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Journal Abstract Search

273 related items for PubMed ID: 9787072

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  • 3. 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
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  • 4. 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
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  • 5. 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
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  • 8. 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
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  • 9. 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 15; 72(4):279-86. PubMed ID: 11286501
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  • 10. Simpson-Golabi-Behmel syndrome: genotype/phenotype analysis of 18 affected males from 7 unrelated families.
    Hughes-Benzie RM, Pilia G, Xuan JY, Hunter AG, Chen E, Golabi M, Hurst JA, Kobori J, Marymee K, Pagon RA, Punnett HH, Schelley S, Tolmie JL, Wohlferd MM, Grossman T, Schlessinger D, MacKenzie AE.
    Am J Med Genet; 1996 Dec 11; 66(2):227-34. PubMed ID: 8958336
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  • 11. A clinical and molecular study of a patient with Simpson-Golabi-Behmel syndrome.
    Okamoto N, Yagi M, Imura K, Wada Y.
    J Hum Genet; 1999 Dec 11; 44(5):327-9. PubMed ID: 10496077
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  • 12. 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
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  • 13. 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
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  • 14. Analysis of exon/intron structure and 400 kb of genomic sequence surrounding the 5'-promoter and 3'-terminal ends of the human glypican 3 (GPC3) gene.
    Huber R, Crisponi L, Mazzarella R, Chen CN, Su Y, Shizuya H, Chen EY, Cao A, Pilia G.
    Genomics; 1997 Oct 01; 45(1):48-58. PubMed ID: 9339360
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  • 15. Large scale deletions in the GPC3 gene may account for a minority of cases of Simpson-Golabi-Behmel syndrome.
    Lindsay S, Ireland M, O'Brien O, Clayton-Smith J, Hurst JA, Mann J, Cole T, Sampson J, Slaney S, Schlessinger D, Burn J, Pilia G.
    J Med Genet; 1997 Jun 01; 34(6):480-3. PubMed ID: 9192268
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  • 16. Transcriptional regulation of OCI-5/Glypican 3: elongation control of confluence-dependent induction.
    Li M, Pullano R, Yang HL, Lee HK, Miyamoto NG, Filmus J, Buick RN.
    Oncogene; 1997 Sep 25; 15(13):1535-44. PubMed ID: 9380405
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  • 17. Characterization of glypican-5 and chromosomal localization of human GPC5, a new member of the glypican gene family.
    Veugelers M, Vermeesch J, Reekmans G, Steinfeld R, Marynen P, David G.
    Genomics; 1997 Feb 15; 40(1):24-30. PubMed ID: 9070915
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  • 18. 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
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  • 19. GPC3 mutation analysis in a spectrum of patients with overgrowth expands the phenotype of Simpson-Golabi-Behmel syndrome.
    Li M, Shuman C, Fei YL, Cutiongco E, Bender HA, Stevens C, Wilkins-Haug L, Day-Salvatore D, Yong SL, Geraghty MT, Squire J, Weksberg R.
    Am J Med Genet; 2001 Aug 01; 102(2):161-8. PubMed ID: 11477610
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  • 20. Mapping of a new SGBS locus to chromosome Xp22 in a family with a severe form of Simpson-Golabi-Behmel syndrome.
    Brzustowicz LM, Farrell S, Khan MB, Weksberg R.
    Am J Hum Genet; 1999 Sep 01; 65(3):779-83. PubMed ID: 10441586
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