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The Hippo Pathway Regulates Wnt/β-Catenin Signaling
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/dbio.2001.0308openalex-snapshot
The Casein Kinase I Family in Wnt Signaling
inferredcites →https://doi.org/10.1007/s00467-007-0504-4openalex-snapshot
Molecular regulation of kidney development: is the answer blowing in the Wnt?
inferredcites →https://doi.org/10.1016/0092-8674(90)90451-jopenalex-snapshot
Spatial expression of the Drosophila segment polarity gene armadillo is posttranscriptionally regulated by wingless
inferredcites →https://doi.org/10.1016/j.bbrc.2004.07.113openalex-snapshot
Interaction between the internal motif KTXXXI of Idax and mDvl PDZ domain
inferredcites →https://doi.org/10.1016/j.ceb.2008.10.001openalex-snapshot
The Hippo–YAP pathway: new connections between regulation of organ size and cancer
inferredcites →https://doi.org/10.1016/j.cell.2005.06.007openalex-snapshot
The Hippo Signaling Pathway Coordinately Regulates Cell Proliferation and Apoptosis by Inactivating Yorkie, the Drosophila Homolog of YAP
inferredcites →https://doi.org/10.1016/j.cell.2006.10.018openalex-snapshot
Wnt/β-Catenin Signaling in Development and Disease
inferredcites →https://doi.org/10.1016/j.cell.2007.07.019openalex-snapshot
Elucidation of a Universal Size-Control Mechanism in Drosophila and Mammals
inferredcites →https://doi.org/10.1016/j.cellsig.2006.08.011openalex-snapshot
Wnt-3a utilizes a novel low dose and rapid pathway that does not require casein kinase 1-mediated phosphorylation of Dvl to activate β-catenin
inferredcites →https://doi.org/10.1016/j.cub.2006.09.004openalex-snapshot
The Tumor-Suppressor Gene fat Controls Tissue Growth Upstream of Expanded in the Hippo Signaling Pathway
inferredcites →https://doi.org/10.1016/j.cub.2006.09.005openalex-snapshot
The Fat Cadherin Acts through the Hippo Tumor-Suppressor Pathway to Regulate Tissue Size
inferredcites →https://doi.org/10.1016/j.cub.2006.09.045openalex-snapshot
Fat Cadherin Modulates Organ Size in Drosophila via the Salvador/Warts/Hippo Signaling Pathway
inferredcites →https://doi.org/10.1016/j.cub.2007.09.062openalex-snapshot
The Salvador-Warts-Hippo Pathway Is Required for Epithelial Proliferation and Axis Specification in Drosophila
inferredcites →https://doi.org/10.1016/j.devcel.2009.02.003openalex-snapshot
The Hippo Signaling Pathway Components Lats and Yap Pattern Tead4 Activity to Distinguish Mouse Trophectoderm from Inner Cell Mass
inferredcites →https://doi.org/10.1016/j.jmb.2007.08.005openalex-snapshot
High-throughput Generation of Synthetic Antibodies from Highly Functional Minimalist Phage-displayed Libraries
inferredcites →https://doi.org/10.1016/j.ydbio.2007.02.004openalex-snapshot
Expanded and fat regulate growth and differentiation in the Drosophila eye through multiple signaling pathways
inferredcites →https://doi.org/10.1016/s0092-8674(00)81991-1openalex-snapshot
Direct and Long-Range Action of a Wingless Morphogen Gradient
inferredcites →https://doi.org/10.1016/s0092-8674(03)00549-xopenalex-snapshot
hippo Encodes a Ste-20 Family Protein Kinase that Restricts Cell Proliferation and Promotes Apoptosis in Conjunction with salvador and warts
inferredcites →https://doi.org/10.1016/s0092-8674(03)00557-9openalex-snapshot
The Drosophila Mst Ortholog, hippo, Restricts Growth and Cell Proliferation and Promotes Apoptosis
inferredcites →https://doi.org/10.1016/s1097-2765(02)00776-1openalex-snapshot
Akt Phosphorylates the Yes-Associated Protein, YAP, to Induce Interaction with 14-3-3 and Attenuation of p73-Mediated Apoptosis
inferredcites →https://doi.org/10.1016/s1097-2765(03)00427-1openalex-snapshot
Direct Binding of the PDZ Domain of Dishevelled to a Conserved Internal Sequence in the C-Terminal Region of Frizzled
inferredcites →https://doi.org/10.1038/msb.2009.72openalex-snapshot
Application of an integrated physical and functional screening approach to identify inhibitors of the Wnt pathway
inferredcites →https://doi.org/10.1038/ncb1339openalex-snapshot
The tumour-suppressor genes NF2/Merlin and Expanded act through Hippo signalling to regulate cell proliferation and apoptosis
inferredcites →https://doi.org/10.1038/ncb1670openalex-snapshot
Kif3a constrains β-catenin-dependent Wnt signalling through dual ciliary and non-ciliary mechanisms
inferredcites →https://doi.org/10.1038/ncb1748openalex-snapshot
TAZ controls Smad nucleocytoplasmic shuttling and regulates human embryonic stem-cell self-renewal
inferredcites →https://doi.org/10.1038/ng.104openalex-snapshot
Dishevelled controls apical docking and planar polarization of basal bodies in ciliated epithelial cells
inferredcites →https://doi.org/10.1038/ng.179openalex-snapshot
Loss of Fat4 disrupts PCP signaling and oriented cell division and leads to cystic kidney disease
inferredcites →https://doi.org/10.1038/ng1887openalex-snapshot
Delineation of a Fat tumor suppressor pathway
inferredcites →https://doi.org/10.1038/sj.cr.7290260openalex-snapshot
Wnt signaling in disease and in development
inferredcites →https://doi.org/10.1038/sj.onc.1204825openalex-snapshot
Early development of polycystic kidney disease in transgenic mice expressing an activated mutant of the β-catenin gene
inferredcites →https://doi.org/10.1038/sj.onc.1208445openalex-snapshot
The Ste20-like kinase Mst2 activates the human large tumor suppressor kinase Lats1
inferredcites →https://doi.org/10.1038/sj.onc.1208956openalex-snapshot
Apc deficiency predisposes to renal carcinoma in the mouse
inferredcites →https://doi.org/10.1073/pnas.0605266104openalex-snapshot
Glomerulocystic kidney disease in mice with a targeted inactivation of Wwtr1
inferredcites →https://doi.org/10.1073/pnas.90.10.4582openalex-snapshot
Simple and efficient production of embryonic stem cell-embryo chimeras by coculture.
