Fahs SA - 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. Among authors: fahs sa. 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: fahs sa. Blood. 2002 Sep 1;100(5):1699-706. doi: 10.1182/blood-2002-03-0789. Blood. 2002. PMID: 12176890 Free article.

3

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: fahs sa. Blood. 1996 Feb 1;87(3):1013-21. Blood. 1996. PMID: 8562925 Free article.

4

von Willebrand factor storage and multimerization: 2 independent intracellular processes.

Haberichter SL, Fahs SA, Montgomery RR. Haberichter SL, et al. Among authors: fahs sa. Blood. 2000 Sep 1;96(5):1808-15. Blood. 2000. PMID: 10961880 Free article.

5

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: fahs sa. Mol Genet Metab. 2003 May;79(1):25-33. doi: 10.1016/s1096-7192(03)00049-0. Mol Genet Metab. 2003. PMID: 12765843

6

Factor VIII inhibitors: von Willebrand factor makes a difference in vitro and in vivo.

Shi Q, Kuether EL, Schroeder JA, Perry CL, Fahs SA, Cox Gill J, Montgomery RR. Shi Q, et al. Among authors: fahs sa. J Thromb Haemost. 2012 Nov;10(11):2328-37. doi: 10.1111/j.1538-7836.2012.04902.x. J Thromb Haemost. 2012. PMID: 22908929 Free PMC article.

7

von Willebrand factor binding to myosin assists in coagulation.

Flood VH, Slobodianuk TL, Keesler D, Lohmeier HK, Fahs S, Zhang L, Simpson P, Montgomery RR. Flood VH, et al. Blood Adv. 2020 Jan 14;4(1):174-180. doi: 10.1182/bloodadvances.2019000533. Blood Adv. 2020. PMID: 31935285 Free PMC article.

8

Re-establishment of VWF-dependent Weibel-Palade bodies in VWD endothelial cells.

Haberichter SL, Merricks EP, Fahs SA, Christopherson PA, Nichols TC, Montgomery RR. Haberichter SL, et al. Among authors: fahs sa. Blood. 2005 Jan 1;105(1):145-52. doi: 10.1182/blood-2004-02-0464. Epub 2004 Aug 26. Blood. 2005. PMID: 15331450 Free PMC article.

9

Factor VIII ectopically targeted to platelets is therapeutic in hemophilia A with high-titer inhibitory antibodies.

Shi Q, Wilcox DA, Fahs SA, Weiler H, Wells CW, Cooley BC, Desai D, Morateck PA, Gorski J, Montgomery RR. Shi Q, et al. Among authors: fahs sa. J Clin Invest. 2006 Jul;116(7):1974-82. doi: 10.1172/JCI28416. J Clin Invest. 2006. PMID: 16823491 Free PMC article.

10

Targeting FVIII expression to endothelial cells regenerates a releasable pool of FVIII and restores hemostasis in a mouse model of hemophilia A.

Shi Q, Fahs SA, Kuether EL, Cooley BC, Weiler H, Montgomery RR. Shi Q, et al. Among authors: fahs sa. Blood. 2010 Oct 21;116(16):3049-57. doi: 10.1182/blood-2010-03-272419. Epub 2010 Jul 6. Blood. 2010. PMID: 20606161 Free PMC article.

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