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220 related items for PubMed ID: 10964473

  • 1. glypican-3 controls cellular responses to Bmp4 in limb patterning and skeletal development.
    Paine-Saunders S, Viviano BL, Zupicich J, Skarnes WC, Saunders S.
    Dev Biol; 2000 Sep 01; 225(1):179-87. PubMed ID: 10964473
    [Abstract] [Full Text] [Related]

  • 2. GPC4, the gene for human K-glypican, flanks GPC3 on xq26: deletion of the GPC3-GPC4 gene cluster in one family with Simpson-Golabi-Behmel syndrome.
    Veugelers M, Vermeesch J, Watanabe K, Yamaguchi Y, Marynen P, David G.
    Genomics; 1998 Oct 01; 53(1):1-11. PubMed ID: 9787072
    [Abstract] [Full Text] [Related]

  • 3. Expression of the cell surface proteoglycan glypican-5 is developmentally regulated in kidney, limb, and brain.
    Saunders S, Paine-Saunders S, Lander AD.
    Dev Biol; 1997 Oct 01; 190(1):78-93. PubMed ID: 9331333
    [Abstract] [Full Text] [Related]

  • 4. Simpson Golabi Behmel syndrome: progress toward understanding the molecular basis for overgrowth, malformation, and cancer predisposition.
    DeBaun MR, Ess J, Saunders S.
    Mol Genet Metab; 2001 Apr 01; 72(4):279-86. PubMed ID: 11286501
    [Abstract] [Full Text] [Related]

  • 5. Overgrowth of a mouse model of the Simpson-Golabi-Behmel syndrome is independent of IGF signaling.
    Chiao E, Fisher P, Crisponi L, Deiana M, Dragatsis I, Schlessinger D, Pilia G, Efstratiadis A.
    Dev Biol; 2002 Mar 01; 243(1):185-206. PubMed ID: 11846487
    [Abstract] [Full Text] [Related]

  • 6. Altered hematopoiesis in glypican-3-deficient mice results in decreased osteoclast differentiation and a delay in endochondral ossification.
    Viviano BL, Silverstein L, Pflederer C, Paine-Saunders S, Mills K, Saunders S.
    Dev Biol; 2005 Jun 01; 282(1):152-62. PubMed ID: 15936336
    [Abstract] [Full Text] [Related]

  • 7. Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome.
    Pilia G, Hughes-Benzie RM, MacKenzie A, Baybayan P, Chen EY, Huber R, Neri G, Cao A, Forabosco A, Schlessinger D.
    Nat Genet; 1996 Mar 01; 12(3):241-7. PubMed ID: 8589713
    [Abstract] [Full Text] [Related]

  • 8. A small interstitial deletion in the GPC3 gene causes Simpson-Golabi-Behmel syndrome in a Dutch-Canadian family.
    Xuan JY, Hughes-Benzie RM, MacKenzie AE.
    J Med Genet; 1999 Jan 01; 36(1):57-8. PubMed ID: 9950367
    [Abstract] [Full Text] [Related]

  • 9. GPC6, a novel member of the glypican gene family, encodes a product structurally related to GPC4 and is colocalized with GPC5 on human chromosome 13.
    Paine-Saunders S, Viviano BL, Saunders S.
    Genomics; 1999 May 01; 57(3):455-8. PubMed ID: 10329016
    [Abstract] [Full Text] [Related]

  • 10. Glypican-3 modulates inhibitory Bmp2-Smad signaling to control renal development in vivo.
    Hartwig S, Hu MC, Cella C, Piscione T, Filmus J, Rosenblum ND.
    Mech Dev; 2005 Jul 01; 122(7-8):928-38. PubMed ID: 15925496
    [Abstract] [Full Text] [Related]

  • 11. Glypican-3 modulates BMP- and FGF-mediated effects during renal branching morphogenesis.
    Grisaru S, Cano-Gauci D, Tee J, Filmus J, Rosenblum ND.
    Dev Biol; 2001 Mar 01; 231(1):31-46. PubMed ID: 11180950
    [Abstract] [Full Text] [Related]

  • 12. Mutational analysis of the GPC3/GPC4 glypican gene cluster on Xq26 in patients with Simpson-Golabi-Behmel syndrome: identification of loss-of-function mutations in the GPC3 gene.
    Veugelers M, Cat BD, Muyldermans SY, Reekmans G, Delande N, Frints S, Legius E, Fryns JP, Schrander-Stumpel C, Weidle B, Magdalena N, David G.
    Hum Mol Genet; 2000 May 22; 9(9):1321-8. PubMed ID: 10814714
    [Abstract] [Full Text] [Related]

  • 13. Glypican-3-deficient mice exhibit developmental overgrowth and some of the abnormalities typical of Simpson-Golabi-Behmel syndrome.
    Cano-Gauci DF, Song HH, Yang H, McKerlie C, Choo B, Shi W, Pullano R, Piscione TD, Grisaru S, Soon S, Sedlackova L, Tanswell AK, Mak TW, Yeger H, Lockwood GA, Rosenblum ND, Filmus J.
    J Cell Biol; 1999 Jul 12; 146(1):255-64. PubMed ID: 10402475
    [Abstract] [Full Text] [Related]

  • 14. Haploinsufficient phenotypes in Bmp4 heterozygous null mice and modification by mutations in Gli3 and Alx4.
    Dunn NR, Winnier GE, Hargett LK, Schrick JJ, Fogo AB, Hogan BL.
    Dev Biol; 1997 Aug 15; 188(2):235-47. PubMed ID: 9268572
    [Abstract] [Full Text] [Related]

  • 15. Expression of GPC3, an X-linked recessive overgrowth gene, is silenced in malignant mesothelioma.
    Murthy SS, Shen T, De Rienzo A, Lee WC, Ferriola PC, Jhanwar SC, Mossman BT, Filmus J, Testa JR.
    Oncogene; 2000 Jan 20; 19(3):410-6. PubMed ID: 10656689
    [Abstract] [Full Text] [Related]

  • 16. Overgrowth syndromes and genomic imprinting: from mouse to man.
    Li M, Squire JA, Weksberg R.
    Clin Genet; 1998 Mar 20; 53(3):165-70. PubMed ID: 9630066
    [Abstract] [Full Text] [Related]

  • 17. Frequent silencing of the GPC3 gene in ovarian cancer cell lines.
    Lin H, Huber R, Schlessinger D, Morin PJ.
    Cancer Res; 1999 Feb 15; 59(4):807-10. PubMed ID: 10029067
    [Abstract] [Full Text] [Related]

  • 18. Expression of the heparan sulfate proteoglycan glypican-1 in the developing rodent.
    Litwack ED, Ivins JK, Kumbasar A, Paine-Saunders S, Stipp CS, Lander AD.
    Dev Dyn; 1998 Jan 15; 211(1):72-87. PubMed ID: 9438425
    [Abstract] [Full Text] [Related]

  • 19. Noggin antagonism of BMP4 signaling controls development of the axial skeleton in the mouse.
    Wijgerde M, Karp S, McMahon J, McMahon AP.
    Dev Biol; 2005 Oct 01; 286(1):149-57. PubMed ID: 16122729
    [Abstract] [Full Text] [Related]

  • 20. Fibroblast growth factor signaling regulates Dach1 expression during skeletal development.
    Horner A, Shum L, Ayres JA, Nonaka K, Nuckolls GH.
    Dev Dyn; 2002 Sep 01; 225(1):35-45. PubMed ID: 12203718
    [Abstract] [Full Text] [Related]

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