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The PCP pathway regulates Baz planar distribution in epithelial cells

https://doi.org/10.1038/srep33420
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/dvdy.21089openalex-snapshot
Isoform‐specific interaction of Flamingo/Starry Night with excess Bazooka affects planar cell polarity in the Drosophila wing
inferredcites →https://doi.org/10.1002/wdev.175openalex-snapshot
Asymmetric cell division in the Drosophila bristle lineage: from the polarization of sensory organ precursor cells to Notch‐mediated binary fate decision
inferredcites →https://doi.org/10.1006/dbio.1993.1243openalex-snapshot
crumbs and stardust Act in a Genetic Pathway That Controls the Organization of Epithelia in Drosophila melanogaster
inferredcites →https://doi.org/10.1007/978-1-59745-583-1_16openalex-snapshot
Imaging Drosophila Pupal Wing Morphogenesis
inferredcites →https://doi.org/10.1007/bf00848156openalex-snapshot
Mutations affecting the pattern of the larval cuticle inDrosophila melanogaster
inferredcites →https://doi.org/10.1007/bf00848157openalex-snapshot
Mutations affecting the pattern of the larval cuticle inDrosophila melanogaster
inferredcites →https://doi.org/10.1016/0092-8674(89)90033-0openalex-snapshot
The FLP recombinase of yeast catalyzes site-specific recombination in the drosophila genome
inferredcites →https://doi.org/10.1016/0092-8674(90)90189-lopenalex-snapshot
crumbs encodes an EGF-like protein expressed on apical membranes of Drosophila epithelial cells and required for organization of epithelia
inferredcites →https://doi.org/10.1016/0092-8674(91)90013-oopenalex-snapshot
The regulatory light chain of nonmuscle myosin is encoded by spaghetti-squash, a gene required for cytokinesis in Drosophila
inferredcites →https://doi.org/10.1016/b978-0-12-385044-7.00007-2openalex-snapshot
Planar Cell Polarity Signaling in the Drosophila Eye
inferredcites →https://doi.org/10.1016/j.bbamem.2007.08.029openalex-snapshot
Polarity complex proteins
inferredcites →https://doi.org/10.1016/j.cell.2005.03.014openalex-snapshot
The Apical Determinants aPKC and dPatj Regulate Frizzled-Dependent Planar Cell Polarity in the Drosophila Eye
inferredcites →https://doi.org/10.1016/j.cell.2007.05.050openalex-snapshot
Planar Polarity and Tissue Morphogenesis
inferredcites →https://doi.org/10.1016/j.cell.2008.04.048openalex-snapshot
Asymmetric Homotypic Interactions of the Atypical Cadherin Flamingo Mediate Intercellular Polarity Signaling
inferredcites →https://doi.org/10.1016/j.cell.2010.02.040openalex-snapshot
aPKC Phosphorylation of Bazooka Defines the Apical/Lateral Border in Drosophila Epithelial Cells
inferredcites →https://doi.org/10.1016/j.cell.2010.05.011openalex-snapshot
Cell Polarity in Eggs and Epithelia: Parallels and Diversity
inferredcites →https://doi.org/10.1016/j.cub.2008.08.063openalex-snapshot
Differential Stability of Flamingo Protein Complexes Underlies the Establishment of Planar Polarity
inferredcites →https://doi.org/10.1016/j.cub.2010.04.049openalex-snapshot
Crumbs/DaPKC-Dependent Apical Exclusion of Bazooka Promotes Photoreceptor Polarity Remodeling
inferredcites →https://doi.org/10.1016/j.cub.2013.09.015openalex-snapshot
Principles of E-Cadherin Supramolecular Organization In Vivo
inferredcites →https://doi.org/10.1016/j.cub.2015.02.073openalex-snapshot
Planar Cell Polarity Breaks the Symmetry of PAR Protein Distribution prior to Mitosis in Drosophila Sensory Organ Precursor Cells
inferredcites →https://doi.org/10.1016/j.devcel.2004.05.003openalex-snapshot
Sequential Roles of Cdc42, Par-6, aPKC, and Lgl in the Establishment of Epithelial Polarity during Drosophila Embryogenesis
inferredcites →https://doi.org/10.1016/j.devcel.2005.03.015openalex-snapshot
Echinoid Is a Component of Adherens Junctions That Cooperates with DE-Cadherin to Mediate Cell Adhesion
inferredcites →https://doi.org/10.1016/j.devcel.2005.11.016openalex-snapshot
