The DOI matches its Crossref record; 30 of the 30 references it cites were found in a registry or an index.
Wnt proteins are lipid-modified and can act as stem cell growth factors
Abstract
Wnt signalling is involved in numerous events in animal development, including the proliferation of stem cells and the specification of the neural crest. Wnt proteins are potentially important reagents in expanding specific cell types, but in contrast to other developmental signalling molecules such as hedgehog proteins and the bone morphogenetic proteins, Wnt proteins have never been isolated in an active form. Although Wnt proteins are secreted from cells, secretion is usually inefficient and previous attempts to characterize Wnt proteins have been hampered by their high degree of insolubility. Here we have isolated active Wnt molecules, including the product of the mouse Wnt3a gene. By mass spectrometry, we found the proteins to be palmitoylated on a conserved cysteine. Enzymatic removal of the palmitate or site-directed and natural mutations of the modified cysteine result in loss of activity, and indicate that the lipid is important for signalling. The purified Wnt3a protein induces self-renewal of haematopoietic stem cells, signifying its potential use in tissue engineering.
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
“Studies have revealed that the Wnt proteins are glycosylated in the endoplasmic reticulum and also are palmitolated.9,10”
From Wnt signal transduction pathways (2008) · cites this paper as [10]
Citations
Cites
Large-scale analysis of the yeast proteome by multidimensional protein identification technology
Washburn, M. P., Wolters, D. A., & Yates, J. R. (2001) · Nature Biotechnology · doi:10.1038/85686 · Cited by 4,768
Self-citationPhase separation of integral membrane proteins in Triton X-114 solution.
Bordier, C. (1981) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)69848-0 · Cited by 3,324
Polakis, P. (2000) · Genes & Development · doi:10.1101/gad.14.15.1837 · Cited by 3,183
Wnt signaling: a common theme in animal development
Cadigan, K. M., & Nusse, R. (1997) · Genes & Development · doi:10.1101/gad.11.24.3286 · Cited by 2,567
Self-citationA role for Wnt signalling in self-renewal of haematopoietic stem cells
Reya, T., Duncan, A. W., Ailles, L., Domen, J., Scherer, D. C., Willert, K., Hintz, L., Nusse, R., & Weissman, I. L. (2003) · Nature · doi:10.1038/nature01593 · Cited by 2,159
Self-citationThe β-Catenin/TCF-4 Complex Imposes a Crypt Progenitor Phenotype on Colorectal Cancer Cells
van de Wetering, M., Sancho, E., Verweij, C., de Lau, W., Oving, I., Hurlstone, A., van der Horn, K., Batlle, E., Coudreuse, D., Haramis, A.-P., et al. (2002) · Cell · doi:10.1016/s0092-8674(02)01014-0 · Cited by 2,030
Tabb, D. L., McDonald, W. H., & Yates, J. R. (2002) · Journal of Proteome Research · doi:10.1021/pr015504q · Cited by 1,369
Self-citationIdentification of a Palmitic Acid-modified Form of Human Sonic hedgehog
Pepinsky, R. B., Zeng, C., Wen, D., Rayhorn, P., Baker, D. P., Williams, K. P., Bixler, S. A., Ambrose, C. M., Garber, E. A., Miatkowski, K., et al. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.22.14037 · Cited by 754
