scholarly article | Q13442814 |
P2093 | author name string | E. Fuchs | |
R. DasGupta | |||
P433 | issue | 20 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Lymphoid enhancer binding factor 1 | Q21498209 |
Transcription factor 7 like 1 (T cell specific, HMG box) | Q21991825 | ||
P304 | page(s) | 4557–4568 | |
P577 | publication date | 1999-10-01 | |
P1433 | published in | Development | Q3025404 |
P1476 | title | Multiple roles for activated LEF/TCF transcription complexes during hair follicle development and differentiation | |
P478 | volume | 126 |
Q39280114 | 'Cyclic alopecia' in Msx2 mutants: defects in hair cycling and hair shaft differentiation |
Q40883157 | 1α,25-dihydroxyvitamin D3 modulates the hair-inductive capacity of dermal papilla cells: therapeutic potential for hair regeneration |
Q37213583 | A Chronic Obstructive Pulmonary Disease Susceptibility Gene, FAM13A, Regulates Protein Stability of β-Catenin |
Q35952286 | A DNA binding mutation in estrogen receptor-α leads to suppression of Wnt signaling via β-catenin destabilization in osteoblasts |
Q42938802 | A SHH-responsive signaling center in the forebrain regulates craniofacial morphogenesis via the facial ectoderm |
Q34695948 | A WNT/beta-catenin signaling activator, R-spondin, plays positive regulatory roles during skeletal myogenesis |
Q36323830 | A developmental conundrum: a stabilized form of beta-catenin lacking the transcriptional activation domain triggers features of hair cell fate in epidermal cells and epidermal cell fate in hair follicle cells |
Q36638955 | A distinct cohort of progenitor cells participates in synovial joint and articular cartilage formation during mouse limb skeletogenesis |
Q36432895 | A dual function for canonical Wnt/β-catenin signaling in the developing mammalian cochlea |
Q34422168 | A molecular basis for classic blond hair color in Europeans |
Q33755851 | A primary cilia-dependent etiology for midline facial disorders. |
Q35341650 | A re-evaluation of two key reagents for in vivo studies of Wnt signaling |
Q36702256 | A role for Wnt/planar cell polarity signaling during lens fiber cell differentiation? |
Q30497823 | A sensitive and bright single-cell resolution live imaging reporter of Wnt/ß-catenin signaling in the mouse. |
Q24809626 | A signaling pathway involving TGF-beta2 and snail in hair follicle morphogenesis |
Q33763816 | Aberrant expression of a beta-catenin gain-of-function mutant induces hyperplastic transformation in the mouse cornea. |
Q33786235 | Abnormal hair follicle development and altered cell fate of follicular keratinocytes in transgenic mice expressing DeltaNp63alpha |
Q28509974 | Acentriolar mitosis activates a p53-dependent apoptosis pathway in the mouse embryo |
Q33580683 | Activation of Wnt Signaling by Mechanical Loading Is Impaired in the Bone of Old Mice |
Q50146261 | Activation of Wnt/β-catenin signaling is involved in hair growth-promoting effect of 655-nm red light and LED in in vitro culture model. |
Q36837854 | Activation of beta-catenin signaling programs embryonic epidermis to hair follicle fate |
Q33957004 | Activation of the Wnt/beta-catenin signaling reporter in developing mouse olfactory nerve layer marks a specialized subgroup of olfactory ensheathing cells |
Q27437626 | Activation of the canonical Wnt/β-catenin pathway in ATF3-induced mammary tumors |
Q41862984 | Activation of vascular smooth muscle parathyroid hormone receptor inhibits Wnt/beta-catenin signaling and aortic fibrosis in diabetic arteriosclerosis |
Q42102894 | Activation of β-catenin/TCF targets following loss of the tumor suppressor SNF5. |
Q24613142 | Actomyosin-mediated cellular tension drives increased tissue stiffness and β-catenin activation to induce epidermal hyperplasia and tumor growth |
Q36909848 | Adenovirus-mediated Wnt5a expression inhibits the telogen-to-anagen transition of hair follicles in mice |
Q42516622 | Adult interfollicular tumour-initiating cells are reprogrammed into an embryonic hair follicle progenitor-like fate during basal cell carcinoma initiation |
Q64981333 | Aging differentially modulates the Wnt pro-survival signalling pathways in vascular smooth muscle cells. |
Q37326916 | Akt2 and SGK3 are both determinants of postnatal hair follicle development. |
Q35843381 | Alterations of beta-catenin pathway in non-melanoma skin tumors: loss of alpha-ABC nuclear reactivity correlates with the presence of beta-catenin gene mutation |
Q24679566 | Altered HOX and WNT7A expression in human lung cancer |
Q33849654 | Altering Glypican-1 levels modulates canonical Wnt signaling during trigeminal placode development |
Q83228837 | An RNAi screen unravels the complexities of Rho GTPase networks in skin morphogenesis |
Q34366558 | An internal ribosome entry site mediates translation of lymphoid enhancer factor-1 |
Q92468922 | An updated classification of hair follicle morphogenesis |
Q36133730 | Analysis of a Jup hypomorphic allele reveals a critical threshold for postnatal viability |
Q58705518 | Anxiety Specific Response and Contribution of Active Hippocampal Neural Stem Cells to Chronic Pain Through Wnt/β-Catenin Signaling in Mice |
Q28505133 | Architectural niche organization by LHX2 is linked to hair follicle stem cell function |
Q35226270 | Atlas of Wnt and R-spondin gene expression in the developing male mouse lower urogenital tract |
Q28534536 | Augmenting endogenous Wnt signaling improves skin wound healing |
Q36811483 | Axin2 expression identifies progenitor cells in the murine prostate |
Q36710713 | Axin2 marks quiescent hair follicle bulge stem cells that are maintained by autocrine Wnt/β-catenin signaling. |
Q41864101 | BMP signaling and its pSMAD1/5 target genes differentially regulate hair follicle stem cell lineages |
Q37222697 | BMP signaling negatively regulates bone mass through sclerostin by inhibiting the canonical Wnt pathway. |
Q35348773 | BMP-FGF signaling axis mediates Wnt-induced epidermal stratification in developing mammalian skin. |
Q31028060 | Barx1-mediated inhibition of Wnt signaling in the mouse thoracic foregut controls tracheo-esophageal septation and epithelial differentiation |
Q33714238 | Beta-catenin deficiency causes DiGeorge syndrome-like phenotypes through regulation of Tbx1. |
Q41291637 | Beta-catenin is necessary to keep cells of ureteric bud/Wolffian duct epithelium in a precursor state |
