In one paragraphArticle in bioRxiv : the preprint server for biology, 2026. 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
11 authors.
Katherine K TjoelkerCellular & Molecular Biology Graduate Program, University of Michigan, Ann Arbor, MI 48109.ORCID 0000-0001-6657-5833 Tamsuk PaulDepartment of Chemistry, Chicago Center for Theoretical Chemistry, Institute for Biophysical Dynamics, and James Franck Institute, The University of Chicago, Chicago, IL 60637.
Babli AdhikaryDepartment of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI 48109.ORCID 0009-0007-0573-1426 Sahithya S IyerDepartment of Chemistry, Chicago Center for Theoretical Chemistry, Institute for Biophysical Dynamics, and James Franck Institute, The University of Chicago, Chicago, IL 60637.ORCID 0009-0000-5591-5177 Kristina M HermanDepartment of Chemistry, Chicago Center for Theoretical Chemistry, Institute for Biophysical Dynamics, and James Franck Institute, The University of Chicago, Chicago, IL 60637.ORCID 0000-0003-4923-5727 Leah M BeelDepartment of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI 48109.ORCID 0009-0009-5761-2861 Gregory A VothDepartment of Chemistry, Chicago Center for Theoretical Chemistry, Institute for Biophysical Dynamics, and James Franck Institute, The University of Chicago, Chicago, IL 60637.ORCID 0000-0002-3267-6748 Allen P LiuCellular & Molecular Biology Graduate Program, University of Michigan, Ann Arbor, MI 48109.ORCID 0000-0002-0309-7018 Ann L MillerCellular & Molecular Biology Graduate Program, University of Michigan, Ann Arbor, MI 48109.ORCID 0000-0002-7293-764X Funding
Cellular and Molecular Biology at MichiganT32GM145470 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI John Chadwick Brenner · 2022 to 2026
$4.1MMultiscale Simulation of Key Biomolecular Processes in the CellR35GM158238 · NIGMS · UNIVERSITY OF CHICAGO · PI VOTH, GREGORY A. · 2025 to 2025
$2.0MUG Diversity Supplement: Epithelial cell-cell junction remodeling in response to cell- and tissue-scale forcesR35GM153204 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Ann Louise Miller · 2024 to 2026
$1.0MEngineering liposomal DNA-driven membrane fusion for efficient protein, nucleic acid, and lipid deliveryR01GM163198 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Allen Po-Chih Liu · 2026 to 2026
$995kSensing and modulating the chemokine environment with synthetic cellsR21AI173559 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LIU, ALLEN PO-CHIH, LUKER, GARY D · 2023 to 2024
$429kInvestigating the emergent dynamics of actin filament branch formation and aging using a multiscale computational approachF32GM161057 · NIGMS · UNIVERSITY OF CHICAGO · PI Kristina Herman · 2025 to 2026
$152kNIAID NIH HHS R21 AI173559NIGMS NIH HHS F32 GM161057NIGMS NIH HHS R01 GM163198NIGMS NIH HHS R35 GM153204NIGMS NIH HHS R35 GM158238NIGMS NIH HHS T32 GM145470
6 · The paper itselfAbstract
The actomyosin cytoskeleton plays important roles in cell-cell adhesion by generating and responding to forces. Actin-binding proteins support actomyosin networks by reinforcing actin filaments, promoting actin remodeling, and transmitting forces to transmembrane adhesion proteins. One family of actin-binding proteins, LIM domain-containing proteins, is recruited to strained actin filaments. Here, we investigate two members of the LIM domain family, Zyxin and Lipoma-Preferred Partner (LPP), using the embryonic epithelium of
Indexed as
actin-binding proteinscell-cell junctionscomputational modelingcytoskeletonLIM domain-containing proteins
Identifiers
PMID42817941
PMCPMC13622051
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