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Wnt signaling in the intestinal epithelium: from endoderm to cancer
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/1097-0177(2000)9999:9999<::aid-dvdy1047>3.3.co;2-yopenalex-snapshot
Molecular mechanisms of development of the gastrointestinal tract
inferredcites →https://doi.org/10.1002/bies.10028openalex-snapshot
The intestinal epithelial stem cell
inferredcites →https://doi.org/10.1002/bies.20007openalex-snapshot
Hedgehog: an unusual signal transducer
inferredcites →https://doi.org/10.1002/dvdy.10091openalex-snapshot
Villin: A marker for development of the epithelial pyloric border
inferredcites →https://doi.org/10.1002/humu.1380020602openalex-snapshot
Mutations of theAPC adenomatous polyposis coli) gene
inferredcites →https://doi.org/10.1002/j.1460-2075.1993.tb06225.xopenalex-snapshot
Mutations in the segment polarity genes wingless and porcupine impair secretion of the wingless protein.
inferredcites →https://doi.org/10.1016/0092-8674(81)90021-0openalex-snapshot
Identification and characterization of the familial adenomatous polyposis coli gene
inferredcites →https://doi.org/10.1016/0092-8674(90)90186-iopenalex-snapshot
A genetic model for colorectal tumorigenesis
inferredcites →https://doi.org/10.1016/j.ccr.2004.09.032openalex-snapshot
An autocrine mechanism for constitutive Wnt pathway activation in human cancer cells
inferredcites →https://doi.org/10.1016/j.devcel.2004.08.022openalex-snapshot
The APC Tumor Suppressor Binds to C-Terminal Binding Protein to Divert Nuclear β-Catenin from TCF
inferredcites →https://doi.org/10.1016/j.semcancer.2004.04.017openalex-snapshot
Notch signaling in the integrated control of keratinocyte growth/differentiation and tumor suppression
inferredcites →https://doi.org/10.1016/s0002-9440(10)64856-0openalex-snapshot
β-Catenin—A Linchpin in Colorectal Carcinogenesis?
inferredcites →https://doi.org/10.1016/s0012-1606(02)00020-9openalex-snapshot
Requirement for tumor suppressor Apc in the morphogenesis of anterior and ventral mouse embryo
inferredcites →https://doi.org/10.1016/s0014-4827(02)00019-8openalex-snapshot
Regulation of tumor suppressors by nuclear-cytoplasmic shuttling
inferredcites →https://doi.org/10.1016/s0092-8674(00)00121-5openalex-snapshot
TGFβ Signaling in Growth Control, Cancer, and Heritable Disorders
inferredcites →https://doi.org/10.1016/s0092-8674(00)00122-7openalex-snapshot
Linking Colorectal Cancer to Wnt Signaling
inferredcites →https://doi.org/10.1016/s0092-8674(00)80112-9openalex-snapshot
XTcf-3 Transcription Factor Mediates β-Catenin-Induced Axis Formation in Xenopus Embryos
inferredcites →https://doi.org/10.1016/s0092-8674(00)80128-2openalex-snapshot
MADR2 Maps to 18q21 and Encodes a TGFβ–Regulated MAD–Related Protein That Is Functionally Mutated in Colorectal Carcinoma
inferredcites →https://doi.org/10.1016/s0092-8674(00)80531-0openalex-snapshot
Wnt Signaling and an APC-Related Gene Specify Endoderm in Early C. elegans Embryos
inferredcites →https://doi.org/10.1016/s0092-8674(00)81208-8openalex-snapshot
GBP, an Inhibitor of GSK-3, Is Implicated in Xenopus Development and Oncogenesis
inferredcites →https://doi.org/10.1016/s0092-8674(00)81333-1openalex-snapshot
Lessons from Hereditary Colorectal Cancer
inferredcites →https://doi.org/10.1016/s0092-8674(00)81664-5openalex-snapshot
PPARδ Is an APC-Regulated Target of Nonsteroidal Anti-Inflammatory Drugs
inferredcites →https://doi.org/10.1016/s0092-8674(00)81730-4openalex-snapshot
Smad3 Mutant Mice Develop Metastatic Colorectal Cancer
inferredcites →https://doi.org/10.1016/s0092-8674(00)81988-1openalex-snapshot
Suppression of Intestinal Polyposis in ApcΔ716 Knockout Mice by Inhibition of Cyclooxygenase 2 (COX-2)
inferredcites →https://doi.org/10.1016/s0092-8674(02)00679-7openalex-snapshot
Wnt/Wingless Signaling Requires BCL9/Legless-Mediated Recruitment of Pygopus to the Nuclear β-Catenin-TCF Complex
inferredcites →https://doi.org/10.1016/s0092-8674(02)00685-2openalex-snapshot
Control of β-Catenin Phosphorylation/Degradation by a Dual-Kinase Mechanism
inferredcites →https://doi.org/10.1016/s0092-8674(02)01014-0openalex-snapshot
The β-Catenin/TCF-4 Complex Imposes a Crypt Progenitor Phenotype on Colorectal Cancer Cells
inferredcites →https://doi.org/10.1016/s0092-8674(02)01015-2openalex-snapshot
β-Catenin and TCF Mediate Cell Positioning in the Intestinal Epithelium by Controlling the Expression of EphB/EphrinB
inferredcites →https://doi.org/10.1016/s0925-4773(03)00069-8openalex-snapshot
Down-regulation of endodermal Shh is required for gland formation in chicken stomach
inferredcites →https://doi.org/10.1016/s0960-9822(00)80016-0openalex-snapshot
A molecular pathway leading to endoderm formation in zebrafish
inferredcites →https://doi.org/10.1016/s0960-9822(06)00340-xopenalex-snapshot
Sonic hedgehog directs specialised mesoderm differentiation in the intestine and pancreas
inferredcites →https://doi.org/10.1016/s0960-9822(98)70226-xopenalex-snapshot
Downregulation of β-catenin by human Axin and its association with the APC tumor suppressor, β-catenin and GSK3β
inferredcites →https://doi.org/10.1016/s0960-9822(99)80091-8openalex-snapshot
The F-box protein β-TrCP associates with phosphorylated β-catenin and regulates its activity in the cell
inferredcites →https://doi.org/10.1016/s0962-8924(03)00147-8openalex-snapshot
Id proteins in development, cell cycle and cancer
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/10.1016/s1097-2765(03)00484-2openalex-snapshot
A Mechanism for Wnt Coreceptor Activation
inferredcites →https://doi.org/10.1016/s1534-5807(02)00206-xopenalex-snapshot
Formation of Multiple Hearts in Mice following Deletion of β-catenin in the Embryonic Endoderm
inferredcites →https://doi.org/10.1016/s1535-6108(02)00035-1openalex-snapshot
ITF-2, a downstream target of the Wnt/TCF pathway, is activated in human cancers with β-catenin defects and promotes neoplastic transformation
inferredcites →https://doi.org/10.1016/s1535-6108(03)00334-9openalex-snapshot
Small-molecule antagonists of the oncogenic Tcf/β-catenin protein complex
inferredcites →https://doi.org/10.1016/s1535-6108(04)00114-xopenalex-snapshot
Induction of HDAC2 expression upon loss of APC in colorectal tumorigenesis
inferredcites →https://doi.org/10.1023/a:1025858928620openalex-snapshot
Lymphoid enhancer factor/T cell factor expression in colorectal cancer
inferredcites →https://doi.org/10.1038/11932openalex-snapshot
Requirement for Wnt3 in vertebrate axis formation
inferredcites →https://doi.org/10.1038/1270openalex-snapshot
