Runnin' with the Dvl: Proteins That Associate with Dsh/Dvl and Their Significance to Wnt Signal Transduction

Activation of β-Catenin-Tcf Signaling in Colon Cancer by Mutations in β-Catenin or APC

Morin, P. J., Sparks, A. B., Kořínek, V., Barker, N., Clevers, H. C., Vogelstein, B., & Kinzler, K. W. (1997) · Science · doi:10.1126/science.275.5307.1787 · Cited by 4,000

Wnt signaling and cancer

Polakis, P. (2000) · Genes & Development · doi:10.1101/gad.14.15.1837 · Cited by 3,183

β‐catenin is a target for the ubiquitin–proteasome pathway

Aberle, H., Bauer, A., Stappert, J., Kispert, A., & Kemler, R. (1997) · The EMBO Journal · doi:10.1093/emboj/16.13.3797 · Cited by 2,586

Control of β-Catenin Phosphorylation/Degradation by a Dual-Kinase Mechanism

Liu, C., Li, Y., Semënov, M. V., Han, C., Baeg, G., Tan, Y., Zhang, Z., Lin, X., & He, X. (2002) · Cell · doi:10.1016/s0092-8674(02)00685-2 · Cited by 2,152

Mutations affecting the pattern of the larval cuticle inDrosophila melanogaster

N�sslein-Volhard, C., Wieschaus, E. F., & Kluding, H. (1984) · Development Genes and Evolution · doi:10.1007/bf00848156 · Cited by 1,552

A new member of the frizzled family from Drosophila functions as a Wingless receptor

Bhanot, P., van den Brink, M. R. M., Samos, C. H., Hsieh, J.-C., Wang, Y., Macke, J. P., Andrew, D. J., Nathans, J., & Nusse, R. (1996) · Nature · doi:10.1038/382225a0 · Cited by 1,504

Binding of GSK3β to the APC-β-Catenin Complex and Regulation of Complex Assembly

Rubinfeld, B., Albert, I., Porfiri, E., Fiol, C. J., Munemitsu, S. M., & Polakis, P. G. (1996) · Science · doi:10.1126/science.272.5264.1023 · Cited by 1,420

Functional Interaction of an Axin Homolog, Conductin, with β-Catenin, APC, and GSK3β

Behrens, J., Jerchow, B., Würtele, M., Grimm, J., Asbrand, C., Wirtz, R. M., Kühl, M., Wedlich, D., & Birchmeier, W. (1998) · Science · doi:10.1126/science.280.5363.596 · Cited by 1,255

Wnt Signaling in Oncogenesis and Embryogenesis--a Look Outside the Nucleus

Peifer, M., & Polakis, P. (2000) · Science · doi:10.1126/science.287.5458.1606 · Cited by 1,253

Axin, a negative regulator of the Wnt signaling pathway, forms a complex with GSK‐3β and β‐catenin and promotes GSK‐3β‐dependent phosphorylation of β‐catenin

Ikeda, S., Kishida, S., Yamamoto, H., Murai, H., Koyama, S., & Kikuchi, A. (1998) · The EMBO Journal · doi:10.1093/emboj/17.5.1371 · Cited by 1,248

Retinal Stem Cells and Regeneration of Vision System

Yip, H. K.-F. (2013) · The Anatomical Record · doi:10.1002/ar.22800 · Cited by 21

GC‐binding factor 2 interacts with dishevelled and regulates Wnt signaling pathways in human carcinoma cell lines

Ohtsuka, H., Oikawa, M., Ariake, K., Rikiyama, T., Motoi, F., Katayose, Y., Unno, M., & Johnson, A. C. (2010) · International Journal of Cancer · doi:10.1002/ijc.25837 · Cited by 22

Evaluation of a chemical library of small-molecule Dishevelled antagonists that suppress tumor growth by down-regulating T-cell factor–mediated transcription

You, L., Xu, Z., Punchihewa, C., Jablons, D. M., & Fujii, N. (2008) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-08-0155 · Cited by 22

Unveiling novel genes upregulated by both rhBMP2 and rhBMP7 during early osteoblastic transdifferentiation of C2C12 cells

