Zobrazeno 1 - 10
of 152
pro vyhledávání: '"L. Harvath"'
Publikováno v:
Cytotherapy. 4:415-418
415 © 2002 ISCT Meeting Report National Heart, Lung, and Blood Institute of the National Institutes of Health forum on immune reconstitution and cellular therapy following hematopoietic stem-cell transplantation D Stroncek1, L Harvath2 and J Barrett
Publikováno v:
Transfusion. 38:867-873
Publikováno v:
Molecular Pathology. 49:M17-M22
Aims—To investigate the heterotypic adhesion of unactivated platelets to chemotactically responsive (migrated) and non-responsive (non-migrated) polymorphonuclear neutrophils (PMN). Methods—Platelets and PMN were isolated from autologous, normal
Publikováno v:
The Journal of Immunology. 152:5447-5456
Laminin, isolated from Engelbreth-Holm-Swarm tumor, and 10 chemically synthesized peptides, corresponding to various regions of the laminin A and B1 chains, were compared for their abilities to stimulate human peripheral blood polymorphonuclear leuko
Autor:
L, Harvath
Publikováno v:
Cytotherapy. 1(4)
Publikováno v:
The Journal of Immunology. 146:949-957
The CD45 Ag family is a group of high m.w. glycoproteins that are expressed on the plasma membranes of all leukocytes. CD45 has protein tyrosine phosphatase activity and appears to regulate signal transduction and lymphocyte activation by specific as
Publikováno v:
The Journal of Immunology. 146:224-232
Neutrophils (PMN) treated with cAMP elevating agents were evaluated for their chemotactic responsiveness to FMLP and leukotriene B4 (LTB4). PGE1 and isoproterenol, increased PMN cyclic AMP production and inhibited chemotaxis to both FMLP and LTB4. In
Autor:
L, Harvath, D A, Terle
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 115
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 115
Publikováno v:
Journal of immunology (Baltimore, Md. : 1950). 152(6)
Mouse alloantibodies to Ia.7 display a cross-reactive idiotype (CRI) recognized by xenogeneic anti-idiotypes. The CRI is expressed on serum Abs in all responding individuals and on all anti-Ia.7 mAbs, from mice of appropriate genetic types. In additi