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Richard A. Flavell
Researcher at Yale University
Publications - 1389
Citations - 223064
Richard A. Flavell is an academic researcher from Yale University. The author has contributed to research in topics: Immune system & T cell. The author has an hindex of 231, co-authored 1328 publications receiving 205119 citations. Previous affiliations of Richard A. Flavell include National Institute for Medical Research & University of Michigan.
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Immune-mediated eradication of tumors through the blockade of transforming growth factor-beta signaling in T cells.
TL;DR: It is demonstrated here that T-cell–specific blockade of TGF-β signaling allows the generation of an immune response capable of eradicating tumors in mice challenged with live tumor cells.
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Interchromosomal associations between alternatively expressed loci
TL;DR: An example of eukaryotic genes located on separate chromosomes associating physically in the nucleus via interactions that may have a function in coordinating gene expression is provided and there seems to be a cell-type-specific dynamic interaction between interacting chromatin partners whereby interchromosomal interactions are apparently lost in favour of intrachromosomal ones upon gene activation.
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Regulatory T cells suppress tumor-specific CD8 T cell cytotoxicity through TGF-β signals in vivo
Mei Ling Chen,Mikael J. Pittet,Leonid Gorelik,Leonid Gorelik,Richard A. Flavell,Ralph Weissleder,Harald von Boehmer,Khashayarsha Khazaie +7 more
TL;DR: Monitoring the homing, expansion, and effector function of both subsets in draining and nondraining lymph nodes shows that CD8 cells expand to the same extent and produce similar levels of IFN-γ in the presence or absence of Ag-specific Treg, which abrogate CD8 T cell-mediated tumor rejection by specifically suppressing the cytotoxicity of expandedCD8 cells.
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Transforming Growth Factor-β Controls Development, Homeostasis, and Tolerance of T Cells by Regulatory T Cell-Dependent and -Independent Mechanisms
TL;DR: In this paper, the role of transforming growth factor-beta (TGF-beta) in inhibiting T cell functions has been studied with dominant negative TGF-β receptor transgenic models.
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The NLR gene family: a standard nomenclature
Jenny P.-Y. Ting,Ruth C. Lovering,Emad S. Alnemri,John Bertin,Jeremy M. Boss,Beckley K. Davis,Richard A. Flavell,Stephen E. Girardin,Adam Godzik,Jonathan A. Harton,Hal M. Hoffman,Jean-Pierre Hugot,Naohiro Inohara,Alex MacKenzie,Lois J. Maltais,Gabriel Núñez,Yasunori Ogura,Luc A. Otten,Dana J. Philpott,John C. Reed,Walter Reith,Stefan Schreiber,Viktor Steimle,Peter A. Ward +23 more
TL;DR: In this article, the nucleotide-binding domain and leucine-rich repeat containing (NLR) gene family was defined and standardized gene designations for all family members were provided.