The DOI matches its Crossref record; 63 of the 63 references it cites were found in a registry or an index.
Mechanical compartmentalization of the intestinal organoid enables crypt folding and collective cell migration
Open accessPublished version of a preprint
Abstract
Intestinal organoids capture essential features of the intestinal epithelium such as crypt folding, cellular compartmentalization and collective movements. Each of these processes and their coordination require patterned forces that are at present unknown. Here we map three-dimensional cellular forces in mouse intestinal organoids grown on soft hydrogels. We show that these organoids exhibit a non-monotonic stress distribution that defines mechanical and functional compartments. The stem cell compartment pushes the extracellular matrix and folds through apical constriction, whereas the transit amplifying zone pulls the extracellular matrix and elongates through basal constriction. The size of the stem cell compartment depends on the extracellular-matrix stiffness and endogenous cellular forces. Computational modelling reveals that crypt shape and force distribution rely on cell surface tensions following cortical actomyosin density. Finally, cells are pulled out of the crypt along a gradient of increasing tension. Our study unveils how patterned forces enable compartmentalization, folding and collective migration in the intestinal epithelium.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“perfusable microfluidic chips have also been developed to promote the long-term culture of organoids21,22,94.”
From Organoids (2022) · cites this paper as [94]
Experimental — accuracy not yet measuredThe check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“It has been shown that by maximizing the mass transfer and minimizing the shear stress in the perfusive soluble microenvironment, cells grown in organ-on-a-chip set-ups upregulate their functions, getting a step closer to a native tissue94,244,245.”
From Organoids (2022) · cites this paper as [94]
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Fiji: an open-source platform for biological-image analysis
Schindelin, J., Arganda-Carreras, I., Frise, E., Kaynig, V., Longair, M., Pietzsch, T., Preibisch, S., Rueden, C., Saalfeld, S., Schmid, B., et al. (2012) · Nature Methods · doi:10.1038/nmeth.2019 · Cited by 66,890
Matrix elasticity directs stem cell lineage specification
Engler, A. J., Sen, S., Sweeney, H. L., & Discher, D. E. (2006) · Cell · doi:10.1016/j.cell.2006.06.044 · Cited by 13,915
Single Lgr5 stem cells build crypt-villus structures in vitro without a mesenchymal niche
Sato, T., Vries, R. G., Snippert, H. J., van de Wetering, M., Barker, N., Stange, D. E., van Es, J. H., Abo, A., Kujala, P., Peters, P. J., et al. (2009) · Nature · doi:10.1038/nature07935 · Cited by 7,204
Identification of stem cells in small intestine and colon by marker gene Lgr5
Barker, N., van Es, J. H., Kuipers, J., Kujala, P., van den Born, M., Cozijnsen, M., Haegebarth, A., Korving, J., Begthel, H., Peters, P. J., et al. (2007) · Nature · doi:10.1038/nature06196 · Cited by 5,687
Cell Shape, Cytoskeletal Tension, and RhoA Regulate Stem Cell Lineage Commitment
McBeath, R., Pirone, D. M., Nelson, C. M., Bhadriraju, K., & Chen, C. S. (2004) · Developmental Cell · doi:10.1016/s1534-5807(04)00075-9 · Cited by 4,182
