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Journal Abstract Search

397 related items for PubMed ID: 20962035

  • 1. Disruption of PCP signaling causes limb morphogenesis and skeletal defects and may underlie Robinow syndrome and brachydactyly type B.
    Wang B, Sinha T, Jiao K, Serra R, Wang J.
    Hum Mol Genet; 2011 Jan 15; 20(2):271-85. PubMed ID: 20962035
    [Abstract] [Full Text] [Related]

  • 2. Prickle1 stunts limb growth through alteration of cell polarity and gene expression.
    Yang T, Bassuk AG, Fritzsch B.
    Dev Dyn; 2013 Nov 15; 242(11):1293-306. PubMed ID: 23913870
    [Abstract] [Full Text] [Related]

  • 3. The Wnt coreceptor Ryk regulates Wnt/planar cell polarity by modulating the degradation of the core planar cell polarity component Vangl2.
    Andre P, Wang Q, Wang N, Gao B, Schilit A, Halford MM, Stacker SA, Zhang X, Yang Y.
    J Biol Chem; 2012 Dec 28; 287(53):44518-25. PubMed ID: 23144463
    [Abstract] [Full Text] [Related]

  • 4. Wnt signaling gradients establish planar cell polarity by inducing Vangl2 phosphorylation through Ror2.
    Gao B, Song H, Bishop K, Elliot G, Garrett L, English MA, Andre P, Robinson J, Sood R, Minami Y, Economides AN, Yang Y.
    Dev Cell; 2011 Feb 15; 20(2):163-76. PubMed ID: 21316585
    [Abstract] [Full Text] [Related]

  • 5. A gradient of ROR2 protein stability and membrane localization confers brachydactyly type B or Robinow syndrome phenotypes.
    Schwarzer W, Witte F, Rajab A, Mundlos S, Stricker S.
    Hum Mol Genet; 2009 Nov 01; 18(21):4013-21. PubMed ID: 19640924
    [Abstract] [Full Text] [Related]

  • 6. The Meckel-Gruber syndrome protein TMEM67 controls basal body positioning and epithelial branching morphogenesis in mice via the non-canonical Wnt pathway.
    Abdelhamed ZA, Natarajan S, Wheway G, Inglehearn CF, Toomes C, Johnson CA, Jagger DJ.
    Dis Model Mech; 2015 Jun 01; 8(6):527-41. PubMed ID: 26035863
    [Abstract] [Full Text] [Related]

  • 7. A mammalian Wnt5a-Ror2-Vangl2 axis controls the cytoskeleton and confers cellular properties required for alveologenesis.
    Zhang K, Yao E, Lin C, Chou YT, Wong J, Li J, Wolters PJ, Chuang PT.
    Elife; 2020 May 12; 9():. PubMed ID: 32394892
    [Abstract] [Full Text] [Related]

  • 8. Non-canonical Wnt5a/Ror2 signaling regulates kidney morphogenesis by controlling intermediate mesoderm extension.
    Yun K, Ajima R, Sharma N, Costantini F, Mackem S, Lewandoski M, Yamaguchi TP, Perantoni AO.
    Hum Mol Genet; 2014 Dec 20; 23(25):6807-14. PubMed ID: 25082826
    [Abstract] [Full Text] [Related]

  • 9. Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2.
    Afzal AR, Rajab A, Fenske CD, Oldridge M, Elanko N, Ternes-Pereira E, Tüysüz B, Murday VA, Patton MA, Wilkie AO, Jeffery S.
    Nat Genet; 2000 Aug 20; 25(4):419-22. PubMed ID: 10932186
    [Abstract] [Full Text] [Related]

  • 10. Ror-family receptor tyrosine kinases in noncanonical Wnt signaling: their implications in developmental morphogenesis and human diseases.
    Minami Y, Oishi I, Endo M, Nishita M.
    Dev Dyn; 2010 Jan 20; 239(1):1-15. PubMed ID: 19530173
    [Abstract] [Full Text] [Related]

  • 11. One gene, two phenotypes: ROR2 mutations in autosomal recessive Robinow syndrome and autosomal dominant brachydactyly type B.
    Afzal AR, Jeffery S.
    Hum Mutat; 2003 Jul 20; 22(1):1-11. PubMed ID: 12815588
    [Abstract] [Full Text] [Related]