inferredcites →https://doi.org/10.1074/jbc.m001713200openalex-snapshot
Crystal Structure of a Conformation-selective Casein Kinase-1 Inhibitor
inferredcites →https://doi.org/10.1093/emboj/16.13.3797openalex-snapshot
β‐catenin is a target for the ubiquitin–proteasome pathway
inferredcites →https://doi.org/10.1093/emboj/19.24.6778openalex-snapshot
TAZ: a novel transcriptional co‐activator regulated by interactions with 14‐3‐3 and PDZ domain proteins
inferredcites →https://doi.org/10.1093/hmg/ddn208openalex-snapshot
Polycystin-1 C-terminal tail associates with β-catenin and inhibits canonical Wnt signaling
inferredcites →https://doi.org/10.1126/science.1105776openalex-snapshot
High-Throughput Mapping of a Dynamic Signaling Network in Mammalian Cells
inferredcites →https://doi.org/10.1126/science.1109374openalex-snapshot
Functional Genomic Analysis of the Wnt-Wingless Signaling Pathway
inferredcites →https://doi.org/10.1126/science.1110955openalex-snapshot
TAZ, a Transcriptional Modulator of Mesenchymal Stem Cell Differentiation
inferredcites →https://doi.org/10.1128/mcb.00254-07openalex-snapshot
TAZ Promotes PC2 Degradation through a SCF β-Trcp E3 Ligase Complex
inferredcites →https://doi.org/10.1128/mcb.01874-07openalex-snapshot
TAZ Promotes Cell Proliferation and Epithelial-Mesenchymal Transition and Is Inhibited by the Hippo Pathway
inferredcites →https://doi.org/10.1128/mcb.26.1.77-87.2006openalex-snapshot
Defects in Yolk Sac Vasculogenesis, Chorioallantoic Fusion, and Embryonic Axis Elongation in Mice with Targeted Disruption of Yap65
inferredcites →https://doi.org/10.1152/ajprenal.00201.2007openalex-snapshot
Multiple renal cysts, urinary concentration defects, and pulmonary emphysematous changes in mice lacking TAZ
inferredcites →https://doi.org/10.1158/0008-5472.can-06-2559openalex-snapshot
Transcriptional Cooperation between the Transforming Growth Factor-β and Wnt Pathways in Mammary and Intestinal Tumorigenesis
inferredcites →https://doi.org/10.1242/dev.015255openalex-snapshot
In vivo regulation of Yorkie phosphorylation and localization
inferredcites →https://doi.org/10.1242/dev.02068openalex-snapshot
The developmental biology of Dishevelled: an enigmatic protein governing cell fate and cell polarity
inferredcites →https://doi.org/10.1242/dev.117.4.1223openalex-snapshot
Analysis of genetic mosaics in developing and adult Drosophila tissues
inferredcites →https://doi.org/10.1242/dev.121.4.1053openalex-snapshot
Identifying tumor suppressors in genetic mosaics: the Drosophila lats gene encodes a putative protein kinase
inferredcites →https://doi.org/10.1371/journal.pone.0001761openalex-snapshot
The Hippo Pathway Promotes Notch Signaling in Regulation of Cell Differentiation, Proliferation, and Oocyte Polarity
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4661071openalex-extracted
Dual States of Bmi1-Expressing Intestinal Stem Cells Drive Epithelial Development
inferred← citeshttps://doi.org/10.1002/9780470015902.a0026054openalex-snapshot
Hippo Growth Control Pathway and Organ Size
inferred← citeshttps://doi.org/10.1002/9781118444122.ch10openalex-snapshot
New Insights about Wnt/β‐Catenin Pathway Mechanisms from Global siRNA Screens
inferred← citeshttps://doi.org/10.1002/adfm.202503903openalex-snapshot
Magnetically Guided Mechanoactive Mineralization Scaffolds for Enhanced Bone Regeneration
inferred← citeshttps://doi.org/10.1002/adhm.202000709openalex-snapshot
The Intersection of Mechanotransduction and Regenerative Osteogenic Materials
inferred← citeshttps://doi.org/10.1002/adhm.202301081openalex-snapshot
Convergence of Calcium Channel Regulation and Mechanotransduction in Skeletal Regenerative Biomaterial Design
inferred← citeshttps://doi.org/10.1002/adma.202312081openalex-snapshot
Magnetic Aggregation‐Induced Bone‐Targeting Nanocarrier with Effects of Piezo1 Activation and Osteogenic–Angiogenic Coupling for Osteoporotic Bone Repair
inferred← citeshttps://doi.org/10.1002/bies.201600037openalex-snapshot
YAP and TAZ in epithelial stem cells: A sensor for cell polarity, mechanical forces and tissue damage
inferred← citeshttps://doi.org/10.1002/biof.1634openalex-snapshot
New insights into the core Hippo signaling and biological macromolecules interactions in the biology of solid tumors
inferred← citeshttps://doi.org/10.1002/dvdy.22590openalex-snapshot
Regulation of leg size and shape: Involvement of the Dachsous‐fat signaling pathway
inferred← citeshttps://doi.org/10.1002/dvdy.22723openalex-snapshot
Hippo signaling in Drosophila: Recent advances and insights
inferred← citeshttps://doi.org/10.1002/dvdy.24234openalex-snapshot
Wnt and FGF mediated epithelial‐mesenchymal crosstalk during lung development
inferred← citeshttps://doi.org/10.1002/dvdy.24589openalex-snapshot
Endothelial‐to‐mesenchymal transition in cardiovascular diseases: Developmental signaling pathways gone awry
inferred← citeshttps://doi.org/10.1002/dvdy.24628openalex-snapshot
