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Function and biological roles of the Dickkopf family of Wnt modulators
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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/dvdy.10491openalex-snapshot
Expression analysis of chick Wnt and frizzled genes and selected inhibitors in early chick patterning
inferredcites →https://doi.org/10.1002/dvdy.20285openalex-snapshot
Dynamic expression of Wnt signaling‐related Dickkopf1, ‐2, and ‐3 mRNAs in the developing mouse tooth
inferredcites →https://doi.org/10.1002/ijc.22033openalex-snapshot
Serum concentrations of Dickkopf‐1 protein are increased in patients with multiple myeloma and reduced after autologous stem cell transplantation
inferredcites →https://doi.org/10.1002/mrd.20314openalex-snapshot
DkkL1 (Soggy), a Dickkopf family member, localizes to the acrosome during mammalian spermatogenesis
inferredcites →https://doi.org/10.1006/bbrc.1999.2067openalex-snapshot
A REIC Gene Shows Down-Regulation in Human Immortalized Cells and Human Tumor-Derived Cell Lines
inferredcites →https://doi.org/10.1006/dbio.1999.9537openalex-snapshot
Zebrafish Dkk1 Functions in Forebrain Specification and Axial Mesendoderm Formation
inferredcites →https://doi.org/10.1006/jmbi.1998.2057openalex-snapshot
A structural homologue of colipase in black mamba venom revealed by NMR floating disulphide bridge analysis
inferredcites →https://doi.org/10.1007/s00427-003-0318-8openalex-snapshot
A genomewide survey of developmentally relevant genes in Ciona intestinalis
inferredcites →https://doi.org/10.1007/s00427-003-0322-zopenalex-snapshot
A genomewide survey of developmentally relevant genes in Ciona intestinalis
inferredcites →https://doi.org/10.1007/s00427-003-0378-9openalex-snapshot
A Dickkopf-3-related gene is expressed in differentiating nematocytes in the basal metazoan Hydra
inferredcites →https://doi.org/10.1007/s00427-004-0436-yopenalex-snapshot
Hypoblast controls mesoderm generation and axial patterning in the gastrulating rabbit embryo
inferredcites →https://doi.org/10.1007/s10735-005-9008-3openalex-snapshot
Dkk1, -2, and -3 expression in mouse craniofacial development
inferredcites →https://doi.org/10.1007/s10735-005-9014-5openalex-snapshot
Developmental expression of Dkk1-3 and Mmp9 and apoptosis in cranial base of mice
inferredcites →https://doi.org/10.1016/j.bbrc.2004.09.001openalex-snapshot
Dickkopf-1 antagonizes Wnt signaling independent of β-catenin in human mesothelioma
inferredcites →https://doi.org/10.1016/j.bbrc.2005.01.009openalex-snapshot
Wnt-independent activation of β-catenin mediated by a Dkk1-Fz5 fusion protein
inferredcites →https://doi.org/10.1016/j.bone.2006.03.017openalex-snapshot
Dkk1-mediated inhibition of Wnt signaling in bone results in osteopenia
inferredcites →https://doi.org/10.1016/j.ceca.2005.06.022openalex-snapshot
Wnt and calcium signaling: β-Catenin-independent pathways
inferredcites →https://doi.org/10.1016/j.conb.2006.01.001openalex-snapshot
Secreted inducers in vertebrate eye development: more functions for old morphogens
inferredcites →https://doi.org/10.1016/j.devbrainres.2004.09.008openalex-snapshot
Characterisation of the Wnt antagonists and their response to conditionally activated Wnt signalling in the developing mouse forebrain
inferredcites →https://doi.org/10.1016/j.devcel.2005.09.011openalex-snapshot
Canonical Wnt Signaling and Its Antagonist Regulate Anterior-Posterior Axis Polarization by Guiding Cell Migration in Mouse Visceral Endoderm
inferredcites →https://doi.org/10.1016/j.ydbio.2004.04.026openalex-snapshot
En1 and Wnt7a interact with Dkk1 during limb development in the mouse
inferredcites →https://doi.org/10.1016/j.ydbio.2005.01.020openalex-snapshot
Growth factor regulation of lens development
inferredcites →https://doi.org/10.1016/s0041-0101(99)00174-9openalex-snapshot
Isolation of a funnel-web spider polypeptide with homology to mamba intestinal toxin 1 and the embryonic head inducer Dickkopf-1
inferredcites →https://doi.org/10.1016/s0092-8674(01)00571-2openalex-snapshot
LDL Receptor-Related Protein 5 (LRP5) Affects Bone Accrual and Eye Development
inferredcites →https://doi.org/10.1016/s0167-4781(01)00168-3openalex-snapshot
Molecular cloning and characterization of Kremen, a novel kringle-containing transmembrane protein
inferredcites →https://doi.org/10.1016/s0378-1119(01)00838-1openalex-snapshot
Reduced expression of the REIC/Dkk-3 gene by promoter-hypermethylation in human tumor cells
inferredcites →https://doi.org/10.1016/s0378-1119(02)01106-xopenalex-snapshot
Kremen2 modulates Dickkopf2 activity during Wnt/lRP6 signaling
inferredcites →https://doi.org/10.1016/s0378-1119(99)00365-0openalex-snapshot
Functional and structural diversity of the human Dickkopf gene family
inferredcites →https://doi.org/10.1016/s0925-4773(00)00433-0openalex-snapshot
Zebrafish Dkk1, induced by the pre-MBT Wnt signaling, is secreted from the prechordal plate and patterns the anterior neural plate
inferredcites →https://doi.org/10.1016/s0925-4773(99)00138-0openalex-snapshot
Dickkopf genes are co-ordinately expressed in mesodermal lineages
inferredcites →https://doi.org/10.1016/s0925-4773(99)00194-xopenalex-snapshot
Expression pattern of Dkk-1 during mouse limb development
inferredcites →https://doi.org/10.1016/s0960-9822(00)00676-xopenalex-snapshot
Evidence for 14 homeobox gene clusters in human genome ancestry
inferredcites →https://doi.org/10.1016/s0960-9822(00)00868-xopenalex-snapshot
Mutual antagonism between dickkopf1 and dickkopf2 regulates Wnt/β-catenin signalling
inferredcites →https://doi.org/10.1016/s0960-9822(01)00290-1openalex-snapshot
Head inducer Dickkopf-1 is a ligand for Wnt coreceptor LRP6
inferredcites →https://doi.org/10.1016/s0960-9822(98)70309-4openalex-snapshot
A colipase fold in the carboxy-terminal domain of the Wnt antagonists – the Dickkopfs
inferredcites →https://doi.org/10.1016/s1044-7431(03)00229-xopenalex-snapshot
Glycogen synthase kinase-3 and Axin function in a β-catenin-independent pathway that regulates neurite outgrowth in neuroblastoma cells
inferredcites →https://doi.org/10.1016/s1084-9521(02)00052-6openalex-snapshot
Non-canonical Wnt signalling and regulation of gastrulation movements
inferredcites →https://doi.org/10.1016/s1097-2765(01)00224-6openalex-snapshot
Low-Density Lipoprotein Receptor-Related Protein-5 Binds to Axin and Regulates the Canonical Wnt Signaling Pathway
inferredcites →https://doi.org/10.1016/s1388-1981(99)00149-3openalex-snapshot
Colipase: structure and interaction with pancreatic lipase
inferredcites →https://doi.org/10.1016/s1534-5807(01)00041-7openalex-snapshot
Dickkopf1 Is Required for Embryonic Head Induction and Limb Morphogenesis in the Mouse
inferredcites →https://doi.org/10.1016/s1534-5807(02)00167-3openalex-snapshot
WNT Signals Are Required for the Initiation of Hair Follicle Development
inferredcites →https://doi.org/10.1016/s1534-5807(03)00055-8openalex-snapshot
Wnt3a Plays a Major Role in the Segmentation Clock Controlling Somitogenesis
inferredcites →https://doi.org/10.1038/34848openalex-snapshot
