ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2026
Sex and the Developmental Environment Shape Molecular Networks Underlying Bronchial Responsiveness in Mice.
Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Sex and the Developmental Environment Shape Molecular Networks Underlying Bronchial Responsiveness in Mice.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026Article
Corrections and comments
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Authors and funding
9 authors.
Funding
Abstract
Epidemiological evidence supports sex-specific prevalence patterns of respiratory disease, yet the molecular basis of these dimorphic patterns under normal physiological conditions remains poorly understood. Using an isogenic murine model, we assessed bronchial responsiveness to methacholine in male and female adult offspring, with and without maternal exposure to air pollution particulates. We confirmed that males exhibit significantly greater bronchial responsiveness than females, independent of maternal exposure. RNA sequencing of lung tissue, coupled with gene co-expression analysis, revealed differentially expressed genes and sex-specific gene network modules associated with this physiological dimorphism. Interestingly, although maternal exposure did not alter the physiological response, it did interact with sex to affect which gene modules are associated with bronchial responsiveness. These findings provide new insight into the molecular architecture of sex-based differences in lung function and highlight the importance of incorporating both sex and developmental context in respiratory research.
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Registered trials
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