Helping Wingless take flight: how WNT proteins are secreted

Wnt/β-Catenin Signaling in Development and Disease

Clevers, H. (2006) · Cell · doi:10.1016/j.cell.2006.10.018 · Cited by 5,568

The Wnt Signaling Pathway in Development and Disease

Logan, C. Y., & Nusse, R. (2004) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.20.010403.113126 · Cited by 5,325

Wnt proteins are lipid-modified and can act as stem cell growth factors

Willert, K., Brown, J. D., Danenberg, E., Duncan, A. W., Weissman, I. L., Reya, T., Yates, J. R., & Nusse, R. (2003) · Nature · doi:10.1038/nature01611 · Cited by 2,257

Many tumors induced by the mouse mammary tumor virus contain a provirus integrated in the same region of the host genome

Nusse, R., & VARMUS, H. E. (1982) · Cell · doi:10.1016/0092-8674(82)90409-3 · Cited by 1,864

A Second Canon

Veeman, M. T., Axelrod, J. D., & Moon, R. T. (2003) · Developmental Cell · doi:10.1016/s1534-5807(03)00266-1 · Cited by 1,359

The Drosophila homology of the mouse mammary oncogene int-1 is identical to the segment polarity gene wingless

Rijsewijk, F. A. M., Schuermann, M., Wagenaar, E., Parren, P. W. H. I., Weigel, D., & Nusse, R. (1987) · Cell · doi:10.1016/0092-8674(87)90038-9 · Cited by 931

Monounsaturated Fatty Acid Modification of Wnt Protein: Its Role in Wnt Secretion

Takada, R., Satomi, Y., Kurata, T., Ueno, N., Norioka, S., Kondoh, H., Takao, T., & Takada, S. (2006) · Developmental Cell · doi:10.1016/j.devcel.2006.10.003 · Cited by 809

Wntless, a Conserved Membrane Protein Dedicated to the Secretion of Wnt Proteins from Signaling Cells

Bänziger, C., Soldini, D., Schütt, C., Zipperlen, P., Hausmann, G., & Basler, K. (2006) · Cell · doi:10.1016/j.cell.2006.02.049 · Cited by 764

Direct and Long-Range Action of a Wingless Morphogen Gradient

Zecca, M., Basler, K., & Struhl, G. (1996) · Cell · doi:10.1016/s0092-8674(00)81991-1 · Cited by 732

Lipoprotein particles are required for Hedgehog and Wingless signalling

Panáková, D., Sprong, H., Marois, É., Thiele, C., & Eaton, S. (2005) · Nature · doi:10.1038/nature03504 · Cited by 703

Wnt/β-Catenin Signaling: Components, Mechanisms, and Diseases

MacDonald, B. T., Tamai, K., & He, X. (2009) · Developmental Cell · doi:10.1016/j.devcel.2009.06.016 · Cited by 5,583

Wnt signal transduction pathways

Komiya, Y., & Habas, R. (2008) · Organogenesis · doi:10.4161/org.4.2.5851 · Cited by 1,528

Wnt signalling and its impact on development and cancer

Klaus, A., & Birchmeier, W. (2008) · Nature Reviews Cancer · doi:10.1038/nrc2389 · Cited by 1,595

Deciphering the function of canonical Wnt signals in development and disease: conditional loss- and gain-of-function mutations of β-catenin in micePreprint

Grigoryan, T., Wend, P., Klaus‐Bergmann, A., & Birchmeier, W. (2008) · Genes & Development · doi:10.1101/gad.1686208 · Cited by 573

Linking Aβ and Tau in Late-Onset Alzheimer's Disease: A Dual Pathway Hypothesis

Small, S. A., & Duff, K. (2008) · Neuron · doi:10.1016/j.neuron.2008.11.007 · Cited by 546

Endosomal sorting and signalling: an emerging role for sorting nexins

Cullen, P. J. (2008) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2427 · Cited by 404

Sorting nexins provide diversity for retromer-dependent trafficking events

Cullen, P. J., & Korswagen, H. C. (2012) · Nature Cell Biology · doi:10.1038/ncb2374 · Cited by 330

