| P2093 | author name string | Rachel K Miller | |
| | Pierre D McCrea | |
| P2860 | cites work | LDL-receptor-related proteins in Wnt signal transduction | Q24290392 |
| | Wnt-4 activates the canonical beta-catenin-mediated Wnt pathway and binds Frizzled-6 CRD: functional implications of Wnt/beta-catenin activity in kidney epithelial cells | Q24299786 |
| | Perinatal lethality with kidney and pancreas defects in mice with a targetted Pkd1 mutation | Q24317412 |
| | Regulation of planar cell polarity by Smurf ubiquitin ligases | Q24317525 |
| | Signal transduction by the Wnt family of ligands | Q24530639 |
| | The planar polarity gene strabismus regulates convergent extension movements in Xenopus | Q24536211 |
| | The TAK1-NLK mitogen-activated protein kinase cascade functions in the Wnt-5a/Ca(2+) pathway to antagonize Wnt/beta-catenin signaling | Q24540545 |
| | Interaction between RGS7 and polycystin | Q24653605 |
| | Coactivation of Rac and Rho by Wnt/Frizzled signaling is required for vertebrate gastrulation | Q24672832 |
| | The ankyrin repeat protein Diversin recruits Casein kinase Iepsilon to the beta-catenin degradation complex and acts in both canonical Wnt and Wnt/JNK signaling | Q24673748 |
| | Hyperactive Wnt signaling changes the developmental potential of embryonic lung endoderm | Q24791466 |
| | Beta-catenin regulates expression of cyclin D1 in colon carcinoma cells | Q27860717 |
| | Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouse | Q28184694 |
| | Convergent extension: the molecular control of polarized cell movement during embryonic development | Q28204202 |
| | Wnt/Frizzled activation of Rho regulates vertebrate gastrulation and requires a novel Formin homology protein Daam1 | Q28214701 |
| | Disruption of scribble (Scrb1) causes severe neural tube defects in the circletail mouse | Q28218970 |
| | The role of RhoA in tissue polarity and Frizzled signalling | Q28238365 |
| | Maternal wnt11 activates the canonical wnt signaling pathway required for axis formation in Xenopus embryos | Q28242317 |
| | Diego and Prickle regulate Frizzled planar cell polarity signalling by competing for Dishevelled binding | Q28254777 |
| | Mutations affecting morphogenesis during gastrulation and tail formation in the zebrafish, Danio rerio | Q28302050 |
| | Evidence for a mitogenic effect of Wnt-1 in the developing mammalian central nervous system | Q72106566 |
| | Distinct functions of Rho and Rac are required for convergent extension during Xenopus gastrulation | Q73691283 |
| | Retinal axon misrouting at the optic chiasm in mice with neural tube closure defects | Q73912821 |
| | Expression patterns of Wnt genes in mouse gut development | Q74107411 |
| | Early development of polycystic kidney disease in transgenic mice expressing an activated mutant of the beta-catenin gene | Q74604719 |
| | Endothelial cell influence on dorsal root ganglion cell formation | Q75225152 |
| | Instructive role of Wnt/beta-catenin in sensory fate specification in neural crest stem cells | Q75236410 |
| | Axial elongation in the mouse and its retardation in homozygous looptail mice | Q76495195 |
| | Molecular regulation of pronephric development | Q77803712 |
| | A mitogen gradient of dorsal midline Wnts organizes growth in the CNS | Q77960718 |
| | Wnt5a is required for cardiac outflow tract septation in mice | Q80362379 |
| | Chick pulmonary Wnt5a directs airway and vascular tubulogenesis | Q80785633 |
| | Signals which build a tubule | Q81441570 |
| | Wnt signals mediate a fate decision between otic placode and epidermis | Q82444199 |
| | Wnt11-R, a protein closely related to mammalian Wnt11, is required for heart morphogenesis in Xenopus | Q28307143 |
| | Wnt5a functions in planar cell polarity regulation in mice | Q28505898 |
| | Wnt5a is required for proper mammary gland development and TGF-beta-mediated inhibition of ductal growth | Q28505930 |
