Zobrazeno 1 - 10
of 17
pro vyhledávání: '"H M, Rosenblatt"'
Publikováno v:
The Journal of allergy and clinical immunology. 106(3)
Peripheral blood CD4(+) and CD8(+) T cells, CD19(+)/20(+) B cells, and serum Igs are known to be altered by the progression of pediatric HIV-1 infection, but their evaluation as predictors of survival needs further definition.To determine the natural
Autor:
J M, Puck, A E, Pepper, P S, Henthorn, F, Candotti, J, Isakov, T, Whitwam, M E, Conley, R E, Fischer, H M, Rosenblatt, T N, Small, R H, Buckley
Publikováno v:
Blood. 89(6)
Severe combined immunodeficiency (SCID) is a syndrome of profoundly impaired cellular and humoral immunity. In humans, SCID is most commonly caused by mutations in the X-linked gene IL2RG, which encodes the common gamma chain, gamma c, of the leukocy
Publikováno v:
Pediatrics. 93(5)
Publikováno v:
Annals of the New York Academy of Sciences. 693
One of the principal targets of HIV infection is the human peripheral blood CD4+ T cell, resulting in progressive CD4+ lymphocyte loss. Hypothesized mechanisms for this loss include apoptosis, cytolytic reactions, V-beta gene deletion of the T-cell r
Publikováno v:
The Pediatric infectious disease journal. 11(8)
Autor:
B. H. Goodman, M. E. Paul, I. C. Hanson, K. L. McClain, R. Broaddus, H. M. Rosenblatt, S. L. Abramson, W. T. Shearer
Publikováno v:
Southern Medical Journal. 89:S9
Publikováno v:
Southern Medical Journal. 84:5
Autor:
S. Kullback, H. M. Rosenblatt
Publikováno v:
Biometrika. 44:67-83
Publikováno v:
Research communications in chemical pathology and pharmacology. 49(1)
Monoclonal anti-actin antibody which is known to stimulate DNA synthesis and cell growth in a murine transformed cell line, L cell, was examined for its ability to modulate the expression of surface antigen on the cell membrane. There was a time depe
Publikováno v:
The Journal of allergy and clinical immunology. 83(1)
We report a case of Burkitt's lymphoma developing in a 7-year-old boy with hyper-IgE syndrome. This is the third reported case of malignancy in the hyper-IgE syndrome. The other two cases were an 18-year-old man with Hodgkin's disease and a 10-year-o