The establishment of spemann's organizer and patterning of the vertebrate embryo

Wnt signaling and cancer

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

Expression cloning of noggin, a new dorsalizing factor localized to the Spemann organizer in Xenopus embryos

Smith, W. C., & Harland, R. M. (1992) · Cell · doi:10.1016/0092-8674(92)90316-5 · Cited by 1,184

Dorsoventral Patterning in Xenopus: Inhibition of Ventral Signals by Direct Binding of Chordin to BMP-4

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

The Mouse Locus Encodes Axin, an Inhibitor of the Wnt Signaling Pathway That Regulates Embryonic Axis Formation

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

Uncoupling the BMP receptor antagonist function from the WNT agonist function of R-spondin 2 using the inhibitory peptide dendrimer RWd

Lee, H.-Y., Sun, R., & Niehrs, C. (2022) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2022.101586 · Cited by 6

Reversal of Xenopus Oct25 Function by Disruption of the POU Domain Structure

Cao, Y., Oswald, F., Wacker, S., Bundschu, K., & Knöchel, W. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.064386 · Cited by 6

Cholesterol-rich membrane microdomains modulate Wnt/β-catenin morphogen gradient during Xenopus development

Reis, A. H., Moreno, M. M., Maia, L. A., de Oliveira, F. P., Santos, A. S., & Abreu, J. G. (2016) · Mechanisms of Development · doi:10.1016/j.mod.2016.09.001 · Cited by 6

The Molecular Basis of the Gastrula Organizer in Amphibians and Cnidarians

Yasuoka, Y., & Taira, M. (2018) · Diversity and commonality in animals · doi:10.1007/978-4-431-56609-0_31 · Cited by 6

Maternal control of axial–paraxial mesoderm patterning via direct transcriptional repression in zebrafish

He, Y., Xu, X., Zhao, S., Ma, S., Sun, L., Liu, Z., & Luo, C. (2013) · Developmental Biology · doi:10.1016/j.ydbio.2013.11.022 · Cited by 6

A Vascular Perspective on Neurogenesis

Selfe, J. S., & Karen, K. Y. (2013) · InTech eBooks · doi:10.5772/54980 · Cited by 7

Induction of tooth and eye by transplantation of activin A-treated, undifferentiated presumptive ectodermal Xenopus cells into the abdomen

Myoishi, Y., Furue, M. K., Fukui, Y., Okamoto, T., & Asashima, M. (2004) · The International Journal of Developmental Biology · doi:10.1387/ijdb.041907ym · Cited by 6

Evo-devo: Hydra raises its Noggin

Chandramore, K., & Ghaskadbi, S. (2011) · Journal of Biosciences · doi:10.1007/s12038-011-9086-1 · Cited by 5

Towards a synthetic view of axis specification mechanisms in vertebrates: insights from the dogfish

Coolen, M., Menuet, A., & Mazan, S. (2008) · Comptes Rendus Biologies · doi:10.1016/j.crvi.2008.07.008 · Cited by 5

The Early Neural Plate Rules over the Mesoderm

Tam, P. (2001) · Developmental Cell · doi:10.1016/s1534-5807(01)00015-6 · Cited by 5

Nodal/Bozozok-independent induction of the dorsal organizer by zebrafish cell lines

Hashiguchi, M., Shinya, M., Tokumoto, M., & Sakai, N. (2008) · Developmental Biology · doi:10.1016/j.ydbio.2008.06.035 · Cited by 5

The secreted EGF-Discoidin factor xDel1 is essential for dorsal development of the Xenopus embryo

Arakawa, A., Matsuo‐Takasaki, M., Takai, A., Inomata, H., Matsumura, M., Ikeya, M., Takahashi, K., Miyachi, Y., Sasai, N., & Sasai, Y. (2007) · Developmental Biology · doi:10.1016/j.ydbio.2007.03.008 · Cited by 5