Hippo‐yap signaling in ocular development and disease
inferred← citeshttps://doi.org/10.1002/embj.201386942openalex-snapshot
A combination of Wnt and growth factor signaling induces Arl4c expression to form epithelial tubular structures
inferred← citeshttps://doi.org/10.1002/ijc.29073openalex-snapshot
Hippo‐YAP signaling pathway: A new paradigm for cancer therapy
inferred← citeshttps://doi.org/10.1002/ijc.29293openalex-snapshot
The H ippo pathway in chemotherapeutic drug resistance
inferred← citeshttps://doi.org/10.1002/ijc.31561openalex-snapshot
A time for YAP1: Tumorigenesis, immunosuppression and targeted therapy
inferred← citeshttps://doi.org/10.1002/jcp.22435openalex-snapshot
The hippo pathway in biological control and cancer development
inferred← citeshttps://doi.org/10.1002/mco2.375openalex-snapshot
Targeting Hippo signaling in cancer: novel perspectives and therapeutic potential
inferred← citeshttps://doi.org/10.1002/med.21286openalex-snapshot
Sleeping Giants: Emerging Roles for the Fat Cadherins in Health and Disease
inferred← citeshttps://doi.org/10.1002/path.2856openalex-snapshot
Altered Hippo signalling in polycystic kidney disease
inferred← citeshttps://doi.org/10.1002/path.4919openalex-snapshot
WWC3 regulates the Wnt and Hippo pathways via Dishevelled proteins and large tumour suppressor 1, to suppress lung cancer invasion and metastasis
inferred← citeshttps://doi.org/10.1002/stem.2432openalex-snapshot
HucMSC Exosome-Delivered 14-3-3ζ Orchestrates Self-Control of the Wnt Response via Modulation of YAP During Cutaneous Regeneration
inferred← citeshttps://doi.org/10.1002/stem.2723openalex-snapshot
Concise Review: Wnt Signaling Pathways in Skin Development and Epidermal Stem Cells
inferred← citeshttps://doi.org/10.1002/wdev.281openalex-snapshot
Signaling and epigenetic mechanisms of intestinal stem cells and progenitors: insight into crypt homeostasis, plasticity, and niches
inferred← citeshttps://doi.org/10.1002/wsbm.140openalex-snapshot
Postgenomic technologies targeting the Wnt signaling network
inferred← citeshttps://doi.org/10.1007/978-1-4614-4370-4_10openalex-snapshot
Other Major Types of Signaling Mediators
inferred← citeshttps://doi.org/10.1007/978-1-4614-4370-4_3openalex-snapshot
Preamble to Cytoplasmic Protein Kinases
inferred← citeshttps://doi.org/10.1007/978-1-4614-4370-4_4openalex-snapshot
Cytoplasmic Protein Tyrosine Kinases
inferred← citeshttps://doi.org/10.1007/978-1-4614-4370-4_5openalex-snapshot
Cytoplasmic Protein Serine/Threonine Kinases
inferred← citeshttps://doi.org/10.1007/978-1-4614-4370-4_6openalex-snapshot
Mitogen-Activated Protein Kinase Module
inferred← citeshttps://doi.org/10.1007/978-1-4614-4370-4_7openalex-snapshot
Dual-Specificity Protein Kinases
inferred← citeshttps://doi.org/10.1007/978-1-4614-4370-4_8openalex-snapshot
Cytosolic Protein Phosphatases
inferred← citeshttps://doi.org/10.1007/978-1-4614-4370-4_9openalex-snapshot
Guanosine Triphosphatases and Their Regulators
inferred← citeshttps://doi.org/10.1007/978-1-4614-6220-0_13openalex-snapshot
Hippo Signaling and Stem Cells
inferred← citeshttps://doi.org/10.1007/978-1-4614-6220-0_15openalex-snapshot
Hippo Signaling in Heart Development
inferred← citeshttps://doi.org/10.1007/978-1-4614-6220-0_17openalex-snapshot
Non-canonical Roles for the Hippo Pathway
inferred← citeshttps://doi.org/10.1007/978-1-4614-6220-0_5openalex-snapshot
Regulation of YAP and TAZ Transcription Co-activators
inferred← citeshttps://doi.org/10.1007/978-1-4614-8232-1_9openalex-snapshot
Drosophila Eye as a Model to Study Regulation of Growth Control: The Discovery of Size Control Pathways
inferred← citeshttps://doi.org/10.1007/978-1-4939-3283-2_18openalex-snapshot
Mathematical and Statistical Techniques for Systems Medicine: The Wnt Signaling Pathway as a Case Study
inferred← citeshttps://doi.org/10.1007/978-1-4939-6747-6_11openalex-snapshot
LUMIER: A Discovery Tool for Mammalian Protein Interaction Networks
inferred← citeshttps://doi.org/10.1007/978-3-030-32656-2_16openalex-snapshot
Wnt/Beta-Catenin Signaling and Prostate Cancer Therapy Resistance
inferred← citeshttps://doi.org/10.1007/978-3-030-36214-0_2openalex-snapshot
Gastric Tumor Microenvironment
inferred← citeshttps://doi.org/10.1007/978-3-030-42246-2_8openalex-snapshot
Drosophila Eye as a Model to Study Regulation of Growth Control: The Discovery of Size Control Pathways
inferred← citeshttps://doi.org/10.1007/978-3-031-97035-1_4openalex-snapshot
Transcriptional Regulation of Lipid Metabolism by Wnt Signaling and Hox Protein Cues
inferred← citeshttps://doi.org/10.1007/978-3-319-46095-6_6openalex-snapshot
Vertebrate Axial Patterning: From Egg to Asymmetry
inferred← citeshttps://doi.org/10.1007/978-3-319-78762-6_18openalex-snapshot
Diversity of Wnt/β-Catenin Signaling in Head and Neck Cancer: Cancer Stem Cells, Epithelial-to-Mesenchymal Transition, and Tumor Microenvironment
inferred← citeshttps://doi.org/10.1007/s00018-014-1742-9openalex-snapshot
