Bruton agammaglobulinemia (disease) tyrosine kinase

Bruton agammaglobulinemia (disease) tyrosine kinase
Bru·ton agammaglobulinemia (disease), tyrosine kinase (brooґtən) [Col. Ogden Carr Bruton, American pediatrician, 1908–2003] see X-linked agammaglobulinemia, under agammaglobulinemia, and see Bruton tyrosine kinase.

Medical dictionary. 2011.

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  • Bruton's tyrosine kinase — (or Btk) is a type of kinase enzyme implicated in the primary immunodeficiency disease X linked agammaglobulinemia (XLA). Its exact mechanism of action remains unknown, but it plays a crucial role in B cell maturation as well as mast cell… …   Wikipedia

  • X-linked agammaglobulinemia — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 1728 ICD10 = ICD10|D|80|0|d|80 ICD9 = ICD9|279.04 ICDO = OMIM = 300300 MedlinePlus = eMedicineSubj = ped eMedicineTopic = 294 eMedicine mult = eMedicine2|derm|858 | MeshID = X linked… …   Wikipedia

  • X-linked agammaglobulinemia — X linked infantile agammaglobulinemia a primary X linked immunodeficiency disorder (gene locus: Xq21.3 q22) caused by mutation of the gene encoding Bruton tyrosine kinase. It is characterized by absence of circulating B lymphocytes, absence of… …   Medical dictionary

  • HNRPH2 — Heterogeneous nuclear ribonucleoprotein H2 (H ), also known as HNRPH2, is a human gene.cite web | title = Entrez Gene: HNRPH2 heterogeneous nuclear ribonucleoprotein H2 (H )| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene… …   Wikipedia

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