The DOI matches its Crossref record; 38 of the 38 references it cites were found in a registry or an index.
Visualization of a short-range Wnt gradient in the intestinal stem-cell niche
Abstract
Mammalian Wnt proteins are believed to act as short-range signals, yet have not been previously visualized in vivo. Self-renewal, proliferation and differentiation are coordinated along a putative Wnt gradient in the intestinal crypt. Wnt3 is produced specifically by Paneth cells. Here we have generated an epitope-tagged, functional Wnt3 knock-in allele. Wnt3 covers basolateral membranes of neighbouring stem cells. In intestinal organoids, Wnt3-transfer involves direct contact between Paneth cells and stem cells. Plasma membrane localization requires surface expression of Frizzled receptors, which in turn is regulated by the transmembrane E3 ligases Rnf43/Znrf3 and their antagonists Lgr4-5/R-spondin. By manipulating Wnt3 secretion and by arresting stem-cell proliferation, we demonstrate that Wnt3 mainly travels away from its source in a cell-bound manner through cell division, and not through diffusion. We conclude that stem-cell membranes constitute a reservoir for Wnt proteins, while Frizzled receptor turnover and 'plasma membrane dilution' through cell division shape the epithelial Wnt3 gradient.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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?
In the citing paper
“Because it was recently reported that Wnt3 transfer requires direct cell contact and has only a very limited range (Farin et al., 2016), the most likely cellular source of Wnts that influence Wnt signaling upon aging might thus be mostly Paneth cells and, in part, mesenchyme.”
From Canonical Wnt Signaling Ameliorates Aging of Intestinal Stem Cells (2017) · cites this paper as Farin et al., 2016
In the citing paper
“Because it was recently reported that Wnt3 transfer requires direct cell contact and has only a very limited range (Farin et al., 2016)”
From Canonical Wnt Signaling Ameliorates Aging of Intestinal Stem Cells (2017) · cites this paper as Farin et al., 2016
Citations
Cites
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
Self-citationIdentification 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
Self-citationPaneth 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
Self-citationSchwank, G., Koo, B.-K., Sasselli, V., Dekkers, J. F., Heo, I., Demircan, T., Sasaki, N., Boymans, S., Cuppen, E., van der Ent, C. K., et al. (2013) · Cell Stem Cell · doi:10.1016/j.stem.2013.11.002 · Cited by 1,424
Self-citationSmall molecule–mediated disruption of Wnt-dependent signaling in tissue regeneration and cancer
Chen, B., Dodge, M. E., Tang, W., Lü, J., Ma, Z., Fan, C.-W., Wei, S., Hao, W., Kilgore, J. A., Williams, N. S., et al. (2009) · Nature Chemical Biology · doi:10.1038/nchembio.137 · Cited by 1,402
The intestinal crypt, a prototype stem cell compartment
Clevers, H. (2013) · Cell · doi:10.1016/j.cell.2013.07.004 · Cited by 1,223
Self-citationTissue‐specific and inducible Cre‐mediated recombination in the gut epithelium
Marjou, F. E., Janssen, K., Chang, B. H., Li, M., Hindie, V., Chan, L., Louvard, D., Chambon, P., METZGER, D., & Robine, S. (2004) · genesis · doi:10.1002/gene.20042 · Cited by 1,087
Tumour suppressor RNF43 is a stem-cell E3 ligase that induces endocytosis of Wnt receptors
