Signaling pathways regulating ectodermal cell fate choices

Molecular architecture of annelid nerve cord supports common origin of nervous system centralization in bilateria

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Ventral and Lateral Regions of the Zebrafish Gastrula, Including the Neural Crest Progenitors, Are Established by abmp2b/swirlPathway of Genes

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An early requirement for FGF signalling in the acquisition of neural cell fate in the chick embryo

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The status of Wnt signalling regulates neural and epidermal fates in the chick embryo

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Progressive induction of caudal neural character by graded Wnt signaling

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A balance of FGF, BMP and WNT signalling positions the future placode territory in the head

Litsiou, A., Hanson, S., & Streit, A. (2005) · Development · doi:10.1242/dev.01964 · Cited by 275 · see citing works

Establishment and maintenance of the border of the neural plate in the chick: involvement of FGF and BMP activity

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Six1 promotes a placodal fate within the lateral neurogenic ectoderm by functioning as both a transcriptional activator and repressor

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Extensive Cell Movements Accompany Formation of the Otic Placode

Streit, A. (2002) · Developmental Biology · doi:10.1006/dbio.2002.0739 · Cited by 210 · see citing works

Neural Induction in Xenopus: Requirement for Ectodermal and Endomesodermal Signals via Chordin, Noggin, β-Catenin, and Cerberus

Kuroda, H., Wessely, O., & Robertis, E. M. D. (2004) · PLoS Biology · doi:10.1371/journal.pbio.0020092 · Cited by 195 · see citing works

Role of FGF andNogginin Neural Crest Induction

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Bimodal functions of Notch-mediated signaling are involved in neural crest formation during avian ectoderm development

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BMP signaling is essential for development of skeletogenic and neurogenic cranial neural crest

Kanzler, B., Foreman, R. K., Labosky, P. A., & Mallo, M. (2000) · Development · doi:10.1242/dev.127.5.1095 · Cited by 182 · see citing works

Differential requirements of BMP and Wnt signalling during gastrulation and neurulation define two steps in neural crest induction

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Progressive restriction of otic fate: the role of FGF and Wnt in resolving inner ear potential

Freter, S., Muta, Y., Mak, S.-S., Rinkwitz, S., & Ladher, R. (2008) · Development · doi:10.1242/dev.026674 · Cited by 163 · see citing works

Identification of Early Requirements for Preplacodal Ectoderm and Sensory Organ Development

Kwon, H., Bhat, N., Sweet, E. M., Cornell, R. A., & Riley, B. B. (2010) · PLoS Genetics · doi:10.1371/journal.pgen.1001133 · Cited by 163 · see citing works

Neural induction: 10 years on since the ‘default model’

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Tissues and signals involved in the induction of placodal Six1 expression in Xenopus laevis

Ahrens, K., & Schlosser, G. (2005) · Developmental Biology · doi:10.1016/j.ydbio.2005.07.022 · Cited by 161 · see citing works

BMP inhibition initiates neural induction via FGF signaling and Zic genes

Marchal, L., Luxardi, G., Thomé, V., & Kodjabachian, L. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0906352106 · Cited by 135 · see citing works

An Early Role for Wnt Signaling in Specifying Neural Patterns of Cdx and Hox Gene Expression and Motor Neuron Subtype Identity

Nordström, U., Maier, E., Jessell, T. M., & Edlund, H. (2006) · PLoS Biology · doi:10.1371/journal.pbio.0040252 · Cited by 130 · see citing works

BMP4 induction of sensory neurons from human embryonic stem cells and reinnervation of sensory epithelium

Shi, F., Corrales, C. E., Liberman, M. C., & Edge, A. S. B. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05909.x · Cited by 127 · see citing works

Wnt-regulated temporal control of BMP exposure directs the choice between neural plate border and epidermal fate

Patthey, C., Edlund, H., & Gunhaga, L. (2008) · Development · doi:10.1242/dev.025890 · Cited by 123 · see citing works

pitx3defines an equivalence domain for lens and anterior pituitary placode

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Epidermal Development in Mammals: Key Regulators, Signals from Beneath, and Stem Cells

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Efficient generation of lens progenitor cells and lentoid bodies from human embryonic stem cells in chemically defined conditions

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β-Catenin specifies the endomesoderm and defines the posterior organizer of the hemichordate Saccoglossus kowalevskii

Darras, S., Gerhart, J. C., Terasaki, M., Kirschner, M. W., & Lowe, C. J. (2011) · Development · doi:10.1242/dev.059493 · Cited by 106 · see citing works

Time of Exposure to BMP Signals Plays a Key Role in the Specification of the Olfactory and Lens Placodes Ex Vivo

