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YAP1 is amplified and up-regulated in hedgehog-associated medulloblastomas and mediates Sonic hedgehog-driven neural precursor proliferation
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1097-4644(19980801)70:2<231::aid-jcb9>3.0.co;2-popenalex-snapshot
Distinct nuclear import and export pathways mediated by members of the karyopherin β family
inferredcites →https://doi.org/10.1002/path.1681openalex-snapshot
Analysis of ovarian cancer cell lines using array‐based comparative genomic hybridization
inferredcites →https://doi.org/10.1002/path.1712openalex-snapshot
Insulin‐like growth factor ligands, receptors, and binding proteins in cancer
inferredcites →https://doi.org/10.1007/bf00165516openalex-snapshot
Cellular and molecular pathology of medulloblastoma
inferredcites →https://doi.org/10.1016/0360-3016(94)00393-yopenalex-snapshot
Brain tumors in children: Long-term survival after radiation treatment
inferredcites →https://doi.org/10.1016/j.bbcan.2006.05.003openalex-snapshot
IGF-I mediated survival pathways in normal and malignant cells
inferredcites →https://doi.org/10.1016/j.ccr.2006.11.008openalex-snapshot
Radiation resistance and stem-like cells in brain tumors
inferredcites →https://doi.org/10.1016/j.ccr.2006.11.020openalex-snapshot
A Perivascular Niche for Brain Tumor Stem Cells
inferredcites →https://doi.org/10.1016/j.ccr.2006.12.007openalex-snapshot
Hit 'Em Where They Live: Targeting the Cancer Stem Cell Niche
inferredcites →https://doi.org/10.1016/j.ccr.2008.02.011openalex-snapshot
The Emerging Role of the Hippo Pathway in Cell Contact Inhibition, Organ Size Control, and Cancer Development in Mammals
inferredcites →https://doi.org/10.1016/j.ccr.2008.12.016openalex-snapshot
Identification of CD15 as a Marker for Tumor-Propagating Cells in a Mouse Model of Medulloblastoma
inferredcites →https://doi.org/10.1016/j.cell.2006.05.030openalex-snapshot
Identification and Validation of Oncogenes in Liver Cancer Using an Integrative Oncogenomic Approach
inferredcites →https://doi.org/10.1016/j.cub.2007.10.039openalex-snapshot
YAP1 Increases Organ Size and Expands Undifferentiated Progenitor Cells
inferredcites →https://doi.org/10.1016/j.molmed.2004.11.008openalex-snapshot
Medulloblastoma: developmental mechanisms out of control
inferredcites →https://doi.org/10.1016/s0896-6273(00)80682-0openalex-snapshot
Control of Neuronal Precursor Proliferation in the Cerebellum by Sonic Hedgehog
inferredcites →https://doi.org/10.1016/s0959-437x(03)00002-9openalex-snapshot
Sonic hedgehog in normal and neoplastic proliferation: insight gained from human tumors and animal models
inferredcites →https://doi.org/10.1023/a:1012260318979openalex-snapshot
A Mouse Model for Medulloblastoma and Basal Cell Nevus Syndrome
inferredcites →https://doi.org/10.1038/ncb1107-1225openalex-snapshot
How size is controlled: from Hippos to Yorkies
inferredcites →https://doi.org/10.1038/ng.336openalex-snapshot
Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastoma
inferredcites →https://doi.org/10.1038/sj.onc.1210636openalex-snapshot
Nuclear insulin receptor substrate-1 activates promoters of cell cycle progression genes
inferredcites →https://doi.org/10.1073/pnas.0605579103openalex-snapshot
Transforming properties of YAP , a candidate oncogene on the chromosome 11q22 amplicon
inferredcites →https://doi.org/10.1073/pnas.0832317100openalex-snapshot
Transcriptional profiling of the Sonic hedgehog response: A critical role for N-myc in proliferation of neuronal precursors
inferredcites →https://doi.org/10.1093/emboj/18.9.2551openalex-snapshot
A WW domain‐containing Yes‐associated protein (YAP) is a novel transcriptional co‐activator
inferredcites →https://doi.org/10.1093/hmg/ddg083openalex-snapshot
A comprehensive search for DNA amplification in lung cancer identifies inhibitors of apoptosis cIAP1 and cIAP2 as candidate oncogenes
inferredcites →https://doi.org/10.1093/neuonc/1.3.232openalex-snapshot
Medulloblastoma: Clinical and biologic aspects
inferredcites →https://doi.org/10.1101/gad.1536007openalex-snapshot
Hippo signaling in organ size control
inferredcites →https://doi.org/10.1101/gad.1602907openalex-snapshot
Inactivation of YAP oncoprotein by the Hippo pathway is involved in cell contact inhibition and tissue growth control
inferredcites →https://doi.org/10.1101/gad.1627008openalex-snapshot
PI3K pathway regulates survival of cancer stem cells residing in the perivascular niche following radiation in medulloblastoma in vivo
inferredcites →https://doi.org/10.1101/gad.1664408openalex-snapshot