Bustos-Valenzuela, J. C., Fujita, A., Halcsik, E., Granjeiro, J. M., & Sogayar, M. C. (2011) · BMC Research Notes · doi:10.1186/1756-0500-4-370 · Cited by 21

Serving up health: How phytochemicals transform food into medicine in the battle against cancer

Sharma, E., Tewari, M., Sati, P., Sharma, I., Attri, D. C., Rana, S., Aldahish, A. A., Călina, D. C., Dhyani, P., Sharifi‐Rad, J., et al. (2024) · Food Frontiers · doi:10.1002/fft2.439 · Cited by 21

Stage‐dependent Dishevelled‐1 expression during mouse spermatogenesis suggests a role in regulating spermatid morphological changes

Ma, P., Wang, H.-Z., Guo, R., Ma, Q., Yu, Z.-R., Jiang, Y., Ge, Y.-H., Ma, J., Xue, S.-P., & Han, D. (2006) · Molecular Reproduction and Development · doi:10.1002/mrd.20468 · Cited by 20

Dishevelled 1, a pivotal positive regulator of the Wnt signalling pathway, mediates 5-fluorouracil resistance in HepG2 cells

Xu, Y.-S., Zhang, C., Liang, H., Hu, S., Li, P., Liu, L., Duan, X., Chen, C., Zhang, Y., & Dai, P. (2018) · Artificial Cells Nanomedicine and Biotechnology · doi:10.1080/21691401.2018.1453827 · Cited by 20

Structure–Function Dissection of the Frizzled Receptor in Drosophila melanogaster Suggests Different Mechanisms of Action in Planar Polarity and Canonical Wnt Signaling

Strutt, D. I., Madder, D., Chaudhary, V., & Artymiuk, P. J. (2012) · Genetics · doi:10.1534/genetics.112.144592 · Cited by 20

Phosphorylation of β-catenin results in lack of β-catenin signaling in melanoma

Kuphal, S. (2011) · International Journal of Oncology · doi:10.3892/ijo.2011.1028 · Cited by 18

Indole-2-amide based biochemical antagonist of Dishevelled PDZ domain interaction down-regulates Dishevelled-driven Tcf transcriptional activity

Mahindroo, N., Punchihewa, C., Bail, A. M., & Fujii, N. (2007) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2007.12.039 · Cited by 19

Effect of activation of canonical Wnt signaling by the Wnt-3a protein on the susceptibility of PC12 cells to oxidative and apoptotic insults

Kawamoto, E. M., Gleichmann, M., Yshii, L., Lima, L. D. S., Mattson, M. P., & Scavone, C. (2011) · Brazilian Journal of Medical and Biological Research · doi:10.1590/s0100-879x2011007500157 · Cited by 18

Placental defects lead to embryonic lethality in mice lacking the Formin and PCP proteins Daam1 and Daam2

Nakaya, M., Gudmundsson, K. O., Komiya, Y., Keller, J. R., Habas, R., Yamaguchi, T. P., & Ajima, R. (2020) · PLoS ONE · doi:10.1371/journal.pone.0232025 · Cited by 16

Protein Kinase A-mediated 14-3-3 Association Impedes Human Dapper1 to Promote Dishevelled Degradation

Chen, H., Liu, L., Ma, B., Ma, T. M., Hou, J.-J., Xie, G.-M., Wu, W., Yang, F.-Q., & Chen, Y. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.211607 · Cited by 18

Dishevelled-3 C-terminal His single amino acid repeats are obligate for Wnt5a activation of non-canonical signaling

Ma, L., Wang, Y., Malbon, C. C., & Wang, H. (2010) · Journal of Molecular Signaling · doi:10.1186/1750-2187-5-19 · Cited by 15

Vertebrate homologues of Frodo are dynamically expressed during embryonic development in tissues undergoing extensive morphogenetic movements

Hunter, N. L., Hikasa, H., Dymecki, S. M., & Sokol, S. Y. (2005) · Developmental Dynamics · doi:10.1002/dvdy.20609 · Cited by 15

