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113 related items for PubMed ID: 19141649

  • 21. The FWD1/beta-TrCP-mediated degradation pathway establishes a 'turning off switch' of a Cdc42 guanine nucleotide exchange factor, FGD1.
    Hayakawa M, Kitagawa H, Miyazawa K, Kitagawa M, Kikugawa K.
    Genes Cells; 2005 Mar; 10(3):241-51. PubMed ID: 15743413
    [Abstract] [Full Text] [Related]

  • 22. 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
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  • 23. Minireview: Role of genetic changes of faciogenital dysplasia protein 1 in human disease.
    Pedigo NG, Van Delden D, Walters L, Farrell CL.
    Physiol Genomics; 2016 Jul 01; 48(7):446-54. PubMed ID: 27199457
    [Abstract] [Full Text] [Related]

  • 24. Caldesmon suppresses cancer cell invasion by regulating podosome/invadopodium formation.
    Yoshio T, Morita T, Kimura Y, Tsujii M, Hayashi N, Sobue K.
    FEBS Lett; 2007 Aug 07; 581(20):3777-82. PubMed ID: 17631293
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  • 25. 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]

  • 26. Faciogenital dysplasia protein (FGD1) regulates export of cargo proteins from the golgi complex via Cdc42 activation.
    Egorov MV, Capestrano M, Vorontsova OA, Di Pentima A, Egorova AV, Mariggiò S, Ayala MI, Tetè S, Gorski JL, Luini A, Buccione R, Polishchuk RS.
    Mol Biol Cell; 2009 May 25; 20(9):2413-27. PubMed ID: 19261807
    [Abstract] [Full Text] [Related]

  • 27. Invadopodia: specialized tumor cell structures for the focal degradation of the extracellular matrix.
    Buccione R, Caldieri G, Ayala I.
    Cancer Metastasis Rev; 2009 Jun 25; 28(1-2):137-49. PubMed ID: 19153671
    [Abstract] [Full Text] [Related]

  • 28. Protease activity at invadopodial focal digestive areas is dependent on NHE1-driven acidic pHe.
    Greco MR, Antelmi E, Busco G, Guerra L, Rubino R, Casavola V, Reshkin SJ, Cardone RA.
    Oncol Rep; 2014 Feb 25; 31(2):940-6. PubMed ID: 24337203
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  • 29. Expression and molecular characterization of alternative transcripts of the ARHGEF5/TIM oncogene specific for human breast cancer.
    Debily MA, Camarca A, Ciullo M, Mayer C, El Marhomy S, Ba I, Jalil A, Anzisi A, Guardiola J, Piatier-Tonneau D.
    Hum Mol Genet; 2004 Feb 01; 13(3):323-34. PubMed ID: 14662653
    [Abstract] [Full Text] [Related]

  • 30. Cellular signaling for activation of Rho GTPase Cdc42.
    Sinha S, Yang W.
    Cell Signal; 2008 Nov 01; 20(11):1927-34. PubMed ID: 18558478
    [Abstract] [Full Text] [Related]

  • 31. A Trio-Rac1-Pak1 signalling axis drives invadopodia disassembly.
    Moshfegh Y, Bravo-Cordero JJ, Miskolci V, Condeelis J, Hodgson L.
    Nat Cell Biol; 2014 Jun 01; 16(6):574-86. PubMed ID: 24859002
    [Abstract] [Full Text] [Related]

  • 32. 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]

  • 33. Invasion of breast cancer cells into collagen matrix requires TGF-α and Cdc42 signaling.
    Kikuchi K, Li X, Zheng Y, Takano Y.
    FEBS Lett; 2011 Jan 21; 585(2):286-90. PubMed ID: 21167153
    [Abstract] [Full Text] [Related]

  • 34. 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]

  • 35. FGD1 exhibits oncogenic properties in hepatocellular carcinoma through regulating cell morphology, autophagy and mitochondrial function.
    Zeng Y, Guo Z, Hu Z, Liu M, Chen Y, Chen S, Peng B, Zhang P, Wu Z, Luo H, Zhong F, Jiang K, Lu Y, Yuan G, He S.
    Biomed Pharmacother; 2020 May 01; 125():110029. PubMed ID: 32106378
    [Abstract] [Full Text] [Related]

  • 36. Proline-rich domain plays a crucial role in extracellular stimuli-responsive translocation of a Cdc42 guanine nucleotide exchange factor, FGD1.
    Oshima T, Fujino T, Ando K, Hayakawa M.
    Biol Pharm Bull; 2010 May 01; 33(1):35-9. PubMed ID: 20045932
    [Abstract] [Full Text] [Related]

  • 37. The matrix corroded: podosomes and invadopodia in extracellular matrix degradation.
    Linder S.
    Trends Cell Biol; 2007 Mar 01; 17(3):107-17. PubMed ID: 17275303
    [Abstract] [Full Text] [Related]

  • 38. 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 01; 121(11):4383-92. PubMed ID: 21965325
    [Abstract] [Full Text] [Related]

  • 39. NaV1.5 Na⁺ channels allosterically regulate the NHE-1 exchanger and promote the activity of breast cancer cell invadopodia.
    Brisson L, Driffort V, Benoist L, Poet M, Counillon L, Antelmi E, Rubino R, Besson P, Labbal F, Chevalier S, Reshkin SJ, Gore J, Roger S.
    J Cell Sci; 2013 Nov 01; 126(Pt 21):4835-42. PubMed ID: 23902689
    [Abstract] [Full Text] [Related]

  • 40. Mathematical modeling of invadopodia formation.
    Saitou T, Rouzimaimaiti M, Koshikawa N, Seiki M, Ichikawa K, Suzuki T.
    J Theor Biol; 2012 Apr 07; 298():138-46. PubMed ID: 22212912
    [Abstract] [Full Text] [Related]

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