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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. 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]
4. 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]
8. 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]
9. 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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
11. 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]
13. 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 [Abstract] [Full Text] [Related]
14. 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]
15. 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 [Abstract] [Full Text] [Related]
16. 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]
18. 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 20; 65(3):779-83. PubMed ID: 10441586 [Abstract] [Full Text] [Related]
19. 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 [Abstract] [Full Text] [Related]