Q37452225 | Beta-catenin signaling levels in progenitors influence the laminar cell fates of projection neurons |
Q36414539 | Beta-catenin/Tcf determines the outcome of thymic selection in response to alphabetaTCR signaling |
Q33559386 | Bioactives in Chinese Proprietary Medicine Modulates 5α-Reductase Activity and Gene Expression Associated with Androgenetic Alopecia |
Q28510349 | Bmp4 is required for tracheal formation: a novel mouse model for tracheal agenesis |
Q33707771 | Bone marrow derived mesenchymal stem cells incorporate into the prostate during regrowth |
Q35103102 | Bone morphogenetic protein signaling regulates postnatal hair follicle differentiation and cycling |
Q37180939 | Brachy-syndactyly caused by loss of Sfrp2 function |
Q37218833 | Building epithelial tissues from skin stem cells |
Q27320065 | CACN-1/Cactin plays a role in Wnt signaling in C. elegans |
Q41633733 | CD133-positive dermal papilla-derived Wnt ligands regulate postnatal hair growth |
Q91909286 | CRISPR/Cas9-mediated VDR knockout plays an essential role in the growth of dermal papilla cells through enhanced relative genes |
Q28505430 | Calcium/NFAT signalling promotes early nephrogenesis |
Q51922368 | Canonical Wnt signaling activity during synovial joint development. |
Q39331082 | Canonical Wnt signaling in diabetic retinopathy. |
Q37698498 | Canonical Wnt signaling is required for ophthalmic trigeminal placode cell fate determination and maintenance |
Q24610934 | Characterization and in vivo pharmacological rescue of a Wnt2-Gata6 pathway required for cardiac inflow tract development |
Q35647585 | Characterization of Lef-1 promoter segments that facilitate inductive developmental expression in skin |
Q41909361 | Characterization of a transient TCF/LEF-responsive progenitor population in the embryonic mouse retina |
Q37377298 | Chromatin protein HMGB2 regulates articular cartilage surface maintenance via beta-catenin pathway |
Q28302606 | Cilia and developmental signaling |
Q41513642 | Cloning and developmental expression of mouse pygopus 2, a putative Wnt signaling component |
Q34652352 | Combined transcriptome analysis of fetal human and mouse cerebral cortex exposed to alcohol |
Q33304986 | Common activation of canonical Wnt signaling in pancreatic adenocarcinoma. |
Q38958604 | Comparison of strain measurement in the mouse forearm using subject-specific finite element models, strain gaging, and digital image correlation |
Q34233989 | Computational biophysical, biochemical, and evolutionary signature of human R-spondin family proteins, the member of canonical Wnt/β-catenin signaling pathway |
Q36328599 | Conditional ablation of beta1 integrin in skin. Severe defects in epidermal proliferation, basement membrane formation, and hair follicle invagination |
Q37412788 | Conditional stabilization of beta-catenin expands the pool of lung stem cells |
Q33999191 | Contrasting expression of canonical Wnt signaling reporters TOPGAL, BATGAL and Axin2(LacZ) during murine lung development and repair. |
Q27300741 | Control of bone mass and remodeling by PTH receptor signaling in osteocytes |
Q42078751 | Convergent extension movements in growth plate chondrocytes require gpi-anchored cell surface proteins |
Q88887679 | Costunolide promotes the proliferation of human hair follicle dermal papilla cells and induces hair growth in C57BL/6 mice |
Q35066919 | Covering the limb--formation of the integument |
Q35208152 | Cranial nerve development requires co-ordinated Shh and canonical Wnt signaling |
Q28587428 | Crosstalk between the p190-B RhoGAP and IGF signaling pathways is required for embryonic mammary bud development |
Q91792135 | Current understanding and dispute on the function of the Wnt signaling pathway effector TCF7L2 in hepatic gluconeogenesis |
Q36407832 | Cutaneous retinoic acid levels determine hair follicle development and downgrowth |
Q27004417 | Cutaneous wound healing: recruiting developmental pathways for regeneration |
Q34959844 | Cytochrome b5 null mouse: a new model for studying inherited skin disorders and the role of unsaturated fatty acids in normal homeostasis |
Q35690673 | Daam2 is required for dorsal patterning via modulation of canonical Wnt signaling in the developing spinal cord |
Q37259094 | Deciphering the function of canonical Wnt signals in development and disease: conditional loss- and gain-of-function mutations of beta-catenin in mice |
Q36773411 | Decoction and Fermentation of Selected Medicinal Herbs Promote Hair Regrowth by Inducing Hair Follicle Growth in Conjunction with Wnts Signaling |
Q36324810 | Defining BMP functions in the hair follicle by conditional ablation of BMP receptor IA. |
Q33891944 | Defining the impact of beta-catenin/Tcf transactivation on epithelial stem cells |
Q28709530 | Delineating a conserved genetic cassette promoting outgrowth of body appendages |
Q64119063 | Dermal Condensate Niche Fate Specification Occurs Prior to Formation and Is Placode Progenitor Dependent |
Q35841035 | Dermal β-catenin activity in response to epidermal Wnt ligands is required for fibroblast proliferation and hair follicle initiation |
Q26866064 | Developing a sense of taste |
Q28756916 | Development of the upper lip: morphogenetic and molecular mechanisms |
Q30978182 | Differential expression of cyclin D1 in the human hair follicle |
Q28506749 | Differential regulation of midbrain dopaminergic neuron development by Wnt-1, Wnt-3a, and Wnt-5a |
Q34993647 | Differential sensitivity of epidermal cell subpopulations to beta-catenin-induced ectopic hair follicle formation |
Q38755954 | Discovery, Diagnosis, and Etiology of Craniofacial Ciliopathies |
Q37679924 | Disrupting hedgehog and WNT signaling interactions promotes cleft lip pathogenesis |
Q92621345 | Disruption of Dhcr7 and Insig1/2 in cholesterol metabolism causes defects in bone formation and homeostasis through primary cilium formation |
Q42861996 | Disruption of E-cadherin-mediated adhesion induces a functionally distinct pathway of dendritic cell maturation |
Q37078665 | Disruption of Smad4 in mouse epidermis leads to depletion of follicle stem cells |
Q33580141 | Disruption of the temporally regulated cloaca endodermal β-catenin signaling causes anorectal malformations. |
Q37450404 | Dissociation of EphB2 signaling pathways mediating progenitor cell proliferation and tumor suppression. |
