This article provides a comprehensive overview of the evolving landscape of RNA secondary structure prediction, a critical task for understanding RNA function in health and disease.
Long non-coding RNAs (lncRNAs), once considered 'genomic dark matter,' are now recognized as crucial regulators of gene expression in physiological and pathological states.
This article explores the groundbreaking discovery of small nuclear RNA (snRNA) glycosylation, a phenomenon that bridges the fields of RNA biology and glycobiology.
This article synthesizes the rapidly advancing field of cell surface RNA localization, a paradigm-shifting concept where nuclear-encoded RNAs are stably displayed on the extracellular face of the plasma membrane.
Adenosine-to-inosine (A-to-I) RNA editing, catalyzed by ADAR enzymes, represents the most prevalent post-transcriptional modification in humans, dynamically expanding transcriptome and proteome diversity.
This article provides a comprehensive overview of the critical roles RNA-binding proteins (RBPs) play in post-transcriptional gene regulation, a rapidly advancing field with profound implications for understanding disease and developing...
This article provides a comprehensive exploration of RNA structure and dynamics, tailored for researchers and drug development professionals.
This article provides a comprehensive overview of glycoRNA, a recently discovered class of small non-coding RNAs modified with glycans.
This article provides a complete roadmap for researchers and drug development professionals designing single-cell RNA sequencing (scRNA-seq) experiments. It covers foundational principles, from understanding cellular heterogeneity and the critical importance of Unique Molecular Identifiers (UMIs) to selecting the appropriate isolation method for your sample type. The guide details step-by-step methodological workflows for both high- and low-throughput platforms, offers solutions for common pitfalls in tissue dissociation and batch effects, and outlines essential techniques for validating scRNA-seq findings through spatial transcriptomics, protein-level assays, and functional studies. By integrating established best practices with the latest advancements, this resource aims to empower scientists to generate robust, reproducible, and biologically insightful single-cell data.
Exploring how BCR-ABL splice variants in chronic myeloid leukemia create treatment resistance and challenge targeted therapy approaches.