Polarized Transport of Frizzled along the Planar Microtubule Arrays in Drosophila Wing Epithelium
inferredcites →https://doi.org/10.1016/j.devcel.2006.09.007openalex-snapshot
Multicellular Rosette Formation Links Planar Cell Polarity to Tissue Morphogenesis
inferredcites →https://doi.org/10.1016/j.devcel.2010.08.004openalex-snapshot
Atypical Cadherins Dachsous and Fat Control Dynamics of Noncentrosomal Microtubules in Planar Cell Polarity
inferredcites →https://doi.org/10.1016/j.devcel.2010.08.011openalex-snapshot
Rho-Kinase Directs Bazooka/Par-3 Planar Polarity during Drosophila Axis Elongation
inferredcites →https://doi.org/10.1016/j.devcel.2012.09.013openalex-snapshot
Anisotropy of Crumbs and aPKC Drives Myosin Cable Assembly during Tube Formation
inferredcites →https://doi.org/10.1016/j.semcdb.2013.03.012openalex-snapshot
Revisiting planar cell polarity in the inner ear
inferredcites →https://doi.org/10.1016/j.ydbio.2009.06.024openalex-snapshot
The apical/basal-polarity determinant Scribble cooperates with the PCP core factor Stbm/Vang and functions as one of its effectors
inferredcites →https://doi.org/10.1016/j.ydbio.2013.09.031openalex-snapshot
Transcriptional regulation of tissue organization and cell morphogenesis: The fly retina as a case study
inferredcites →https://doi.org/10.1016/j.ymeth.2014.03.017openalex-snapshot
Methods for studying planar cell polarity
inferredcites →https://doi.org/10.1016/s0092-8674(00)80046-xopenalex-snapshot
Flamingo, a Seven-Pass Transmembrane Cadherin, Regulates Planar Cell Polarity under the Control of Frizzled
inferredcites →https://doi.org/10.1016/s0092-8674(01)00298-7openalex-snapshot
Drosophila Rho-Associated Kinase (Drok) Links Frizzled-Mediated Planar Cell Polarity Signaling to the Actin Cytoskeleton
inferredcites →https://doi.org/10.1016/s0092-8674(01)00444-5openalex-snapshot
The Partner of Inscuteable/Discs-Large Complex Is Required to Establish Planar Polarity during Asymmetric Cell Division in Drosophila
inferredcites →https://doi.org/10.1016/s0092-8674(02)00715-8openalex-snapshot
Prickle Mediates Feedback Amplification to Generate Asymmetric Planar Cell Polarity Signaling
inferredcites →https://doi.org/10.1016/s0960-9822(02)00841-2openalex-snapshot
Asymmetric Localization of Frizzled and the Determination of Notch-Dependent Cell Fate in the Drosophila Eye
inferredcites →https://doi.org/10.1016/s0960-9822(03)00244-6openalex-snapshot
Mammalian Lgl Forms a Protein Complex with PAR-6 and aPKC Independently of PAR-3 to Regulate Epithelial Cell Polarity
inferredcites →https://doi.org/10.1016/s0960-9822(99)80505-3openalex-snapshot
Flamingo controls the planar polarity of sensory bristles and asymmetric division of sensory organ precursors in Drosophila
inferredcites →https://doi.org/10.1016/s1097-2765(01)00184-8openalex-snapshot
Asymmetric Localization of Frizzled and the Establishment of Cell Polarity in the Drosophila Wing
inferredcites →https://doi.org/10.1016/s1534-5807(01)00010-7openalex-snapshot
The Ankyrin Repeat Protein Diego Mediates Frizzled-Dependent Planar Polarization
inferredcites →https://doi.org/10.1016/s1534-5807(02)00147-8openalex-snapshot
The Atypical Cadherin Flamingo Links Frizzled and Notch Signaling in Planar Polarity Establishment in the Drosophila Eye
inferredcites →https://doi.org/10.1016/s1534-5807(02)00197-1openalex-snapshot
Convergent Extension
inferredcites →https://doi.org/10.1016/s1534-5807(02)00363-5openalex-snapshot
Nonautonomous Planar Polarity Patterning in Drosophila
inferredcites →https://doi.org/10.1016/s1534-5807(04)00060-7openalex-snapshot
Patterned Gene Expression Directs Bipolar Planar Polarity in Drosophila
inferredcites →https://doi.org/10.1038/30265openalex-snapshot
Frizzled signalling controls orientation of asymmetric sense organ precursor cell divisions in Drosophila
inferredcites →https://doi.org/10.1038/329549a0openalex-snapshot
