Ginsburg D - Search Results

1

Bleeding due to disruption of a cargo-specific ER-to-Golgi transport complex.

Zhang B, Cunningham MA, Nichols WC, Bernat JA, Seligsohn U, Pipe SW, McVey JH, Schulte-Overberg U, de Bosch NB, Ruiz-Saez A, White GC, Tuddenham EG, Kaufman RJ, Ginsburg D. Zhang B, et al. Among authors: ginsburg d. Nat Genet. 2003 Jun;34(2):220-5. doi: 10.1038/ng1153. Nat Genet. 2003. PMID: 12717434

2

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.

3

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.

4

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.

5

Molecular characterization of a unique von Willebrand disease variant. A novel mutation affecting von Willebrand factor/factor VIII interaction.

Cacheris PM, Nichols WC, Ginsburg D. Cacheris PM, et al. Among authors: ginsburg d. J Biol Chem. 1991 Jul 25;266(21):13499-502. J Biol Chem. 1991. PMID: 1906877 Free article.

In previous studies, we have mapped the epitope for an anti-vWF monoclonal antibody which inhibits the interaction between FVIII and vWF to a region spanning Thr78 to Thr96 of the mature protein (Bahou, W.F., Ginsburg, D., Sikkink, R., Litwiller, R., and Fass, D …

In previous studies, we have mapped the epitope for an anti-vWF monoclonal antibody which inhibits the interaction between FVIII and vWF to …

6

Structure of pre-pro-von Willebrand factor and its expression in heterologous cells.

Bonthron DT, Handin RI, Kaufman RJ, Wasley LC, Orr EC, Mitsock LM, Ewenstein B, Loscalzo J, Ginsburg D, Orkin SH. Bonthron DT, et al. Among authors: ginsburg d. Nature. 1986 Nov 20-26;324(6094):270-3. doi: 10.1038/324270a0. Nature. 1986. PMID: 3491324

7

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

Nichols WC, Cooney KA, Mohlke KL, Ballew JD, Yang A, Bruck ME, Reddington M, Novak EK, Swank RT, Ginsburg D. Nichols WC, et al. Among authors: ginsburg d. Blood. 1994 Jun 1;83(11):3225-31. Blood. 1994. PMID: 8193357 Free article.

8

Conserved linkage of neurotrophin-3 and von Willebrand factor on mouse chromosome 6.

Barrow LL, Simin K, Mohlke K, Nichols WC, Ginsburg D, Meisler MH. Barrow LL, et al. Among authors: ginsburg d. Mamm Genome. 1993;4(6):343-5. doi: 10.1007/BF00357095. Mamm Genome. 1993. PMID: 8318738 Free article. No abstract available.

9

Neonatal purpura fulminans in association with factor V R506Q mutation.

Pipe SW, Schmaier AH, Nichols WC, Ginsburg D, Bozynski ME, Castle VP. Pipe SW, et al. Among authors: ginsburg d. J Pediatr. 1996 May;128(5 Pt 1):706-9. doi: 10.1016/s0022-3476(96)80142-9. J Pediatr. 1996. PMID: 8627449

10

Moderation of hemophilia A phenotype by the factor V R506Q mutation.

Nichols WC, Amano K, Cacheris PM, Figueiredo MS, Michaelides K, Schwaab R, Hoyer L, Kaufman RJ, Ginsburg D. Nichols WC, et al. Among authors: ginsburg d. Blood. 1996 Aug 15;88(4):1183-7. Blood. 1996. PMID: 8695835 Free article.

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