The Retromer Complex Influences Wnt Secretion by Recycling Wntless from Endosomes to the Trans-Golgi Network

Belenkaya, T. Y., Wu, Y., Tang, X., Zhou, B., Cheng, L., Sharma, Y. V., Yan, D., Selva, E. M., & Lin, X. (2007) · Developmental Cell · doi:10.1016/j.devcel.2007.12.003 · Cited by 327

Crosstalk between hepatic tumor cells and macrophages via Wnt/β-catenin signaling promotes M2-like macrophage polarization and reinforces tumor malignant behaviors

Yang, Y., Ye, Y., Chen, Y., Zhao, J., Gao, C.-C., Han, H., Liu, W., & Qin, H. (2018) · Cell Death and Disease · doi:10.1038/s41419-018-0818-0 · Cited by 310

YAP Partially Reprograms Chromatin Accessibility to Directly Induce Adult Cardiogenesis In Vivo

Monroe, T. O., Hill, M. C., Morikawa, Y., Leach, J. P., Heallen, T., Cao, S., Krijger, P. H. L., de Laat, W., Wehrens, X. H. T., Rodney, G. G., et al. (2019) · Developmental Cell · doi:10.1016/j.devcel.2019.01.017 · Cited by 289

Wingless secretion promotes and requires retromer-dependent cycling of Wntless

Port, F., Kuster, M., Herr, P., Furger, E., Bänziger, C., Hausmann, G., & Basler, K. (2008) · Nature Cell Biology · doi:10.1038/ncb1687 · Cited by 278

Wnt Signaling Requires Retromer-Dependent Recycling of MIG-14/Wntless in Wnt-Producing Cells

Yang, P., Lorenowicz, M. J., Macůrková, M., Coudreuse, D. Y. M., Betist, M. C., & Korswagen, H. C. (2007) · Developmental Cell · doi:10.1016/j.devcel.2007.12.004 · Cited by 259

Wingless secretion requires endosome-to-Golgi retrieval of Wntless/Evi/Sprinter by the retromer complex

Franch‐Marro, X., Wendler, F., Guidato, S., Griffith, J. M., Baena-López, L. A., Itasaki, N., Maurice, M. M., & Vincent, J. (2008) · Nature Cell Biology · doi:10.1038/ncb1678 · Cited by 260

Wnt and the Wnt signaling pathway in bone development and disease

Wang, Y. (2014) · Frontiers in bioscience · doi:10.2741/4214 · Cited by 255

International Union of Basic and Clinical Pharmacology. LXXX. The Class Frizzled Receptors

Schulte, G. (2010) · Pharmacological Reviews · doi:10.1124/pr.110.002931 · Cited by 237

WLS-dependent secretion of WNT3A requires Ser209 acylation and vacuolar acidification

Coombs, G. S., Yu, J., Canning, C. A., Veltri, C. A., Covey, T. M., Cheong, J. K., Utomo, V., Banerjee, N., Zhang, Z. H., Jadulco, R. C., et al. (2010) · Journal of Cell Science · doi:10.1242/jcs.072132 · Cited by 214

C. elegans AP-2 and Retromer Control Wnt Signaling by Regulating MIG-14/Wntless

Pan, C., Baum, P. D., Gu, M., Jørgensen, E. M., Clark, S. G., & Garriga, G. (2007) · Developmental Cell · doi:10.1016/j.devcel.2007.12.001 · Cited by 208

Wnt/β-catenin signaling in kidney injury and repair: a double-edged sword

Zhou, D. F., Tan, R. J., Fu, H., & Liu, Y. (2015) · Laboratory Investigation · doi:10.1038/labinvest.2015.153 · Cited by 204

Wnt Signaling in Bone Development and Disease: Making Stronger Bone with WntsPreprint

Regard, J. B., Zhong, Z. A., Williams, B. O., & Yang, Y. (2012) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a007997 · Cited by 202