The Molecular Nature of Spemann’s Organizer

Robertis, E. M. D., & Wessely, O. (2004) · Springer eBooks · doi:10.1007/978-3-662-10416-3_5 · Cited by 5

Foxj3 represses TGF-β signals-responsive transcriptions in Xenopus early development

Yoon, G., Kim, M. S., & Choi, S. (2025) · Genes & Genomics · doi:10.1007/s13258-025-01654-7 · Cited by 4

Subcellular mass spectrometry reveals proteome remodeling in an asymmetrically dividing (frog) embryonic stem cell

Shen, B., Pade, L. R., Zhou, F., & Nemes, P. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2518372123 · Cited by 4

Germ layer formation during Xenopus embryogenesis: the balance between pluripotency and differentiation

Cao, Y. (2015) · Science China Life Sciences · doi:10.1007/s11427-015-4799-2 · Cited by 4

Zbtb21 is required for the anterior-posterior patterning of neural tissue in the early Xenopus embryo

Takebayashi‐Suzuki, K., Uchida, M., & Suzuki, A. (2022) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2022.09.048 · Cited by 4

Interactions between genistein and Wnt pathway in colon adenocarcinoma and early embryos

Azbazdar, Y., Sosa, E., Monka, J., Kurmangaliyev, Y. Z., & Tejeda‐Muñoz, N. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e32243 · Cited by 5

Self-organization of an organizer: Whole-body regeneration from reaggregated cells in cnidarians

Narayanaswamy, S., & Technau, U. (2025) · Cells and Development · doi:10.1016/j.cdev.2025.204024 · Cited by 4

A novel Kinesin‐like protein, Surhe is associated with dorsalization in the zebrafish embryos

Kim, E. J., Ro, H., Huh, T., Lee, C. J., Choi, J., & Rhee, M. (2008) · Animal Cells and Systems · doi:10.1080/19768354.2008.9647176 · Cited by 4

Characterization of small RNAs in X. tropicalis gastrulae

Faunes, F., Almonacid, L. I., Melo, F., & Larraı́n, J. (2012) · genesis · doi:10.1002/dvg.22027 · Cited by 4

Identification and expression patterns ofkif3bzduring the zebrafish embryonic development

Lee, A., & Rhee, M. (2009) · Animal Cells and Systems · doi:10.1080/19768354.2009.9647237 · Cited by 4

Activin/Nodal signals mediate the ventral expression of myf-5 in Xenopus gastrula embryos

Chen, Y., Lin, G., Hu, R., Chen, Y., & Ding, X. (2003) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2003.08.127 · Cited by 4

Recent perspectives on the genetic background of neural tube defects with special regard to iniencephaly

Joó, J. G. (2009) · Expert Review of Molecular Diagnostics · doi:10.1586/erm.09.4 · Cited by 4

Anomalien der Nägel und Zähne als Schlüssel für die Diagnose von Genodermatosen

Itin, P. H. (2014) · Der Hautarzt · doi:10.1007/s00105-013-2713-z · Cited by 4

Ottogi Inhibits Wnt/β-catenin Signaling by Regulating Cell Membrane Trafficking of Frizzled8

Kim, H.-T., Lee, M., Jeong, Y.-M., Ro, H., Kim, D.-I., Shin, Y., Kim, J., Hwang, K.-S., Choi, J.-H., Bahn, M., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-13429-6 · Cited by 4

Sprouty and Cerberus proteins in urogenital system development

Chi, L. (2007) · Cited by 4

Wnt Signals and Antagonists: The Molecular Nature of Spemann’s Head Organizer

Niehrs, C. (2004) · Springer eBooks · doi:10.1007/978-3-662-10416-3_9 · Cited by 4

maea affects head formation through β‐catenin degradation during early Xenopus laevis development

Goto, T., & Shibuyà, H. (2022) · Development Growth & Differentiation · doi:10.1111/dgd.12828 · Cited by 2

