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Richard M. Siegel

Researcher at National Institutes of Health

Publications -  249
Citations -  23557

Richard M. Siegel is an academic researcher from National Institutes of Health. The author has contributed to research in topics: Apoptosis & T cell. The author has an hindex of 68, co-authored 243 publications receiving 21301 citations. Previous affiliations of Richard M. Siegel include Rutgers University & University of Pennsylvania.

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Encoding of spatial location by posterior parietal neurons.

TL;DR: The cortex of the inferior parietal lobule in primates is important for spatial perception and spatially oriented behavior and recordings of single neurons in this area in behaving monkeys showed that the visual sensitivity of the retinotopic receptive fields changes systematically with the angle of gaze.
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Interleukin-2 Signaling via STAT5 Constrains T Helper 17 Cell Generation

TL;DR: It is demonstrated that in addition to the promotion of activation-induced cell death of lymphocytes and the generation of Treg cells, inhibition of Th17 polarization appears to be an important function of IL-2.
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Mature T lymphocyte apoptosis--immune regulation in a dynamic and unpredictable antigenic environment.

TL;DR: Immunological, cellular, and molecular evidence indicates that throughout the life of a T cell, apoptosis may be evoked in excessive, harmful, or useless clonotypes to preserve a healthy and balanced immune system.
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A domain in TNF receptors that mediates ligand-independent receptor assembly and signaling.

TL;DR: A conserved domain in the extracellular region of the 60- and 80-kilodalton tumor necrosis factor receptors was identified that mediates specific ligand-independent assembly of receptor trimers.
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Pembrolizumab versus paclitaxel for previously treated, advanced gastric or gastro-oesophageal junction cancer (KEYNOTE-061): a randomised, open-label, controlled, phase 3 trial

Kohei Shitara, +152 more
- 14 Jul 2018 - 
TL;DR: Pembrolizumab did not significantly improve overall survival compared with paclitaxel as second-line therapy for advanced gastric or gastro-oesophageal junction cancer with PD-L1 CPS of 1 or higher and had a better safety profile than pac litaxel.