Wnt Signaling and an APC-Related Gene Specify Endoderm in Early C. elegans Embryos
Rocheleau, C. E., Downs, W. D., Lin, R., Wittmann, C., Bei, Y., Cha, Y.-H., Ali, M., Priess, J. R., & Mello, C. C. (1997) · Cell · doi:10.1016/s0092-8674(00)80531-0 · Cited by 660
Shotgun identification of protein modifications from protein complexes and lens tissue
MacCoss, M. J., McDonald, W. H., Saraf, A., Sadygov, R. G., Clark, J., Tasto, J. J., Gould, K. L., Wolters, D. A., Washburn, M. P., Weiss, A., et al. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.122231399 · Cited by 593
Self-citation
Cited by
Sorted by citations
Items 901–1,000 of 1,003
Carboxylesterase Notum Is a Druggable Target to Modulate Wnt Signaling
Bayle, E. D., Svensson, F., Atkinson, B. N., Steadman, D., Willis, N. J., Woodward, H. L., Whiting, P. J., Vincent, J., & Fish, P. V. (2021) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.0c01974 · Cited by 53
A Human Pleiotropic Multiorgan Condition Caused by Deficient Wnt Secretion
Chai, G., Szenker‐Ravi, E., Chung, C., Li, Z., Wang, L., Khatoo, M., Marshall, T. G., Jiang, N., Yang, X., McEvoy‐Venneri, J., et al. (2021) · New England Journal of Medicine · doi:10.1056/nejmoa2033911 · Cited by 50
Self-citationTrevant, B., Gaur, T., Hussain, S., Symons, J., Komm, B. S., Bodine, P. V. N., Stein, G. S., & Lian, J. B. (2008) · Journal of Cellular Physiology · doi:10.1002/jcp.21482 · Cited by 52
Song, L., Li, Y., He, B., & Gong, Y. (2015) · Clinical Colorectal Cancer · doi:10.1016/j.clcc.2015.02.001 · Cited by 51
Wheway, G., Abdelhamed, Z., Natarajan, S., Toomes, C., Inglehearn, C. F., & Johnson, C. A. (2013) · Developmental Biology · doi:10.1016/j.ydbio.2013.02.015 · Cited by 49
NMR Structure of the WIF Domain of the Human Wnt-Inhibitory Factor-1
Liepinsh, E., Bányai, L., Patthy, L., & Otting, G. (2006) · Journal of Molecular Biology · doi:10.1016/j.jmb.2006.01.047 · Cited by 50
Wnt/β-catenin pathway activation and myogenic differentiation are induced by cholesterol depletion
Mermelstein, C., Portilho, D. M., Mendes, F. A., Costa, M. L., & Abreu, J. G. (2006) · Differentiation · doi:10.1111/j.1432-0436.2006.00129.x · Cited by 50
Membrane bound O-acyltransferases and their inhibitors.
Masumoto, N., Lanyon-Hogg, T., Rodgers, U., Konitsiotis, A., Magee, A., & Tate, E. (2015) · Biochemical Society Transactions · doi:10.1042/bst20150018 · Cited by 42
Iqbal, W., Alkarim, S., Al-Hejin, A. M., Mukhtar, H., & Saini, K. S. (2016) · Oncotarget · doi:10.18632/oncotarget.10942 · Cited by 50
Kulkarni, M. M., Leszczynska, A., Wei, G., Winkler, M. A., Tang, J., Funari, V. A., Deng, N., Liu, Z., Punj, V., Deng, S. X., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-03449-7 · Cited by 50
TMEM59 potentiates Wnt signaling by promoting signalosome formation
Gerlach, J. P., Jordens, I., Tauriello, D. V. F., Kuper, I., Bugter, J. M., Noordstra, I., van der Kooij, J., Low, T. Y., Pimentel‐Muiños, F. X., Xanthakis, D., et al. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1721321115 · Cited by 50
Pleiotropic function of FGF‐4: Its role in development and stem cells
