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Publication : Distinct gene expression signature in Btk-defective T1 B-cells.

First Author  Lindvall JM Year  2006
Journal  Biochem Biophys Res Commun Volume  346
Issue  2 Pages  461-9
PubMed ID  16764821 Mgi Jnum  J:110533
Mgi Id  MGI:3640455 Doi  10.1016/j.bbrc.2006.05.146
Citation  Lindvall JM, et al. (2006) Distinct gene expression signature in Btk-defective T1 B-cells. Biochem Biophys Res Commun 346(2):461-9
abstractText  Bruton's tyrosine kinase (Btk) is a cytoplasmic tyrosine kinase important for B-lymphocyte maturation. Mutations in Btk give rise to the primary immunodeficiency disease X-linked agammaglobulinemia (XLA) in man and X-linked immunodeficiency (Xid) in mice. Recent studies have subdivided the mouse immature, or transitional, B-cells into two distinct subsets according to their respective surface markers. Transitional type 1 (T1) and transitional type 2 (T2) cells are also located in distinct anatomic locations. Based on a limited number of markers it has previously been reported that the earliest phenotypic sign of Btk deficiency is manifested at the T2 stage in mice. Here, we report on distinct genome-wide transcriptomic signature differences found in T1 B-lymphocytes from Btk-defective compared to normal mice and demonstrate that Btk deficiency is visible already at this stage.
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