Koo, B.-K., Spit, M., Jordens, I., Low, T. Y., Stange, D. E., van de Wetering, M., van Es, J. H., Mohammed, S., Heck, A. J. R., Maurice, M. M., et al. (2012) · Nature · doi:10.1038/nature11308 · Cited by 980
Self-citationZNRF3 promotes Wnt receptor turnover in an R-spondin-sensitive manner
Hao, H.-X., Xie, Y., Zhang, Y., Charlat, O., Oster, E., Avello, M., Lei, H., Mickanin, C., Liu, D., Ruffner, H., et al. (2012) · Nature · doi:10.1038/nature11019 · Cited by 962
Structural Basis of Wnt Recognition by Frizzled
Janda, C. Y., Waghray, D., Levin, A. M., Thomas, C., & García, K. C. (2012) · Science · doi:10.1126/science.1222879 · Cited by 901
Flagged first, then by citations
Cited by
Sorted by citations
Items 401–500 of 525
Hydrogel design for intestinal organoids: principles governing translational regenerative medicine
Wang, Y., Cao, Z., Li, B., Huang, Y., Wang, G., & Chen, Q. (2025) · Biomaterials Science · doi:10.1039/d5bm00926j · Cited by 3
Application and prospects of organoid-on-a-chip in research on the intestinal mucosal barrier
Qian, K., Wang, Y., Li, R. Q., Zhuang, M., Zhao, Z., Meng, C., Zhou, J., Wang, W., & Sun, Y. J. (2026) · Burns & Trauma · doi:10.1093/burnst/tkag029 · Cited by 4
Rewinding the clock: mechanisms of dedifferentiation
Raz, A. A., & Yamashita, Y. M. (2025) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2025.102353 · Cited by 3
Archana, R., Rajendran, R. L., Gangadaran, P., & Raja, N. S. (2025) · Gene · doi:10.1016/j.gene.2025.149640 · Cited by 3
Shinozuka, T., Okubo, T., Sasai, N., & Takada, S. (2025) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2025.1571770 · Cited by 3
Developmental Biology-Based 3D Bioprinting: An Off-the-Shelf Strategy to Induce Tissue Regeneration
Chakraborty, J., & Ghosh, S. (2025) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.5c00213 · Cited by 4
Planar cell polarity emerges through polarized accumulation of Wnt11
Mii, Y., Suzuki, M., Koyama, H., Nakayama, K., Takada, R., Kobayashi, T., Tsutsumi, M., Nemoto, T., Matsuyama, M., Fujimori, T., et al. (2026) · Science Advances · doi:10.1126/sciadv.aea0326 · Cited by 3
Heparan Sulfate Clusters Regulate Distribution and Signaling of Wnt Morphogens
Mii, Y. (2020) · Trends in Glycoscience and Glycotechnology · doi:10.4052/tigg.2006.7e · Cited by 3
A Holistic Analysis of the Intestinal Stem Cell Niche NetworkPreprint
Hansen, D. M., Meneses-Giles, P., He, X., Chen, S., Paulson, A., Dekaney, C. M., Wang, J. X., Hu, D., Venkatraman, A., Kim, W., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2019.12.12.871756 · Cited by 3
van de Grift, Y. V. D., Aarts, M. T., Wiese, K. E., Heijmans, N., Hooijkaas, I. B., Pritchard, C. E. J., Henneman, L., Krimpenfort, P., van Boxtel, A. V., & van Amerongen, R. (2025) · bioRxiv · doi:10.1101/2025.04.11.648333 · Cited by 1
Ghasemi, N., Azizi, H., & Skutella, T. (2025) · IntechOpen eBooks · doi:10.5772/intechopen.1010865 · Cited by 3
Scharr, M., Scherer, S., Fuchs, J., Hirt, B., & Neckel, P. H. (2025) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2025.101642 · Cited by 2
From Embryo to Colony: The Role of Wnt Signaling Pathways in Body Plan Formation in Cnidaria
Vetrova, A. A., & Kremnyov, S. V. (2025) · Paleontological Journal · doi:10.1134/s0031030125600775 · Cited by 2
Philippi, M., Dohle, J., Watrinet, I., Holtmannspötter, M., Li, J., Birkholz, O., Miao, Y., Rothbauer, U., García, K. C., Kurre, R., et al. (2026) · Science Signaling · doi:10.1126/scisignal.adr8141 · Cited by 3
