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209 related items for PubMed ID: 10906777

  • 1. Skeletal-specific expression of Fgd1 during bone formation and skeletal defects in faciogenital dysplasia (FGDY; Aarskog syndrome).
    Gorski JL, Estrada L, Hu C, Liu Z.
    Dev Dyn; 2000 Aug; 218(4):573-86. PubMed ID: 10906777
    [Abstract] [Full Text] [Related]

  • 2. Isolation, characterization, and mapping of the mouse and human Fgd2 genes, faciogenital dysplasia (FGD1; Aarskog syndrome) gene homologues.
    Pasteris NG, Gorski JL.
    Genomics; 1999 Aug 15; 60(1):57-66. PubMed ID: 10458911
    [Abstract] [Full Text] [Related]

  • 3. Genomic organization of the faciogenital dysplasia (FGD1; Aarskog syndrome) gene.
    Pasteris NG, Buckler J, Cadle AB, Gorski JL.
    Genomics; 1997 Aug 01; 43(3):390-4. PubMed ID: 9268645
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. 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 25; 121(11):4383-92. PubMed ID: 21965325
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. 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]

  • 8. Novel alternative splicing of human faciogenital dysplasia 1 gene.
    Yanagi K, Kaname T, Chinen Y, Naritomi K.
    Congenit Anom (Kyoto); 2004 Sep 15; 44(3):137-41. PubMed ID: 15327482
    [Abstract] [Full Text] [Related]

  • 9. Two novel mutations confirm FGD1 is responsible for the Aarskog syndrome.
    Schwartz CE, Gillessen-Kaesbach G, May M, Cappa M, Gorski J, Steindl K, Neri G.
    Eur J Hum Genet; 2000 Nov 15; 8(11):869-74. PubMed ID: 11093277
    [Abstract] [Full Text] [Related]

  • 10. Isolation and characterization of the faciogenital dysplasia (Aarskog-Scott syndrome) gene: a putative Rho/Rac guanine nucleotide exchange factor.
    Pasteris NG, Cadle A, Logie LJ, Porteous ME, Schwartz CE, Stevenson RE, Glover TW, Wilroy RS, Gorski JL.
    Cell; 1994 Nov 18; 79(4):669-78. PubMed ID: 7954831
    [Abstract] [Full Text] [Related]

  • 11. First case of deletion of the faciogenital dysplasia 1 (FGD1) gene in a patient with Aarskog-Scott syndrome.
    Bedoyan JK, Friez MJ, DuPont B, Ahmad A.
    Eur J Med Genet; 2009 Nov 18; 52(4):262-4. PubMed ID: 19110080
    [Abstract] [Full Text] [Related]

  • 12. The Caenorhabditis elegans homolog of FGD1, the human Cdc42 GEF gene responsible for faciogenital dysplasia, is critical for excretory cell morphogenesis.
    Gao J, Estrada L, Cho S, Ellis RE, Gorski JL.
    Hum Mol Genet; 2001 Dec 15; 10(26):3049-62. PubMed ID: 11751687
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. 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]

  • 15. Unilateral focal polymicrogyria in a patient with classical Aarskog-Scott syndrome due to a novel missense mutation in an evolutionary conserved RhoGEF domain of the faciogenital dysplasia gene FGD1.
    Bottani A, Orrico A, Galli L, Karam O, Haenggeli CA, Ferey S, Conrad B.
    Am J Med Genet A; 2007 Oct 01; 143A(19):2334-8. PubMed ID: 17847065
    [Abstract] [Full Text] [Related]

  • 16. Ets transcription factors and targets in osteogenesis.
    Raouf A, Seth A.
    Oncogene; 2000 Dec 18; 19(55):6455-63. PubMed ID: 11175361
    [Abstract] [Full Text] [Related]

  • 17. Faciogenital dysplasia protein (FGD1) and Vav, two related proteins required for normal embryonic development, are upstream regulators of Rho GTPases.
    Olson MF, Pasteris NG, Gorski JL, Hall A.
    Curr Biol; 1996 Dec 01; 6(12):1628-33. PubMed ID: 8994827
    [Abstract] [Full Text] [Related]

  • 18. Expression of Semaphorin-3A and its receptors in endochondral ossification: potential role in skeletal development and innervation.
    Gomez C, Burt-Pichat B, Mallein-Gerin F, Merle B, Delmas PD, Skerry TM, Vico L, Malaval L, Chenu C.
    Dev Dyn; 2005 Oct 01; 234(2):393-403. PubMed ID: 16145665
    [Abstract] [Full Text] [Related]

  • 19. Expression of interstitial collagenase during skeletal development of the mouse is restricted to osteoblast-like cells and hypertrophic chondrocytes.
    Gack S, Vallon R, Schmidt J, Grigoriadis A, Tuckermann J, Schenkel J, Weiher H, Wagner EF, Angel P.
    Cell Growth Differ; 1995 Jun 01; 6(6):759-67. PubMed ID: 7669731
    [Abstract] [Full Text] [Related]

  • 20. Skeletogenesis in Xenopus tropicalis: characteristic bone development in an anuran amphibian.
    Miura S, Hanaoka K, Togashi S.
    Bone; 2008 Nov 01; 43(5):901-9. PubMed ID: 18692165
    [Abstract] [Full Text] [Related]

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