Kosaka, N., Sakamoto, H., Terada, M., & Ochiya, T. (2008) · Developmental Dynamics · doi:10.1002/dvdy.21699 · Cited by 50
Hematopoiesis and stem cell renewal in long-term bone marrow cultures containing catalase
Gupta, R., Karpatkin, S., & Basch, R. S. (2005) · Blood · doi:10.1182/blood-2005-03-1180 · Cited by 53
Wnt Signaling in Cardiac Disease
Hermans, K. C. M., & Blankesteijn, W. M. (2015) · Comprehensive physiology · doi:10.1002/cphy.c140060 · Cited by 56
Wnt5a in cancer-associated fibroblasts promotes colorectal cancer progression
Hirashima, T., Karasawa, H., Aizawa, T., Suzuki, T., Yamamura, A., Suzuki, H., Kajiwara, T., Musha, H., Funayama, R., Shirota, M., et al. (2021) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2021.06.062 · Cited by 52
Sileo, P., Simonin, C., Melnyk, P., Chartier‐Harlin, M., & Cotelle, P. (2022) · Cells · doi:10.3390/cells11223631 · Cited by 56
Wnt acylation and its functional implication in Wnt signalling regulation
Janda, C. Y., & García, K. C. (2015) · Biochemical Society Transactions · doi:10.1042/bst20140249 · Cited by 49
Sukowati, C. H. C., Rosso, N., Crocè, L. S., & Tiribelli, C. (2010) · World Journal of Hepatology · doi:10.4254/wjh.v2.i3.114 · Cited by 49
Gujral, T. S., & MacBeath, G. (2010) · PLoS ONE · doi:10.1371/journal.pone.0010024 · Cited by 49
Epigenetic abnormalities in myeloproliferative neoplasms: a target for novel therapeutic strategies
Mascarenhas, J. O., Roper, N., Chaurasia, P., & Hoffman, R. (2011) · Clinical Epigenetics · doi:10.1007/s13148-011-0050-6 · Cited by 51
Dishevelled-2 docks and activates Src in a Wnt-dependent manner
Yokoyama, N. N., & Malbon, C. C. (2009) · Journal of Cell Science · doi:10.1242/jcs.051847 · Cited by 49
Planutiene, M., Planutis, K., & Holcombe, R. F. (2011) · Vascular Cell · doi:10.1186/2045-824x-3-28 · Cited by 50
A truncated Wnt7a retains full biological activity in skeletal muscle
von Maltzahn, J., Zinoviev, R. I., Chang, N. C., Bentzinger, C. F., & Rudnicki, M. A. (2013) · Nature Communications · doi:10.1038/ncomms3869 · Cited by 49
PORCN Moonlights in a Wnt-Independent Pathway That Regulates Cancer Cell Proliferation
Covey, T. M., Kaur, S. J., Ong, T. T., Proffitt, K. D., Wu, Y., Tan, P. B. O., & Virshup, D. M. (2012) · PLoS ONE · doi:10.1371/journal.pone.0034532 · Cited by 49
Macůrková, M., Port, F., Harterink, M., Basler, K., & Korswagen, H. C. (2010) · The EMBO Journal · doi:10.1038/emboj.2010.278 · Cited by 52
Kim, Y. S., Jeong, H.-Y., Kim, A. R., Kim, W., Cho, H., Um, J., Seo, Y., Kang, W. S., Jin, S., Kim, M. C., et al. (2016) · Scientific Reports · doi:10.1038/srep30726 · Cited by 48
Dattilo, R., Mottini, C., Camera, E., Lamolinara, A., Auslander, N., Doglioni, G., Muscolini, M., Tang, W., Planque, M., Ercolani, C., et al. (2020) · Cancer Research · doi:10.1158/0008-5472.can-19-1184 · Cited by 48
Stearoyl-CoA desaturase 5 (SCD5), a Δ-9 fatty acyl desaturase in search of a function
Igal, R. A., & Sinner, D. I. (2020) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2020.158840 · Cited by 49
Trimeric G protein-dependent signaling by Frizzled receptors in animal development
Egger‐Adam, D. (2008) · Frontiers in bioscience · doi:10.2741/3036 · Cited by 48
Notch Signaling in Hematopoietic Stem Cells