Multitasking Paneth Cells in the Intestinal Stem Cell Niche
Schewe, M., & Fodde, R. (2018) · Advances in stem cells and their niches · doi:10.1016/bs.asn.2017.12.001 · Cited by 2
Visualizing WNT signaling in mammalian systems
van der Wal, T., & van Amerongen, R. (2023) · Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2023.02.001 · Cited by 2
Responses of organ precursors to correct and incorrect inductive signals
Yang, Y., Li, S., & Luo, L. (2023) · Trends in Cell Biology · doi:10.1016/j.tcb.2023.08.008 · Cited by 2
In toto biological framework: Modeling interconnectedness during human development
Yoneyama, Y., Wu, Y., Mori, K., & Takebe, T. (2025) · Developmental Cell · doi:10.1016/j.devcel.2024.09.027 · Cited by 2
WNT7B drives a program for pancreatic cancer subtype switching and progression
Sprangers, J., Bugter, J. M., Xanthakis, D., Boekhout, M., Kok, R. N. U., Geurts, V., Clevers, H. C., Brosens, L. A. A., Dijk, F., Colman, M. J. R., et al. (2026) · iScience · doi:10.1016/j.isci.2026.115050 · Cited by 3
Self-citationIntestinal Stem Cells and Their Defining Niche
Trentesaux, C., & Romagnolo, B. (2018) · Advances in stem cells and their niches · doi:10.1016/bs.asn.2017.12.003 · Cited by 2
Epigenetically distinct sister chromatids and asymmetric generation of tumor initiating cells
Liu, Y., Siles, L., Postigo, A. A., & Dean, D. C. (2018) · Cell Cycle · doi:10.1080/15384101.2018.1532254 · Cited by 2
Agent-Based Modelling to Delineate Spatiotemporal Control Mechanisms of the Stem Cell Niche
Mines, R. C., Chen, K., & Shen, X. (2019) · Methods in molecular biology · doi:10.1007/978-1-4939-9224-9_1 · Cited by 2
Tiny Drosophila intestinal stem cells, big power
Zhai, J., Li, W., Liu, X., Wang, D., Zhang, D., Liu, Y., Liang, X., & Chen, Z. (2022) · Cell Biology International · doi:10.1002/cbin.11911 · Cited by 2
Suzuki, M., Takada, S., & Mii, Y. (2024) · Development Growth & Differentiation · doi:10.1111/dgd.12915 · Cited by 2
Esposito, A. (2021) · Royal Society Open Science · doi:10.1098/rsos.201532 · Cited by 2
Evidence of functional long-range Wnt/Wg in the developing Drosophila wing epitheliumPreprint
Chaudhary, V., & Boutros, M. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/412627 · Cited by 2
Establishment of Wnt ligand-receptor organization and cell polarity in the C. elegans embryoPreprint
Recouvreux, P., Pai, P., Torro, R., Ludányi, M., Mélénec, P., Boughzala, M., Bertrand, V., & Lenne, P. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.01.17.524363 · Cited by 2
Cadherin-linked morphogen gradient actualizes robust tissue patterning
Ishitani, T. (2023) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2023.102275 · Cited by 1
Mechanics of serotonin-producing human entero-endocrine cells
Evers, T. M. J., Beumer, J., Clevers, H. C., & Mashaghi, A. (2024) · Mechanobiology in Medicine · doi:10.1016/j.mbm.2024.100044 · Cited by 2
Self-citationWang, Y.-W., Li, Q.-Y., Liu, L.-F., Tan, X., Wang, W., Sun, J., & Wang, W. (2025) · Gastroenterology report · doi:10.1093/gastro/goaf031 · Cited by 1
Ruan, F., Li, L., Wu, M., Xue, F., Fu, Z., Zhang, F., Zuo, Z., Bu, L., Zeng, F., & He, C. (2025) · ACS Applied Bio Materials · doi:10.1021/acsabm.5c00910 · Cited by 1
Eli, S., Rauso, G., Ghezzi, P., Szczerkowski, J. L. A., Bruzzi, M., Rizzelli, F., Iommazzo, F., Loffreda, A., Castagna, F., Donà, F., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-65775-z · Cited by 1