A global double-fluorescent Cre reporter mouse
Muzumdar, M. D., Tasic, B., Miyamichi, K., Li, L., & Luo, L. (2007) · genesis · doi:10.1002/dvg.20335 · Cited by 3,491
Paneth cells constitute the niche for Lgr5 stem cells in intestinal crypts
Sato, T., van Es, J. H., Snippert, H. J., Stange, D. E., Vries, R. G., van den Born, M., Barker, N., Shroyer, N. F., van de Wetering, M., & Clevers, H. (2011) · Nature · doi:10.1038/nature09637 · Cited by 2,510
Snippert, H. J., van der Flier, L. G., Sato, T., van Es, J. H., van den Born, M., Kroon-Veenboer, C., Barker, N., Klein, A. M., van Rheenen, J., Simons, B. D., et al. (2010) · Cell · doi:10.1016/j.cell.2010.09.016 · Cited by 1,951
Advanced methods of microscope control using μManager software
Edelstein, A., Tsuchida, M. A., Amodaj, N., Pinkard, H., Vale, R. D., & Stuurman, N. (2014) · Journal of Biological Methods · doi:10.14440/jbm.2014.36 · Cited by 1,927
Directed differentiation of human pluripotent stem cells into intestinal tissue in vitro
Spence, J. R., Mayhew, C. N., Rankin, S. A., Kuhar, M. F., Vallance, J. E., Tolle, K. A., Hoskins, E. E., Kalinichenko, V. V., Wells, S. I., Zorn, A. M., et al. (2010) · Nature · doi:10.1038/nature09691 · Cited by 1,911
Designer matrices for intestinal stem cell and organoid culture
Gjorevski, N., Sachs, N., Manfrin, A., Giger, S., Bragina, M. E., Ordóñez-Morán, P., Clevers, H., & Lutolf, M. P. (2016) · Nature · doi:10.1038/nature20168 · Cited by 1,426
The intestinal crypt, a prototype stem cell compartment
Clevers, H. (2013) · Cell · doi:10.1016/j.cell.2013.07.004 · Cited by 1,223
Physical forces during collective cell migration
Trepat, X., Wasserman, M. R., Angelini, T. E., Millet, E. J., Weitz, D. A., Butler, J. P., & Fredberg, J. J. (2009) · Nature Physics · doi:10.1038/nphys1269 · Cited by 1,198
Self-citationGrowing Self-Organizing Mini-Guts from a Single Intestinal Stem Cell: Mechanism and Applications
Sato, T., & Clevers, H. (2013) · Science · doi:10.1126/science.1234852 · Cited by 1,170
Collective cell guidance by cooperative intercellular forces
Tambe, D. T., Hardin, C., Angelini, T. E., Rajendran, K., Park, C. Y., Serra‐Picamal, X., Zhou, E. H., Zaman, M. H., Butler, J. P., Weitz, D. A., et al. (2010) · Nature Materials · doi:10.1038/nmat3025 · Cited by 942
Self-citationForce mapping in epithelial cell migration
du Roure, O., Saez, A., Buguin, A., Austin, R. H., Chavrier, P., Silberzan, P., & Ladoux, B. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0408482102 · Cited by 780
Homeostatic mini-intestines through scaffold-guided organoid morphogenesis
Nikolaev, M., Mitrofanova, O., Broguiere, N., Geraldo, S., Dutta, D., Tabata, Y., Elci, B., Brandenberg, N., Kolotuev, I., Gjorevski, N., et al. (2020) · Nature · doi:10.1038/s41586-020-2724-8 · Cited by 755
Development of a primary human Small Intestine-on-a-Chip using biopsy-derived organoids
Kasendra, M., Tovaglieri, A., Sontheimer-Phelps, A., Jalili-Firoozinezhad, S., Bein, A., Chalkiadaki, A., Scholl, W., Zhang, C., Rickner, H., Richmond, C. A., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-21201-7 · Cited by 754
Measurement of mechanical tractions exerted by cells in three-dimensional matrices
Legant, W. R., Miller, J. S., Blakely, B. L., Cohen, D. M., Genin, G. M., & Chen, C. S. (2010) · Nature Methods · doi:10.1038/nmeth.1531 · Cited by 657
