Article in The Journal of cell biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it
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 registry
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.
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
5 · Who and what money
Authors and funding
40 authors.
Inna A Belyantseva *Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, USA.ORCID 0000-0001-5030-9784
Chang Liu *Department of Otolaryngology-Head and Neck Surgery, Indiana University School of Medicine, Indianapolis, IN, USA.ORCID 0000-0003-3604-2010
Abigail K DragichDepartment of Physiology, University of Kentucky, College of Medicine, Lexington, KY, USA.ORCID 0000-0002-5181-3074
Takushi MiyoshiLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, USA.ORCID 0000-0001-5236-0807
Sayaka InagakiLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, USA.ORCID 0000-0001-9064-0762
Ayesha ImtiazLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, USA.ORCID 0000-0002-2643-6879
Risa TonaLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, USA.ORCID 0000-0003-0878-8587
Karen Sofia Zuluaga-OsorioDepartment of Physiology, University of Kentucky, College of Medicine, Lexington, KY, USA.ORCID 0009-0000-5094-5908
Shadan HadiDepartment of Physiology, University of Kentucky, College of Medicine, Lexington, KY, USA.ORCID 0000-0002-7482-0250
Elizabeth WilsonLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, USA.ORCID 0000-0002-0035-5341
Eva MorozkoLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, USA.ORCID 0000-0002-1820-0399
Rafal OlszewskiAuditory Development and Restoration Program, National Institute on Deafness and Other Communication Disorders, NIH , Bethesda, MD, USA.ORCID 0000-0001-8134-9009
Rizwan YousafLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, USA.ORCID 0000-0003-2323-0004
Yuliya SokolovaAdvanced Imaging Core, National Institute on Deafness and Other Communication Disorders, NIH, Bethesda, MD, USA.ORCID 0000-0003-0448-7226
Gavin P RiordanLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, USA.ORCID 0000-0002-3400-3571
S Andrew AstonData Science Core, National Institute on Deafness and Other Communication Disorders, NIH, Bethesda, MD, USA.ORCID 0000-0002-3409-8486
Atteeq U RehmanLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, USA.ORCID 0000-0002-1165-1568
Cristina Fenollar FerrerLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, USA.ORCID 0000-0003-4953-8891
Jan WisniewskiConfocal Microscopy and Digital Imaging Facility, Experimental Immunology Branch, NCI, NIH , Bethesda, MD, USA.ORCID 0000-0002-9131-0711
Shoujun GuAuditory Development and Restoration Program, National Institute on Deafness and Other Communication Disorders, NIH , Bethesda, MD, USA.ORCID 0000-0003-1041-3813
Richard J GoodyearSchool of Life Sciences, University of Sussex , Brighton, UK.ORCID 0000-0001-6698-4127
Jinan LiDepartment of Otolaryngology-Head and Neck Surgery, Indiana University School of Medicine, Indianapolis, IN, USA.ORCID 0000-0002-3021-972X
Jocelyn F KreyOregon Hearing Research Center, Oregon Health & Science University , Portland, OR, USA.ORCID 0000-0002-3015-4081
Talah WafaMouse Auditory Testing Core, National Institute on Deafness and Other Communication Disorders, NIH, Bethesda, MD, USA.ORCID 0000-0001-6943-2205
Rabia FaridiLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, USA.ORCID 0000-0001-7788-8755
Samuel Mawuli AdadeyLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, USA.ORCID 0000-0002-1993-2786
Meghan DrummondLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, USA.ORCID 0009-0001-5182-8065
Benjamin PerrinDepartment of Biology, Indiana University Indianapolis, Indianapolis, IN, USA.ORCID 0000-0003-1921-4861
Dennis C WinklerAdvanced Imaging Core, National Institute on Deafness and Other Communication Disorders, NIH, Bethesda, MD, USA.ORCID 0000-0003-1445-6554
Matthew F StarostDivision of Veterinary Resources, Office of Research Services, NIH, Bethesda, MD, USA.ORCID 0000-0002-6234-4875
Hui ChengData Science Core, National Institute on Deafness and Other Communication Disorders, NIH, Bethesda, MD, USA.ORCID 0000-0001-5380-2830