Depletion of epithelial stem-cell compartments in the small intestine of mice lacking Tcf-4
inferredcites →https://doi.org/10.1038/1717openalex-snapshot
Sonic hedgehog is essential to foregut development
inferredcites →https://doi.org/10.1038/18884openalex-snapshot
β-Catenin regulates expression of cyclin D1 in colon carcinoma cells
inferredcites →https://doi.org/10.1038/21666openalex-snapshot
MAP kinase and Wnt pathways converge to downregulate an HMG-domain repressor in Caenorhabditis elegans
inferredcites →https://doi.org/10.1038/21674openalex-snapshot
The TAK1–NLK–MAPK-related pathway antagonizes signalling between β-catenin and transcription factor TCF
inferredcites →https://doi.org/10.1038/22336openalex-snapshot
The cell-surface proteoglycan Dally regulates Wingless signalling in Drosophila
inferredcites →https://doi.org/10.1038/26982openalex-snapshot
Drosophila Tcf and Groucho interact to repress Wingless signalling activity
inferredcites →https://doi.org/10.1038/26989openalex-snapshot
The Xenopus Wnt effector XTcf-3 interacts with Groucho-related transcriptional repressors
inferredcites →https://doi.org/10.1038/35023605openalex-snapshot
Nuclear-cytoplasmic shuttling of APC regulates β-catenin subcellular localization and turnover
inferredcites →https://doi.org/10.1038/35035110openalex-snapshot
arrow encodes an LDL-receptor-related protein essential for Wingless signalling
inferredcites →https://doi.org/10.1038/35035117openalex-snapshot
LDL-receptor-related proteins in Wnt signal transduction
inferredcites →https://doi.org/10.1038/35035124openalex-snapshot
An LDL-receptor-related protein mediates Wnt signalling in mice
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/10.1038/382225a0openalex-snapshot
A new member of the frizzled family from Drosophila functions as a Wingless receptor
inferredcites →https://doi.org/10.1038/382638a0openalex-snapshot
Functional interaction of β-catenin with the transcription factor LEF-1
inferredcites →https://doi.org/10.1038/71657openalex-snapshot
Control of endodermal endocrine development by Hes-1
inferredcites →https://doi.org/10.1038/79859openalex-snapshot
Mutations in AXIN2 cause colorectal cancer with defective mismatch repair by activating β-catenin/TCF signalling
inferredcites →https://doi.org/10.1038/88919openalex-snapshot
Germline mutations of the gene encoding bone morphogenetic protein receptor 1A in juvenile polyposis
inferredcites →https://doi.org/10.1038/nature01570openalex-snapshot
Chibby, a nuclear β-catenin-associated antagonist of the Wnt/Wingless pathway
inferredcites →https://doi.org/10.1038/nature01611openalex-snapshot
Wnt proteins are lipid-modified and can act as stem cell growth factors
inferredcites →https://doi.org/10.1038/nature01972openalex-snapshot
Widespread requirement for Hedgehog ligand stimulation in growth of digestive tract tumours
inferredcites →https://doi.org/10.1038/nature02009openalex-snapshot
Hedgehog is an early and late mediator of pancreatic cancer tumorigenesis
inferredcites →https://doi.org/10.1038/ncb1141openalex-snapshot
Pygopus and Legless target Armadillo/β-catenin to the nucleus to enable its transcriptional co-activator function
inferredcites →https://doi.org/10.1038/ncb1240openalex-snapshot
Wnt signalling induces maturation of Paneth cells in intestinal crypts
inferredcites →https://doi.org/10.1038/ncb786openalex-snapshot
A new nuclear component of the Wnt signalling pathway
inferredcites →https://doi.org/10.1038/ng0501-53openalex-snapshot
β-catenin–sensitive isoforms of lymphoid enhancer factor-1 are selectively expressed in colon cancer
inferredcites →https://doi.org/10.1038/ng1304openalex-snapshot
Indian Hedgehog is an antagonist of Wnt signaling in colonic epithelial cell differentiation
inferredcites →https://doi.org/10.1038/ng1330openalex-snapshot
Epigenetic inactivation of SFRP genes allows constitutive WNT signaling in colorectal cancer
inferredcites →https://doi.org/10.1038/ng1430openalex-snapshot
BMP signaling inhibits intestinal stem cell self-renewal through suppression of Wnt–β-catenin signaling
inferredcites →https://doi.org/10.1038/nm1026openalex-snapshot
Peroxisome proliferator–activated receptor-δ attenuates colon carcinogenesis
inferredcites →https://doi.org/10.1038/nm993openalex-snapshot
Activation of nuclear hormone receptor peroxisome proliferator–activated receptor-δ accelerates intestinal adenoma growth
inferredcites →https://doi.org/10.1038/nrg1178openalex-snapshot
From developmental disorder to heritable cancer: it's all in the BMP/TGF-β family
inferredcites →https://doi.org/10.1038/nrg1427openalex-snapshot
WNT and β-catenin signalling: diseases and therapies
inferredcites →https://doi.org/10.1038/sj.emboj.7600191openalex-snapshot
Hindgut defects and transformation of the gastro‐intestinal tract in Tcf4−/−/Tcf1−/− embryos
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.embor.embor865openalex-snapshot
Specific inhibition of gene expression using a stably integrated, inducible small‐interfering‐RNA vector
inferredcites →https://doi.org/10.1038/sj.onc.1208143openalex-snapshot
PPARδ status and Apc-mediated tumourigenesis in the mouse intestine
inferredcites →https://doi.org/10.1038/sj.onc.1208237openalex-snapshot
β-Catenin activates the growth factor endothelin-1 in colon cancer cells
inferredcites →https://doi.org/10.1042/bc0970001openalex-snapshot
What's new for Biology of the Cell in 2005?
inferredcites →https://doi.org/10.1042/bc20040094openalex-snapshot
Wnt, stem cells and cancer in the intestine
inferredcites →https://doi.org/10.1053/gast.1996.v111.pm8898652openalex-snapshot
Somatic alterations of the DPC4 gene in human colorectal cancers in vivo
inferredcites →https://doi.org/10.1053/gast.2002.32990openalex-snapshot
Inactivation of the transcription factor Elf3 in mice results in dysmorphogenesis and altered differentiation of intestinal epithelium
inferredcites →https://doi.org/10.1053/j.gastro.2003.10.067openalex-snapshot
Bone morphogenetic protein 2 is expressed by, and acts upon, mature epithelial cells in the colon
inferredcites →https://doi.org/10.1053/j.gastro.2004.03.020openalex-snapshot
Inducible cre-mediated control of gene expression in the murine gastrointestinal tract: effect of loss of β-catenin
inferredcites →https://doi.org/10.1073/pnas.2536800100openalex-snapshot
Essential requirement for Wnt signaling in proliferation of adult small intestine and colon revealed by adenoviral expression of Dickkopf-1
inferredcites →https://doi.org/10.1073/pnas.92.10.4482openalex-snapshot
Loss of Apc heterozygosity and abnormal tissue building in nascent intestinal polyps in mice carrying a truncated Apc gene.