Distinct molecular profile of the chick organizer as a stem zone during axial elongation

Wood, T. R., Kuciński, I., & Voiculescu, O. (2024) · Open Biology · doi:10.1098/rsob.240139 · Cited by 3

Third Week: Becoming Trilaminar and Establishing Body Axes

Schoenwolf, G. C., Bleyl, S. B., Brauer, P. R., & Francis‐West, P. H. (2009) · Elsevier eBooks · doi:10.1016/b978-0-443-06811-9.10003-x · Cited by 3

The regulatory proteins DSCR6 and Ezh2 oppositely regulate Stat3 transcriptional activity in mesoderm patterning during Xenopus development

Loreti, M., Shi, D., & Carron, C. (2020) · Journal of Biological Chemistry · doi:10.1074/jbc.ra119.010719 · Cited by 3

ccr7 affects both morphogenesis and differentiation during early Xenopus embryogenesis

Goto, T., Michiue, T., & Shibuyà, H. (2022) · Development Growth & Differentiation · doi:10.1111/dgd.12790 · Cited by 3

Cell biology of fetal tissues and fundamental medicine

Repin, V. S., Saburina, I. N., & Sukhikh, G. T. (2007) · Bulletin of Experimental Biology and Medicine · doi:10.1007/s10517-007-0268-7 · Cited by 3

Vg1 has specific processing requirements that restrict its action to body axis patterning centers

Thomas, J. T., & Moos, M. C. (2007) · Developmental Biology · doi:10.1016/j.ydbio.2007.07.032 · Cited by 3

Conference on Cadherins, Catenins and Cancer

Birchmeier, W. (2014) · Cited by 3

Transcriptional Repression in Spemann’s Organizer and the Formation of Dorsal Mesoderm

Yaklichkin, S., Steiner, A. B., & Kessler, D. S. (2004) · Springer eBooks · doi:10.1007/978-3-662-10416-3_8 · Cited by 3

ccl19 and ccl21 affect cell movements and differentiation in early Xenopus development

Goto, T., Michiue, T., & Shibuyà, H. (2023) · Development Growth & Differentiation · doi:10.1111/dgd.12847 · Cited by 2

Signaling mechanisms that direct cell fate specification and morphogenesis in human embryonic stem cells-based models of human gastrulation

Stringa, B., & Solnica‐Krezel, L. (2023) · Emerging Topics in Life Sciences · doi:10.1042/etls20230084 · Cited by 3

Établissement des axes embryonnaires au cours du développement du poisson zèbre

Thisse, B., & Thisse, C. (2002) · médecine/sciences · doi:10.1051/medsci/2002182193 · Cited by 2

A genomic view of TGF‐β signal transduction in an invertebrate deuterostome organism and lessons from the functional analyses of Nodal and BMP2/4 during sea urchin development

Lapraz, F., Duboc, V., & Lepage, T. (2007) · Signal Transduction · doi:10.1002/sita.200600125 · Cited by 2

INTEGRATING MECHANICAL CONTROL THEORY INTO MODELS OF BIOLOGICAL DEVELOPMENT — ANALYTICAL REVIEW

Petrov, V. G., & Aegerter, C. M. (2011) · Journal of Mechanics in Medicine and Biology · doi:10.1142/s0219519411004162 · Cited by 2

Wnt Signaling during EarlyXenopusDevelopment

Fagotto, F. (2014) · Wiley eBooks · doi:10.1002/9781118492833.ch8 · Cited by 2

Mosaic versus regulation development in avian blastoderms depends on the spatial distribution of Rauber's sickle material

Callebaut, M., Nueten, E. V., Harrisson, F., & Bortier, H. E. (2007) · Journal of Morphology · doi:10.1002/jmor.10528 · Cited by 2

La mise en place des axes embryonnaires des vertébrés : un problème fascinant en passe d'être résolu ?

