| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/EJI.1830220136 |
| P953 | full work available at URL | https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Feji.1830220136 |
| https://onlinelibrary.wiley.com/doi/full/10.1002/eji.1830220136 | ||
| P698 | PubMed publication ID | 1730252 |
| P2093 | author name string | Vossen JM | |
| Timmers E | |||
| Schuurman RK | |||
| Kenter MJ | |||
| Raaphorst FM | |||
| Van Tol MJ | |||
| P2860 | cites work | A comprehensive set of sequence analysis programs for the VAX | Q26778432 |
| A VH gene is located within 95 Kb of the human immunoglobulin heavy chain constant region genes | Q28291466 | ||
| Somatic generation of antibody diversity | Q29616439 | ||
| Sequence homologies, N sequence insertion and JH gene utilization in VHDJH joining: implications for the joining mechanism and the ontogenetic timing of Ly1 B cell and B-CLL progenitor generation | Q33764048 | ||
| Preferential utilization of specific immunoglobulin heavy chain diversity and joining segments in adult human peripheral blood B lymphocytes | Q36229896 | ||
| Lack of N regions in fetal and neonatal mouse immunoglobulin V-D-J junctional sequences | Q36353825 | ||
| Proceedings of the National Academy of Sciences of the United States of America | Q1146531 | ||
| Early human IgH gene assembly in Epstein-Barr virus-transformed fetal B cell lines. Preferential utilization of the most JH-proximal D segment (DQ52) and two unusual VH-related rearrangements | Q36356085 | ||
| Novel rearrangements at the immunoglobulin D locus. Inversions and fusions add to IgH somatic diversity | Q36356579 | ||
| Organization of the Ig VH locus in mice and humans | Q38706470 | ||
| The mechanism of antigen receptor gene assembly | Q38722451 | ||
| Nucleotide sequences of the cDNAs encoding the V-regions of H- and L-chains of a human monoclonal antibody specific to HIV-1-gp41. | Q40522741 | ||
| Content and organization of the human Ig VH locus: definition of three new VH families and linkage to the Ig CH locus | Q41091501 | ||
| VH gene family utilization is regulated by a locus outside of the VH region | Q41955992 | ||
| Are anti-arsonate antibody N-segments selected at both the protein and the DNA level? | Q47688240 | ||
| Diversity of immunoglobulin heavy chain gene segment rearrangement in B lymphoblastoid cell lines from X-linked agammaglobulinemia patients | Q48207079 | ||
| Developmentally controlled expression of immunoglobulin VH genes | Q48380478 | ||
| Junctional sequences of T cell receptor gamma delta genes: implications for gamma delta T cell lineages and for a novel intermediate of V-(D)-J joining. | Q52244112 | ||
| Preferential expression of VH5 and VH6 immunoglobulin genes in early human B-cell ontogeny | Q69796815 | ||
| Organization and evolution of variable region genes of the human immunoglobulin heavy chain | Q70313336 | ||
| At least five DH genes of human immunoglobulin heavy chains are encoded in 9-kilobase DNA fragments | Q70387473 | ||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | immunology | Q101929 |
| lymphocyte | Q715347 | ||
| gene rearrangement | Q65350917 | ||
| immunoglobulin genes | Q70688789 | ||
| P304 | page(s) | 247-251 | |
| P577 | publication date | 1992-01-01 | |
| P1433 | published in | European Journal of Immunology | Q5412727 |
| P1476 | title | Restricted utilization of germ-line VH3 genes and short diverse third complementarity-determining regions (CDR3) in human fetal B lymphocyte immunoglobulin heavy chain rearrangements | |
| P478 | volume | 22 |
| Q73481209 | Age‐related impaired affinity maturation and differential D‐JH gene usage in human VH6‐expressing B lymphocytes from healthy individuals |
| Q78427270 | An unrelated cytogenetic karyotype and intra-lineage shift at relapse of an aggressive paediatric B-precursor ALL |
| Q35428887 | Analysis of human monoclonal antibodies elicited by vaccination with a Cryptococcus neoformans glucuronoxylomannan capsular polysaccharide vaccine. |
