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Journal Abstract Search

230 related items for PubMed ID: 19481194

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  • 3. Altered hematopoiesis in glypican-3-deficient mice results in decreased osteoclast differentiation and a delay in endochondral ossification.
    Viviano BL, Silverstein L, Pflederer C, Paine-Saunders S, Mills K, Saunders S.
    Dev Biol; 2005 Jun 01; 282(1):152-62. PubMed ID: 15936336
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  • 4. 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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  • 5. 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 01; 173(5):1400-1405. PubMed ID: 28371070
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  • 7. Five siblings expand the spectrum of GPC6-related skeletal dysplasia.
    Crenshaw MM, Meyers ML, Brown K, Slegesky V, Duis J, Elias ER, Saenz M, Shi W, Filmus J, Meeks NJL.
    Am J Med Genet A; 2023 Oct 01; 191(10):2571-2577. PubMed ID: 37353964
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  • 8. 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
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  • 9. 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 17; 12(3):241-7. PubMed ID: 8589713
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  • 10. Glypican-6 promotes the growth of developing long bones by stimulating Hedgehog signaling.
    Capurro M, Izumikawa T, Suarez P, Shi W, Cydzik M, Kaneiwa T, Gariepy J, Bonafe L, Filmus J.
    J Cell Biol; 2017 Sep 04; 216(9):2911-2926. PubMed ID: 28696225
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  • 11. Allelic imbalance at 13q31 is associated with reduced GPC6 in Chinese with sporadic retinoblastoma.
    Lau CS, Yu CB, Wong HK, Fan DS, Mak HT, Wong KW, Lam DS, Pang CP, Choy KW.
    Br J Ophthalmol; 2010 Mar 04; 94(3):357-62. PubMed ID: 19726429
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  • 12. 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 Mar 04; 53(1):45-9. PubMed ID: 19941983
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  • 13. Glypicans in growth control and cancer.
    Filmus J.
    Glycobiology; 2001 Mar 04; 11(3):19R-23R. PubMed ID: 11320054
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  • 14. Glypican-6 and Glypican-4 stimulate embryonic stomach growth by regulating Hedgehog and noncanonical Wnt signaling.
    Shi W, Filmus J.
    Dev Dyn; 2022 Dec 04; 251(12):2015-2028. PubMed ID: 36057966
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  • 15. Pathogenic Variants in GPC4 Cause Keipert Syndrome.
    Amor DJ, Stephenson SEM, Mustapha M, Mensah MA, Ockeloen CW, Lee WS, Tankard RM, Phelan DG, Shinawi M, de Brouwer APM, Pfundt R, Dowling C, Toler TL, Sutton VR, Agolini E, Rinelli M, Capolino R, Martinelli D, Zampino G, Dumić M, Reardon W, Shaw-Smith C, Leventer RJ, Delatycki MB, Kleefstra T, Mundlos S, Mortier G, Bahlo M, Allen NJ, Lockhart PJ.
    Am J Hum Genet; 2019 May 02; 104(5):914-924. PubMed ID: 30982611
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  • 16. 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 02; 213(4):431-9. PubMed ID: 9853964
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  • 17. 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 02; 44(5):327-9. PubMed ID: 10496077
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  • 18. 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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  • 19. 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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  • 20. 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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