Schneider‐Maunoury, S., & Charnay, P. (2001) · médecine/sciences · doi:10.4267/10608/1965 · Cited by 2

[A new method for the synthesis of theobromine, caffeine and 7-methylxanthine].

WOJCIECHOWSKI, J. (1961) · PubMed · Cited by 2

Neural induction: New insight into the default model and an extended four‐step model in vertebrate embryos

Sagha, M. (2025) · Developmental Dynamics · doi:10.1002/dvdy.70002 · Cited by 1

Artesunate disrupts germ layer formation by inhibiting BMP signaling pathway

Kim, M. S., Yoon, G., & Choi, S. (2025) · Animal Cells and Systems · doi:10.1080/19768354.2025.2504940 · Cited by 1

One Wnt to lead them all: a Wnt1 primer

Lekven, A. C., Empie, S., & Saoud, R. (2025) · Differentiation · doi:10.1016/j.diff.2025.100884 · Cited by 1

Diversification of amphioxus and vertebrate Cerberus protein function in modulating Nodal, BMP and Wnt signals

Zhang, Y., & Shi, D. (2020) · Marine Life Science & Technology · doi:10.1007/s42995-019-00024-z · Cited by 1

“Evolution” of Embryogenesis: Complexity of the Early Developmental Stages in the Animal Kingdom

Liebich, S. (2020) · OBM Genetics · doi:10.21926/obm.genet.2003113 · Cited by 2

Xenopus cell-free extracts and their applications in cell biology study

Liu, J., & Zhang, C. (2023) · Biophysics Reports · doi:10.52601/bpr.2023.230016 · Cited by 1

Zbtb11 interacts with Otx2 and patterns the anterior neuroectoderm in Xenopus

Satou-Kobayashi, Y., Takahashi, S., Haramoto, Y., Asashima, M., & Taira, M. (2024) · PLoS ONE · doi:10.1371/journal.pone.0293852 · Cited by 1

Self-organization from organs to embryoids by activin in early amphibian development

Asashima, M., Satou-Kobayashi, Y., Haramoto, Y., & Ariizumi, T. (2025) · Cells and Development · doi:10.1016/j.cdev.2025.203996 · Cited by 1

Regulation of Spemann’s Organizer Formation

Fainsod, A., & Levy, V. (2004) · Springer eBooks · doi:10.1007/978-3-662-10416-3_7 · Cited by 1

Anteriore Musterbildung im Wirbeltierembryo - Die Induktion von Vorderhirn und Herz

Wittler, L. (2003) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-599 · Cited by 1

Function of the CHD4/Mi-2ß chromatin remodelling ATPase during neural development of Xenopus laevis

Nieberler, M. (2012) · Electronic Theses of LMU Munich (Ludwig-Maximilians-Universität München) · doi:10.5282/edoc.13954 · Cited by 1

Anosmin-1 is a regionally restricted component of basement membranes and interstitial matrices during organogenesis: Implications for the developmental anomalies of X chromosome-linked Kallmann syndrome

Hardelin, J., Julliard, A., Moniot, B., Soussi‐Yanicostas, N., Verney, C., Schwanzel‐Fukuda, M., Lièvre, C. A., & Petit, C. (1999) · Developmental Dynamics · doi:10.1002/(sici)1097-0177(199905)215:1 · Cited by 146

A tale of tails

Niehrs, C. (2003) · Nature · doi:10.1038/424375a · Cited by 1

Regulation of Embryogenesis

Lee, M., Warburton, D., & Minoo, P. (2016) · Elsevier eBooks · doi:10.1016/b978-0-323-35214-7.00004-4 · Cited by 1

The effects of DNA damage caused by sperm cryopreservation in Xenopus

Morrow, S. (2015) · Cited by 1

Ectodermal Dysplasias

Itin, P. H. (2016) · Wiley eBooks · doi:10.1002/9781118441213.rtd0068 · Cited by 1