Reciprocal regulation of Wnt and Gpr177/mouse Wntless is required for embryonic axis formation

Fu, J., Jiang, M., Mirando, A. J., Yu, H. I., & Hsu, W. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0904894106 · Cited by 196

Notum Is Required for Neural and Head Induction via Wnt Deacylation, Oxidation, and Inactivation

Zhang, X., Cheong, S.-M., Amado, N. G., Reis, A. H., MacDonald, B. T., Zebisch, M., Jones, E. Y., Abreu, J. G., & He, X. (2015) · Developmental Cell · doi:10.1016/j.devcel.2015.02.014 · Cited by 184

Wntless functions in mature osteoblasts to regulate bone mass

Zhong, Z. A., Diegel, C. R., Schumacher, C. A., Baker, J. J., Carpenter, A. C., Rao, S., Yao, W., Guan, M., Helms, J. A., Lane, N. E., et al. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1120407109 · Cited by 180

Progress and renewal in gustation: new insights into taste bud development

Barlow, L. A. (2015) · Development · doi:10.1242/dev.120394 · Cited by 178

Deletion of mouse Porcn blocks Wnt ligand secretion and reveals an ectodermal etiology of human focal dermal hypoplasia/Goltz syndrome

Barrott, J. J., Cash, G. M., Smith, A. P., Barrow, J. R., & Murtaugh, L. C. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1006437108 · Cited by 173

Tiki1 Is Required for Head Formation via Wnt Cleavage-Oxidation and Inactivation

Zhang, X., Abreu, J. G., Yokota, C., MacDonald, B. T., Singh, S. A., Coburn, K. L. A., Cheong, S.-M., Zhang, M. M., Ye, Q.-Z., Hang, H. C., et al. (2012) · Cell · doi:10.1016/j.cell.2012.04.039 · Cited by 150

Wnt/β-catenin Signaling in Normal and Cancer Stem Cells

Valkenburg, K. C., Graveel, C. R., Diegel, C. R., Zhong, Z. A., & Williams, B. O. (2011) · Cancers · doi:10.3390/cancers3022050 · Cited by 144

WNT and NOTCH signaling in human trophoblast development and differentiation

Dietrich, B., Haider, S., Meinhardt, G., Pollheimer, J., & Knöfler, M. (2022) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-022-04285-3 · Cited by 141

A Comprehensive Overview of Skeletal Phenotypes Associated with Alterations in Wnt/β-catenin Signaling in Humans and Mice

Maupin, K. A., Droscha, C. J., & Williams, B. O. (2013) · Bone Research · doi:10.4248/br201301004 · Cited by 133

Reggie‐1/flotillin‐2 promotes secretion of the long‐range signalling forms of Wingless and Hedgehog in Drosophila

Katanaev, V. L., Solis, G. P., Hausmann, G., Buestorf, S., Katanayeva, N., Schrock, Y., Stuermer, C. A. O., & Basler, K. (2008) · The EMBO Journal · doi:10.1038/sj.emboj.7601981 · Cited by 115

Wnt/β-catenin signaling in melanoma: Preclinical rationale and novel therapeutic insights

Xue, G., Romano, E., Massi, D., & Mandalà, M. (2016) · Cancer Treatment Reviews · doi:10.1016/j.ctrv.2016.06.009 · Cited by 113

Motor Neurons with Axial Muscle Projections Specified by Wnt4/5 Signaling

Agalliu, D., Takada, S., Agalliu, I., McMahon, A. P., & Jessell, T. M. (2009) · Neuron · doi:10.1016/j.neuron.2008.12.026 · Cited by 110

Class III phosphatidylinositol 3–kinase and its catalytic product P tdIns3 P in regulation of endocytic membrane traffic

Raiborg, C., Schink, K. O., & Stenmark, H. (2013) · FEBS Journal · doi:10.1111/febs.12116 · Cited by 107

