Cutting edge: B cell linker protein is dispensable for the allelic exclusion of immunoglobulin heavy chain locus but required for the persistence of CD5+ B cells

Journal of Immunology

Volumn 165, Issue 8, 2000, Pages 4153-4157

  Xu, S ^a   Wong, S C ^a   Lam, K P ^a  

^a INSTITUTE OF MOLECULAR AND CELL BIOLOGY   (Singapore)

Author keywords

[No Author keywords available]

Indexed keywords

B LYMPHOCYTE RECEPTOR; CD5 ANTIGEN; IMMUNOGLOBULIN HEAVY CHAIN; LINK PROTEIN; PROTEIN TYROSINE KINASE;

ALLELE; ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; B LYMPHOCYTE DIFFERENTIATION; CELL MATURATION; CELL RENEWAL; CONTROLLED STUDY; GENE LOCUS; MOUSE; NONHUMAN; PERITONEAL CAVITY; PRIORITY JOURNAL; PROTEIN EXPRESSION; SIGNAL TRANSDUCTION; TRANSGENE;

EID: 0034667788     PISSN: 00221767     EISSN: None     Source Type: Journal    
DOI: 10.4049/jimmunol.165.8.4153     Document Type: Article

References (30)

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6. Targeted disruption of the μ-chain membrane exon causes loss of heavy-chain allelic exclusion
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22. B cell antigen receptor specificity and surface density together determine B-1 versus B-2 cell development
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29. + B cell precursor in B-1 cell differentiation
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