Positionsinformation, Musterbildung und embryonale Induktion

Müller, W. A., & Hassel, M. (2003) · Springer-Lehrbuch · doi:10.1007/978-3-662-07055-0_12

Characterizing the roles of Memo in TGFߠSignalling

Sosu-Sedzorme, W. (2004) · Summit (Simon Fraser University)

Signaling cross-talk by bone morphogenetic proteins

Ghosh‐Choudhury, N., & Ghosh-Choudhury, G. (2008) · Birkhäuser Basel eBooks · doi:10.1007/978-3-7643-8552-1_9

A GENE NETWORK FOR HEAD ORGANIZER FORMATION

Soligo, S. (2010) · Padua Research Archive (University of Padova)

Gene Expression and Regulation in Early Vertebrate Development

Li, X. (2007)

Sostdc1 Plays an Essential Role in Mammalian Tooth Patterning: Insight into the Rodent Dental Evolution

Munne, P. (2010) · Työväentutkimus Vuosikirja

Regulation of Zebrafish Hindbrain Development by Fibroblast Growth Factor and Retinoic Acid: A Dissertation

Roy, N. M. (2003) · The Journal of the American Medical Association (JAMA) Network (American Medical Association) · doi:10.13028/0841-mq56

Generating Cell Diversity

Chitnis, A. B. (2005) · doi:10.1002/9783527619689.ch8

Characterization of a Cdc42 effector protein (Cep4l) and a novel role for Cdc42 in Xenopus neurogenesis and Fgf signaling

Hulstrand, A. M. (2013) · doi:10.17077/etd.vys5pbkr

Entwicklung bedeutsamer Modellorganismen I: Wirbellose

Müller, W. A., & Hassel, M. (2012) · Springer-Lehrbuch · doi:10.1007/978-3-642-28383-3_4

Transcriptome analysis of adult neural stem cells and functional analysis of the candidate genes TSP-4 and Uhrf1

Bayam, E. (2014) · Elektronische Hochschulschriften der LMU München (Ludwig-Maximilians-Universität München) · doi:10.5282/edoc.17632

Molecular basis for specification of the vertebrate head field

Yamamoto, A. (2010) · Springer eBooks · doi:10.1007/978-4-431-99644-6_4

Developmental Mechanisms that Support Genome Stability and Embryonic Survival in Stress-tolerant Embryos of the Annual Killifish Austrofundulus limnaeus

Wagner, J. T. (2000) · doi:10.15760/etd.2517

Bone Morphogenetic Protein (BMP) Signaling in the Neuroectoderm

Mizutani, C. M., & Bier, E. (2009) · Elsevier eBooks · doi:10.1016/b978-008045046-9.01047-0

Mechanisms of Wnt signaling: from embryonic stem cells to dopaminergic neurons

Čajánek, L. (2011) · Figshare

A message to the back side

Driever, W. (2005) · Nature · doi:10.1038/438926b

Regulation of Wnt and FGF Signaling within the Endoplasmic Reticulum for Head Formation

Yamamoto, A. (2006) · Journal of Oral Biosciences · doi:10.1016/s1349-0079(06)80015-0

The Mitotic Activity of Embryonic Tissues During Gastrulation and Nevrulation inTriturus Vulgaris L.Embryos

Georgiev, P., & Necheva, V. (2009) · Biotechnology & Biotechnological Equipment · doi:10.1080/13102818.2009.10818510

Characterization of the Visceral Endoderm Components in Early Post-Implantation Mouse Embryo Development: A Dissertation

Huang, T. (2014) · eScholarship@UMassChan · doi:10.13028/m26g63

XenopusEmbryo: Mesoderm Induction

Dale, L., & Wardle, F. C. (2015) · Encyclopedia of Life Sciences · doi:10.1002/9780470015902.a0000730.pub3

Functional studies of novel genes involved in embryogenesis of the vertebrate Xenopus laevis

