ArticlemBio2025
Article in mBio, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
Abstract
Red-spotted grouper nervous necrosis virus (RGNNV) is an intensely virulent pathogen affecting cultured fish, capable of infecting various reared marine and freshwater species worldwide and causing severe financial losses in the aquaculture business. The capsid protein (CP) of RGNNV, as the viral surface's sole structural protein, is essential for mediating RGNNV binding to susceptible host cells. However, the cellular receptors involved in RGNNV entry are still mostly unknown. In this study, immunoprecipitation-mass spectrometry (IP-MS) was employed to screen for candidate proteins that could interact with RGNNV-CP. The IMPORTANCE: Red-spotted grouper nervous necrosis virus (RGNNV) is the most prevalent genotype in Betanodavirus and infects numerous fish species in warm water environments. In the viral infectious life cycle, virus-receptor recognition and interactions play a crucial role. Nevertheless, the host interaction proteins involved in RGNNV infection are still not completely understood. Therefore, further research is required to identify additional host proteins involved in RGNNV invasion to refine our understanding of its pathogenic mechanisms. In this study, we identified
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.