Suzuki, T., & Chiba, S. (2005) · International Journal of Hematology · doi:10.1532/ijh97.05115 · Cited by 49
Hanson, M. L., Brundage, K. M., Schafer, R., Tou, J. C. L., & Barnett, J. B. (2009) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2009.09.023 · Cited by 49
Tumor-secreted exosomal Wnt2B activates fibroblasts to promote cervical cancer progression
Liang, L.-J., Yang, Y., Wei, W.-F., Wu, X., Yan, R.-M., Zhou, C.-F., Chen, X., Wu, S., Wang, W., & Fan, L. (2021) · Oncogenesis · doi:10.1038/s41389-021-00319-w · Cited by 48
Regulation of Wnt receptor activity: Implications for therapeutic development in colon cancer
Zhong, Z. A., Michalski, M. N., Stevens, P. D., Sall, E. A., & Williams, B. O. (2021) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2021.100782 · Cited by 49
Yao, W., Wang, Z., Ma, H., Lin, Y., Liu, X., Li, P., & He, X. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e34269 · Cited by 48
Sailing with the Wnt: Charting the Wnt processing and secretion route
Lorenowicz, M. J., & Korswagen, H. C. (2009) · Experimental Cell Research · doi:10.1016/j.yexcr.2009.06.015 · Cited by 48
Wnt5a Inhibits the Proliferation and Melanogenesis of Melanocytes
Zhang, J., Li, Y., Wu, Y., Yang, T., Yang, K., Wang, R., Yang, J., & Guo, H. (2013) · International Journal of Medical Sciences · doi:10.7150/ijms.5664 · Cited by 48
Functional Characterization of Melanocyte Stem Cells in Hair Follicles
Nishikawa‐Torikai, S., Osawa, M., & Nishikawa, S. (2011) · Journal of Investigative Dermatology · doi:10.1038/jid.2011.195 · Cited by 49
Wnt Signaling Is Regulated by Endoplasmic Reticulum Retention
Zoltewicz, J. S., Ashique, A. M., Choe, Y., Lee, G., Taylor, S., Phamluong, K., Solloway, M. J., & Peterson, A. S. (2009) · PLoS ONE · doi:10.1371/journal.pone.0006191 · Cited by 48
Update on ghrelin biology in birds
Kaiya, H., Kangawa, K., & Miyazato, M. (2013) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2013.04.014 · Cited by 48
Wnt Signaling in Normal and Malignant Stem Cells
Bhavanasi, D., & Klein, P. S. (2016) · Current Stem Cell Reports · doi:10.1007/s40778-016-0068-y · Cited by 48
Wnt/β Catenin-Mediated Signaling Commonly Altered in Colorectal Cancer
Deitrick, J., & Pruitt, W. M. (2016) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2016.09.010 · Cited by 48
The thyroid hormone nuclear receptors and the Wnt/β-catenin pathway: An intriguing liaison
Skah, S., Uchuya-Castillo, J., Sirakov, M., & Plateroti, M. (2017) · Developmental Biology · doi:10.1016/j.ydbio.2017.01.003 · Cited by 47
Ge, Y., Wang, C., Hu, F., Pan, L., Min, J., Niu, K., Zhang, L., Li, J., & Xu, T. (2017) · Journal of Cellular Physiology · doi:10.1002/jcp.25853 · Cited by 46
Glycogen synthase kinase-3 (GSK-3) activity regulates mRNA methylation in mouse embryonic stem cells
Faulds, K. J., Egelston, J. N., Sedivy, L. J., Mitchell, M., Garimella, S., Kozlowski, H., D’Alessandro, A., Hansen, K. C., Balsbaugh, J. L., & Phiel, C. J. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.ra117.001298 · Cited by 47
Inositol Pentakisphosphate Mediates Wnt/β-Catenin Signaling
Gao, Y., & Wang, H. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m702106200 · Cited by 48