Delicate Analysis of Post-Translational Modifications on Dishevelled 3

Wu, C., Wei, W., Li, C., Li, Q., Sheng, Q., & Zeng, R. (2012) · Journal of Proteome Research · doi:10.1021/pr300314d · Cited by 14

Wnt Signaling Mediates Diverse Developmental Processes in Zebrafish

Verkade, H. M., & Heath, J. K. (2008) · Methods in molecular biology · doi:10.1007/978-1-60327-469-2_17 · Cited by 14

Morphogenetic cell movements shaping the zebrafish gastrula

Jessen, J. R., & Solnica‐Krezel, L. (2005) · Advances in developmental biology · doi:10.1016/s1574-3349(05)14007-1 · Cited by 14

Probing the physical nature and composition of signalsomes

Wang, H., & Malbon, C. C. (2011) · Journal of Molecular Signaling · doi:10.1186/1750-2187-6-1 · Cited by 14

Dishevelled‐3 activates p65 to upregulate p120‐catenin transcription via a p38‐dependent pathway in non‐small cell lung cancer

Zhao, H., Zhao, Y., Jiang, G., Zhang, X., Zhang, Y., Dong, Q., Luan, L., Papavassiliou, P., Wang, E., & Wang, E. (2014) · Molecular Carcinogenesis · doi:10.1002/mc.22196 · Cited by 13

It takes more than two to tango: Dishevelled polymerization and Wnt signaling

Roberts, D. M., Slep, K. C., & Peifer, M. A. (2007) · Nature Structural & Molecular Biology · doi:10.1038/nsmb0607-463 · Cited by 13

Matrigel and Activin A promote cell-cell contact and anti-apoptotic activity in cultured human retinal pigment epithelium cells

Guo, X., Zhu, D., Lian, R., Han, Y., Guo, Y., Li, Z., Tang, S., & Chen, J. (2016) · Experimental Eye Research · doi:10.1016/j.exer.2016.04.021 · Cited by 13

AXIN1 Expression and Localization in Meningiomas and Association to Changes of APC and E-cadherin

Pećina‐Šlaus, N., Kafka, A., Vladušić, T., Pećina, H. I., & Hrašćan, R. (2016) · Anticancer Research · doi:10.21873/anticanres.11007 · Cited by 13

Cell-autonomous, myristyl-independent activity of the Drosophila Wnt/Wingless antagonist Naked cuticle (Nkd)

Chan, C., Zhang, S., Çağatay, T., & Wharton, K. A. (2007) · Developmental Biology · doi:10.1016/j.ydbio.2007.09.002 · Cited by 13

Origin and function of fluctuations in cell behaviour and the emergence of patterns

Mateus, A. M., Gorfinkiel, N., & Arias, A. M. (2009) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2009.07.009 · Cited by 13

Germline predisposition in multiple myeloma

Rodrigues, F. M., Jasielec, J. K., Perpich, M., Kim, A., Moma, L., Li, Y., Storrs, E. P., Wendl, M. C., Jayasinghe, R. G., Fiala, M. A., et al. (2024) · iScience · doi:10.1016/j.isci.2024.111620 · Cited by 12

Dishevelled 2 regulates cancer cell proliferation and T cell mediated immunity in HER2-positive breast cancer

Rasha, F. A., Boligala, G. P., Yang, M. V., Martinez‐Marin, D., Castro‐Piedras, I., Furr, K. L., Snitman, A., Khan, S. Y., Brandi, L., Castro, M., et al. (2023) · BMC Cancer · doi:10.1186/s12885-023-10647-2 · Cited by 11

TMED3 exerts a protumor function in non-small cell lung cancer by enhancing the Wnt/β-catenin pathway via regulation of AKT

Zhang, D., Sun, L., & Zhang, J. (2021) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2021.115793 · Cited by 12

Dorsal closure and convergent extension: two polarised morphogenetic movements controlled by similar mechanisms?