The mammalian Hippo pathway: regulation and function of YAP1 and TAZ
inferred← citeshttps://doi.org/10.1007/s00424-017-2004-0openalex-snapshot
Cross talk between the Crumbs complex and Hippo signaling in renal epithelial cells
inferred← citeshttps://doi.org/10.1007/s10571-019-00762-9openalex-snapshot
Recent Advances of the Hippo/YAP Signaling Pathway in Brain Development and Glioma
inferred← citeshttps://doi.org/10.1007/s11010-021-04174-6openalex-snapshot
Wnt/β-catenin signaling pathway in uterine leiomyoma: role in tumor biology and targeting opportunities
inferred← citeshttps://doi.org/10.1007/s11033-025-10372-yopenalex-snapshot
Molecular mechanisms of Hippo pathway in tumorigenesis: therapeutic implications
inferred← citeshttps://doi.org/10.1007/s11160-021-09656-wopenalex-snapshot
Maturation in Atlantic salmon (Salmo salar, Salmonidae): a synthesis of ecological, genetic, and molecular processes
inferred← citeshttps://doi.org/10.1007/s11427-021-2018-7openalex-snapshot
REGγ drives Lgr5+ stem cells to potentiate radiation induced intestinal regeneration
inferred← citeshttps://doi.org/10.1007/s12015-019-09931-1openalex-snapshot
An Insight into Reprogramming Barriers to iPSC Generation
inferred← citeshttps://doi.org/10.1007/s12038-024-00445-8openalex-snapshot
The first embryo, the origin of cancer and animal phylogeny. III. The totipotency as revealed by morphogenesis and the neoplasia controlled by cellular differentiation
inferred← citeshttps://doi.org/10.1007/s12265-015-9630-8openalex-snapshot
Mechanotransduction Mechanisms for Intraventricular Diastolic Vortex Forces and Myocardial Deformations: Part 2
inferred← citeshttps://doi.org/10.1007/s12307-019-00222-4openalex-snapshot
Mechanobiology of Cancer Stem Cells and Their Niche
inferred← citeshttps://doi.org/10.1007/s12672-026-04860-1openalex-snapshot
Expression of CSNK1D in lung adenocarcinoma and its prognostic value after surgery
inferred← citeshttps://doi.org/10.1007/s13238-010-0138-3openalex-snapshot
Structural and functional insights into the TEAD-YAP complex in the Hippo signaling pathway
inferred← citeshttps://doi.org/10.1007/s13238-012-2913-9openalex-snapshot
Hippo pathway in intestinal homeostasis and tumorigenesis
inferred← citeshttps://doi.org/10.1007/s40778-020-00183-1openalex-snapshot
Biomechanical Regulation of Stem Cell Fate
inferred← citeshttps://doi.org/10.1016/b978-0-12-385944-0.00005-8openalex-snapshot
Analyzing the Structure, Function and Information Flow in Signaling Networks using Quantitative Cellular Signatures
inferred← citeshttps://doi.org/10.1016/b978-0-12-386035-4.00002-1openalex-snapshot
New Insights into the Mechanism of Wnt Signaling Pathway Activation
inferred← citeshttps://doi.org/10.1016/b978-0-12-394311-8.00017-0openalex-snapshot
Beta-Catenin Versus the Other Armadillo Catenins
inferred← citeshttps://doi.org/10.1016/b978-0-12-415853-5.00018-2openalex-snapshot
WNT Signaling in Skeletal Homeostasis and Diseases
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.11187-0openalex-snapshot
Wnt Signaling in Cartilage Development
inferred← citeshttps://doi.org/10.1016/b978-0-12-809954-4.00005-0openalex-snapshot
The Role of Hippo Signaling in Intestinal Homeostasis
inferred← citeshttps://doi.org/10.1016/b978-0-12-813073-5.00012-5openalex-snapshot
WNT signaling in skeletal homeostasis and diseases
inferred← citeshttps://doi.org/10.1016/b978-0-443-33623-2.00001-5openalex-snapshot
Modulation of Hippo signaling pathway dysregulation through nanotechnology for neurodegenerative disorders
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2014.11.018openalex-snapshot
Nuclear Signaling from Cadherin Adhesion Complexes
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2018.11.010openalex-snapshot
Wnt-signaling in skeletal development
inferred← citeshttps://doi.org/10.1016/j.ajog.2019.12.016openalex-snapshot
From 2646 to 15: differentially regulated microRNAs between progenitors from normal myometrium and leiomyoma
inferred← citeshttps://doi.org/10.1016/j.ajpath.2011.10.032openalex-snapshot
The Influence of Skeletal Muscle on the Regulation of Liver:Body Mass and Liver Regeneration
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2024.741857openalex-snapshot
Negative regulation of hippo-mediated antiviral response targeted WSSV in Penaeus vannamei
inferred← citeshttps://doi.org/10.1016/j.bbadis.2011.05.005openalex-snapshot
Polycystic kidney disease: The complexity of planar cell polarity and signaling during tissue regeneration and cyst formation
inferred← citeshttps://doi.org/10.1016/j.bbadis.2020.165839openalex-snapshot
Ubiquitin ligases and medulloblastoma: genetic markers of the four consensus subgroups identified through transcriptome datasets
inferred← citeshttps://doi.org/10.1016/j.bbagen.2012.07.005openalex-snapshot
Stem cell regulation by the Hippo pathway
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2016.10.001openalex-snapshot