Dickkopf-1 is a member of a new family of secreted proteins and functions in head induction
inferredcites →https://doi.org/10.1038/35035124openalex-snapshot
An LDL-receptor-related protein mediates Wnt signalling in mice
inferredcites →https://doi.org/10.1038/35077108openalex-snapshot
LDL-receptor-related protein 6 is a receptor for Dickkopf proteins
inferredcites →https://doi.org/10.1038/35083081openalex-snapshot
Novel mechanism of Wnt signalling inhibition mediated by Dickkopf-1 interaction with LRP6/Arrow
inferredcites →https://doi.org/10.1038/39092openalex-snapshot
Head induction by simultaneous repression of Bmp and Wnt signalling in Xenopus
inferredcites →https://doi.org/10.1038/nature00921openalex-snapshot
Wnt-11 activation of a non-canonical Wnt signalling pathway is required for cardiogenesis
inferredcites →https://doi.org/10.1038/nature01522openalex-snapshot
Wnt-mediated axon guidance via the Drosophila Derailed receptor
inferredcites →https://doi.org/10.1038/nature04170openalex-snapshot
Casein kinase 1 γ couples Wnt receptor activation to cytoplasmic signal transduction
inferredcites →https://doi.org/10.1038/nature04185openalex-snapshot
A dual-kinase mechanism for Wnt co-receptor phosphorylation and activation
inferredcites →https://doi.org/10.1038/nature756openalex-snapshot
Kremen proteins are Dickkopf receptors that regulate Wnt/β-catenin signalling
inferredcites →https://doi.org/10.1038/ng1099openalex-snapshot
Notch1 functions as a tumor suppressor in mouse skin
inferredcites →https://doi.org/10.1038/ng1614openalex-snapshot
Dkk2 has a role in terminal osteoblast differentiation and mineralized matrix formation
inferredcites →https://doi.org/10.1038/nrg1347openalex-snapshot
Regionally specific induction by the Spemann–Mangold organizer
inferredcites →https://doi.org/10.1038/nrg1427openalex-snapshot
WNT and β-catenin signalling: diseases and therapies
inferredcites →https://doi.org/10.1038/sj.bjc.6602008openalex-snapshot
Transcriptional silencing of the Dickkopfs-3 (Dkk-3) gene by CpG hypermethylation in acute lymphoblastic leukaemia
inferredcites →https://doi.org/10.1038/sj.emboj.7600460openalex-snapshot
FGF‐20 and DKK1 are transcriptional targets of β‐catenin and FGF‐20 is implicated in cancer and development
inferredcites →https://doi.org/10.1038/sj.onc.1203503openalex-snapshot
Dickkopf-1, an inhibitor of the Wnt signaling pathway, is induced by p53
inferredcites →https://doi.org/10.1038/sj.onc.1205138openalex-snapshot
Human Dkk-1, a gene encoding a Wnt antagonist, responds to DNA damage and its overexpression sensitizes brain tumor cells to apoptosis following alkylation damage of DNA
inferredcites →https://doi.org/10.1038/sj.onc.1208138openalex-snapshot
Dickkopf-3/REIC functions as a suppressor gene of tumor growth
inferredcites →https://doi.org/10.1038/sj.onc.1208303openalex-snapshot
The Wnt antagonist DICKKOPF-1 gene is a downstream target of β-catenin/TCF and is downregulated in human colon cancer
inferredcites →https://doi.org/10.1038/sj.onc.1208479openalex-snapshot
An integrated data analysis approach to characterize genes highly expressed in hepatocellular carcinoma
inferredcites →https://doi.org/10.1038/sj.onc.1209279openalex-snapshot
Systematic search for gastric cancer-specific genes based on SAGE data: melanoma inhibitory activity and matrix metalloproteinase-10 are novel prognostic factors in patients with gastric cancer
inferredcites →https://doi.org/10.1038/sj.onc.1209439openalex-snapshot
Epigenetic inactivation of the Wnt antagonist DICKKOPF-1 (DKK-1) gene in human colorectal cancer
inferredcites →https://doi.org/10.1038/sj.onc.1209661openalex-snapshot
Regulation of prostate cell growth and morphogenesis by Dickkopf-3
inferredcites →https://doi.org/10.1046/j.1365-2443.2003.00662.xopenalex-snapshot
The receptor tyrosine kinase Ror2 is involved in non‐canonical Wnt5a/JNK signalling pathway
inferredcites →https://doi.org/10.1056/nejmoa013444openalex-snapshot
High Bone Density Due to a Mutation in LDL-Receptor–Related Protein 5
inferredcites →https://doi.org/10.1056/nejmoa030847openalex-snapshot
The Role of the Wnt-Signaling Antagonist DKK1 in the Development of Osteolytic Lesions in Multiple Myeloma
inferredcites →https://doi.org/10.1073/pnas.011513398openalex-snapshot
Gene expression profiles in normal and Otx2 −/− early gastrulating mouse embryos
inferredcites →https://doi.org/10.1073/pnas.0501963102openalex-snapshot
Crooked tail ( Cd ) model of human folate-responsive neural tube defects is mutated in Wnt coreceptor lipoprotein receptor-related protein 6
inferredcites →https://doi.org/10.1073/pnas.0836141100openalex-snapshot
Dispersal of NK homeobox gene clusters in amphioxus and humans
inferredcites →https://doi.org/10.1074/jbc.274.27.19465openalex-snapshot
Isolation and Biochemical Characterization of the Human Dkk-1 Homologue, a Novel Inhibitor of Mammalian Wnt Signaling
inferredcites →https://doi.org/10.1074/jbc.m002036200openalex-snapshot
Cloning, Expression, and Functional Characterization of the Substrate Binding Subunit of Rat Type II Iodothyronine 5′-Deiodinase
inferredcites →https://doi.org/10.1074/jbc.m111131200openalex-snapshot
Second Cysteine-rich Domain of Dickkopf-2 Activates Canonical Wnt Signaling Pathway via LRP-6 Independently of Dishevelled
inferredcites →https://doi.org/10.1074/jbc.m300191200openalex-snapshot
Functional Characterization of WNT7A Signaling in PC12 Cells
inferredcites →https://doi.org/10.1074/jbc.m406275200openalex-snapshot
Dkk-1-derived Synthetic Peptides and Lithium Chloride for the Control and Recovery of Adult Stem Cells from Bone Marrow
inferredcites →https://doi.org/10.1083/jcb.200201089openalex-snapshot
Cbfa1-independent decrease in osteoblast proliferation, osteopenia, and persistent embryonic eye vascularization in mice deficient in Lrp5, a Wnt coreceptor
inferredcites →https://doi.org/10.1083/jcb.200311122openalex-snapshot
Mesenchymal–epithelial interactions in the skin
inferredcites →https://doi.org/10.1093/carcin/bgg190openalex-snapshot
A functional genomics approach for the identification of putative tumor suppressor genes: Dickkopf-1 as suppressor of HeLa cell transformation
inferredcites →https://doi.org/10.1093/emboj/21.5.966openalex-snapshot
The Wnt antagonist Dickkopf‐1 is regulated by Bmp signaling and c‐Jun and modulates programmed cell death
inferredcites →https://doi.org/10.1093/nar/28.20.3982openalex-snapshot
Soggy, a spermatocyte-specific gene, lies 3.8 kb upstream of and antipodal to TEAD-2, a transcription factor expressed at the beginning of mouse development
inferredcites →https://doi.org/10.1097/01.ju.0000101047.64379.d4openalex-snapshot
Decreased Expression of REIC/Dkk-3 in Human Renal Clear Cell Carcinoma
inferredcites →https://doi.org/10.1097/01.lab.0000059926.66359.bdopenalex-snapshot
Overexpression of Human Dickkopf-1, an Antagonist of wingless/WNT Signaling, in Human Hepatoblastomas and Wilms' Tumors
inferredcites →https://doi.org/10.1101/gad.10.3.313openalex-snapshot
Analysis of the vestigial tail mutation demonstrates that Wnt-3a gene dosage regulates mouse axial development.
