226 related articles for article (PubMed ID: 12913069)
1. 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; 12(16):1981-93. PubMed ID: 12913069
[TBL] [Abstract][Full Text] [Related]
2. Effect of Fgd1 on cortactin in Arp2/3 complex-mediated actin assembly.
Kim K; Hou P; Gorski JL; Cooper JA
Biochemistry; 2004 Mar; 43(9):2422-7. PubMed ID: 14992579
[TBL] [Abstract][Full Text] [Related]
3. 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; 242(1-2):237-47. PubMed ID: 10721717
[TBL] [Abstract][Full Text] [Related]
4. 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; 60(1):57-66. PubMed ID: 10458911
[TBL] [Abstract][Full Text] [Related]
5. 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; 10(26):3049-62. PubMed ID: 11751687
[TBL] [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; 10(5):485-95. PubMed ID: 11181572
[TBL] [Abstract][Full Text] [Related]
7. Genomic organization of the faciogenital dysplasia (FGD1; Aarskog syndrome) gene.
Pasteris NG; Buckler J; Cadle AB; Gorski JL
Genomics; 1997 Aug; 43(3):390-4. PubMed ID: 9268645
[TBL] [Abstract][Full Text] [Related]
8. 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
[TBL] [Abstract][Full Text] [Related]
9. Cortactin interacts with WIP in regulating Arp2/3 activation and membrane protrusion.
Kinley AW; Weed SA; Weaver AM; Karginov AV; Bissonette E; Cooper JA; Parsons JT
Curr Biol; 2003 Mar; 13(5):384-93. PubMed ID: 12620186
[TBL] [Abstract][Full Text] [Related]
10. Cortactin localization to sites of actin assembly in lamellipodia requires interactions with F-actin and the Arp2/3 complex.
Weed SA; Karginov AV; Schafer DA; Weaver AM; Kinley AW; Cooper JA; Parsons JT
J Cell Biol; 2000 Oct; 151(1):29-40. PubMed ID: 11018051
[TBL] [Abstract][Full Text] [Related]
11. Association of mouse actin-binding protein 1 (mAbp1/SH3P7), an Src kinase target, with dynamic regions of the cortical actin cytoskeleton in response to Rac1 activation.
Kessels MM; Engqvist-Goldstein AE; Drubin DG
Mol Biol Cell; 2000 Jan; 11(1):393-412. PubMed ID: 10637315
[TBL] [Abstract][Full Text] [Related]
12. Regulated interactions between dynamin and the actin-binding protein cortactin modulate cell shape.
McNiven MA; Kim L; Krueger EW; Orth JD; Cao H; Wong TW
J Cell Biol; 2000 Oct; 151(1):187-98. PubMed ID: 11018064
[TBL] [Abstract][Full Text] [Related]
13. Erk/Src phosphorylation of cortactin acts as a switch on-switch off mechanism that controls its ability to activate N-WASP.
Martinez-Quiles N; Ho HY; Kirschner MW; Ramesh N; Geha RS
Mol Cell Biol; 2004 Jun; 24(12):5269-80. PubMed ID: 15169891
[TBL] [Abstract][Full Text] [Related]
14. Actin-binding protein-1 interacts with WASp-interacting protein to regulate growth factor-induced dorsal ruffle formation.
Cortesio CL; Perrin BJ; Bennin DA; Huttenlocher A
Mol Biol Cell; 2010 Jan; 21(1):186-97. PubMed ID: 19910490
[TBL] [Abstract][Full Text] [Related]
15. 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; 121(11):4383-92. PubMed ID: 21965325
[TBL] [Abstract][Full Text] [Related]
16. 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; 79(4):669-78. PubMed ID: 7954831
[TBL] [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; 6(12):1628-33. PubMed ID: 8994827
[TBL] [Abstract][Full Text] [Related]
18. A Cortactin-CD2-associated protein (CD2AP) complex provides a novel link between epidermal growth factor receptor endocytosis and the actin cytoskeleton.
Lynch DK; Winata SC; Lyons RJ; Hughes WE; Lehrbach GM; Wasinger V; Corthals G; Cordwell S; Daly RJ
J Biol Chem; 2003 Jun; 278(24):21805-13. PubMed ID: 12672817
[TBL] [Abstract][Full Text] [Related]
19. The faciogenital dysplasia gene product FGD1 functions as a Cdc42Hs-specific guanine-nucleotide exchange factor.
Zheng Y; Fischer DJ; Santos MF; Tigyi G; Pasteris NG; Gorski JL; Xu Y
J Biol Chem; 1996 Dec; 271(52):33169-72. PubMed ID: 8969170
[TBL] [Abstract][Full Text] [Related]
20. Identification of a novel cortactin SH3 domain-binding protein and its localization to growth cones of cultured neurons.
Du Y; Weed SA; Xiong WC; Marshall TD; Parsons JT
Mol Cell Biol; 1998 Oct; 18(10):5838-51. PubMed ID: 9742101
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
