M. E. Bruck

Impaired intracellular transport produced by a subset of type IIA von Willebrand disease mutations.

D. Ginsburg, E. Bowie, S. E. Lyons, 1992, The Journal of biological chemistry.

The molecular defect in type IIB von Willebrand disease. Identification of four potential missense mutations within the putative GpIb binding domain.

K. Cooney, H. Gralnick, D. Ginsburg, 1991, The Journal of clinical investigation.

Analysis of the relationship of von Willebrand disease (vWD) and hereditary hemorrhagic telangiectasia and identification of a potential type IIA vWD mutation (IIe865 to Thr).

F. Collins, M. Boehnke, M. Iannuzzi, 1991, American journal of human genetics.

Purification of Thermus aquaticus DNA polymerase expressed in Escherichia coli.

D. Engelke, D. Ginsburg, D. Ginsburg, 1990, Analytical biochemistry.

von Willebrand disease in the RIIIS/J mouse is caused by a defect outside of the von Willebrand factor gene.

K. Cooney, K. Mohlke, D. Ginsburg, 1995, Blood.