Directional non-cell autonomy and the transmission of polarity information by the frizzled gene of Drosophila
inferredcites →https://doi.org/10.1038/35001108openalex-snapshot
Localization of apical epithelial determinants by the basolateral PDZ protein Scribble
inferredcites →https://doi.org/10.1038/35050550openalex-snapshot
DmPAR-6 directs epithelial polarity and asymmetric cell division of neuroblasts in Drosophila
inferredcites →https://doi.org/10.1038/35050558openalex-snapshot
Frizzled regulates localization of cell-fate determinants and mitotic spindle rotation during asymmetric cell division
inferredcites →https://doi.org/10.1038/nature01618openalex-snapshot
Identification of Vangl2 and Scrb1 as planar polarity genes in mammals
inferredcites →https://doi.org/10.1038/nature02952openalex-snapshot
Surface mechanics mediate pattern formation in the developing retina
inferredcites →https://doi.org/10.1038/nature14603openalex-snapshot
A self-organized biomechanical network drives shape changes during tissue morphogenesis
inferredcites →https://doi.org/10.1038/ncb1055openalex-snapshot
Discs-Large and Strabismus are functionally linked to plasma membrane formation
inferredcites →https://doi.org/10.1038/ncb2224openalex-snapshot
Spatial regulation of Dia and Myosin-II by RhoGEF2 controls initiation of E-cadherin endocytosis during epithelial morphogenesis
inferredcites →https://doi.org/10.1038/ncb2685openalex-snapshot
Monomeric α-catenin links cadherin to the actin cytoskeleton
inferredcites →https://doi.org/10.1038/ncb896openalex-snapshot
Interactions between the crumbs, lethal giant larvae and bazooka pathways in epithelial polarization
inferredcites →https://doi.org/10.1038/ncb897openalex-snapshot
Integrated activity of PDZ protein complexes regulates epithelial polarity
inferredcites →https://doi.org/10.1038/nmeth.2019openalex-snapshot
Fiji: an open-source platform for biological-image analysis
inferredcites →https://doi.org/10.1038/nmeth.2692openalex-snapshot
ScientiFig: a tool to build publication-ready scientific figures
inferredcites →https://doi.org/10.1038/nrm2222openalex-snapshot
Cell surface mechanics and the control of cell shape, tissue patterns and morphogenesis
inferredcites →https://doi.org/10.1073/pnas.0900641106openalex-snapshot
Directed, efficient, and versatile modifications of the Drosophila genome by genomic engineering
inferredcites →https://doi.org/10.1073/pnas.261408198openalex-snapshot
A protein trap strategy to detect GFP-tagged proteins expressed from their endogenous loci in Drosophila
inferredcites →https://doi.org/10.1083/jcb.200203080openalex-snapshot
Crumbs interacts with moesin and βHeavy-spectrin in the apical membrane skeleton of Drosophila
inferredcites →https://doi.org/10.1083/jcb.200311031openalex-snapshot
DaPKC-dependent phosphorylation of Crumbs is required for epithelial cell polarity in Drosophila
inferredcites →https://doi.org/10.1083/jcb.200505127openalex-snapshot
The positioning and segregation of apical cues during epithelial polarity establishment in Drosophila
inferredcites →https://doi.org/10.1083/jcb.201408039openalex-snapshot
The cell biology of planar cell polarity
inferredcites →https://doi.org/10.1093/genetics/150.1.199openalex-snapshot
Van Gogh: A New Drosophila Tissue Polarity Gene
inferredcites →https://doi.org/10.1098/rspb.1960.0094openalex-snapshot
The ultra-structure of the developing eye of Drosophila
inferredcites →https://doi.org/10.1101/gad.13.17.2315openalex-snapshot
The balance between isoforms of the Prickle LIM domain protein is critical for planar polarity in Drosophila imaginal discs
inferredcites →https://doi.org/10.1101/gad.890501openalex-snapshot
Unipolar membrane association of Dishevelled mediates Frizzled planar cell polarity signaling
inferredcites →https://doi.org/10.1126/science.2035025openalex-snapshot
Site-Specific Recombination Between Homologous Chromosomes in Drosophila