inferredcites →https://doi.org/10.1101/gad.1044903openalex-snapshot
EctodermalWnt3/β-cateninsignaling is required for the establishment and maintenance of the apical ectodermal ridge
inferredcites →https://doi.org/10.1101/gad.11.24.3286openalex-snapshot
Wnt signaling: a common theme in animal development
inferredcites →https://doi.org/10.1101/gad.1217404openalex-snapshot
Segmentation in vertebrates: clock and gradient finally joined
inferredcites →https://doi.org/10.1101/gad.263003openalex-snapshot
Genetic interaction between Wnt/β-catenin and BMP receptor signaling during formation of the AER and the dorsal–ventral axis in the limb
inferredcites →https://doi.org/10.1101/gad.269103openalex-snapshot
Dkk1 and noggin cooperate in mammalian head induction
inferredcites →https://doi.org/10.1101/gad.855501openalex-snapshot
Inhibition of Wnt activity induces heart formation from posterior mesoderm
inferredcites →https://doi.org/10.1101/gad.855601openalex-snapshot
Wnt antagonism initiates cardiogenesis in Xenopus laevis
inferredcites →https://doi.org/10.1124/mol.65.3.582openalex-snapshot
Structural Determinants Required for the Bioactivities of Prokineticins and Identification of Prokineticin Receptor Antagonists
inferredcites →https://doi.org/10.1128/mcb.22.17.6100-6110.2002openalex-snapshot
Regulation of Wnt/LRP Signaling by Distinct Domains of Dickkopf Proteins
inferredcites →https://doi.org/10.1128/mcb.25.12.4946-4955.2005openalex-snapshot
Reduced Affinity to and Inhibition by DKK1 Form a Common Mechanism by Which High Bone Mass-Associated Missense Mutations in LRP5 Affect Canonical Wnt Signaling
inferredcites →https://doi.org/10.1128/mcb.25.9.3475-3482.2005openalex-snapshot
The Mechanism of Endogenous Receptor Activation Functionally Distinguishes Prototype Canonical and Noncanonical Wnts
inferredcites →https://doi.org/10.1128/mcb.26.6.2317-2326.2006openalex-snapshot
Generation and Characterization of dickkopf3 Mutant Mice
inferredcites →https://doi.org/10.1146/annurev.cellbio.20.011403.154124openalex-snapshot
DORSAL-VENTRAL PATTERNING AND NEURAL INDUCTION IN XENOPUS EMBRYOS
inferredcites →https://doi.org/10.1158/0008-5472.can-03-1952openalex-snapshot
Dickkopf 3 Inhibits Invasion and Motility of Saos-2 Osteosarcoma Cells by Modulating the Wnt-β-Catenin Pathway
inferredcites →https://doi.org/10.1158/0008-5472.can-04-4407openalex-snapshot
Functional Epigenomics Identifies Genes Frequently Silenced in Prostate Cancer
inferredcites →https://doi.org/10.1158/0008-5472.can-05-0829openalex-snapshot
Adenovirus-Mediated Overexpression of REIC/Dkk-3 Selectively Induces Apoptosis in Human Prostate Cancer Cells through Activation of c-Jun-NH2-Kinase
inferredcites →https://doi.org/10.1159/000082277openalex-snapshot
Wnt/Frizzled Signaling during Vertebrate Retinal Development
inferredcites →https://doi.org/10.1172/jci28551openalex-snapshot
Regulation of bone mass by Wnt signaling
inferredcites →https://doi.org/10.1210/en.2002-220823openalex-snapshot
Divergent Expression of Type 2 Deiodinase and the Putative Thyroxine-Binding Protein p29, in Rat Brain, Suggests that They Are Functionally Unrelated Proteins
inferredcites →https://doi.org/10.1242/dev.00154openalex-snapshot
Kremen proteins interact with Dickkopf1 to regulate anteroposterior CNS patterning
inferredcites →https://doi.org/10.1242/dev.00674openalex-snapshot
Wise, a context-dependent activator and inhibitor of Wnt signalling
inferredcites →https://doi.org/10.1242/dev.01117openalex-snapshot
LDL receptor-related proteins 5 and 6 in Wnt/β-catenin signaling:Arrows point the way
inferredcites →https://doi.org/10.1242/dev.01126openalex-snapshot
Hypomorphic expression ofDkk1in thedoubleridgemouse: dose dependence and compensatory interactions withLrp6
inferredcites →https://doi.org/10.1242/dev.01137openalex-snapshot
The Wnt co-receptors Lrp5 and Lrp6 are essential for gastrulation in mice
inferredcites →https://doi.org/10.1242/dev.01405openalex-snapshot
Skeletal defects inringelschwanzmutant mice reveal that Lrp6 is required for proper somitogenesis and osteogenesis
inferredcites →https://doi.org/10.1242/dev.02265openalex-snapshot
An ancient Wnt-Dickkopf antagonism inHydra
inferredcites →https://doi.org/10.1242/dev.02381openalex-snapshot
Dkk2 plays an essential role in the corneal fate of the ocular surface epithelium
inferredcites →https://doi.org/10.1242/dev.127.22.4981openalex-snapshot
The role of Xenopus dickkopf1 in prechordal plate specification and neural patterning
inferredcites →https://doi.org/10.1242/jcs.00623openalex-snapshot
Secreted antagonists of the Wnt signalling pathway
inferredcites →https://doi.org/10.1242/jcs.02826openalex-snapshot
Wnt signaling: complexity at the surface
inferredcites →https://doi.org/10.1359/jbmr.040907openalex-snapshot
Decreased BMD and Limb Deformities in Mice Carrying Mutations in Both Lrp5 and Lrp6
inferredcites →https://doi.org/10.1359/jbmr.050614openalex-snapshot
Downregulation of Wnt Signaling by Increased Expression of Dickkopf-1 and -2 is a Prerequisite for Late-Stage Osteoblast Differentiation of KS483 Cells
inferredcites →https://doi.org/10.1359/jbmr.060311openalex-snapshot
Deletion of a Single Allele of the Dkk1 Gene Leads to an Increase in Bone Formation and Bone Mass
inferredcites →https://doi.org/10.1359/jbmr.2003.18.6.960openalex-snapshot
High Bone Mass in Mice Expressing a Mutant LRP5 Gene
inferredcites →https://doi.org/10.1371/journal.pbio.0040115openalex-snapshot
Purified Wnt5a Protein Activates or Inhibits β-Catenin–TCF Signaling Depending on Receptor Context
inferredcites →https://doi.org/10.1387/ijdb.12455630openalex-snapshot
Wnt signalling during limb development
inferredcites →https://doi.org/10.1523/jneurosci.1381-04.2004openalex-snapshot
Induction of Dickkopf-1, a Negative Modulator of the Wnt Pathway, Is Associated with Neuronal Degeneration in Alzheimer's Brain
inferredcites →https://doi.org/10.1523/jneurosci.5230-04.2005openalex-snapshot
Induction of Dickkopf-1, a Negative Modulator of the Wnt Pathway, Is Required for the Development of Ischemic Neuronal Death
inferredcites →https://doi.org/10.3892/ijo.19.1.117openalex-snapshot
Reduced expression of REIC/Dkk-3 gene in non-small cell lung cancer
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/9781118444122.ch13openalex-snapshot
Secreted Wnt Inhibitors or Modulators
inferred← citeshttps://doi.org/10.1002/9781118444122.ch2openalex-snapshot
Wnt Signaling at the Membrane
inferred← citeshttps://doi.org/10.1002/9781118444122.ch8openalex-snapshot
Modulation of Wnt Signaling by Endocytosis of Receptor Complexes
