gene loci act as a single pool encoding recognition of the polymorphic alleles of the species major histocompatibility complex | Q36711567 | ||
| Crossing the SJL lambda locus into kappa-knockout mice reveals a dysfunction of the lambda 1-containing immunoglobulin receptor in B cell differentiation | Q37628799 | ||
| The protecton: the unit of humoral immunity selected by evolution | Q37949412 | ||
| Diversity 1990. | Q37949426 | ||
| The E-T (elephant-tadpole) paradox necessitates the concept of a unit of B-cell function: the protection | Q38705452 | ||
| Bursectomy in ovo blocks the generation of immunoglobulin diversity | Q39515193 | ||
| The immune system: a weapon of mass destruction invented by evolution to even the odds during the war of the DNAs | Q40638252 | ||
| Recognition of a specific self-peptide: self-MHC class II complex is critical for positive selection of thymocytes expressing the D10 TCR. | Q40681845 | ||
| A theory of the ontogeny of the chicken humoral immune system: the consequences of diversification by gene hyperconversion and its extension to rabbit | Q40811965 | ||
| On the Genetic Dissection of a Specific Humoral Immune Response to (1,3) Dextran | Q41292460 | ||
| Diversity in the CDR3 region of V(H) is sufficient for most antibody specificities | Q41753346 | ||
| Regulation of the antibody repertoire through control of HCDR3 diversity. | Q41961202 | ||
| A point mutation in the constant region of Ig lambda1 prevents normal B cell development due to defective BCR signaling | Q43899250 | ||
| Porcine reproductive and respiratory syndrome virus subverts repertoire development by proliferation of germline-encoded B cells of all isotypes bearing hydrophobic heavy chain CDR3. | Q45397373 | ||
| Ligand recognition by alpha beta T cell receptors | Q46222293 | ||
| A single DH gene segment creates its own unique CDR-H3 repertoire and is sufficient for B cell development and immune function | Q46792429 | ||
| D-J joining and D-J proteins in B cells and T cells | Q47688665 | ||
| The chicken D locus and its contribution to the immunoglobulin heavy chain repertoire | Q48201720 | ||
| A hyperconversion mechanism generates the chicken light chain preimmune repertoire | Q48349399 | ||
| A single rearrangement event generates most of the chicken immunoglobulin light chain diversity | Q48381680 | ||
| Sequences of immunoglobulin lambda 1 genes in a lambda 1 defective mouse strain | Q48403926 | ||
| Identification and nucleotide sequence of a diversity DNA segment (D) of immunoglobulin heavy-chain genes | Q48409965 | ||
| An immunoglobulin heavy chain variable region gene is generated from three segments of DNA: VH, D and JH. | Q48413837 | ||
| T cell development in TCR-alpha beta transgenic mice. Analysis using V(D)J recombination substrates. | Q52208354 | ||
| Positive and negative selection of an antigen receptor on T cells in transgenic mice. | Q52249517 | ||
| A strong propensity toward loop formation characterizes the expressed reading frames of the D segments at the Ig H and T cell receptor loci. | Q52862325 | ||
| DH reading frame bias: evolutionary selection, antigen selection or both? Evolutionary selection. | Q52862882 | ||
| TCR alpha-chain usage can determine antigen-selected TCR beta-chain repertoire diversity. | Q52891426 | ||
| Somatic hyperconversion diversifies the single Vh gene of the chicken with a high incidence in the D region | Q69235085 | ||
| Has immunoglobulin come to a sticky end? | Q70140185 | ||
| Immune capacity of the chicken bursectomized at 60 hr of incubation; production of the immunoglobulins and specific antibodies | Q72673082 | ||
| A few comments about the Cohn and Langman theory of the ontogeny of the chicken humoral immune system | Q72761222 | ||
| D is for different-differences between H and L chain rearrangement | Q74569859 | ||
| Antibody repertoire development in fetal and neonatal piglets: XIX. Undiversified B cells with hydrophobic HCDR3s preferentially proliferate in the porcine reproductive and respiratory syndrome | Q80257367 | ||
| Reading of D genes in variable frames as a source of antibody diversity | Q85701216 | ||
| P433 | issue | 7 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 1779-1787 | |
| P577 | publication date | 2008-07-01 | |
| P1433 | published in | European Journal of Immunology | Q5412727 |
| P1476 | title | A hypothesis accounting for the paradoxical expression of the D gene segment in the BCR and the TCR. | |
| P478 | volume | 38 |
| Q30652074 | Challenging the Tritope Model of T cell receptor structure-function relationships with classical data on 'super' and 'allo-MHC' antigens |
| Q37776272 | Genetic control of DH reading frame and its effect on B-cell development and antigen-specifc antibody production |
| Q34899954 | On the logic of restrictive recognition of peptide by the T-cell antigen receptor |
| Q35747546 | Partial versus productive immunoglobulin heavy locus rearrangements in chronic lymphocytic leukemia: implications for B-cell receptor stereotypy |
| Q37186530 | Preferential use of DH reading frame 2 alters B cell development and antigen-specific antibody production |
| Q37186575 | Regulation of repertoire development through genetic control of DH reading frame preference |
| Q82282859 | Ten experiments that would make a difference in understanding immune mechanisms |
| Q36822711 | The link between antibodies to OxLDL and natural protection against pneumococci depends on D(H) gene conservation. |
| Q84926012 | What is so special about thinking; after all, we all do it! |
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