C. elegans as a model for membrane traffic

Sato, K. (2014) · WormBook · doi:10.1895/wormbook.1.77.2 · Cited by 103

Making, Exporting, and Modulating Wnts

Langton, P. F., Kakugawa, S., & Vincent, J. (2016) · Trends in Cell Biology · doi:10.1016/j.tcb.2016.05.011 · Cited by 98

Gpr177/mouse Wntless is essential for Wnt‐mediated craniofacial and brain development

Fu, J., Yu, H. I., Maruyama, T., Mirando, A. J., & Hsu, W. (2011) · Developmental Dynamics · doi:10.1002/dvdy.22541 · Cited by 97

Porcupine-mediated lipid-modification regulates the activity and distribution of Wnt proteins in the chick neural tube

Galli, L. M., Barnes, T. L., Secrest, S. S., Kadowaki, T., & Burrus, L. W. (2007) · Development · doi:10.1242/dev.02881 · Cited by 102

The VPS35 gene and Parkinson's disease

Deng, H., Gao, K., & Jankovic, J. J. (2013) · Movement Disorders · doi:10.1002/mds.25430 · Cited by 96

WNT6 is a novel target gene of caveolin-1 promoting chemoresistance to epirubicin in human gastric cancer cells

Yuan, G., Regel, I., Lian, F., Friedrich, T., Hitkova, I., Hofheinz, R., Ströbel, P., Langer, R., Keller, G., Röcken, C., et al. (2012) · Oncogene · doi:10.1038/onc.2012.40 · Cited by 93

Retromer Retrieves Wntless

Eaton, S. (2008) · Developmental Cell · doi:10.1016/j.devcel.2007.12.014 · Cited by 93

Wnt Signaling in Cell Motility and Invasion: Drawing Parallels between Development and Cancer

Sedgwick, A., & D’Souza‐Schorey, C. (2016) · Cancers · doi:10.3390/cancers8090080 · Cited by 85

From endosomes to the trans-Golgi network

Lü, L., & Hong, W. (2014) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2014.04.024 · Cited by 81

Wnt/β-catenin Signaling Inhibitors

Zhang, X., Dong, N., & Hu, X. (2023) · Current Topics in Medicinal Chemistry · doi:10.2174/1568026623666230303101810 · Cited by 68

The emerging role of substance P/neurokinin-1 receptor signaling pathways in growth and development of tumor cells

Javid, H., Mohammadi, F., Zahiri, E., & Hashemy, S. I. (2019) · Journal of Physiology and Biochemistry · doi:10.1007/s13105-019-00697-1 · Cited by 64

A Cryptic Frizzled Module in Cell Surface Collagen 18 Inhibits Wnt/β−Catenin Signaling

Quélard, D., Lavergne, E., Hendaoui, I., Elamaa, H., Tiirola, U., Heljäsvaara, R., Pihlajaniemi, T. A., Clément, B., & Musso, O. C. (2008) · PLoS ONE · doi:10.1371/journal.pone.0001878 · Cited by 67

Interaction of the mu-opioid receptor with GPR177 (Wntless) inhibits Wnt secretion: potential implications for opioid dependence

Jin, J., Kittanakom, S., Wong, V., Reyes, B. A. S., Bockstaele, E. J. V., Štagljar, I., Berrettini, W. H., & Levenson, R. G. (2010) · BMC Neuroscience · doi:10.1186/1471-2202-11-33 · Cited by 60

Role of Adhesion in Arthropod Immune Recognition

Schmidt, O., Söderhäll, K., Theopold, U., & Faye, I. (2009) · Annual Review of Entomology · doi:10.1146/annurev.ento.54.110807.090618 · Cited by 58

Identification of an Endocytosis Motif in an Intracellular Loop of Wntless Protein, Essential for Its Recycling and the Control of Wnt Protein Signaling

Gasnereau, I., Herr, P., Chia, P. Z. C., Basler, K., & Gleeson, P. A. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.307231 · Cited by 57

Somatic Tissue Engineering in Mouse Models Reveals an Actionable Role for WNT Pathway Alterations in Prostate Cancer Metastasis