| | Wnt7b stimulates embryonic lung growth by coordinately increasing the replication of epithelium and mesenchyme | Q28506294 |
| | Wnt/beta-catenin signaling regulates nephron induction during mouse kidney development | Q28506499 |
| | Induction of ureter branching as a response to Wnt-2b signaling during early kidney organogenesis | Q28506528 |
| | Dishevelled 2 is essential for cardiac outflow tract development, somite segmentation and neural tube closure | Q28507430 |
| | Modulation of morphogenesis by noncanonical Wnt signaling requires ATF/CREB family-mediated transcriptional activation of TGFbeta2 | Q28507487 |
| | Guidance of trunk neural crest migration requires neuropilin 2/semaphorin 3F signaling | Q28507757 |
| | Wnt-6 is expressed in the ureter bud and induces kidney tubule development in vitro | Q28507791 |
| | Canonical WNT signaling promotes mammary placode development and is essential for initiation of mammary gland morphogenesis | Q28508102 |
| | Epithelial transformation of metanephric mesenchyme in the developing kidney regulated by Wnt-4 | Q28508296 |
| | beta-Catenin is required for specification of proximal/distal cell fate during lung morphogenesis | Q28508592 |
| | Regulation of polarized extension and planar cell polarity in the cochlea by the vertebrate PCP pathway | Q28509023 |
| | Lef1 is required for the transition of Wnt signaling from mesenchymal to epithelial cells in the mouse embryonic mammary gland | Q28510734 |
| | Wnt9b plays a central role in the regulation of mesenchymal to epithelial transitions underlying organogenesis of the mammalian urogenital system | Q28511083 |
| | Independent functions and mechanisms for homeobox gene Barx1 in patterning mouse stomach and spleen | Q28511280 |
| | Murine dishevelled 3 functions in redundant pathways with dishevelled 1 and 2 in normal cardiac outflow tract, cochlea, and neural tube development | Q28511382 |
| | Beta-catenin is essential for pancreatic acinar but not islet development | Q28512693 |
| | Wnt5a is essential for intestinal elongation in mice | Q28584757 |
| | Neuropilin-mediated neural crest cell guidance is essential to organise sensory neurons into segmented dorsal root ganglia | Q28584790 |
| | Transcriptional profiling of Wnt4 mutant mouse kidneys identifies genes expressed during nephron formation | Q28585730 |
| | Ciliary proteins link basal body polarization to planar cell polarity regulation | Q28585995 |
| | The Wnt-1 (int-1) proto-oncogene is required for development of a large region of the mouse brain | Q28586297 |
| | Dishevelled genes mediate a conserved mammalian PCP pathway to regulate convergent extension during neurulation | Q28587130 |
| | Loss of Apc in vivo immediately perturbs Wnt signaling, differentiation, and migration | Q28587140 |
| | The stomach mesenchymal transcription factor Barx1 specifies gastric epithelial identity through inhibition of transient Wnt signaling | Q28587498 |
| | Vangl2 acts via RhoA signaling to regulate polarized cell movements during development of the proximal outflow tract | Q28587502 |
| | A Wnt7b-dependent pathway regulates the orientation of epithelial cell division and establishes the cortico-medullary axis of the mammalian kidney | Q28587526 |
| | Expression of Tcf/Lef and sFrp and localization of beta-catenin in the developing mouse lung | Q28587734 |
| | Canonical Wnt signaling functions in second heart field to promote right ventricular growth | Q28588651 |
| | The Wnt signaling receptor Lrp5 is required for mammary ductal stem cell activity and Wnt1-induced tumorigenesis | Q28589724 |
| | Beta-catenin directly regulates Islet1 expression in cardiovascular progenitors and is required for multiple aspects of cardiogenesis | Q28590588 |
| | Dishevelled controls apical docking and planar polarization of basal bodies in ciliated epithelial cells | Q30491381 |
| | Pulsed contractions of an actin-myosin network drive apical constriction | Q30493161 |
