This study introduces ​​gPRINT​​ (generalized approach for cell subtype Identification with single cell's voicePRINT), a novel algorithm designed to unify the annotation of disease-specific cell subtypes (DSCSs) across heterogeneous single-cell datasets(scRNA-seq). By integrating gene expression levels and chromosomal positional information into unique "gene prints," gPRINT overcomes the limitations of conventional annotation methods, enabling high-precision identification of cell subtypes in complex diseases such as fibrosis and tendinopathy.Validated across multiple platforms and tissues, gPRINT achieved an external validation accuracy of ​​98.37%​​, surpassing existing tools and offering transformative potential for precision medicine.

Scientists developed a smartphone-compatible ethanol sensor using a metal–organic framework called Cu-MOF-74. The sensor visually detects ethanol concentrations across a wide range, with no electronics or lab tools required. This technology has promising applications in environmental monitoring, healthcare, industrial processes, and alcohol breath analysis.

A collection of cutting-edge papers in the May 2025 issue of Brain Medicine synthesizes current evidence on the alarming accumulation of microplastics in the human brain and proposes multiple pathways by which these particles, particularly abundant in ultra-processed foods, might contribute to rising rates of depression, dementia, and other neurological disorders through inflammatory and oxidative mechanisms shared with known dietary impacts on mental health.

Scientists have discovered that small RNA fragments derived from transfer RNA (tRNA) act as key regulators protecting neurons from death during botulinum neurotoxin type A (BoNT/A) intoxication. The study reveals these fragments block ferroptosis, a form of cell death, while maintaining paralysis effects, potentially opening new avenues for treating neuromuscular disorders.

A comprehensive review published in Genomic Psychiatry synthesizes the latest understanding of Prader-Willi syndrome, revealing how this rare genetic disorder provides a unique framework for exploring the relationship between autism spectrum disorder and psychotic spectrum disorders through genetic mechanisms, neuroimaging findings, and emerging cellular models.