Kroner PA - Search Results

1

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.

Kroner PA, Friedman KD, Fahs SA, Scott JP, Montgomery RR. Kroner PA, et al. J Biol Chem. 1991 Oct 15;266(29):19146-9. J Biol Chem. 1991. PMID: 1918030 Free article.

2

The role of the D1 domain of the von Willebrand factor propeptide in multimerization of VWF.

Rosenberg JB, Haberichter SL, Jozwiak MA, Vokac EA, Kroner PA, Fahs SA, Kawai Y, Montgomery RR. Rosenberg JB, et al. Among authors: kroner pa. Blood. 2002 Sep 1;100(5):1699-706. doi: 10.1182/blood-2002-03-0789. Blood. 2002. PMID: 12176890 Free article.

3

Genetic mutations in von Willebrand disease identified by DHPLC and DNA sequence analysis.

Kakela JK, Friedman KD, Haberichter SL, Buchholz NP, Christopherson PA, Kroner PA, Gill JC, Montgomery RR, Bellissimo DB. Kakela JK, et al. Among authors: kroner pa. Mol Genet Metab. 2006 Mar;87(3):262-71. doi: 10.1016/j.ymgme.2005.09.016. Mol Genet Metab. 2006. PMID: 16321553

4

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

Kroner PA, Kluessendorf ML, Scott JP, Montgomery RR. Kroner PA, et al. Blood. 1992 Apr 15;79(8):2048-55. Blood. 1992. PMID: 1373334 Free article.

5

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.

Kroner PA, Foster PA, Fahs SA, Montgomery RR. Kroner PA, et al. Blood. 1996 Feb 1;87(3):1013-21. Blood. 1996. PMID: 8562925 Free article.

6

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

Rosenberg JB, Foster PA, Kaufman RJ, Vokac EA, Moussalli M, Kroner PA, Montgomery RR. Rosenberg JB, et al. Among authors: kroner pa. J Clin Invest. 1998 Feb 1;101(3):613-24. doi: 10.1172/JCI1250. J Clin Invest. 1998. PMID: 9449695 Free PMC article.

7

von Willebrand disease: a common pediatric disorder.

Montgomery RR, Kroner PA. Montgomery RR, et al. Among authors: kroner pa. Pediatr Ann. 2001 Sep;30(9):534-40. doi: 10.3928/0090-4481-20010901-08. Pediatr Ann. 2001. PMID: 11554262 Review. No abstract available.

8

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

Shi Q, Wilcox DA, Fahs SA, Kroner PA, Montgomery RR. Shi Q, et al. Among authors: kroner pa. Mol Genet Metab. 2003 May;79(1):25-33. doi: 10.1016/s1096-7192(03)00049-0. Mol Genet Metab. 2003. PMID: 12765843

9

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.

Mancuso DJ, Kroner PA, Christopherson PA, Vokac EA, Gill JC, Montgomery RR. Mancuso DJ, et al. Among authors: kroner pa. Blood. 1996 Oct 1;88(7):2559-68. Blood. 1996. PMID: 8839848 Free article.

10

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

Kroner PA, Frey AB. Kroner PA, et al. Biochemistry. 1996 Oct 15;35(41):13460-8. doi: 10.1021/bi9610313. Biochemistry. 1996. PMID: 8873615

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