Arg60 to Leu mutation of the human thromboxane A2 receptor in a dominantly inherited bleeding disorder.

Những quyển sách tương tự

• Two thromboxane A2 receptor isoforms in human platelets. Opposite coupling to adenylyl cyclase with different sensitivity to Arg60 to Leu mutation.
  Bằng: Hirata, T, et al.
  Được phát hành: (1996)
• Binding of a radioiodinated 13-azapinane thromboxane antagonist to platelets: correlation with antiaggregatory activity in different species.
  Bằng: Narumiya, S., et al.
  Được phát hành: (1986)
• Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis.
  Bằng: Soutar, A K, et al.
  Được phát hành: (1992)
• Molecular characterization of a mouse prostaglandin D receptor and functional expression of the cloned gene.
  Bằng: Hirata, M, et al.
  Được phát hành: (1994)
• Characterization of an autosomal dominant bleeding disorder caused by a thrombomodulin mutation
  Bằng: Dargaud, Yesim, et al.
  Được phát hành: (2015)