Lawrence, N. J., & Morel, V. (2003) · Mechanisms of Development · doi:10.1016/j.mod.2003.07.004 · Cited by 11

Small-molecule modulators of Hh and Wnt signaling pathways

Kiselyov, A. S., Tkachenko, S. E., Balakin, K. V., & Ivachtchenko, A. V. (2007) · Expert Opinion on Therapeutic Targets · doi:10.1517/14728222.11.8.1087 · Cited by 13

Quantitative Mass Spectrometry Characterizes Client Spectra of Components for Targeting of Membrane Proteins to and Their Insertion into the Membrane of the Human ER

Jung, M., & Zimmermann, R. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241814166 · Cited by 10

Dact3 inhibits the malignant phenotype of non-small cell lung cancer through downregulation of c-Myb.

Zhao, H., Yang, L.-H., Han, Y., Li, H., Ling, Z., Wang, Y., Wang, E., & Wu, G. (2017) · PubMed Central · Cited by 11

Anticancer Activity of (S)-5-Chloro-3-((3,5-dimethylphenyl)sulfonyl)-N-(1-oxo-1-((pyridin-4-ylmethyl)amino)propan-2-yl)-1H-indole-2-carboxamide (RS4690), a New Dishevelled 1 Inhibitor

Coluccia, A., Bufano, M., Regina, G. L., Puxeddu, M., Toto, A., Paone, A., Bouzidi, A., Musto, G., Badolati, N., Orlando, V., et al. (2022) · Cancers · doi:10.3390/cancers14051358 · Cited by 11

CWN-1 functions with DSH-2 to regulate C. elegans asymmetric neuroblast division in a β-catenin independent Wnt pathway

Hingwing, K., Lee, S., Nykilchuk, L., Walston, T., Hardin, J. D., & Hawkins, N. (2009) · Developmental Biology · doi:10.1016/j.ydbio.2009.01.025 · Cited by 11

Neuroglobin Regulates Wnt/β-Catenin and NFκB Signaling Pathway through Dvl1

Xun, Y., Li, Z., Tang, Y., Yang, M., Long, S., Shu, P., Li, J., Xiao, Y., Tang, F., Wei, C., et al. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19072133 · Cited by 11

Dvl proteins regulate SMAD1, AHR, mTOR, BRD7 protein expression while differentially regulating canonical and non-canonical Wnt signaling pathways in CML cell lines

Çalışkan, C., Yüce, Z., & Sercan, H. O. (2022) · Gene · doi:10.1016/j.gene.2022.147109 · Cited by 10

Inhibiting the Wnt Signaling Pathway with Small Molecules

Lee, H., Zhang, X., & Zheng, J. (2010) · Springer eBooks · doi:10.1007/978-1-4419-8023-6_9 · Cited by 10

Role and Function of Wnts in the Regulation of Myogenesis: When Wnt Meets Myostatin

Fédon, Y., Bonnieu, A., Gay, S., Vernus, B., Bacou, F., & Bernardi, H. (2012) · InTech eBooks · doi:10.5772/48330 · Cited by 11

Knockdown of DEPDC1B inhibits the development of glioblastoma

Xu, C., Guo, Z., Cao, D., Chen, Y., & Chen, J. (2020) · Cancer Cell International · doi:10.1186/s12935-020-01404-7 · Cited by 9

DEPDC1B promotes colorectal cancer via facilitating cell proliferation and migration while inhibiting apoptosis

Han, F., Cheng, C., Xu, Q., Chen, J., Yang, Z., & Liu, J. (2022) · Cell Cycle · doi:10.1080/15384101.2022.2110439 · Cited by 9

Mouse naked cuticle 2 (mNkd2) as a direct transcriptional target of Hoxc8 in vivo

Lei, H., Juan, A. H., Kim, M., & Ruddle, F. H. (2006) · Journal of Experimental Zoology Part A Ecological Genetics and Physiology · doi:10.1002/jez.a.327 · Cited by 9

Dishevelled: An emerging therapeutic oncogene in human cancers

Alshahrani, S. H., Rakhimov, N., Rana, A., Alsaab, H. O., Hjazi, A. M., Adile, M., Abosaooda, M., Alazbjee, A. A. A., Alsalamy, A., & Mahmoudi, R. (2023) · Pathology - Research and Practice · doi:10.1016/j.prp.2023.154793 · Cited by 8

Genome-wide network analysis of Wnt signaling in three pediatric cancers

Bao, J., Lee, H., & Zheng, J. (2013) · Scientific Reports · doi:10.1038/srep02969 · Cited by 8

Implication of Wnt signaling in neuronal polarization

Yang, G., & Luo, Z. (2010) · Developmental Neurobiology · doi:10.1002/dneu.20851 · Cited by 8

PDZ domain from Dishevelled -- a specificity study.