Q35091279 | Distinct DNA binding sites contribute to the TCF transcriptional switch in C. elegans and Drosophila. |
Q41887923 | Distinct functions for Wnt/β-catenin in hair follicle stem cell proliferation and survival and interfollicular epidermal homeostasis |
Q30538615 | Divergent roles for Wnt/β-catenin signaling in epithelial maintenance and breakdown during semicircular canal formation |
Q28589659 | Dlg5 maintains apical aPKC and regulates progenitor differentiation during lung morphogenesis |
Q37424528 | Dosage-dependent hedgehog signals integrated with Wnt/beta-catenin signaling regulate external genitalia formation as an appendicular program. |
Q41820010 | Dynamic expression of Lgr5, a Wnt target gene, in the developing and mature mouse cochlea |
Q36101565 | Dynamic expression of a LEF-EGFP Wnt reporter in mouse development and cancer |
Q33580134 | Dysregulation of Wnt inhibitory factor 1 (Wif1) expression resulted in aberrant Wnt-β-catenin signaling and cell death of the cloaca endoderm, and anorectal malformations. |
Q37367925 | E-cadherin controls adherens junctions in the epidermis and the renewal of hair follicles |
Q64105690 | EGFR Controls Hair Shaft Differentiation in a p53-Independent Manner |
Q37470392 | Effect of retinoic acid signaling on Wnt/beta-catenin and FGF signaling during body axis extension |
Q33787188 | Elevated circulation levels of an antiangiogenic SERPIN in patients with diabetic microvascular complications impair wound healing through suppression of Wnt signaling |
Q36594267 | Embryonic attenuated Wnt/β-catenin signaling defines niche location and long-term stem cell fate in hair follicle |
Q35174984 | Emerging interactions between skin stem cells and their niches |
Q34786853 | Endothelial cell-specific deletion of transcription factor FoxM1 increases urethane-induced lung carcinogenesis |
Q34314234 | Epidermal Wnt controls hair follicle induction by orchestrating dynamic signaling crosstalk between the epidermis and dermis |
Q26823139 | Epidermal development in mammals: key regulators, signals from beneath, and stem cells |
Q24654755 | Epidermal homeostasis: a balancing act of stem cells in the skin |
Q36528809 | Epidermal stem cells of the skin |
Q41109067 | Epithelial Skin Biology: Three Decades of Developmental Biology, a Hundred Questions Answered and a Thousand New Ones to Address |
Q41865262 | Epithelial Wnt ligand secretion is required for adult hair follicle growth and regeneration |
Q34579328 | Epithelial Wnt/β-catenin signaling regulates palatal shelf fusion through regulation of Tgfβ3 expression |
Q36690919 | Epithelial stem cells: turning over new leaves |
Q39437645 | Essential roles of fibronectin in the development of the left-right embryonic body plan |
Q33429012 | Estradiol activates beta-catenin dependent transcription in neurons |
Q34335928 | Estrogen leads to reversible hair cycle retardation through inducing premature catagen and maintaining telogen |
Q36678664 | Evaluation of the current knowledge limitations in breast cancer research: a gap analysis |
Q41825988 | Evidence for an early role for BMP4 signaling in thymus and parathyroid morphogenesis |
Q42775592 | Experimental myocardial infarction triggers canonical Wnt signaling and endothelial-to-mesenchymal transition |
Q53561362 | Expression of Wnt/β-catenin signaling, stem-cell markers and proliferating cell markers in rat whisker hair follicles. |
Q36919874 | Expression of Wnt9b and activation of canonical Wnt signaling during midfacial morphogenesis in mice |
Q37352900 | Expression of Wnts in the developing murine secondary palate |
Q35190520 | Expression patterns of astrocyte elevated gene-1 (AEG-1) during development of the mouse embryo |
Q37170606 | FGF-regulated BMP signaling is required for eyelid closure and to specify conjunctival epithelial cell fate |
Q34422788 | FGF10 controls the patterning of the tracheal cartilage rings via Shh. |
Q24641842 | FOXC2 controls formation and maturation of lymphatic collecting vessels through cooperation with NFATc1 |
Q28593038 | Fgf10 dosage is critical for the amplification of epithelial cell progenitors and for the formation of multiple mesenchymal lineages during lung development |
Q36660211 | Fgf20 governs formation of primary and secondary dermal condensations in developing hair follicles |
Q36387418 | Fibroblast growth factor 10 is critical for liver growth during embryogenesis and controls hepatoblast survival via beta-catenin activation |
Q47113121 | Follicular Cell Implantation: An Emerging Cell Therapy for Hair Loss. |
Q30890395 | Forensic hair analysis to identify animal species on a case of pet animal abuse |
Q28509325 | Formation and differentiation of multiple mesenchymal lineages during lung development is regulated by beta-catenin signaling |
Q36277296 | Foxm1 mediates cross talk between Kras/mitogen-activated protein kinase and canonical Wnt pathways during development of respiratory epithelium |
Q57177200 | Foxn1 in Skin Development, Homeostasis and Wound Healing |
Q35978882 | Function of Wnt/β-catenin in counteracting Tcf3 repression through the Tcf3-β-catenin interaction |
Q28512924 | GATA-3: an unexpected regulator of cell lineage determination in skin |
Q34374129 | GSK3 takes centre stage more than 20 years after its discovery |
Q39138179 | Gata6 promotes hair follicle progenitor cell renewal by genome maintenance during proliferation |
Q37381860 | Gene Expression Architecture of Mouse Dorsal and Tail Skin Reveals Functional Differences in Inflammation and Cancer. |
Q28594537 | Generation of mice with a conditional null allele for Wntless |
Q34318169 | Genetic interplays between Msx2 and Foxn1 are required for Notch1 expression and hair shaft differentiation |
Q24307581 | Glucagon-like peptide-1 activation of TCF7L2-dependent Wnt signaling enhances pancreatic beta cell proliferation |
Q30362607 | Glycogen synthase kinase-3beta haploinsufficiency mimics the behavioral and molecular effects of lithium |
Q34753930 | Gsk3β is required in the epithelium for palatal elevation in mice |
Q35187105 | Gsα enhances commitment of mesenchymal progenitors to the osteoblast lineage but restrains osteoblast differentiation in mice. |
Q42468016 | Hair follicle morphogenesis and epidermal homeostasis in we/we wal/wal mice with postnatal alopecia. |