BET bromodomain is a novel regulator of TAZ and its activity
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2022.119305openalex-snapshot
Nuclear Dishevelled: An enigmatic role in governing cell fate and Wnt signaling
inferred← citeshttps://doi.org/10.1016/j.bbcan.2026.189621openalex-snapshot
The role of Hippo pathway in cancer progression: Implications for cancer stem cells and EMT
inferred← citeshttps://doi.org/10.1016/j.bbrc.2018.05.127openalex-snapshot
Biophysical studies and modelling indicate the binding preference of TAZ WW domain for LATS1 PPxY motif
inferred← citeshttps://doi.org/10.1016/j.bbrc.2018.09.112openalex-snapshot
Olfactomedin-like protein OLFML1 inhibits Hippo signaling and mineralization in osteoblasts
inferred← citeshttps://doi.org/10.1016/j.biochi.2024.03.008openalex-snapshot
The molecular crosstalk of the hippo cascade in breast cancer: A potential central susceptibility
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2015.01.078openalex-snapshot
On human pluripotent stem cell control: The rise of 3D bioengineering and mechanobiology
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2024.122713openalex-snapshot
Transcriptomic profiling of human mesenchymal stem cells using a pulsed electromagnetic-wave motion bioreactor system for enhanced osteogenic commitment and therapeutic potentials
inferred← citeshttps://doi.org/10.1016/j.biopha.2017.04.019openalex-snapshot
Icariin stimulates osteogenic differentiation of rat bone marrow stromal stem cells by increasing TAZ expression
inferred← citeshttps://doi.org/10.1016/j.biopha.2021.112102openalex-snapshot
Ex vivo expansion and functional activity preservation of adult hematopoietic stem cells by a diarylheptanoid from Curcuma comosa
inferred← citeshttps://doi.org/10.1016/j.biopha.2022.113144openalex-snapshot
Hippo signaling pathway: A comprehensive gene expression profile analysis in breast cancer
inferred← citeshttps://doi.org/10.1016/j.biopha.2024.116703openalex-snapshot
YAP in development and disease: Navigating the regulatory landscape from retina to brain
inferred← citeshttps://doi.org/10.1016/j.bone.2018.04.001openalex-snapshot
The YAP/TAZ transcriptional co-activators have opposing effects at different stages of osteoblast differentiation
inferred← citeshttps://doi.org/10.1016/j.canlet.2010.12.008openalex-snapshot
Hippo signaling in oval cells and hepatocarcinogenesis
inferred← citeshttps://doi.org/10.1016/j.canlet.2017.08.005openalex-snapshot
A miR-135b-TAZ positive feedback loop promotes epithelial–mesenchymal transition (EMT) and tumorigenesis in osteosarcoma
inferred← citeshttps://doi.org/10.1016/j.canlet.2018.01.062openalex-snapshot
The Hippo pathway as a drug target in gastric cancer
inferred← citeshttps://doi.org/10.1016/j.ccell.2017.03.007openalex-snapshot
TIAM1 Antagonizes TAZ/YAP Both in the Destruction Complex in the Cytoplasm and in the Nucleus to Inhibit Invasion of Intestinal Epithelial Cells
inferred← citeshttps://doi.org/10.1016/j.ccr.2014.01.010openalex-snapshot
A Peptide Mimicking VGLL4 Function Acts as a YAP Antagonist Therapy against Gastric Cancer
inferred← citeshttps://doi.org/10.1016/j.ceb.2012.12.006openalex-snapshot
The Hippo superhighway: signaling crossroads converging on the Hippo/Yap pathway in stem cells and development
inferred← citeshttps://doi.org/10.1016/j.ceb.2014.09.001openalex-snapshot
Signaling pathway cooperation in TGF-β-induced epithelial–mesenchymal transition
inferred← citeshttps://doi.org/10.1016/j.ceb.2017.04.005openalex-snapshot
Hippo signalling in intestinal regeneration and cancer
inferred← citeshttps://doi.org/10.1016/j.ceb.2025.102476openalex-snapshot
The recent advances and implications in cancer therapy for the hippo pathway
inferred← citeshttps://doi.org/10.1016/j.cell.2012.11.026openalex-snapshot
β-Catenin-Driven Cancers Require a YAP1 Transcriptional Complex for Survival and Tumorigenesis
inferred← citeshttps://doi.org/10.1016/j.cell.2012.11.027openalex-snapshot
Role of TAZ as Mediator of Wnt Signaling
inferred← citeshttps://doi.org/10.1016/j.cell.2014.06.013openalex-snapshot
YAP/TAZ Incorporation in the β-Catenin Destruction Complex Orchestrates the Wnt Response
inferred← citeshttps://doi.org/10.1016/j.cell.2015.07.013openalex-snapshot
Alternative Wnt Signaling Activates YAP/TAZ
inferred← citeshttps://doi.org/10.1016/j.cellsig.2013.11.006openalex-snapshot
Role of extracellular matrix and YAP/TAZ in cell fate determination
inferred← citeshttps://doi.org/10.1016/j.cellsig.2016.08.004openalex-snapshot
The roles of the Hippo pathway in cancer metastasis
inferred← citeshttps://doi.org/10.1016/j.cellsig.2016.09.004openalex-snapshot
Sphingosylphosphorylcholine regulates the Hippo signaling pathway in a dual manner
inferred← citeshttps://doi.org/10.1016/j.cellsig.2020.109815openalex-snapshot
New insights in Hippo signalling alteration in human papillomavirus-related cancers