| Q48166985 | Analysis of immunoglobulin variable region genes from human IgG anti-DNA hybridomas |
| Q48083576 | B precursor acute lymphoblastic leukemia third complementarity-determining regions predominantly represent an unbiased recombination repertoire: leukemic transformation frequently occurs in fetal life |
| Q41146630 | Characterization of anti-sperm antibodies and their coding cDNA sequences by Epstein-Barr virus transformed B cell lines from lymphocytes of infertile women possessing anti-sperm antibodies |
| Q33192836 | Chromosomal organization of the heavy chain variable region gene segments comprising the human fetal antibody repertoire |
| Q36341119 | 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 hypermutation |
| Q52507703 | Concurrent presence of inv(14)(q11q32) and t(4;11)(q21;q23) in pre-B acute lymphoblastic leukemia. |
| Q38462172 | Development of the early B cell population in Xenopus |
| Q36902130 | Developmental progression of equine immunoglobulin heavy chain variable region diversity |
| Q35763473 | Ethnic differences of polymorphism of an immunoglobulin VH3 gene |
| Q47213323 | Ig heavy chain CDR3 size diversities are similar after conventional peripheral blood and ex vivo expanded hematopoietic cell transplants |
| Q74074341 | Immunoglobulin heavy chain junctional diversity in young and aged humans |
| Q49829351 | In-Depth Analysis of Human Neonatal and Adult IgM Antibody Repertoires |
| Q34384371 | Invariance and restriction toward a limited set of self-antigens characterize neonatal IgM antibody repertoires and prevail in autoreactive repertoires of healthy adults |
| Q48075371 | Location and sequence of rearranged immunoglobulin genes in human thymus |
| Q74774303 | Long-term kinetics of adult human antibody repertoires |
| Q36774868 | Mechanisms that generate human immunoglobulin diversity operate from the 8th week of gestation in fetal liver |
| Q52005635 | Memory B lymphocytes determine repertoire oligoclonality early after haematopoietic stem cell transplantation. |
| Q41401910 | Molecular characterization of monoclonal IgM derived from human B cell lines expressing the 4C9 rheumatoid factor associated idiotype |
| Q41339873 | Molecular mechanisms governing reading frame choice of immunoglobulin diversity genes |
| Q73923498 | Negative selection at the pre-BCR checkpoint elicited by human mu heavy chains with unusual CDR3 regions |
| Q68176920 | New nucleotide sequence data on the EMBL File Server |
| Q40676106 | Normal B lymphocyte differentiation |
| Q48056941 | Rabbit DQ52 and DH gene expression in early B-cell development |
| Q28290642 | Reconsidering the human immunoglobulin heavy-chain locus: 1. An evaluation of the expressed human IGHD gene repertoire |
| Q34981948 | Regulation and chance in the ontogeny of B and T cell antigen receptor repertoires |
| Q74128116 | Repertoire analysis in human immunoglobulin heavy chain minilocus transgenic, muMT/muMT mice |
| Q58393545 | Self-reactive antibodies (natural autoantibodies) in healthy individuals |
| Q48067974 | The VDJ repertoire expressed in human preB cells reflects the selection of bona fide heavy chains |
| Q41829277 | The human neonatal B cell response to respiratory syncytial virus uses a biased antibody variable gene repertoire that lacks somatic mutations |
| Q28247264 | The mechanism of V(D)J joining: lessons from molecular, immunological, and comparative analyses |
| Q39035263 | Timely and spatially regulated maturation of B and T cell repertoire during human fetal development |
| Q41545122 | Unequal signal and coding joint formation in human V(D)J recombination |
| Q52219682 | Usage of TCRAV and TCRBV gene families in human fetal and adult TCR rearrangements. |
| Q35884584 | Use of D gene segments with irregular spacers in terminal deoxynucleotidyltransferase (TdT)+/+ and TdT-/- mice carrying a human Ig heavy chain transgenic minilocus |
| Q41544908 | What limits affinity maturation of antibodies in Xenopus--the rate of somatic mutation or the ability to select mutants? |
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