Heparan sulfate proteoglycans: Coordinators of multiple signaling pathways during chondrogenesis
Kirn‐Safran, C. B., Gomes, R. R., Brown, A. J., & Carson, D. D. (2004) · Birth Defects Research Part C Embryo Today Reviews · doi:10.1002/bdrc.20005 · Cited by 50
Hemogenic endothelium: Origins, regulation, and implications for vascular biology
Zape, J. P., & Zovein, A. C. (2011) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2011.10.003 · Cited by 50
Human Osteoblast–Derived Factors Induce Early Osteogenic Markers in Human Mesenchymal Stem Cells
Ilmer, M., Karow, M., Geißler, C., Jochum, M., & Neth, P. (2009) · Tissue Engineering Part A · doi:10.1089/ten.tea.2008.0427 · Cited by 47
Despeaux, M., Chicanne, G., Rouer, É., de Toni, F., Bertrand, J., Mas, V. M., Vergnolle, N., Eaves, C. J., Payrastre, B., Girault, J., et al. (2012) · Stem Cells · doi:10.1002/stem.1157 · Cited by 47
Malhotra, S., & Kincade, P. W. (2008) · Experimental Hematology · doi:10.1016/j.exphem.2008.08.008 · Cited by 46
The Secreted Signaling Protein Wnt3 Is Associated with Membrane Domains In Vivo: A SPIM-FCS Study
Ng, X. W., Teh, C., Korzh, V. P., & Wohland, T. (2016) · Biophysical Journal · doi:10.1016/j.bpj.2016.06.021 · Cited by 47
Porcupine inhibitors impair trabecular and cortical bone mass and strength in mice
Funck‐Brentano, T., Nilsson, K. H., Brommage, R., Henning, P., Lerner, U. H., Koskela, A., Tuukkanen, J., Cohen-Solal, M. E., Movérare‐Skrtic, S., & Ohlsson, C. (2018) · Journal of Endocrinology · doi:10.1530/joe-18-0153 · Cited by 50
Role of WNT signaling in normal and malignant hematopoiesis.
Khan, N. I., & Bendall, L. J. (2006) · PubMed · doi:10.14670/hh-21.761 · Cited by 47
Kilander, M. B. C., Halleskog, C., & Schulte, G. (2011) · Acta Physiologica · doi:10.1111/j.1748-1716.2011.02324.x · Cited by 47
Protein Depalmitoylation Is Induced by Wnt5a and Promotes Polarized Cell Behavior
Wang, W., Runkle, K. B., Terkowski, S. M., Ekaireb, R. I., & Witze, E. S. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.639609 · Cited by 46
The Role of SOX9 Transcription Factor in Pancreatic and Duodenal Development
Belo, J., Krishnamurthy, M., Oakie, A., & Wang, R. (2013) · Stem Cells and Development · doi:10.1089/scd.2013.0106 · Cited by 46
MATSUOKA, Y., Nakatsuka, R., Sumide, K., Kawamura, H., Takahashi, M., Fujioka, T., Uemura, Y., Asano, H., Sasaki, Y., Inoue, M., et al. (2014) · Stem Cells · doi:10.1002/stem.1941 · Cited by 46
Dema, A., Schröter, M. F., Perets, E., Skroblin, P., Moutty, M. C., Deàk, V. A., Birchmeier, W., & Klußmann, E. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.738047 · Cited by 47
Suciu, R. M., Cognetta, A. B., Potter, Z. E., & Cravatt, B. F. (2018) · ACS Medicinal Chemistry Letters · doi:10.1021/acsmedchemlett.8b00191 · Cited by 45
Resham, K., & Sharma, S. S. (2019) · Journal of Pain · doi:10.1016/j.jpain.2019.04.010 · Cited by 46
Understanding stem cells and its pivotal role in regenerative medicine
Sarkar, A., Saha, S., Paul, A., Maji, A., Roy, P., & Maity, T. K. (2021) · Life Sciences · doi:10.1016/j.lfs.2021.119270 · Cited by 47
Patterns of Wnt/Fzd/LRP Gene Expression During Embryonic Hematopoiesis