Q38968636 | Hair follicle stem cell proliferation, Akt and Wnt signaling activation in TPA-induced hair regeneration. |
Q33595234 | Hairless is a nuclear receptor corepressor essential for skin function |
Q34078641 | Hairless triggers reactivation of hair growth by promoting Wnt signaling |
Q38039734 | Hairy tale of signaling in hair follicle development and cycling |
Q35859575 | Heavy Metal Ion Regulation of Gene Expression: MECHANISMS BY WHICH LEAD INHIBITS OSTEOBLASTIC BONE-FORMING ACTIVITY THROUGH MODULATION OF THE Wnt/β-CATENIN SIGNALING PATHWAY. |
Q35080487 | Hedgehog modulates cell cycle regulators in stem cells to control hematopoietic regeneration |
Q41814485 | Hematopoietic stem cell development requires transient Wnt/β-catenin activity |
Q35025268 | Hmgb3 regulates the balance between hematopoietic stem cell self-renewal and differentiation |
Q37992833 | Home sweet home: skin stem cell niches |
Q36752936 | Hopx expression defines a subset of multipotent hair follicle stem cells and a progenitor population primed to give rise to K6+ niche cells |
Q52105638 | Hox in hair growth and development |
Q36462558 | Hoxc8 initiates an ectopic mammary program by regulating Fgf10 and Tbx3 expression and Wnt/β-catenin signaling |
Q24791466 | Hyperactive Wnt signaling changes the developmental potential of embryonic lung endoderm |
Q49791135 | Id2 determines intestinal identity through repression of the foregut transcription factor, Irx5. |
Q34466213 | Identification and dissection of an enhancer controlling epithelial gene expression in skin |
Q28506100 | Impaired Wnt-beta-catenin signaling disrupts adult renal homeostasis and leads to cystic kidney ciliopathy |
Q35661164 | In vivo mechanical loading rapidly activates β-catenin signaling in osteocytes through a prostaglandin mediated mechanism |
Q90474945 | In-Vivo Nucleus Pulposus-Specific Regulation of Adult Murine Intervertebral Disc Degeneration via Wnt/Beta-Catenin Signaling |
Q24620091 | Indian hedgehog and beta-catenin signaling: role in the sebaceous lineage of normal and neoplastic mammalian epidermis |
Q24595260 | Inhibition of Bmp signaling affects growth and differentiation in the anagen hair follicle |
Q51901609 | Inhibition of Wnt signaling by Wise (Sostdc1) and negative feedback from Shh controls tooth number and patterning. |
Q36299831 | Inhibition of Wnt/β-catenin pathway promotes regenerative repair of cutaneous and cartilage injury. |
Q35041009 | Inhibition of beta-catenin signaling by Pb leads to incomplete fracture healing |
Q37085648 | Inhibition of beta-catenin signaling causes defects in postnatal cartilage development |
Q30480583 | Integrin-linked kinase is required for epidermal and hair follicle morphogenesis |
Q44980229 | Interactions between FGF and Wnt signals and Tbx3 gene expression in mammary gland initiation in mouse embryos |
Q34770625 | Intervertebral disc development is regulated by Wnt/β-catenin signaling |
Q24791486 | Intestine in the lung |
Q36796873 | Intra-epithelial requirement of canonical Wnt signaling for tooth morphogenesis |
Q36952062 | Investigating molecular mechanisms of embryonic mammary gland development by bead-implantation in embryonic flank explant cultures - a protocol |
Q46292185 | Investigating tonic Wnt signaling throughout the adult CNS and in the hippocampal neurogenic niche of BatGal and ins-TopGal mice |
Q42205603 | Investigation of Frizzled-5 during embryonic neural development in mouse |
Q43375935 | Involvement of WNT Signaling in the Regulation of Gestational Age-Dependent Umbilical Cord-Derived Mesenchymal Stem Cell Proliferation. |
Q34341443 | Involvement of Wnt, Eda and Shh at defined stages of sweat gland development |
Q37698545 | In vivo transcriptional governance of hair follicle stem cells by canonical Wnt regulators |
Q42712637 | Isolated lymphoid follicles in colon: switch points between inflammation and colorectal cancer? |
Q28910190 | Kindlin-1 controls Wnt and TGF-β availability to regulate cutaneous stem cell proliferation |
Q34624546 | Klotho inhibits transforming growth factor-beta1 (TGF-beta1) signaling and suppresses renal fibrosis and cancer metastasis in mice |
Q35001290 | LEF1 identifies androgen-independent epithelium in the developing prostate |
Q21560941 | LGR5 is a negative regulator of tumourigenicity, antagonizes Wnt signalling and regulates cell adhesion in colorectal cancer cell lines |
Q28259213 | Lack of plakoglobin in epidermis leads to keratoderma |
Q28506843 | Laminin-511 is an epithelial message promoting dermal papilla development and function during early hair morphogenesis |
Q36800919 | Lef1 contributes to the differentiation of bulge stem cells by nuclear translocation and cross-talk with the Notch signaling pathway |
Q34663671 | Lentiviral-mediated transgene expression can potentiate intestinal mesenchymal-epithelial signaling. |
Q33793283 | Lhx2 differentially regulates Sox9, Tcf4 and Lgr5 in hair follicle stem cells to promote epidermal regeneration after injury |
Q36688765 | Lhx2 maintains stem cell character in hair follicles |
Q90384306 | Lineage-Specific Wnt Reporter Elucidates Mesenchymal Wnt Signaling during Bone Repair |
Q36713589 | Links between signal transduction, transcription and adhesion in epithelial bud development |
Q35653124 | Load/strain distribution between ulna and radius in the mouse forearm compression loading model |
Q30558570 | Local Dkk1 crosstalk from breeding ornaments impedes regeneration of injured male zebrafish fins. |
Q37124573 | Localized Fgf10 expression is not required for lung branching morphogenesis but prevents differentiation of epithelial progenitors |
Q35435068 | Loss-of-function of ACVR1 in osteoblasts increases bone mass and activates canonical Wnt signaling through suppression of Wnt inhibitors SOST and DKK1. |
Q39490738 | Lrp4 and Wise interplay controls the formation and patterning of mammary and other skin appendage placodes by modulating Wnt signaling |
Q37381682 | Macrophage migration inhibitory factor promotes proliferation and neuronal differentiation of neural stem/precursor cells through Wnt/β-catenin signal pathway |
Q30415959 | Making sense of Wnt signaling-linking hair cell regeneration to development |
Q35050344 | Mammary cells with active Wnt signaling resist ErbB2-induced tumorigenesis |
Q33735595 | Mammary development and breast cancer: the role of stem cells |
