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PUBMED FOR HANDHELDS

Journal Abstract Search


152 related items for PubMed ID: 17567778

  • 1. Huntingtin-deficient zebrafish exhibit defects in iron utilization and development.
    Lumsden AL, Henshall TL, Dayan S, Lardelli MT, Richards RI.
    Hum Mol Genet; 2007 Aug 15; 16(16):1905-20. PubMed ID: 17567778
    [Abstract] [Full Text] [Related]

  • 2. C1q-like inhibits p53-mediated apoptosis and controls normal hematopoiesis during zebrafish embryogenesis.
    Mei J, Zhang QY, Li Z, Lin S, Gui JF.
    Dev Biol; 2008 Jul 15; 319(2):273-84. PubMed ID: 18514183
    [Abstract] [Full Text] [Related]

  • 3. A novel endothelial-specific heat shock protein HspA12B is required in both zebrafish development and endothelial functions in vitro.
    Hu G, Tang J, Zhang B, Lin Y, Hanai J, Galloway J, Bedell V, Bahary N, Han Z, Ramchandran R, Thisse B, Thisse C, Zon LI, Sukhatme VP.
    J Cell Sci; 2006 Oct 01; 119(Pt 19):4117-26. PubMed ID: 16968741
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  • 4. Striatal specificity of gene expression dysregulation in Huntington's disease.
    Thomas EA.
    J Neurosci Res; 2006 Nov 01; 84(6):1151-64. PubMed ID: 16983659
    [Abstract] [Full Text] [Related]

  • 5. Decreased BDNF levels are a major contributor to the embryonic phenotype of huntingtin knockdown zebrafish.
    Diekmann H, Anichtchik O, Fleming A, Futter M, Goldsmith P, Roach A, Rubinsztein DC.
    J Neurosci; 2009 Feb 04; 29(5):1343-9. PubMed ID: 19193881
    [Abstract] [Full Text] [Related]

  • 6. Transferrin-a modulates hepcidin expression in zebrafish embryos.
    Fraenkel PG, Gibert Y, Holzheimer JL, Lattanzi VJ, Burnett SF, Dooley KA, Wingert RA, Zon LI.
    Blood; 2009 Mar 19; 113(12):2843-50. PubMed ID: 19047682
    [Abstract] [Full Text] [Related]

  • 7. Chondroitin 4-O-sulfotransferase-1 is required for somitic muscle development and motor axon guidance in zebrafish.
    Mizumoto S, Mikami T, Yasunaga D, Kobayashi N, Yamauchi H, Miyake A, Itoh N, Kitagawa H, Sugahara K.
    Biochem J; 2009 Apr 15; 419(2):387-99. PubMed ID: 19125692
    [Abstract] [Full Text] [Related]

  • 8. Global changes to the ubiquitin system in Huntington's disease.
    Bennett EJ, Shaler TA, Woodman B, Ryu KY, Zaitseva TS, Becker CH, Bates GP, Schulman H, Kopito RR.
    Nature; 2007 Aug 09; 448(7154):704-8. PubMed ID: 17687326
    [Abstract] [Full Text] [Related]

  • 9. The lim domain only protein 7 is important in zebrafish heart development.
    Ott EB, van den Akker NM, Sakalis PA, Gittenberger-de Groot AC, Te Velthuis AJ, Bagowski CP.
    Dev Dyn; 2008 Dec 09; 237(12):3940-52. PubMed ID: 19035355
    [Abstract] [Full Text] [Related]

  • 10. The Wilms tumor genes wt1a and wt1b control different steps during formation of the zebrafish pronephros.
    Perner B, Englert C, Bollig F.
    Dev Biol; 2007 Sep 01; 309(1):87-96. PubMed ID: 17651719
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  • 12. The chianti zebrafish mutant provides a model for erythroid-specific disruption of transferrin receptor 1.
    Wingert RA, Brownlie A, Galloway JL, Dooley K, Fraenkel P, Axe JL, Davidson AJ, Barut B, Noriega L, Sheng X, Zhou Y, Zon LI.
    Development; 2004 Dec 01; 131(24):6225-35. PubMed ID: 15563524
    [Abstract] [Full Text] [Related]

  • 13. The A2A adenosine receptor rescues the urea cycle deficiency of Huntington's disease by enhancing the activity of the ubiquitin-proteasome system.
    Chiang MC, Chen HM, Lai HL, Chen HW, Chou SY, Chen CM, Tsai FJ, Chern Y.
    Hum Mol Genet; 2009 Aug 15; 18(16):2929-42. PubMed ID: 19443488
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  • 16. Discovery and characterization of three novel synuclein genes in zebrafish.
    Sun Z, Gitler AD.
    Dev Dyn; 2008 Sep 15; 237(9):2490-5. PubMed ID: 18521955
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  • 18. Selective neuronal requirement for huntingtin in the developing zebrafish.
    Henshall TL, Tucker B, Lumsden AL, Nornes S, Lardelli MT, Richards RI.
    Hum Mol Genet; 2009 Dec 15; 18(24):4830-42. PubMed ID: 19797250
    [Abstract] [Full Text] [Related]

  • 19. The transcription factor Six1a plays an essential role in the craniofacial myogenesis of zebrafish.
    Lin CY, Chen WT, Lee HC, Yang PH, Yang HJ, Tsai HJ.
    Dev Biol; 2009 Jul 15; 331(2):152-66. PubMed ID: 19409884
    [Abstract] [Full Text] [Related]

  • 20. Deficiency of ribosomal protein S19 during early embryogenesis leads to reduction of erythrocytes in a zebrafish model of Diamond-Blackfan anemia.
    Uechi T, Nakajima Y, Chakraborty A, Torihara H, Higa S, Kenmochi N.
    Hum Mol Genet; 2008 Oct 15; 17(20):3204-11. PubMed ID: 18653748
    [Abstract] [Full Text] [Related]


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