inferred← citeshttps://doi.org/10.1002/9781118492833.ch13openalex-snapshot
Development of Neural Tissues inXenopus laevis
inferred← citeshttps://doi.org/10.1002/9781119266594.ch9openalex-snapshot
Recent Developments in Understanding the Role of Wnt Signaling in Skeletal Development and Disease
inferred← citeshttps://doi.org/10.1002/ajmg.a.60694openalex-snapshot
Cenani–Lenz syndrome and other related syndactyly disorders due to variants in LRP4, GREM1/FMN1, and APC: Insight into the pathogenesis and the relationship to polyposis through the WNT and BMP antagonistic pathways
inferred← citeshttps://doi.org/10.1002/ange.202015009openalex-snapshot
Sulfur‐Coordinated Organoiridium(III) Complexes Exert Breast Anticancer Activity via Inhibition of Wnt/β‐Catenin Signaling
inferred← citeshttps://doi.org/10.1002/anie.202015009openalex-snapshot
Sulfur‐Coordinated Organoiridium(III) Complexes Exert Breast Anticancer Activity via Inhibition of Wnt/β‐Catenin Signaling
inferred← citeshttps://doi.org/10.1002/ar.24069openalex-snapshot
Differential Changes in the Number and Morphology of the New Neurons after Chronic Infusion of Wnt7a, Wnt5a, and Dkk‐1 in the Adult Hippocampus In Vivo
inferred← citeshttps://doi.org/10.1002/art.27357openalex-snapshot
Control of Dkk‐1 ameliorates chondrocyte apoptosis, cartilage destruction, and subchondral bone deterioration in osteoarthritic knees
inferred← citeshttps://doi.org/10.1002/art.30625openalex-snapshot
R-spondins are newly recognized players in osteoarthritis that regulate Wnt signaling in osteoblasts
inferred← citeshttps://doi.org/10.1002/art.34481openalex-snapshot
Dkk‐1 expression in chondrocytes inhibits experimental osteoarthritic cartilage destruction in mice
inferred← citeshttps://doi.org/10.1002/bdra.20495openalex-snapshot
Wnt signaling in caudal dysgenesis and diabetic embryopathy
inferred← citeshttps://doi.org/10.1002/brb3.1589openalex-snapshot
The role of serum Dickkopf‐1 in predicting 30‐day death in severe traumatic brain injury
inferred← citeshttps://doi.org/10.1002/cam4.6992openalex-snapshot
Dickkopf 1 is expressed in normal fibroblasts during early stages of colorectal tumorigenesis
inferred← citeshttps://doi.org/10.1002/cam4.702openalex-snapshot
Combined detection of serum Dickkopf‐1 and its autoantibodies to diagnose esophageal squamous cell carcinoma
inferred← citeshttps://doi.org/10.1002/cncr.24491openalex-snapshot
Wnt antagonist gene polymorphisms and renal cancer
inferred← citeshttps://doi.org/10.1002/cncr.25666openalex-snapshot
DICKKOPF‐4 activates the noncanonical c‐Jun‐NH2 kinase signaling pathway while inhibiting the Wnt‐canonical pathway in human renal cell carcinoma
inferred← citeshttps://doi.org/10.1002/cne.22169openalex-snapshot
Mapping of Wnt, frizzled, and Wnt inhibitor gene expression domains in the avian otic primordium
inferred← citeshttps://doi.org/10.1002/ctm2.1239openalex-snapshot
O‐GlcNAcylated LARP1 positively regulated by circCLNS1A facilitates hepatoblastoma progression through DKK4/β‐catenin signalling
inferred← citeshttps://doi.org/10.1002/dneu.22135openalex-snapshot
Integration of anterior neural plate patterning and morphogenesis by the Wnt signaling pathway
inferred← citeshttps://doi.org/10.1002/dneu.22211openalex-snapshot
sox21a directs lateral line patterning by modulating FGF signaling
inferred← citeshttps://doi.org/10.1002/dvdy.21198openalex-snapshot
Expression of Frizzled5, Frizzled7, and Frizzled10 during early mouse development and interactions with canonical Wnt signaling
inferred← citeshttps://doi.org/10.1002/dvdy.21491openalex-snapshot
Members of the WNT signaling pathways are widely expressed in mouse ovaries, oocytes, and cleavage stage embryos
inferred← citeshttps://doi.org/10.1002/dvdy.21784openalex-snapshot
To β or not to β: Canonical β‐catenin signaling pathway and ovarian development
inferred← citeshttps://doi.org/10.1002/dvdy.21934openalex-snapshot
Expression of WNT signalling pathway genes during chicken craniofacial development
inferred← citeshttps://doi.org/10.1002/dvdy.22033openalex-snapshot
Signaling “cross‐talk” is integrated by transcription factors in the development of the anterior segment in the eye
inferred← citeshttps://doi.org/10.1002/dvdy.22106openalex-snapshot
Patterns of Wnt pathway activity in the mouse incisor indicate absence of Wnt/β‐catenin signaling in the epithelial stem cells
inferred← citeshttps://doi.org/10.1002/dvdy.22325openalex-snapshot
Loss of adenomatous polyposis coli (apc) results in an expanded ciliary marginal zone in the zebrafish eye
inferred← citeshttps://doi.org/10.1002/dvdy.234openalex-snapshot
Epithelial morphogenesis in the perinatal mouse uterus
inferred← citeshttps://doi.org/10.1002/dvdy.23973openalex-snapshot
Activation of canonical Wnt/β‐catenin signaling stimulates proliferation in neuromasts in the zebrafish posterior lateral line
inferred← citeshttps://doi.org/10.1002/dvg.20369openalex-snapshot
Sfrp1, Sfrp2, and Sfrp5 regulate the Wnt/β‐catenin and the planar cell polarity pathways during early trunk formation in mouse
inferred← citeshttps://doi.org/10.1002/glia.21022openalex-snapshot
Microglia promote colonization of brain tissue by breast cancer cells in a Wnt‐dependent way
inferred← citeshttps://doi.org/10.1002/hep.24740openalex-snapshot
Dickkopf 4 positively regulated by the thyroid hormone receptor suppresses cell invasion in human hepatoma cells
inferred← citeshttps://doi.org/10.1002/iid3.232openalex-snapshot
Elevated blood levels of Dickkopf‐1 are associated with acute infections
inferred← citeshttps://doi.org/10.1002/ijc.23721openalex-snapshot
Acquired cisplatin resistance in the head–neck cancer cell line Cal27 is associated with decreased DKK1 expression and can partially be reversed by overexpression of DKK1
inferred← citeshttps://doi.org/10.1002/ijc.23913openalex-snapshot
Dkk3 , downregulated in cervical cancer, functions as a negative regulator of β‐catenin
inferred← citeshttps://doi.org/10.1002/ijc.24276openalex-snapshot
Nmi (N‐Myc interactor) inhibits Wnt/β‐catenin signaling and retards tumor growth
inferred← citeshttps://doi.org/10.1002/ijc.24865openalex-snapshot
Dickkopf‐1 is overexpressed in human pancreatic ductal adenocarcinoma cells and is involved in invasive growth
inferred← citeshttps://doi.org/10.1002/ijc.25507openalex-snapshot
Wnt antagonist DKK1 acts as a tumor suppressor gene that induces apoptosis and inhibits proliferation in human renal cell carcinoma
inferred← citeshttps://doi.org/10.1002/ijc.26449openalex-snapshot
Dickkopf1: A tumor suppressor or metastasis promoter?
