Hillery CA - Search Results

1

Single-chain antibody fragments derived from a human synthetic phage-display library bind thrombospondin and inhibit sickle cell adhesion.

Watkins NA, Du LM, Scott JP, Ouwehand WH, Hillery CA. Watkins NA, et al. Among authors: hillery ca. Blood. 2003 Jul 15;102(2):718-24. doi: 10.1182/blood-2002-11-3497. Epub 2003 Mar 27. Blood. 2003. PMID: 12663449 Free article.

2

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. Blood. 1996 Jun 1;87(11):4879-86. Blood. 1996. PMID: 8639862 Free article.

3

Hydroxyurea therapy in children severely affected with sickle cell disease.

Scott JP, Hillery CA, Brown ER, Misiewicz V, Labotka RJ. Scott JP, et al. Among authors: hillery ca. J Pediatr. 1996 Jun;128(6):820-8. doi: 10.1016/s0022-3476(96)70335-9. J Pediatr. 1996. PMID: 8648542

4

Mechanisms of stroke in sickle cell disease: sickle erythrocytes decrease cerebral blood flow in rats after nitric oxide synthase inhibition.

French JA 2nd, Kenny D, Scott JP, Hoffmann RG, Wood JD, Hudetz AG, Hillery CA. French JA 2nd, et al. Among authors: hillery ca. Blood. 1997 Jun 15;89(12):4591-9. Blood. 1997. PMID: 9192784 Free article.

5

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. Blood. 1998 Mar 1;91(5):1572-81. Blood. 1998. PMID: 9473222 Free article.

6

Potential therapeutic approaches for the treatment of vaso-occlusion in sickle cell disease.

Hillery CA. Hillery CA. Curr Opin Hematol. 1998 Mar;5(2):151-5. doi: 10.1097/00062752-199803000-00011. Curr Opin Hematol. 1998. PMID: 9570709 Review.

7

The carboxy-terminal cell-binding domain of thrombospondin is essential for sickle red blood cell adhesion.

Hillery CA, Scott JP, Du MC. Hillery CA, et al. Blood. 1999 Jul 1;94(1):302-9. Blood. 1999. PMID: 10381526 Free article.

8

Hydroxyurea therapy decreases the in vitro adhesion of sickle erythrocytes to thrombospondin and laminin.

Hillery CA, Du MC, Wang WC, Scott JP. Hillery CA, et al. Br J Haematol. 2000 May;109(2):322-7. doi: 10.1046/j.1365-2141.2000.02040.x. Br J Haematol. 2000. PMID: 10848818 Free article.

9

Bleeding disorders: A common cause of menorrhagia in adolescents.

Bevan JA, Maloney KW, Hillery CA, Gill JC, Montgomery RR, Scott JP. Bevan JA, et al. Among authors: hillery ca. J Pediatr. 2001 Jun;138(6):856-61. doi: 10.1067/mpd.2001.113042. J Pediatr. 2001. PMID: 11391329

10

Altered erythrocyte endothelial adherence and membrane phospholipid asymmetry in hereditary hydrocytosis.

Gallagher PG, Chang SH, Rettig MP, Neely JE, Hillery CA, Smith BD, Low PS. Gallagher PG, et al. Among authors: hillery ca. Blood. 2003 Jun 1;101(11):4625-7. doi: 10.1182/blood-2001-12-0329. Epub 2003 Jan 30. Blood. 2003. PMID: 12560240 Free article.

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