ArticleiScience2026
Molecular signatures of cell diversity modulated by long noncoding RNAs in the human fetal spinal cord.
Article in iScience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
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Who cites it
2 citing papers in PubMed.
- The Prospective Regulatory Functions of lncRNAs and Their ceRNA Networks in the Development of Motor Neurons and Associated Diseases.Biomolecules · 2026Review
- Making multi-axis Gaussian graphical models scalable to millions of cells.Bioinformatics (Oxford, England) · 2026Article
Corrections and comments
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Authors and funding
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The human spinal cord controls sophisticated sensory perception and motor response across its extensive length. However, the spatial and temporal regulation of the generation of various motor neurons (MNs) and glial cells remains obscure. Using single-cell RNA sequencing (scRNA-seq) and single-cell Stereo RNA sequencing (scStereo RNA-seq), we here investigated and annotated molecular signatures of three neural stem cell (NSC) lineages, MNs, astrocytes, and oligodendrocytes, in the human fetal spinal cord from gestational week 8 (GW8) to GW12. We also found that some long noncoding RNAs (lncRNAs) have overlapping or reciprocal expression patterns with their adjacent coding genes, which are enriched with the promoter, enhancer, and CCCTC-binding factor (CTCF) in the same cell cluster. Our study generated a rich spatial expression library of molecular diversity of lncRNAs and their adjacent genes in neurons and glia in the human fetal spinal cord.
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Registered trials
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