Structural basis of Wnt signalosome extracellular complex assembly
Yue, D., Sun, G., Cao, Y., Li, H., Yang, Y., Pan, Z., Xue, L., Zhang, L., Wang, Z., & Xu, W. (2026) · Cell · doi:10.1016/j.cell.2026.05.006 · Cited by 2
Cell differentiation can underpin the reproducibility of morphogenesis
Devlin, D. K., Ganley, A. R. D., & Takeuchi, N. (2026) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1014361 · Cited by 1
Translational insights and clinical challenges of targeting cancer stem cells
Ahmed, M., Al-Haidari, A., Agarwal, S., Sun, J., Hammarlund, E. U., Rönnstrand, L., Pienta, K. J., Tatlı, Ö., & Kazi, J. U. (2026) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-026-02887-y · Cited by 1
Haemodynamic control of zonated liver function via instructive vascular Wnt signalling
Lee, K. H., Jakab, M., Uvarovskii, A., Papageorgiou, D. N., Inverso, D., Shi, J., Riedel, M., Gehrs, S., Kulkarni, S., Bobe, S., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-76966-7 · Cited by 1
Biophysics of lumen morphogenesis
Lee, B. H., Mukenhirn, M., Guyomar, T., Maggipinto, Y., Tanida, S., Fuji, K., Lu, L., Rømer, F., Nonomura, M., Hiraiwa, T., et al. (2026) · Development · doi:10.1242/dev.205628 · Cited by 1
Seeing is believing: Wnt3 localization in the gut epithelium
Gregorieff, A., & Wrana, J. L. (2016) · Cell Research · doi:10.1038/cr.2016.41 · Cited by 1
Takata, N., Sakakura, E., Sakuma, T., & Yamamoto, T. (2017) · Methods in molecular biology · doi:10.1007/978-1-4939-7108-4_19 · Cited by 1
Paneth cell differentiation associated with neoadjuvant therapy in esophageal adenocarcinoma
Ramineni, M., Findeis, S. K., Ye, J., & Hao, Y. (2024) · American Journal of Clinical Pathology · doi:10.1093/ajcp/aqae098 · Cited by 1
Synthetically programming natural cell–cell communication pathways for tissue engineering
Wallach, L. A., Thomas, C. D., & Li, P. (2024) · Current Opinion in Biomedical Engineering · doi:10.1016/j.cobme.2024.100554 · Cited by 1
Wang, L., Guo, W., Tian, Y., Wang, J., Xu, S., Shu, W., Liang, H., & Chen, M. (2024) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2024.135129 · Cited by 1
Hayashi, S., Suzuki, H., Takada, S., & Takemoto, T. (2024) · Developmental Biology · doi:10.1016/j.ydbio.2025.03.015 · Cited by 1
The interplay between genetics, the microbiome, DNA‐methylation & gene‐expression
Bonder, M. J. (2017) · Cited by 1
Recreating stem-cell niches using self-assembling biomaterials
Avolio, L. N., Sipes, D., Stephanopoulos, N., & Sur, S. (2018) · Elsevier eBooks · doi:10.1016/b978-0-08-102015-9.00021-6 · Cited by 1
Spatial Patterning from an Integrated Wnt/β-catenin and Notch/Delta Gene Circuit
Mines, R. C., Dohlman, A. B., Lim, S.-X., Tung, K., Wang, E., & Shen, X. (2018) · Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) · doi:10.1109/embc.2018.8513462 · Cited by 1
Inter-cellular Interactions and Patterns: Vertebrate Development and Embryonic Stem CellsPreprint
Siggia, E. D. (2018) · arXiv (Cornell University) · doi:10.48550/arxiv.1801.09142 · Cited by 2
Fontenete, S., Christensen, J., Martínez-Silgado, A., Zarzuela, E., Muñoz, J., Megı́as, D., Castellana, D., Loewe, R. P., & Pérez‐Moreno, M. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.07.17.209338 · Cited by 1
Philippi, M., Dohle, J., Watrinet, I., Holtmannspötter, M., Li, J., Birkholz, O., Miao, Y., Rothbauer, U., García, K. C., Kurre, R., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.06.18.599024 · Cited by 1