TEAD mediates YAP-dependent gene induction and growth control
inferredcites →https://doi.org/10.1101/gad.1726608openalex-snapshot
YAP regulates neural progenitor cell number via the TEA domain transcription factor
inferredcites →https://doi.org/10.1126/science.1073733openalex-snapshot
Medulloblastoma Growth Inhibition by Hedgehog Pathway Blockade
inferredcites →https://doi.org/10.1128/mcb.20.23.9055-9067.2000openalex-snapshot
Sonic hedgehog Promotes G 1 Cyclin Expression and Sustained Cell Cycle Progression in Mammalian Neuronal Precursors
inferredcites →https://doi.org/10.1146/annurev.ne.18.030195.002125openalex-snapshot
Mechanisms of Neural Patterning and Specification in the Development Cerebellum
inferredcites →https://doi.org/10.1155/2005/407216openalex-snapshot
Chromosomal Changes in relation to Clinical Outcome in Larynx and Pharynx Squamous Cell Carcinoma
inferredcites →https://doi.org/10.1158/0008-5472.can-04-1813openalex-snapshot
The SmoA1 Mouse Model Reveals That Notch Signaling Is Critical for the Growth and Survival of Sonic Hedgehog-Induced Medulloblastomas
inferredcites →https://doi.org/10.1158/0008-5472.can-05-1513openalex-snapshot
Multiple Microalterations Detected at High Frequency in Oral Cancer
inferredcites →https://doi.org/10.1158/0008-5472.can-08-4710openalex-snapshot
The miR-17/92 Polycistron Is Up-regulated in Sonic Hedgehog–Driven Medulloblastomas and Induced by N-myc in Sonic Hedgehog–Treated Cerebellar Neural Precursors
inferredcites →https://doi.org/10.1242/dev.00182openalex-snapshot
Nmyc upregulation by sonic hedgehog signaling promotes proliferation in developing cerebellar granule neuron precursors
inferredcites →https://doi.org/10.1242/dev.00891openalex-snapshot
Hedgehog and PI-3 kinase signaling converge on Nmyc1 to promote cell cycle progression in cerebellar neuronal precursors
inferredcites →https://doi.org/10.1242/dev.022871openalex-snapshot
Insulin receptor substrate 1 is an effector of sonic hedgehog mitogenic signaling in cerebellar neural precursors
inferredcites →https://doi.org/10.1242/dev.027151openalex-snapshot
Mammalian Tead proteins regulate cell proliferation and contact inhibition as transcriptional mediators of Hippo signaling
inferredcites →https://doi.org/10.1242/dev.126.14.3089openalex-snapshot
Sonic hedgehog regulates the growth and patterning of the cerebellum
inferredcites →https://doi.org/10.1242/dev.126.17.3915openalex-snapshot
Regulation of Gli2 and Gli3 activities by an amino-terminal repression domain: implication of Gli2 and Gli3 as primary mediators of Shh signaling
inferredcites →https://doi.org/10.1371/journal.pone.0003088openalex-snapshot
Integrated Genomics Identifies Five Medulloblastoma Subtypes with Distinct Genetic Profiles, Pathway Signatures and Clinicopathological Features
inferredcites →https://doi.org/10.1593/neo.04586openalex-snapshot
Array-Based Comparative Genomic Hybridization Identifies Localized DNA Amplifications and Homozygous Deletions in Pancreatic Cancer
inferredcites →https://doi.org/10.3171/foc.2005.19.5.8openalex-snapshot
Modeling medulloblastoma with genetically engineered mice
inferredcites →https://doi.org/10.4161/cc.6.21.4822openalex-snapshot
Morphogens and the Control of Cell Proliferation and Patterning in the Spinal Cord
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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The Calcium Binding Protein S100β Marks Hedgehog-Responsive Perivascular Stem Cells That Contribute to Intimal Thickening Following Iatrogenic Flow Restriction
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The TEAD4–YAP/TAZ Protein–Protein Interaction: Expected Similarities and Unexpected Differences
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Effect of Nutrient Availability on Progenitor Cells in Zebrafish (Danio Rerio)
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YAP maintains the production of intermediate progenitor cells and upper‐layer projection neurons in the mouse cerebral cortex
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The role of Hippo‐YAP/TAZ signaling in brain development
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YAP1 and VGLL3, encoding two cofactors of TEAD transcription factors, are amplified and overexpressed in a subset of soft tissue sarcomas
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Yes-associated protein regulates the hepatic response after bile duct ligation
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Hedgehog regulates yes‐associated protein 1 in regenerating mouse liver
inferred← citeshttps://doi.org/10.1002/ijc.28330openalex-snapshot
