The DOI matches its Crossref record; 115 of the 115 references it cites were found in a registry or an index.
The establishment of spemann's organizer and patterning of the vertebrate embryo
Open accessAbstract
Molecular studies have begun to unravel the sequential cell-cell signalling events that establish the dorsal-ventral, or 'back-to-belly', axis of vertebrate animals. In Xenopus and zebrafish, these events start with the movement of membrane vesicles associated with dorsal determinants. This mediates the induction of mesoderm by generating gradients of growth factors. Dorsal mesoderm then becomes a signalling centre, the Spemann's organizer, which secretes several antagonists of growth-factor signalling. Recent studies have led to new models for the regulation of cell-cell signalling during development, which may also apply to the homeostasis of adult tissues.
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
“For example, overexpression of Xwnt8, Dsh, β-catenin or dominant-negative GSK3 can induce secondary axis formation.56”
From Wnt signal transduction pathways (2008) · cites this paper as [56]
Citations
Cites
Polakis, P. (2000) · Genes & Development · doi:10.1101/gad.14.15.1837 · Cited by 3,183
A molecular mechanism for the effect of lithium on development.
Klein, P. S., & Melton, D. A. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.16.8455 · Cited by 2,334
MECHANISMS OF WNT SIGNALING IN DEVELOPMENT
Wodarz, A., & Nusse, R. (1998) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.14.1.59 · Cited by 2,030
XTcf-3 Transcription Factor Mediates β-Catenin-Induced Axis Formation in Xenopus Embryos
Molenaar, M., van de Wetering, M., Oosterwegel, M., Peterson-Maduro, J., Godsave, S., Korinek, V., Roose, J., Destrée, O., & Clevers, H. (1996) · Cell · doi:10.1016/s0092-8674(00)80112-9 · Cited by 1,824
The Spemann Organizer Signal noggin Binds and Inactivates Bone Morphogenetic Protein 4
Zimmerman, L. B., Jesús-Escobar, J. M. D., & Harland, R. M. (1996) · Cell · doi:10.1016/s0092-8674(00)80133-6 · Cited by 1,639
Dickkopf-1 is a member of a new family of secreted proteins and functions in head induction
Glinka, A., Wu, W., Delius, H., Monaghan, A. P., Blumenstock, C., & Niehrs, C. (1998) · Nature · doi:10.1038/34848 · Cited by 1,608
Smith, W. C., & Harland, R. M. (1992) · Cell · doi:10.1016/0092-8674(92)90316-5 · Cited by 1,184
Piccolo, S., Sasai, Y., Lu, B., & Robertis, E. M. D. (1996) · Cell · doi:10.1016/s0092-8674(00)80132-4 · Cited by 1,127
Xenopus chordin: A novel dorsalizing factor activated by organizer-specific homeobox genes
Sasai, Y. (1994) · Cell · doi:10.1016/0092-8674(94)90068-x · Cited by 1,122
Zeng, L., Fagotto, F., Zhang, T., Hsu, W., Vasicek, T. J., Perry, W. L., Lee, J. J., Tilghman, S. M., Gumbiner, B. M., & Costantini, F. D. (1997) · Cell · doi:10.1016/s0092-8674(00)80324-4 · Cited by 907
Cited by
Sorted by citations
Wnt signal transduction pathways
Komiya, Y., & Habas, R. (2008) · Organogenesis · doi:10.4161/org.4.2.5851 · Cited by 1,528