| | Wnt/Frizzled signaling controls C. elegans gastrulation by activating actomyosin contractility | Q30497437 |
| | The role of the polycystins in kidney development | Q33691019 |
| | Towards a molecular anatomy of the Xenopus pronephric kidney. | Q33759889 |
| | Side-branching in the mammary gland: the progesterone-Wnt connection. | Q33843842 |
| | Wnt signalling in mammalian development and cancer | Q33870394 |
| | Requirement of a neural tube signal for the differentiation of neural crest cells into dorsal root ganglia | Q43788176 |
| | Differentiation and maturation of zebrafish dorsal root and sympathetic ganglion neurons | Q43947348 |
| | Essential function of Wnt-4 for tubulogenesis in the Xenopus pronephric kidney. | Q44079507 |
| | Selective binding of lectins to embryonic chicken vasculature | Q44409385 |
| | beta-Catenin signals regulate cell growth and the balance between progenitor cell expansion and differentiation in the nervous system | Q44472635 |
| | Xenopus Dishevelled signaling regulates both neural and mesodermal convergent extension: parallel forces elongating the body axis. | Q45980748 |
| | Mesodermal Wnt2b signalling positively regulates liver specification. | Q45995605 |
| | Regulation of convergent extension in Xenopus by Wnt5a and Frizzled-8 is independent of the canonical Wnt pathway | Q46041157 |
| | Sensory nerves determine the pattern of arterial differentiation and blood vessel branching in the skin | Q46623662 |
| | Pancreas-specific deletion of beta-catenin reveals Wnt-dependent and Wnt-independent functions during development. | Q46708971 |
| | Drosophila Rho-associated kinase (Drok) links Frizzled-mediated planar cell polarity signaling to the actin cytoskeleton. | Q47070036 |
| | The ankyrin repeat protein Diego mediates Frizzled-dependent planar polarization | Q47070692 |
| | Patterned gene expression directs bipolar planar polarity in Drosophila | Q47071305 |
| | Control of tracheal tubulogenesis by Wingless signaling. | Q47072501 |
| | Dual roles of zygotic and maternal Scribble1 in neural migration and convergent extension movements in zebrafish embryos | Q47073230 |
| | Cystic kidney gene seahorse regulates cilia-mediated processes and Wnt pathways | Q47073543 |
| | Zebrafish Rho kinase 2 acts downstream of Wnt11 to mediate cell polarity and effective convergence and extension movements | Q47073597 |
| | A genetic screen in zebrafish identifies cilia genes as a principal cause of cystic kidney | Q47074132 |
| | Wnt signal transduction: more than one wat to skin a (beta-)cat? | Q47986655 |
| | The neural tube patterns vessels developmentally using the VEGF signaling pathway. | Q48005094 |
| | Wnt-10b directs hypermorphic development and transformation in mammary glands of male and female mice | Q48041933 |
| | JNK and ROKalpha function in the noncanonical Wnt/RhoA signaling pathway to regulate Xenopus convergent extension movements | Q48148721 |
| | Blood vessels form a scaffold for neuroblast migration in the adult olfactory bulb. | Q48151551 |
| | Role of beta-catenin in the developing cortical and hippocampal neuroepithelium | Q48155430 |
| | Expression of multiple novel Wnt-1/int-1-related genes during fetal and adult mouse development | Q48841883 |
| | Long-term time-lapse fluorescence imaging of developing zebrafish. | Q50647707 |
| | Progressive restriction of otic fate: the role of FGF and Wnt in resolving inner ear potential. | Q50776563 |
| | Imaging neural crest cell dynamics during formation of dorsal root ganglia and sympathetic ganglia. | Q50784026 |
| | Wnt7b regulates mesenchymal proliferation and vascular development in the lung. | Q51701912 |
| | Wnt11r is required for cranial neural crest migration. | Q51947640 |
| | GATA transcription factors integrate Wnt signalling during heart development. | Q51950738 |
