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• W4200449141 endingPage "40" @default.
• W4200449141 startingPage "22" @default.
• W4200449141 abstract "CD95/Fas controls multiple cellular programs in immune cells by triggering apoptotic as well as nonapoptotic pathways. CD95 mutations can lead to immune system defects and certain autoimmune diseases. Mutations in different domains of CD95 affect all stages of CD95 signaling, from CD95L binding to assembly of the receptor complex. Recently resolved 3D crystal structures of human CD95 provide remarkable insights into the presumed effects of mutations on altered CD95-mediated signaling in certain autoimmune diseases. CD95/Fas/APO-1 can trigger apoptotic as well as nonapoptotic pathways in immune cells. CD95 signaling in humans can be inhibited by several mechanisms, including mutations in the gene encoding CD95. CD95 mutations lead to autoimmune disorders, such as autoimmune lymphoproliferative syndrome (ALPS). Gaining further insight into the reported mutations of CD95 and resulting alterations of its signaling networks may provide further understanding of their presumed role in certain autoimmune diseases. For illustrative purposes and to better understand the potential outcomes of CD95 mutations, here we assign their positions to the recently determined 3D structures of human CD95. Based on this, we make certain predictions and speculate on the putative role of CD95 mutation defects in CD95-mediated signaling for certain autoimmune diseases. CD95/Fas/APO-1 can trigger apoptotic as well as nonapoptotic pathways in immune cells. CD95 signaling in humans can be inhibited by several mechanisms, including mutations in the gene encoding CD95. CD95 mutations lead to autoimmune disorders, such as autoimmune lymphoproliferative syndrome (ALPS). Gaining further insight into the reported mutations of CD95 and resulting alterations of its signaling networks may provide further understanding of their presumed role in certain autoimmune diseases. For illustrative purposes and to better understand the potential outcomes of CD95 mutations, here we assign their positions to the recently determined 3D structures of human CD95. Based on this, we make certain predictions and speculate on the putative role of CD95 mutation defects in CD95-mediated signaling for certain autoimmune diseases. program of lymphocyte elimination in the down phase of an immune response. genetic autoimmune disorder characterized by the inability of the immune system to maintain lymphocyte homeostasis. rare disorder characterized by lymph node enlargement. inhibitor of procaspase-8 activation. multiprotein complex comprising DR, FADD, procaspase-8, and c-FLIP. adaptor protein at the DISC. single copy of the wild-type allele, insufficient for producing the wild-type protein. domain preventing spontaneous activation of CD95. initiator caspase in extrinsic apoptosis." @default.
• W4200449141 created "2021-12-31" @default.
• W4200449141 creator A5010473847 @default.
• W4200449141 creator A5023414847 @default.
• W4200449141 creator A5029566293 @default.
• W4200449141 creator A5054417011 @default.
• W4200449141 creator A5076841276 @default.
• W4200449141 date "2022-01-01" @default.
• W4200449141 modified "2023-10-01" @default.
• W4200449141 title "Impact of human CD95 mutations on cell death and autoimmunity: a model" @default.
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