inferredcites →https://doi.org/10.1073/pnas.94.19.10330openalex-snapshot
β-Catenin mutations in cell lines established from human colorectal cancers
inferredcites →https://doi.org/10.1073/pnas.94.4.1402openalex-snapshot
Intestinal tumorigenesis is suppressed in mice lacking the metalloproteinase matrilysin
inferredcites →https://doi.org/10.1073/pnas.96.10.5522openalex-snapshot
The cyclin D1 gene is a target of the β-catenin/LEF-1 pathway
inferredcites →https://doi.org/10.1074/jbc.m104366200openalex-snapshot
Foxl1 Controls the Wnt/β-Catenin Pathway by Modulating the Expression of Proteoglycans in the Gut
inferredcites →https://doi.org/10.1074/jbc.m107742200openalex-snapshot
Id2 Is a Target of the β-Catenin/T Cell Factor Pathway in Colon Carcinoma
inferredcites →https://doi.org/10.1074/jbc.m200139200openalex-snapshot
Activation of AXIN2 Expression by β-Catenin-T Cell Factor
inferredcites →https://doi.org/10.1074/jbc.m310876200openalex-snapshot
Identification of BMP and Activin Membrane-bound Inhibitor (BAMBI), an Inhibitor of Transforming Growth Factor-β Signaling, as a Target of the β-Catenin Pathway in Colorectal Tumor Cells
inferredcites →https://doi.org/10.1083/jcb.149.2.249openalex-snapshot
The Transcriptional Coactivator Cbp Interacts with β-Catenin to Activate Gene Expression
inferredcites →https://doi.org/10.1086/323703openalex-snapshot
Germline Mutations in BMPR1A/ALK3 Cause a Subset of Cases of Juvenile Polyposis Syndrome and of Cowden and Bannayan-Riley-Ruvalcaba Syndromes*
inferredcites →https://doi.org/10.1093/carcin/20.11.2045openalex-snapshot
Introduction of full-length APC modulates cyclooxygenase-2 expression in HT-29 human colorectal carcinoma cells at the translational level
inferredcites →https://doi.org/10.1093/emboj/18.8.2196openalex-snapshot
Hes1 and Hes5 as Notch effectors in mammalian neuronal differentiation
inferredcites →https://doi.org/10.1093/emboj/18.9.2401openalex-snapshot
An F‐box protein, FWD1, mediates ubiquitin‐dependent proteolysis of β‐catenin
inferredcites →https://doi.org/10.1093/emboj/19.8.1839openalex-snapshot
The p300/CBP acetyltransferases function as transcriptional coactivators of β‐catenin in vertebrates
inferredcites →https://doi.org/10.1093/emboj/20.17.4935openalex-snapshot
The chromatin remodelling factor Brg‐1 interacts with β‐catenin to promote target gene activation
inferredcites →https://doi.org/10.1093/emboj/cdg105openalex-snapshot
Nuclear export of the APC tumour suppressor controls β‐catenin function in transcription
inferredcites →https://doi.org/10.1101/gad.10.24.3116openalex-snapshot
The segment polarity gene porcupine encodes a putative multitransmembrane protein involved in Wingless processing.
inferredcites →https://doi.org/10.1101/gad.11.12.1583openalex-snapshot
The mesenchymal winged helix transcription factor Fkh6 is required for the control of gastrointestinal proliferation and differentiation.
inferredcites →https://doi.org/10.1101/gad.1260605openalex-snapshot
Foxl1 is a mesenchymal Modifier of Min in carcinogenesis of stomach and colon
inferredcites →https://doi.org/10.1101/gad.13.3.270openalex-snapshot
The SCFbeta -TRCP-ubiquitin ligase complex associates specifically with phosphorylated destruction motifs in Ikappa Balpha and beta -catenin and stimulates Ikappa Balpha ubiquitination in vitro
inferredcites →https://doi.org/10.1101/gad.13.6.709openalex-snapshot
Wnt3a-/--like phenotype and limb deficiency in Lef1-/-Tcf1-/- mice
inferredcites →https://doi.org/10.1101/gad.14.14.1741openalex-snapshot
Inhibition of Wnt signaling by ICAT, a novel β-catenin-interacting protein
inferredcites →https://doi.org/10.1101/gad.227502openalex-snapshot
Nr-CAM is a target gene of the β-catenin/LEF-1 pathway in melanoma and colon cancer and its expression enhances motility and confers tumorigenesis
inferredcites →https://doi.org/10.1101/gad.229102openalex-snapshot
Disruption of the gene encoding the latent transforming growth factor-β binding protein 4 (LTBP-4) causes abnormal lung development, cardiomyopathy, and colorectal cancer
inferredcites →https://doi.org/10.1101/gad.230302openalex-snapshot
Axin-mediated CKI phosphorylation of β-catenin at Ser 45: a molecular switch for the Wnt pathway
inferredcites →https://doi.org/10.1101/gad.267103openalex-snapshot
Canonical Wnt signals are essential for homeostasis of the intestinal epithelium
inferredcites →https://doi.org/10.1101/gad.287404openalex-snapshot
Loss of Apc in vivo immediately perturbs Wnt signaling, differentiation, and migration
inferredcites →https://doi.org/10.1101/gad.326705openalex-snapshot
Frat is dispensable for canonical Wnt signaling in mammals
inferredcites →https://doi.org/10.1126/science.1065718openalex-snapshot
Requirement of Math1 for Secretory Cell Lineage Commitment in the Mouse Intestine
inferredcites →https://doi.org/10.1126/science.1082808openalex-snapshot
Dishevelled 2 Recruits ß-Arrestin 2 to Mediate Wnt5A-Stimulated Endocytosis of Frizzled 4
inferredcites →https://doi.org/10.1126/science.1093587openalex-snapshot
De Novo Crypt Formation and Juvenile Polyposis on BMP Inhibition in Mouse Intestine
inferredcites →https://doi.org/10.1126/science.1651562openalex-snapshot
Identification of FAP Locus Genes from Chromosome 5q21
inferredcites →https://doi.org/10.1126/science.272.5264.1023openalex-snapshot
Binding of GSK3β to the APC-β-Catenin Complex and Regulation of Complex Assembly
inferredcites →https://doi.org/10.1126/science.275.5307.1784openalex-snapshot
Constitutive Transcriptional Activation by a β-Catenin-Tcf Complex in APC −/− Colon Carcinoma
inferredcites →https://doi.org/10.1126/science.275.5307.1787openalex-snapshot
Activation of β-Catenin-Tcf Signaling in Colon Cancer by Mutations in β-Catenin or APC
inferredcites →https://doi.org/10.1126/science.281.5382.1509openalex-snapshot
Identification of c- MYC as a Target of the APC Pathway
inferredcites →https://doi.org/10.1126/science.285.5435.1923openalex-snapshot
Synergy Between Tumor Suppressor APC and the β-Catenin-Tcf4 Target Tcf1
inferredcites →https://doi.org/10.1126/science.7761852openalex-snapshot
Inactivation of the Type II TGF-β Receptor in Colon Cancer Cells with Microsatellite Instability
inferredcites →https://doi.org/10.1126/science.8259518openalex-snapshot
Association of the APC Gene Product with β-Catenin
inferredcites →https://doi.org/10.1128/mcb.22.4.1172-1183.2002openalex-snapshot
Wnt/β-Catenin/Tcf Signaling Induces the Transcription of Axin2, a Negative Regulator of the Signaling Pathway