  • 12. The PTK7 and ROR2 Protein Receptors Interact in the Vertebrate WNT/Planar Cell Polarity (PCP) Pathway.
    Martinez S, Scerbo P, Giordano M, Daulat AM, Lhoumeau AC, Thomé V, Kodjabachian L, Borg JP.
    J Biol Chem; 2015 Dec 18; 290(51):30562-72. PubMed ID: 26499793
    [Abstract] [Full Text] [Related]

  • 13. WNT5A mutations in patients with autosomal dominant Robinow syndrome.
    Person AD, Beiraghi S, Sieben CM, Hermanson S, Neumann AN, Robu ME, Schleiffarth JR, Billington CJ, van Bokhoven H, Hoogeboom JM, Mazzeu JF, Petryk A, Schimmenti LA, Brunner HG, Ekker SC, Lohr JL.
    Dev Dyn; 2010 Jan 18; 239(1):327-37. PubMed ID: 19918918
    [Abstract] [Full Text] [Related]

  • 14. The non-canonical Wnt receptor Ror2 is required for cartilage cell polarity and morphogenesis of the craniofacial skeleton in zebrafish.
    Dranow DB, Le Pabic P, Schilling TF.
    Development; 2023 Apr 15; 150(8):. PubMed ID: 37039156
    [Abstract] [Full Text] [Related]

  • 15. Clinical and molecular characterization of seven Egyptian families with autosomal recessive robinow syndrome: Identification of four novel ROR2 gene mutations.
    Aglan M, Amr K, Ismail S, Ashour A, Otaify GA, Mehrez MA, Aboul-Ezz EH, El-Ruby M, Mazen I, Abdel-Hamid MS, Temtamy SA.
    Am J Med Genet A; 2015 Dec 15; 167A(12):3054-61. PubMed ID: 26284319
    [Abstract] [Full Text] [Related]

  • 16. Disheveled mediated planar cell polarity signaling is required in the second heart field lineage for outflow tract morphogenesis.
    Sinha T, Wang B, Evans S, Wynshaw-Boris A, Wang J.
    Dev Biol; 2012 Oct 01; 370(1):135-44. PubMed ID: 22841628
    [Abstract] [Full Text] [Related]

  • 17. The apical ectodermal ridge of the mouse model of ectrodactyly Dlx5;Dlx6-/- shows altered stratification and cell polarity, which are restored by exogenous Wnt5a ligand.
    Conte D, Garaffo G, Lo Iacono N, Mantero S, Piccolo S, Cordenonsi M, Perez-Morga D, Orecchia V, Poli V, Merlo GR.
    Hum Mol Genet; 2016 Feb 15; 25(4):740-54. PubMed ID: 26685160
    [Abstract] [Full Text] [Related]

  • 18. Structure and function of the ROR2 cysteine-rich domain in vertebrate noncanonical WNT5A signaling.
    Griffiths SC, Tan J, Wagner A, Blazer LL, Adams JJ, Srinivasan S, Moghisaei S, Sidhu SS, Siebold C, Ho HH.
    Elife; 2024 May 23; 13():. PubMed ID: 38780011
    [Abstract] [Full Text] [Related]

  • 19. The mutation ROR2W749X, linked to human BDB, is a recessive mutation in the mouse, causing brachydactyly, mediating patterning of joints and modeling recessive Robinow syndrome.
    Raz R, Stricker S, Gazzerro E, Clor JL, Witte F, Nistala H, Zabski S, Pereira RC, Stadmeyer L, Wang X, Gowen L, Sleeman MW, Yancopoulos GD, Canalis E, Mundlos S, Valenzuela DM, Economides AN.
    Development; 2008 May 23; 135(9):1713-23. PubMed ID: 18353862
    [Abstract] [Full Text] [Related]

  • 20. Genetic interactions between Ror2 and Wnt9a, Ror1 and Wnt9a and Ror2 and Ror1: Phenotypic analysis of the limb skeleton and palate in compound mutants.
    Weissenböck M, Latham R, Nishita M, Wolff LI, Ho HH, Minami Y, Hartmann C.
    Genes Cells; 2019 Apr 23; 24(4):307-317. PubMed ID: 30801848
    [Abstract] [Full Text] [Related]

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