Tissue Geometry Determines Sites of Mammary Branching Morphogenesis in Organotypic Cultures
Nelson, C. M., VanDuijn, M. M., Inman, J. L., Fletcher, D. A., & Bissell, M. J. (2006) · Science · doi:10.1126/science.1131000 · Cited by 616
Villification: How the Gut Gets Its Villi
Shyer, A. E., Tallinen, T., Nerurkar, N. L., Wei, Z., Gil, E. S., Kaplan, D. L., Tabin, C. J., & Mahadevan, L. (2013) · Science · doi:10.1126/science.1238842 · Cited by 549
MorphoGraphX: A platform for quantifying morphogenesis in 4D
de Reuille, P. B., Routier‐Kierzkowska, A., Kierzkowski, D., Bassel, G. W., Schuepbach, T., Tauriello, G., Bajpai, N., Strauss, S., Weber, A. R., Kiss, A., et al. (2015) · eLife · doi:10.7554/elife.05864 · Cited by 542
Interplay between metabolic identities in the intestinal crypt supports stem cell function
Rodríguez-Colman, M. J., Schewe, M., Meerlo, M., Stigter, E., Gerrits, J., Pras-Raves, M., Sacchetti, A., Hornsveld, M., Oost, K. C., Snippert, H. J., et al. (2017) · Nature · doi:10.1038/nature21673 · Cited by 522
Apical constriction: themes and variations on a cellular mechanism driving morphogenesis
Martin, A. C., & Goldstein, B. (2014) · Development · doi:10.1242/dev.102228 · Cited by 502
Intestinal crypt homeostasis revealed at single-stem-cell level by in vivo live imaging
Ritsma, L., Ellenbroek, S. I. J., Zomer, A., Snippert, H. J. G., de Sauvage, F. J., Simons, B. D., Clevers, H. C., & van Rheenen, J. (2014) · Nature · doi:10.1038/nature12972 · Cited by 501
Vertex models: from cell mechanics to tissue morphogenesis
Alt, S., Ganguly, P. S., & Salbreux, G. (2017) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2015.0520 · Cited by 433
Hydraulic control of mammalian embryo size and cell fate
Chan, C. J., Costanzo, M., Ruiz-Herrero, T., Mönke, G., Petrie, R. J., Bergert, M., Diz-Muñoz, A., Mahadevan, L., & Hiiragi, T. (2019) · Nature · doi:10.1038/s41586-019-1309-x · Cited by 344
Lifeact mice for studying F-actin dynamics
Riedl, J., Flynn, K. C., Raducanu, A., Gärtner, F. C., Beck, G., Bösl, M. R., Bradke, F., Maßberg, S., Aszódi, A., Sixt, M., et al. (2010) · Nature Methods · doi:10.1038/nmeth0310-168 · Cited by 333
Active superelasticity in three-dimensional epithelia of controlled shape
Latorre, E., Kale, S., Casares, L., Gómez‐González, M., Uroz, M., Valon, L., Nair, R. V., Garreta, E., Montserrat, N., del Campo, A., et al. (2018) · Nature · doi:10.1038/s41586-018-0671-4 · Cited by 324
Self-citationChase-and-run between adjacent cell populations promotes directional collective migration
Théveneau, E., Steventon, B., Scarpa, E., García, S., Trepat, X., Streit, A., & Mayor, R. (2013) · Nature Cell Biology · doi:10.1038/ncb2772 · Cited by 321
Self-citationQuantifying cellular traction forces in three dimensions
Maskarinec, S. A., Franck, C., Tirrell, D. A., & Ravichandran, G. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0904565106 · Cited by 297
Growth of Epithelial Organoids in a Defined Hydrogel
Broguiere, N., Isenmann, L., Hirt, C., Ringel, T., Placzek, S., Cavalli, E., Ringnalda, F., Villiger, L., Züllig, R., Lehmann, R., et al. (2018) · Advanced Materials · doi:10.1002/adma.201801621 · Cited by 282
Theory of epithelial sheet morphology in three dimensions
Hannezo, É., Prost, J., & Joanny, J. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1312076111 · Cited by 256