inferredcites →https://doi.org/10.1128/mcb.22.4.1184-1193.2002openalex-snapshot
Negative Feedback Loop of Wnt Signaling through Upregulation of Conductin/Axin2 in Colorectal and Liver Tumors
inferredcites →https://doi.org/10.1128/mcb.24.17.7598-7611.2004openalex-snapshot
Cyclin D1 Genetic Heterozygosity Regulates Colonic Epithelial Cell Differentiation and Tumor Number in ApcMin Mice
inferredcites →https://doi.org/10.1136/jmg.2004.018598openalex-snapshot
The prevalence of MADH4 and BMPR1A mutations in juvenile polyposis and absence of BMPR2, BMPR1B, and ACVR1 mutations
inferredcites →https://doi.org/10.1146/annurev.cellbio.14.1.59openalex-snapshot
MECHANISMS OF WNT SIGNALING IN DEVELOPMENT
inferredcites →https://doi.org/10.1146/annurev.cellbio.15.1.393openalex-snapshot
Vertebrate Endoderm Development
inferredcites →https://doi.org/10.1146/annurev.cellbio.20.010403.092805openalex-snapshot
SIGNALING PATHWAYS IN INTESTINAL DEVELOPMENT AND CANCER
inferredcites →https://doi.org/10.1146/annurev.cellbio.20.012103.094541openalex-snapshot
THE ADENOMATOUS POLYPOSIS COLI PROTEIN: The Achilles Heel of the Gut Epithelium
inferredcites →https://doi.org/10.1152/ajpcell.1999.277.2.c183openalex-snapshot
Myofibroblasts. II. Intestinal subepithelial myofibroblasts
inferredcites →https://doi.org/10.1158/0008-5472.can-03-1346openalex-snapshot
The Wnt Antagonist sFRP1 in Colorectal Tumorigenesis
inferredcites →https://doi.org/10.1158/0008-5472.can-04-2095openalex-snapshot
Id2 Drives Differentiation and Suppresses Tumor Formation in the Intestinal Epithelium
inferredcites →https://doi.org/10.1172/jci13588openalex-snapshot
Epimorphin expression in intestinal myofibroblasts induces epithelial morphogenesis
inferredcites →https://doi.org/10.1172/jci200213588openalex-snapshot
Epimorphin expression in intestinal myofibroblasts induces epithelial morphogenesis
inferredcites →https://doi.org/10.1172/jci9476openalex-snapshot
Gastrin is a target of the β-catenin/TCF-4 growth-signaling pathway in a model of intestinal polyposis
inferredcites →https://doi.org/10.1186/jbiol3openalex-snapshot
Hyperactive Wnt signaling changes the developmental potential of embryonic lung endoderm
inferredcites →https://doi.org/10.1210/en.2004-0051openalex-snapshot
Minireview: Development and Differentiation of Gut Endocrine Cells
inferredcites →https://doi.org/10.1242/dev.00703openalex-snapshot
Manipulation of stem cell proliferation and lineage commitment:visualisation of label-retaining cells in wholemounts of mouse epidermis
inferredcites →https://doi.org/10.1242/dev.00762openalex-snapshot
PP2A:B56ϵ is required for Wnt/β-catenin signaling during embryonic development
inferredcites →https://doi.org/10.1242/dev.01176openalex-snapshot
Sox17 and β-catenin cooperate to regulate the transcription of endodermal genes
inferredcites →https://doi.org/10.1242/dev.01576openalex-snapshot
Epithelial hedgehog signals pattern the intestinal crypt-villus axis
inferredcites →https://doi.org/10.1242/dev.01700openalex-snapshot
Crypt-restricted proliferation and commitment to the Paneth cell lineage following Apc loss in the mouse intestine
inferredcites →https://doi.org/10.1242/dev.115.3.717openalex-snapshot
Developmental regulation of villin gene expression in the epithelial cell lineages of mouse digestive and urogenital tracts
inferredcites →https://doi.org/10.1242/dev.126.10.2215openalex-snapshot
Targeted disruption of the homeobox transcription factor Nkx2-3 in mice results in postnatal lethality and abnormal development of small intestine and spleen
inferredcites →https://doi.org/10.1242/dev.127.12.2763openalex-snapshot
Hedgehog signals regulate multiple aspects of gastrointestinal development
inferredcites →https://doi.org/10.1242/dev.127.14.3009openalex-snapshot
β-catenin mediates the specification of endoderm cells in ascidian embryos
inferredcites →https://doi.org/10.1242/dev.127.21.4551openalex-snapshot
Hes1 is a negative regulator of inner ear hair cell differentiation
inferredcites →https://doi.org/10.1242/dev.127.9.1971openalex-snapshot
The concentric structure of the developing gut is regulated by Sonic hedgehog derived from endodermal epithelium
inferredcites →https://doi.org/10.1242/dev.129.10.2367openalex-snapshot
Depletion of definitive gut endoderm in Sox17 -null mutant mice
inferredcites →https://doi.org/10.1242/dev.129.11.2565openalex-snapshot
Pygopus, a nuclear PHD-finger protein required for Wingless signaling inDrosophila
inferredcites →https://doi.org/10.1242/dev.129.11.2619openalex-snapshot
The zinc-finger transcription factor Klf4 is required for terminal differentiation of goblet cells in the colon
inferredcites →https://doi.org/10.1242/jcs.00623openalex-snapshot
Secreted antagonists of the Wnt signalling pathway
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113476zenodo-depositor-declared
Undescribed isoquinolines from Zanthoxylum nitidum and their antiproliferative effects against human cancer cell lines
inferred← citeshttps://doi.org/10.1002/9781118512074.ch2openalex-snapshot
Stem Cells and Tissue Renewal
inferred← citeshttps://doi.org/10.1002/9781118695746.ch1openalex-snapshot
Wnt Signaling in Regulation of Stem Cells
inferred← citeshttps://doi.org/10.1002/9783527627523.ch16openalex-snapshot
Gastrointestinal Polyposis Syndromes
inferred← citeshttps://doi.org/10.1002/bies.20581openalex-snapshot
The diverse functions of Krüppel‐like factors 4 and 5 in epithelial biology and pathobiology
inferred← citeshttps://doi.org/10.1002/biof.1133openalex-snapshot
Berberine acts as a natural inhibitor of Wnt/β‐catenin signaling—Identification of more active 13‐arylalkyl derivatives
inferred← citeshttps://doi.org/10.1002/dvdy.434openalex-snapshot
Morphogen regulation of stem cell plasticity in intestinal regeneration and carcinogenesis
inferred← citeshttps://doi.org/10.1002/emmm.201201773openalex-snapshot
Antimicrobial peptides and gut microbiota in homeostasis and pathology
inferred← citeshttps://doi.org/10.1002/gcc.20567openalex-snapshot
Concomitant activation of Wnt pathway and loss of mismatch repair function in human melanoma
inferred← citeshttps://doi.org/10.1002/hep.21523openalex-snapshot
Liver-specific loss of β-catenin results in delayed hepatocyte proliferation after partial hepatectomy
inferred← citeshttps://doi.org/10.1002/hep.30795openalex-snapshot
A Noncoding Regulatory RNAs Network Driven by Circ‐CDYL Acts Specifically in the Early Stages Hepatocellular Carcinoma
inferred← citeshttps://doi.org/10.1002/ibd.20698openalex-snapshot
Is there a role for defensins in IBD?