| | DM-GRASP/ALCAM/CD166 is required for cardiac morphogenesis and maintenance of cardiac identity in first heart field derived cells. | Q51953129 |
| | Frizzled5/8 is required in secondary mesenchyme cells to initiate archenteron invagination during sea urchin development. | Q52029441 |
| | Expression pattern of Wnt signaling components in the adult intestine. | Q52042359 |
| | Dickkopf-1 (DKK1) reveals that fibronectin is a major target of Wnt signaling in branching morphogenesis of the mouse embryonic lung. | Q52061734 |
| | Identification of the mammary line in mouse by Wnt10b expression. | Q52094358 |
| | Wnt signaling during development of the gastrointestinal tract. | Q52102720 |
| | Nuclear signaling by Rac and Rho GTPases is required in the establishment of epithelial planar polarity in the Drosophila eye. | Q52165280 |
| | WNT11 promotes cardiac tissue formation of early mesoderm. | Q52174716 |
| | Wnt signalling required for expansion of neural crest and CNS progenitors. | Q52192233 |
| | Wnt-4 expression induces a pregnancy-like growth pattern in reconstituted mammary glands in virgin mice. | Q52206864 |
| | Hu neuronal proteins are expressed in proliferating neurogenic cells. | Q52219021 |
| | Wingless and its signalling pathway have common and separable functions during tracheal development. | Q52582885 |
| | From cilia to cyst. | Q55036761 |
| | Xwnt11 is a target of Xenopus Brachyury: regulation of gastrulation movements via Dishevelled, but not through the canonical Wnt pathway. | Q33898502 |
| | Wnt antagonism initiates cardiogenesis in Xenopus laevis | Q33931613 |
| | Seven Wnt homologues in Drosophila: a case study of the developing tracheae | Q33951975 |
| | Shaping the mammalian auditory sensory organ by the planar cell polarity pathway | Q34154050 |
| | Neurovascular congruence results from a shared patterning mechanism that utilizes Semaphorin3A and Neuropilin-1. | Q34181370 |
| | Crypt-restricted proliferation and commitment to the Paneth cell lineage following Apc loss in the mouse intestine. | Q34395279 |
| | Common mechanisms of nerve and blood vessel wiring | Q34433723 |
| | The developmental biology of Dishevelled: an enigmatic protein governing cell fate and cell polarity | Q34455099 |
| | Regulation of early lung morphogenesis: questions, facts and controversies | Q34513653 |
| | It takes guts: the Drosophila hindgut as a model system for organogenesis | Q34532395 |
| | Polycystic kidney disease: cell division without a c(l)ue? | Q34544069 |
| | Gene function in mouse embryogenesis: get set for gastrulation | Q34612511 |
| | Nodal flow and the generation of left-right asymmetry. | Q34652060 |
| | Phases of canonical Wnt signaling during the development of mouse intestinal epithelium | Q34660140 |
| | Non-canonical Wnt signaling in Xenopus: regulation of axis formation and gastrulation | Q34758581 |
| | Non-canonical Wnt signalling and regulation of gastrulation movements | Q34758596 |
| | Convergence and extension in vertebrate gastrulae: cell movements according to or in search of identity? | Q34783796 |
| | The Xenopus pronephros as a model system for the study of kidney development and pathophysiology. | Q34974054 |
| | Tube morphogenesis: making and shaping biological tubes | Q35044542 |
| | Tube or not tube: remodeling epithelial tissues by branching morphogenesis | Q35046568 |
| | Essential requirement for Wnt signaling in proliferation of adult small intestine and colon revealed by adenoviral expression of Dickkopf-1. | Q35122385 |
| | Developmental stage-specific biphasic roles of Wnt/beta-catenin signaling in cardiomyogenesis and hematopoiesis | Q35544524 |
| | Tube morphogenesis: closure, but many openings remain | Q35587483 |
| | Planar cell polarity genes and neural tube closure. | Q35639986 |
| | Wnt signaling regulates pancreatic beta cell proliferation | Q35741102 |
| | Biphasic role for Wnt/beta-catenin signaling in cardiac specification in zebrafish and embryonic stem cells | Q35808417 |
