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
1 · What the graph read from itWhat 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.
Arantxa Cebrian-SillaEli and Edythe Broad Institute for Stem Cell Research and Regeneration Medicine, University of California, San Francisco, CA 94143, USA.ORCID 0000-0003-4623-7655 Fiona R Dale-HuangEli and Edythe Broad Institute for Stem Cell Research and Regeneration Medicine, University of California, San Francisco, CA 94143, USA.
Stephanie A RedmondEli and Edythe Broad Institute for Stem Cell Research and Regeneration Medicine, University of California, San Francisco, CA 94143, USA.ORCID 0000-0002-5580-6269 Carmen Elena Aragon OrtizEli and Edythe Broad Institute for Stem Cell Research and Regeneration Medicine, University of California, San Francisco, CA 94143, USA.ORCID 0009-0004-6626-0320 Juan MorianosEli and Edythe Broad Institute for Stem Cell Research and Regeneration Medicine, University of California, San Francisco, CA 94143, USA.ORCID 0000-0001-6781-340X Marcos Assis NascimentoEli and Edythe Broad Institute for Stem Cell Research and Regeneration Medicine, University of California, San Francisco, CA 94143, USA.ORCID 0000-0002-9830-9801 Zhenmeiyu LiEli and Edythe Broad Institute for Stem Cell Research and Regeneration Medicine, University of California, San Francisco, CA 94143, USA.ORCID 0000-0002-4132-7486 Cristina GuintoEli and Edythe Broad Institute for Stem Cell Research and Regeneration Medicine, University of California, San Francisco, CA 94143, USA.
Susana González-GraneroBTELab, Research Foundation of the General University Hospital of Valencia, Valencia,46014, Spain.ORCID 0000-0003-1531-550X Ricardo Romero-RodriguezEli and Edythe Broad Institute for Stem Cell Research and Regeneration Medicine, University of California, San Francisco, CA 94143, USA.
Cathryn R CadwellDepartment of Neurological Surgery, University of California, San Francisco, CA 94143, USA.ORCID 0000-0003-1963-8285 Vicente Herranz-PérezLaboratory of Comparative Neurobiology, Cavanilles Institute of Biodiversity and Evolutionary Biology, University of Valencia and CIBERNED-ISCIII, Paterna, Valencia, 46980, Spain.ORCID 0000-0002-1969-1214 Jose Manuel Garcia-VerdugoLaboratory of Comparative Neurobiology, Cavanilles Institute of Biodiversity and Evolutionary Biology, University of Valencia and CIBERNED-ISCIII, Paterna, Valencia, 46980, Spain.ORCID 0000-0001-9872-6499 Arnold KriegsteinEli and Edythe Broad Institute for Stem Cell Research and Regeneration Medicine, University of California, San Francisco, CA 94143, USA.ORCID 0000-0001-5742-2990 Arturo Alvarez-BuyllaEli and Edythe Broad Institute for Stem Cell Research and Regeneration Medicine, University of California, San Francisco, CA 94143, USA.ORCID 0000-0003-4426-8925 Funding
NEUROGENESIS IN THE ADULT VERTEBRATE BRAINR01NS028478 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ALVAREZ-BUYLLA, ARTURO · 1996 to 2024
$8.6MThe Developmental Transition of Neural Stem Cell Niches in the Human BrainR35NS143000 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Arturo Alvarez-Buylla · 2025 to 2026
$2.4MStructure and function of a novel population of regenerating ependymal cellsR01NS113910 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ALVAREZ-BUYLLA, ARTURO · 2020 to 2024
$2.2MThe role of retinoic acid signaling in patterning the human cerebral cortexK08NS126573 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Cathryn Rene Cadwell · 2022 to 2026
$1.2MInvestigating Functional Ependymal Cell Heterogeneity in the Ventricular SystemK99NS121273 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI REDMOND, STEPHANIE · 2021 to 2022
$304kNINDS NIH HHS K08 NS126573NINDS NIH HHS K99 NS121273NINDS NIH HHS R01 NS028478NINDS NIH HHS R01 NS113910NINDS NIH HHS R35 NS143000
6 · The paper itselfAbstract
Ependymal (E1) cells, with their tufts of ~50 motile cilia, line the walls of the brain ventricles and help propel the cerebrospinal fluid (CSF). The CSF is rich in signaling molecules, but the cellular targets that detect these signals and their function remain unknown. Here, we describe a distinct population of ependymal cells (E2) in the forebrain of mice and humans, the majority having only 1 or 2 cilia. These cilia were motile, but unlike E1 cells' cilia, their pattern of motility and high expression of Arl13b and Inpp5e suggest a sensory function. E2 cells were characterized by an enormous, donut-like basal body that contained an increased number and size of subdistal appendages. In mice, E2 cells were mostly born in the embryo, but completed their differentiation in juveniles and young adults; they were found at higher densities in regions of high CSF flow and neurogenesis. E2 cilia contained the G protein-coupled receptor Smoothened, which accumulated in their cilia upon exposure to Sonic Hedgehog (Shh). Together, these findings identify E2 cells as a novel CSF-sensing ependymal cell type and provide a cellular target for the CSF signaling.
Indexed as
Cerebrospinal FluidCilia BeatingE1 cellsE2 cellsEpendymocytesShh signalingSubdistal AppendagesVentricular Zone
Identifiers
PMID42845561
PMCPMC13640753
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