Active cell migration is critical for steady-state epithelial turnover in the gut
Krndija, D., Marjou, F. E., Guirao, B., Richon, S., Leroy, O., Bellaı̈che, Y., Hannezo, É., & Vignjevic, D. M. (2019) · Science · doi:10.1126/science.aau3429 · Cited by 234
Self-citationActive wetting of epithelial tissues
Gonzalez, C. P., Alert, R., Blanch-Mercader, C., Gómez-González, M., Kolodziej, T., Bazellières, E., Casademunt, J., & Trepat, X. (2018) · Nature Physics · doi:10.1038/s41567-018-0279-5 · Cited by 221
Self-citationMorphogenesis and Compartmentalization of the Intestinal Crypt
Sumigray, K., Terwilliger, M., & Lechler, T. (2018) · Developmental Cell · doi:10.1016/j.devcel.2018.03.024 · Cited by 202
Signaling in the stem cell niche: regulating cell fate, function and plasticity
Chacón‐Martínez, C. A., Koester, J., & Wickström, S. A. (2018) · Development · doi:10.1242/dev.165399 · Cited by 197
Mouse models of MYH9-related disease: mutations in nonmuscle myosin II-A
Zhang, Y., Conti, M. A., Malide, D. A., Dong, F., Wang, A., Shmist, Y. A., Liu, C., Zerfas, P. M., Daniels, M. P., Chan, C., et al. (2011) · Blood · doi:10.1182/blood-2011-06-358853 · Cited by 185
Cell fate coordinates mechano-osmotic forces in intestinal crypt formation
Yang, Q., Xue, S.-L., Chan, C. J., Rempfler, M., Vischi, D., Maurer-Gutierrez, F., Hiiragi, T., Hannezo, E., & Liberali, P. (2021) · Nature Cell Biology · doi:10.1038/s41556-021-00700-2 · Cited by 183
Thorne, C. A., Chen, I. W., Sanman, L. E., Cobb, M. H., Wu, L. F., & Altschuler, S. J. (2018) · Developmental Cell · doi:10.1016/j.devcel.2018.01.024 · Cited by 174
Engineered Tissue Folding by Mechanical Compaction of the Mesenchyme
Hughes, A. J., Miyazaki, H., Coyle, M. C., Zhang, J., Laurie, M. T., Chu, D. B., Vavrušová, Z., Schneider, R. A., Klein, O. D., & Gartner, Z. J. (2017) · Developmental Cell · doi:10.1016/j.devcel.2017.12.004 · Cited by 173
Instabilities of Monolayered Epithelia: Shape and Structure of Villi and Crypts
Hannezo, É., Prost, J., & Joanny, J. (2011) · Physical Review Letters · doi:10.1103/physrevlett.107.078104 · Cited by 171
Hedgehog-responsive mesenchymal clusters direct patterning and emergence of intestinal villi
Walton, K. D., Kolterud, Å., Czerwinski, M. J., Bell, M. J., Prakash, A., Kushwaha, J. S., Grosse, A. S., Schnell, S. D., & Gumucio, D. L. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1205669109 · Cited by 166
Sui, L., Alt, S., WEIGERT, M. G., Dye, N. A., Eaton, S., Jug, F., Myers, E. W., Jülicher, F., Salbreux, G., & Dahmann, C. (2018) · Nature Communications · doi:10.1038/s41467-018-06497-3 · Cited by 165
Altay, G., Larrañaga, E., Tosi, S., Barriga, F. M., Batlle, E., Fernández‐Majada, V., & Martínez, E. (2019) · Scientific Reports · doi:10.1038/s41598-019-46497-x · Cited by 141
Self-citationMicrofluidic chest cavities reveal that transmural pressure controls the rate of lung development
Nelson, C. M., Gleghorn, J. P., Pang, M.-F., Jaslove, J. M., Goodwin, K., Varner, V. D., Miller, E. E., Radisky, D. C., & Stone, H. A. (2017) · Development · doi:10.1242/dev.154823 · Cited by 131
A geometrically controlled rigidity transition in a model for confluent 3D tissues
Merkel, M., & Manning, M. L. (2018) · New Journal of Physics · doi:10.1088/1367-2630/aaaa13 · Cited by 129