inferred← citeshttps://doi.org/10.1002/ijc.22145openalex-snapshot
Mucin‐depleted foci are modulated by dietary treatments and show deregulation of proliferative activity in carcinogen‐treated rodents
inferred← citeshttps://doi.org/10.1002/ijc.22750openalex-snapshot
SFRP1 suppressed hepatoma cells growth through Wnt canonical signaling pathway
inferred← citeshttps://doi.org/10.1002/ijc.24802openalex-snapshot
Lef‐1 isoforms regulate different target genes and reduce cellular adhesion
inferred← citeshttps://doi.org/10.1002/ijc.28008openalex-snapshot
Identification of a novel promyelocytic leukemia zinc‐finger isoform required for colorectal cancer cell growth and survival
inferred← citeshttps://doi.org/10.1002/jcp.21766openalex-snapshot
The APC tumor suppressor is required for epithelial integrity in the mouse mammary gland
inferred← citeshttps://doi.org/10.1002/jcp.30325openalex-snapshot
DOCK4 stimulates MUC2 production through its effect on goblet cell differentiation
inferred← citeshttps://doi.org/10.1002/jemt.22534openalex-snapshot
Depletion of enteroendocrine and mucus‐secreting cells is associated with colorectal carcinogenesis severity and impaired intestinal motility in rats
inferred← citeshttps://doi.org/10.1002/mc.22196openalex-snapshot
Dishevelled‐3 activates p65 to upregulate p120‐catenin transcription via a p38‐dependent pathway in non‐small cell lung cancer
inferred← citeshttps://doi.org/10.1002/mc.22294openalex-snapshot
Hepatocyte nuclear factor 4α suppresses the aggravation of colon carcinoma
inferred← citeshttps://doi.org/10.1002/path.2475openalex-snapshot
Gastrointestinal stem cells in development and cancer
inferred← citeshttps://doi.org/10.1002/path.5437openalex-snapshot
Deficiency in IκBα in the intestinal epithelium leads to spontaneous inflammation and mediates apoptosis in the gut
inferred← citeshttps://doi.org/10.1002/pmic.201800132openalex-snapshot
Proteomic Profiling of Enteroid Cultures Skewed toward Development of Specific Epithelial Lineages
inferred← citeshttps://doi.org/10.1002/ptr.3469openalex-snapshot
Persicaria hydropiper (L.) Spach and its Flavonoid Components, Isoquercitrin and Isorhamnetin, Activate the Wnt/β‐catenin Pathway and Inhibit Adipocyte Differentiation of 3T3‐L1 Cells
inferred← citeshttps://doi.org/10.1002/stem.1344openalex-snapshot
Wnt and Notch Signals Guide Embryonic Stem Cell Differentiation into the Intestinal Lineages
inferred← citeshttps://doi.org/10.1002/stem.2307openalex-snapshot
BVES Regulates Intestinal Stem Cell Programs and Intestinal Crypt Viability after Radiation
inferred← citeshttps://doi.org/10.1002/tox.22674openalex-snapshot
Melatonin reduces lung cancer stemness through inhibiting of PLC, ERK, p38, β‐catenin, and Twist pathways
inferred← citeshttps://doi.org/10.1002/wsbm.1176openalex-snapshot
Gut stem cells in tissue renewal and disease: methods, markers, and myths
inferred← citeshttps://doi.org/10.1002/wsbm.45openalex-snapshot
Agent‐based models in translational systems biology
inferred← citeshttps://doi.org/10.1007/164_2021_524openalex-snapshot
Frizzled7 Activates β-Catenin-Dependent and β-Catenin-Independent Wnt Signalling Pathways During Developmental Morphogenesis: Implications for Therapeutic Targeting in Colorectal Cancer
inferred← citeshttps://doi.org/10.1007/978-0-387-49518-7_28openalex-snapshot
Cell Regeneration in Lung Injury
inferred← citeshttps://doi.org/10.1007/978-0-387-68561-8_10openalex-snapshot
Wnt Signaling in Neurite Development
inferred← citeshttps://doi.org/10.1007/978-0-387-69080-3_25openalex-snapshot
Vitamin D3 and Colorectal Cancer
inferred← citeshttps://doi.org/10.1007/978-0-387-69182-4_20openalex-snapshot
Prostaglandin and Transforming Growth Factor β Signaling in Gastric Cancer
inferred← citeshttps://doi.org/10.1007/978-0-387-72114-9_2openalex-snapshot
Molecular Genetics of Lung and Pleural Neoplasms
inferred← citeshttps://doi.org/10.1007/978-0-387-89611-3_8openalex-snapshot
Stem Cells and Lung Cancer
inferred← citeshttps://doi.org/10.1007/978-1-4020-6826-3_4openalex-snapshot
The adenomatous polyposis coli tumour-suppressor protein in normal gut tissue maintenance and cancer
inferred← citeshttps://doi.org/10.1007/978-1-4419-8023-6openalex-snapshot
Targeting the Wnt Pathway in Cancer
inferred← citeshttps://doi.org/10.1007/978-1-4419-8023-6_5openalex-snapshot
Dysregulation of the Wnt Pathway in Solid Tumors
inferred← citeshttps://doi.org/10.1007/978-1-4939-0706-9_15openalex-snapshot
Epigenetic Mechanisms of Colon Cancer Prevention: What Can Nutrition Do?
inferred← citeshttps://doi.org/10.1007/978-1-4939-8859-4_13openalex-snapshot
Notch Signaling in the Normal Intestine and Intestinal Cancer
inferred← citeshttps://doi.org/10.1007/978-1-59745-510-7_8openalex-snapshot
Medulloblastoma, Primitive Neuroectodermal Tumors, and Pineal Tumors
inferred← citeshttps://doi.org/10.1007/978-1-59745-510-7_9openalex-snapshot
Key Mechanisms and Pathways
inferred← citeshttps://doi.org/10.1007/978-1-59745-561-9_20openalex-snapshot
Use of RNA Aptamers for the Modulation of Cancer Cell Signaling
inferred← citeshttps://doi.org/10.1007/978-1-60327-933-8_4openalex-snapshot
Wnt Signaling in Cancer: From Embryogenesis to Stem Cell Self-Renewal
inferred← citeshttps://doi.org/10.1007/978-1-60327-933-8_7openalex-snapshot
Stem Cell Chromatin Patterns and DNA Hypermethylation
inferred← citeshttps://doi.org/10.1007/978-3-030-56510-7_13openalex-snapshot
Multiscale and Tissue Realistic Translational Modeling of Gut Inflammation
inferred← citeshttps://doi.org/10.1007/978-3-030-93333-3_2openalex-snapshot
MicroRNA as a Versatile Regulator of Wnt the Signaling Pathway in Colorectal Cancer
inferred← citeshttps://doi.org/10.1007/978-3-319-19986-3_11openalex-snapshot
Epithelial to Mesenchymal Transition (EMT) and Intestinal Tumorigenesis
inferred← citeshttps://doi.org/10.1007/978-3-319-41342-6_10openalex-snapshot
Plumbagin and Its Role in Chronic Diseases
inferred← citeshttps://doi.org/10.1007/978-3-319-59885-7_11openalex-snapshot
Pathogenesis of Colorectal Cancer
inferred← citeshttps://doi.org/10.1007/978-3-540-33177-3_16openalex-snapshot
Adhesion Molecules in the Vascular Cell Cross-Talk
inferred← citeshttps://doi.org/10.1007/978-3-540-49433-1_28openalex-snapshot
Cell Regeneration in Lung Injury
inferred← citeshttps://doi.org/10.1007/978-3-540-69414-4_9openalex-snapshot
Tiermodelle in der biomedizinischen Forschung
inferred← citeshttps://doi.org/10.1007/978-3-642-04935-4_2openalex-snapshot
Epidemiologie, Ätiologie und Pathogenese
inferred← citeshttps://doi.org/10.1007/978-3-642-41787-0_10openalex-snapshot
Plant Compounds Acting on the Cytoskeleton
inferred← citeshttps://doi.org/10.1007/978-4-431-56068-5_14openalex-snapshot
The Role of Chronic Inflammation in the Promotion of Gastric Tumourigenesis
inferred← citeshttps://doi.org/10.1007/s00018-010-0366-yopenalex-snapshot
Beta-catenin/TCF4 transactivates miR-30e during intestinal cell differentiation
inferred← citeshttps://doi.org/10.1007/s00253-016-7885-xopenalex-snapshot
Design and validation of an orally administrated active L. fermentum-L. acidophilus probiotic formulation using colorectal cancer Apc Min/+ mouse model