Zhao, H. (2002) · DuEPublico (University of Duisburg-Essen)

Mechanisms of Wnt8 function in zebrafish mesoderm patterning

Ramel, M. (2006) · OakTrust (Texas A&M University Libraries)

Spemann's organizer and self- regulation in amphibian embryos

Oversold, L. (2006)

The role of HyBMP5-8b, a BMP5-8 orthologue, during axial patterning and tentacle formation in Hydra

Reinhardt, B. (2006) · Multimedialen Archiv und Publikationsserver der Christian-Albrechts-Universität zu Kiel (Christian-Albrechts-Universität zu Kiel)

Annals of morphology fields and prepatterns. Editorial Festschrift for John C. Carey, MD, MPH

Opitz, J. M. (2016) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.37810

TGFβ and Signaling through Receptor Serine/Threonine Protein Kinases

Kramer, I. M. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-394803-8.00017-6

The Role of Claudin-5 on Xenopus Heart Development

Zhang, B. (2009) · NCSU Libraries Repository (North Carolina State University Libraries)

An evolutionarily conserved system that regulates dorsal-ventral patterning via the BMP, Chordin, Tolloid and Twisted gastrulation proteins

Robertis, E. M. D., Pera, E. M., Garcia-Abreu, J., Larraı́n, J., Oelgeschläger, M., & Coffinier, C. (2001) · The International Journal of Developmental Biology · doi:10.1387/ijdb.01450025

Investigating the Role of Wnt in the Activation and Localization of Nkd1

Larraguibel, J. I. (2013) · The Atrium (University of Guelph)

RAPGEF5 regulates nuclear translocation of β-cateninPreprint

Griffin, J. N., del Viso, F., Duncan, A. R., Robson, A., Kulkarni, S., Liu, K. J., & Khokha, M. K. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/152892

Analysis of Naked in the Canonical Wnt Pathway

Lau, G. (2008) · TSpace (University of Toronto)

An early role for zebrafish hoxd4a and its cofactors in hematopoiesis

Zhang, C. (2017) · doi:10.32657/10356/73069

Developmental Patterning of the Inner Ear

Thiede, B. R. (2014) · doi:10.18130/v3f81g

Early Mouse Development

Kispert, A., & Gossler, A. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-382008-2.00006-4

Identification and expression patterns ofkif3az during the zebrafish embryonic development

Rhee, M. (2009) · Genes & Genomics · doi:10.1007/bf03191861

Three-Modal Theory of Early Embryo Asymmetric Cleavage Determination

Liebich, S. (2021) · Cosmos and history

脊索動物か,脊索を持った動物たちか : 古生物学と分子生物学の統合

安井, 金., & 舒, 徳. (2004) · 化石 · doi:10.14825/kaseki.76.0_7

A T-box Protein Interacting with the TCF Transcriptional Switch of Wnt Signaling in Xenopus Dorsal Axis Development.

Yang, Y. X. (2014) · Deep Blue (University of Michigan)

The Vertebrate Organizer

(2004) · Springer eBooks · doi:10.1007/978-3-662-10416-3 · Cited by 22

The Spemann-Mangold organizer: the control of fate specification and morphogenetic rearrangements during gastrulation in Xenopus

Bouwmeester, T. (2001) · The International Journal of Developmental Biology · doi:10.1387/ijdb.11291854 · Cited by 32

Cell signaling pathways controlling an axis organizing center in the zebrafish

Jones, W. D., & Mullins, M. C. (2022) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2022.03.005 · Cited by 23

Signaling Components in Dorsal-Ventral Patterning and the Organizer in Xenopus

Robertis, E. M. D., & Tejeda‐Muñoz, N. (2022) · CRC Press eBooks · doi:10.1201/9781003050230-5

Formation of the vertebrate embryo: Moving beyond the Spemann organizer

Thisse, B., & Thisse, C. (2015) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2015.05.007 · Cited by 39