Parker, A., Maclaren, O. J., Fletcher, A. G., Muraro, D., Kreuzaler, P. A., Byrne, H. M., Maini, P. K., Watson, A. J. M., & Pin, C. (2016) · The FASEB Journal · doi:10.1096/fj.201601002 · Cited by 124
Buckling of an Epithelium Growing under Spherical Confinement
Trushko, A., Meglio, I. D., Merzouki, A., Blanch-Mercader, C., Abuhattum, S., Guck, J. R., Alessandri, K., Nassoy, P., Kruse, K., Bastien Chopard, B., et al. (2020) · Developmental Cell · doi:10.1016/j.devcel.2020.07.019 · Cited by 120
Buckling Instabilities of One-Layered Growing Tissues
Drasdo, D. (2000) · Physical Review Letters · doi:10.1103/physrevlett.84.4244 · Cited by 118
Planar Differential Growth Rates Initiate Precise Fold Positions in Complex Epithelia
Tozluoǧlu, M., Duda, M., Kirkland, N. J., Barrientos, R., Burden, J. J., Muñoz, J. J., & Mao, Y. (2019) · Developmental Cell · doi:10.1016/j.devcel.2019.09.009 · Cited by 103
Verhulsel, M., Simon, A. Y., Bernheim-Dennery, M., Gannavarapu, V. R., Gérémie, L., Ferraro, D., Krndija, D., Talini, L., Viovy, J., Vignjevic, D. M., et al. (2020) · Lab on a Chip · doi:10.1039/d0lc00672f · Cited by 103
Self-citationActive wetting of epithelial tissues
Gonzalez, C. P., Alert Zenón, R., Blanch-Mercader, C., Gómez González, M., Kołodziej, T., Bazellières, E., Casademunt i Viader, J., & Trepat Guixer, X. (2017) · Dipòsit Digital de la Universitat de Barcelona (Universitat de Barcelona) · Cited by 99
Self-citationRadially patterned cell behaviours during tube budding from an epithelium
Sánchez-Corrales, Y. E., Blanchard, G. B., & Röper, K. (2018) · eLife · doi:10.7554/elife.35717 · Cited by 96
McKinley, K. L., Stuurman, N., Royer, L. A., Schartner, C., Castillo‐Azofeifa, D., Delling, M., Klein, O. D., & Vale, R. D. (2018) · eLife · doi:10.7554/elife.36739 · Cited by 95
Uncoupling apical constriction from tissue invagination
Chung, S., Kim, S., & Andrew, D. J. (2017) · eLife · doi:10.7554/elife.22235 · Cited by 91
A Protocol for Lentiviral Transduction and Downstream Analysis of Intestinal Organoids
de Jeude, J. F. V. L., Vermeulen, J. L. M., Montenegro-Miranda, P. S., BRINK, G. R. V. D., & Heijmans, J. (2015) · Journal of Visualized Experiments · doi:10.3791/52531 · Cited by 81
Collective cell guidance by cooperative intercellular forcesPreprint
Tambe, D. T., Hardin, C. C., Fredberg, J. J., & Trepat, X. (2010) · Nature Precedings · doi:10.1038/npre.2010.5405.1 · Cited by 55
Self-citationMonolayer culture of intestinal epithelium sustains Lgr5+ intestinal stem cells
Liu, Y., Qi, Z., Li, X., Du, Y., & Chen, Y. (2018) · Cell Discovery · doi:10.1038/s41421-018-0036-z · Cited by 51
Geometric constraints alter cell arrangements within curved epithelial tissues
Rupprecht, J.-F., Ong, K. H., Yin, J., Huang, A., Dinh, H.-H.-Q., Singh, A. P., Zhang, S., Yu, W., & Saunders, T. E. (2017) · Molecular Biology of the Cell · doi:10.1091/mbc.e17-01-0060 · Cited by 50
Almet, A. A., Maini, P. K., Moulton, D. E., & Byrne, H. M. (2020) · Current Opinion in Biomedical Engineering · doi:10.1016/j.cobme.2019.12.012 · Cited by 26
Cell fate coordinates mechano-osmotic forces in intestinal crypt morphogenesisPreprint
Yang, Q., Xue, S.-L., Chan, C. J., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.05.13.094359 · Cited by 21
Buckling of epithelium growing under spherical confinementPreprint
