Ginsburg D - Search Results

1

Molecular genetic analysis of porcine von Willebrand disease: tight linkage to the von Willebrand factor locus.

Bahou WF, Bowie EJ, Fass DN, Ginsburg D. Bahou WF, et al. Among authors: ginsburg d. Blood. 1988 Jul;72(1):308-13. Blood. 1988. PMID: 2898953 Free article.

2

Fine mapping of monoclonal antibody epitopes on human von Willebrand factor using a recombinant peptide library.

Ginsburg D, Bockenstedt PL, Allen EA, Fox DA, Foster PA, Ruggeri ZM, Zimmerman TS, Montgomery RR, Bahou WF, Johnson TA, et al. Ginsburg D, et al. Thromb Haemost. 1992 Jan 23;67(1):166-71. Thromb Haemost. 1992. PMID: 1377414

3

Biology of inherited coagulopathies: von Willebrand factor.

Ginsburg D. Ginsburg D. Hematol Oncol Clin North Am. 1992 Oct;6(5):1011-20. Hematol Oncol Clin North Am. 1992. PMID: 1400069 Review.

4

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

Lyons SE, Bruck ME, Bowie EJ, Ginsburg D. Lyons SE, et al. Among authors: ginsburg d. J Biol Chem. 1992 Mar 5;267(7):4424-30. J Biol Chem. 1992. PMID: 1537829 Free article.

5

Functional analysis of a type IIB von Willebrand disease missense mutation: increased binding of large von Willebrand factor multimers to platelets.

Cooney KA, Lyons SE, Ginsburg D. Cooney KA, et al. Among authors: ginsburg d. Proc Natl Acad Sci U S A. 1992 Apr 1;89(7):2869-72. doi: 10.1073/pnas.89.7.2869. Proc Natl Acad Sci U S A. 1992. PMID: 1557393 Free PMC article.

6

Molecular genetics of von Willebrand disease.

Ginsburg D, Bowie EJ. Ginsburg D, et al. Blood. 1992 May 15;79(10):2507-19. Blood. 1992. PMID: 1586703 Free article. Review. No abstract available.

7

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

Cooney KA, Nichols WC, Bruck ME, Bahou WF, Shapiro AD, Bowie EJ, Gralnick HR, Ginsburg D. Cooney KA, et al. Among authors: ginsburg d. J Clin Invest. 1991 Apr;87(4):1227-33. doi: 10.1172/JCI115123. J Clin Invest. 1991. PMID: 1672694 Free PMC article.

8

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).

Iannuzzi MC, Hidaka N, Boehnke M, Bruck ME, Hanna WT, Collins FS, Ginsburg D. Iannuzzi MC, et al. Among authors: ginsburg d. Am J Hum Genet. 1991 Apr;48(4):757-63. Am J Hum Genet. 1991. PMID: 1673047 Free PMC article.

9

Severe von Willebrand disease due to a defect at the level of von Willebrand factor mRNA expression: detection by exonic PCR-restriction fragment length polymorphism analysis.

Nichols WC, Lyons SE, Harrison JS, Cody RL, Ginsburg D. Nichols WC, et al. Among authors: ginsburg d. Proc Natl Acad Sci U S A. 1991 May 1;88(9):3857-61. doi: 10.1073/pnas.88.9.3857. Proc Natl Acad Sci U S A. 1991. PMID: 1673793 Free PMC article.

10

Prognostic significance of Philadelphia chromosome-positive cells detected by the polymerase chain reaction after allogeneic bone marrow transplant for chronic myelogenous leukemia.

Roth MS, Antin JH, Ash R, Terry VH, Gotlieb M, Silver SM, Ginsburg D. Roth MS, et al. Among authors: ginsburg d. Blood. 1992 Jan 1;79(1):276-82. Blood. 1992. PMID: 1728316 Free article.

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