79 results match your criteria: "The John Hopkins University School of Medicine.[Affiliation]"

Csk is constitutively associated with a 60-kDa tyrosine-phosphorylated protein in human T cells.

J Biol Chem

April 1996

Division of Clinical Immunology, Johns Hopkins Asthma and Allergy Center, The John Hopkins University School of Medicine, Baltimore, Maryland 21224, USA.

The protein-tyrosine kinase Csk is one of the main down-regulators of the Src family of kinases. Csk may be involved in the down-regulation of T cell receptor (TCR) signaling by C-terminal tyrosine phosphorylation of Lck and Fyn; however, it is not known how Csk activity is regulated or how it targets these Src family members. We used Jurkat T cells and normal human T cells to examine proteins that bind to the SH2 domain of Csk.

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The 4-kDa beta-amyloid peptide (Abeta), a principal component of parenchymal amyloid deposits in Alzheimer's disease, is derived from amyloid precursor proteins (APP). To identify potential intracellular compartments involved in Abeta production, we expressed human APP-695 (APPwt) and APP-695 harboring the Swedish double mutation (APPswe) associated with familial early-onset Alzheimer's disease, in mouse N2a cells. We demonstrate that cells expressing APPswe secrete high levels of Abeta peptides and beta-secretase-generated soluble APP derivatives (APP s beta) relative to cells expressing APPwt.

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The restriction of phosphatidylserine (PtdSer) to the inner surface of the plasma membrane bilayer is lost early during apoptosis. Since PtdSer is a potent surface procoagulant, and since there is an increased incidence of coagulation events in patients with systemic lupus erythematosus (SLE) who have anti-phospholipid antibodies, we addressed whether apoptotic cells are procoagulant and whether anti-phospholipid antibodies influence this. Apoptotic HeLa cells, human endothelial cells, and a murine pre-B-cell line were markedly procoagulant in a modified Russell viper venom assay.

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Isotype-specific regulation of the IgE response by IgE-binding factors.

Immunol Today

July 1983

The John Hopkins University School of Medicine, Departments of Medicine and Immunology, The Good Samaritan Hospital, Baltimore, MD 21239, USA.

The IgE response is regulated by antigen-speck helper and suppressor T cells. Here Kimishige Ishizaka and his colleagues discuss recent work which indicates that soluble IgE-binding T-cell factors provide an additional, isotypespecific level of control on the antibody response.

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