Neogenin1 is a sonic hedgehog target in medulloblastoma and is necessary for cell cycle progression
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/iub.2052openalex-snapshot
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The hippo pathway in biological control and cancer development
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Role of Hippo Signaling in Cancer Stem Cells
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Yes‐associated protein mediates human embryonic stem cell‐derived cardiomyocyte proliferation: Involvement of epidermal growth factor receptor signaling
inferred← citeshttps://doi.org/10.1002/jcp.28981openalex-snapshot
Mu‐KRAS attenuates Hippo signaling pathway through PKCι to sustain the growth of pancreatic cancer
inferred← citeshttps://doi.org/10.1002/jnr.24551openalex-snapshot
The emerging role of Hippo signaling in neurodegeneration
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Invited reply on PBC-13-0662.R2: Biomarkers and wilms tumor
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Overexpression of TEAD4 in atypical teratoid/rhabdoid tumor: New insight to the pathophysiology of an aggressive brain tumor
inferred← citeshttps://doi.org/10.1002/tox.23025openalex-snapshot
Shh‐Yap signaling controls hepatic ductular reactions in CCl4 ‐induced liver injury
inferred← citeshttps://doi.org/10.1007/978-1-4419-8435-7_8openalex-snapshot
Hedgehog Signaling in Pediatric Brain Tumors
inferred← citeshttps://doi.org/10.1007/978-1-4614-6220-0_11openalex-snapshot
Hippo and Mouse Models for Cancer
inferred← citeshttps://doi.org/10.1007/978-1-4614-6220-0_13openalex-snapshot
Hippo Signaling and Stem Cells
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Medulloblastoma and CNS Primitive Neuroectodermal Tumors
inferred← citeshttps://doi.org/10.1007/978-3-031-11665-0_9openalex-snapshot
Ciliopathies: Their Role in Pediatric Kidney Disease
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Medulloblastoma: Pathology
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Cancer Stem Cell: From Conjecture to Reality
inferred← citeshttps://doi.org/10.1007/978-3-662-52972-0_11openalex-snapshot
Ciliopathies: Their Role in Pediatric Renal Disease
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The Hippo Signaling Pathway: A Candidate New Drug Target for Malignant Tumors
inferred← citeshttps://doi.org/10.1007/978-981-15-8473-2_4openalex-snapshot
Sonic Hedgehog Cell Signaling Pathway and Medulloblastoma
inferred← citeshttps://doi.org/10.1007/978-981-16-1247-3_93-1openalex-snapshot
Targeting Signaling Pathways in Cancer Stem Cells for Therapy of Cancer
inferred← citeshttps://doi.org/10.1007/978-981-16-5422-0_93openalex-snapshot
Targeting Signaling Pathways in Cancer Stem Cells for Therapy of Cancer
inferred← citeshttps://doi.org/10.1007/978-981-96-2763-9_5openalex-snapshot
Hippo LATS Pathway in Cancer and Its Role as a Potential Target for Anti-cancer Drugs
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/s00018-016-2412-xopenalex-snapshot
Role of YAP/TAZ transcriptional regulators in resistance to anti-cancer therapies
inferred← citeshttps://doi.org/10.1007/s00018-023-04892-8openalex-snapshot
Proteomic investigation of neural stem cell to oligodendrocyte precursor cell differentiation reveals phosphorylation-dependent Dclk1 processing
inferred← citeshttps://doi.org/10.1007/s00381-012-1704-1openalex-snapshot
Matching mice to malignancy: molecular subgroups and models of medulloblastoma
inferred← citeshttps://doi.org/10.1007/s00381-012-2014-3openalex-snapshot
A contemporary review of molecular candidates for the development and treatment of childhood medulloblastoma
inferred← citeshttps://doi.org/10.1007/s00401-010-0751-5openalex-snapshot
Molecular diagnostics of CNS embryonal tumors
inferred← citeshttps://doi.org/10.1007/s00401-011-0800-8openalex-snapshot
Medulloblastoma: clinicopathological correlates of SHH, WNT, and non-SHH/WNT molecular subgroups
inferred← citeshttps://doi.org/10.1007/s00401-012-0946-zopenalex-snapshot
An essential role for p38 MAPK in cerebellar granule neuron precursor proliferation
inferred← citeshttps://doi.org/10.1007/s00432-021-03577-8openalex-snapshot
Blockage of glioma cell survival by truncated TEAD-binding domain of YAP
inferred← citeshttps://doi.org/10.1007/s00784-018-2693-6openalex-snapshot
Yes-associated protein (YAP) molecule expression in odontogenic epithelium of ameloblastoma
inferred← citeshttps://doi.org/10.1007/s10072-018-3327-0openalex-snapshot
The association of NF2 (neurofibromin 2) gene polymorphism and the risk of medulloblastomas