| | Canonical Wnt signaling is a positive regulator of mammalian cardiac progenitors | Q35865003 |
| | Making tubes in the Drosophila embryo | Q36042641 |
| | Prickle and Strabismus form a functional complex to generate a correct axis during planar cell polarity signaling | Q36065784 |
| | Epithelial morphogenesis | Q36093263 |
| | Wnt signaling through canonical and non-canonical pathways: recent progress | Q36194509 |
| | Morphogens in motion: growth control of the neural tube | Q36206016 |
| | Planar cell polarity and a potential role for a Wnt morphogen gradient in stereociliary bundle orientation in the mammalian inner ear. | Q36206053 |
| | Activities of the Wnt-1 class of secreted signaling factors are antagonized by the Wnt-5A class and by a dominant negative cadherin in early Xenopus development | Q36236916 |
| | Severe neural tube defects in the loop-tail mouse result from mutation of Lpp1, a novel gene involved in floor plate specification | Q28591062 |
| | A local Wnt-3a signal is required for development of the mammalian hippocampus | Q28591198 |
| | Wnt-dependent regulation of inner ear morphogenesis is balanced by the opposing and supporting roles of Shh. | Q28591489 |
| | Asymmetric localization of Vangl2 and Fz3 indicate novel mechanisms for planar cell polarity in mammals | Q28591957 |
| | Depletion of epithelial stem-cell compartments in the small intestine of mice lacking Tcf-4 | Q28592260 |
| | Effects of Wnt1 signaling on proliferation in the developing mid-/hindbrain region | Q28592616 |
| | Dynamic recruitment of axin by Dishevelled protein assemblies | Q28592772 |
| | Identification of Vangl2 and Scrb1 as planar polarity genes in mammals | Q28593071 |
| | The role of Frizzled3 and Frizzled6 in neural tube closure and in the planar polarity of inner-ear sensory hair cells | Q28593180 |
| | Wnt5a participates in distal lung morphogenesis | Q28593390 |
| | Essential function of Wnt-4 in mammary gland development downstream of progesterone signaling | Q28594185 |
| | Protein kinase C is differentially stimulated by Wnt and Frizzled homologs in a G-protein-dependent manner | Q28613361 |
| | Ca(2+)/calmodulin-dependent protein kinase II is stimulated by Wnt and Frizzled homologs and promotes ventral cell fates in Xenopus | Q28613481 |
| | Role of frizzled 7 in the regulation of convergent extension movements during gastrulation in Xenopus laevis | Q28613539 |
| | Dishevelled activates JNK and discriminates between JNK pathways in planar polarity and wingless signaling | Q28616347 |
| | Differential recruitment of Dishevelled provides signaling specificity in the planar cell polarity and Wingless signaling pathways | Q28616373 |
| | Planar cell polarity signaling: from fly development to human disease | Q28749129 |
| | Mechanisms of Wnt signaling in development | Q29547537 |
| | The vertebrate primary cilium in development, homeostasis, and disease | Q29614609 |
| | Inversin, the gene product mutated in nephronophthisis type II, functions as a molecular switch between Wnt signaling pathways | Q29614619 |
| | The cyclin D1 gene is a target of the beta-catenin/LEF-1 pathway | Q29615176 |
| | Many tumors induced by the mouse mammary tumor virus contain a provirus integrated in the same region of the host genome | Q29616165 |
| | A dual-kinase mechanism for Wnt co-receptor phosphorylation and activation | Q29618700 |
| | A series of normal stages in the development of the chick embryo. 1951 | Q29618726 |
| | A second canon. Functions and mechanisms of beta-catenin-independent Wnt signaling | Q29619294 |
| | Dishevelled controls cell polarity during Xenopus gastrulation | Q29619295 |
| | Silberblick/Wnt11 mediates convergent extension movements during zebrafish gastrulation | Q29619296 |
| | Mapping Wnt/beta-catenin signaling during mouse development and in colorectal tumors | Q29619814 |
