P. Kroner

发表

Expressed full-length von Willebrand factor containing missense mutations linked to type IIB von Willebrand disease shows enhanced binding to platelets.

J. Scott, R. Montgomery, P. Kroner, 1992, Blood.

Expressed full-length von Willebrand factor containing missense mutations linked to type IIB von Willebrand disease shows enhanced binding to platelets

J. Scott, R. Montgomery, P. Kroner, 1992 .

Abnormal binding of factor VIII is linked with the substitution of glutamine for arginine 91 in von Willebrand factor in a variant form of von Willebrand disease.

J. Scott, R. Montgomery, S. Fahs, 1991, The Journal of biological chemistry.

Analysis of the structure and function of the von Willebrand factor A1 domain using targeted deletions and alanine-scanning mutagenesis.

A. Frey, P. Kroner, P. Kroner, 1996, Biochemistry.

von Willebrand disease: a common pediatric disorder.

R. Montgomery, P. Kroner, 2001, Pediatric annals.

The defective interaction between von Willebrand factor and factor VIII in a patient with type 1 von Willebrand disease is caused by substitution of Arg19 and His54 in mature von Willebrand factor.

P. Foster, R. Montgomery, S. Fahs, 1996, Blood.

Type 2M:Milwaukee-1 von Willebrand disease: an in-frame deletion in the Cys509-Cys695 loop of the von Willebrand factor A1 domain causes deficient binding of von Willebrand factor to platelets.

R. Montgomery, J. Gill, D. Mancuso, 1996, Blood.

Expression of human factor VIII under control of the platelet-specific alphaIIb promoter in megakaryocytic cell line as well as storage together with VWF.

R. Montgomery, S. Fahs, P. Kroner, 2003, Molecular genetics and metabolism.

causes deficient binding of von Willebrand factor to platelets the Cys509-Cys695 loop of the von Willebrand factor A1 domain Type 2M:Milwaukee-1 von Willebrand disease: an in-frame deletion in

R. Montgomery, J. Gill, D. Mancuso, 2011 .

The human multimerin gene MMRN maps to chromosome 4q22

P. Kroner, P. van Tuinen, M. D. Torres, 2000, Cytogenetic and Genome Research.

Intracellular trafficking of factor VIII to von Willebrand factor storage granules.

R. Kaufman, P. Foster, R. Montgomery, 1998, The Journal of clinical investigation.