Śmietana, K., Mateja, A., Krężel, A., & Otlewski, J. (2011) · Acta Biochimica Polonica · doi:10.18388/abp.2011_2272 · Cited by 8

Dishevelled-3 phosphorylation is governed by HIPK2/PP1Cα/ITCH axis and the non-phosphorylated form promotes cancer stemness via LGR5 in hepatocellular carcinoma

Tsui, Y., Sze, K. M., Tung, E. K. K., Ho, D. W., Lee, T. K., & Ng, I. O. (2017) · Oncotarget · doi:10.18632/oncotarget.17049 · Cited by 8

Identification and Validation of DEPDC1B as an Independent Early Diagnostic and Prognostic Biomarker in Liver Hepatocellular Carcinoma

Fan, X., Wen, J., Bao, L., Gao, F., Li, Y., & He, D. (2022) · Frontiers in Genetics · doi:10.3389/fgene.2021.681809 · Cited by 7

Linking Fold, Function and Phylogeny: A Comparative Genomics View on Protein (Domain) Evolution

Velthuis, A. J. W. T., & Bagowski, C. P. (2008) · Current Genomics · doi:10.2174/138920208784139537 · Cited by 7

Regulation of Focal Adhesion Dynamics by Wnt5a Signaling

Matsumoto, S., & Kikuchi, A. (2011) · Methods in molecular biology · doi:10.1007/978-1-61779-510-7_17 · Cited by 7

Dishevelled proteins and CYLD reciprocally regulate each other in CML cell lines

Çalışkan, C., Pehli̇van, M., Yüce, Z., & Sercan, H. O. (2017) · Molecular Biology Reports · doi:10.1007/s11033-017-4122-3 · Cited by 7

Oridonin inhibits growth and induces apoptosis of human neurocytoma cells via the Wnt/β‑catenin pathway

Liang, J., Wang, W., Wei, L., Gao, S., & Wang, Y. (2018) · Oncology Letters · doi:10.3892/ol.2018.8977 · Cited by 7

Specification and patterning of the animal‐vegetal axis in sea urchins by the canonical Wnt signaling pathway

Kumburegama, S., & Wikramanayake, A. H. (2007) · Signal Transduction · doi:10.1002/sita.200600127 · Cited by 7

Secondary Structure, 1H, 13C and 15N Resonance Assignments and Molecular Interactions of the Dishevelled DIX Domain

Capelluto, D. G. S., & Overduin, M. (2005) · BMB Reports · doi:10.5483/bmbrep.2005.38.2.243 · Cited by 7

A transgenic Cre mouse line for the study of cortical and hippocampal development

Zhou, W., Zhang, Y., Li, Y., Wei, Y., Liu, G., Liu, D., Pleasure, S. J., Xie, W., & Zhao, C. (2010) · genesis · doi:10.1002/dvg.20611 · Cited by 6

Intracellular Signaling Pathways Implicated in the Pathophysiology of Depression

Réus, G. Z., Generoso, J. S., Rodrigues, A. L. S., & Quevedo, J. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-813333-0.00010-x · Cited by 6

Recent discoveries in vertebrate non‐canonical Wnt signaling: Towards a Wnt signaling network

Pandur, P. (2005) · Advances in developmental biology · doi:10.1016/s1574-3349(05)14005-8 · Cited by 5

Inhibition on JNK Mimics Silencing of Wnt-11 Mediated Cellular Response in Androgen-Independent Prostate Cancer Cells

Arısan, E. D., Rencüzoğulları, Ö., Keskin, B., Grant, G. H., & Onganer, P. U. (2020) · Biology · doi:10.3390/biology9070142 · Cited by 5