inferred← citeshttps://doi.org/10.1016/j.cellsig.2020.109858openalex-snapshot
Regulation of Hippo signaling pathway in cancer: A MicroRNA perspective
inferred← citeshttps://doi.org/10.1016/j.cellsig.2025.112023openalex-snapshot
Crosstalk between hippo and Wnt pathways in intestinal stem cells regeneration
inferred← citeshttps://doi.org/10.1016/j.cellsig.2025.112057openalex-snapshot
A FUT2-β-catenin axis mediates chemoresistance and cancer stemness in lung adenocarcinoma
inferred← citeshttps://doi.org/10.1016/j.celrep.2012.09.016openalex-snapshot
Regulation of CD133 by HDAC6 Promotes β-Catenin Signaling to Suppress Cancer Cell Differentiation
inferred← citeshttps://doi.org/10.1016/j.celrep.2013.05.029openalex-snapshot
SOX2 Regulates YAP1 to Maintain Stemness and Determine Cell Fate in the Osteo-Adipo Lineage
inferred← citeshttps://doi.org/10.1016/j.celrep.2013.11.037openalex-snapshot
LATS2 Suppresses Oncogenic Wnt Signaling by Disrupting β-Catenin/BCL9 Interaction
inferred← citeshttps://doi.org/10.1016/j.celrep.2014.07.040openalex-snapshot
Hipk2 and PP1c Cooperate to Maintain Dvl Protein Levels Required for Wnt Signal Transduction
inferred← citeshttps://doi.org/10.1016/j.celrep.2019.04.047openalex-snapshot
The Hippo Pathway Blocks Mammalian Retinal Müller Glial Cell Reprogramming
inferred← citeshttps://doi.org/10.1016/j.clml.2019.09.620openalex-snapshot
Emerging Insights Into the Role of the Hippo Pathway in Multiple Myeloma and Associated Bone Disease
inferred← citeshttps://doi.org/10.1016/j.cmet.2019.10.003openalex-snapshot
TAZ Is a Negative Regulator of PPARγ Activity in Adipocytes and TAZ Deletion Improves Insulin Sensitivity and Glucose Tolerance
inferred← citeshttps://doi.org/10.1016/j.colsurfb.2017.01.039openalex-snapshot
YAP-mediated mechanotransduction regulates osteogenic and adipogenic differentiation of BMSCs on hierarchical structure
inferred← citeshttps://doi.org/10.1016/j.copbio.2010.09.001openalex-snapshot
Interactive proteomics research technologies: recent applications and advances
inferred← citeshttps://doi.org/10.1016/j.csbj.2019.12.015openalex-snapshot
Cross-talk between Hippo and Wnt signalling pathways in intestinal crypts: Insights from an agent-based model
inferred← citeshttps://doi.org/10.1016/j.cub.2012.06.074openalex-snapshot
Homeodomain-Interacting Protein Kinase Regulates Yorkie Activity to Promote Tissue Growth
inferred← citeshttps://doi.org/10.1016/j.cub.2012.12.021openalex-snapshot
Intestinal Regeneration: YAP—Tumor Suppressor and Oncoprotein?
inferred← citeshttps://doi.org/10.1016/j.cub.2015.08.064openalex-snapshot
The Hippo Pathway Core Cassette Regulates Asymmetric Cell Division
inferred← citeshttps://doi.org/10.1016/j.cub.2015.12.043openalex-snapshot
Cell Competition Drives the Growth of Intestinal Adenomas in Drosophila
inferred← citeshttps://doi.org/10.1016/j.devcel.2010.04.003openalex-snapshot
TAZ-Mediated Crosstalk between Wnt and Hippo Signaling
inferred← citeshttps://doi.org/10.1016/j.devcel.2010.09.011openalex-snapshot
The Hippo Signaling Pathway in Development and Cancer
inferred← citeshttps://doi.org/10.1016/j.devcel.2010.11.012openalex-snapshot
The Crumbs Complex Couples Cell Density Sensing to Hippo-Dependent Control of the TGF-β-SMAD Pathway
inferred← citeshttps://doi.org/10.1016/j.devcel.2013.08.013openalex-snapshot
YAP and TAZ, Hippo Signaling Targets, Act as a Rheostat for Nuclear SHP2 Function
inferred← citeshttps://doi.org/10.1016/j.devcel.2014.06.003openalex-snapshot
The Hippo Pathway Effector Yap Controls Patterning and Differentiation of Airway Epithelial Progenitors
inferred← citeshttps://doi.org/10.1016/j.devcel.2015.01.031openalex-snapshot
FOXKs Promote Wnt/β-Catenin Signaling by Translocating DVL into the Nucleus
inferred← citeshttps://doi.org/10.1016/j.devcel.2016.03.002openalex-snapshot
SETD7 Controls Intestinal Regeneration and Tumorigenesis by Regulating Wnt/β-Catenin and Hippo/YAP Signaling
inferred← citeshttps://doi.org/10.1016/j.devcel.2016.09.005openalex-snapshot
Acetylation of VGLL4 Regulates Hippo-YAP Signaling and Postnatal Cardiac Growth
inferred← citeshttps://doi.org/10.1016/j.devcel.2018.06.017openalex-snapshot
Yorkie Functions at the Cell Cortex to Promote Myosin Activation in a Non-transcriptional Manner
inferred← citeshttps://doi.org/10.1016/j.devcel.2025.03.014openalex-snapshot
Dual states of murine Bmi1-expressing intestinal stem cells drive epithelial development utilizing non-canonical Wnt signaling
inferred← citeshttps://doi.org/10.1016/j.ejmech.2025.118299openalex-snapshot
Discovery of repurposed ethacrynic acid and its derivatives as novel TEAD inhibitors
inferred← citeshttps://doi.org/10.1016/j.exer.2013.06.012openalex-snapshot
What do mechanotransduction, Hippo, Wnt, and TGFβ have in common? YAP and TAZ as key orchestrating molecules in ocular health and disease
inferred← citeshttps://doi.org/10.1016/j.gendis.2014.09.001openalex-snapshot
Wnt versus Hippo: A balanced act or dynamic duo?
