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WNT signalling molecules act in axis formation in the diploblastic metazoan Hydra

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Hox genes and chordate evolution.

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Evolution of Key Cell Signaling and Adhesion Protein Families Predates Animal Origins

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Origins of Bilateral Symmetry: Hox and Dpp Expression in a Sea Anemone

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Xwnt-8, a Xenopus Wnt-1/int-1-related gene responsive to mesoderminducing growth factors, may play a role in ventral mesodermal patterning during embryogenesis

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Differential expression of WNT4 in testicular and ovarian development in a marsupial

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Conserved and novel Wnt clusters in the basal eumetazoan Nematostella vectensis

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Xenacoelomorpha Survey Reveals That All 11 Animal Homeobox Gene Classes Were Present in the First Bilaterians

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Molecular cloning, characterization and expression analysis of Wnt4, Wnt5, Wnt6, Wnt7, Wnt10 and Wnt16 from Litopenaeus vannamei

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Wnts talking with the TGF-β superfamily: WISPers about modulation of osteoarthritis

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Targeting the Versatile Wnt/β-Catenin Pathway in Cancer Biology and Therapeutics: From Concept to Actionable Strategy

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An organizing region in metamorphosing hydrozoan planula larvae - stimulation of axis formation in both larval and in adult tissue

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Symmetry and the tentacular apparatus in Cnidaria

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The molecular basis of differential morphology and bleaching thresholds in two morphs of the coral Pocillopora acuta

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Nucleation of the destruction complex on the centrosome accelerates degradation of β-catenin and regulates Wnt signal transmission

Lach, R. S., Qiu, C., Kajbaf, E. Z., Baxter, N. J., Han, D., Wang, A., Lock, H., Chirikian, O., Pruitt, B. L., & Wilson, M. Z. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2204688119 · Cited by 28

Cell adhesion and signal transduction in cancer

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Developmental Progression in the CoralAcropora digitiferaIs Controlled by Differential Expression of Distinct Regulatory Gene Networks

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A bipolar role of the transcription factor ERG for cnidarian germ layer formation and apical domain patterning

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Punctuated Emergences of Genetic and Phenotypic Innovations in Eumetazoan, Bilaterian, Euteleostome, and Hominidae Ancestors

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Identification and In Vivo Characterization of NvFP-7R, a Developmentally Regulated Red Fluorescent Protein of Nematostella vectensis

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BAC library for the amphipod crustacean, Parhyale hawaiensis

Parchem, R. J., Poulin, F., Stuart, A. B., Amemiya, C. T., & Patel, N. H. (2010) · Genomics · doi:10.1016/j.ygeno.2010.03.005 · Cited by 30

The cytochrome P450 (CYP) superfamily in cnidarians

Pankov, K., McArthur, A. G., Gold, D. A., Nelson, D. R., Goldstone, J. V., & Wilson, J. Y. (2021) · Scientific Reports · doi:10.1038/s41598-021-88700-y · Cited by 27

Comparative analysis of septic injury-inducible genes in phylogenetically distant model organisms of regeneration and stem cell research, the planarian Schmidtea mediterranea and the cnidarian Hydra vulgaris

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Genomic analysis of the tryptome reveals molecular mechanisms of gland cell evolution

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Effect of Interventions in WNT Signaling on Healing of Cardiac Injury: A Systematic Review

Daskalopoulos, E. P., & Blankesteijn, W. M. (2021) · Cells · doi:10.3390/cells10020207 · Cited by 26

Developmental processes in Ediacara macrofossils

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Long-range morphogen gradient formation by cell-to-cell signal propagation

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The Flavonol Quercitrin Hinders GSK3 Activity and Potentiates the Wnt/β-Catenin Signaling Pathway

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Methodological approaches for nanotoxicology using cnidarian models

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T‐box and homeobox genes from the ctenophore Pleurobrachia pileus: Comparison of Brachyury, Tbx2/3 and Tlx in basal metazoans and bilaterians

Martinelli, C., & Spring, J. (2005) · FEBS Letters · doi:10.1016/j.febslet.2005.08.008 · Cited by 27

Approaching marine bioprospecting in hexacorals by RNA deep sequencing

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Wnt Signaling in Cnidarians

Holstein, T. W. (2008) · Methods in molecular biology · doi:10.1007/978-1-60327-469-5 · Cited by 25

Where Simplicity Meets Complexity: Hydra, a Model for Host–Microbe Interactions

Augustin, R., Fraune, S., Franzenburg, S., & Bosch, T. C. G. (2011) · Advances in experimental medicine and biology · doi:10.1007/978-1-4419-5638-5_8 · Cited by 26

Molecular characterisation of a cellular conveyor belt in Clytia medusae

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Detection and Phylogenetic Assessment of Conserved Synteny Derived from Whole Genome Duplications