Q29619814 | Mapping Wnt/beta-catenin signaling during mouse development and in colorectal tumors |
Q26824956 | Mesenchymal-epithelial interactions during hair follicle morphogenesis and cycling |
Q35669707 | Mice cloned from skin cells |
Q38539859 | MicroRNAs (miRNAs) in the control of HF development and cycling: the next frontiers in hair research |
Q27021818 | Mitotic and mitogenic Wnt signalling |
Q64261434 | Modeling Edar expression reveals the hidden dynamics of tooth signaling center patterning |
Q49805610 | Modeling the Role of Wnt Signaling in Human and Drosophila Stem Cells. |
Q24815112 | Molecular dissection of mesenchymal-epithelial interactions in the hair follicle |
Q28729265 | Molecular organization and timing of Wnt1 expression define cohorts of midbrain dopamine neuron progenitors in vivo |
Q41855870 | Monitoring Wnt/β-Catenin Signaling in Skin |
Q37216344 | Mouse R-spondin2 is required for apical ectodermal ridge maintenance in the hindlimb |
Q34632384 | Mouse Tenm4 is required for mesoderm induction |
Q36761867 | Msx2 exerts bone anabolism via canonical Wnt signaling |
Q42717983 | Msx2 promotes cardiovascular calcification by activating paracrine Wnt signals |
Q39969977 | Multi-potentiality of a new immortalized epithelial stem cell line derived from human hair follicles |
Q38685435 | Multiple modes of Lrp4 function in modulation of Wnt/β-catenin signaling during tooth development. |
Q41851264 | Multiple roles for HOXA3 in regulating thymus and parathyroid differentiation and morphogenesis in mouse |
Q47674940 | Myc cooperates with β-catenin to drive gene expression in nephron progenitor cells. |
Q42948857 | Mycophenolate antagonizes IFN-γ-induced catagen-like changes via β-catenin activation in human dermal papilla cells and hair follicles. |
Q37325961 | Nas transgenic mouse line allows visualization of Notch pathway activity in vivo. |
Q33604836 | Neural Wiskott-Aldrich syndrome protein modulates Wnt signaling and is required for hair follicle cycling in mice |
Q36321576 | Neural crest stem cell maintenance by combinatorial Wnt and BMP signaling |
Q90677927 | Neuropsin (OPN5) Mediates Local Light-Dependent Induction of Circadian Clock Genes and Circadian Photoentrainment in Exposed Murine Skin |
Q35229097 | Neutrophil transmigration triggers repair of the lung epithelium via beta-catenin signaling. |
Q26823824 | New insight into the mechanisms underlying the function of the incretin hormone glucagon-like peptide-1 in pancreatic β-cells: the involvement of the Wnt signaling pathway effector β-catenin |
Q35858253 | Next stop, the twilight zone: hedgehog network regulation of mammary gland development |
Q34341676 | Nkx2-5 regulates cardiac growth through modulation of Wnt signaling by R-spondin3 |
Q30675556 | Non-contact strain measurement in the mouse forearm loading model using digital image correlation (DIC) |
Q33462524 | Nonthermal atmospheric pressure plasma enhances mouse limb bud survival, growth, and elongation |
Q35226585 | Normal and abnormal epithelial differentiation in the female reproductive tract. |
Q47138802 | Novel insights into the pathways regulating the canine hair cycle and their deregulation in alopecia X. |
Q42114886 | Nuclear Factor I-C Regulates TGF-β-dependent Hair Follicle Cycling* |
Q35684848 | Nuclear β-catenin is increased in systemic sclerosis pulmonary fibrosis and promotes lung fibroblast migration and proliferation |
Q42033503 | Obligatory participation of macrophages in an angiopoietin 2-mediated cell death switch |
Q28593311 | Ocular coloboma and dorsoventral neuroretinal patterning defects in Lrp6 mutant eyes |
Q42740079 | Ontogeny and Homeostasis of Adult Epithelial Skin Stem Cells |
Q33236624 | Optic cup and facial patterning defects in ocular ectoderm beta-catenin gain-of-function mice |
Q36595560 | Osteocytes, mechanosensing and Wnt signaling |
Q30503629 | Otic ablation of smoothened reveals direct and indirect requirements for Hedgehog signaling in inner ear development |
Q36112948 | Overview of genetic tools and techniques to study Notch signaling in mice. |
Q41130183 | PCDH24-induced contact inhibition involves downregulation of beta-catenin signaling |
Q37263731 | PKA inhibits WNT signalling in adrenal cortex zonation and prevents malignant tumour development |
Q35064196 | Paneth cell marker expression in intestinal villi and colon crypts characterizes dietary induced risk for mouse sporadic intestinal cancer |
Q35484934 | Parabronchial smooth muscle constitutes an airway epithelial stem cell niche in the mouse lung after injury |
Q36340155 | Parathyroid hormone-related protein activates Wnt signaling to specify the embryonic mammary mesenchyme |
Q36359286 | Partial promoter substitutions generating transcriptional sentinels of diverse signaling pathways in embryonic stem cells and mice |
Q30496391 | Patterning by heritage in mouse molar row development |
Q33393402 | Patterning of palatal rugae through sequential addition reveals an anterior/posterior boundary in palatal development |
Q64974008 | Peroxisome Proliferator-Activated Receptor-γ Knockdown Impairs Bone Morphogenetic Protein-2-Induced Critical-Size Bone Defect Repair. |
Q34170531 | Pinin modulates expression of an intestinal homeobox gene, Cdx2, and plays an essential role for small intestinal morphogenesis |
Q28586689 | Pitx2 regulates cardiac left-right asymmetry by patterning second cardiac lineage-derived myocardium |
Q36077325 | Polycomb-Mediated Repression and Sonic Hedgehog Signaling Interact to Regulate Merkel Cell Specification during Skin Development |
Q64286282 | Possible Contribution of Wnt-Responsive Chondroprogenitors to the Postnatal Murine Growth Plate |
Q35282985 | Post-natal effect of overexpressed DKK1 on mandibular molar formation |
Q36952066 | Prenatal morphogenesis of mammary glands in mouse and rabbit |
Q37036226 | Primary cilia maintain corneal epithelial homeostasis by regulation of the Notch signaling pathway |
Q28550463 | Protein O-Glucosyltransferase 1 (POGLUT1) Promotes Mouse Gastrulation through Modification of the Apical Polarity Protein CRUMBS2 |
Q34932642 | R-Spondin1 protects mice from chemotherapy or radiation-induced oral mucositis through the canonical Wnt/beta-catenin pathway |
Q37174807 | RNAi screens in mice identify physiological regulators of oncogenic growth |
