In one paragraphArticle in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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.
2 · The registryThe 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.
3 · Its place in the literatureWho cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
4 · The recordCorrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
5 · Who and what moneyAuthors and funding
16 authors.
Aidan FenixInstitute of Stem Cell and Regenerative Medicine, University of Washington, Seattle, WA, USA.ORCID 0000-0002-1564-7347 Daphnée M MarciniakDepartment of Pharmacology, University of Washington, Seattle, WA, USA.
Qiaoyi LinDepartment of Pharmacology, University of Washington, Seattle, WA, USA.
Sara BianchiMolecular Biotechnology Center "Guido Tarone", Department of Molecular Biotechnology and Health Sciences, University of Turin, Torino, Italy.
Shuai LiDepartment of Pharmacology, University of Washington, Seattle, WA, USA.
Brian J BeliveauInstitute of Stem Cell and Regenerative Medicine, University of Washington, Seattle, WA, USA.ORCID 0000-0003-1314-3118 Alessandro BerteroMolecular Biotechnology Center "Guido Tarone", Department of Molecular Biotechnology and Health Sciences, University of Turin, Torino, Italy.ORCID 0000-0002-4919-9087 Charles E MurryInstitute of Stem Cell and Regenerative Medicine, University of Washington, Seattle, WA, USA.ORCID 0000-0003-3862-6773 Funding
Pharmacological Sciences SupplementT32GM007750 · NIGMS · UNIVERSITY OF WASHINGTON · PI ATKINS, WILLIAM M · 1985 to 2023
$12.6MProbing the dynamics of chromosome organization in single cellsR35GM137916 · NIGMS · UNIVERSITY OF WASHINGTON · PI Brian Joseph Beliveau · 2020 to 2026
$2.9MFunction, composition, and mechanism of RNA splicing factories in cardiomyopathyR01HL160825 · NHLBI · UNIVERSITY OF WASHINGTON · PI Charles E Murry · 2023 to 2026
$2.3MOligonucleotide-directed in situ proximity biotinylation: a unified method for mapping RNA-interacting proteomes, transcriptomes and genomic loci within intact cells.R01GM138799 · NIGMS · UNIVERSITY OF WASHINGTON · PI SHECHNER, DAVID MICHAEL · 2020 to 2024
$1.7MTechnology for evaluating drug-binding responses to small-molecule perturbationR35GM150919 · NIGMS · UNIVERSITY OF WASHINGTON · PI Devin Karl Schweppe · 2023 to 2026
$1.6MA NanoLC-Orbitrap Tribrid Instrument for Comprehensive Proteomics AnalysesS10OD021502 · OD · UNIVERSITY OF WASHINGTON · PI ONG, SHAO-EN · 2017 to 2017
$906kLeica SP8 WWL Confocal MicroscopeS10OD016240 · OD · UNIVERSITY OF WASHINGTON · PI CATTERALL, WILLIAM A · 2014 to 2014
$581kNHLBI NIH HHS R01 HL160825NIGMS NIH HHS R01 GM138799NIGMS NIH HHS R35 GM137916NIGMS NIH HHS R35 GM150919NIGMS NIH HHS T32 GM007750NIH HHS S10 OD016240NIH HHS S10 OD021502
6 · The paper itselfAbstract
Eukaryotic nuclei adopt a highly compartmentalized architecture that influences nearly all genomic processes. Understanding how this architecture impacts gene expression has been hindered by a lack of tools for elucidating the molecular interactions at individual genomic loci. Here, we adapt oligonucleotide-mediated proximity-interactome mapping (O-MAP) to biochemically characterize discrete, micron-scale nuclear neighborhoods. By targeting O-MAP to introns within the
Identifiers
PMID39574693
PMCPMC11580901
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