S. Zheng

发表

Platelet adhesion to multimerin 1 in vitro: influences of platelet membrane receptors, von Willebrand factor and shear

J. Miller, F. Adam, S. Tasneem, 2009, Journal of thrombosis and haemostasis : JTH.

Platelets from patients with the Quebec platelet disorder contain and secrete abnormal amounts of urokinase-type plasminogen activator.

T. Podor, G. Rivard, M. Pai, 2001, Blood.

An autosomal dominant, qualitative platelet disorder associated with multimerin deficiency, abnormalities in platelet factor V, thrombospondin, von Willebrand factor, and fibrinogen and an epinephrine aggregation defect.

J. Kelton, G. Rivard, J. Drouin, 1996, Blood.

Monitoring Human Copper/Zinc Superoxide Dismutase Misfolding/Aggregation in Mammalian Cells

Inchan Kwon, Jacob A. Irwin, S. Zheng, 2012 .

Studies of multimerin in human endothelial cells.

R. Stead, T. Podor, C. Hayward, 1998, Blood.

The storage defects in grey platelet syndrome and alphadelta-storage pool deficiency affect alpha-granule factor V and multimerin storage without altering their proteolytic processing.

B. Lages, P. Harrison, C. Hayward, 2001, British journal of haematology.

Multimerin processing by cells with and without pathways for regulated protein secretion.

M. Pai, C. Hayward, E. Cramer, 1999, Blood.

Studies of a second family with the Quebec platelet disorder: evidence that the degradation of the alpha-granule membrane and its soluble contents are not secondary to a defect in targeting proteins to alpha-granules.

G. Rivard, C. Hayward, E. Cramer, 1997, Blood.

Fibrinogen degradation products in patients with the Quebec platelet disorder

G. Rivard, C. Hayward, S. Zheng, 1997, British journal of haematology.