Tracy FitzgeraldMouse Auditory Testing Core, National Institute on Deafness and Other Communication Disorders, NIH, Bethesda, MD, USA.ORCID 0000-0002-4402-5029
Guy P RichardsonSchool of Life Sciences, University of Sussex , Brighton, UK.ORCID 0000-0001-8476-0223
Lijin DongGenetic Engineering Core, National Eye Institute, NIH , Bethesda, MD, USA.ORCID 0000-0001-7401-9511
Peter G Barr-GillespieOregon Hearing Research Center, Oregon Health & Science University , Portland, OR, USA.ORCID 0000-0002-9787-5860
Michael HoaAuditory Development and Restoration Program, National Institute on Deafness and Other Communication Disorders, NIH , Bethesda, MD, USA.ORCID 0000-0001-7469-2909
Gregory I FrolenkovDepartment of Physiology, University of Kentucky, College of Medicine, Lexington, KY, USA.ORCID 0000-0002-9810-5024
Thomas B FriedmanLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, USA.ORCID 0000-0003-4614-6630
Bo ZhaoDepartment of Otolaryngology-Head and Neck Surgery, Indiana University School of Medicine, Indianapolis, IN, USA.ORCID 0000-0003-2881-5714
Funding
Mouse Auditory Testing Core FacilityZICDC000080 · NIDCD · NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS · PI FITZGERALD, TRACY · 2012 to 2025
$8.0M
Identification of Genes Causing Syndromic And Nonsyndromic Hearing ImpairmentZ01DC000039 · NIDCD · NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS · PI FRIEDMAN, THOMAS BAER · 1997 to 2008
$7.2M
Taperin-based macromolecular complex at the base of stereociliaR01DC017147 · NIDCD · INDIANA UNIVERSITY INDIANAPOLIS · PI Gregory I Frolenkov, Bo Zhao · 2018 to 2026
$3.9M
Cytoskeletal stability in stereocilia maintenanceR01DC015495 · NIDCD · INDIANA UNIVERSITY INDIANAPOLIS · PI BENJAMIN J PERRIN · 2017 to 2026
$3.9M
GIPC3, multifunctional myosin adaptor in mammalian auditory hair cellsR01DC019054 · NIDCD · UNIVERSITY OF KENTUCKY · PI FROLENKOV, GREGORY I, VANDER KOOI, CRAIG · 2020 to 2024
$2.8M
Molecular Mechanisms of Aminoglycoside OtotoxicityR01DC018785 · NIDCD · INDIANA UNIVERSITY INDIANAPOLIS · PI Bo Zhao · 2022 to 2026
$2.8M
Repair of mechano-electrical transduction in mammalian auditory hair cellsR01DC014658 · NIDCD · UNIVERSITY OF KENTUCKY · PI FROLENKOV, GREGORY I · 2015 to 2019
$2.0M
Advanced microscope technologies for single-molecule functional analyses of stereocilia components necessary for normal human hearingR00DC019949 · NIDCD · SOUTHERN ILLINOIS UNIVERSITY CARBONDALE · PI Takushi Miyoshi · 2024 to 2026
$728k
SPEECH AND HEARING SCIENCEST32DC000039 · NIDCD · CUNY GRADUATE SCH AND UNIV CTR · PI SCHWARTZ, RICHARD G · 1992 to 2002
$429k
High-Pressure Freezing / Freeze-Substitution SystemS10OD025130 · OD · UNIVERSITY OF KENTUCKY · PI FROLENKOV, GREGORY I · 2018 to 2018
Stereocilia are rod-like mechanosensory projections consisting of unidirectionally oriented actin filaments that extend into the inner ear hair cell cytoskeleton, forming dense rootlets. Taperin (TPRN) localizes to the narrowed-down base of stereocilia, where they pivot in response to sound and gravity. We show that TPRN-deficient mice have progressive deafness characterized by gradual asynchronous retraction and fusion of outer and inner hair cell stereocilia, followed by synaptic abnormalities. Stereocilia that lack TPRN develop warped rootlets with gradual loss of TRIOBP-5 and ANKRD24 from mechanosensory rows starting postnatally. In contrast, TPRN overexpression causes excessive F-actin bundling, extra rows, and over-elongation of stereocilia during development. Purified full-length mouse TPRN cross-links F-actin into bendable bundles reflecting in vivo data. This F-actin-bundling ability is attributed to the TPRN N-terminal region. TPRN interacts with the membrane receptor PTPRQ, connecting the F-actin core to the plasma membrane, stabilizing stereocilia. Thus, TPRN is a specialized F-actin bundler strategically located to augment stereocilia rootlet formation and their pivot point flexibility for sustained sound-induced deflections.
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 Socratic graph.
Taperin bundles F-actin at stereocilia pivot points enabling optimal lifelong mechanosensitivity. · full record | Socratic