inferred← citeshttps://doi.org/10.1007/s00277-012-1595-yopenalex-snapshot
Methylation of Wnt antagonist genes: a useful prognostic marker for myelodysplastic syndrome
inferred← citeshttps://doi.org/10.1007/s00281-012-0353-5openalex-snapshot
The role of PGE2-associated inflammatory responses in gastric cancer development
inferred← citeshttps://doi.org/10.1007/s00292-012-1660-2openalex-snapshot
Plastizität der WNT-Signalwegaktivität im Kolonkarzinom
inferred← citeshttps://doi.org/10.1007/s00432-009-0669-2openalex-snapshot
SFRP4 was overexpressed in colorectal carcinoma
inferred← citeshttps://doi.org/10.1007/s00439-009-0665-2openalex-snapshot
Barrett’s oesophagus: an ideal model to study cancer genetics
inferred← citeshttps://doi.org/10.1007/s00441-013-1562-5openalex-snapshot
The flavonoid chrysin attenuates colorectal pathological remodeling reducing the number and severity of pre-neoplastic lesions in rats exposed to the carcinogen 1,2-dimethylhydrazine
inferred← citeshttps://doi.org/10.1007/s00740-013-0091-xopenalex-snapshot
Plastizität der WNT-Signalwegaktivität im Kolonkarzinom
inferred← citeshttps://doi.org/10.1007/s00774-007-0824-2openalex-snapshot
Signal transduction and transcriptional regulation during mesenchymal cell differentiation
inferred← citeshttps://doi.org/10.1007/s00795-012-0002-zopenalex-snapshot
Identification of DNA-dependent protein kinase catalytic subunit as a novel interaction partner of lymphocyte enhancer factor 1
inferred← citeshttps://doi.org/10.1007/s10123-020-00128-yopenalex-snapshot
Identification of the role of toxin B in the virulence of Clostridioides difficile based on integrated bioinformatics analyses
inferred← citeshttps://doi.org/10.1007/s10126-024-10296-xopenalex-snapshot
DNA Methylation Analysis Reveals Potential Mechanism in Takifugu rubripes Against Cryptocaryon irritans Infection
inferred← citeshttps://doi.org/10.1007/s10456-019-09688-8openalex-snapshot
Cancer-associated fibroblast-derived WNT2 increases tumor angiogenesis in colon cancer
inferred← citeshttps://doi.org/10.1007/s10495-019-01519-xopenalex-snapshot
Combination treatment of podophyllotoxin and rutin promotes mouse Lgr5+ ve intestinal stem cells survival against lethal radiation injury through Wnt signaling
inferred← citeshttps://doi.org/10.1007/s10555-018-9733-1openalex-snapshot
Functional link between plasma membrane spatiotemporal dynamics, cancer biology, and dietary membrane-altering agents
inferred← citeshttps://doi.org/10.1007/s10571-012-9841-3openalex-snapshot
Investigating Tonic Wnt Signaling Throughout the Adult CNS and in the Hippocampal Neurogenic Niche of BatGal and Ins-TopGal Mice
inferred← citeshttps://doi.org/10.1007/s10585-008-9156-4openalex-snapshot
The upstream components of the Wnt signalling pathway in the dynamic EMT and MET associated with colorectal cancer progression
inferred← citeshttps://doi.org/10.1007/s10585-014-9666-1openalex-snapshot
Mutational profiling of the RAS, PI3K, MET and b-catenin pathways in cancer of unknown primary: a retrospective study of the Hellenic Cooperative Oncology Group
inferred← citeshttps://doi.org/10.1007/s10620-011-1885-6openalex-snapshot
Molecular Mechanisms of Barrett’s Esophagus
inferred← citeshttps://doi.org/10.1007/s10620-018-5286-yopenalex-snapshot
Active β-Catenin Signaling in the Small Intestine of Humans During Infancy
inferred← citeshttps://doi.org/10.1007/s10637-009-9359-9openalex-snapshot
Luteolin inhibits cell proliferation during Azoxymethane-induced experimental colon carcinogenesis via Wnt/ β-catenin pathway
inferred← citeshttps://doi.org/10.1007/s10637-021-01079-5openalex-snapshot
Histone deacetylase inhibitor chidamide regulates the Wnt/β-catenin pathway by MYCN/DKK3 in B-ALL
inferred← citeshttps://doi.org/10.1007/s10689-010-9408-8openalex-snapshot
Linkage to chromosome 2q32.2-q33.3 in familial serrated neoplasia (Jass syndrome)
inferred← citeshttps://doi.org/10.1007/s11427-021-1943-9openalex-snapshot
Low-density lipoprotein receptor-related protein 1 is a CROPs-associated receptor for Clostridioides infection toxin B
inferred← citeshttps://doi.org/10.1007/s11888-006-0002-2openalex-snapshot
Molecular genetics of colorectal cancer: An overview
inferred← citeshttps://doi.org/10.1007/s11888-012-0145-2openalex-snapshot
n-3 PUFAs as Modulators of Stem Cells in Prevention of Colorectal Cancer
inferred← citeshttps://doi.org/10.1007/s11888-013-0194-1openalex-snapshot
Stem Cell Signaling Pathways in Colorectal Cancer
inferred← citeshttps://doi.org/10.1007/s12032-022-01823-8openalex-snapshot
Association between cancer genes and germ layer specificity
inferred← citeshttps://doi.org/10.1007/s12253-010-9268-4openalex-snapshot
The Plasminogen System in Microdissected Colonic Mucosa Distant from an Isolated Adenoma
inferred← citeshttps://doi.org/10.1007/s13659-015-0053-7openalex-snapshot
Cycloartane Glycosides from the Roots of Cimicifuga foetida with Wnt Signaling Pathway Inhibitory Activity
inferred← citeshttps://doi.org/10.1007/s13659-015-0056-4openalex-snapshot
Biflavone Ginkgetin, a Novel Wnt Inhibitor, Suppresses the Growth of Medulloblastoma
inferred← citeshttps://doi.org/10.1007/s40778-016-0068-yopenalex-snapshot
Wnt Signaling in Normal and Malignant Stem Cells
inferred← citeshttps://doi.org/10.1016/b978-0-12-375098-3.50018-4openalex-snapshot
Wnt Signaling in Bone
inferred← citeshttps://doi.org/10.1016/b978-0-12-382026-6.00009-9openalex-snapshot
Developmental Signaling Networks
inferred← citeshttps://doi.org/10.1016/b978-0-12-384860-4.00005-8openalex-snapshot
Regeneration of Digestive, Respiratory and Urinary Tissues
inferred← citeshttps://doi.org/10.1016/b978-0-12-394447-4.40011-8openalex-snapshot
Vertical Integration
inferred← citeshttps://doi.org/10.1016/b978-0-12-397884-4.00014-8openalex-snapshot
Agent-Based Modeling and Translational Systems Biology
inferred← citeshttps://doi.org/10.1016/b978-0-12-398523-1.00035-5openalex-snapshot
Intestinal Regeneration
inferred← citeshttps://doi.org/10.1016/b978-0-12-809954-4.00003-7openalex-snapshot
Growth Factors in the Intestinal Tract
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/b978-0-12-816137-1.00087-8openalex-snapshot
Soft Tissue Engineering
inferred← citeshttps://doi.org/10.1016/b978-0-323-05385-3.50019-2openalex-snapshot
Digestive and Respiratory Systems and Body Cavities
inferred← citeshttps://doi.org/10.1016/b978-0-323-90195-6.00002-4openalex-snapshot
Cancer cell development, migratory response, and the role of the tumor microenvironment in invasion and metastasis
inferred← citeshttps://doi.org/10.1016/b978-0-443-06811-9.10014-4openalex-snapshot
Development of the Gastrointestinal Tract
inferred← citeshttps://doi.org/10.1016/b978-0-443-13870-6.00021-0openalex-snapshot
Impact of the microbiome on colorectal cancer development
inferred← citeshttps://doi.org/10.1016/b978-012088394-3/50011-8openalex-snapshot
Developmental Signaling Networks Wnt/β-Catenin Signaling in the Gastrointestinal Tract
inferred← citeshttps://doi.org/10.1016/b978-012370544-0.50019-7openalex-snapshot
Wnt Signaling in Bone
inferred← citeshttps://doi.org/10.1016/b978-1-4557-2794-0.00015-2openalex-snapshot