Corrigan, P. M., Dobbin, E., Freeburn, R. W., & Wheadon, H. (2008) · Stem Cells and Development · doi:10.1089/scd.2008.0270 · Cited by 47
Hedgehog signalling as a target in cancer stem cells
Médina, V., Blanco, M., Díaz‐Prado, S., & Espada, J. (2009) · Clinical & Translational Oncology · doi:10.1007/s12094-009-0341-y · Cited by 45
Membrane targeting of palmitoylated Wnt and Hedgehog revealed by chemical probes
Gao, X., Arenas-Ramirez, N., Scales, S. J., & Hannoush, R. N. (2011) · FEBS Letters · doi:10.1016/j.febslet.2011.06.033 · Cited by 45
Live imaging of active fluorophore labelled Wnt proteins
Holzer, T., Liffers, K., Rahm, K., Trageser, B., Özbek, S., & Gradl, D. (2012) · FEBS Letters · doi:10.1016/j.febslet.2012.04.035 · Cited by 45
Biomaterial Strategies for Stem Cell Maintenance During In Vitro Expansion
Yan, X., van den Beucken, J. J. J. P., Both, S. K., Yang, P.-S., Jansen, J. A., & Yang, F. (2013) · Tissue Engineering Part B Reviews · doi:10.1089/ten.teb.2013.0349 · Cited by 46
Ullmann, U., Gilles, C., Rycke, M. D., de Velde, H. V., Sermon, K., & Liebaers, I. (2008) · Molecular Human Reproduction · doi:10.1093/molehr/gan001 · Cited by 45
Groen, R. W. J., Oud, M. E. C. M., Schilder-Tol, E. J. M., Overdijk, M. B., ten Berge, D., Nusse, R., Spaargaren, M., & Pals, S. T. (2008) · Cancer Research · doi:10.1158/0008-5472.can-08-1322 · Cited by 44
Self-citationDifferences in the secretion and transport of Wnt proteins
Takada, S., Fujimori, S., Shinozuka, T., Takada, R., & Mii, Y. (2016) · The Journal of Biochemistry · doi:10.1093/jb/mvw071 · Cited by 45
Wnt Signaling in Thyroid Homeostasis and Carcinogenesis
Ely, K., Bischoff, L. A., & Weiss, V. L. (2018) · Genes · doi:10.3390/genes9040204 · Cited by 46
Ou, H., Chen, Z., Xiang, L., Fang, Y., Xu, Y., Liu, Q., Hu, Z., Li, X., Huang, Y., & Yang, D. (2019) · Cancer Science · doi:10.1111/cas.13949 · Cited by 45
Kreuser, U., Buchert, J., Haase, A., Richter, W., & Diederichs, S. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.581331 · Cited by 44
Molecular pathways in the development of HPV-induced cervical cancer
Rasi Bonab, F., Baghbanzadeh, A., Ghaseminia, M., Bolandi, N., Mokhtarzadeh, A., Amini, M., Dadashzadeh, K., Hajiasgharzadeh, K., Baradaran, B., & Baghi, H. B. (2021) · EXCLI journal · doi:10.17179/excli2021-3365 · Cited by 50
Acyltransferases for secreted signalling proteins (Review)
Chang, S., & Magee, A. I. (2009) · Molecular Membrane Biology · doi:10.1080/09687680802706432 · Cited by 46
Specificity of WNT-receptor interactions
Hsieh, J.-C. (2004) · Frontiers in bioscience · doi:10.2741/1321 · Cited by 46
Gαi2-induced conductin/axin2 condensates inhibit Wnt/β-catenin signaling and suppress cancer growth
Miete, C., Solis, G. P., Koval, A., Brückner, M., Katanaev, V. L., Behrens, J., & Bernkopf, D. B. (2022) · Nature Communications · doi:10.1038/s41467-022-28286-9 · Cited by 45
Cheng, J., Li, M., & Bai, R. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.954454 · Cited by 46
Goodnough, L. H., Dinuoscio, G. J., Ferguson, J. W., Williams, T., Lang, R. A., & Atit, R. P. (2014) · PLoS Genetics · doi:10.1371/journal.pgen.1004152 · Cited by 44