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The transcriptome of the colonial marine hydroid Hydractinia echinata

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Aryl hydrocarbon receptor (AHR) in the cnidarian Nematostella vectensis: comparative expression, protein interactions, and ligand binding

Reitzel, A. M., Passamaneck, Y. J., Karchner, S. I., Franks, D. G., Martindale, M. Q., Tarrant, A. M., & Hahn, M. E. (2013) · Development Genes and Evolution · doi:10.1007/s00427-013-0458-4 · Cited by 27

A surprising abundance of human disease genes in a simple “basal” animal, the starlet sea anemone (Nematostella vectensis)

Sullivan, J. C., & Finnerty, J. R. (2007) · Genome · doi:10.1139/g07-045 · Cited by 25

A Suppressor/Enhancer Screen in Drosophila Reveals a Role for Wnt-Mediated Lipid Metabolism in Primordial Germ Cell Migration

McElwain, M. A., Ko, D. C., Gordon, M. D., Fyrst, H., Saba, J. D., & Nusse, R. (2011) · PLoS ONE · doi:10.1371/journal.pone.0026993 · Cited by 24

Rho Family of Ras-Like GTPases in Early-Branching Animals

Beljan, S., Bosnar, M. H., & Ćetković, H. (2020) · Cells · doi:10.3390/cells9102279 · Cited by 23

Genome-Wide Identification and Expression Profiling of Wnt Family Genes in the Silkworm, Bombyx mori

Ding, X. S., Liu, J., Zheng, L., Song, J., Li, N., Hu, H., Tong, X., & Dai, F. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20051221 · Cited by 24

A Reference Genome from the Symbiotic Hydrozoan, Hydra viridissima

Hamada, M., Satoh, N., & Khalturin, K. (2020) · G3 Genes Genomes Genetics · doi:10.1534/g3.120.401411 · Cited by 25

Wnt6 expression in epidermis and epithelial tissues during Xenopus organogenesis

Lavery, D. L., Davenport, I. R., Turnbull, Y. D., Wheeler, G. N., & Hoppler, S. (2008) · Developmental Dynamics · doi:10.1002/dvdy.21440 · Cited by 24

Animal Evolution: Trichoplax, Trees, and Taxonomic Turmoil

Miller, D. J., & Ball, E. E. (2008) · Current Biology · doi:10.1016/j.cub.2008.09.016 · Cited by 24

Origin and Evolution of Dishevelled

Dillman, A. R., Minor, P. J., & Sternberg, P. W. (2013) · G3 Genes Genomes Genetics · doi:10.1534/g3.112.005314 · Cited by 23

Lineage‐specific evolution of cnidarian Wnt ligands

Hensel, K., Lotan, T., Sanders, S. M., Cartwright, P., & Uri Frank, A. (2014) · Evolution & Development · doi:10.1111/ede.12089 · Cited by 23

Does the High Gene Density in the Sponge NK Homeobox Gene Cluster Reflect Limited Regulatory Capacity?

Fahey, B., Larroux, C., Woodcroft, B. J., & Degnan, B. M. (2008) · Biological Bulletin · doi:10.2307/25470664 · Cited by 23

Preparation Techniques for Transmission Electron Microscopy of Hydra

Holstein, T. W., Hess, M. W., & Salvenmoser, W. (2010) · Methods in cell biology · doi:10.1016/s0091-679x(10)96013-5 · Cited by 22

TGF-β superfamily members from the helminth Fasciola hepatica show intrinsic effects on viability and development

Japa, O., Hodgkinson, J. E., Emes, R. D., & Flynn, R. J. (2015) · Veterinary Research · doi:10.1186/s13567-015-0167-2 · Cited by 21

A WNTer wonderland in Snowbird

He, X., & Axelrod, J. D. (2006) · Development · doi:10.1242/dev.02452 · Cited by 22

Whole body regeneration deploys a rewired embryonic gene regulatory network logicPreprint

Johnston, H., Warner, J. F., Amiel, A., Nedoncelle, K., Carvalho, J. E., & Röttinger, É. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/658930 · Cited by 36

Wnt3a-Modified Nanofiber Scaffolds Facilitate Tendon Healing by Driving Macrophage Polarization during Repair

Wei, Y., Yun, X., Guan, Y., Cao, S., Li, X., Wang, Y., Meng, H., Liu, Y.-J., Quan, Q., & Wei, M. (2023) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.2c20386 · Cited by 24

Diversity, Phylogeny and Expression Patterns of Pou and Six Homeodomain Transcription Factors in Hydrozoan Jellyfish Craspedacusta sowerbyi

Hradilová, M., Vojta, P., Strnad, H., Krejčík, Z., Rídl, J., Pačes, J., Vlček, Č., & Pačes, V. (2012) · PLoS ONE · doi:10.1371/journal.pone.0036420 · Cited by 21