inferredcites →https://doi.org/10.1146/annurev-cellbio-092910-154033openalex-snapshot
The Apical Polarity Protein Network in Drosophila Epithelial Cells: Regulation of Polarity, Junctions, Morphogenesis, Cell Growth, and Survival
inferredcites →https://doi.org/10.1146/annurev.biochem.77.061906.092014openalex-snapshot
Super-Resolution Fluorescence Microscopy
inferredcites →https://doi.org/10.1146/annurev.genet.42.110807.091432openalex-snapshot
Planar Cell Polarity Signaling: From Fly Development to Human Disease
inferredcites →https://doi.org/10.1242/dev.00411openalex-snapshot
Strabismus requires Flamingo and Prickle function to regulate tissue polarity in theDrosophilaeye
inferredcites →https://doi.org/10.1242/dev.00526openalex-snapshot
Strabismus is asymmetrically localised and binds to Prickle and Dishevelled duringDrosophilaplanar polarity patterning
inferredcites →https://doi.org/10.1242/dev.00928openalex-snapshot
The planar cell polarity protein Strabismus promotes Pins anterior localization during asymmetric division of sensory organ precursor cells in Drosophila
inferredcites →https://doi.org/10.1242/dev.01317openalex-snapshot
Diego interacts with Prickle and Strabismus/Van Gogh to localize planar cell polarity complexes
inferredcites →https://doi.org/10.1242/dev.01645openalex-snapshot
aPKC, Crumbs3 and Lgl2 control apicobasal polarity in early vertebrate development
inferredcites →https://doi.org/10.1242/dev.122.10.3133openalex-snapshot
par-6, a gene involved in the establishment of asymmetry in early C. elegans embryos, mediates the asymmetric localization of PAR-3
inferredcites →https://doi.org/10.1242/dev.125.6.1149openalex-snapshot
strabismus, a novel gene that regulates tissue polarity and cell fate decisions in Drosophila
inferredcites →https://doi.org/10.1242/dev.126.1.127openalex-snapshot
PAR-6 is a conserved PDZ domain-containing protein that colocalizes with PAR-3 in Caenorhabditis elegans embryos
inferredcites →https://doi.org/10.1242/dev.126.23.5421openalex-snapshot
The Drosophila tissue polarity gene starry night encodes a member of the protocadherin family
inferredcites →https://doi.org/10.1242/jcs.03170openalex-snapshot
PAR3 acts as a molecular organizer to define the apical domain of chick neuroepithelial cells
inferredcites →https://doi.org/10.1242/jcs.047183openalex-snapshot
Crumbs stabilises epithelial polarity during tissue remodelling
inferredcites →https://doi.org/10.1242/jcs.086694openalex-snapshot
Differential regulation of adherens junction dynamics during apical–basal polarization
inferredcites →https://doi.org/10.1366/11-06398openalex-snapshot
Review of Super-Resolution Fluorescence Microscopy for Biology
inferredcites →https://doi.org/10.1523/jneurosci.4680-05.2006openalex-snapshot
Asymmetric Localization of Vangl2 and Fz3 Indicate Novel Mechanisms for Planar Cell Polarity in Mammals
inferredcites →https://doi.org/10.1534/genetics.106.065961openalex-snapshot
The Carnegie Protein Trap Library: A Versatile Tool for Drosophila Developmental Studies
inferredcites →https://doi.org/10.1534/genetics.106.065995openalex-snapshot
Exploring Strategies for Protein Trapping in Drosophila

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4648583openalex-extracted
inferred← citeshttps://doi.org/10.1002/9780470015902.a0029229openalex-snapshot
Drosophila Retinal Patterning
inferred← citeshttps://doi.org/10.1007/978-3-030-42246-2_7openalex-snapshot
Adhesion and the Cytoskeleton in the Drosophila Pupal Eye
inferred← citeshttps://doi.org/10.1016/j.cdev.2021.203747openalex-snapshot
Cell cycle expression of polarity genes features Rb targeting of Vang
inferred← citeshttps://doi.org/10.1016/j.devcel.2025.04.026openalex-snapshot
Disrupted endosomal trafficking of the Vangl-Celsr polarity complex underlies congenital anomalies in Xenopus trachea-esophageal morphogenesis
inferred← citeshttps://doi.org/10.1016/j.neuro.2025.103346openalex-snapshot