| | In vivo imaging of embryonic vascular development using transgenic zebrafish | Q29619921 |
| | Mechanisms of convergence and extension by cell intercalation | Q30306607 |
| | The planar cell polarity gene strabismus regulates convergence and extension and neural fold closure in Xenopus | Q30309547 |
| | The genetic control of tissue polarity in Drosophila | Q30311367 |
| | Model systems for the study of kidney development: use of the pronephros in the analysis of organ induction and patterning | Q30428197 |
| | Cell migration during gastrulation | Q30437765 |
| | Roles for Rac1 and Cdc42 in planar polarization and hair outgrowth in the wing of Drosophila | Q30442177 |
| | Planar cell polarity signalling couples cell division and morphogenesis during neurulation. | Q30477078 |
| | Wnt/beta-catenin signaling promotes expansion of Isl-1-positive cardiac progenitor cells through regulation of FGF signaling | Q30479587 |
| | Zebrafish trilobite identifies new roles for Strabismus in gastrulation and neuronal movements. | Q30481137 |
| | Planar cell polarization: an emerging model points in the right direction | Q36280306 |
| | Delta N89 beta-catenin induces precocious development, differentiation, and neoplasia in mammary gland | Q36360340 |
| | Dishevelled activates Ca2+ flux, PKC, and CamKII in vertebrate embryos. | Q36381456 |
| | Vang-like 2 and noncanonical Wnt signaling in outflow tract development. | Q36394655 |
| | The left-right axis in the mouse: from origin to morphology | Q36467624 |
| | The role of Wnt signalling in cardiac development and tissue remodelling in the mature heart | Q36543886 |
| | Mechanisms of Disease: autosomal dominant and recessive polycystic kidney diseases | Q36577116 |
| | Planar cell polarity, ciliogenesis and neural tube defects | Q36599301 |
| | Planar cell polarity signaling: a common mechanism for cellular polarization. | Q36606892 |
| | Gastrulation: Wnts signal constriction. | Q36631009 |
| | The Scribble and Par complexes in polarity and migration: friends or foes? | Q36635733 |
| | Wnts as ligands: processing, secretion and reception | Q36672661 |
| | Multiplicity of the interactions of Wnt proteins and their receptors | Q36692201 |
| | Tissue/planar cell polarity in vertebrates: new insights and new questions | Q36720615 |
| | Intestinal morphogenesis | Q36724562 |
| | Molecular regulation of kidney development: is the answer blowing in the Wnt? | Q36842478 |
| | Zebrafish gastrulation: cell movements, signals, and mechanisms | Q36845712 |
| | Planar polarity and tissue morphogenesis | Q36851258 |
| | Wnt/beta-catenin signaling and cardiogenesis: timing does matter | Q36869551 |
| | Renal abnormalities and their developmental origin | Q36945522 |
| | The first steps towards hearing: mechanisms of otic placode induction. | Q36950097 |
| | Gastrulation in C. elegans | Q37020481 |
| | Wnt signaling in breast organogenesis | Q37080183 |
| | Wnt signaling: an essential regulator of cardiovascular differentiation, morphogenesis and progenitor self-renewal | Q37080793 |
| | Wnt/beta-catenin and noncanonical Wnt signaling interact in tissue evagination in the simple eumetazoan Hydra | Q37106903 |
| | Wnt/beta-catenin signaling: new (and old) players and new insights | Q37109729 |
| | Requirement of Wnt/beta-catenin signaling in pronephric kidney development | Q37197987 |
| | Loss of TGF-beta or Wnt5a results in an increase in Wnt/beta-catenin activity and redirects mammary tumour phenotype | Q37208778 |
| | Endothelial cells promote migration and proliferation of enteric neural crest cells via beta1 integrin signaling | Q37213009 |
| | Neurovascular congruence during cerebral cortical development | Q37220151 |
| | Regulated adhesion as a driving force of gastrulation movements | Q37308883 |
| | Primary cilia in planar cell polarity regulation of the inner ear | Q37369343 |
| | Wnt signaling pathways meet Rho GTPases. | Q37388913 |