Oliveira, L. F. S., Khetani, R. S., Makogonov, N., Partan, E. S., Wu, Y.-S., Dasuri, V. S., Harrington, A. W., Olaloye, O. O., Goldsmith, J. D., Breault, D. T., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.09.25.612672 · Cited by 1
Coupling cell differentiation to dewetting can explain villus elongationPreprint
Devlin, D. K., Ishihara, S., Ganley, A. R. D., & Takeuchi, N. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.05.14.725076 · Cited by 1
Delayed activation of the DNA replication licensing system in Lgr5(+) intestinal stem cellsPreprint
Carroll, T. D., Newton, I. P., Chen, Y., Blow, J. J., & Näthke, I. S. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/177477
Defining the Intestinal Stem Cell Niche for Tissue Engineering and Disease Modeling
Kim, S. W., Banerjee, A., Starchenko, A., Yilmaz, Ö. H., & Lau, K. S. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.65482-x · Cited by 1
Intestinal stem cells: current understanding of functions andregulation
YeHua, L. I., & Chen, Y. (2018) · Scientia Sinica Vitae · doi:10.1360/n052018-00108
EGFR confers exquisite specificity of Wnt9a-Fzd9b signaling in hematopoietic stem cell developmentPreprint
Grainger, S. J., Nguyen, N. A., Richter, J., Setayesh, J., Lonquich, B., Oon, C. H., Wozniak, J. M., Barahona, R. A., Kamei, C. N., Houston, J., et al. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/387043
Austin, K. (2017) · TSpace (University of Toronto)
MR to Ultrasound Registration for Image-Guided Prostate Biopsy
Sun, Y. (2014) · Scholarship@Western (Western University)
Maselli, K. M., Schlieve, C. R., Frey, M. R., & Grikscheit, T. C. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-818422-6.00039-3
Aripaka, K. (2019) · KTH Publication Database DiVA (KTH Royal Institute of Technology)
Constructing roadmaps towards functional cell types using organoids
Beumer, J. (2020) · Utrecht University Repository (Utrecht University) · doi:10.33540/125
Effective Potential Description of the Interaction between Single Stem Cells and Localized Ligands
Bordeu, I., Garcin, C. L., Habib, S. J., & Pruessner, G. (2020) · Physical Review X · doi:10.1103/physrevx.10.041022
Utilizing organoids to study general and tissue-specific adult stem cell profiles
Boonekamp, K. E. (2020) · Utrecht University Repository (Utrecht University) · doi:10.33540/280
Elucidating the Molecular Mechanism of FZD5 Essentiality in RNF43 mutant Pancreatic Cancer
Zhang, M. (2020) · TSpace (University of Toronto)
Nishiya, N., & Yonezawa, H. (2021) · The Journal of Antibiotics · doi:10.1038/s41429-021-00461-y
Az embrionális fejlődés során zajló sejtmozgások szabályozásának vizsgálata zebradánió modellben
Zsigmond, Á. (2018) · Eötvös Loránd Tudományegyetem · doi:10.15476/elte.2017.122
Mohamed, R. (2021) · Carleton University's Institutional Repository (MacOdrum Library, Carleton University) · doi:10.22215/etd/2021-14744
Angers, S. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.736771607.793566890
Self-citationAdrenal glands stem cells: general signaling pathways
Glazova, O., Vorontsova, M. V., Shevkova, L., Sakr, N., Onyanov, N., Kaziakhmedova, S., & Volchkov, P. (2021) · Problems of Endocrinology · doi:10.14341/probl12819
Hornef, M. W. (2018) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.733879009.793551960
Seeber, F., & Blume, M. (2018) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.733504696.793551808