The significance of sponges for comparative studies of developmental evolution

Colgren, J. J., & Nichols, S. (2019) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.359 · Cited by 18

The Path Less Explored: Innate Immune Reactions in Cnidarians

Bosch, T. C. G. (2007) · Nucleic acids and molecular biology · doi:10.1007/978-3-540-73930-2_2 · Cited by 20

Functional conservation of Nematostella Wnts in canonical and noncanonical Wnt-signaling

Rigo‐Watermeier, T., Kraft, B. N., Ritthaler, M., Wallkamm, V., Holstein, T. W., & Wedlich, D. (2011) · Biology Open · doi:10.1242/bio.2011021 · Cited by 24

Structure, function and disease relevance of Wnt inhibitory factor 1, a secreted protein controlling the Wnt and hedgehog pathways

Kerekes, K., Bányai, L., Trexler, M., & Patthy, L. (2019) · Growth Factors · doi:10.1080/08977194.2019.1626380 · Cited by 20

Wnt Gene Expression During Early Embryogenesis in the Nymphalid Butterfly Bicyclus anynana

Holzem, M., Braak, N., Brattström, O., McGregor, A. P., & Breuker, C. J. (2019) · Frontiers in Ecology and Evolution · doi:10.3389/fevo.2019.00468 · Cited by 20

Molecular analysis of heparan sulfate biosynthetic enzyme machinery and characterization of heparan sulfate structure in Nematostella vectensis

Feta, A., Do, A.-T., Rentzsch, F., Technau, U., & Kusche‐Gullberg, M. (2009) · Biochemical Journal · doi:10.1042/bj20082081 · Cited by 20

Detection of Expression Patterns in Hydra Pattern Formation

Bode, H. R., Lengfeld, T., Hobmayer, B., & Holstein, T. W. (2008) · Methods in molecular biology · doi:10.1007/978-1-60327-469-2_7 · Cited by 20

Pathological role of long non-coding (lnc) RNA in the regulation of Wnt/β-catenin signaling pathway during epithelial-mesenchymal transition (EMT)

Alsaab, H. O. (2023) · Pathology - Research and Practice · doi:10.1016/j.prp.2023.154566 · Cited by 19

Sense and anti-sense: Role of FAM83A and FAM83A-AS1 in Wnt, EGFR, PI3K, EMT pathways and tumor progression

Zhao, C., Li, X., Zhang, R., Lyu, H., Xiao, S., Guo, D. S., Ali, D. W., Michalak, M., Chen, X., Zhou, C., et al. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.116372 · Cited by 19

Nanotoxicology using the sea anemoneNematostella vectensis: from developmental toxicity to genotoxicology

Ambrosone, A., Marchesano, V., Mazzarella, V., & Tortiglione, C. (2013) · Nanotoxicology · doi:10.3109/17435390.2013.802386 · Cited by 19

Key transitions in animal evolution.

DeSalle, R., & Schierwater, B. (2010) · Integrative and Comparative Biology · doi:10.1093/icb/icm042 · Cited by 25

Canonical Wnt Signaling in the Pathology of Iron Overload‐Induced Oxidative Stress and Age‐Related Diseases

Armstrong, A. T., Mandala, A., Malhotra, M., & Gnana‐Prakasam, J. P. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/7163326 · Cited by 18

Subfunctionalization and neofunctionalization of vertebrate Lef/Tcf transcription factors

Klingel, S., Morath, I., Strietz, J., Menzel, K., Holstein, T. W., & Gradl, D. (2012) · Developmental Biology · doi:10.1016/j.ydbio.2012.05.012 · Cited by 18

Wnt affects symmetry and morphogenesis during post-embryonic development in colonial chordates

Maio, A. D., Setar, L., Tiozzo, S., & Tomaso, A. W. D. (2015) · EvoDevo · doi:10.1186/s13227-015-0009-3 · Cited by 18

Incorporating tree‐thinking and evolutionary time scale into developmental biology

Kuraku, S., Feiner, N., Keeley, S. D., & Hara, Y. (2016) · Development Growth & Differentiation · doi:10.1111/dgd.12258 · Cited by 17

Differential regulation of myc homologs by Wnt/β‐Catenin signaling in the early metazoan Hydra

Hartl, M., Glasauer, S. M. K., Gufler, S., Raffeiner, A., Puglisi, K., Breuker, K., Bister, K., & Hobmayer, B. (2019) · FEBS Journal · doi:10.1111/febs.14812 · Cited by 18

Ectopic activation of GABAB receptors inhibits neurogenesis and metamorphosis in the cnidarian Nematostella vectensis

Levy, S., Brekhman, V., Bakhman, A. F., Malik, A., Sebé-Pedrós, A., Kosloff, M., & Lotan, T. (2020) · Nature Ecology & Evolution · doi:10.1038/s41559-020-01338-3 · Cited by 19

Expression of Wnt pathway genes in polyps and medusa‐like structures of Ectopleura larynx ( C nidaria: Hydrozoa)

Nawrocki, A. M., & Cartwright, P. (2013) · Evolution & Development · doi:10.1111/ede.12045 · Cited by 18

Implications of cnidarian gene expression patterns for the origins of bilaterality is the glass half full or half empty?