| | Guidance of vascular development: lessons from the nervous system. | Q37402196 |
| | Noncanonical Wnt/PCP signaling during vertebrate gastrulation | Q37416717 |
| | Division of labor during trunk neural crest development | Q37732864 |
| | The polycystic kidney disease-1 promoter is a target of the beta-catenin/T-cell factor pathway | Q38288606 |
| | beta-catenin/TCF/Lef controls a differentiation-associated transcriptional program in renal epithelial progenitors | Q38299235 |
| | Prickle 1 regulates cell movements during gastrulation and neuronal migration in zebrafish | Q38352359 |
| | Zebrafish prickle, a modulator of noncanonical Wnt/Fz signaling, regulates gastrulation movements. | Q38520593 |
| | The planar cell-polarity gene stbm regulates cell behaviour and cell fate in vertebrate embryos. | Q38523609 |
| | The prickle-related gene in vertebrates is essential for gastrulation cell movements | Q39750801 |
| | Wnt5a and Wnt11 interact in a maternal Dkk1-regulated fashion to activate both canonical and non-canonical signaling in Xenopus axis formation | Q39752731 |
| | The function and mechanism of convergent extension during gastrulation of Xenopus laevis | Q39805739 |
| | Canonical Wnt signals are essential for homeostasis of the intestinal epithelium | Q39895829 |
| | Initiation of Wnt signaling: control of Wnt coreceptor Lrp6 phosphorylation/activation via frizzled, dishevelled and axin functions. | Q40036004 |
| | Canonical WNT signaling during kidney development | Q40134356 |
| | Scribble associates with two polarity proteins, Lgl2 and Vangl2, via distinct molecular domains | Q40264123 |
| | Peripheral nerve-derived VEGF promotes arterial differentiation via neuropilin 1-mediated positive feedback. | Q40465024 |
| | Endothelial cells stimulate self-renewal and expand neurogenesis of neural stem cells | Q40570664 |
| | Wnt signaling components in the chicken intestinal tract | Q40598525 |
| | Wnt11 and Ret/Gdnf pathways cooperate in regulating ureteric branching during metanephric kidney development. | Q40642802 |
| | Wnt-11 activation of a non-canonical Wnt signalling pathway is required for cardiogenesis | Q40712030 |
| | Induced repatterning of type XVIII collagen expression in ureter bud from kidney to lung type: association with sonic hedgehog and ectopic surfactant protein C. | Q40814557 |
| | Wnt-4 is a mesenchymal signal for epithelial transformation of metanephric mesenchyme in the developing kidney | Q41006079 |
| | Gut reaction to Wnt signaling in worms | Q41588808 |
| | Think globally, act locally: the making of a mouse mammary gland. | Q41705141 |
| | Wnt11-R signaling regulates a calcium sensitive EMT event essential for dorsal fin development of Xenopus | Q42041530 |
| | JNK functions in the non-canonical Wnt pathway to regulate convergent extension movements in vertebrates | Q42113998 |
| | Notch signaling augments the canonical Wnt pathway to specify the size of the otic placode | Q42226422 |
| | Ciliogenesis defects in embryos lacking inturned or fuzzy function are associated with failure of planar cell polarity and Hedgehog signaling | Q42491186 |
| | Regional expression, pattern and timing of convergence and extension during gastrulation of Xenopus laevis | Q42514448 |
| | The behaviour and function of bottle cells during gastrulation of Xenopus laevis | Q42514455 |
| | Delamination of cells from neurogenic placodes does not involve an epithelial-to-mesenchymal transition | Q42520714 |
| | Wnt signaling in gut organogenesis | Q42652916 |
| | Dishevelled proteins lead to two signaling pathways. Regulation of LEF-1 and c-Jun N-terminal kinase in mammalian cells | Q42823306 |
| P433 | issue | 1 | |
| P304 | page(s) | 77-93 | |
| P577 | publication date | 2010-01-01 | |
| P1433 | published in | Developmental Dynamics | Q59752 |
| P1476 | title | Wnt to build a tube: contributions of Wnt signaling to epithelial tubulogenesis | |
| P478 | volume | 239 | |