inferred← citeshttps://doi.org/10.1007/s10555-013-9463-3openalex-snapshot
The dual functions of YAP-1 to promote and inhibit cell growth in human malignancy
inferred← citeshttps://doi.org/10.1007/s10555-026-10349-8openalex-snapshot
The Hippo signaling pathway in pediatric brain tumors: molecular mechanisms and therapeutic opportunities
inferred← citeshttps://doi.org/10.1007/s10571-017-0498-9openalex-snapshot
Exploration of Involved Key Genes and Signaling Diversity in Brain Tumors
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/s11033-013-2939-yopenalex-snapshot
Construction, characterization and expression of full length cDNA clone of sheep YAP1 gene
inferred← citeshttps://doi.org/10.1007/s11033-025-10299-4openalex-snapshot
Decoding gene expression profiles of Hippo signaling pathway components in breast cancer
inferred← citeshttps://doi.org/10.1007/s11060-014-1654-4openalex-snapshot
RETRACTED ARTICLE: Mst1 regulates glioma cell proliferation via the AKT/mTOR signaling pathway
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Hugl-1 inhibits glioma cell growth in intracranial model
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It’s all downstream from here: RTK/Raf/MEK/ERK pathway resistance mechanisms in glioblastoma
inferred← citeshttps://doi.org/10.1007/s13193-025-02246-3openalex-snapshot
GLI1-VENTX Expression Pattern as a Prognostic Value for Non-Metastatic Early Esophageal Squamous Cell Carcinoma
inferred← citeshttps://doi.org/10.1007/s13238-012-2919-3openalex-snapshot
The Hippo pathway regulates stem cell proliferation, self-renewal, and differentiation
inferred← citeshttps://doi.org/10.1007/s13238-020-00742-6openalex-snapshot
SHANK2 is a frequently amplified oncogene with evolutionarily conserved roles in regulating Hippo signaling
inferred← citeshttps://doi.org/10.1007/s13277-013-0751-xopenalex-snapshot
Clinical and prognostic significance of Yes-associated protein in colorectal cancer
inferred← citeshttps://doi.org/10.1007/s13277-015-3297-2openalex-snapshot
Role of Yes-associated protein 1 in gliomas: pathologic and therapeutic aspects
inferred← citeshttps://doi.org/10.1007/s13277-016-5318-1openalex-snapshot
Expression and significance of Hippo/YAP signaling in glioma progression
inferred← citeshttps://doi.org/10.1007/s13577-025-01308-6openalex-snapshot
Establishment of human histiocytic sarcoma organoids dependent on the SHH/YAP pathway
inferred← citeshttps://doi.org/10.1007/s40675-014-0008-2openalex-snapshot
Sleep and Oligodendrocyte Functions
inferred← citeshttps://doi.org/10.1016/j.ajhg.2014.01.001openalex-snapshot
Heterozygous Loss-of-Function Mutations in YAP1 Cause Both Isolated and Syndromic Optic Fissure Closure Defects
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.bbagrm.2018.10.003openalex-snapshot
Heterogeneous ribonucleoprotein F regulates YAP expression via a G-tract in 3′UTR
inferred← citeshttps://doi.org/10.1016/j.bbrc.2020.06.105openalex-snapshot
Hippo pathway cooperates with ChREBP to regulate hepatic glucose utilization
inferred← citeshttps://doi.org/10.1016/j.biopha.2024.116873openalex-snapshot
Therapeutic implications of signaling pathways and tumor microenvironment interactions in esophageal cancer
inferred← citeshttps://doi.org/10.1016/j.biopha.2024.117569openalex-snapshot
Buparlisib and ponatinib inhibit aggressiveness of cholangiocarcinoma cells via suppression of IRS1-related pathway by targeting oxidative stress resistance
inferred← citeshttps://doi.org/10.1016/j.brainres.2013.08.049openalex-snapshot
Spinal expression of Hippo signaling components YAP and TAZ following peripheral nerve injury in rats
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.2021.03.006openalex-snapshot
Hippo pathway: Regulation, deregulation and potential therapeutic targets in cancer
inferred← citeshttps://doi.org/10.1016/j.ccell.2016.05.005openalex-snapshot
YAP/TAZ at the Roots of Cancer
inferred← citeshttps://doi.org/10.1016/j.ccell.2019.07.009openalex-snapshot
Single-Cell Transcriptomics in Medulloblastoma Reveals Tumor-Initiating Progenitors and Oncogenic Cascades during Tumorigenesis and Relapse
inferred← citeshttps://doi.org/10.1016/j.ccell.2025.04.014openalex-snapshot
Genetic modeling of ELP1-associated Sonic hedgehog medulloblastoma identifies MDM2 as a selective therapeutic target
inferred← citeshttps://doi.org/10.1016/j.ccell.2026.01.005openalex-snapshot
Male-biased Yap1-Cd276/B7-H3 axis for immune evasion in medulloblastoma
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.cell.2014.06.003openalex-snapshot
Yap1 Activation Enables Bypass of Oncogenic Kras Addiction in Pancreatic Cancer
