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Article

The Pseudokinase MLKL and the Kinase RIPK3 Have Distinct Roles in Autoimmune Disease Caused by Loss of Death-Receptor-Induced Apoptosis

12 Aug 2016

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 27523270
DOI: 10.1016/j.immuni.2016.07.016

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Related research

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The Pseudokinase MLKL and the Kinase RIPK3 Have Distinct Roles in Autoimmune Disease Caused by Loss of Death-Receptor-Induced ApoptosisPMID 27523270Read ↗

The Killer Pseudokinase Mixed Lineage Kinase Domain-Like Protein (MLKL).Semantic proximity Read ↗

The pseudokinase MLKL mediates programmed hepatocellular necrosis independently of RIPK3 during hepatitisSemantic proximity Read ↗

Post-translational control of RIPK3 and MLKL mediated necroptotic cell deathSemantic proximity Read ↗

Sequential Engagement of Distinct MLKL Phosphatidylinositol-Binding Sites Executes NecroptosisSemantic proximity Read ↗

Necroptosis: a crucial pathogenic mediator of human diseaseSemantic proximity Read ↗

Necroptosis molecular mechanisms: Recent findings regarding novel necroptosis regulatorsSemantic proximity Read ↗

Conformational interconversion of MLKL and disengagement from RIPK3 precede cell death by necroptosis.Semantic proximity Read ↗

Necroptosis in development and diseases.Semantic proximity Read ↗

Membrane permeabilization is mediated by distinct epitopes in mouse and human orthologs of the necroptosis effector, MLKLSemantic proximity Read ↗

Caspase-8-Dependent Inflammatory Responses Are Controlled by Its Adaptor, FADD, and Necroptosis.Semantic proximity Read ↗

Activation of the pseudokinase MLKL unleashes the four-helix bundle domain to induce membrane localization and necroptotic cell death.Semantic proximity Read ↗

Caspases at the crossroads of immune-cell life and deathSemantic proximity Read ↗

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