Leibold, J., Ruscetti, M. A., Cao, Z., Ho, Y.-J., Baslan, T., Zou, M., Abida, W. M., Feucht, J., Han, T., Barriga, F. M., et al. (2020) · Cancer Discovery · doi:10.1158/2159-8290.cd-19-1242 · Cited by 56

Motoneuron Wnts regulate neuromuscular junction development

Shen, C., Li, L., Zhao, K., Bai, L., Wang, A., Shu, X., Xiao, Y., Zhang, J., Zhang, K., Hui, T., et al. (2018) · eLife · doi:10.7554/elife.34625 · Cited by 53

The use of porcupine inhibitors to target Wnt-driven cancers

Ho, S. Y., & Keller, T. H. (2015) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2015.10.032 · Cited by 54

Trimeric G protein-dependent signaling by Frizzled receptors in animal development

Egger‐Adam, D. (2008) · Frontiers in bioscience · doi:10.2741/3036 · Cited by 48

Wnt Signaling Is Regulated by Endoplasmic Reticulum Retention

Zoltewicz, J. S., Ashique, A. M., Choe, Y., Lee, G., Taylor, S., Phamluong, K., Solloway, M. J., & Peterson, A. S. (2009) · PLoS ONE · doi:10.1371/journal.pone.0006191 · Cited by 48

Carboxypeptidase E: a negative regulator of the canonical Wnt signaling pathway

Skalka, N., Caspi, M., Caspi, E., Loh, Y. P., & Rosin‐Arbesfeld, R. (2012) · Oncogene · doi:10.1038/onc.2012.308 · Cited by 47

Blocking Wnt Secretion Reduces Growth of Hepatocellular Carcinoma Cell Lines Mostly Independent of β-Catenin Signaling

Wang, W., Xu, L., Liu, P., Jairam, K., Yin, Y., Chen, K., Sprengers, D., Peppelenbosch, M. P., Pan, Q., & Smits, R. (2016) · Neoplasia · doi:10.1016/j.neo.2016.10.004 · Cited by 47

Decoding the molecular pathways governing trophoblast migration and placental development; a literature review

Liu, L., Tang, L., Chen, D., Zheng, L., & Ma, X. (2024) · Frontiers in Endocrinology · doi:10.3389/fendo.2024.1486608 · Cited by 52

Synaptic Activity-Regulated Wnt Signaling in Synaptic Plasticity, Glial Function and Chronic Pain

Tang, S. (2014) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/1871527312666131223114457 · Cited by 43

Take the Wnt out of the inflammatory sails: modulatory effects of Wnt in airway diseases

Reuter, S., Beckert, H., & Taube, C. (2015) · Laboratory Investigation · doi:10.1038/labinvest.2015.143 · Cited by 42

Osteogenesis and Bone Regeneration

Yang, H. (2019) · IntechOpen eBooks · doi:10.5772/intechopen.73955 · Cited by 42

Wnt signaling and neurite outgrowth: Insights and questions

Endo, Y., & Rubin, J. S. (2007) · Cancer Science · doi:10.1111/j.1349-7006.2007.00536.x · Cited by 40

Wnt-β-Catenin Signaling in Human Dendritic Cells Mediates Regulatory T-Cell Responses to Fungi via the PD-L1 Pathway

Karnam, A., Bonam, S. R., Rambabu, N., Wong, S. S. W., Aimanianda, V., & Bayry, J. (2021) · mBio · doi:10.1128/mbio.02824-21 · Cited by 39

Analyses of mental dysfunction-related ACSl4 in Drosophila reveal its requirement for Dpp/BMP production and visual wiring in the brain

Zhang, Y., Chen, D., & Wang, Z. (2009) · Human Molecular Genetics · doi:10.1093/hmg/ddp332 · Cited by 37

Expression of Gpr177, a Wnt trafficking regulator, in mouse embryogenesis

Yu, H. I., Jin, Y., Fu, J., & Hsu, W. (2010) · Developmental Dynamics · doi:10.1002/dvdy.22336 · Cited by 35