The development of molecular diagnostics for breast cancer

Israyelyan, A. (2003) · doi:10.31390/gradschool_theses.3503 · Cited by 5

Dishevelled2 activates WGEF via its interaction with a unique internal peptide motif of the GEF

Omble, A., Mahajan, S., Bhoite, A., & Kulkarni, K. A. (2024) · Communications Biology · doi:10.1038/s42003-024-06194-6 · Cited by 3

Wnt Signaling Networks and Embryonic Patterning

Klymkowsky, M. W. (2007) · Springer eBooks · doi:10.1007/0-387-28671-3_18 · Cited by 4

Stem Cells in Brain Tumour Development and Therapy- Two-Sides of the Same Coin

Lee, C., Dunn, S. E., & Yip, S. S. F. (2012) · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · doi:10.1017/s0317167100013159 · Cited by 3

Formin Binding Protein 1 (FNBP1) regulates non-canonical Wnt signaling and vertebrate gastrulation

Zeni, C., Komiya, Y., & Habas, R. (2024) · Developmental Biology · doi:10.1016/j.ydbio.2024.06.019 · Cited by 4

Basic mechanism of mobilizing cell movement during invasion of glioblastoma and target selection of targeted therapy

Xu, J., Shi, P., Yang, L., & Cui, H. (2025) · Journal of Advanced Research · doi:10.1016/j.jare.2025.04.042 · Cited by 3

Proteomic Analysis of Wnt-Dependent Dishevelled-Based Supermolecular Complexes

Yokoyama, N. N. (2012) · InTech eBooks · doi:10.5772/30271 · Cited by 2

Treatment with Gaoziban Tablet Ameliorates Depression by Promoting GSK-3β Phosphorylation to Enhance the Wnt/β-catenin Activation in the Hippocampus of Rats

Zou, X.-S., Yin, H.-L., Shi, L., Li, H., Wang, M., Song, W., Luo, Y., Chen, W., Wu, H., Yang, Y., et al. (2021) · Journal of Exploratory Research in Pharmacology · doi:10.14218/jerp.2021.00016 · Cited by 2

Role of Wnt Signaling Pathways in Multiple Myeloma Pathogenesis

Fulciniti, M., & Carrasco, D. R. (2012) · Springer eBooks · doi:10.1007/978-1-4614-4666-8_5 · Cited by 2

Limb Development

Mackem, S. (2005) · Wiley eBooks · doi:10.1002/9783527619689.ch15 · Cited by 2

The Wnt signaling network in cancer

Apfel-Starke, J., Parikh, J. R., Reischmann, P., Ewing, R. M., Müller, O. J., Xia, Y., & Dominguez, I. M. (2015) · Cambridge University Press eBooks · doi:10.1017/cbo9780511979811.016 · Cited by 2

Identification and Characterization of the Rat DVL2 Gene Using Bioinformatic Tools

Varışlı, L., & Çen, O. (2007) · DergiPark (Istanbul University) · Cited by 1

Biochemical Assays to Detect Activation of Small GTPases Rho, Rac, and Cdc42 during Morphogenesis

Berns, M. L., & Habas, R. (2022) · Methods in molecular biology · doi:10.1007/978-1-0716-2035-9_5 · Cited by 1

DEPDC1B enhances malignant phenotypes of multiple myeloma through upregulating CCNB1 and inhibiting p53 signaling pathway

Fei, H., Shi, X., Li, S., Li, Y., Yin, X., Wu, Z., Wang, W., Shi, H., & Li, R. (2023) · Tissue and Cell · doi:10.1016/j.tice.2023.102263 · Cited by 1

Activation of p53 by Dishevelled independent of Wnt or planar polarity pathways

Ding, V. W., Lin, L.-P., Chiang, A. L., & McCormick, F. P. (2007) · Journal of Molecular Medicine · doi:10.1007/s00109-007-0228-8 · Cited by 1

Noncanonical Wnt Signaling and Neural

Montcouquiol, M., & Kelley, M. W. (2006) · Cited by 1

Wnt/β-catenin Signaling Pathway

Kaykas, A., & Moon, R. T. (2006) · Springer eBooks · doi:10.1007/3-540-29623-9_1050 · Cited by 1