Digestive and Respiratory Systems and Body Cavities
inferred← citeshttps://doi.org/10.1016/b978-141604059-0.50011-4openalex-snapshot
Congenital and Developmental Disorders of the GI Tract
inferred← citeshttps://doi.org/10.1016/bs.pmbts.2016.10.001openalex-snapshot
Molecular Changes Associated With Tumor Initiation and Progression of Soft Tissue Sarcomas
inferred← citeshttps://doi.org/10.1016/j.ajpath.2013.03.017openalex-snapshot
Spdef Null Mice Lack Conjunctival Goblet Cells and Provide a Model of Dry Eye
inferred← citeshttps://doi.org/10.1016/j.ajpath.2019.10.024openalex-snapshot
Haploinsufficiency of Casitas B-Lineage Lymphoma Augments the Progression of Colon Cancer in the Background of Adenomatous Polyposis Coli Inactivation
inferred← citeshttps://doi.org/10.1016/j.ajpath.2020.09.009openalex-snapshot
Requirement of Bccip for the Regeneration of Intestinal Progenitors
inferred← citeshttps://doi.org/10.1016/j.aninu.2025.04.008openalex-snapshot
New insights into methionine’s role in maintaining intestinal stem cell regeneration via autophagy regulation
inferred← citeshttps://doi.org/10.1016/j.bbadis.2010.12.010openalex-snapshot
Emerging actions of the nuclear receptor LRH-1 in the gut
inferred← citeshttps://doi.org/10.1016/j.bbadis.2010.12.020openalex-snapshot
The thyroid hormones and their nuclear receptors in the gut: From developmental biology to cancer
inferred← citeshttps://doi.org/10.1016/j.bbadis.2015.05.009openalex-snapshot
Adenomatous polyposis coli (APC)-induced apoptosis of HT29 colorectal cancer cells depends on mitochondrial oxidative metabolism
inferred← citeshttps://doi.org/10.1016/j.bbadis.2015.06.011openalex-snapshot
Kaiso overexpression promotes intestinal inflammation and potentiates intestinal tumorigenesis in ApcMin/+ mice
inferred← citeshttps://doi.org/10.1016/j.bbagen.2009.12.007openalex-snapshot
Insulin alters the expression of components of the Wnt signaling pathway including TCF-4 in the intestinal cells
inferred← citeshttps://doi.org/10.1016/j.bbagen.2012.08.008openalex-snapshot
TGF-β family signaling in stem cells
inferred← citeshttps://doi.org/10.1016/j.bbcan.2022.188736openalex-snapshot
E3 ligases and deubiquitinating enzymes regulating the MAPK signaling pathway in cancers
inferred← citeshttps://doi.org/10.1016/j.bbrc.2006.02.193openalex-snapshot
β-Catenin control of T-cell transcription factor 4 (Tcf4) importation from the cytoplasm to the nucleus contributes to Tcf4-mediated transcription in 293 cells
inferred← citeshttps://doi.org/10.1016/j.bbrc.2009.01.124openalex-snapshot
Smad4 restoration leads to a suppression of Wnt/β-catenin signaling activity and migration capacity in human colon carcinoma cells
inferred← citeshttps://doi.org/10.1016/j.bbrc.2011.04.045openalex-snapshot
Phosphatidylinositol 5-phosphate 4-kinase type II beta is required for vitamin D receptor-dependent E-cadherin expression in SW480 cells
inferred← citeshttps://doi.org/10.1016/j.bbrc.2018.03.064openalex-snapshot
Regulation by commensal bacteria of neurogenesis in the subventricular zone of adult mouse brain
inferred← citeshttps://doi.org/10.1016/j.bioorg.2024.107178openalex-snapshot
Discovery of a stilbenoid-flavanone hybrid as an antitumor Wnt/β-catenin signaling pathway inhibitor
inferred← citeshttps://doi.org/10.1016/j.biopha.2023.114950openalex-snapshot
Natural products targeting Nrf2/ARE signaling pathway in the treatment of inflammatory bowel disease
inferred← citeshttps://doi.org/10.1016/j.bmcl.2015.03.038openalex-snapshot
BMS-871: A novel orally active pan-Notch inhibitor as an anticancer agent
inferred← citeshttps://doi.org/10.1016/j.bpj.2019.09.009openalex-snapshot
AdipoRon Attenuates Wnt Signaling by Reducing Cholesterol-Dependent Plasma Membrane Rigidity
inferred← citeshttps://doi.org/10.1016/j.canlet.2008.02.061openalex-snapshot
Signal-dependent regulation of gene expression as a target for cancer treatment: Inhibiting p38α in colorectal tumors
inferred← citeshttps://doi.org/10.1016/j.canlet.2008.07.001openalex-snapshot
Calcium, calcium-sensing receptor and colon cancer
inferred← citeshttps://doi.org/10.1016/j.canlet.2014.03.023openalex-snapshot
Resistance to irinotecan (CPT-11) activates epidermal growth factor receptor/nuclear factor kappa B and increases cellular metastasis and autophagy in LoVo colon cancer cells
inferred← citeshttps://doi.org/10.1016/j.canlet.2015.07.002openalex-snapshot
The sulfiredoxin–peroxiredoxin (Srx–Prx) axis in cell signal transduction and cancer development
inferred← citeshttps://doi.org/10.1016/j.canrad.2019.06.002openalex-snapshot
Gene therapy and cell therapy for the management of radiation damages to healthy tissues: Rationale and early results
inferred← citeshttps://doi.org/10.1016/j.ccr.2007.01.003openalex-snapshot
The Morphogenetic Code and Colon Cancer Development
inferred← citeshttps://doi.org/10.1016/j.ccr.2009.01.018openalex-snapshot
Oncogenic Function of ATDC in Pancreatic Cancer through Wnt Pathway Activation and β-Catenin Stabilization
inferred← citeshttps://doi.org/10.1016/j.ceb.2008.01.011openalex-snapshot
Eph–ephrin signalling in adult tissues and cancer
inferred← citeshttps://doi.org/10.1016/j.cell.2006.01.053openalex-snapshot
Parafibromin/Hyrax Activates Wnt/Wg Target Gene Transcription by Direct Association with β-catenin/Armadillo
inferred← citeshttps://doi.org/10.1016/j.cell.2008.12.044openalex-snapshot
Disrupted in Schizophrenia 1 Regulates Neuronal Progenitor Proliferation via Modulation of GSK3β/β-Catenin Signaling
inferred← citeshttps://doi.org/10.1016/j.cell.2009.01.031openalex-snapshot
Transcription Factor Achaete Scute-Like 2 Controls Intestinal Stem Cell Fate
inferred← citeshttps://doi.org/10.1016/j.cell.2009.05.014openalex-snapshot
Cytokine/Jak/Stat Signaling Mediates Regeneration and Homeostasis in the Drosophila Midgut
inferred← citeshttps://doi.org/10.1016/j.cellsig.2018.03.014openalex-snapshot
Inhibition of DNMT suppresses the stemness of colorectal cancer cells through down-regulating Wnt signaling pathway
inferred← citeshttps://doi.org/10.1016/j.cellsig.2025.111605openalex-snapshot
Non-coding RNAs as mediators of epithelial to mesenchymal transition in metastatic colorectal cancers
inferred← citeshttps://doi.org/10.1016/j.celrep.2014.08.034openalex-snapshot
Prox1 Promotes Expansion of the Colorectal Cancer Stem Cell Population to Fuel Tumor Growth and Ischemia Resistance
inferred← citeshttps://doi.org/10.1016/j.celrep.2017.02.056openalex-snapshot
Canonical Wnt Signaling Ameliorates Aging of Intestinal Stem Cells
inferred← citeshttps://doi.org/10.1016/j.celrep.2023.113407openalex-snapshot
Single-cell resolution of the adult zebrafish intestine under conventional conditions and in response to an acute Vibrio cholerae infection
inferred← citeshttps://doi.org/10.1016/j.critrevonc.2015.12.005openalex-snapshot
The Wnt signaling pathway in cancer
inferred← citeshttps://doi.org/10.1016/j.critrevonc.2024.104544openalex-snapshot
Origin, development and therapy of colorectal cancer from the perspective of a biologist and an oncologist
inferred← citeshttps://doi.org/10.1016/j.critrevonc.2026.105562openalex-snapshot
