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121 related items for PubMed ID: 11566272

  • 1. 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; 20(5-6):375-85. PubMed ID: 11566272
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 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. 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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  • 5. Glypican-6, a new member of the glypican family of cell surface heparan sulfate proteoglycans.
    Veugelers M, De Cat B, Ceulemans H, Bruystens AM, Coomans C, Dürr J, Vermeesch J, Marynen P, David G.
    J Biol Chem; 1999 Sep 17; 274(38):26968-77. PubMed ID: 10480909
    [Abstract] [Full Text] [Related]

  • 6. An interstitial duplication of chromosome 13q31.3q32.1 further delineates the critical region for postaxial polydactyly type A2.
    van der Zwaag PA, Dijkhuizen T, Gerssen-Schoorl KB, Colijn AW, Broens PM, Flapper BC, van Ravenswaaij-Arts CM.
    Eur J Med Genet; 2010 Sep 17; 53(1):45-9. PubMed ID: 19941983
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. GPC5 is a possible target for the 13q31-q32 amplification detected in lymphoma cell lines.
    Yu W, Inoue J, Imoto I, Matsuo Y, Karpas A, Inazawa J.
    J Hum Genet; 2003 Feb 15; 48(6):331-335. PubMed ID: 12721791
    [Abstract] [Full Text] [Related]

  • 9. 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
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. 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]

  • 12. Mutations in the heparan-sulfate proteoglycan glypican 6 (GPC6) impair endochondral ossification and cause recessive omodysplasia.
    Campos-Xavier AB, Martinet D, Bateman J, Belluoccio D, Rowley L, Tan TY, Baxová A, Gustavson KH, Borochowitz ZU, Innes AM, Unger S, Beckmann JS, Mittaz L, Ballhausen D, Superti-Furga A, Savarirayan R, Bonafé L.
    Am J Hum Genet; 2009 Jun 28; 84(6):760-70. PubMed ID: 19481194
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  • 17. 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 28; 12(3):241-7. PubMed ID: 8589713
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  • 18. Mapping of the rat glypican genes.
    Szpirer C, Szpirer J, Rivière M, Van Vooren P, Veugelers M, David G.
    Cytogenet Cell Genet; 2001 Mar 28; 93(1-2):83-6. PubMed ID: 11474185
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  • 20. 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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