Sjödal, M., Edlund, H., & Gunhaga, L. (2007) · Developmental Cell · doi:10.1016/j.devcel.2007.04.020 · Cited by 102 · see citing works

Differential distribution of competence for panplacodal and neural crest induction to non-neural and neural ectoderm

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FGF/MAPK signaling is required in the gastrula epiblast for avian neural crest induction

Stuhlmiller, T. J., & García‐Castro, M. I. (2011) · Development · doi:10.1242/dev.070276 · Cited by 96 · see citing works

Early regionalization of the otic placode and its regulation by the Notch signaling pathway

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Differential BMP signaling controls formation and differentiation of multipotent preplacodal ectoderm progenitors from human embryonic stem cells

Leung, A. W., Morest, D. K., & Li, J. Y. H. (2013) · Developmental Biology · doi:10.1016/j.ydbio.2013.04.023 · Cited by 81 · see citing works

Early Development of the Central and Peripheral Nervous Systems Is Coordinated by Wnt and BMP Signals

Patthey, C., Gunhaga, L., & Edlund, H. (2008) · PLoS ONE · doi:10.1371/journal.pone.0001625 · Cited by 77 · see citing works

Mutual repression between Gbx2 and Otx2 in sensory placodes reveals a general mechanism for ectodermal patterning

Steventon, B., Mayor, R., & Streit, A. (2012) · Developmental Biology · doi:10.1016/j.ydbio.2012.04.025 · Cited by 77 · see citing works

Neural induction in Xenopus requires inhibition of Wnt-β-catenin signaling

Heeg‐Truesdell, E., & LaBonne, C. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2006.06.015 · Cited by 68 · see citing works

A gene network that coordinates preplacodal competence and neural crest specification in zebrafish

Bhat, N., Kwon, H., & Riley, B. B. (2012) · Developmental Biology · doi:10.1016/j.ydbio.2012.10.012 · Cited by 67 · see citing works

Fate map and morphogenesis of presumptive neural crest and dorsal neural tube

Ezin, A. M., Fraser, S. E., & Bronner-Fraser, M. E. (2009) · Developmental Biology · doi:10.1016/j.ydbio.2009.03.018 · Cited by 63 · see citing works

dlx3b/4b are required for the formation of the preplacodal region and otic placode through local modulation of BMP activity

Esterberg, R., & Fritz, A. (2008) · Developmental Biology · doi:10.1016/j.ydbio.2008.10.017 · Cited by 61 · see citing works

Neural crests are actively precluded from the anterior neural fold by a novel inhibitory mechanism dependent on Dickkopf1 secreted by the prechordal mesoderm

Carmona‐Fontaine, C., Acuña, G., Ellwanger, K., Niehrs, C., & Mayor, R. (2007) · Developmental Biology · doi:10.1016/j.ydbio.2007.07.006 · Cited by 60 · see citing works

Body-plan evolution in the Bilateria: early antero-posterior patterning and the deuterostome–protostome dichotomy

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Evolution of Axis Specification Mechanisms in Jawed Vertebrates: Insights from a Chondrichthyan

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SNW1 Is a Critical Regulator of Spatial BMP Activity, Neural Plate Border Formation, and Neural Crest Specification in Vertebrate Embryos

Wu, M., Ramel, M., Howell, M. T., & Hill, C. S. (2011) · PLoS Biology · doi:10.1371/journal.pbio.1000593 · Cited by 50 · see citing works

Early neural crest induction requires an initial inhibition of Wnt signals

Steventon, B., & Mayor, R. (2012) · Developmental Biology · doi:10.1016/j.ydbio.2012.02.029 · Cited by 48 · see citing works

An Intermediate Level of BMP Signaling Directly Specifies Cranial Neural Crest Progenitor Cells in Zebrafish

Schumacher, J. A., Hashiguchi, M., Nguyen, V., & Mullins, M. C. (2011) · PLoS ONE · doi:10.1371/journal.pone.0027403 · Cited by 46 · see citing works

Specification and regionalisation of the neural plate border

Patthey, C., & Gunhaga, L. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07871.x · Cited by 41 · see citing works

Craniofacial development in the talpid3 chicken mutant

Buxton, P., Francis‐West, P. H., Davey, M. G., Tickle, C. A., Paton, I. R., Morrice, D., & Burt, D. W. (2004) · Differentiation · doi:10.1111/j.1432-0436.2004.07207006.x · Cited by 39 · see citing works

BMP‐induced L‐Maf regulates subsequent BMP‐independent differentiation of primary lens fibre cells

Pandit, T., Jidigam, V. K., & Gunhaga, L. (2011) · Developmental Dynamics · doi:10.1002/dvdy.22692 · Cited by 25 · see citing works

Directed Differentiation of Neural and Sensory Tissues from Embryonic Stem Cells In Vitro

Sasai, Y. (2006) · Springer eBooks · doi:10.1007/3-540-37644-5_7 · Cited by 7 · see citing works

The cellular and molecular mechanisms of vertebrate lens development

Cvekl, A., & Ashery-Padan, R. (2014) · Development · doi:10.1242/dev.107953 · Cited by 227 · see citing works

Ectodermal dysplasias: Classification and organization by phenotype, genotype and molecular pathway.