inferred← citeshttps://doi.org/10.1016/j.gendis.2022.07.011openalex-snapshot
Wnt signaling: Essential roles in osteoblast differentiation, bone metabolism and therapeutic implications for bone and skeletal disorders
inferred← citeshttps://doi.org/10.1016/j.gendis.2023.03.012openalex-snapshot
The Wnt-dependent and Wnt-independent functions of BCL9 in development, tumorigenesis, and immunity: Implications in therapeutic opportunities
inferred← citeshttps://doi.org/10.1016/j.gene.2019.144005openalex-snapshot
Structure, regulation, and (patho-)physiological functions of the stress-induced protein kinase CK1 delta (CSNK1D)
inferred← citeshttps://doi.org/10.1016/j.gene.2024.148424openalex-snapshot
Breast cancer drug resistance: Decoding the roles of Hippo pathway crosstalk
inferred← citeshttps://doi.org/10.1016/j.isci.2018.01.003openalex-snapshot
Transcriptional Co-activator Functions of YAP and TAZ Are Inversely Regulated by Tyrosine Phosphorylation Status of Parafibromin
inferred← citeshttps://doi.org/10.1016/j.isci.2020.101860openalex-snapshot
YAP/TAZ Are Required to Suppress Osteogenic Differentiation of Vascular Smooth Muscle Cells
inferred← citeshttps://doi.org/10.1016/j.jcmgh.2020.04.007openalex-snapshot
Are Wnt/β-Catenin and PI3K/AKT/mTORC1 Distinct Pathways in Colorectal Cancer?
inferred← citeshttps://doi.org/10.1016/j.jgg.2011.09.009openalex-snapshot
Hippo signaling: A hub of growth control, tumor suppression and pluripotency maintenance
inferred← citeshttps://doi.org/10.1016/j.jhep.2015.11.028openalex-snapshot
RNAi-nanoparticulate manipulation of gene expression as a new functional genomics tool in the liver
inferred← citeshttps://doi.org/10.1016/j.jia.2023.09.031openalex-snapshot
Biology of Hippo signaling pathway: Skeletal muscle development and beyond
inferred← citeshttps://doi.org/10.1016/j.jip.2018.09.007openalex-snapshot
Impact of the microsporidian Nosema ceranae on the gut epithelium renewal of the honeybee, Apis mellifera
inferred← citeshttps://doi.org/10.1016/j.jot.2024.12.003openalex-snapshot
Role of YAP/TAZ in bone diseases: A transductor from mechanics to biology
inferred← citeshttps://doi.org/10.1016/j.lfs.2021.119298openalex-snapshot
Microenvironmental regulation of intestinal stem cells in the inflamed intestine
inferred← citeshttps://doi.org/10.1016/j.lfs.2023.121980openalex-snapshot
MicroRNAs: The key players regulating the crosstalk between Hippo and Wnt/β-catenin pathways in breast cancer
inferred← citeshttps://doi.org/10.1016/j.lfs.2024.123240openalex-snapshot
SIRT7 stabilizes β-catenin and promotes canonical Wnt activation via upregulating FZD7
inferred← citeshttps://doi.org/10.1016/j.mce.2015.06.020openalex-snapshot
The LH/CG receptor activates canonical signaling pathway when expressed in Drosophila
inferred← citeshttps://doi.org/10.1016/j.mce.2021.111460openalex-snapshot
Overexpression of Lin28a induces a primary ovarian insufficiency phenotype via facilitation of primordial follicle activation in mice
inferred← citeshttps://doi.org/10.1016/j.mcn.2013.10.005openalex-snapshot
p21-Activated kinase (PAK) is required for Bone Morphogenetic Protein (BMP)-induced dendritogenesis in cortical neurons
inferred← citeshttps://doi.org/10.1016/j.mod.2015.08.001openalex-snapshot
The transcriptional coactivator Taz regulates proximodistal patterning of the pronephric tubule in zebrafish
inferred← citeshttps://doi.org/10.1016/j.molcel.2017.10.010openalex-snapshot
Regulation of the Hippo-YAP Pathway by Glucose Sensor O-GlcNAcylation
inferred← citeshttps://doi.org/10.1016/j.molimm.2025.12.013openalex-snapshot
Hippo signaling as a therapeutic switch for T cell functions and tumor immunity
inferred← citeshttps://doi.org/10.1016/j.mvr.2018.04.003openalex-snapshot
YAP1-TEAD1 signaling controls angiogenesis and mitochondrial biogenesis through PGC1α
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2017.09.002openalex-snapshot
Paving the Rho in cancer metastasis: Rho GTPases and beyond
inferred← citeshttps://doi.org/10.1016/j.phymed.2024.156156openalex-snapshot
Yes-associated protein indispensably mediates hirsutine-induced inhibition on cell growth and Wnt/β-catenin signaling in colorectal cancer
inferred← citeshttps://doi.org/10.1016/j.preteyeres.2018.11.008openalex-snapshot
Wnt Signaling in vascular eye diseases
inferred← citeshttps://doi.org/10.1016/j.prp.2023.154539openalex-snapshot
Dysregulation of P53 in breast cancer: Causative factors and treatment strategies
inferred← citeshttps://doi.org/10.1016/j.prp.2024.155547openalex-snapshot
MicroRNA-135b mainly functions as an oncogene during tumor progression
inferred← citeshttps://doi.org/10.1016/j.regen.2019.100025openalex-snapshot
Transcriptional analysis of scar-free wound healing during early stages of tail regeneration in the green anole lizard, Anolis carolinensis
