Ginsburg D - Search Results

1

Localization of the gene for familial primary pulmonary hypertension to chromosome 2q31-32.

Nichols WC, Koller DL, Slovis B, Foroud T, Terry VH, Arnold ND, Siemieniak DR, Wheeler L, Phillips JA 3rd, Newman JH, Conneally PM, Ginsburg D, Loyd JE. Nichols WC, et al. Among authors: ginsburg d. Nat Genet. 1997 Mar;15(3):277-80. doi: 10.1038/ng0397-277. Nat Genet. 1997. PMID: 9054941

2

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.

3

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.

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

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.

6

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 …

7

Linkage relationship of X-linked juvenile retinoschisis with Xp22.1-p22.3 probes.

Sieving PA, Bingham EL, Roth MS, Young MR, Boehnke M, Kuo CY, Ginsburg D. Sieving PA, et al. Among authors: ginsburg d. Am J Hum Genet. 1990 Oct;47(4):616-21. Am J Hum Genet. 1990. PMID: 1977307 Free PMC article.

8

Molecular characterization of anti-idiotype antibody-resistant variants of a murine B cell lymphoma.

Roth MS, Weiner GJ, Allen EA, Terry VH, Harnden CE, Boehnke M, Kaminski MS, Ginsburg D. Roth MS, et al. Among authors: ginsburg d. J Immunol. 1990 Jul 15;145(2):768-77. J Immunol. 1990. PMID: 2114449

9

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.

10

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.

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