inferred← citeshttps://doi.org/10.1002/ijc.27798openalex-snapshot
Gene expression and epigenetic discovery screen reveal methylation of SFRP2 in prostate cancer
inferred← citeshttps://doi.org/10.1002/ijc.28321openalex-snapshot
Genome‐wide methylation analyses identify a subset of mantle cell lymphoma with a high number of methylated CpGs and aggressive clinicopathological features
inferred← citeshttps://doi.org/10.1002/ijc.34250openalex-snapshot
Dickkopf‐1 expression is repressed by oncogenic human papillomaviruses ( HPVs) and regulates the Cisplatin sensitivity of HPV ‐positive cancer cells in a JNK ‐dependent manner
inferred← citeshttps://doi.org/10.1002/iub.1062openalex-snapshot
The Wnt pathway and the roles for its antagonists, DKKS, in angiogenesis
inferred← citeshttps://doi.org/10.1002/jbm.a.36704openalex-snapshot
Sustained‐release of sclerostin single‐chain antibody fragments using poly(lactic‐co‐glycolic acid) microspheres for osteoporotic fracture repair
inferred← citeshttps://doi.org/10.1002/jbmr.1583openalex-snapshot
Misexpression of Dickkopf-1 in endothelial cells, but not in chondrocytes or hypertrophic chondrocytes, causes defects in endochondral ossification
inferred← citeshttps://doi.org/10.1002/jbmr.358openalex-snapshot
Elevated Dickkopf-2 levels contribute to the abnormal phenotype of human osteoarthritic osteoblasts
inferred← citeshttps://doi.org/10.1002/jbt.70587openalex-snapshot
METTL14 Mediates Malignant Progression and Docetaxel Resistance of Lung Cancer by Regulating DKK4 Expression Through m6A Methylation Modification
inferred← citeshttps://doi.org/10.1002/jcb.24708openalex-snapshot
Wnt Pathway in Osteosarcoma, from Oncogenic to Therapeutic
inferred← citeshttps://doi.org/10.1002/jcb.28251openalex-snapshot
Perspective into the regulation of cell‐generated forces toward stem cell migration and differentiation
inferred← citeshttps://doi.org/10.1002/jcla.24360openalex-snapshot
MiR‐363‐3p promotes prostate cancer tumor progression by targeting Dickkopf 3
inferred← citeshttps://doi.org/10.1002/jcp.21625openalex-snapshot
Protease activated receptor‐1, PAR1, promotes placenta trophoblast invasion and β‐catenin stabilization
inferred← citeshttps://doi.org/10.1002/jcp.24436openalex-snapshot
Inhibition of Wnt/β‐ C atenin Signaling Promotes Engraftment of Mesenchymal Stem Cells to Repair Lung Injury
inferred← citeshttps://doi.org/10.1002/jcp.26313openalex-snapshot
Dickkopf homolog 3 ( DKK3 ): A candidate for detection and treatment of cancers?
inferred← citeshttps://doi.org/10.1002/jcp.27137openalex-snapshot
Therapeutic potency of Wnt signaling antagonists in the pathogenesis of prostate cancer, current status and perspectives
inferred← citeshttps://doi.org/10.1002/jcsm.13829openalex-snapshot
ZBED6 Knockout Prevents Ageing‐ and Dexamethasone‐Induced Muscle Atrophy via Dkk3 in Pig and Mice
inferred← citeshttps://doi.org/10.1002/jgh3.12177openalex-snapshot
Dickkopf‐4 gene expression is associated with differentiation and lymph node metastasis in colorectal cancer
inferred← citeshttps://doi.org/10.1002/jgm.3466openalex-snapshot
Genome wide analysis of dexamethasone stimulated mineralization in human dental pulp cells by RNA sequencing
inferred← citeshttps://doi.org/10.1002/jlb.3ri0721-385ropenalex-snapshot
Dickkopf proteins in pathological inflammatory diseases
inferred← citeshttps://doi.org/10.1002/jnr.24757openalex-snapshot
Corneal nonmyelinating Schwann cells illuminated by single‐cell transcriptomics and visualized by protein biomarkers
inferred← citeshttps://doi.org/10.1002/jor.22626openalex-snapshot
Research perspectives: The 2013 AAOS/ORS research symposium on Bone Quality and Fracture Prevention
inferred← citeshttps://doi.org/10.1002/mc.20729openalex-snapshot
Wnt antagonist DICKKOPF‐3 (Dkk‐3) induces apoptosis in human renal cell carcinoma
inferred← citeshttps://doi.org/10.1002/mrd.22257openalex-snapshot
Changes in WNT signaling‐related gene expression associated with development and cloning in bovine extra‐embryonic and endometrial tissues during the peri‐implantation period
inferred← citeshttps://doi.org/10.1002/path.70117openalex-snapshot
A transition zone enriched WIF1 + basal cell subtype is associated with benign prostatic hyperplasia
inferred← citeshttps://doi.org/10.1002/pmic.200900218openalex-snapshot
Comparative analysis of the secretory proteome of human adipose stromal vascular fraction cells during adipogenesis
inferred← citeshttps://doi.org/10.1002/pros.20711openalex-snapshot
Dysregulation of Dkk‐3 expression in benign and malignant prostatic tissue
inferred← citeshttps://doi.org/10.1002/pros.22691openalex-snapshot
Dickkopf‐related protein 3 promotes pathogenic stromal remodeling in benign prostatic hyperplasia and prostate cancer
inferred← citeshttps://doi.org/10.1002/stem.1525openalex-snapshot
Partial Proteasome Inhibitors Induce Hair Follicle Growth by Stabilizing β-Catenin
inferred← citeshttps://doi.org/10.1002/stem.2313openalex-snapshot
Systems Genetics Analysis of a Recombinant Inbred Mouse Cell Culture Panel Reveals Wnt Pathway Member Lrp6 as a Regulator of Adult Hippocampal Precursor Cell Proliferation
inferred← citeshttps://doi.org/10.1007/978-0-387-69179-4_24openalex-snapshot
Unique Effects of Wnt Signaling on Prostate Cancer Cells: Modulation of the Androgen Signaling Pathway by Interactions of the Androgen Receptor Gene and Protein with Key Components of the Canonical Wnt Signaling Pathway
inferred← citeshttps://doi.org/10.1007/978-1-4419-7656-7_3openalex-snapshot
Gene Discovery by MMTV Mediated Insertional Mutagenesis
inferred← citeshttps://doi.org/10.1007/978-2-8178-0466-8_4openalex-snapshot
Wnt/Frizzled Signaling in the Vasculature
inferred← citeshttps://doi.org/10.1007/978-3-030-12040-5_13openalex-snapshot
Adding Insult to Injury: Improving the Regenerative Capacity of the Aged Thymus Following Clinically Induced Damage
inferred← citeshttps://doi.org/10.1007/978-3-030-16624-3_1openalex-snapshot
Cancer Stem Cells: From Birth to Death
inferred← citeshttps://doi.org/10.1007/978-3-030-21573-6_258-1openalex-snapshot
Low-Density Lipoprotein Receptor Gene Family
inferred← citeshttps://doi.org/10.1007/978-3-030-57401-7_258openalex-snapshot
Low-Density Lipoprotein Receptor Gene Family
inferred← citeshttps://doi.org/10.1007/978-3-031-07634-3_13openalex-snapshot
The Cross-Talk between Epigenetic Gene Regulation and Signaling Pathways Regulates Cancer Pathogenesis
inferred← citeshttps://doi.org/10.1007/978-3-319-13611-0_1openalex-snapshot
Inflammation-Associated Carcinogenesis Involves Interaction Between the iNOS/NO and Wnt/β-catenin Signaling Pathways
inferred← citeshttps://doi.org/10.1007/978-3-319-19530-8_13openalex-snapshot
Mechanisms of Bone Remodelling in Psoriatic Arthritis
inferred← citeshttps://doi.org/10.1007/978-3-319-45514-3_11openalex-snapshot
Blood Vessels in the Brain: A Signaling Hub in Brain Tumor Inflammation
inferred← citeshttps://doi.org/10.1007/s00005-008-0029-yopenalex-snapshot
Role of the Wnt/β-catenin network in regulating hematopoiesis
inferred← citeshttps://doi.org/10.1007/s00109-007-0266-2openalex-snapshot
The complex pathways of Wnt 5a in cancer progression
inferred← citeshttps://doi.org/10.1007/s00109-020-01978-9openalex-snapshot
Wnt signaling in kidney: the initiator or terminator?
