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Silence or correct mutations: e.g., SNCA and LRRK2 via RNA interference (RNAi) or CRISPR-Cas9 (Niethammer et al., 2017

Engineering N-terminal CPD to facilitate the desired cleavage at the design site Based on this intriguing observation, we next chose Fusion 2 as the initial template to engineer the CPD tag, aiming to achieve the neatly hydrolyzed product of Xaa-POI

Insulin-like growth factor-1 and site-specific cancers: A mendelian randomization study

In brief, male mice were deeply anaesthetized with an intraperitoneal injection of 7% chloral hydrate and transcardially perfused with a modified ice-cold artificial cerebrospinal fluid (aCSF) (described below)