MicroRNA control of signal transduction
Inui, M., Martello, G., & Piccolo, S. (2010) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2868 · Cited by 1,272
Mapping Wnt/β-catenin signaling during mouse development and in colorectal tumors
Maretto, S., Cordenonsi, M., Dupont, S., Braghetta, P., Broccoli, V., Hassan, A. B., Volpin, D., Bressan, G. M., & Piccolo, S. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0434590100 · Cited by 759
Morphogen gradient interpretation
Gurdon, J. B., & Bourillot, P.-Y. (2001) · Nature · doi:10.1038/35101500 · Cited by 746
DORSAL-VENTRAL PATTERNING AND NEURAL INDUCTION IN XENOPUS EMBRYOS
De Robertis, E. M., & Kuroda, H. (2004) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.20.011403.154124 · Cited by 671
Balancing cell adhesion and Wnt signaling, the key role of β-catenin
Brembeck, F. H., Rosário, M., & Birchmeier, W. (2005) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2005.12.007 · Cited by 677
A Maternal-Zygotic Effect Gene, Zfp57, Maintains Both Maternal and Paternal Imprints
Li, X., Ito, M., Zhou, F., Youngson, N. A., Zuo, X., Leder, P., & Ferguson‐Smith, A. C. (2008) · Developmental Cell · doi:10.1016/j.devcel.2008.08.014 · Cited by 647
Extracellular Regulation of BMP Signaling in Vertebrates: A Cocktail of Modulators
Balemans, W., & Hul, W. V. (2002) · Developmental Biology · doi:10.1006/dbio.2002.0779 · Cited by 616
Kiecker, C. M., & Niehrs, C. (2001) · Development · doi:10.1242/dev.128.21.4189 · Cited by 515
The evolution of signalling pathways in animal development
Pires-daSilva, A., & Sommer, R. J. (2003) · Nature Reviews Genetics · doi:10.1038/nrg977 · Cited by 466
Reprogramming metastatic tumour cells with embryonic microenvironments
Hendrix, M. J. C., Seftor, E. A., Seftor, R. E. B., Kasemeier‐Kulesa, J. C., Kulesa, P. M., & Postovit, L.-M. M. (2007) · Nature reviews. Cancer · doi:10.1038/nrc2108 · Cited by 475
Early Steps in the Development of the Forebrain
Wilson, S. W., & Houart, C. (2004) · Developmental Cell · doi:10.1016/s1534-5807(04)00027-9 · Cited by 460
Topczewski, J., Sepich, D. S., Myers, D. C., Walker, C., Amores, A., Lele, Z., Hammerschmidt, M., Postlethwait, J. H., & Solnica‐Krezel, L. (2001) · Developmental Cell · doi:10.1016/s1534-5807(01)00005-3 · Cited by 454
Embryonic and tumorigenic pathways converge via Nodal signaling: role in melanoma aggressiveness
Topczewska, J. M., Postovit, L.-M. M., Margaryan, N. V., Sam, A., Hess, A. R., Wheaton, W. W., Nickoloff, B. J., Topczewski, J., & Hendrix, M. J. C. (2006) · Nature Medicine · doi:10.1038/nm1448 · Cited by 438
Integration of IGF, FGF, and anti-BMP signals via Smad1 phosphorylation in neural inductionPreprint
Pera, E. M., Ikeda, A., Eivers, E., & Robertis, E. M. D. (2003) · Genes & Development · doi:10.1101/gad.1153603 · Cited by 421
Conserved Patterns of Cell Movements during Vertebrate Gastrulation
Solnica-Krezel, L. (2005) · Current Biology · doi:10.1016/j.cub.2005.03.016 · Cited by 391
Intracellular BMP Signaling Regulation in Vertebrates: Pathway or Network?