inferred← citeshttps://doi.org/10.1007/s00193-013-0480-5openalex-snapshot
Molecular changes after shockwave therapy in osteoarthritic knee in rats
inferred← citeshttps://doi.org/10.1007/s00223-017-0338-4openalex-snapshot
Homozygous Dkk1 Knockout Mice Exhibit High Bone Mass Phenotype Due to Increased Bone Formation
inferred← citeshttps://doi.org/10.1007/s00223-022-01020-9openalex-snapshot
New Emerging Biomarkers for Bone Disease: Sclerostin and Dickkopf-1 (DKK1)
inferred← citeshttps://doi.org/10.1007/s00395-015-0481-xopenalex-snapshot
Dickkopf-3 protects against cardiac dysfunction and ventricular remodelling following myocardial infarction
inferred← citeshttps://doi.org/10.1007/s00404-019-05126-8openalex-snapshot
Wnt signaling pathway in early- and late-onset preeclampsia: evaluation with Dickkopf-1 and R-Spondin-3 glycoproteins
inferred← citeshttps://doi.org/10.1007/s00418-007-0278-6openalex-snapshot
Dickkopf-3 is expressed in a subset of adult human pancreatic beta cells
inferred← citeshttps://doi.org/10.1007/s00427-015-0487-2openalex-snapshot
Identification of a Ly-6 superfamily gene expressed in lateral line neuromasts in zebrafish
inferred← citeshttps://doi.org/10.1007/s00428-009-0769-zopenalex-snapshot
Altered expression of CD44 and DKK1 in the progression of Barrett’s esophagus to esophageal adenocarcinoma
inferred← citeshttps://doi.org/10.1007/s00428-009-0772-4openalex-snapshot
Overexpression of Dickkopf 3 in hepatoblastomas and hepatocellular carcinomas
inferred← citeshttps://doi.org/10.1007/s00428-010-0926-4openalex-snapshot
Immunohistochemically detectable dickkopf-3 expression in tumor vessels predicts survival in gastric cancer
inferred← citeshttps://doi.org/10.1007/s00432-010-0916-6openalex-snapshot
Expression of the Wnt antagonist DKK3 is frequently suppressed in sporadic epithelial ovarian cancer
inferred← citeshttps://doi.org/10.1007/s00432-014-1642-2openalex-snapshot
The expression of Wnt-inhibitor DKK1 (Dickkopf 1) is determined by intercellular crosstalk and hypoxia in human malignant gliomas
inferred← citeshttps://doi.org/10.1007/s00432-019-03114-8openalex-snapshot
Crosstalk of estrogen receptors and Wnt/β-catenin signaling in endometrial cancer
inferred← citeshttps://doi.org/10.1007/s00436-016-5033-2openalex-snapshot
Identification of host proteins, Spata3 and Dkk2, interacting with Toxoplasma gondii micronemal protein MIC3
inferred← citeshttps://doi.org/10.1007/s00441-014-1996-4openalex-snapshot
Wnt signalling in neuronal differentiation and development
inferred← citeshttps://doi.org/10.1007/s00441-019-03113-8openalex-snapshot
Dickkopf3 (Dkk3) is required for maintaining the integrity of secretory vesicles in the mouse adrenal medulla
inferred← citeshttps://doi.org/10.1007/s00467-025-06696-3openalex-snapshot
Urinary Dickkopf-related protein 3 as a novel biomarker for kidney function decline in children with Alport syndrome
inferred← citeshttps://doi.org/10.1007/s00774-010-0202-3openalex-snapshot
Targeted overexpression of Dkk1 in osteoblasts reduces bone mass but does not impair the anabolic response to intermittent PTH treatment in mice
inferred← citeshttps://doi.org/10.1007/s10059-010-0017-zopenalex-snapshot
Downregulation of Wnt-Mediated ROS Generation Is Causally Implicated in Leprechaunism
inferred← citeshttps://doi.org/10.1007/s10067-017-3640-7openalex-snapshot
Association between serum and synovial fluid Dickkopf-1 levels with radiographic severity in primary knee osteoarthritis patients
inferred← citeshttps://doi.org/10.1007/s10585-011-9393-9openalex-snapshot
Dickkopf-1 is frequently overexpressed in ovarian serous carcinoma and involved in tumor invasion
inferred← citeshttps://doi.org/10.1007/s10620-019-05606-6openalex-snapshot
Comprehensive Analysis of the Canonical and Non-canonical Wnt Signaling Pathways in Gastric Cancer
inferred← citeshttps://doi.org/10.1007/s10735-011-9347-1openalex-snapshot
Dickkopf-1 is involved in invasive growth of esophageal cancer cells
inferred← citeshttps://doi.org/10.1007/s10735-016-9703-2openalex-snapshot
Expression analysis of Dickkopf-related protein 3 (Dkk3) suggests its pleiotropic roles for a secretory glycoprotein in adult mouse
inferred← citeshttps://doi.org/10.1007/s11033-013-2800-3openalex-snapshot
Polymorphisms of the bovine DKK2 and their associations with body measurement traits and meat quality traits in Qinchuan cattle
inferred← citeshttps://doi.org/10.1007/s11055-020-00938-7openalex-snapshot
Dickkopf-1 and Norrin Suppress Long-Term Potentiation in Vivo in the Rat Hippocampus
inferred← citeshttps://doi.org/10.1007/s11064-008-9710-0openalex-snapshot
The Wnt Antagonist, Dickkopf-1, as a Target for the Treatment of Neurodegenerative Disorders
inferred← citeshttps://doi.org/10.1007/s11481-012-9359-yopenalex-snapshot
Wnt/beta-Catenin Signaling in Glioma
inferred← citeshttps://doi.org/10.1007/s11626-023-00809-8openalex-snapshot
WAY-262611 ameliorates the inflammatory bowel disease by activating Wnt/β-catenin pathway
inferred← citeshttps://doi.org/10.1007/s11626-024-00856-9openalex-snapshot
Understanding and manipulating extracellular behaviors of Wnt ligands
inferred← citeshttps://doi.org/10.1007/s11626-024-00858-7openalex-snapshot
Wnt/β-catenin signaling pathway in liver biology and tumorigenesis
inferred← citeshttps://doi.org/10.1007/s11670-011-0183-3openalex-snapshot
