Zobrazeno 1 - 10
of 269
pro vyhledávání: '"Peter J Newman"'
Publikováno v:
PLoS ONE, Vol 10, Iss 8, p e0135738 (2015)
IgG immune complexes contribute to the etiology and pathogenesis of numerous autoimmune disorders, including heparin-induced thrombocytopenia, systemic lupus erythematosus, rheumatoid- and collagen-induced arthritis, and chronic glomerulonephritis. P
Externí odkaz:
https://doaj.org/article/3d2d7c3aed69436e949d5c0b6101daa2
Autor:
Yongwei Zheng, Tamara Adams, Huiying Zhi, Mei Yu, Renren Wen, Peter J Newman, Demin Wang, Debra K Newman
Publikováno v:
PLoS ONE, Vol 10, Iss 3, p e0119739 (2015)
Receptor-mediated platelet activation requires phospholipase C (PLC) activity to elevate intracellular calcium and induce actin cytoskeleton reorganization. PLCs are classified into structurally distinct β, γ, δ, ε, ζ, and η isoforms. There are
Externí odkaz:
https://doaj.org/article/ee6d8127081545fd81da6f3bbe186adc
Autor:
Peter J. Newman, Alyssa J. Moroi
Publikováno v:
J Thromb Haemost
BACKGROUND: Thrombocytopenia leading to life-threatening excessive bleeding can be treated by platelet transfusion. Currently, such treatments are totally dependent on donor-derived platelets. To support future applications in the use of in vitro-der
Publikováno v:
Arterioscler Thromb Vasc Biol
Objective:PECAM-1 (platelet endothelial cell adhesion molecule 1) is a 130 kDa member of the immunoglobulin (Ig) gene superfamily that is expressed on the surfaces of platelets and leukocytes and concentrated at the intercellular junctions of conflue
Publikováno v:
Journal of Cellular and Molecular Medicine
Despite the recent advancements in transfusion medicine, red blood cell (RBC) alloimmunization remains a challenge for multiparous women and chronically transfused patients. At times, diagnostic laboratories depend on difficult‐to‐procure rare re
Publikováno v:
Blood Adv
Fetal/neonatal alloimmune thrombocytopenia (FNAIT) is a life-threatening bleeding disorder caused by maternal antibodies directed against paternally inherited antigens present on the surface of fetal platelets. The human platelet alloantigen HPA-1a (
Publikováno v:
Blood. 140:2828-2828
Autor:
Nicole M. J. Zwifelhofer, D. Woodrow Benson, Ke Yan, Robert A. Niebler, Debra K. Newman, John P. Scott, Alyssa J. Moroi, Pippa Simpson, Eckehard A. D. Stuth, Peter J. Newman, Ronald K. Woods, Rachel S. Bercovitz, Regina Cole
Publikováno v:
Thromb Haemost
Thrombocytopenia and platelet dysfunction induced by extracorporeal blood circulation are thought to contribute to postsurgical bleeding complications in neonates undergoing cardiac surgery with cardiopulmonary bypass (CPB). In this study, we examine
Autor:
Nanyan Zhang, Peter J. Newman
Publikováno v:
Journal of Tissue Engineering and Regenerative Medicine. 13:244-252
The contents of platelet α-granules arrive via a number of pathways; some are synthesized by megakaryocytes (MKs), for example, von Willebrand factor (VWF), whereas others are endocytosed from plasma, for example, fibrinogen (Fgn) and factor V (FV).
Autor:
Peter J. Newman, Aye Myat Myat Thinn, Brian R. Curtis, Bjørn Skogen, Jieqing Zhu, Huiying Zhi, Hartmut Weiler, Maria Therese Ahlen
Publikováno v:
Blood Advances. 2:3001-3011
Antibodies to platelet-specific antigens are responsible for 2 clinically important bleeding disorders: posttransfusion purpura and fetal/neonatal alloimmune thrombocytopenia (FNAIT). The human platelet-specific alloantigen 1a/1b (HPA-1a/1b; also kno