Involvement of canonical Wnt/β-catenin signaling in the extinction of auditory fear conditioning in male mice

Xu, N., Geng, L., Yan, X., Niu, A., Yu, H., & Su, B. (2023) · Behavioural Brain Research · doi:10.1016/j.bbr.2023.114378 · Cited by 1

PDZ Domains: Intracellular Mediators of Carboxy‐Terminal Protein Recognition and Scaffolding

Lasky, L. A., Skelton, N. J., & Sidhu, S. S. (2008) · Wiley eBooks · doi:10.1002/9783527610754.pp03 · Cited by 1

Molecular Pharmacology of Frizzleds—with Implications for Possible Therapy

Schulte, G. (2010) · Wiley eBooks · doi:10.1002/9780470627327.ch5 · Cited by 1

Identification and functional characterization of PTK7 ligands in Xenopus laevis

Peradziryi, H. (2011) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-3158 · Cited by 1

Requirement for Wnt and Planar Cell Polarity pathway genes in asymmetric neuroblast division in Caenorhabditis elegans

Roh‐Johnson, M. (2004) · Summit (Simon Fraser University) · Cited by 1

Characterizing the role of C. elegans dsh-2 in asymmetric cell division and embryonic development

Lee, S. C.-H. (2005) · Summit (Simon Fraser University) · Cited by 1

Counterintuitive Binding of Phosphorylated DEP Domain from Dishevelled Protein to Negatively Charged MembranesPreprint

Falginella, F. L., Drabinová, M., Bryja, V., & Vácha, R. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.01.27.525887 · Cited by 1

Functional networks of events that modulate phenotypic manifestation of cancer

Thiagalingam, S. (2015) · Cambridge University Press eBooks · doi:10.1017/cbo9780511979811.012

Domain Architecture in Homolog Identification

Song, N., Sedgewick, R. D., & Durand, D. (2006) · Lecture notes in computer science · doi:10.1007/11864127_2

Progenitor cell maturation and initiation of neurogenesis in the developing vertebrate neural retina.

Yang, H. (2009) · University of Minnesota Digital Conservancy (University of Minnesota)

Dact genes in mouse kidney development

Lee, W. (2009) · ERA

The role of Wnt signalling in excitatory hippocampal synapse formation and function

Anane, D. (2012) · UCL Discovery (University College London)

Análise dos genes diferencialmente expressos durante a osteodiferenciação induzida por proteínas morfogenéticas de osso (BMP2 e BMP7) em células C2C12 e super-expressão de rhBMP2 e rhBMP7 em células de mamíferos

Bustos-Valenzuela, J. C. (2008) · doi:10.11606/t.46.2008.tde-31072009-140027

IKK and Beta-Catenin in Breast Cancer

Teo, M. (2002) · Defense Technical Information Center (DTIC) · doi:10.21236/ada407807

Oncogenic β-catenin signaling networks in colorectal cancer

Fuchs, S. Y., Ougolkov, A. V., Spiegelman, V. S., & Minamoto, T. (2006) · Institutional Repositories DataBase (IRDB)

Efeitos comportamentais e bioquímicos da dieta intermitente na vigência de um estímulo inflamatório no hipocampo de ratos.

Vasconcelos, A. R. (2011) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.42.2011.tde-10022012-100857

Nuclear receptor and Wnt function in developing dopaminergic neurons

Sousa, K. M. (2007) · Figshare

Synthesis of potential cancer therapeutic and diagnostic agents

Tohid, & Farah, S. (2011) · ORCA Online Research @Cardiff (Cardiff University)

Molecular mechanism of Indian Hedgehog signalling in human sebocytes

Séquaris, G. (2010) · Kölner Universitäts PublikationsServer (Universität zu Köln)

functiona novel regulator of Wnt signaling required for Naked cuticle

Bernards, R., Creyghton, M. P., Roël, G., Hijmans, E. M., Maurer, I., & Destrée, O. (2006)

The identification of MIG-5/dishevelled as a CACN-1 interacting protein in C. elegans, using in vivo and in vitro approaches

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