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Journal Abstract Search

262 related items for PubMed ID: 10814714

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  • 5. 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; 72(4):279-86. PubMed ID: 11286501
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  • 7. Molecular analysis of a novel intragenic deletion in GPC3 in three cousins with Simpson-Golabi-Behmel syndrome.
    Schmidt J, Hollstein R, Kaiser FJ, Gillessen-Kaesbach G.
    Am J Med Genet A; 2017 May; 173(5):1400-1405. PubMed ID: 28371070
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  • 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
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  • 11. 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
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  • 12. 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 12; 36(1):57-8. PubMed ID: 9950367
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  • 13. A 4-Mb BAC/PAC contig and complete genomic structure of the GPC5/GPC6 gene cluster on chromosome 13q32.
    Veugelers M, De Cat B, Delande N, Esselens C, Bonk I, Vermeesch J, Marynen P, Fryns JP, David G.
    Matrix Biol; 2001 Sep 12; 20(5-6):375-85. PubMed ID: 11566272
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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. Familial Simpson-Golabi-Behmel syndrome: studies of X-chromosome inactivation and clinical phenotypes in two female individuals with GPC3 mutations.
    Yano S, Baskin B, Bagheri A, Watanabe Y, Moseley K, Nishimura A, Matsumoto N, Ray PN.
    Clin Genet; 2011 Nov 01; 80(5):466-71. PubMed ID: 20950395
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  • 16. 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 Nov 01; 44(5):327-9. PubMed ID: 10496077
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  • 17. 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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  • 18. Duplications of GPC3 and GPC4 genes in symptomatic female carriers of Simpson-Golabi-Behmel syndrome type 1.
    Schirwani S, Novelli A, Digilio MC, Bourn D, Wilson V, Roberts C, Dallapiccola B, Hobson E.
    Eur J Med Genet; 2019 Apr 15; 62(4):243-247. PubMed ID: 30048822
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  • 19. Overgrowth syndromes and genomic imprinting: from mouse to man.
    Li M, Squire JA, Weksberg R.
    Clin Genet; 1998 Mar 15; 53(3):165-70. PubMed ID: 9630066
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  • 20. Novel nonsense mutation of GPC3 gene in a patient with Simpson-Golabi-Behmel syndrome.
    Ratbi I, Elalaoui SC, Moizard MP, Raynaud M, Sefiani A.
    Turk J Pediatr; 2010 Mar 15; 52(5):525-8. PubMed ID: 21434539
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