Wright, J. T., Fete, M., Schneider, H., Zinser, M., Koster, M. I., Clarke, A. J., Hadj‐Rabia, S., Tadini, G., Pagnan, N., Visinoni, A. F., et al. (2019) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.61045 · Cited by 185 · see citing works

Signaling and Gene Regulatory Networks in Mammalian Lens Development

Cvekl, A., & Zhang, X. (2017) · Trends in Genetics · doi:10.1016/j.tig.2017.08.001 · Cited by 168 · see citing works

Self-organizing neuruloids model developmental aspects of Huntington’s disease in the ectodermal compartment

Haremaki, T., Metzger, J. J., Rito, T., Ozair, M. Z., Etoc, F., & Brivanlou, A. H. (2019) · Nature Biotechnology · doi:10.1038/s41587-019-0237-5 · Cited by 157 · see citing works

WNT/β-catenin signaling mediates human neural crest induction via a pre-neural border intermediate

Leung, A. W., Murdoch, B., Salem, A. F., Prasad, M. S., Gomez, G. A., & García‐Castro, M. I. (2016) · Development · doi:10.1242/dev.130849 · Cited by 146 · see citing works

TGF-β Family Signaling in Epithelial Differentiation and Epithelial–Mesenchymal TransitionPreprint

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Neural crest cell signaling pathways critical to cranial bone development and pathology

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Cell fate decisions, transcription factors and signaling during early retinal development

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Amniogenesis occurs in two independent waves in primates

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Lens Development and Crystallin Gene Expression

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Building inner ears: recent advances and future challenges for in vitro organoid systems

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Functional integration of eye tissues and refractive eye development: mechanisms and pathways

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Behavioral alterations of zebrafish larvae after early embryonic exposure to ketamine

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PFKFB4 controls embryonic patterning via Akt signalling independently of glycolysis

Pegoraro, C., Figueiredo, A. L., Maczkowiak, F., Pouponnot, C., Eychène, A., & Monsoro-Burq, A. H. (2015) · Nature Communications · doi:10.1038/ncomms6953 · Cited by 48 · see citing works

The mouse Foxi3 transcription factor is necessary for the development of posterior placodes

Birol, O., Ohyama, T., Edlund, R. K., Drakou, K., Georgiades, P., & Groves, A. K. (2015) · Developmental Biology · doi:10.1016/j.ydbio.2015.09.022 · Cited by 46 · see citing works

Intracellular attenuation of BMP signaling via CKIP-1/Smurf1 is essential during neural crest induction

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Foxi3 is necessary for the induction of the chick otic placode in response to FGF signaling

Khatri, S. B., Edlund, R. K., & Groves, A. K. (2014) · Developmental Biology · doi:10.1016/j.ydbio.2014.04.014 · Cited by 43 · see citing works

WNT/β-CATENIN modulates the axial identity of ES derived human neural crest

Gomez, G. A., Prasad, M. S., Wong, M., Charney, R. M., Shelar, P. B., Sandhu, N., Hackland, J. O. S., Hernández, J. C., Leung, A. W., & García‐Castro, M. I. (2019) · Development · doi:10.1242/dev.175604 · Cited by 43 · see citing works

Signalling pathways involved in the process of mesenchymal stem cells differentiating into hepatocytes

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Specifying neural crest cells: From chromatin to morphogens and factors in between

Rogers, C. D., & Nie, S. (2018) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.322 · Cited by 36 · see citing works

Insights into Bone Morphogenetic Protein—(BMP-) Signaling in Ocular Lens Biology and Pathology

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Transcriptome and proteome characterization of surface ectoderm cells differentiated from human iPSCs

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Post-transcriptional tuning of FGF signaling mediates neural crest induction

Copeland, J., & Simoes-Costa, M. (2020) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.2009997117 · Cited by 22 · see citing works