Genetic variants in MMP9 and TCF2 contribute to susceptibility to lung cancer
inferred← citeshttps://doi.org/10.1007/s12013-024-01620-2openalex-snapshot
TOP2A Promotes Proliferation, Migration, and Inflammatory Response in M5-Treated Keratinocytes by Binding CTBP1 to Activate Wnt/β-Catenin Signaling
inferred← citeshttps://doi.org/10.1007/s12015-007-0001-yopenalex-snapshot
The Wnt Signal Transduction Pathway in Stem Cells and Cancer Cells: Influence on Cellular Invasion
inferred← citeshttps://doi.org/10.1007/s12015-021-10256-1openalex-snapshot
Basal Cells in the Epidermis and Epidermal Differentiation
inferred← citeshttps://doi.org/10.1007/s12015-024-10788-2openalex-snapshot
Dynamics of Neurogenic Signals as Biological Switchers of Brain Plasticity
inferred← citeshttps://doi.org/10.1007/s12035-014-8940-1openalex-snapshot
Inhibitory Effects of Bisphenol-A on Neural Stem Cells Proliferation and Differentiation in the Rat Brain Are Dependent on Wnt/β-Catenin Pathway
inferred← citeshttps://doi.org/10.1007/s12035-015-9596-1openalex-snapshot
Increased Wnt Signaling and Reduced Viability in a Neuronal Model of Progranulin-Deficient Frontotemporal Lobar Degeneration
inferred← citeshttps://doi.org/10.1007/s12035-018-1162-1openalex-snapshot
Wnt-7a Stimulates Dendritic Spine Morphogenesis and PSD-95 Expression Through Canonical Signaling
inferred← citeshttps://doi.org/10.1007/s12035-020-02274-wopenalex-snapshot
Müller Glia-Mediated Retinal Regeneration
inferred← citeshttps://doi.org/10.1007/s12265-021-10116-wopenalex-snapshot
Dickkopf 3: a Novel Target Gene of miR-25-3p in Promoting Fibrosis-Related Gene Expression in Myocardial Fibrosis
inferred← citeshttps://doi.org/10.1007/s12272-009-2200-3openalex-snapshot
Wnt/β-catenin signaling: A novel target for therapeutic intervention of fibrotic kidney disease
inferred← citeshttps://doi.org/10.1007/s12272-026-01622-zopenalex-snapshot
M2 microglial exosomal miR-1949 ameliorates sepsis-associated encephalopathy through DKK1/Wnt/β-catenin-mediated microglial repolarization
inferred← citeshttps://doi.org/10.1007/s12307-008-0010-7openalex-snapshot
Bone Marrow Microenvironment and Tumor Progression
inferred← citeshttps://doi.org/10.1007/s13258-022-01351-9openalex-snapshot
CDK9 inhibitors downregulate DKK1 expression to suppress the metastatic potential of HCC cells
inferred← citeshttps://doi.org/10.1007/s13277-015-4379-xopenalex-snapshot
Transcriptomic changes associated with DKK4 overexpression in pancreatic cancer cells detected by RNA-Seq
inferred← citeshttps://doi.org/10.1007/s13312-019-1649-5openalex-snapshot
Correlation of Dickkopf-1 with Inflammation in Crohn Disease
inferred← citeshttps://doi.org/10.1016/b978-0-12-373884-4.00013-6openalex-snapshot
Wnt Signaling and Bone
inferred← citeshttps://doi.org/10.1016/b978-0-12-374145-5.00227-8openalex-snapshot
Interactions Between Wnt/β-Catenin/Fgf and Chemokine Signaling in Lateral Line Morphogenesis
inferred← citeshttps://doi.org/10.1016/b978-0-12-381978-9.10013-7openalex-snapshot
Vitamin D and Wnt/β-Catenin Signaling
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/b978-0-12-407173-5.00004-2openalex-snapshot
The Transcription Factor FOXM1 (Forkhead box M1)
inferred← citeshttps://doi.org/10.1016/b978-0-12-809963-6.00099-7openalex-snapshot
Vitamin D and Colon Cancer
inferred← citeshttps://doi.org/10.1016/b978-0-12-820472-6.00097-9openalex-snapshot
The Pharmacology of WNT Signaling
inferred← citeshttps://doi.org/10.1016/b978-0-323-85545-7.00010-7openalex-snapshot
Induced pluripotent stem cells-derived craniofacial mesenchymal progenitor cells
inferred← citeshttps://doi.org/10.1016/b978-0-323-91338-6.00039-2openalex-snapshot
Vitamin D and colorectal cancer
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2023.01.004openalex-snapshot
Got WNTS? Insight into bone health from a WNT perspective
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2023.01.006openalex-snapshot
The logistics of Wnt production and delivery
inferred← citeshttps://doi.org/10.1016/j.abb.2008.04.025openalex-snapshot
Advanced glycation end-product-inhibited cell proliferation and protein expression of β-catenin and cyclin D1 are dependent on glycogen synthase kinase 3β in LLC-PK1 cells
inferred← citeshttps://doi.org/10.1016/j.ajpath.2023.05.009openalex-snapshot
Dickkopf1 Promotes Pulmonary Fibrosis upon Bleomycin-Induced Lung Injury
inferred← citeshttps://doi.org/10.1016/j.aquatox.2021.106039openalex-snapshot
Chlorogenic acid alleviates thioacetamide-induced toxicity and promotes liver development in zebrafish (Danio rerio) through the Wnt signaling pathway
inferred← citeshttps://doi.org/10.1016/j.archoralbio.2017.04.008openalex-snapshot
Lysophosphatidic acid induces expression of genes in human oral keratinocytes involved in wound healing
inferred← citeshttps://doi.org/10.1016/j.archoralbio.2021.105322openalex-snapshot
Wnt signaling in dental pulp homeostasis and dentin regeneration
inferred← citeshttps://doi.org/10.1016/j.arr.2017.06.001openalex-snapshot
The emerging role of Wnt signaling dysregulation in the understanding and modification of age-associated diseases
inferred← citeshttps://doi.org/10.1016/j.atherosclerosis.2011.05.015openalex-snapshot
Circulating Dickkopf-1 in acute ischemic stroke and clinically stable cerebrovascular disease
inferred← citeshttps://doi.org/10.1016/j.atherosclerosis.2020.03.024openalex-snapshot
atherosclerosis: gone with the Wnt?
