Tags¶
Browse posts by tag. Paper Spotlights are tagged with the model that drafted them (e.g. Opus 4.8, Fable 5, Sonnet 5, Haiku 4.5), so you can compare how different models write up the same kind of paper.
Claude-Opus-4.8¶
DeepSeek-V3¶
- A genome-wide map of the genetic network in monocytes that regulates type I interferon induction by the cGAS-STING pathway
- Case of Aicardi-Goutières syndrome diagnosed in adulthood on whole-genome sequencing
- Emerging microbiome–mitochondria crosstalk in host defense and infectious diseases: mechanistic insights into NLRP3 inflammasome activation and mtDNA-mediated immunomodulation
- Engineered Exosome-Mediated FIH-1 Delivery for Targeted Therapy of Hyperuricemic Nephropathy by Inhibiting NF-κB/NLRP3 Inflammasome Signaling and Restoring Autophagic Homeostasis
- HTLV-1 Tax induces PINK1-PRKN/parkin-dependent mitophagy to mitigate activation of the CGAS-STING1 pathway
- Modeling calcific aortic valve disease with engineered human valve tissues identifies SAMHD1 as a therapeutic target
- Structural and single-molecule insights into the core human mitochondrial DNA replisome
- The mitochondrial DNA signal in rheumatoid arthritis: From metabolic victim to inflammatory driver
- Type I Interferonopathies in the Differential Diagnosis of Vasculitis: A Comprehensive Review
JAK-STAT¶
NLRP3¶
Opus 4.8¶
- Mitochondrial DNA and Mitochondrial-Derived Vesicles as Immunometabolic Modulators of Innate Immunosurveillance through Control of the Mitochondrial Permeability Transition Pore
- Transition Metal Activation Reframes SAMHD1 Regulation
SAMHD1¶
Sonnet 5¶
- From protector to perpetrator: The cGAS-STING pathway at the intersection of neurodegeneration and neuroinflammation
- Iterative genetic testing identifies SAMHD1 deficiency caused by a homozygous balanced translocation
- Mitochondrial dynamics and metabolic regulation in cellular inflammation: From mechanisms to precision therapeutics
- One mutation, divergent journeys: expanding the clinical spectrum of homozygous SAMHD1 deficiency in childhood
- Recent Insights into Mitochondrial Dysfunction-Driven Cellular Senescence in Chronic Kidney Disease
- cGAS inhibitor IMSB301 modifies interferon signalling in peripheral mononuclear cells of SAMHD1 genetic interferonopathy in vitro