Q36666693 | Rac1 activation controls nuclear localization of beta-catenin during canonical Wnt signaling. |
Q44662531 | Rac1 modulates mammalian lung branching morphogenesis in part through canonical Wnt signaling |
Q28586747 | Reciprocal requirements for EDA/EDAR/NF-kappaB and Wnt/beta-catenin signaling pathways in hair follicle induction |
Q38142568 | Regenerating the skin: a task for the heterogeneous stem cell pool and surrounding niche |
Q89514224 | Regeneration of skin appendages and nerves: current status and further challenges |
Q35941330 | Regional Fluctuation in the Functional Consequence of LINE-1 Insertion in the Mitf Gene: The Black Spotting Phenotype Arisen from the Mitfmi-bw Mouse Lacking Melanocytes |
Q37351025 | Regulation of trachebronchial tissue-specific stem cell pool size |
Q33865835 | Replicating adenoviruses that target tumors with constitutive activation of the wnt signaling pathway |
Q28586947 | Repression of Nanog gene transcription by Tcf3 limits embryonic stem cell self-renewal |
Q28246772 | Restrictive loss of plakoglobin in cardiomyocytes leads to arrhythmogenic cardiomyopathy |
Q33712611 | Retinoic acid signaling in perioptic mesenchyme represses Wnt signaling via induction of Pitx2 and Dkk2 |
Q28395832 | Roles for β-catenin and doxycycline in the regulation of respiratory epithelial cell frequency and function |
Q28590882 | Runx1 modulates adult hair follicle stem cell emergence and maintenance from distinct embryonic skin compartments |
Q37418536 | Runx2 and bone morphogenic protein 2 regulate the expression of an alternative Lef1 transcript during osteoblast maturation |
Q34855927 | SMAD4-mediated WNT signaling controls the fate of cranial neural crest cells during tooth morphogenesis |
Q24647707 | Scratching the surface of skin development |
Q36602402 | Secreted frizzled-related protein 3 regulates activity-dependent adult hippocampal neurogenesis |
Q36108383 | Self-renewing diploid Axin2(+) cells fuel homeostatic renewal of the liver |
Q36301662 | Separate and distinctive roles for Wnt5a in tongue, lingual tissue and taste papilla development |
Q27312464 | Sfrp controls apicobasal polarity and oriented cell division in developing gut epithelium |
Q37351698 | Sfrp1 and Sfrp2 are not involved in Wnt/β-catenin signal silencing during lens induction but are required for maintenance of Wnt/β-catenin signaling in lens epithelial cells |
Q24816701 | Sgk3 links growth factor signaling to maintenance of progenitor cells in the hair follicle |
Q39892897 | Signaling Networks among Stem Cell Precursors, Transit-Amplifying Progenitors, and their Niche in Developing Hair Follicles. |
Q37535695 | Signaling involved in hair follicle morphogenesis and development |
Q28275914 | Skin shedding and tissue regeneration in African spiny mice (Acomys) |
Q36404865 | Skin stem cells: rising to the surface |
Q91739345 | Skin transcriptome profiling of Changthangi goats highlights the relevance of genes involved in Pashmina production |
Q36056415 | Soluble epoxide hydrolase regulates hematopoietic progenitor cell function via generation of fatty acid diols |
Q37652779 | Somatic stem cell heterogeneity: diversity in the blood, skin and intestinal stem cell compartments |
Q41397974 | Sox2 in the dermal papilla niche controls hair growth by fine-tuning BMP signaling in differentiating hair shaft progenitors |
Q28584894 | Sox2 is required for development of taste bud sensory cells |
Q36948830 | Sox2+ stem cells contribute to all epithelial lineages of the tooth via Sfrp5+ progenitors |
Q41558641 | Spatial and temporal expression of molecular markers and cell signals during normal development of the mouse patellar tendon |
Q37677008 | Spatiotemporal antagonism in mesenchymal-epithelial signaling in sweat versus hair fate decision |
Q42457488 | Stabilized beta-catenin in lung epithelial cells changes cell fate and leads to tracheal and bronchial polyposis |
Q34393703 | Stem cell dynamics in the hair follicle niche |
Q36943373 | Stem cells and TCF proteins: a role for beta-catenin--independent functions |
Q35571486 | Stem cells for skin tissue engineering and wound healing |
Q34582093 | Stem cells of the skin epithelium |
Q41891219 | Stromal cell-derived factor-1 promotes survival of pancreatic beta cells by the stabilisation of beta-catenin and activation of transcription factor 7-like 2 (TCF7L2). |
Q33611142 | Stromal transforming growth factor-beta signaling mediates prostatic response to androgen ablation by paracrine Wnt activity |
Q39741986 | Suppression of Wnt signaling by Dkk1 attenuates PTH-mediated stromal cell response and new bone formation |
Q33708229 | TCF7L1 promotes skin tumorigenesis independently of β-catenin through induction of LCN2. |
Q33701577 | TIEG1 modulates β-catenin sub-cellular localization and enhances Wnt signaling in bone |
Q37497352 | Targeted disruption of the protein kinase SGK3/CISK impairs postnatal hair follicle development |
Q37597645 | Tbx20 acts upstream of Wnt signaling to regulate endocardial cushion formation and valve remodeling during mouse cardiogenesis |
Q35079614 | Tcf3 and Lef1 regulate lineage differentiation of multipotent stem cells in skin. |
Q28591794 | Tcf3 and Tcf4 are essential for long-term homeostasis of skin epithelia |
Q34341321 | Tcf3 expression marks both stem and progenitor cells in multiple epithelia |
Q33736914 | Tcf3 promotes cell migration and wound repair through regulation of lipocalin 2. |
Q38533900 | Tcf7l1 is required for spinal cord progenitor maintenance |
Q50033429 | Temporal Layering of Signaling Effectors Drives Chromatin Remodeling during Hair Follicle Stem Cell Lineage Progression. |
Q37453525 | The Hair Growth-Promoting Effect of Rumex japonicus Houtt. Extract. |
Q34027866 | The LEF1/beta -catenin complex activates movo1, a mouse homolog of Drosophila ovo required for epidermal appendage differentiation |
Q30540974 | The Meckel syndrome protein meckelin (TMEM67) is a key regulator of cilia function but is not required for tissue planar polarity. |
Q27021525 | The R-spondin protein family |
Q39155089 | The T-box transcription factor Eomesodermin is essential for AVE induction in the mouse embryo |
Q92339564 | The Wave complex controls epidermal morphogenesis and proliferation by suppressing Wnt-Sox9 signaling |