von Bubnoff, A., & Cho, K. W. Y. (2001) · Developmental Biology · doi:10.1006/dbio.2001.0388 · Cited by 392
Structural Biology and Evolution of the TGF-β FamilyPreprint
Hinck, A. P., Mueller, T. D., & Springer, T. A. (2016) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a022103 · Cited by 381
Gastrulation: Making and Shaping Germ Layers
Solnica‐Krezel, L., & Sepich, D. S. (2011) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-092910-154043 · Cited by 373
Smed- β catenin-1 Is Required for Anteroposterior Blastema Polarity in Planarian Regeneration
Petersen, C. P., & Reddien, P. W. (2008) · Science · doi:10.1126/science.1149943 · Cited by 364
Germ-Layer Specification and Control of Cell Growth by Ectodermin, a Smad4 Ubiquitin Ligase
Dupont, S., Zacchigna, L., Cordenonsi, M., Soligo, S., Adorno, M., Rugge, M., & Piccolo, S. (2005) · Cell · doi:10.1016/j.cell.2005.01.033 · Cited by 367
Nodal and BMP2/4 Signaling Organizes the Oral-Aboral Axis of the Sea Urchin Embryo
Duboc, V., Röttinger, É., Besnardeau, L., & Lepage, T. (2004) · Developmental Cell · doi:10.1016/s1534-5807(04)00056-5 · Cited by 353
Planar Cell Polarity: Coordinating Morphogenetic Cell Behaviors with Embryonic Polarity
Gray, R. S., Roszko, I., & Solnica‐Krezel, L. (2011) · Developmental Cell · doi:10.1016/j.devcel.2011.06.011 · Cited by 328
Essential role of BCL9-2 in the switch between β-catenin's adhesive and transcriptional functionsPreprint
Brembeck, F. H., Schwarz, T., Bakkers, J., Wilhelm, S., Hammerschmidt, M., & Birchmeier, W. (2004) · Genes & Development · doi:10.1101/gad.317604 · Cited by 318
Nodal antagonists regulate formation of the anteroposterior axis of the mouse embryo
Yamamoto, M., Saijoh, Y., Perea-Gómez, A., Shawlot, W., Behringer, R. R., Ang, S., Hamada, H., & Meno, C. (2004) · Nature Cell Biology · doi:10.1038/nature02418 · Cited by 304
T‐box genes in early embryogenesis
Showell, C., Binder, O., & Conlon, F. L. (2003) · Developmental Dynamics · doi:10.1002/dvdy.10480 · Cited by 310
Regionally specific induction by the Spemann–Mangold organizer
Niehrs, C. (2004) · Nature Reviews Genetics · doi:10.1038/nrg1347 · Cited by 294
Neural induction in Xenopus requires early FGF signalling in addition to BMP inhibition
Delaune, E. A., Lemaire, P., & Kodjabachian, L. (2004) · Development · doi:10.1242/dev.01582 · Cited by 290
Spemann's organizer and self-regulation in amphibian embryos
De Robertis, E. M. (2006) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1855 · Cited by 267
Adamska, M., Degnan, S. M., Green, K. M., Adamski, M., Craigie, A., Larroux, C., & Degnan, B. M. (2007) · PLoS ONE · doi:10.1371/journal.pone.0001031 · Cited by 257
Axial patterning in cephalochordates and the evolution of the organizer
Yu, J., Satou, Y., Holland, N. D., Shin‐I, T., Kohara, Y., Satoh, N., Bronner-Fraser, M. E., & Holland, L. Z. (2007) · Nature · doi:10.1038/nature05472 · Cited by 256
Maternal Control of Vertebrate Development before the Midblastula Transition
Dosch, R., Wagner, D. S., Mintzer, K. A., Runke, G., Wiemelt, A. P., & Mullins, M. C. (2004) · Developmental Cell · doi:10.1016/j.devcel.2004.05.002 · Cited by 251
Kinder, S. J., Tsang, T. E., Wakamiya, M., Sasaki, H., Behringer, R. R., Nagy, A., & Tam, P. (2001) · Development · doi:10.1242/dev.128.18.3623 · Cited by 247
Nodal Signaling in Early Vertebrate Embryos
Whitman, M. (2001) · Developmental Cell · doi:10.1016/s1534-5807(01)00076-4 · Cited by 243
