Single‐molecule DNA flow‐stretch assays for high‐throughput DNA–protein interaction studies
We describe an optimised single‐molecule DNA flow‐stretch assay that visualises DNA–protein interactions in real time. Linear DNA fragments are tethered to a surface and stretched by buffer flow for fluorescence imaging. Using λ and φX174 DNA, this protocol enhances reproducibility and accessibility, providing a versatile approach for studying diverse ...
Ayush Kumar Ganguli +8 more
wiley +1 more source
Ethyl methanesulfonate mutagenesis in fungi: genetic mechanisms, applications, and implications for agricultural biotechnology. [PDF]
Holman DE +9 more
europepmc +1 more source
This study investigated a novel WST‐8‐based assay for evaluating d‐Amino acid oxidase (DAO) inhibitors. We confirmed its effectiveness using known inhibitors and found that uremic toxins possess relatively weak inhibitory activity compared to existing drugs.
Kahoko Miyake +4 more
wiley +1 more source
A Comprehensive Analysis of the Agreement and Performance of Variant Annotation Programs in Equine Genomes. [PDF]
Marlowe JL +6 more
europepmc +1 more source
This paper reveals how human lactoferrin–albumin fusion (hLF‐HSA) potently suppresses lung adenocarcinoma cell migration. hLF‐HSA upregulates NHE7, leading to Golgi alkalization, disruption of the Golgi secretome, downregulation of MMP1, and reversal of EMT. These findings suggest a novel Golgi‐targeting strategy to suppress cancer cell migration.
Hana Nopia +3 more
wiley +1 more source
Multi-ancestry polygenic risk scores for the prediction of type 2 diabetes and complications in diverse ancestries. [PDF]
Huerta-Chagoya A +39 more
europepmc +1 more source
Compressing the collective knowledge of ESM into a single protein language model. [PDF]
Dinh T, Jang SK, Zaitlen N, Ntranos V.
europepmc +1 more source
An increased number of heterozygous calls in the AxiomTM Equine Genotyping Array. [PDF]
Gmel AI +3 more
europepmc +1 more source
Polygenic Risk Scores for Breast Cancer Among African American Women With High Risk.
Sun Y +10 more
europepmc +1 more source
A de novo start-loss variant in the NIPBL gene causing mild type 1 Cornelia de Lange syndrome in an Iranian family: A Case Report. [PDF]
Mir A +8 more
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