inferred← citeshttps://doi.org/10.1016/j.athoracsur.2020.08.068openalex-snapshot
Wnt Signaling Mediates Pro-Fibrogenic Activity in Human Aortic Valve Interstitial Cells
inferred← citeshttps://doi.org/10.1016/j.bbadis.2017.08.031openalex-snapshot
Wnt/β-catenin signaling links embryonic lung development and asthmatic airway remodeling
inferred← citeshttps://doi.org/10.1016/j.bbapap.2013.02.016openalex-snapshot
Biological significance of a thyroid hormone-regulated secretome
inferred← citeshttps://doi.org/10.1016/j.bbcan.2011.09.003openalex-snapshot
Targeting the Wnt pathway in cancer: The emerging role of Dickkopf-3
inferred← citeshttps://doi.org/10.1016/j.bbcan.2026.189722openalex-snapshot
WNT/β-catenin signaling: implications for homeostasis and tumorigenesis in the esophagus
inferred← citeshttps://doi.org/10.1016/j.bbrc.2008.08.079openalex-snapshot
An N-terminal 78 amino acid truncation of REIC/Dkk-3 effectively induces apoptosis
inferred← citeshttps://doi.org/10.1016/j.bbrc.2009.10.113openalex-snapshot
Neucrin is a novel neural-specific secreted antagonist to canonical Wnt signaling
inferred← citeshttps://doi.org/10.1016/j.bbrc.2017.04.123openalex-snapshot
TCF7L1 recruits CtBP and HDAC1 to repress DICKKOPF4 gene expression in human colorectal cancer cells
inferred← citeshttps://doi.org/10.1016/j.bbrc.2019.08.024openalex-snapshot
YAP balances the osteogenic and adipogenic differentiation of hPDLSCs in vitro partly through the Wnt/β-catenin signaling pathway
inferred← citeshttps://doi.org/10.1016/j.bbrc.2025.152806openalex-snapshot
Molecular mechanisms and clinical implications of Wnt pathway inhibition
inferred← citeshttps://doi.org/10.1016/j.biocel.2022.106191openalex-snapshot
Wnt antagonist as therapeutic targets in ovarian cancer
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2014.08.005openalex-snapshot
A platform technique for growth factor delivery with novel mode of action
inferred← citeshttps://doi.org/10.1016/j.bioorg.2018.06.018openalex-snapshot
Design and synthesis of gallocyanine inhibitors of DKK1/LRP6 interactions for treatment of Alzheimer’s disease
inferred← citeshttps://doi.org/10.1016/j.biopha.2019.109336openalex-snapshot
Negative regulators of Wnt signaling in non-small cell lung cancer: Theoretical basis and therapeutic potency
inferred← citeshttps://doi.org/10.1016/j.biopha.2020.111099openalex-snapshot
The role of miRNAs in colorectal cancer progression and chemoradiotherapy
inferred← citeshttps://doi.org/10.1016/j.biopha.2024.116792openalex-snapshot
Enhancing motor functional recovery in spinal cord injury through pharmacological inhibition of Dickkopf-1 with BHQ880 antibody
inferred← citeshttps://doi.org/10.1016/j.biopsych.2011.08.004openalex-snapshot
Analysis of Target Genes Regulated by Chronic Electroconvulsive Therapy Reveals Role for Fzd6 in Depression
inferred← citeshttps://doi.org/10.1016/j.blre.2013.08.002openalex-snapshot
Dickkopf-1 is a key regulator of myeloma bone disease: Opportunities and challenges for therapeutic intervention
inferred← citeshttps://doi.org/10.1016/j.bone.2015.02.009openalex-snapshot
Wnt signaling in bone and muscle
inferred← citeshttps://doi.org/10.1016/j.bone.2017.01.023openalex-snapshot
The chronic kidney disease — Mineral bone disorder (CKD-MBD): Advances in pathophysiology
inferred← citeshttps://doi.org/10.1016/j.bone.2017.03.044openalex-snapshot
LRP5: From bedside to bench to bone
inferred← citeshttps://doi.org/10.1016/j.canlet.2008.11.003openalex-snapshot
Dickkopf-4 is frequently down-regulated and inhibits growth of colorectal cancer cells
inferred← citeshttps://doi.org/10.1016/j.canlet.2014.01.010openalex-snapshot
Dickkopf-1 as a mediator and novel target in malignant bone disease
inferred← citeshttps://doi.org/10.1016/j.cca.2012.07.003openalex-snapshot
Clinical significance of serum and tissue Dickkopf-1 levels in patients with gastric cancer
inferred← citeshttps://doi.org/10.1016/j.cca.2021.07.009openalex-snapshot
Emerging role of serum dickkopf-1 in prognosis of aneurysmal subarachnoid hemorrhage
inferred← citeshttps://doi.org/10.1016/j.cell.2026.05.006openalex-snapshot
Structural basis of Wnt signalosome extracellular complex assembly
inferred← citeshttps://doi.org/10.1016/j.cellsig.2013.08.016openalex-snapshot
Transglutaminase 2 as a novel activator of LRP6/β-catenin signaling
inferred← citeshttps://doi.org/10.1016/j.cellsig.2017.08.008openalex-snapshot
Complexity of the Wnt/β‑catenin pathway: Searching for an activation model
inferred← citeshttps://doi.org/10.1016/j.cellsig.2024.111576openalex-snapshot
Tumor cells induce neural DKK1 expression to promote MDSC infiltration and subsequent T cell suppression
inferred← citeshttps://doi.org/10.1016/j.celrep.2014.08.011openalex-snapshot
β-Catenin Fluctuates in Mouse ESCs and Is Essential for Nanog-Mediated Reprogramming of Somatic Cells to Pluripotency
inferred← citeshttps://doi.org/10.1016/j.celrep.2018.11.017openalex-snapshot
Regional Control of Hairless versus Hair-Bearing Skin by Dkk2
inferred← citeshttps://doi.org/10.1016/j.clim.2022.109156openalex-snapshot
Dickkopf-1 as a promising therapeutic target for autoimmune diseases
inferred← citeshttps://doi.org/10.1016/j.clinbiochem.2013.03.010openalex-snapshot
Folate-receptor 1 (FOLR1) protein is elevated in the serum of ovarian cancer patients
inferred← citeshttps://doi.org/10.1016/j.conb.2018.06.003openalex-snapshot
Wnt proteins as modulators of synaptic plasticity
inferred← citeshttps://doi.org/10.1016/j.cpt.2026.09.002openalex-snapshot
DKK1-CKAP4 axis functions as an immunometabolic checkpoint linking tumor-intrinsic signaling with immune suppression
inferred← citeshttps://doi.org/10.1016/j.csbj.2022.07.008openalex-snapshot
Crystallographic mining of ASK1 regulators to unravel the intricate PPI interfaces for the discovery of small molecule
inferred← citeshttps://doi.org/10.1016/j.cub.2016.07.024openalex-snapshot
Reversal of Synapse Degeneration by Restoring Wnt Signaling in the Adult Hippocampus
inferred← citeshttps://doi.org/10.1016/j.devcel.2008.04.015openalex-snapshot
Wnt3a and Dkk1 Regulate Distinct Internalization Pathways of LRP6 to Tune the Activation of β-Catenin Signaling
inferred← citeshttps://doi.org/10.1016/j.devcel.2008.10.002openalex-snapshot
Wnt/β-Catenin and Fgf Signaling Control Collective Cell Migration by Restricting Chemokine Receptor Expression
inferred← citeshttps://doi.org/10.1016/j.devcel.2011.09.003openalex-snapshot
Structural Basis of Wnt Signaling Inhibition by Dickkopf Binding to LRP5/6
inferred← citeshttps://doi.org/10.1016/j.diff.2009.06.003openalex-snapshot
Members of the miR-290 cluster modulate in vitro differentiation of mouse embryonic stem cells
inferred← citeshttps://doi.org/10.1016/j.diff.2017.08.003openalex-snapshot
Extrinsic control of Wnt signaling in the intestine
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