Khokha, M. K., Yeh, J., Grammer, T. C., & Harland, R. M. (2005) · Developmental Cell · doi:10.1016/j.devcel.2005.01.013 · Cited by 230
Neural and Head Induction by Insulin-like Growth Factor Signals
Pera, E. M., Wessely, O., Li, S.-Y., & Robertis, E. M. D. (2001) · Developmental Cell · doi:10.1016/s1534-5807(01)00069-7 · Cited by 229
Self-citationIntegration of Smad and MAPK pathways: a link and a linker revisitedPreprint
Massagué, J. (2003) · Genes & Development · doi:10.1101/gad.1167003 · Cited by 229
Piotrowska, K., Wianny, F., Pedersen, R. A., & Zernicka‐Goetz, M. (2001) · Development · doi:10.1242/dev.128.19.3739 · Cited by 225
Constructing the hindbrain: Insights from the zebrafish
Moens, C. B., & Prince, V. (2002) · Developmental Dynamics · doi:10.1002/dvdy.10086 · Cited by 225
Models of Biological Pattern Formation: From Elementary Steps to the Organization of Embryonic Axes
Meinhardt, H. (2007) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(07)81001-5 · Cited by 219
Mesoderm induction: from caps to chips
Kimelman, D. (2006) · Nature Reviews Genetics · doi:10.1038/nrg1837 · Cited by 210
Neurodevelopmental effects of insulin-like growth factor signaling
OʼKusky, J. R., & Ye, P. (2012) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2012.06.002 · Cited by 219
The role of the zebrafishnodal-related genessquintandcyclopsin patterning of mesendoderm
Dougan, S. T., Warga, R. M., Kane, D. A., Schier, A. F., & Talbot, W. S. (2003) · Development · doi:10.1242/dev.00400 · Cited by 200
Kuroda, H., Wessely, O., & Robertis, E. M. D. (2004) · PLoS Biology · doi:10.1371/journal.pbio.0020092 · Cited by 195
Self-citationUSP15 is a deubiquitylating enzyme for receptor-activated SMADs
Inui, M., Manfrin, A., Mamidi, A., Martello, G., Morsut, L., Soligo, S., Enzo, E., Moro, S., Polo, S., Dupont, S., et al. (2011) · Nature Cell Biology · doi:10.1038/ncb2346 · Cited by 193
Schwarz-Romond, T., Asbrand, C., Bakkers, J., Kühl, M., Schaeffer, H.-J., Huelsken, J., Behrens, J., Hammerschmidt, M., & Birchmeier, W. (2002) · Genes & Development · doi:10.1101/gad.230402 · Cited by 192
MicroRNA control of Nodal signalling
Martello, G., Zacchigna, L., Inui, M., Montagner, M., Adorno, M., Mamidi, A., Morsut, L., Soligo, S., Tran, U., Dupont, S., et al. (2007) · Nature · doi:10.1038/nature06100 · Cited by 188
Self-citationA WNT of things to come: Evolution of Wnt signaling and polarity in cnidarians
LEE, P., PANG, K., Matus, D. Q., & Martindale, M. Q. (2006) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2006.05.002 · Cited by 180
Morkel, M., Huelsken, J., Wakamiya, M., Ding, J., van de Wetering, M., Clevers, H. C., Taketo, M. M., Behringer, R. R., Shen, M. M., & Birchmeier, W. (2003) · Development · doi:10.1242/dev.00859 · Cited by 189
Yamamoto, A., Nagano, T., Takehara, S., Hibi, M., & Aizawa, S. (2005) · Cell · doi:10.1016/j.cell.2004.11.051 · Cited by 191
Stat3 Controls Cell Movements during Zebrafish Gastrulation
Yamashita, S., Miyagi, C., Carmany-Rampey, A., Shimizu, T., Fujii, R., Schier, A. F., & Hirano, T. (2002) · Developmental Cell · doi:10.1016/s1534-5807(02)00126-0 · Cited by 178
Myers, D. C., Sepich, D. S., & Solnica‐Krezel, L. (2002) · Trends in Genetics · doi:10.1016/s0168-9525(02)02725-7 · Cited by 176
Turner, D. A., Hayward, P. C., Baillie‐Johnson, P., Rué, P., Broome, R., Faunes, F., & Arias, A. M. (2014) · Development · doi:10.1242/dev.112979 · Cited by 158
