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Titlebook: Alternate Programmed Cell Death Signaling in Antiviral Host Defense; Edward S. Mocarski,Pratyusha Mandal Book 2023 Springer Nature Switzer

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發(fā)表于 2025-3-23 11:55:56 | 只看該作者
Kevin M. Riggle MD,Kenneth W. Gow MD-containing proteins such as RIPK1. To ensure lifelong infection in the host, HSV carries out sophisticated molecular?strategies to evade host cell death responses during viral infection. HSV-1 is a well-characterized pathogen that encodes potent viral inhibitors that modulate both caspase activatio
12#
發(fā)表于 2025-3-23 14:08:03 | 只看該作者
Guy F. Brisseau MD, MEd, FAAP, FACS, FRCS(C) or variola virus manifests through subversion of MLKL activation. Recently described viral mimics of MLKL in other chordopoxviruses inhibit all three modes of necroptotic cell death. As with inhibition of apoptosis, the evolution of potentially redundant viral mechanisms to inhibit programmed necro
13#
發(fā)表于 2025-3-23 20:53:53 | 只看該作者
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發(fā)表于 2025-3-24 00:18:30 | 只看該作者
0070-217X oded inhibitor was shown to prevent the recruitment of RIPK3 (RIP3). This transformative evidence identified a novel pathway acting independent of TNF, interferon or RIPK1 that can stop virus from infecting its978-3-031-45280-2978-3-031-45278-9Series ISSN 0070-217X Series E-ISSN 2196-9965
15#
發(fā)表于 2025-3-24 04:55:01 | 只看該作者
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發(fā)表于 2025-3-24 08:34:59 | 只看該作者
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發(fā)表于 2025-3-24 11:41:17 | 只看該作者
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發(fā)表于 2025-3-24 16:15:54 | 只看該作者
19#
發(fā)表于 2025-3-24 21:37:50 | 只看該作者
Manipulation of Host Cell Death Pathways by Herpes Simplex Virus,-containing proteins such as RIPK1. To ensure lifelong infection in the host, HSV carries out sophisticated molecular?strategies to evade host cell death responses during viral infection. HSV-1 is a well-characterized pathogen that encodes potent viral inhibitors that modulate both caspase activatio
20#
發(fā)表于 2025-3-25 02:02:15 | 只看該作者
Subversion of Programed Cell Death by Poxviruses, or variola virus manifests through subversion of MLKL activation. Recently described viral mimics of MLKL in other chordopoxviruses inhibit all three modes of necroptotic cell death. As with inhibition of apoptosis, the evolution of potentially redundant viral mechanisms to inhibit programmed necro
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