Heparan Sulfate Clusters Regulate Distribution and Signaling of Wnt Morphogens
Mii, Y. (2020) · Trends in Glycoscience and Glycotechnology · doi:10.4052/tigg.2006.7j
Xi, R. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.733685205.793557862
Yadav, A., & Chaturvedi, R. K. (2017) · Springer eBooks · doi:10.1007/978-3-319-67199-4_101790
Chang, C. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.737781764.793577613
Yadav, A., & Chaturvedi, R. K. (2016) · Springer eBooks · doi:10.1007/978-1-4614-6438-9_101790-1
Fritzsch, B. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.728375625.793558092
Sawa, H. (2018) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.733814364.793549824
Alison, M. R. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.737406582.793571991
Li, L. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.733789469.793554894
Yang, Z., & Li, L. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-821618-7.00163-2
Intestinal myofibroblasts regulate intestinal epithelial cell plasticity via YAP/TAZPreprint
Pastuła, A., Janssen, K., Steiger, K., Slotta‐Huspenina, J., Friedman, R. A., Hauck, S. M., Ruiz-Fernandez, M. J. A., Fottner, M., Borgmann, M., Ehmer, U., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.10.07.511327
Efeito do desmame precoce sobre marcadores moleculares e desenvolvimento da mucosa intestinal.
da Costa, A. V. (2021) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.42.2021.tde-28012022-155015
Intestinal Paneth cell differentiation relies on asymmetric regulation of Wnt signaling by Daam1/2Preprint
Colozza, G., Lee, H., Merenda, A., Wu, S.-H. S., Català-Bordes, A., Radaszkiewicz, T. W., Jordens, I., Lee, J., Bamford, A.-D., Farnhammer, F., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.01.24.525366
Self-citationMosa, M. H., Michels, B. E., Menche, C., Nicolas, A. M., Darvishi, T., Greten, F. R., & Farin, H. F. (2023) · doi:10.1158/0008-5472.c.6512463
Self-citationMosa, M. H., Michels, B. E., Menche, C., Nicolas, A. M., Darvishi, T., Greten, F. R., & Farin, H. F. (2023) · doi:10.1158/0008-5472.c.6512463.v1
Self-citationDevelopment of the Neocortical Area Map
Grove, E. A. (2023) · Wiley eBooks · doi:10.1002/9781119860914.ch22
Ramos-Junior, J. L. P., Monteiro, O., Santos, N. C., Correa, R., Cavalcanti, D. P., Martins, J., Boldrini, L., Granjeiro, J. M., & Folgueras-Flatschart, Á. V. (2023) · Journal of Physics Conference Series · doi:10.1088/1742-6596/2606/1/012017
Sensory progenitors influence patterning of the mammalian auditory sensory epitheliumPreprint
Young, C. A., Burt, E. K., & Munnamalai, V. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.11.13.566920
A cochlear progenitor pool influences patterning of the mammalian sensory epithelium via MYBL2
Young, C. A., Burt, E. K., & Munnamalai, V. (2024) · Development · doi:10.1242/dev.202635
Sankova, M. V., Nikolenko, V. N., Bolotskaya, A. A., Oganesyan, M. V., Rizaeva, N. A., Sankov, A. V., Zharikova, T. S., Pontes‐Silva, A., Beeraka, N. M., R, H. V. P., et al. (2025) · Current Medicinal Chemistry · doi:10.2174/0109298673357073250526104619
Secretion and signaling properties of Wnt11 and Wnt3 are determined by their N-terminusPreprint
Voloshanenko, O., Dhonnar, N., Aponte-Santamaria, D., Seidl, C., Wolf, L., Kranz, D., Ivanova, A., Marquez, E. J. F., Pokrandt, B., Augustin, I., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.07.02.662750
