Zobrazeno 1 - 10
of 51
pro vyhledávání: '"G. J. Roth"'
Autor:
G J Roth, Andreas Schnapp, Nveed Chaudhary, Antje Prasse, Joachim Müller-Quernheim, Frank Hilberg, John Edward Park, Gernot Zissel
Publikováno v:
European Respiratory Journal. 29:976-985
BIBF 1000 is a small molecule inhibitor targeting the receptor kinases of platelet-derived growth factor (PDGF), basic fibroblast growth factor and vascular endothelial growth factor, which have known roles in the pathogenesis of pulmonary fibrosis.
Autor:
S D, Russell, G J, Roth
Publikováno v:
Blood. 81:1787-1791
Pseudo (platelet-type)-von Willebrand disease is an autosomal dominant bleeding disorder caused by the hyperfunction of a receptor on the platelet surface. The abnormal receptor, glycoprotein Ib, displays increased affinity for its ligand, von Willeb
Autor:
G. J. Roth, M. Yagi
Publikováno v:
Journal of thrombosis and haemostasis : JTH. 4(9)
Summary. Background: During differentiation, megakaryocytes (MK), the bone marrow precursors of circulating blood platelets, undergo polyploidization, repeated rounds of DNA replication without cell division. Mature normal MK may contain a DNA conten
Autor:
B M, Trost, G J, Roth
Publikováno v:
Organic letters. 1(1)
[formula: see text] A synthesis of gamma-amino acids and their cyclic derivatives, 3-pyrrolinones, from alpha-amino acids employs a ruthenium-catalyzed Alder ene reaction as a key step in the sequence. Cyclopentadienylruthenium (1,4-cyclooctadiene) c
Publikováno v:
SAE Technical Paper Series.
Autor:
D C, Calverley, G J, Roth
Publikováno v:
Hematology/oncology clinics of North America. 12(6)
Aspirin is the most widely employed antithrombotic agent in use today and has a proven role in the prevention and acute management of atherosclerosis-associated arterial thrombotic events. More recently developed antiplatelet agents have been found t
Publikováno v:
Blood. 91(4)
The initiation of primary hemostasis is mediated by interaction of the platelet glycoprotein Ib (GPIb) surface receptor and its arterial subendothelial von Willebrand factor (vWF) ligand. The intracellular signaling immediately following GPIb recepto
Publikováno v:
Thrombosis and haemostasis. 76(5)
Bernard-Soulier syndrome is a rare congenital platelet disorder that affects a surface membrane adhesion receptor, glycoprotein (GP) Ib-V-IX. Both the genetic defects and the bleeding diatheses associated with the syndrome are heterogeneous due, in p
Autor:
G J, Roth
Publikováno v:
Comptes rendus de l'Academie des sciences. Serie III, Sciences de la vie. 319(9)
Bernard-Soulier syndrome involves a multicomponent adhesion receptor on the surface of human platelets. Patients with this disorder bleed excessively from the skin and mucous membranes; and in occasional cases, the bleeding is fatal. At a molecular l
Publikováno v:
Stem cells (Dayton, Ohio). 14
Platelet glycoproteins (GPs) Ib-V-IX form the surface receptor for von Willebrand factor, and this receptor-ligand interaction mediates the shear-dependent adhesion of platelets to damaged arterial vessel walls. The receptor is a multicomponent struc