Oxidative stress and retinal damage induced by cobalt chloride in Drosophila melanogaster: Insights into cone cell susceptibility and stress gene responses
inferred← citeshttps://doi.org/10.1016/j.ydbio.2021.07.004openalex-snapshot
Hexagonal patterning of the Drosophila eye
inferred← citeshttps://doi.org/10.1038/s41580-022-00465-yopenalex-snapshot
Apical–basal polarity and the control of epithelial form and function
inferred← citeshttps://doi.org/10.1091/mbc.e19-09-0523openalex-snapshot
Cell-type-specific mechanical response and myosin dynamics during retinal lens development in Drosophila
inferred← citeshttps://doi.org/10.1101/2023.10.11.561909openalex-snapshot
Disrupted Endosomal Trafficking of the Vangl-Celsr Polarity Complex Underlies Congenital Anomalies in Trachea-Esophageal Morphogenesis
inferred← citeshttps://doi.org/10.1101/328385openalex-snapshot
Theoretical Tool Bridging Cell Polarities with Development of Robust Morphologies
inferred← citeshttps://doi.org/10.1101/477760openalex-snapshot
E-cadherin endocytosis is modulated by p120-catenin through the opposing actions of RhoA and Arf1
inferred← citeshttps://doi.org/10.1101/558593openalex-snapshot
Cell-type specific mechanical response and myosin dynamics during retinal lens development in Drosophila
inferred← citeshttps://doi.org/10.1101/564708openalex-snapshot
Neph/Nephrin-like adhesion and tissue level pulling forces regulate cell intercalation during Drosophila retina development
inferred← citeshttps://doi.org/10.1242/dev.196386openalex-snapshot
Planar polarization of cilia in the zebrafish floor-plate involves Par3-mediated posterior localization of highly motile basal bodies
inferred← citeshttps://doi.org/10.1242/dev.197301openalex-snapshot
A combination of Notch signaling, preferential adhesion and endocytosis induces a slow mode of cell intercalation in the Drosophila retina
inferred← citeshttps://doi.org/10.3389/fcell.2019.00209openalex-snapshot
Planar Asymmetries in the C. elegans Embryo Emerge by Differential Retention of aPARs at Cell-Cell Contacts
inferred← citeshttps://doi.org/10.3390/cells13171403openalex-snapshot
Centriole Translational Planar Polarity in Monociliated Epithelia
inferred← citeshttps://doi.org/10.70675/45004e64z3cdbz4307z818bz78f3b59c136eopenalex-snapshot
How cellulose and microtubules contribute to plant cell and organ growth : a temporal and spatial multi-scale analysis
inferred← citeshttps://doi.org/10.70675/7b46d312z85bbz4378za962z0721959eeb6fopenalex-snapshot
Mechanical basis of cell shapes and cell arrangements during retinal morphogenesis in Drosophila
inferred← citeshttps://doi.org/10.70675/acc1a95cz8229z4c8dz98a0zb840ff0fb208openalex-snapshot
Planar polarization of a mono-ciliated epithelium : the zebrafish floor-plate
inferred← citeshttps://doi.org/10.70675/b6eb2d91z239fz4d4dz9824z27fdda94d3a9openalex-snapshot
Cooperation between Toll receptors and the GPCR Cirl in the control of planar polarized cell contractility during morphogenesis
inferred← citeshttps://doi.org/10.7554/elife.22796openalex-snapshot
Patterned cortical tension mediated by N-cadherin controls cell geometric order in the Drosophila eye
inferred← citeshttps://doi.org/10.7554/elife.25014openalex-snapshot
Meru couples planar cell polarity with apical-basal polarity during asymmetric cell division
inferred← citeshttps://doi.org/10.7554/elife.37881openalex-snapshot
Par3 interacts with Prickle3 to generate apical PCP complexes in the vertebrate neural plate
inferred← citeshttps://doi.org/10.7554/elife.38407openalex-snapshot
Theoretical tool bridging cell polarities with development of robust morphologies
inferred← citeshttps://doi.org/10.7554/elife.54927openalex-snapshot
Par protein localization during the early development of Mnemiopsis leidyi suggests different modes of epithelial organization in the metazoa
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