Ball, E. E., de Jong, D. M., Schierwater, B., Shinzato, C., Hayward, D. C., & Miller, D. J. (2007) · Integrative and Comparative Biology · doi:10.1093/icb/icm028 · Cited by 18

Wnt/β-catenin signaling participates in the regulation of lipogenesis in the liver of juvenile turbot (Scophthalmus maximus L.)

Liu, D., Mai, K., Zhang, Y., Xu, W., & Ai, Q. (2016) · Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology · doi:10.1016/j.cbpb.2015.11.002 · Cited by 15

Embryonic expression of priapulid Wnt genes

Hogvall, M., Vellutini, B. C., Martín-Durán, J. M., Hejnol, A., Budd, G. E., & Janßen, R. (2019) · Development Genes and Evolution · doi:10.1007/s00427-019-00636-6 · Cited by 17

Genome-wide identification and expression profiling analysis of Wnt family genes affecting adipocyte differentiation in cattle

Pan, C., Wang, S., Yang, C., Hu, C., Sheng, H., Xue, X., Hu, H., Lei, Z., Yang, M., & Ma, Y. (2022) · Scientific Reports · doi:10.1038/s41598-021-04468-1 · Cited by 17

Asymmetric requirement of surface epithelial β‐catenin during the upper and lower jaw development

Sun, Y., Teng, I., Huo, R., Rosenfeld, M. G., Olson, L. E., Li, X., & Li, X. (2012) · Developmental Dynamics · doi:10.1002/dvdy.23755 · Cited by 17

Evolution of Metazoan Life Cycles and the Origin of Pelagic Larvae

Malakhov, V. V., Bogomolova, E., Kuzmina, T. V., & Temereva, E. N. (2019) · Russian Journal of Developmental Biology · doi:10.1134/s1062360419060043 · Cited by 17

TMEM79/MATTRIN defines a pathway for Frizzled regulation and is required for Xenopus embryogenesis

Chen, M., Amado, N. G., Tan, J., Reis, A. H., Ge, M., Abreu, J. G., & He, X. (2020) · eLife · doi:10.7554/elife.56793 · Cited by 16

The centipede Strigamia maritima possesses a large complement of Wnt genes with diverse expression patterns

Hayden, L., & Arthur, W. (2014) · Evolution & Development · doi:10.1111/ede.12073 · Cited by 17

Qualitative shift to indirect development in the parasitic sea anemone Edwardsiella lineata

Reitzel, A. M., Sullivan, J. C., & Finnerty, J. R. (2006) · Integrative and Comparative Biology · doi:10.1093/icb/icl032 · Cited by 17

Expression profiles of urbilaterian genes uniquely shared between honey bee and vertebrates

Matsui, T., Yamamoto, T., Wyder, S., Zdobnov, E. M., & Kadowaki, T. (2009) · BMC Genomics · doi:10.1186/1471-2164-10-17 · Cited by 17

A food's-eye view of the transition from basal metazoans to bilaterians

Blackstone, N. W. (2007) · Integrative and Comparative Biology · doi:10.1093/icb/icm056 · Cited by 17

Are we degenerate tetraploids? More genomes, new facts

Abbasi, A. A. (2008) · Biology Direct · doi:10.1186/1745-6150-3-50 · Cited by 16

Identification and expression characterization of WntA during intestinal regeneration in the sea cucumber Apostichopus japonicus

Li, X., Sun, L., Yang, H., Zhang, L., Miao, T., Xing, L., & Huo, D. (2017) · Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology · doi:10.1016/j.cbpb.2017.06.005 · Cited by 16

Extracellular matrix and morphogenesis in cnidarians: a tightly knit relationship

Bergheim, B. G., & Özbek, S. (2019) · Essays in Biochemistry · doi:10.1042/ebc20190021 · Cited by 16

Expression of galaxin and oncogene homologs in growth anomaly in the coral Montipora capitata

Spies, N. P., & Takabayashi, M. (2013) · Diseases of Aquatic Organisms · doi:10.3354/dao02603 · Cited by 16

Cnidaria

Technau, U., Genikhovich, G., & Kraus, J. E. M. (2015) · Springer eBooks · doi:10.1007/978-3-7091-1862-7_6 · Cited by 17

Comparative analysis of zygotic developmental genes in Rhodnius prolixus genome shows conserved features on the tracheal developmental pathway

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