inferred← citeshttps://doi.org/10.1016/j.cell.2015.10.044openalex-snapshot
Hippo Pathway in Organ Size Control, Tissue Homeostasis, and Cancer
inferred← citeshttps://doi.org/10.1016/j.celrep.2016.02.021openalex-snapshot
Yap1 Regulates Multiple Steps of Chondrocyte Differentiation during Skeletal Development and Bone Repair
inferred← citeshttps://doi.org/10.1016/j.celrep.2023.112338openalex-snapshot
Matrix stiffness regulates tumor cell intravasation through expression and ESRP1-mediated alternative splicing of MENA
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.115381openalex-snapshot
YAP1 is a key regulator of EWS::FLI1-dependent malignant transformation upon IGF-1-mediated reprogramming of bone mesenchymal stem cells
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.115673openalex-snapshot
Chromatin modification abnormalities by CHD7 and KMT2C loss promote medulloblastoma progression
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.2017.08.019openalex-snapshot
YAP/TAZ and Hedgehog Coordinate Growth and Patterning in Gastrointestinal Mesenchyme
inferred← citeshttps://doi.org/10.1016/j.devcel.2019.06.003openalex-snapshot
The Hippo Signaling Pathway in Development and Disease
inferred← citeshttps://doi.org/10.1016/j.ebiom.2020.102655openalex-snapshot
Recent insights into the biology of pancreatic cancer
inferred← citeshttps://doi.org/10.1016/j.exphem.2019.11.002openalex-snapshot
Yap1 promotes proliferation of transiently amplifying stress erythroid progenitors during erythroid regeneration
inferred← citeshttps://doi.org/10.1016/j.gendis.2019.11.003openalex-snapshot
The Hippo Tumor Suppressor Pathway (YAP/TAZ/TEAD/MST/LATS) and EGFR-RAS-RAF-MEK in cancer metastasis
inferred← citeshttps://doi.org/10.1016/j.gep.2019.119068openalex-snapshot
Expression of transcription factors and signaling molecules in the cerebellar granule cell development
inferred← citeshttps://doi.org/10.1016/j.humgen.2024.201269openalex-snapshot
In silico analysis of hippo signaling pathway associated microRNAs in breast cancer
inferred← citeshttps://doi.org/10.1016/j.humpath.2011.12.001openalex-snapshot
Expression of Yes-associated protein modulates Survivin expression in primary liver malignancies
inferred← citeshttps://doi.org/10.1016/j.isci.2023.106152openalex-snapshot
Moesin is an effector of tau-induced actin overstabilization, cell cycle activation, and neurotoxicity in Alzheimer’s disease
inferred← citeshttps://doi.org/10.1016/j.isci.2023.107449openalex-snapshot
The circadian clock protein Cryptochrome 1 is a direct target and feedback regulator of the Hippo pathway
inferred← citeshttps://doi.org/10.1016/j.jalz.2017.08.012openalex-snapshot
A systematic integrated analysis of brain expression profiles reveals YAP1 and other prioritized hub genes as important upstream regulators in Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.jfma.2015.03.011openalex-snapshot
The role of Hippo signaling in tooth development
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.2015.05.031openalex-snapshot
Accumulation of duct cells with activated YAP parallels fibrosis progression in non-alcoholic fatty liver disease
inferred← citeshttps://doi.org/10.1016/j.jhep.2015.07.008openalex-snapshot
Emerging evidence on the role of the Hippo/YAP pathway in liver physiology and cancer
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.jprot.2017.03.022openalex-snapshot
Proteomic profiling of isogenic primary and metastatic medulloblastoma cell lines reveals differential expression of key metastatic factors
inferred← citeshttps://doi.org/10.1016/j.mod.2012.05.007openalex-snapshot
Regulation of Yorkie activity in Drosophila imaginal discs by the Hedgehog receptor gene patched
inferred← citeshttps://doi.org/10.1016/j.ncrna.2024.06.006openalex-snapshot
Interaction of noncoding RNAs with hippo signaling pathway in cancer cells and cancer stem cells
inferred← citeshttps://doi.org/10.1016/j.neuint.2025.105929openalex-snapshot
Understanding the intricacies of cellular mechanisms in remyelination: The role of circadian rhythm
inferred← citeshttps://doi.org/10.1016/j.pan.2020.12.003openalex-snapshot
Association of subcellular localization of TEAD transcription factors with outcome and progression in pancreatic ductal adenocarcinoma
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2024.108673openalex-snapshot
Mechanistic insights into medulloblastoma relapse
inferred← citeshttps://doi.org/10.1016/j.phrs.2015.11.025openalex-snapshot
Targeting the Hippo pathway: Clinical implications and therapeutics
inferred← citeshttps://doi.org/10.1016/j.phrs.2019.03.018openalex-snapshot