Jin, G., Westphalen, C. B., Hayakawa, Y., Worthley, D. L., Asfaha, S., Yang, X., Chen, X., Si, Y., Wang, H., Tailor, Y. H., et al. (2013) · Gastroenterology · doi:10.1053/j.gastro.2013.07.034 · Cited by 44
Targeting the Cancer Initiating Cell: The Ultimate Target for Cancer Therapy
McCubrey, J. A., Steelman, L. S., Abrams, S. L., Misaghian, N., Chappell, W. H., Mijatović, S., Montalto, G., Cervello, M., Laidler, P. M., Bonati, A., et al. (2012) · Current Pharmaceutical Design · doi:10.2174/138161212799859701 · Cited by 44
Winding back Wnt signalling: potential therapeutic targets for treating gastric cancers
Flanagan, D. J., Vincan, E., & Phesse, T. J. (2017) · British Journal of Pharmacology · doi:10.1111/bph.13890 · Cited by 42
Sadeghi, R. S., Kulej, K., Kathayat, R. S., Garcia, B. A., Dickinson, B. C., Brady, D. C., & Witze, E. S. (2018) · eLife · doi:10.7554/elife.34362 · Cited by 44
Wnt/-Catenin Signaling and Liver Regeneration: Circuit, Biology, and Opportunities
Hu, S., & Monga, S. P. (2021) · Gene Expression · doi:10.3727/105221621x16111780348794 · Cited by 43
Multiple PPPS/TP motifs act in a combinatorial fashion to transduce Wnt signaling through LRP6
Wolf, J., Palmby, T. R., Gavard, J., Williams, B. O., & Gutkind, J. S. (2007) · FEBS Letters · doi:10.1016/j.febslet.2007.12.013 · Cited by 45
Xu, J., Suzuki, M., Niwa, Y., Hiraga, J., Nagasaka, T., Ito, M., Nakamura, S., Tomita, A., Abe, A., Kiyoi, H., et al. (2008) · British Journal of Haematology · doi:10.1111/j.1365-2141.2007.06914.x · Cited by 45
Nikolova, T., Wu, M., Brumbarov, K., Alt, R., Opitz, H., Boheler, K. R., Cross, M. A., & Wobus, A. M. (2006) · Differentiation · doi:10.1111/j.1432-0436.2006.00119.x · Cited by 43
Stem cells and cancer: a deadly mix
Alison, M. R., Murphy, G., & Leedham, S. J. (2007) · Cell and Tissue Research · doi:10.1007/s00441-007-0510-7 · Cited by 45
Regulatory mechanisms of cytoneme-based morphogen transport
Daly, C. A., Hall, E. T., & Ogden, S. K. (2022) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-022-04148-x · Cited by 43
ANGPTL7 regulates the expansion and repopulation of human hematopoietic stem and progenitor cells
Xiao, Y., Jiang, Z., Li, Y., Ye, W., Jia, B., Zhang, M., Xu, Y., Wu, D., Lai, L., Chen, Y., et al. (2015) · Haematologica · doi:10.3324/haematol.2014.118612 · Cited by 42
Wnt signal transduction pathways: modules, development and evolution
Nayak, L., Bhattacharyya, N. P., & De, R. K. (2016) · BMC Systems Biology · doi:10.1186/s12918-016-0299-7 · Cited by 41
WNT-3A–induced β-catenin signaling does not require signaling through heterotrimeric G proteins
Bowin, C.-F., Inoue, A., & Schulte, G. (2019) · Journal of Biological Chemistry · doi:10.1074/jbc.ac119.009412 · Cited by 43
CBX7 binds the E-box to inhibit TWIST-1 function and inhibit tumorigenicity and metastatic potential
Li, J., Alvero, A. B., Nuti, S. V., Tedja, R., Roberts, C. M., Pitruzzello, M. C., Li, Y., Xiao, Q., Zhang, S., Gan, Y., et al. (2020) · Oncogene · doi:10.1038/s41388-020-1269-5 · Cited by 43
Hematopoietic stem cells: generation and manipulation
Nakano, T. (2003) · Trends in Immunology · doi:10.1016/j.it.2003.09.003 · Cited by 43
