Use of zinc-finger nucleases to knock out the WAS gene in K562 cells: a human cellular model for Wiskott-Aldrich syndrome

• Asıl Yazarlar: Miguel G. Toscano (Yazar), Per Anderson (Yazar), Pilar Muñoz (Yazar), Gema Lucena (Yazar), Marién Cobo (Yazar), Karim Benabdellah (Yazar), Philip D. Gregory (Yazar), Michael C. Holmes (Yazar), Francisco Martin (Yazar)
• Materyal Türü: Kitap
• Baskı/Yayın Bilgisi: The Company of Biologists, 2013-03-01T00:00:00Z.
• Konular: article
• Online Erişim: Connect to this object online.

SUMMARY Mutations in the WAS gene cause Wiskott-Aldrich syndrome (WAS), which is characterized by eczema, immunodeficiency and microthrombocytopenia. Although the role of WASP in lymphocytes and myeloid cells is well characterized, its role on megakaryocyte (MK) development is poorly understood. In...