Dysregulation of the Hippo pathway signaling in aging and cancer
inferred← citeshttps://doi.org/10.1016/j.phrs.2022.106523openalex-snapshot
Role of Hedgehog and Hippo signaling pathways in cancer: A special focus on non-coding RNAs
inferred← citeshttps://doi.org/10.1016/j.semcancer.2021.07.006openalex-snapshot
The two sides of Hippo pathway in cancer
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.2012.05.004openalex-snapshot
The YAP and TAZ transcription co-activators: Key downstream effectors of the mammalian 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.stemcr.2015.03.004openalex-snapshot
GRM7 Regulates Embryonic Neurogenesis via CREB and YAP
inferred← citeshttps://doi.org/10.1016/j.tcb.2010.04.005openalex-snapshot
Yorkie: the final destination of Hippo signaling
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.2012.04.006openalex-snapshot
The Hippo signaling pathway and stem cell biology
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.tibs.2010.05.010openalex-snapshot
Modularity in the Hippo signaling pathway
inferred← citeshttps://doi.org/10.1016/j.tranon.2014.02.005openalex-snapshot
Hippo Signaling Mediates Proliferation, Invasiveness, and Metastatic Potential of Clear Cell Renal Cell Carcinoma
inferred← citeshttps://doi.org/10.1016/j.trecan.2021.01.008openalex-snapshot
Drivers of Gene Expression Dysregulation in Pancreatic Cancer
inferred← citeshttps://doi.org/10.1016/j.ydbio.2011.10.017openalex-snapshot
Negative regulation of Yap during neuronal differentiation
inferred← citeshttps://doi.org/10.1016/j.ydbio.2014.01.018openalex-snapshot
Yap1, transcription regulator in the Hippo signaling pathway, is required for Xenopus limb bud regeneration
inferred← citeshttps://doi.org/10.1016/j.ydbio.2018.05.017openalex-snapshot
The versatile hippo pathway in oral-maxillofacial development and bone remodeling
inferred← citeshttps://doi.org/10.1016/j.ydbio.2019.07.018openalex-snapshot
YAP1 is involved in replenishment of granule cell precursors following injury to the neonatal cerebellum
inferred← citeshttps://doi.org/10.1016/j.ydbio.2019.10.002openalex-snapshot
Yap/Taz are required for establishing the cerebellar radial glia scaffold and proper foliation
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.2014.04.004openalex-snapshot
ANKHD1, a novel component of the Hippo signaling pathway, promotes YAP1 activation and cell cycle progression in prostate cancer cells
inferred← citeshttps://doi.org/10.1016/j.yexcr.2017.06.009openalex-snapshot
SRSF3-regulated miR-132/212 controls cell migration and invasion by targeting YAP1
inferred← citeshttps://doi.org/10.1021/acs.biochem.5b01014openalex-snapshot
YAP and TAZ Take Center Stage in Cancer
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.8b01402openalex-snapshot
Antiproliferative and Antimigratory Effects of a Novel YAP–TEAD Interaction Inhibitor Identified Using in Silico Molecular Docking
inferred← citeshttps://doi.org/10.1021/jm501615vopenalex-snapshot
The Hippo Pathway and YAP/TAZ–TEAD Protein–Protein Interaction as Targets for Regenerative Medicine and Cancer Treatment
inferred← citeshttps://doi.org/10.1021/ml500160mopenalex-snapshot
Structure-Based Design and Synthesis of Potent Cyclic Peptides Inhibiting the YAP–TEAD Protein–Protein Interaction
inferred← citeshttps://doi.org/10.1038/jid.2012.430openalex-snapshot
Yap Controls Stem/Progenitor Cell Proliferation in the Mouse Postnatal Epidermis
inferred← citeshttps://doi.org/10.1038/ncb2303openalex-snapshot
The Hippo pathway in organ size control, tissue regeneration and stem cell self-renewal
inferred← citeshttps://doi.org/10.1038/ncb2306openalex-snapshot
The tumour suppressor L(3)mbt inhibits neuroepithelial proliferation and acts on insulator elements
inferred← citeshttps://doi.org/10.1038/ncb3164openalex-snapshot
Inactivation of a Gαs–PKA tumour suppressor pathway in skin stem cells initiates basal-cell carcinogenesis
inferred← citeshttps://doi.org/10.1038/ncomms5005openalex-snapshot
Identification of genes involved in the biology of atypical teratoid/rhabdoid tumours using Drosophila melanogaster
inferred← citeshttps://doi.org/10.1038/ng.3542openalex-snapshot
Cis-regulatory architecture of a brain signaling center predates the origin of chordates
inferred← citeshttps://doi.org/10.1038/nrd4161openalex-snapshot
The two faces of Hippo: targeting the Hippo pathway for regenerative medicine and cancer treatment
inferred← citeshttps://doi.org/10.1038/nrgastro.2016.59openalex-snapshot
The Hippo pathway in intestinal regeneration and disease
inferred← citeshttps://doi.org/10.1038/nrm2902openalex-snapshot