The role of chordin/Bmp signals in mammalian pharyngeal development and DiGeorge syndrome
Bachiller, D., Klingensmith, J., Shneyder, N., Tran, U., Anderson, R. M., Rossant, J., & Robertis, E. M. D. (2003) · Development · doi:10.1242/dev.00581 · Cited by 167
Larraı́n, J., Oelgeschläger, M., Ketpura, N. I., Reversade, B., Zakin, L., & Robertis, E. M. D. (2001) · Development · doi:10.1242/dev.128.22.4439 · Cited by 156
Self-citationRTK and TGF-β signaling pathways genes in the sea urchin genome
Lapraz, F., Röttinger, É., Duboc, V., Range, R., Duloquin, L., Walton, K. D., Wu, S.-Y., Bradham, C. A., Loza‐Coll, M., Hibino, T., et al. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2006.08.048 · Cited by 158
Chordin Is Required for the Spemann Organizer Transplantation Phenomenon in Xenopus Embryos
Oelgeschläger, M., Kuroda, H., Reversade, B., & Robertis, E. M. D. (2003) · Developmental Cell · doi:10.1016/s1534-5807(02)00404-5 · Cited by 145
Self-citationReversade, B., Kuroda, H., Lee, H. X., Mays, A. N., & Robertis, E. M. D. (2005) · Development · doi:10.1242/dev.01901 · Cited by 147
Evolutionary crossroads in developmental biology: amphioxus
Bertrand, S., & Escrivá, H. (2011) · Development · doi:10.1242/dev.066720 · Cited by 151
Axis formation and patterning in zebrafish
Schier, A. F. (2001) · Current Opinion in Genetics & Development · doi:10.1016/s0959-437x(00)00209-4 · Cited by 141
Recent Development of Wnt Signaling Pathway Inhibitors for Cancer Therapeutics
Harb, J. F., Lin, P.-J., & Hao, J. (2019) · Current Oncology Reports · doi:10.1007/s11912-019-0763-9 · Cited by 139
Kalantry, S., Manning, S., Haub, O., Tomihara-Newberger, C., Lee, H.-G., Fangman, J., Distèche, C. M., Manova, K., & Lacy, E. (2001) · Nature Genetics · doi:10.1038/86912 · Cited by 138
Akiyama‐Oda, Y., & Oda, H. (2006) · Development · doi:10.1242/dev.02400 · Cited by 139
Graham, S. J. L., Wicher, K. B., Jędrusik, A., Guo, G., Herath, W. B., Robson, P., & Zernicka‐Goetz, M. (2014) · Nature Communications · doi:10.1038/ncomms6667 · Cited by 126
Ethanol exposure affects gene expression in the embryonic organizer and reduces retinoic acid levels
Yelin, R., Schyr, R. B., Kot-Leibovich, H., Rousso, S. Z., Frumkin, A., Pillemer, G., & Fainsod, A. (2005) · Developmental Biology · doi:10.1016/j.ydbio.2004.12.014 · Cited by 124
Wessely, O., Agius, E., Oelgeschläger, M., Pera, E. M., & Robertis, E. M. D. (2001) · Developmental Biology · doi:10.1006/dbio.2001.0258 · Cited by 124
Self-citationTwo FGFRL-Wnt circuits organize the planarian anteroposterior axis
Scimone, M. L., Cote, L. E., Rogers, T., & Reddien, P. W. (2016) · eLife · doi:10.7554/elife.12845 · Cited by 121
Blum, M., Andre, P., Feistel, K., Schweickert, A., Fischer, A., Bitzer, E., Bogusch, S., Beyer, T., van Straaten, H. W. M., & Viebahn, C. (2006) · Differentiation · doi:10.1111/j.1432-0436.2006.00124.x · Cited by 123
On the evolution of bilaterality
Genikhovich, G., & Technau, U. (2017) · Development · doi:10.1242/dev.141507 · Cited by 118
Nodal signaling and the evolution of deuterostome gastrulation
Chea, H. K., Wright, C. V. E., & Swalla, B. J. (2005) · Developmental Dynamics · doi:10.1002/dvdy.20549 · Cited by 119
Minn, K. T., Fu, Y. C., He, S., Dietmann, S., George, S. C., Anastasio, M. A., Morris, S. A., & Solnica‐Krezel, L. (2020) · eLife · doi:10.7554/elife.59445 · Cited by 112