Modulating mesendoderm competence during human germ layer differentiation

Valcourt, J. R., Huang, R. E., Kundu, S., Venkatasubramanian, D., Kingston, R. E., & Ramanathan, S. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109990 · Cited by 22 · see citing works

Modeling, applications and challenges of inner ear organoid

Qi, J., Zhang, L., Wang, X., Chen, X., Li, Y., Wang, T., Wu, P., & Chai, R. (2024) · Smart Medicine · doi:10.1002/smmd.20230028 · Cited by 21 · see citing works

The Role of Foxi Family Transcription Factors in the Development of the Ear and Jaw

Edlund, R. K., Birol, O., & Groves, A. K. (2015) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2014.11.014 · Cited by 20 · see citing works

Deletion of the Dishevelled family of genes disrupts anterior-posterior axis specification and selectively prevents mesoderm differentiation

Ngo, J., Hashimoto, M., Hamada, H., & Wynshaw-Boris, A. J. (2020) · Developmental Biology · doi:10.1016/j.ydbio.2020.05.010 · Cited by 16 · see citing works

Only accessible information is useful: insights from gradient-mediated patterning

Tikhonov, M., Little, S. C., & Gregor, T. (2015) · Royal Society Open Science · doi:10.1098/rsos.150486 · Cited by 15 · see citing works

Building an Artificial Stem Cell Niche: Prerequisites for Future 3D‐Formation of Inner Ear Structures—Toward 3D Inner Ear Biotechnology

de Groot, S. C., Sliedregt, K., van Benthem, P. P. G., Rivolta, M. N., & Huisman, M. A. (2019) · The Anatomical Record · doi:10.1002/ar.24067 · Cited by 15 · see citing works

The differentiation effect of bone morphogenetic protein (BMP) on human amniotic epithelial stem cells to express ectodermal lineage markers

Biniazan, F., Manzari‐Tavakoli, A., Safaeinejad, F., Moghimi, A., Rajaei, F., & Niknejad, H. (2020) · Cell and Tissue Research · doi:10.1007/s00441-020-03280-z · Cited by 12 · see citing works

Three-dimensional analysis for detection of pulp stones in a Saudi population using cone beam computed tomography

Kaabi, H. H., Riyahi, A. M., Al-Maflehi, N. S., Alrumayyan, S. F., Bakrman, A. K., & Almutaw, Y. A. (2023) · Journal of Oral Science · doi:10.2334/josnusd.23-0091 · Cited by 12 · see citing works

A possible connection between reactive oxygen species and the unfolded protein response in lens development: From insight to foresight

Gao, L., Jin, N., Ye, Z., Ma, T., Huang, Y. X. R., Li, H., Du, J., & Li, Z. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.820949 · Cited by 8 · see citing works

The Reconstruction of Peripheral Auditory Circuit: Recent Advances and Future Challenges

Li, Z., Zhang, Y., Xiao, Z., & Qi, J. (2025) · Advanced Science · doi:10.1002/advs.202410494 · Cited by 7 · see citing works

Confirmation of a Phenotypic Entity for TSPEAR Variants in Egyptian Ectodermal Dysplasia Patients and Role of Ethnicity

Rabie, E., Sayed, I. S. M., Amr, K. S., Ahmed, H. A., Mostafa, M. I., Hassib, N. F., El-Sayed, H. M., Zada, S. K., & El‐Kamah, G. Y. (2022) · Genes · doi:10.3390/genes13061056 · Cited by 7 · see citing works

Modeling of human neurulation using bioengineered pluripotent stem cell culture

Xue, X., Wang, R. P., & Fu, J. (2020) · Current Opinion in Biomedical Engineering · doi:10.1016/j.cobme.2020.02.002 · Cited by 7 · see citing works

Controlling neural territory patterning from pluripotency using a systems developmental biology approach

Sears, K. E., Gullapalli, K., Trivedi, D., Mihas, A. K., Bukys, M. A., & Jensen, J. N. (2022) · iScience · doi:10.1016/j.isci.2022.104133 · Cited by 6 · see citing works

Amphibian Zic Genes

Merzdorf, C., & Forecki, J. (2018) · Advances in experimental medicine and biology · doi:10.1007/978-981-10-7311-3_7 · Cited by 5 · see citing works

Caregiver‐reported dental manifestations in individuals with genetic neurodevelopmental disorders

Ming, N. R., Noble, D., Chussid, S., Ziegler, A. C., & Chung, W. K. (2023) · International Journal of Paediatric Dentistry · doi:10.1111/ipd.13116 · Cited by 4 · see citing works

Overview of chromatin regulatory processes during surface ectodermal development and homeostasis