Q28505604 | The Wnt receptor, Lrp5, is expressed by mouse mammary stem cells and is required to maintain the basal lineage |
Q39281127 | The Wnt signaling pathway effector TCF7L2 is upregulated by insulin and represses hepatic gluconeogenesis |
Q37202364 | The a"MAZE"ing world of lung-specific transgenic mice. |
Q33781347 | The aging mouse partially models the aging human spine: lumbar and coccygeal disc height, composition, mechanical properties, and Wnt signaling in young and old mice |
Q89865196 | The aging skin microenvironment dictates stem cell behavior |
Q34159158 | The canonical Wnt signaling activator, R-spondin2, regulates craniofacial patterning and morphogenesis within the branchial arch through ectodermal-mesenchymal interaction |
Q27302956 | The cochlear sensory epithelium derives from Wnt responsive cells in the dorsomedial otic cup |
Q35088148 | The critical roles of serum/glucocorticoid-regulated kinase 3 (SGK3) in the hair follicle morphogenesis and homeostasis: the allelic difference provides novel insights into hair follicle biology |
Q35054504 | The emerging face of primary cilia |
Q36515479 | The evolving roles of canonical WNT signaling in stem cells and tumorigenesis: implications in targeted cancer therapies |
Q58713924 | The inconsistent regulation of HOXC13 on different keratins and the regulation mechanism on HOXC13 in cashmere goat (Capra hircus) |
Q35089503 | The inductive role of Wnt-β-Catenin signaling in the formation of oral apparatus |
Q36309053 | The involvement of the wnt signaling pathway and TCF7L2 in diabetes mellitus: The current understanding, dispute, and perspective |
Q37852897 | The lens: a classical model of embryonic induction providing new insights into cell determination in early development |
Q24293633 | The linear ubiquitin-specific deubiquitinase gumby regulates angiogenesis |
Q34000983 | The mammary bud as a skin appendage: unique and shared aspects of development |
Q26865781 | The many faces and functions of β-catenin |
Q37532129 | The possible role of isolated lymphoid follicles in colonic mucosal repair |
Q28511400 | The role of Axin2 in calvarial morphogenesis and craniosynostosis |
Q36193707 | The role of the Wnt signaling pathway in incretin hormone production and function |
Q36731651 | The transcription factors c-rel and RelA control epidermal development and homeostasis in embryonic and adult skin via distinct mechanisms. |
Q36539705 | The tumor suppressor PTEN and the PDK1 kinase regulate formation of the columnar neural epithelium |
Q33316045 | The vitamin D receptor is a Wnt effector that controls hair follicle differentiation and specifies tumor type in adult epidermis |
Q28247148 | The vitamin D receptor is required for activation of cWnt and hedgehog signaling in keratinocytes |
Q47180702 | Therapeutic targeting of oncogenic transcription factors by natural products in eye cancer. |
Q34276643 | Three decades of Wnts: a personal perspective on how a scientific field developed |
Q26778749 | Tissue patterning and cellular mechanics |
Q28589704 | Tissue-specific requirements of beta-catenin in external genitalia development |
Q35008320 | Tissue-specific roles of Axin2 in the inhibition and activation of Wnt signaling in the mouse embryo |
Q33722825 | To beta or not to beta: canonical beta-catenin signaling pathway and ovarian development |
Q28730162 | Transcript profiling identifies dynamic gene expression patterns and an important role for Nrf2/Keap1 pathway in the developing mouse esophagus |
Q36269064 | Transcription Factor CTIP2 Maintains Hair Follicle Stem Cell Pool and Contributes to Altered Expression of LHX2 and NFATC1 |
Q33356256 | Transcriptional profiling of putative human epithelial stem cells |
Q37113911 | Transforming growth factor-beta stimulates cyclin D1 expression through activation of beta-catenin signaling in chondrocytes |
Q50622869 | Transgenic flash mice for in vivo quantitative monitoring of canonical Wnt signaling to track hair follicle cycle dynamics. |
Q37248343 | Transient Inhibition of FGFR2b-ligands signaling leads to irreversible loss of cellular β-catenin organization and signaling in AER during mouse limb development |
Q50150344 | Transient activation of Wnt/β-catenin signaling reporter in fibrotic scar formation after compression spinal cord injury in adult mice. |
Q35965329 | Transient activation of beta -catenin signaling in cutaneous keratinocytes is sufficient to trigger the active growth phase of the hair cycle in mice. |
Q35595485 | Trps1 activates a network of secreted Wnt inhibitors and transcription factors crucial to vibrissa follicle morphogenesis |
Q28298678 | Unlimited in vitro expansion of adult bi-potent pancreas progenitors through the Lgr5/R-spondin axis |
Q37777092 | Unveiling Hair Follicle Stem Cells |
Q28482239 | Valproic acid induces hair regeneration in murine model and activates alkaline phosphatase activity in human dermal papilla cells |
Q30477778 | Visualizing canonical Wnt signaling during mouse craniofacial development |
Q35839632 | Vitamin D receptor is essential for normal keratinocyte stem cell function |
Q30750471 | WNT-SHH Antagonism Specifies and Expands Stem Cells prior to Niche Formation |
Q24650922 | WNT1-inducible signaling protein-1 mediates pulmonary fibrosis in mice and is upregulated in humans with idiopathic pulmonary fibrosis |
Q33786543 | WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation |
Q41901057 | WNT7B promotes bone formation in part through mTORC1. |
Q28511517 | WNT7b mediates macrophage-induced programmed cell death in patterning of the vasculature |
Q33666778 | WT1 regulates the development of the posterior taste field |
Q47699592 | Wnt Signaling in Kidney Development and Disease. |
Q34037153 | Wnt activation in nail epithelium couples nail growth to digit regeneration. |
Q35156225 | Wnt inhibitors Dkk1 and Sost are downstream targets of BMP signaling through the type IA receptor (BMPRIA) in osteoblasts. |
Q41567458 | Wnt ligand presentation and reception: from the stem cell niche to tissue engineering. |
Q34119907 | Wnt ligand/Frizzled 2 receptor signaling regulates tube shape and branch-point formation in the lung through control of epithelial cell shape |
Q35157491 | Wnt ligands from the embryonic surface ectoderm regulate 'bimetallic strip' optic cup morphogenesis in mouse |
Q36991705 | Wnt pathway in pulmonary fibrosis in the bleomycin mouse model |
