Zobrazeno 1 - 10
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pro vyhledávání: '"C L Sidman"'
Autor:
C L Sidman, J B Roths
Publikováno v:
Infection and Immunity. 61:1641-1649
Homozygous mutant scid/scid (severe combined immunodeficiency) mice (referred to as scid mice) lack both specific humoral and cell-mediated immune functions and are exemplary in vivo models for analysis of host-parasite relationships. In our colony,
Publikováno v:
The Journal of Experimental Medicine
Mice homozygous for the mutant allele scid (severe combined immunodeficiency) have been described as excellent models for Pneumocystis carinii (Pc) pneumonia (PCP), a major health problem in patients with acquired immune deficiency syndrome (AIDS) an
Autor:
V S Prasad, C L Sidman
Publikováno v:
The Journal of Immunology. 147:4200-4206
Homozygosity for either of the mutations lpr (lymphoproliferation) or gld (generalized lymphoproliferative disease) in mice results in lymphoproliferation and autoimmune disease. To investigate the site and time of excessive lymphocyte proliferation
Germline V genes encode viable motheaten mouse autoantibodies against thymocytes and red blood cells
Publikováno v:
The Journal of Immunology. 145:2304-2311
Autoantibodies against thymocytes and RBC may contribute to the pathophysiology of homozygous viable motheaten (mev) autoimmune disease. Whether the production of these autoantibodies in mev mouse results from polyclonal nonspecific B cell activation
Publikováno v:
Infection and Immunity. 61:1586-1588
scid mice naturally infected with Pneumocystis carinii and inoculated with a normally apathogenic pneumovirus had significantly higher P. carinii cyst counts and developed significantly more severe P. carinii-related disease than did sham-inoculated,
Publikováno v:
Bone marrow transplantation. 22(4)
This report describes a child with a severe phenotype of autoimmune lymphoproliferative syndrome (ALPS) who developed progressive disease requiring stem cell transplantation. This severe form of ALPS was associated with a novel Fas gene splice site m
Publikováno v:
Molecular carcinogenesis. 18(2)
E(mu)-myc transgenic mice carry a constitutively overexpressed c-myc oncogene and develop B-lineage lymphomas. Previous studies have shown that c-myc overexpression can lead to in vitro apoptosis. Here, we investigated the in vivo effects of altered
Publikováno v:
Cytometry. 23(2)
The clinically important issue of tumor heterogeneity was studied in C57BL/6-E mu-myc transgenic mice, which provide a genetically uniform model system in which all animals eventually develop B cell lymphomas after additional genetic changes beyond e
Publikováno v:
Bone marrow transplantation. 15(4)
Although many cytokines have been previously implicated in graft-versus-host disease (GVHD), no study to date has comprehensively evaluated their expression over time or in different tissues affected by GVHD. Using a semi-quantitative reverse transcr
Publikováno v:
Journal of immunology (Baltimore, Md. : 1950). 152(4)
Homozygosity for either of the autosomal recessive mutations, lpr or gld, confers an autoimmune syndrome characterized by massive lymphoid hyperplasia and extensive autoantibody production. Despite the similarities in disease progression, functional