Quantitative high-resolution imaging of mouse nephron formation to study Wnt signaling dynamicsPreprint
Tsuchida-Straeten, N., Hammer, S., Halavatyi, A. A., Tischer, C., Pereira, G., & Simons, M. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.06.30.662340
Organoids: New Research Tool in Cancer Diagnostics and Therapeutics
Potdar, P. D. (2025) · BENTHAM SCIENCE PUBLISHERS eBooks · doi:10.2174/9789815238693125010009
Engineering the curve of fate: How geometry directs paneth cell localization in intestinal organoids
Bakht, S. M., & Mano, J. F. (2025) · Matter · doi:10.1016/j.matt.2025.102255
The Genetic Basis of Hippocampal Development
Tole, S., Mandal, A., & Singh, A. (2025) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-101123-094216
Sheikh, A., Setu, B., Joardar, N., Martin, J. C., Rosa, B. A., Mitreva, M., & Fleckenstein, J. M. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.10.02.680135
Oliveira, L. F. S., Khetani, R. S., Makogonov, N., Partan, E. S., Wu, Y.-S., Dasuri, V. S., Harrington, A. W., Olaloye, O., Goldsmith, J., Breault, D. T., et al. (2025) · eLife · doi:10.7554/elife.108645
Cataloguing the postnatal small intestinal transcriptome during the first postnatal monthPreprint
Oliveira, L. F. S., Khetani, R. S., Wu, Y.-S., Dasuri, V. S., Harrington, A. W., Olaloye, O. O., Goldsmith, J. D., Breault, D. T., Konnikova, L., Sui, S. J. H., et al. (2025) · eLife · doi:10.7554/elife.108645.1
Ren, Z., Lantermans, H. C., Kuil, A., Kraan, W., Arenzana‐Seisdedos, F., Kersten, M. J., Spaargaren, M., & Pals, S. T. (2021) · Figshare · doi:10.6084/m9.figshare.13566005
Metadata
- Authors
- Farin, H. F., Jordens, I., Mosa, M. H., Basak, O., Korving, J., Tauriello, D. V. F., de Punder, K., Angers, S., Peters, P. J., Maurice, M. M., & Clevers, H.
- Affiliations
- Royal Netherlands Academy of Arts and Sciences (NL)
- University Medical Center Utrecht (NL)
- German Cancer Research Center (DE)
- Maastricht University (NL)
- Corresponding author
- Farin, Henner F.
- Clevers, Hans
- ORCID
- Venue
- Nature
- Published
- 2016-02
- Volume
- 530
- Issue
- 7590
- Pages
- 340-343
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2258083311
- Cited by
- 525
- References
- 38
- Citations by year
- 2026: 27 · 2025: 41 · 2024: 31 · 2023: 48 · 2022: 47 · 2021: 46 · 2020: 55 · 2019: 56 · 2018: 76 · 2017: 62 · 2016: 35
- FWCI
- 39.70
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- KNAW Research Portal (The Royal Netherlands Academy of Arts and Sciences) (publishedVersion)
- Data Archiving and Networked Services (DANS) (submittedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Research Publications (Maastricht University) (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Wnt/β-catenin signaling in development and cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Hedgehog Signaling Pathway Studies
- Keywords
- Wnt3, Wnt signaling, intestinal stem cells, Paneth cells, short-range signaling, intestinal crypts, intestinal organoids, Frizzled receptors, cell division, stem cell self-renewal
- MeSH terms
- Alleles, Animals, Cell Adhesion, Cell Division, Cell Membrane, Diffusion, Female, Intestinal Mucosa, Male, Organoids, Stem Cells, Paneth Cells, Intercellular Signaling Peptides and Proteins, Receptors, G-Protein-Coupled, Ubiquitin-Protein Ligases, Frizzled Receptors, Mice, Stem Cell Niche, Gene Knock-In Techniques, Wnt Signaling Pathway, Wnt3 Protein
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