Role of Bruton's tyrosine kinase in immunodeficiency
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Abstract
References (64)
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The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases
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Expression of Bruton's agammaglobulinemia tyrosine kinase gene, BTK, is selectively down-regulated in T lymphocytes and plasma cells.
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Mutation analysis of the Bruton's tyrosine kinase gene in X-linked agammaglobulinemia: identification of a mutation which affects the same codon as is altered in immunodeficient xid mice
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Development of autoimmune disease in SCID mice populated with long-term "in vitro" proliferating (NZB x NZW)F1 pre-B cells.
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Bruton's Tyrosine Kinase is a Key Regulator in B‐Cell Development
1994 • 107 citations
Tyrosine phosphorylation is required for mast cell activation by Fc epsilon RI cross-linking.
1992 • 101 citations
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1994 • 101 citations
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Deletion within the Src homology domain 3 of Bruton's tyrosine kinase resulting in X-linked agammaglobulinemia (XLA).
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IL-5 receptor positive B cells, but not eosinophils, are functionally and numerically influenced in mice carrying the X-linked immune defect
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1993 • 61 citations
Identification of a closely linked DNA marker, DXS178, to further refine the X-linked agammaglobulinemia locus
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1993 • 37 citations
Bone marrow cells in X-linked agammaglobulinemia express pre-B-specific genes (lambda-like and V pre-B) and present immunoglobulin V-D-J gene usage strongly biased to a fetal-like repertoire.
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