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Michael C. Byrne

Researcher at Pfizer

Publications -  23
Citations -  8835

Michael C. Byrne is an academic researcher from Pfizer. The author has contributed to research in topics: T cell & IL-2 receptor. The author has an hindex of 15, co-authored 23 publications receiving 8135 citations. Previous affiliations of Michael C. Byrne include Genetics Institute, Inc..

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CD4+CD25+ Immunoregulatory T Cells: Gene Expression Analysis Reveals a Functional Role for the Glucocorticoid-Induced TNF Receptor

TL;DR: A number of genes that antagonize signaling, including members of the SOCS family, may contribute to their anergic phenotype and GITR abrogated suppression, demonstrating a functional role for this receptor in regulating the CD4(+)CD25(+) T cell subset.
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Transcriptional mechanisms underlying lymphocyte tolerance.

TL;DR: It is shown that the Ca2+-regulated transcription factor NFAT has an integral role in both aspects of lymphocyte function and in the absence of AP-1, NFAT imposes a genetic program of lymphocytes anergy that counters the program of productive activation mediated by the cooperative NFAT:AP-1 complex.
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Microbial Lipopeptides Induce the Production of IL-17 in Th Cells

TL;DR: Cytometric single-cell analysis of Th cell cytokine production revealed that IL-17 cannot be categorized as either Th1 or Th2 cytokine, and almost allIL-17-producing Th cells simultaneously produced TNF-α and most IL- 17+ Th cells also produced GM-CSF, also observed in humans.
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An essential role in liver development for transcription factor XBP-1

TL;DR: XBP-1 is a CREB/ATF family transcription factor highly expressed in hepatocellular carcinomas that is essential for liver growth and specific target genes of XBP- 1 in the liver were identified as alphaFP, which may be a regulator of hepatocyte growth, and three acute phase protein family members.