Polymorphisms in ACVRL1 and Endoglin genes are not associated with sporadic and HHT related brain AVMs in Dutch patients

Podobne knjige/članki

• Endothelial Depletion of Acvrl1 in Mice Leads to Arteriovenous Malformations Associated with Reduced Endoglin Expression
  od: Tual-Chalot, Simon, et al.
  Izdano: (2014)
• SMAD4 mutations found in unselected HHT patients
  od: Gallione, C J, et al.
  Izdano: (2006)
• Structural Basis of the Human Endoglin-BMP9 Interaction: Insights into BMP Signaling and HHT1
  od: Saito, Takako, et al.
  Izdano: (2017)
• A hereditary haemorrhagic telangiectasia family with pulmonary involvement is unlinked to the known HHT genes, endoglin and ALK-1
  od: Wallace, G, et al.
  Izdano: (2000)
• The ACVRL1 c.314-35A>G Polymorphism is Associated with Organ Vascular Malformations in Hereditary Hemorrhagic Telangiectasia Patients with ENG Mutations, but not in Patients with ACVRL1 Mutations
  od: Pawlikowska, Ludmila, et al.
  Izdano: (2015)