390 related articles for article (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; 20(2):271-85. PubMed ID: 20962035
[TBL] [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; 242(11):1293-306. PubMed ID: 23913870
[TBL] [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; 287(53):44518-25. PubMed ID: 23144463
[TBL] [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; 20(2):163-76. PubMed ID: 21316585
[TBL] [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; 18(21):4013-21. PubMed ID: 19640924
[TBL] [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; 8(6):527-41. PubMed ID: 26035863
[TBL] [Abstract][Full Text] [Related]
7. A mammalian
Zhang K; Yao E; Lin C; Chou YT; Wong J; Li J; Wolters PJ; Chuang PT
Elife; 2020 May; 9():. PubMed ID: 32394892
[TBL] [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; 23(25):6807-14. PubMed ID: 25082826
[TBL] [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; 25(4):419-22. PubMed ID: 10932186
[TBL] [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; 239(1):1-15. PubMed ID: 19530173
[TBL] [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; 22(1):1-11. PubMed ID: 12815588
[TBL] [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; 290(51):30562-72. PubMed ID: 26499793
[TBL] [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; 239(1):327-37. PubMed ID: 19918918
[TBL] [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; 150(8):. PubMed ID: 37039156
[TBL] [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; 167A(12):3054-61. PubMed ID: 26284319
[TBL] [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; 370(1):135-44. PubMed ID: 22841628
[TBL] [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; 25(4):740-54. PubMed ID: 26685160
[TBL] [Abstract][Full Text] [Related]
18. 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; 135(9):1713-23. PubMed ID: 18353862
[TBL] [Abstract][Full Text] [Related]
19. 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; 24(4):307-317. PubMed ID: 30801848
[TBL] [Abstract][Full Text] [Related]
20. Wnt5a-Ror2 signaling between osteoblast-lineage cells and osteoclast precursors enhances osteoclastogenesis.
Maeda K; Kobayashi Y; Udagawa N; Uehara S; Ishihara A; Mizoguchi T; Kikuchi Y; Takada I; Kato S; Kani S; Nishita M; Marumo K; Martin TJ; Minami Y; Takahashi N
Nat Med; 2012 Feb; 18(3):405-12. PubMed ID: 22344299
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]