Trushko, A., Meglio, I. D., Merzouki, A., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/513119 · Cited by 15
Cited by
Sorted by citations
Zhao, Z., Chen, X., Dowbaj, A. M., Sljukic, A., Bratlie, K., Lin, L., Fong, E. L. S., Balachander, G. M., Chen, Z., Soragni, A., et al. (2022) · Nature Reviews Methods Primers · doi:10.1038/s43586-022-00174-y · Cited by 1,082
Cell fate coordinates mechano-osmotic forces in intestinal crypt formation
Yang, Q., Xue, S.-L., Chan, C. J., Rempfler, M., Vischi, D., Maurer-Gutierrez, F., Hiiragi, T., Hannezo, E., & Liberali, P. (2021) · Nature Cell Biology · doi:10.1038/s41556-021-00700-2 · Cited by 183
Curvature in Biological Systems: Its Quantification, Emergence, and Implications across the Scales
Schamberger, B., Ziege, R., Anselme, K., Amar, M. B., Bykowski, M., Castro, A. P. G., Cipitria, A., Coles, R., Dimova, R., Eder, M., et al. (2022) · Advanced Materials · doi:10.1002/adma.202206110 · Cited by 174
Self-citationHarnessing Mechanobiology for Tissue Engineering
Kim, S., Uroz, M., Bays, J., & Chen, C. S. (2021) · Developmental Cell · doi:10.1016/j.devcel.2020.12.017 · Cited by 141
Mechanical state transitions in the regulation of tissue form and function
Mao, Y., & Wickström, S. A. (2024) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-024-00719-x · Cited by 143
Metadata
- Authors
- Pérez-González, C., Ceada, G., Greco, F., Matejčić, M., Gómez-González, M., Castro, N., Menendez, A., Kale, S., Krndija, D., Clark, A. G., Gannavarapu, V. R., Álvarez-Varela, A., Roca-Cusachs, P., Batlle, E., Vignjevic, D. M., Arroyo, M., & Trepat, X.
- Affiliations
- Barcelona Institute of Science and Technology (ES)
- Universitat Politècnica de Catalunya (ES)
- Virginia Tech (US)
- Centre National de la Recherche Scientifique (FR)
- Institute for Research in Biomedicine (ES)
- Institució Catalana de Recerca i Estudis Avançats (ES)
- International Center for Numerical Methods in Engineering (ES)
- Corresponding author
- Vignjevic, Danijela Matic
- Arroyo, Marino
- Trepat, Xavier
- ORCID
- Venue
- Nature Cell Biology
- Published
- 2021-06-21
- Volume
- 23
- Issue
- 7
- Pages
- 745-757
- ISSN
- 1465-7392 (ISSN-L)
- 1476-4679
- PMC
- PMC7611697
- OpenAlex
- W3174575177
- Cited by
- 225
- References
- 61
- Citations by year
- 2026: 33 · 2025: 57 · 2024: 46 · 2023: 31 · 2022: 42 · 2021: 16
- FWCI
- 17.63
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nature Cell Biology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- HAL (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
- Physical Sciences › Engineering › Biomedical Engineering › 3D Printing in Biomedical Research
- Health Sciences › Medicine › Oncology › Cancer Cells and Metastasis
- Keywords
- intestinal organoids, collective cell migration, cellular forces, extracellular matrix stiffness, stem cell compartment, transit amplifying cells, apical constriction, cell surface tension, hydrogel substrates, intestinal epithelium
- MeSH terms
- Animals, Cell Communication, Cell Movement, Cells, Cultured, Computer Simulation, Epithelial Cells, Female, Intestinal Mucosa, Male, Mice, Transgenic, Models, Biological, Organoids, Stress, Mechanical, Surface Tension, Time Factors, Microscopy, Confocal, Cell-Matrix Junctions, Mechanotransduction, Cellular
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review