When pathways collide: collaboration and connivance among signalling proteins in development
inferred← citeshttps://doi.org/10.1038/nrneurol.2012.78openalex-snapshot
The clinical implications of medulloblastoma subgroups
inferred← citeshttps://doi.org/10.1038/onc.2010.454openalex-snapshot
Mitogenic Sonic hedgehog signaling drives E2F1-dependent lipogenesis in progenitor cells and medulloblastoma
inferred← citeshttps://doi.org/10.1038/onc.2010.564openalex-snapshot
Divergent functions for eIF4E and S6 kinase by sonic hedgehog mitogenic signaling in the developing cerebellum
inferred← citeshttps://doi.org/10.1038/onc.2010.571openalex-snapshot
BMI-1 suppresses contact inhibition and stabilizes YAP in Ewing sarcoma
inferred← citeshttps://doi.org/10.1038/onc.2011.363openalex-snapshot
Integrating developmental signals: a Hippo in the (path)way
inferred← citeshttps://doi.org/10.1038/onc.2011.379openalex-snapshot
Oncogenic YAP promotes radioresistance and genomic instability in medulloblastoma through IGF2-mediated Akt activation
inferred← citeshttps://doi.org/10.1038/onc.2011.8openalex-snapshot
The Hippo pathway transcriptional co-activator, YAP, is an ovarian cancer oncogene
inferred← citeshttps://doi.org/10.1038/onc.2012.231openalex-snapshot
YAP modifies cancer cell sensitivity to EGFR and survivin inhibitors and is negatively regulated by the non-receptor type protein tyrosine phosphatase 14
inferred← citeshttps://doi.org/10.1038/onc.2013.433openalex-snapshot
Hedgehog signaling induces osteosarcoma development through Yap1 and H19 overexpression
inferred← citeshttps://doi.org/10.1038/onc.2014.281openalex-snapshot
Kaposi sarcoma-associated herpesvirus promotes tumorigenesis by modulating the Hippo pathway
inferred← citeshttps://doi.org/10.1038/onc.2015.491openalex-snapshot
YB-1 is elevated in medulloblastoma and drives proliferation in Sonic hedgehog-dependent cerebellar granule neuron progenitor cells and medulloblastoma cells
inferred← citeshttps://doi.org/10.1038/onc.2016.108openalex-snapshot
SMARCA4/Brg1 coordinates genetic and epigenetic networks underlying Shh-type medulloblastoma development
inferred← citeshttps://doi.org/10.1038/onc.2017.257openalex-snapshot
TEAD1/4 exerts oncogenic role and is negatively regulated by miR-4269 in gastric tumorigenesis
inferred← citeshttps://doi.org/10.1038/oncsis.2014.27openalex-snapshot
The Yes-associated protein controls the cell density regulation of Hedgehog signaling
inferred← citeshttps://doi.org/10.1038/oncsis.2017.83openalex-snapshot
TNFα-YAP/p65-HK2 axis mediates breast cancer cell migration
inferred← citeshttps://doi.org/10.1038/s41388-020-01454-1openalex-snapshot
Combined inhibition of JAK2-STAT3 and SMO-GLI1/tGLI1 pathways suppresses breast cancer stem cells, tumor growth, and metastasis
inferred← citeshttps://doi.org/10.1038/s41388-025-03418-9openalex-snapshot
Synthetic lethality through Gsk3β inhibition in glioma stem cells via the WNT-WWC1-YAP axis
inferred← citeshttps://doi.org/10.1038/s41416-022-02106-9openalex-snapshot
Hyperglycaemia induces metabolic reprogramming into a glycolytic phenotype and promotes epithelial-mesenchymal transitions via YAP/TAZ-Hedgehog signalling axis in pancreatic cancer
inferred← citeshttps://doi.org/10.1038/s41417-019-0100-3openalex-snapshot
CTGF expression is indicative of better survival rates in patients with medulloblastoma
inferred← citeshttps://doi.org/10.1038/s41419-018-1141-5openalex-snapshot
Plau and Tgfbr3 are YAP-regulated genes that promote keratinocyte proliferation
inferred← citeshttps://doi.org/10.1038/s41421-022-00430-1openalex-snapshot
Spatiotemporal regulation of insulin signaling by liquid–liquid phase separation
inferred← citeshttps://doi.org/10.1038/s41467-019-09597-wopenalex-snapshot
Identification of the kinase STK25 as an upstream activator of LATS signaling
inferred← citeshttps://doi.org/10.1038/s41467-019-11884-5openalex-snapshot
YAP1 subgroup supratentorial ependymoma requires TEAD and nuclear factor I-mediated transcriptional programmes for tumorigenesis
inferred← citeshttps://doi.org/10.1038/s41536-021-00120-8openalex-snapshot
The calcium binding protein S100β marks hedgehog-responsive resident vascular stem cells within vascular lesions
inferred← citeshttps://doi.org/10.1038/s41580-023-00644-5openalex-snapshot
Control of stem cell renewal and fate by YAP and TAZ
inferred← citeshttps://doi.org/10.1038/s41598-017-04052-6openalex-snapshot
The Hippo pathway acts downstream of the Hedgehog signaling to regulate follicle stem cell maintenance in the Drosophila ovary
inferred← citeshttps://doi.org/10.1038/s41598-018-29319-4openalex-snapshot
