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173 related items for PubMed ID: 21911474

  • 1. The Aarskog-Scott syndrome protein Fgd1 regulates podosome formation and extracellular matrix remodeling in transforming growth factor β-stimulated aortic endothelial cells.
    Daubon T, Buccione R, Génot E.
    Mol Cell Biol; 2011 Nov; 31(22):4430-41. PubMed ID: 21911474
    [Abstract] [Full Text] [Related]

  • 2. FGD1 as a central regulator of extracellular matrix remodelling--lessons from faciogenital dysplasia.
    Genot E, Daubon T, Sorrentino V, Buccione R.
    J Cell Sci; 2012 Jul 15; 125(Pt 14):3265-70. PubMed ID: 22854039
    [Abstract] [Full Text] [Related]

  • 3. MLK3 regulates bone development downstream of the faciogenital dysplasia protein FGD1 in mice.
    Zou W, Greenblatt MB, Shim JH, Kant S, Zhai B, Lotinun S, Brady N, Hu DZ, Gygi SP, Baron R, Davis RJ, Jones D, Glimcher LH.
    J Clin Invest; 2011 Nov 15; 121(11):4383-92. PubMed ID: 21965325
    [Abstract] [Full Text] [Related]

  • 4. Transforming growth factor beta induces rosettes of podosomes in primary aortic endothelial cells.
    Varon C, Tatin F, Moreau V, Van Obberghen-Schilling E, Fernandez-Sauze S, Reuzeau E, Kramer I, Génot E.
    Mol Cell Biol; 2006 May 15; 26(9):3582-94. PubMed ID: 16611998
    [Abstract] [Full Text] [Related]

  • 5. ALK5 and ALK1 play antagonistic roles in transforming growth factor β-induced podosome formation in aortic endothelial cells.
    Curado F, Spuul P, Egaña I, Rottiers P, Daubon T, Veillat V, Duhamel P, Leclercq A, Gontier E, Génot E.
    Mol Cell Biol; 2014 Dec 15; 34(24):4389-403. PubMed ID: 25266657
    [Abstract] [Full Text] [Related]

  • 6. A novel, putatively null, FGD1 variant leading to Aarskog-Scott syndrome in a family from UAE.
    Hamzeh AR, Saif F, Nair P, Binjab AJ, Mohamed M, Al-Ali MT, Bastaki F.
    BMC Pediatr; 2017 Jan 19; 17(1):31. PubMed ID: 28103835
    [Abstract] [Full Text] [Related]

  • 7. Fgd1, the Cdc42 GEF responsible for Faciogenital Dysplasia, directly interacts with cortactin and mAbp1 to modulate cell shape.
    Hou P, Estrada L, Kinley AW, Parsons JT, Vojtek AB, Gorski JL.
    Hum Mol Genet; 2003 Aug 15; 12(16):1981-93. PubMed ID: 12913069
    [Abstract] [Full Text] [Related]

  • 8. FGD1-related Aarskog-Scott syndrome: Identification of four novel variations and a literature review of clinical and molecular aspects.
    Li S, Tian A, Wen Y, Gu W, Li W, Qiao X, Zhang C, Luo X.
    Eur J Pediatr; 2024 May 15; 183(5):2257-2272. PubMed ID: 38411716
    [Abstract] [Full Text] [Related]

  • 9. Faciogenital dysplasia protein Fgd1 regulates invadopodia biogenesis and extracellular matrix degradation and is up-regulated in prostate and breast cancer.
    Ayala I, Giacchetti G, Caldieri G, Attanasio F, Mariggiò S, Tetè S, Polishchuk R, Castronovo V, Buccione R.
    Cancer Res; 2009 Feb 01; 69(3):747-52. PubMed ID: 19141649
    [Abstract] [Full Text] [Related]

  • 10. Fgd1, the Cdc42 guanine nucleotide exchange factor responsible for faciogenital dysplasia, is localized to the subcortical actin cytoskeleton and Golgi membrane.
    Estrada L, Caron E, Gorski JL.
    Hum Mol Genet; 2001 Mar 01; 10(5):485-95. PubMed ID: 11181572
    [Abstract] [Full Text] [Related]

