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Journal Abstract Search

353 related items for PubMed ID: 10402475

  • 1.
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  • 2. OCI-5/GPC3, a glypican encoded by a gene that is mutated in the Simpson-Golabi-Behmel overgrowth syndrome, induces apoptosis in a cell line-specific manner.
    Gonzalez AD, Kaya M, Shi W, Song H, Testa JR, Penn LZ, Filmus J.
    J Cell Biol; 1998 Jun 15; 141(6):1407-14. PubMed ID: 9628896
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  • 3. 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 Jun 15; 44(5):327-9. PubMed ID: 10496077
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  • 5. 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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  • 7. 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
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  • 8. Overgrowth syndromes and genomic imprinting: from mouse to man.
    Li M, Squire JA, Weksberg R.
    Clin Genet; 1998 Mar 01; 53(3):165-70. PubMed ID: 9630066
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  • 9. 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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  • 10. 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
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  • 11. Gpc3 expression correlates with the phenotype of the Simpson-Golabi-Behmel syndrome.
    Pellegrini M, Pilia G, Pantano S, Lucchini F, Uda M, Fumi M, Cao A, Schlessinger D, Forabosco A.
    Dev Dyn; 1998 Dec 01; 213(4):431-9. PubMed ID: 9853964
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  • 12. Glypican 3 and glypican 4 are juxtaposed in Xq26.1.
    Huber R, Mazzarella R, Chen CN, Chen E, Ireland M, Lindsay S, Pilia G, Crisponi L.
    Gene; 1998 Dec 28; 225(1-2):9-16. PubMed ID: 9931407
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  • 13. 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 28; 72(4):279-86. PubMed ID: 11286501
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  • 15. 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 28; 36(1):57-8. PubMed ID: 9950367
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  • 16. 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 28; 65(3):779-83. PubMed ID: 10441586
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  • 17. Mouse mutant embryos overexpressing IGF-II exhibit phenotypic features of the Beckwith-Wiedemann and Simpson-Golabi-Behmel syndromes.
    Eggenschwiler J, Ludwig T, Fisher P, Leighton PA, Tilghman SM, Efstratiadis A.
    Genes Dev; 1997 Dec 01; 11(23):3128-42. PubMed ID: 9389646
    [Abstract] [Full Text] [Related]

  • 18. Multiple Sp1 sites efficiently drive transcription of the TATA-less promoter of the human glypican 3 (GPC3) gene.
    Huber R, Schlessinger D, Pilia G.
    Gene; 1998 Jul 03; 214(1-2):35-44. PubMed ID: 9651473
    [Abstract] [Full Text] [Related]

  • 19. Genotype/phenotype correlations of males affected by Simpson-Golabi-Behmel syndrome with GPC3 gene mutations: patient report and review of the literature.
    Mariani S, Iughetti L, Bertorelli R, Coviello D, Pellegrini M, Forabosco A, Bernasconi S.
    J Pediatr Endocrinol Metab; 2003 Feb 03; 16(2):225-32. PubMed ID: 12713262
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  • 20. 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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