Branch, M. C., Weber, M., Li, M.-Y., Flora, P., & Ezhkova, E. (2024) · Developmental Biology · doi:10.1016/j.ydbio.2024.07.001 · Cited by 4 · see citing works

Dental Phenotype with Minor Ectodermal Symptoms Suggestive of WNT10A Deficiency

García-Martínez, V.-E., Galiana-Vallés, X., Alcalá, O. Z., Rodríguez‐López, R., Llena, C., Martínez‐Romero, M. D. C., & Guillén‐Navarro, E. (2023) · Children · doi:10.3390/children10020356 · Cited by 3 · see citing works

Modern In Vitro Techniques for Modeling Hearing Loss

Shah, J. J., Jaramillo, C. J., Lybrand, Z. R., Yuan, T. T., & Erbele, I. D. (2024) · Bioengineering · doi:10.3390/bioengineering11050425 · Cited by 3 · see citing works

NR6A1 is essential for neural crest cell specification, formation and survival

Moore, E. L., Muñoz, W. A., Dennis, J. F., Bhatt, S., Sakai, D., Achilleos, A., Zhao, R., Lamb, M. C., Price, A. J., Seidel, C. W., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-68647-2 · Cited by 2 · see citing works

Streamlining cell fate decisions during chondrogenesis

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A New Wnt1-CRE Tomato Rosa Embryonic Stem Cell Line: A Tool for Studying Neural Crest Cell Integration Capacity

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Changing the Waddington landscape to control mesendoderm competencePreprint

Valcourt, J. R., Huang, R. E., Kundu, S., Venkatasubramanian, D., Kingston, R. E., & Ramanathan, S. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/867010 · Cited by 1 · see citing works

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

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First-Trimester Embryology: An Overview

Jones, C., Penzkover, D., Pollard, R., & Kuhlmann, R. S. (2015) · Springer eBooks · doi:10.1007/978-3-319-20203-7_4

Autism human neural precursor cells exhibit common defects in neurite outgrowth, cell migration, and mTOR signaling

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Modelagem celular>i< in vitro>/i< da Doença de Huntington com ácido 3-nitropropiônico e ácido quinolínico & Avaliação das funções neuroprotetoras da adenosina

Marques, L. B. (2022) · doi:10.11606/d.46.2022.tde-06092022-130610

Corneal Development

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Loss of Atoh8 Affects Neurocranial and Axial Skeleton Development in Zebrafish

Fragale, N., Divvela, S. S. K., Williams, V. C., & Brand‐Saberi, B. (2025) · Frontiers in Bioscience-Landmark · doi:10.31083/fbl26806

Étude fonctionnelle de l'induction neurale chez le céphalochordé Branchiostoma lanceolatum

Pétillon, Y. L. (2014) · doi:10.70675/c49ba4abz06b2z4a62z8728zf50902e98b30

Control of cell specification and migration during early frog development by PFKFB4, a key glycolysis regulator

Figueiredo, A. L. (2015) · doi:10.70675/d28eea5az4010z4696zb3a8zdcb78c323ae4

Selective advantages, selective mismatches, chronic inflammation, obesity, and type 2 diabetes: a new hypothesis to explain the effects of natural selection on genetic variation at the ectodysplasin A receptor locus

Coletta, D. K., Hlusko, L. J., Scott, G. R., Klimentidis, Y. C., Pastore, A. J., Palumbo, S., FATIMA, N., & Mandarino, L. J. (2026) · BMJ Open Diabetes Research & Care · doi:10.1136/bmjdrc-2026-005937

Neural stem cells: From fly to vertebrates

Doe, C. Q., Fuerstenberg, S., & Peng, C. (1998) · Journal of Neurobiology · doi:10.1002/(sici)1097-4695(199808)36:2 · Cited by 85 · see citing works

Epidermal, Neuronal and Glial Cell Fate Choice in the Embryo

Moreau, M., Cochard, P., & Duprat, A. (2004) · Springer eBooks · doi:10.1007/978-3-662-10416-3_19 · Cited by 1 · see citing works

The choice between epidermal and neural fate: a matter of calcium.

Moreau, M., & Leclerc, C. (2004) · The International Journal of Developmental Biology · doi:10.1387/ijdb.15272372 · Cited by 63 · see citing works

Cell Fate Decisions in Early Embryonic Development

Zhang, X. (2013) · Digital Access to Scholarship at Harvard (DASH) (Harvard University)

Novel signals guiding endodermal progenitor cells toward pancreatic fate

Spagnoli, F. M., Petzold, K. M., & Brivanlou, A. H. (2009) · Developmental Biology · doi:10.1016/j.ydbio.2009.05.470