Development of Normal and Cleft Palate: A Central Role for Connective Tissue Growth Factor (CTGF)/CCN2

Tarr, J. T., Lambi, A. G., Bradley, J. P., Barbe, M. F., & Popoff, S. N. (2018) · Journal of Developmental Biology · doi:10.3390/jdb6030018 · Cited by 34

A Role for Frizzled and Their Post-Translational Modifications in the Mammalian Central Nervous System

Vargas, P. P., & Salinas, P. C. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.692888 · Cited by 33

Wnt Secretion and Gradient Formation

Solis, G. P., Lüchtenborg, A., & Katanaev, V. (2013) · International Journal of Molecular Sciences · doi:10.3390/ijms14035130 · Cited by 34

The long and the short of Wnt signaling in C. elegans

Hardin, J. D., & King, R. S. (2008) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2008.06.006 · Cited by 32

β-Catenin: A Key Molecule in Osteoblast Differentiation

Wróbel, E., Wojdasiewicz, P., Mikulska, A., & Szukiewicz, D. (2025) · Biomolecules · doi:10.3390/biom15071043 · Cited by 33

Establishment of a CpG island microarray for analyses of genome-wide DNA methylation in Chinese hamster ovary cells

Wippermann, A., Klausing, S., Rupp, O., Albaum, S. P., Büntemeyer, H., Noll, T., & Hoffrogge, R. (2013) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-013-5282-2 · Cited by 28

Mesenchymal Wnt signaling promotes formation of sternum and thoracic body wall

Snowball, J. M., Ambalavanan, M. S., Cornett, B., Lang, R. A., Whitsett, J. A., & Sinner, D. I. (2015) · Developmental Biology · doi:10.1016/j.ydbio.2015.02.014 · Cited by 27

Secretion of Hedgehog-Related Peptides and WNT DuringCaenorhabditis elegansDevelopment

Kolotuev, I., Apaydin, A., & Labouesse, M. (2009) · Traffic · doi:10.1111/j.1600-0854.2008.00871.x · Cited by 27

Wnt-expressing cells in the intestines: guides for tissue remodeling

Miyoshi, H. (2016) · The Journal of Biochemistry · doi:10.1093/jb/mvw070 · Cited by 30

Wls promotes the proliferation of breast cancer cells via Wnt signaling

Lu, D., Li, Y., Liu, Q., Wu, Q., Zhang, H., Xie, P., & Wang, Q. (2015) · Medical Oncology · doi:10.1007/s12032-015-0585-z · Cited by 25

MOR Is Not Enough: Identification of Novel mu-Opioid Receptor Interacting Proteins Using Traditional and Modified Membrane Yeast Two-Hybrid Screens

Petko, J., Justice-Bitner, S., Jin, J., Wong, V., Kittanakom, S., Ferraro, T. N., Štagljar, I., & Levenson, R. G. (2013) · PLoS ONE · doi:10.1371/journal.pone.0067608 · Cited by 24

Rab8 attenuates Wnt signaling and is required for mesenchymal differentiation into adipocytes

Stypulkowski, E., Feng, Q., Joseph, I., Farrell, V., Flores, J., Yu, S., Sakamori, R., Sun, J., Bandyopadhyay, S., Das, S., et al. (2021) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2021.100488 · Cited by 22

Lipid modification in Wnt structure and function

Ke, J., Xu, H. E., & Williams, B. O. (2013) · Current Opinion in Lipidology · doi:10.1097/mol.0b013e32835df2bf · Cited by 23

ACSL5, a prognostic factor in acute myeloid leukemia, modulates the activity of Wnt/β-catenin signaling by palmitoylation modification

Ye, W., Wang, J., Huang, J., He, X. D., Ma, Z., Li, X., Huang, X., Li, F., Huang, S., Pan, J., et al. (2023) · Frontiers of Medicine · doi:10.1007/s11684-022-0942-1 · Cited by 20

Low expression of D2R and Wntless correlates with high motivation for heroin.

