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Protein & Cell ; (12): 811-817, 2012.
Article in English | WPRIM | ID: wpr-757853

ABSTRACT

Programmed necrosis, also known as necroptosis, has recently drawn great attention. As an important cellular regulation mechanism, knowledge of its signaling components is expanding. Necroptosisis demonstrated to be regulated by the RIP1 and RIP3 kinases, and its pathophysiological importance has been confirmed in a number of disease models. Here we review the new members of this necroptosis pathway, MLKL, PGAM5, Drp1 and DAI, and discuss some of their possible applications according to recent findings.


Subject(s)
Animals , Humans , Carrier Proteins , Metabolism , DNA-Binding Proteins , Metabolism , GTP Phosphohydrolases , Metabolism , Microtubule-Associated Proteins , Metabolism , Mitochondrial Proteins , Metabolism , Necrosis , Phosphoprotein Phosphatases , Protein Kinases , Chemistry , Metabolism , Receptor-Interacting Protein Serine-Threonine Kinases , Metabolism , Signal Transduction , Tumor Necrosis Factors , Metabolism
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