Q35858238 | Wnt proteins in mammary development and cancer |
Q35111651 | Wnt signaling and pulmonary fibrosis |
Q42652916 | Wnt signaling in gut organogenesis |
Q28586329 | Wnt signaling in heart valve development and osteogenic gene induction |
Q37080180 | Wnt signaling in lung organogenesis |
Q36555217 | Wnt signaling in skin development, homeostasis, and disease |
Q34346883 | Wnt signaling in the niche enforces hematopoietic stem cell quiescence and is necessary to preserve self-renewal in vivo. |
Q25257722 | Wnt signaling induces epithelial differentiation during cutaneous wound healing |
Q28594655 | Wnt signaling interacts with Shh to regulate taste papilla development |
Q35193923 | Wnt signaling maintains the hair-inducing activity of the dermal papilla |
Q42546329 | Wnt signaling mediates pathological vascular growth in proliferative retinopathy |
Q34578573 | Wnt signaling promotes regeneration in the retina of adult mammals. |
Q24653563 | Wnt signaling: the good and the bad |
Q33917414 | Wnt some lose some: transcriptional governance of stem cells by Wnt/β-catenin signaling |
Q24319714 | Wnt-5a inhibits the canonical Wnt pathway by promoting GSK-3-independent beta-catenin degradation |
Q28591489 | Wnt-dependent regulation of inner ear morphogenesis is balanced by the opposing and supporting roles of Shh. |
Q35197379 | Wnt-inhibitory factor 1 dysregulation of the bone marrow niche exhausts hematopoietic stem cells |
Q37032393 | Wnt-pathway activation during the early stage of neurodegeneration in FTDP-17 mice |
Q33389500 | Wnt-reporter expression pattern in the mouse intestine during homeostasis |
Q38105461 | Wnt-signalling in the embryonic mammary gland |
Q36943968 | Wnt/Frizzled family members mediate olfactory sensory neuron axon extension |
Q37318020 | Wnt/Rspondin/β-catenin signals control axonal sorting and lineage progression in Schwann cell development |
Q36323709 | Wnt/Tcf1 pathway restricts embryonic stem cell cycle through activation of the Ink4/Arf locus |
Q33581270 | Wnt/beta-catenin and retinoic acid receptor signaling pathways interact to regulate chondrocyte function and matrix turnover |
Q39748866 | Wnt/beta-catenin signaling directs multiple stages of tooth morphogenesis |
Q28510414 | Wnt/beta-catenin signaling is sufficient and necessary for synovial joint formation |
Q41954082 | Wnt/beta-catenin signaling plays an essential role in activation of odontogenic mesenchyme during early tooth development |
Q30479587 | Wnt/beta-catenin signaling promotes expansion of Isl-1-positive cardiac progenitor cells through regulation of FGF signaling |
Q38874087 | Wnt/β-catenin pathway in tissue injury: roles in pathology and therapeutic opportunities for regeneration |
Q28507052 | Wnt/β-catenin signaling in dermal condensates is required for hair follicle formation |
Q34382103 | Wnt/β-catenin signaling in the dental mesenchyme regulates incisor development by regulating Bmp4 |
Q35647471 | Wnt/β-catenin signaling is differentially regulated by Gα proteins and contributes to fibrous dysplasia |
Q42050708 | Wnt1 expression temporally allocates upper rhombic lip progenitors and defines their terminal cell fate in the cerebellum |
Q34232889 | Wnt1/βcatenin injury response activates the epicardium and cardiac fibroblasts to promote cardiac repair. |
Q34484392 | Wnt11 promotes cardiomyocyte development by caspase-mediated suppression of canonical Wnt signals |
Q35842633 | Wnt3a regulates Lef-1 expression during airway submucosal gland morphogenesis. |
Q34491576 | Wnt4 is essential to normal mammalian lung development |
Q28510199 | Wnt5a and Wnt11 regulate mammalian anterior-posterior axis elongation |
Q34286592 | Wnt5a can both activate and repress Wnt/β-catenin signaling during mouse embryonic development |
Q36002416 | Wnt5a inhibits canonical Wnt signaling in hematopoietic stem cells and enhances repopulation |
Q28584757 | Wnt5a is essential for intestinal elongation in mice |
Q37381865 | Wnt5a mediates nerve growth factor-dependent axonal branching and growth in developing sympathetic neurons |
Q41490403 | Wnt5a regulates directional cell migration and cell proliferation via Ror2-mediated noncanonical pathway in mammalian palate development |
Q35431848 | Wnt7b is an important intrinsic regulator of hair follicle stem cell homeostasis and hair follicle cycling. |
Q35893650 | Wnt9b-dependent FGF signaling is crucial for outgrowth of the nasal and maxillary processes during upper jaw and lip development |
Q38056451 | Wound healing in development |
Q33811160 | Wounding the cornea to learn how it heals |
Q36271500 | Wt1 and β-catenin cooperatively regulate diaphragm development in the mouse |
Q41667526 | alphaE-catenin is not a significant regulator of beta-catenin signaling in the developing mammalian brain |
Q35143165 | beta-Catenin initiates tooth neogenesis in adult rodent incisors |
Q42641674 | beta-Catenin is not necessary for maintenance or repair of the bronchiolar epithelium |
Q36992952 | beta-Catenin protects the epidermis from mechanical stresses |
Q34068062 | beta-Catenin stabilization dysregulates mesenchymal cell proliferation, motility, and invasiveness and causes aggressive fibromatosis and hyperplastic cutaneous wounds |
Q33947497 | beta-catenin activity in the dermal papilla regulates morphogenesis and regeneration of hair |
Q39998628 | beta-catenin-dependent and -independent effects of DeltaN-plakoglobin on epidermal growth and differentiation. |
Q42854255 | miR-24 affects hair follicle morphogenesis targeting Tcf-3. |
Q92351765 | p120-catenin regulates WNT signaling and EMT in the mouse embryo |
Q36210483 | β-Catenin determines upper airway progenitor cell fate and preinvasive squamous lung cancer progression by modulating epithelial-mesenchymal transition |
Q33575146 | β-Catenin is required for hair-cell differentiation in the cochlea |
Q36398917 | β-Catenin signaling regulates temporally discrete phases of anterior taste bud development |
Q34353437 | β-catenin contributes to lung tumor development induced by EGFR mutations |
Q35070223 | β-catenin dosage is a critical determinant of tracheal basal cell fate determination |
Q37070081 | β-catenin in the alveolar epithelium protects from lung fibrosis after intratracheal bleomycin |
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