Hippo Signaling Pathway Dysregulation in Human Huntington’s Disease Brain and Neuronal Stem Cells
inferred← citeshttps://doi.org/10.1038/s41598-019-40495-9openalex-snapshot
Differential gene expression induced by Verteporfin in endometrial cancer cells
inferred← citeshttps://doi.org/10.1038/s41598-019-50088-1openalex-snapshot
Upregulation of the chromatin remodeler HELLS is mediated by YAP1 in Sonic Hedgehog Medulloblastoma
inferred← citeshttps://doi.org/10.1038/s41598-022-24140-6openalex-snapshot
Bioinformatics analysis of miRNAs in the neuroblastoma 11q-deleted region reveals a role of miR-548l in both 11q-deleted and MYCN amplified tumour cells
inferred← citeshttps://doi.org/10.1038/srep23208openalex-snapshot
The Hippo pathway member YAP enhances human neural crest cell fate and migration
inferred← citeshttps://doi.org/10.1042/bse0530111openalex-snapshot
The Hippo pathway: key interaction and catalytic domains in organ growth control, stem cell self-renewal and tissue regeneration
inferred← citeshttps://doi.org/10.1053/j.gastro.2013.02.009openalex-snapshot
Yes-Associated Protein Up-regulates Jagged-1 and Activates the NOTCH Pathway in Human Hepatocellular Carcinoma
inferred← citeshttps://doi.org/10.1053/j.gastro.2016.10.047openalex-snapshot
Hippo Signaling in the Liver Regulates Organ Size, Cell Fate, and Carcinogenesis
inferred← citeshttps://doi.org/10.1071/ch22241openalex-snapshot
Hippo signaling in cancer: regulatory mechanisms and therapeutic strategies
inferred← citeshttps://doi.org/10.1073/pnas.1415330111openalex-snapshot
Substratum-induced differentiation of human pluripotent stem cells reveals the coactivator YAP is a potent regulator of neuronal specification
inferred← citeshttps://doi.org/10.1074/jbc.m110.194019openalex-snapshot
PP1 Cooperates with ASPP2 to Dephosphorylate and Activate TAZ
inferred← citeshttps://doi.org/10.1074/jbc.m111.310334openalex-snapshot
Dimerization and Cytoplasmic Localization Regulate Hippo Kinase Signaling Activity in Organ Size Control
inferred← citeshttps://doi.org/10.1074/jbc.m111.329268openalex-snapshot
Yap1 Protein Regulates Vascular Smooth Muscle Cell Phenotypic Switch by Interaction with Myocardin
inferred← citeshttps://doi.org/10.1074/jbc.m114.624411openalex-snapshot
Oncoprotein YAP Regulates the Spindle Checkpoint Activation in a Mitotic Phosphorylation-dependent Manner through Up-regulation of BubR1
inferred← citeshttps://doi.org/10.1080/15384101.2016.1164371openalex-snapshot
The G protein Gα s acts as a tumor suppressor in sonic hedgehog signaling-driven tumorigenesis
inferred← citeshttps://doi.org/10.1080/15513815.2019.1627629openalex-snapshot
Infantile Epithelioid Sarcoma with Genomic Segmental Amplification of BIRC3/YAP1 as Double Minutes Plus Trisomy 2: A Case Report
inferred← citeshttps://doi.org/10.1080/23723556.2017.1295127openalex-snapshot
YAP and the Hippo pathway in pediatric cancer
inferred← citeshttps://doi.org/10.1083/jcb.201309141openalex-snapshot
Coupling of Hedgehog and Hippo pathways promotes stem cell maintenance by stimulating proliferation
inferred← citeshttps://doi.org/10.1089/dna.2018.4340openalex-snapshot
Dual Role of a C-Terminally Truncated Isoform of Large Tumor Suppressor Kinase 1 in the Regulation of Hippo Signaling and Tissue Growth
inferred← citeshttps://doi.org/10.1093/abbs/gmu109openalex-snapshot
Hippo signaling in stress response and homeostasis maintenance
inferred← citeshttps://doi.org/10.1093/abbs/gmu110openalex-snapshot
The regulation and function of YAP transcription co-activator
inferred← citeshttps://doi.org/10.1093/annonc/mdv101openalex-snapshot
Searching for targets for the systemic therapy of mesothelioma
inferred← citeshttps://doi.org/10.1093/carcin/bgq254openalex-snapshot
YAP is a candidate oncogene for esophageal squamous cell carcinoma
inferred← citeshttps://doi.org/10.1093/jb/mvr021openalex-snapshot
Mammalian Hippo pathway: from development to cancer and beyond
inferred← citeshttps://doi.org/10.1093/jb/mvr080openalex-snapshot
The growing role of the Hippo-NDR kinase signalling in neuronal development and disease
inferred← citeshttps://doi.org/10.1093/neuonc/not147openalex-snapshot
The rationale for targeted therapies in medulloblastoma
inferred← citeshttps://doi.org/10.1093/noajnl/vdz023openalex-snapshot
The therapeutic and diagnostic potential of regulatory noncoding RNAs in medulloblastoma
inferred← citeshttps://doi.org/10.1096/fj.202002284rropenalex-snapshot
The hippo pathway: A master regulator of liver metabolism, regeneration, and disease
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