Zobrazeno 1 - 10
of 31
pro vyhledávání: '"J. F. Casella"'
Publikováno v:
Blood. 84:1157-1163
The platelet antigens, PlA1 and PlA2, are responsible for most cases of posttransfusion purpura (PTP) and neonatal alloimmune thrombocytopenia (NAIT) in the caucasian population and are determined by two allelic forms of the platelet glycoprotein GPI
Publikováno v:
Blood. 93(9)
The human platelet alloantigen 1 system (HPA-1) is determined by a polymorphism at position 33 in the N-terminus of human glycoprotein IIIa (GPIIIa). This naturally occurring substitution creates a conformation in the HPA-1a allelic form that can be
Publikováno v:
Journal of pediatric hematology/oncology. 20(5)
Purpose Autoimmune hemolytic anemia (AIHA) due to warm-reactive immunoglobulin M (IgM) antibodies is rare in adults and has never been described in children. This report describes a pediatric patient with warm AIHA due to high-titer complete IgM anti
Publikováno v:
Tissue antigens. 51(2)
The human platelet alloantigen HPA-1a (PlA1) is responsible for most cases of post-transfusion purpura and neonatal alloimmune thrombocytopenia in the Caucasian population. HPA-1a and HPA-1b are two allelic forms of the platelet membrane glycoprotein
Publikováno v:
Blood. 88(9)
The PLA1 epitope on platelet GPIIIa has a sulfhydryl-dependent conformation and is dependent on a leucine 33/proline33 polymorphism. Monoclonal antibody LK-4 differentiates PLA1/PLA1 from PLA2/PLA2 platelet lysates on solid phase enzyme-linked immuno
Publikováno v:
The Journal of biological chemistry. 270(37)
From a human retinal cDNA library, we have isolated cDNAs that are homologs for the alpha 2 and beta subunits of chicken Cap Z. The derived human alpha subunit shares 95% amino acid identity with the chicken alpha 2 subunit; the beta subunit is 99% i
Publikováno v:
The American journal of pediatric hematology/oncology. 16(2)
We describe certain clinical, epidemiologic, and host-susceptibility features of Yersinia enterocolitica infection in the context of a patient with underlying risk factors.A 10-year-old black girl with sickle cell disease receiving chelation therapy
Autor:
J F, Casella, M A, Torres
Publikováno v:
The Journal of biological chemistry. 269(9)
Cap Z is a widely distributed, highly conserved, heterodimeric protein that binds to the barbed ends of actin filaments, but does not sever filaments. In chicken, two variant cDNAs (alpha 1 and alpha 2) encoding proteins homologous to the alpha subun
Publikováno v:
Pediatrics. 93(2)
To determine whether continuous epidural analgesia could effectively decrease pain and thereby improve the management of severe vaso-occlusive crisis in children with sickle cell disease who were unresponsive to conventional analgesic therapy.Retrosp
Autor:
J F, Casella, J A, Cooper
Publikováno v:
Methods in enzymology. 196