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RIP1-Dependent and Independent Effects of Necrostatin-1 in Necrosis and T Cell Activation

Overview of attention for article published in PLOS ONE, August 2011
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Title
RIP1-Dependent and Independent Effects of Necrostatin-1 in Necrosis and T Cell Activation
Published in
PLOS ONE, August 2011
DOI 10.1371/journal.pone.0023209
Pubmed ID
Authors

YoungSik Cho, Thomas McQuade, Haibing Zhang, Jianke Zhang, Francis Ka-Ming Chan

Abstract

Programmed necrosis/necroptosis is an emerging form of cell death that plays important roles in mammalian development and the immune system. The pro-necrotic kinases in the receptor interacting protein (RIP) family are crucial mediators of programmed necrosis. Recent advances in necrosis research have been greatly aided by the identification of chemical inhibitors that block programmed necrosis. Necrostatin-1 (Nec-1) and its derivatives were previously shown to target the pro-necrotic kinase RIP1/RIPK1. The protective effect conferred by Nec-1 and its derivatives in many experimental model systems was often attributed to the inhibition of RIP1 function.

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The data shown below were compiled from readership statistics for 152 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 3 2%
Belgium 2 1%
Brazil 2 1%
Germany 1 <1%
Netherlands 1 <1%
Australia 1 <1%
United Kingdom 1 <1%
Hungary 1 <1%
France 1 <1%
Other 3 2%
Unknown 136 89%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 36 24%
Researcher 31 20%
Student > Master 19 13%
Student > Bachelor 16 11%
Student > Doctoral Student 9 6%
Other 25 16%
Unknown 16 11%
Readers by discipline Count As %
Agricultural and Biological Sciences 69 45%
Medicine and Dentistry 18 12%
Biochemistry, Genetics and Molecular Biology 18 12%
Chemistry 8 5%
Immunology and Microbiology 8 5%
Other 10 7%
Unknown 21 14%