Sunyaev, S. R., Liska, A. J., Golod, A., Shevchenko, A., & Shevchenko, A. (2003) · Analytical Chemistry · doi:10.1021/ac026199a · Cited by 116
Repression of the vertebrate organizer by Wnt8 is mediated by Vent and Vox
Ramel, M., & Lekven, A. C. (2004) · Development · doi:10.1242/dev.01277 · Cited by 116
On the nature and function of organizers
Arias, A. M., & Steventon, B. (2018) · Development · doi:10.1242/dev.159525 · Cited by 115
Hayes, M. N., Naito, M., Daulat, A. M., Angers, S., & Ciruna, B. G. (2013) · Development · doi:10.1242/dev.090183 · Cited by 117
Ogon/Secreted Frizzled functions as a negative feedback regulator of Bmp signaling
Yabe, T., Shimizu, T., Muraoka, O., Bae, Y., Hirata, T., Nojima, H., Kawakami, A., Hirano, T., & Hibi, M. (2003) · Development · doi:10.1242/dev.00506 · Cited by 110
Rentzsch, F., Zhang, J., Kramer, C., Sebald, W., & Hammerschmidt, M. (2006) · Development · doi:10.1242/dev.02250 · Cited by 107
Darras, S., Gerhart, J. C., Terasaki, M. R., Kirschner, M. W., & Lowe, C. J. (2011) · Development · doi:10.1242/dev.059493 · Cited by 107
The route to spinal cord cell types: a tale of signals and switches
Gouti, M., Metzis, V., & Briscoe, J. (2015) · Trends in Genetics · doi:10.1016/j.tig.2015.03.001 · Cited by 106
Tsukushi Functions as an Organizer Inducer by Inhibition of BMP Activity in Cooperation with Chordin
Ohta, K., Lupo, G., Kuriyama, S., Keynes, R. J., Holt, C. E., Harris, W. A., Tanaka, H., & Ohnuma, S. (2004) · Developmental Cell · doi:10.1016/j.devcel.2004.08.014 · Cited by 102
Engert, S., Burtscher, I., Liao, W. P., Dulev, S., Schotta, G., & Lickert, H. (2013) · Development · doi:10.1242/dev.088765 · Cited by 101
Dynamics of Notch-Dependent Transcriptional Bursting in Its Native Context
Lee, C., Shin, H., & Kimble, J. E. (2019) · Developmental Cell · doi:10.1016/j.devcel.2019.07.001 · Cited by 93
Biglycan is a new extracellular component of the Chordin–BMP4 signaling pathway
Moreno, M., Muñoz, R., Aroca, F., Labarca, M., Brandan, E., & Larraı́n, J. (2005) · The EMBO Journal · doi:10.1038/sj.emboj.7600615 · Cited by 99
Self-citationLefty acts as an essential modulator of Nodal activity during sea urchin oral–aboral axis formation
Duboc, V., Lapraz, F., Besnardeau, L., & Lepage, T. (2008) · Developmental Biology · doi:10.1016/j.ydbio.2008.04.012 · Cited by 96
Syntabulin, a motor protein linker, controls dorsal determination
Nojima, H., Rothhämel, S., Shimizu, T., Kim, C., Yonemura, S., Marlow, F. L., & Hibi, M. (2010) · Development · doi:10.1242/dev.046425 · Cited by 95
Dkk1 and noggin cooperate in mammalian head inductionPreprint
Barrantes, I. D. B., Davidson, G. R., Gröne, H., Westphal, H., & Niehrs, C. (2003) · Genes & Development · doi:10.1101/gad.269103 · Cited by 94
Organizer activity of the polar cells duringDrosophilaoogenesis
Grammont, M., & Irvine, K. D. (2002) · Development · doi:10.1242/dev.129.22.5131 · Cited by 92
RAPGEF5 Regulates Nuclear Translocation of β-Catenin
Griffin, J. N., Viso, F. D., Duncan, A. R., Robson, A., Hwang, W. Y., Kulkarni, S. S., Liu, K. J., & Khokha, M. K. (2017) · Developmental Cell · doi:10.1016/j.devcel.2017.12.001 · Cited by 93
PP2A:B56ϵ is required for Wnt/β-catenin signaling during embryonic development
Yang, J., Wu, J., Tan, C. L., & Klein, P. S. (2003) · Development · doi:10.1242/dev.00762 · Cited by 91
Symmetry breakage in the vertebrate embryo: When does it happen and how does it work?