Luis, T. C., Naber, B. A. E., Fibbe, W. E., van Dongen, J. J. M., & Staal, F. J. T. (2010) · Blood · doi:10.1182/blood-2010-04-282624 · Cited by 43
Wang, Y., Arvanites, A. C., Davidow, L. S., Blanchard, J., Lam, K., Yoo, J. W., Coy, S., Rubin, L. L., & McMahon, A. P. (2012) · ACS Chemical Biology · doi:10.1021/cb300028a · Cited by 45
Kinetics of Wnt-driven β-catenin stabilization revealed by quantitative and temporal imaging
Hannoush, R. N. (2008) · PLoS ONE · doi:10.1371/journal.pone.0003498 · Cited by 42
Lysophosphatidic Acid Induces Erythropoiesis through Activating Lysophosphatidic Acid Receptor 3
Chiang, C., Chen, S.-S. A., Lee, S., Tsao, K.-C., Chu, P., Wen, C., Hwang, S., Yao, C., & Lee, H. (2011) · Stem Cells · doi:10.1002/stem.733 · Cited by 42
Sca-1-Expressing Nonmyogenic Cells Contribute to Fibrosis in Aged Skeletal Muscle
Hidestrand, M., Richards-Malcolm, S. A., Gurley, C. M., Nolen, G. T., Grimes, B. A., Waterstrat, A., Zant, G. E. V., & Peterson, C. A. (2008) · The Journals of Gerontology Series A · doi:10.1093/gerona/63.6.566 · Cited by 41
The Interaction of the Wnt and Notch Pathways Modulates Natural Killer Versus T Cell Differentiation
Aoyama, K., Delaney, C. S., Varnum‐Finney, B., Kohn, A. D., Moon, R. T., & Bernstein, I. D. (2007) · Stem Cells · doi:10.1634/stemcells.2007-0102 · Cited by 42
Scott, A., Rouch, J. D., Jabaji, Z. B., Khalil, H. A., Solorzano, S., Lewis, M. S., Martı́n, M. G., Stelzner, M. G., & Dunn, J. (2016) · Journal of Pediatric Surgery · doi:10.1016/j.jpedsurg.2016.02.074 · Cited by 42
Metadata
- Authors
- Willert, K., Brown, J. D., Danenberg, E., Duncan, A. W., Weissman, I. L., Reya, T., Yates, J. R., & Nusse, R.
- Affiliations
- Howard Hughes Medical Institute (US)
- Duke University (US)
- Stanford Medicine (US)
- Scripps Research Institute (US)
- ORCID
- Venue
- Nature
- Published
- 2003-04-27
- Volume
- 423
- Issue
- 6938
- Pages
- 448-452
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2147864074
- Cited by
- 2,257
- References
- 30
- Citations by year
- 2026: 40 · 2025: 42 · 2024: 48 · 2023: 54 · 2022: 63 · 2021: 63 · 2020: 78 · 2019: 87 · 2018: 86 · 2017: 90 · 2016: 100 · 2015: 101 · 2014: 99 · 2013: 106 · 2012: 133
- FWCI
- 48.13
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK067834)
- 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 › Hedgehog Signaling Pathway Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Keywords
- Wnt proteins, Wnt3a, palmitoylation, lipid modification, cysteine modification, Wnt signaling, hematopoietic stem cells, stem cell self-renewal, stem cell growth factor, tissue engineering, neural crest specification, protein purification
- MeSH terms
- Amino Acid Sequence, Animals, Cell Differentiation, Cell Division, Cysteine, Cytoskeletal Proteins, Drosophila melanogaster, Growth Substances, Hematopoietic Stem Cells, L Cells, Molecular Sequence Data, Palmitic Acids, Proteins, Solubility, Xenopus laevis, Signal Transduction, Trans-Activators, Mutagenesis, Site-Directed, Conserved Sequence, Hematopoietic Stem Cell Transplantation, Xenopus Proteins, Zebrafish Proteins, Lipid Metabolism, Wnt Proteins, beta Catenin, Mice, Wnt3 Protein, Wnt3A 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