Bruton's tyrosine kinase

The gene associated with this defect is also named after him: Btk, abbreviation for Bruton's tyrosine kinase.

ARID3A has been shown to interact with E2F1 and Bruton's tyrosine kinase.

The motif is named after Bruton's tyrosine kinase (Btk), an enzyme which is essential for B cell maturation in humans and mice.

Mammalian Bruton's tyrosine kinase (Btk), a protein tyrosine kinase involved in modulation of diverse cellular processes.

XLA is caused by a mutation on the X chromosome of a single gene identified in 1993 which produces an enzyme known as Bruton's tyrosine kinase, or Btk.

Protein kinase D1 has been shown to interact with Centaurin, alpha 1, C1QBP, YWHAQ, Metallothionein 2A and Bruton's tyrosine kinase.

Bruton's tyrosine kinase (abbreviated Btk or BTK) is a type of kinase enzyme implicated in the primary immunodeficiency disease X-linked agammaglobulinemia (Bruton's agammaglobulinemia).

GNAQ has been shown to interact with Sodium-hydrogen antiporter 3 regulator 1, RIC8A, RGS16, Beta adrenergic receptor kinase, RGS4 and Bruton's tyrosine kinase.

GTF2I has been shown to interact with USF1 (human gene), Histone deacetylase 2, PRKG1, Myc, MAPK3, HDAC3, Serum response factor and Bruton's tyrosine kinase.

He and his collaborators contributed to the identification of several genes associated with Primary immunodeficiency diseases located on the X chromosome, including CD40L, Wiskott-Aldrich syndrome protein, Bruton's tyrosine kinase, and FOXP3.