Montgomery RR - Search Results

1

Critical independent regions in the VWF propeptide and mature VWF that enable normal VWF storage.

Haberichter SL, Jacobi P, Montgomery RR. Haberichter SL, et al. Among authors: montgomery rr. Blood. 2003 Feb 15;101(4):1384-91. doi: 10.1182/blood-2002-07-2281. Epub 2002 Oct 10. Blood. 2003. PMID: 12393513 Free article.

2

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. Among authors: montgomery rr. Blood. 1992 Apr 15;79(8):2048-55. Blood. 1992. PMID: 1373334 Free article.

3

The effect of DDAVP on plasma levels of von Willebrand antigen II in normal individuals and patients with von Willebrand's disease.

McCarroll DR, Ruggeri ZM, Montgomery RR. McCarroll DR, et al. Among authors: montgomery rr. Blood. 1984 Mar;63(3):532-5. Blood. 1984. PMID: 6607754 Free article.

4

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. Among authors: montgomery rr. Blood. 1996 Feb 1;87(3):1013-21. Blood. 1996. PMID: 8562925 Free article.

5

Increased adhesion of erythrocytes to components of the extracellular matrix: isolation and characterization of a red blood cell lipid that binds thrombospondin and laminin.

Hillery CA, Du MC, Montgomery RR, Scott JP. Hillery CA, et al. Among authors: montgomery rr. Blood. 1996 Jun 1;87(11):4879-86. Blood. 1996. PMID: 8639862 Free article.

6

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: montgomery rr. Blood. 1996 Oct 1;88(7):2559-68. Blood. 1996. PMID: 8839848 Free article.

7

A dinucleotide deletion results in defective membrane anchoring and circulating soluble glycoprotein Ib alpha in a novel form of Bernard-Soulier syndrome.

Kenny D, Newman PJ, Morateck PA, Montgomery RR. Kenny D, et al. Among authors: montgomery rr. Blood. 1997 Oct 1;90(7):2626-33. Blood. 1997. PMID: 9326229 Free article.

8

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: montgomery rr. J Clin Invest. 1998 Feb 1;101(3):613-24. doi: 10.1172/JCI1250. J Clin Invest. 1998. PMID: 9449695 Free PMC article.

9

Type 2M von Willebrand disease: F606I and I662F mutations in the glycoprotein Ib binding domain selectively impair ristocetin- but not botrocetin-mediated binding of von Willebrand factor to platelets.

Hillery CA, Mancuso DJ, Evan Sadler J, Ponder JW, Jozwiak MA, Christopherson PA, Cox Gill J, Paul Scott J, Montgomery RR. Hillery CA, et al. Among authors: montgomery rr. Blood. 1998 Mar 1;91(5):1572-81. Blood. 1998. PMID: 9473222 Free article.

10

Naturally occurring mutations in glycoprotein Ibalpha that result in defective ligand binding and synthesis of a truncated protein.

Kenny D, Jónsson OG, Morateck PA, Montgomery RR. Kenny D, et al. Among authors: montgomery rr. Blood. 1998 Jul 1;92(1):175-83. Blood. 1998. PMID: 9639514 Free article.

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