Blum, M., Schweickert, A., Vick, P., Wright, C. V. E., & Danilchik, M. V. (2014) · Developmental Biology · doi:10.1016/j.ydbio.2014.06.014 · Cited by 90
Essential roles of a zebrafishprdm1/blimp1homolog in embryo patterning and organogenesis
Wilm, T. P., & Solnica‐Krezel, L. (2004) · Development · doi:10.1242/dev.01572 · Cited by 90
Mechanical Forces Reshape Differentiation Cues That Guide Cardiomyogenesis
Happe, C. L., & Engler, A. J. (2016) · Circulation Research · doi:10.1161/circresaha.115.305139 · Cited by 93
The pivotal role of TGF-β/Smad pathway in fibrosis pathogenesis and treatment
Chen, F., Lyu, L., Xing, C., Chen, Y., Hu, S., Wang, M., & Ai, Z. (2025) · Frontiers in Oncology · doi:10.3389/fonc.2025.1649179 · Cited by 99
Xenopus: An Undervalued Model Organism to Study and Model Human Genetic Disease
Blum, M., & Ott, T. (2018) · Cells Tissues Organs · doi:10.1159/000490898 · Cited by 88
Gratsch, T. E., & O’Shea, K. S. (2002) · Developmental Biology · doi:10.1006/dbio.2002.0629 · Cited by 85
Goosecoid promotes head organizer activity by direct repression of Xwnt8 in Spemann’s organizer
Yao, J., & Kessler, D. S. (2001) · Development · doi:10.1242/dev.128.15.2975 · Cited by 82
Yu, J., Holland, L. Z., & Holland, N. D. (2002) · Evolution & Development · doi:10.1046/j.1525-142x.2002.02030.x · Cited by 84
Nucleo-cytoplasmic Shuttling of Axin, a Negative Regulator of the Wnt-β-Catenin Pathway
Wiechens, N., Heinle, K., Englmeier, L., Schohl, A., & Fagotto, F. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m307253200 · Cited by 84
Single-cell internalization during zebrafish gastrulation
Carmany-Rampey, A., & Schier, A. F. (2001) · Current Biology · doi:10.1016/s0960-9822(01)00353-0 · Cited by 80
The maternally expressed zebrafish T-box gene eomesodermin regulates organizer formation
Bruce, A. E. E., Howley, C., Zhou, Y., Vickers, S. L., Silver, L. M., King, M. L., & Ho, R. K. (2003) · Development · doi:10.1242/dev.00763 · Cited by 77
Metadata
- Authors
- De Robertis, E. M., Larraín, J., Oelgeschläger, M., & Wessely, O.
- Affiliations
- Howard Hughes Medical Institute (US)
- Venue
- Nature Reviews Genetics
- Published
- 2000-12
- Volume
- 1
- Issue
- 3
- Pages
- 171-181
- ISSN
- 1471-0056 (ISSN-L)
- 1471-0064
- PMC
- PMC2291143
- OpenAlex
- W1533376056
- Cited by
- 429
- References
- 115
- Citations by year
- 2026: 3 · 2025: 10 · 2024: 8 · 2023: 8 · 2022: 9 · 2021: 11 · 2020: 16 · 2019: 7 · 2018: 6 · 2017: 13 · 2016: 13 · 2015: 13 · 2014: 18 · 2013: 9 · 2012: 18
- FWCI
- 2.06
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Reviews Genetics (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (R37HD021502)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- 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 › Planarian Biology and Electrostimulation
- Keywords
- Spemann's organizer, dorsal-ventral axis, embryonic patterning, cell-to-cell communication, mesoderm induction, growth factor gradients, Xenopus, zebrafish, tissue homeostasis
- MeSH terms
- Amino Acid Sequence, Animals, Glycoproteins, Molecular Sequence Data, Vertebrates, Sequence Homology, Amino Acid, Body Patterning, Intercellular Signaling Peptides and Proteins
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