Zobrazeno 1 - 10
of 14
pro vyhledávání: '"R. K. Andrews"'
Autor:
J. M. Trevillyan, E. E. Gardiner, R. K. Andrews, A. Maisa, A. C. Hearps, M. Al-Tamimi, S. M. Crowe, J. F. Hoy
Publikováno v:
Platelets, Vol 28, Iss 3, Pp 301-304 (2017)
HIV-positive patients are at increased risk for coronary artery disease (CAD); changes in platelet activation may play a role. This study was performed to determine if levels of soluble glycoprotein VI (sGPVI), a platelet-specific marker of activatio
Externí odkaz:
https://doaj.org/article/ebcf251aebf9481b9c1eaa56e97a4537
Autor:
J. F. Arthur, Y. Shen, Y. Chen, J. Qiao, R. Ni, Y. Lu, R. K. Andrews, E. E. Gardiner, J. Cheng
Publikováno v:
Journal of Diabetes Research, Vol 2013 (2013)
Thrombosis is a life-threatening complication of diabetes. Platelet reactivity is crucial to thrombus formation, particularly in arterial vessels and in thrombotic complications causing myocardial infarction or ischaemic stroke, but diabetic patients
Externí odkaz:
https://doaj.org/article/4a7219424424406f9693d320056f2436
Autor:
M. De Luca, G. M. Veldman, R. K. Andrews, Michael C. Berndt, L. C. Dunlop, J. V. Flannery, D. A. Cumming, R. Ettling
Publikováno v:
Journal of Biological Chemistry. 270:26734-26737
Initial rolling of circulating neutrophils on a blood vessel wall prior to adhesion and transmigration to damaged tissue is dependent upon P-selectin expressed on endothelial cells and its specific neutrophil receptor, the P-selectin glycoprotein lig
Publikováno v:
Biochemical Journal. 304:113-119
Endothelin receptors with endothelin-A (ETa) specificity were present in neonatal rat ventricle. However, in both receptor-binding studies and studies of inositol phosphate accumulation, these receptors had lower affinity for endothelin-1 than ETa re
Publikováno v:
The Journal of biological chemistry. 275(36)
Platelet-type von Willebrand disease is a bleeding disorder resulting from gain-of-function mutations of glycoprotein (GP) Ibalpha that increase its affinity for von Willebrand factor (vWf). The two known naturally occurring mutations, G233V and M239
Autor:
Y, Shen, G M, Romo, J F, Dong, A, Schade, L V, McIntire, D, Kenny, J C, Whisstock, M C, Berndt, J A, López, R K, Andrews
Publikováno v:
Blood. 95(3)
The platelet glycoprotein (GP) Ib-IX-V complex mediates adhesion to von Willebrand factor (vWf) in (patho)physiologic thrombus formation. The vWf-binding site on GP Ib-IX-V is within the N-terminal 282 residues of GP Ibalpha, which consist of an N-te
Autor:
M, De Luca, D A, Facey, E J, Favaloro, M S, Hertzberg, J C, Whisstock, T, McNally, R K, Andrews, M C, Berndt
Publikováno v:
Blood. 95(1)
Binding of the adhesive glycoprotein, von Willebrand factor (vWf), to the platelet membrane glycoprotein (GP) Ib-IX-V complex initiates platelet adhesion and aggregation at high shear stress in hemostasis and thrombosis. In this study, the GP Ib-IX-V
Autor:
F C, Stomski, M, Dottore, W, Winnall, M A, Guthridge, J, Woodcock, C J, Bagley, D T, Thomas, R K, Andrews, M C, Berndt, A F, Lopez
Publikováno v:
Blood. 94(6)
The common beta chain (beta(c)) of the granulocyte-macrophage colony-stimulating factor (GM-CSF), interleukin-3 (IL-3), and IL-5 receptors is the major signaling subunit of these receptors coupling ligand binding to multiple biological activities. It
Autor:
R K, Andrews, M C, Berndt
Publikováno v:
Histology and histopathology. 13(3)
Cell-cell and cell-extracellular matrix adhesion are critical aspects of platelet function, regulating interactions between circulating platelets in the bloodstream with the blood vessel wall. In haemostasis, platelets adhere to the subendothelial ma
Publikováno v:
Blood. 91(12)