inferred← citeshttps://doi.org/10.1016/j.rhum.2024.09.013openalex-snapshot
Les mécanismes de l’ostéoformation dans la spondyloarthrite ankylosante
inferred← citeshttps://doi.org/10.1016/j.semcancer.2015.02.005openalex-snapshot
Evasion of anti-growth signaling: A key step in tumorigenesis and potential target for treatment and prophylaxis by natural compounds
inferred← citeshttps://doi.org/10.1016/j.semcancer.2017.04.010openalex-snapshot
The NDR/LATS protein kinases in immunology and cancer biology
inferred← citeshttps://doi.org/10.1016/j.semcdb.2012.04.006openalex-snapshot
Integration of intercellular signaling through the Hippo pathway
inferred← citeshttps://doi.org/10.1016/j.semcdb.2012.08.001openalex-snapshot
Hippo signaling in mammalian stem cells
inferred← citeshttps://doi.org/10.1016/j.semcdb.2019.09.004openalex-snapshot
Upstream regulation of the Hippo-Yap pathway in cardiomyocyte regeneration
inferred← citeshttps://doi.org/10.1016/j.semcdb.2021.10.001openalex-snapshot
An emergent Wnt5a/YAP/TAZ regulatory circuit and its possible role in cancer
inferred← citeshttps://doi.org/10.1016/j.stem.2017.03.023openalex-snapshot
An FAK-YAP-mTOR Signaling Axis Regulates Stem Cell-Based Tissue Renewal in Mice
inferred← citeshttps://doi.org/10.1016/j.stem.2020.03.002openalex-snapshot
Lats1/2 Sustain Intestinal Stem Cells and Wnt Activation through TEAD-Dependent and Independent Transcription
inferred← citeshttps://doi.org/10.1016/j.stemcr.2020.03.021openalex-snapshot
The Snakeskin-Mesh Complex of Smooth Septate Junction Restricts Yorkie to Regulate Intestinal Homeostasis in Drosophila
inferred← citeshttps://doi.org/10.1016/j.stemcr.2024.02.010openalex-snapshot
MST1/2 regulates fibro/adipogenic progenitor fate decisions in skeletal muscle regeneration
inferred← citeshttps://doi.org/10.1016/j.tcb.2011.10.002openalex-snapshot
Coordinating developmental signaling: novel roles for the Hippo pathway
inferred← citeshttps://doi.org/10.1016/j.tcb.2013.03.007openalex-snapshot
Crossroads of Wnt and Hippo in epithelial tissues
inferred← citeshttps://doi.org/10.1016/j.tcb.2015.05.002openalex-snapshot
YAP and TAZ: a nexus for Hippo signaling and beyond
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2012.08.018openalex-snapshot
Possible involvement of Wnt/β-catenin signaling pathway in hatching and trophectoderm differentiation of pig blastocysts
inferred← citeshttps://doi.org/10.1016/j.tibs.2010.05.010openalex-snapshot
Modularity in the Hippo signaling pathway
inferred← citeshttps://doi.org/10.1016/j.tibs.2020.08.012openalex-snapshot
YAP and TAZ Are Not Identical Twins
inferred← citeshttps://doi.org/10.1016/j.tibs.2021.07.008openalex-snapshot
Regulation of Dishevelled protein activity and stability by post-translational modifications and autophagy
inferred← citeshttps://doi.org/10.1016/j.tips.2013.08.006openalex-snapshot
Regulation of the Hippo pathway and implications for anticancer drug development
inferred← citeshttps://doi.org/10.1016/j.tox.2024.153815openalex-snapshot
Exposure to the phthalate metabolite MEHP impacts survival and growth of human ovarian follicles in vitro
inferred← citeshttps://doi.org/10.1016/j.trecan.2022.08.002openalex-snapshot
TAZ/YAP fusion proteins: mechanistic insights and therapeutic opportunities
inferred← citeshttps://doi.org/10.1016/j.visres.2017.02.007openalex-snapshot
Canonical Wnt signaling in diabetic retinopathy
inferred← citeshttps://doi.org/10.1016/j.ydbio.2015.08.001openalex-snapshot
G protein-coupled receptors Flop1 and Flop2 inhibit Wnt/β-catenin signaling and are essential for head formation in Xenopus
inferred← citeshttps://doi.org/10.1016/j.ydbio.2020.12.018openalex-snapshot
YAP1 and its fusion proteins in cancer initiation, progression and therapeutic resistance
inferred← citeshttps://doi.org/10.1016/j.ydbio.2022.05.005openalex-snapshot
Mechanosignaling in vertebrate development
inferred← citeshttps://doi.org/10.1016/j.ydbio.2025.04.013openalex-snapshot
Canonical Wnt pathway modulation is required to correctly execute multiple independent cellular dynamic programs during cranial neural tube closure
inferred← citeshttps://doi.org/10.1016/j.ydbio.2026.02.003openalex-snapshot
Deciphering the single-cell transcriptomic atlas of donkey (Equus asinus) gonad development in early gestation
inferred← citeshttps://doi.org/10.1016/j.yexcr.2012.05.005openalex-snapshot
YAP regulates neuronal differentiation through Sonic hedgehog signaling pathway
inferred← citeshttps://doi.org/10.1016/j.yexcr.2014.09.005openalex-snapshot
Insight into planar cell polarity
inferred← citeshttps://doi.org/10.1016/j.yexcr.2015.10.034openalex-snapshot
Role of YAP/TAZ in cell-matrix adhesion-mediated signalling and mechanotransduction
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