Tacelosky, D. M., Alexander, D. N., Morse, M., Hajnal, A. S., Berg, A. S., Levenson, R. G., & Grigson, P. S. (2015) · Behavioral Neuroscience · doi:10.1037/bne0000104 · Cited by 20

Wntless (GPR177) expression correlates with poor prognosis in B-cell precursor acute lymphoblastic leukemia via Wnt signaling

Chiou, S., Wang, L., Huang, S., Chai, C., Wang, S., Liao, Y., Lin, P., Liu, K.-Y., & Hsu, S. (2014) · Carcinogenesis · doi:10.1093/carcin/bgu166 · Cited by 19

Wnt3 Is Lipidated at Conserved Cysteine and Serine Residues in Zebrafish Neural Tissue

Dhasmana, D., Veerapathiran, S., Azbazdar, Y., Nelanuthala, A. V. S., Teh, C., Özhan, G., & Wohland, T. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.671218 · Cited by 17

Knockdown of SERPINB2 enhances the osteogenic differentiation of human bone marrow mesenchymal stem cells via activation of the Wnt/β-catenin signalling pathway

Hang, K., Li, Y., Bai, J., Wang, Y., Kuang, Z., Xue, D., & Pan, Z. (2021) · Stem Cell Research & Therapy · doi:10.1186/s13287-021-02581-6 · Cited by 17

Gpr177 Deficiency Impairs Mammary Development and Prohibits Wnt-Induced Tumorigenesis

Maruyama, E. O., Yu, H., Jiang, M., Fu, J., & Hsu, W. (2013) · PLoS ONE · doi:10.1371/journal.pone.0056644 · Cited by 16

A sandwich ELISA for the detection of Wnt5a

Kummitha, C. M., Mayle, K. M., Christman, M. A., Deosarkar, S. P., Schwartz, A. L., McCall, K. D., Kohn, L. D., Malgor, R., & Goetz, D. J. (2009) · Journal of Immunological Methods · doi:10.1016/j.jim.2009.11.005 · Cited by 16

Subcellular localisation of retromer in post‐endocytic pathways of polarised Madin–Darby canine kidney cells

Mellado-López, M., Cuartero, Y., Brugada, R., & Vergés, M. (2014) · Biology of the Cell · doi:10.1111/boc.201400011 · Cited by 16

Harmony of Wnt pathway in Alzheimer's: Navigating the multidimensional progression from preclinical to clinical stages

Varshini, M. S., Reddy, R. A., Krishnamurthy, P. T., & Wadhwani, A. (2024) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2024.105863 · Cited by 13

Retromer in Polarized Protein Transport

Vergés, M. (2016) · International review of cytology · doi:10.1016/bs.ircmb.2015.12.005 · Cited by 13

TAp63, a methotrexate target in CD4+ T cells, suppresses Foxp3 expression and exacerbates autoimmune arthritis

Suga, K., Suto, A., Tanaka, S., Sugawara, Y., Kageyama, T., Ishikawa, J., Sanayama, Y., Ikeda, K., Furuta, S., Kagami, S., et al. (2023) · JCI Insight · doi:10.1172/jci.insight.164778 · Cited by 14

Mutations in the WLS are associated with dental anomalies, torus palatinus, and torus mandibularis

Kantaputra, P. N., Tripuwabhrut, K., Jatooratthawichot, P., Adisornkanj, P., Hatsadaloi, A., Porntrakoolsaree, N., Kaewgaya, M., Olsen, B. R., Tongsima, S., Ngamphiw, C., et al. (2022) · European Journal of Orthodontics · doi:10.1093/ejo/cjac068 · Cited by 13

Coordinate Gα13 and Wnt6-β-catenin signaling in F9 embryonal carcinoma cells is required for primitive endoderm differentiation

Krawetz, R. J., & Kelly, G. M. (2009) · Biochemistry and Cell Biology · doi:10.1139/o09-014 · Cited by 13

Subepithelial Stromal Cells: Their Roles and Interactions with Intestinal Epithelial Cells during Gut Mucosal Homeostasis and Regeneration

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Chapter 4 Retromer

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