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Thymocyte development is normal in CTLA-4-deficient mice

Data up to Jan 2025

Published1997
Citations147
References54

Total Citations Per Year

Abstract

References (54)

Loss of CTLA-4 leads to massive lymphoproliferation and fatal multiorgan tissue destruction, revealing a critical negative regulatory role of CTLA-4

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B7 expression on thymic medullary epithelium correlates with epithelium-mediated deletion of V beta 5+ thymocytes.

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CD28 expression is not essential for positive and negative selection of thymocytes or peripheral T cell tolerance.

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Both immature and mature T cells mobilize Ca2+ in response to antigen receptor crosslinking

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Differing roles for B7 and intercellular adhesion molecule-1 in negative selection of thymocytes.

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Medullary thymic epithelium expresses a ligand for CTLA4 in situ and in vitro.

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CD28-B7 interactions are not required for intrathymic clonal deletion

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CD28-mediated signaling in vivo prevents activation-induced apoptosis in the thymus and alters peripheral lymphocyte homeostasis.

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A positively selecting thymic epithelial cell line lacks costimulatory activity.

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A positively selecting thymic epithelial cell line lacks costimulatory activity.

1994 • 14 citations

The balance between deletion and activation of CD4+8+ thymocytes is controlled by T cell receptor‐antigen interactions and is affected by cyclosporin A

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Exogenous Mtv-7 superantigen transgene expression in major histocompatibility complex class II I-E- mice reconstituted with embryonic stem cell-derived hematopoietic stem cells.

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Thymocyte development is normal in CTLA-4-deficient mice (1997) – Proceedings of the National Academy of Sciences | Metascience Observatory Explorer