Novel clinical intervention pathway based on the pathogenesis mechanism of Enterotoxigenic Bacteroides fragilis
inferred← citeshttps://doi.org/10.1016/j.cub.2006.09.034openalex-snapshot
CK2 Controls the Recruitment of Wnt Regulators to Target Genes In Vivo
inferred← citeshttps://doi.org/10.1016/j.devcel.2022.07.006openalex-snapshot
N6-adenomethylation of GsdmC is essential for Lgr5+ stem cell survival to maintain normal colonic epithelial morphogenesis
inferred← citeshttps://doi.org/10.1016/j.diff.2008.09.008openalex-snapshot
Differences in goblet cell differentiation between Crohn's disease and ulcerative colitis
inferred← citeshttps://doi.org/10.1016/j.ejca.2006.01.061openalex-snapshot
Overexpression of poly(ADP-ribose) polymerase-1 (PARP-1) in the early stage of colorectal carcinogenesis
inferred← citeshttps://doi.org/10.1016/j.ejca.2012.12.014openalex-snapshot
Down-regulation of programmed cell death 4 leads to epithelial to mesenchymal transition and promotes metastasis in mice
inferred← citeshttps://doi.org/10.1016/j.ejmech.2014.05.071openalex-snapshot
Synthesis and biological evaluation of imidazo[1,2-a]pyrimidines and imidazo[1,2-a]pyridines as new inhibitors of the Wnt/β-catenin signaling
inferred← citeshttps://doi.org/10.1016/j.ejmech.2022.114789openalex-snapshot
Recent advances of β-catenin small molecule inhibitors for cancer therapy: Current development and future perspectives
inferred← citeshttps://doi.org/10.1016/j.exer.2024.110022openalex-snapshot
Wnt/β-catenin signaling in corneal epithelium development, homeostasis, and pathobiology
inferred← citeshttps://doi.org/10.1016/j.fct.2016.04.014openalex-snapshot
Food-grade titanium dioxide exposure exacerbates tumor formation in colitis associated cancer model
inferred← citeshttps://doi.org/10.1016/j.febslet.2010.11.002openalex-snapshot
An overview of epigenetics and chemoprevention
inferred← citeshttps://doi.org/10.1016/j.gde.2022.101977openalex-snapshot
Intestinal epithelial organoids: regeneration and maintenance of the intestinal epithelium
inferred← citeshttps://doi.org/10.1016/j.gene.2013.01.015openalex-snapshot
DISC1-related signaling pathways in adult neurogenesis of the hippocampus
inferred← citeshttps://doi.org/10.1016/j.genrep.2021.101465openalex-snapshot
Performance of KLF4 and Wnt1 genes expression fluctuations in tumoral and margin tissues of colorectal cancer in an Iranian population
inferred← citeshttps://doi.org/10.1016/j.humpath.2012.03.018openalex-snapshot
β-Catenin mutations in 2 nested stromal epithelial tumors of the liver—a neoplasia with defective mesenchymal-epithelial transition
inferred← citeshttps://doi.org/10.1016/j.ijmm.2009.08.011openalex-snapshot
Innate antimicrobial host defense in small intestinal Crohn's disease
inferred← citeshttps://doi.org/10.1016/j.immuni.2007.02.012openalex-snapshot
The Toll–Interleukin-1 Receptor Member SIGIRR Regulates Colonic Epithelial Homeostasis, Inflammation, and Tumorigenesis
inferred← citeshttps://doi.org/10.1016/j.isci.2020.101461openalex-snapshot
SIRT7 Facilitates CENP-A Nucleosome Assembly and Suppresses Intestinal Tumorigenesis
inferred← citeshttps://doi.org/10.1016/j.jaci.2021.04.024openalex-snapshot
DEP-induced ZEB2 promotes nasal polyp formation via epithelial-to-mesenchymal transition
inferred← citeshttps://doi.org/10.1016/j.jbc.2022.102735openalex-snapshot
SOX9 and TCF transcription factors associate to mediate Wnt/β-catenin target gene activation in colorectal cancer
inferred← citeshttps://doi.org/10.1016/j.jbc.2024.107424openalex-snapshot
Intestinal lysozyme engagement of Salmonella Typhimurium stimulates the release of barrier-impairing InvE and Lpp1
inferred← citeshttps://doi.org/10.1016/j.jbi.2007.12.001openalex-snapshot
SEGS: Search for enriched gene sets in microarray data
inferred← citeshttps://doi.org/10.1016/j.jcmgh.2017.02.004openalex-snapshot
Hypoxia Inducible Factor (HIF) Hydroxylases as Regulators of Intestinal Epithelial Barrier Function
inferred← citeshttps://doi.org/10.1016/j.jcmgh.2024.02.002openalex-snapshot
Telocytes in the Luminal GI Tract
inferred← citeshttps://doi.org/10.1016/j.jgg.2011.09.003openalex-snapshot
Chemical genetics and drug screening in Drosophila cancer models
inferred← citeshttps://doi.org/10.1016/j.jmb.2007.01.020openalex-snapshot
Developmental Regulators Containing the I-mfa Domain Interact with T cyclins and Tat and Modulate Transcription
inferred← citeshttps://doi.org/10.1016/j.jtbi.2012.08.002openalex-snapshot
A theoretical investigation of the effect of proliferation and adhesion on monoclonal conversion in the colonic crypt
inferred← citeshttps://doi.org/10.1016/j.jtbi.2013.04.018openalex-snapshot
Stem cell population asymmetry can reduce rate of replicative aging
inferred← citeshttps://doi.org/10.1016/j.jtbi.2020.110535openalex-snapshot
A mathematical model of cell fate selection on a dynamic tissue
inferred← citeshttps://doi.org/10.1016/j.mam.2013.01.002openalex-snapshot
Mammalian iron transporters: Families SLC11 and SLC40
inferred← citeshttps://doi.org/10.1016/j.molcel.2011.05.014openalex-snapshot
SHP2 Tyrosine Phosphatase Converts Parafibromin/Cdc73 from a Tumor Suppressor to an Oncogenic Driver
inferred← citeshttps://doi.org/10.1016/j.molmed.2010.05.003openalex-snapshot
Learning from Jekyll to control Hyde: Hedgehog signaling in development and cancer
inferred← citeshttps://doi.org/10.1016/j.molmed.2015.06.003openalex-snapshot
Three cheers for the goblet cell: maintaining homeostasis in mucosal epithelia
inferred← citeshttps://doi.org/10.1016/j.molmed.2018.03.008openalex-snapshot
RNA Binding Proteins in Intestinal Epithelial Biology and Colorectal Cancer
inferred← citeshttps://doi.org/10.1016/j.mpdhp.2010.03.005openalex-snapshot
Molecular pathology of gastrointestinal neuroendocrine tumours – selected topics
inferred← citeshttps://doi.org/10.1016/j.neo.2016.08.006openalex-snapshot
90K Glycoprotein Promotes Degradation of Mutant β-Catenin Lacking the ISGylation or Phosphorylation Sites in the N-terminus
inferred← citeshttps://doi.org/10.1016/j.phrs.2020.105243openalex-snapshot
The Nrf2 in the pathophysiology of the intestine: Molecular mechanisms and therapeutic implications for inflammatory bowel diseases
inferred← citeshttps://doi.org/10.1016/j.phrs.2023.106976openalex-snapshot
The Eph/ephrin system symphony of gut inflammation
inferred← citeshttps://doi.org/10.1016/j.phymed.2013.03.006openalex-snapshot
Characterization of xanthatin: Anticancer properties and mechanisms of inhibited murine melanoma in vitro and in vivo
inferred← citeshttps://doi.org/10.1016/j.procbio.2022.02.006openalex-snapshot
Cancer stem cells: An overview of the pathophysiological and prognostic roles in colorectal cancer
inferred← citeshttps://doi.org/10.1016/j.semcancer.2014.02.005openalex-snapshot
Epithelial stem cells and intestinal cancer
inferred← citeshttps://doi.org/10.1016/j.stem.2010.11.016openalex-snapshot
Tissue-Resident Adult Stem Cell Populations of Rapidly Self-Renewing Organs
inferred← citeshttps://doi.org/10.1016/j.stem.2012.09.009openalex-snapshot
Identifying the Stem Cell of the Intestinal Crypt: Strategies and Pitfalls
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