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Multiplexed genome editing by CRISPR-Un1Cas12f1 restores dystrophin expression in a mouse model of Duchenne muscular dystrophy

10 September 2026 at 08:00
Koo and colleagues demonstrate that Un1Cas12f1 recognizes an expanded PAMs, and enables multiplexed genome editing from a single CRISPR array. Delivered as an all-in-one AAV, this compact Un1Cas12f1 system excises Dmd exon 23 in vivo, restores the reading frame and dystrophin expression in a mouse model of Duchenne muscular dystrophy.

A Linguistics-Aware LLM Watermarking via Syntactic Predictability

arXiv:2510.13829v2 Announce Type: replace-cross Abstract: As large language models (LLMs) continue to advance rapidly, reliable governance tools have become critical. Publicly verifiable watermarking is particularly essential for fostering a trustworthy AI ecosystem. A central challenge persists: balancing text quality against detection robustness. Recent studies have sought to navigate this trade-off by leveraging signals from model output distributions (e.g., token-level entropy); however, their reliance on these model-specific signals presents a significant barrier to public verification, as the detection process requires access to the logits of the underlying model. We introduce STELA, a novel framework that aligns watermark strength with the linguistic degrees of freedom inherent in language. STELA dynamically modulates the signal using part-of-speech (POS) n-gram-modeled linguistic indeterminacy, weakening it in grammatically constrained contexts to preserve quality and strengthen it in contexts with greater linguistic flexibility to enhance detectability. Our detector operates without access to any model logits, thus facilitating publicly verifiable detection. Through extensive experiments on typologically diverse languages-analytic English, isolating Chinese, and agglutinative Korean-we show that STELA surpasses prior methods in detection robustness. Our code is available at https://github.com/Shinwoo-Park/stela_watermark.
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