  • 11. Novel insights into FGD3, a putative GEF for Cdc42, that undergoes SCF(FWD1/beta-TrCP)-mediated proteasomal degradation analogous to that of its homologue FGD1 but regulates cell morphology and motility differently from FGD1.
    Hayakawa M, Matsushima M, Hagiwara H, Oshima T, Fujino T, Ando K, Kikugawa K, Tanaka H, Miyazawa K, Kitagawa M.
    Genes Cells; 2008 Apr 01; 13(4):329-42. PubMed ID: 18363964
    [Abstract] [Full Text] [Related]

  • 12. [Analysis of FGD1 gene variant in a child with Aarskog-Scott syndrome].
    Wang R, Pei J, Jiang X, Guo B, Guo C.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Aug 10; 38(8):757-760. PubMed ID: 34365618
    [Abstract] [Full Text] [Related]

  • 13. Aarskog-Scott syndrome: first report of a duplication in the FGD1 gene.
    Ronce N, Maystadt I, Hubert C, Vonwill S, Devriendt K, Moizard MP, Raynaud M.
    Clin Genet; 2012 Jul 10; 82(1):93-6. PubMed ID: 22211847
    [No Abstract] [Full Text] [Related]

  • 14. A novel splice site mutation of FGD1 gene in an Aarskog-Scott syndrome patient with a large anterior fontanel.
    Parıltay E, Hazan F, Ataman E, Demir K, Etlik Ö, Özbek E, Özkan B.
    J Pediatr Endocrinol Metab; 2016 Sep 01; 29(9):1111-4. PubMed ID: 27544718
    [Abstract] [Full Text] [Related]

  • 15. The Cdc42 guanine nucleotide exchange factor FGD1 regulates osteogenesis in human mesenchymal stem cells.
    Gao L, Gorski JL, Chen CS.
    Am J Pathol; 2011 Mar 01; 178(3):969-74. PubMed ID: 21356349
    [Abstract] [Full Text] [Related]

  • 16. Aarskog-Scott syndrome: a novel mutation in the FGD1 gene associated with severe craniofacial dysplasia.
    Völter C, Martínez R, Hagen R, Kress W.
    Eur J Pediatr; 2014 Oct 01; 173(10):1373-6. PubMed ID: 24770546
    [Abstract] [Full Text] [Related]

  • 17. Fraternal twins with Aarskog-Scott syndrome due to maternal germline mosaicism.
    Pilozzi-Edmonds L, Maher TA, Basran RK, Milunsky A, Al-Thihli K, Braverman NE, Alfares A.
    Am J Med Genet A; 2011 Aug 01; 155A(8):1987-90. PubMed ID: 21739585
    [Abstract] [Full Text] [Related]

  • 18. Isolation, characterization, and mapping of the mouse Fgd3 gene, a new Faciogenital Dysplasia (FGD1; Aarskog Syndrome) gene homologue.
    Pasteris NG, Nagata K, Hall A, Gorski JL.
    Gene; 2000 Jan 25; 242(1-2):237-47. PubMed ID: 10721717
    [Abstract] [Full Text] [Related]

  • 19. The First Korean Family with Aarskog-Scott Syndrome Harboring a Novel Mutation in FGD1 Diagnosed via Targeted Gene Panel Sequencing.
    Bae GY, Kim MS, Kim JY, Jang JH, Lee SM, Cho SY, Jin DK.
    Ann Clin Lab Sci; 2020 Sep 25; 50(5):691-698. PubMed ID: 33067218
    [Abstract] [Full Text] [Related]

  • 20. Sodium fluoride induces podosome formation in endothelial cells.
    Tatin F, Grise F, Reuzeau E, Genot E, Moreau V.
    Biol Cell; 2010 Jul 06; 102(9):489-98. PubMed ID: 20504277
    [Abstract] [Full Text] [Related]

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