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Journal Abstract Search

176 related items for PubMed ID: 11478809

  • 1. The paralemmin protein family: identification of paralemmin-2, an isoform differentially spliced to AKAP2/AKAP-KL, and of palmdelphin, a more distant cytosolic relative.
    Hu B, Copeland NG, Gilbert DJ, Jenkins NA, Kilimann MW.
    Biochem Biophys Res Commun; 2001 Aug 03; 285(5):1369-76. PubMed ID: 11478809
    [Abstract] [Full Text] [Related]

  • 2. Molecular characterization and immunohistochemical localization of palmdelphin, a cytosolic isoform of the paralemmin protein family implicated in membrane dynamics.
    Hu B, Petrasch-Parwez E, Laue MM, Kilimann MW.
    Eur J Cell Biol; 2005 Nov 03; 84(11):853-66. PubMed ID: 16323283
    [Abstract] [Full Text] [Related]

  • 3. Human and Xenopus cingulin share a modular organization of the coiled-coil rod domain: predictions for intra- and intermolecular assembly.
    Citi S, D'Atri F, Parry DA.
    J Struct Biol; 2000 Aug 03; 131(2):135-45. PubMed ID: 11042084
    [Abstract] [Full Text] [Related]

  • 4. Identification and characterization of human FCHSD1 and FCHSD2 genes in silico.
    Katoh M, Katoh M.
    Int J Mol Med; 2004 May 03; 13(5):749-54. PubMed ID: 15067381
    [Abstract] [Full Text] [Related]

  • 5. Identification and characterization of Crumbs homolog 2 gene at human chromosome 9q33.3.
    Katoh M, Katoh M.
    Int J Oncol; 2004 Mar 03; 24(3):743-9. PubMed ID: 14767562
    [Abstract] [Full Text] [Related]

  • 6. PALML, a novel paralemmin-related gene mapping on human chromosome 1p21.
    Andreu N, Escarceller M, Feather S, Devriendt K, Wolf AS, Estivill X, Sumoy L.
    Gene; 2001 Oct 31; 278(1-2):33-40. PubMed ID: 11707320
    [Abstract] [Full Text] [Related]

  • 7. Molecular cloning, expression and chromosomal localization of a novel human REG family gene, REG III.
    Nata K, Liu Y, Xu L, Ikeda T, Akiyama T, Noguchi N, Kawaguchi S, Yamauchi A, Takahashi I, Shervani NJ, Onogawa T, Takasawa S, Okamoto H.
    Gene; 2004 Sep 29; 340(1):161-70. PubMed ID: 15556304
    [Abstract] [Full Text] [Related]

  • 8. Bin2, a functionally nonredundant member of the BAR adaptor gene family.
    Ge K, Prendergast GC.
    Genomics; 2000 Jul 15; 67(2):210-20. PubMed ID: 10903846
    [Abstract] [Full Text] [Related]

  • 9. Conservation and expression of an alternative 3' exon of Runx2 encoding a novel proline-rich C-terminal domain.
    Terry A, Kilbey A, Vaillant F, Stewart M, Jenkins A, Cameron E, Neil JC.
    Gene; 2004 Jul 07; 336(1):115-25. PubMed ID: 15225881
    [Abstract] [Full Text] [Related]

  • 10. Structure of the human paralemmin gene (PALM), mapping to human chromosome 19p13.3 and mouse chromosome 10, and exclusion of coding mutations in grizzled, mocha, jittery, and hesitant mice.
    Burwinkel B, Miglierini G, Jenne DE, Gilbert DJ, Copeland NG, Jenkins NA, Ring HZ, Francke U, Kilimann MW.
    Genomics; 1998 May 01; 49(3):462-6. PubMed ID: 9615234
    [Abstract] [Full Text] [Related]

  • 11. Molecular cloning and characterization of the mouse Acdp gene family.
    Wang CY, Yang P, Shi JD, Purohit S, Guo D, An H, Gu JG, Ling J, Dong Z, She JX.
    BMC Genomics; 2004 Jan 15; 5(1):7. PubMed ID: 14723793
    [Abstract] [Full Text] [Related]

  • 12. Characterization of RUSC1 and RUSC2 genes in silico.
    Katoh M, Katoh M.
    Oncol Rep; 2004 Oct 15; 12(4):933-8. PubMed ID: 15375525
    [Abstract] [Full Text] [Related]

  • 13. KIAA1735 gene on human chromosome 11q23.1 encodes a novel protein with myosine-tail homologous domain and C-terminal DIX domain.
    Katoh M, Katoh M.
    Int J Oncol; 2003 Jul 15; 23(1):145-50. PubMed ID: 12792787
    [Abstract] [Full Text] [Related]

  • 14. Proteins encoded by human Down syndrome critical region gene 1-like 2 (DSCR1L2) mRNA and by a novel DSCR1L2 mRNA isoform interact with cardiac troponin I (TNNI3).
    Canaider S, Facchin F, Griffoni C, Casadei R, Vitale L, Lenzi L, Frabetti F, D'Addabbo P, Carinci P, Zannotti M, Strippoli P.
    Gene; 2006 May 10; 372():128-36. PubMed ID: 16516408
    [Abstract] [Full Text] [Related]

  • 15. Novel splicing isoforms of synaptotagmin-like proteins 2 and 3: identification of the Slp homology domain.
    Fukuda M, Saegusa C, Mikoshiba K.
    Biochem Biophys Res Commun; 2001 May 04; 283(2):513-9. PubMed ID: 11327731
    [Abstract] [Full Text] [Related]

  • 16. The breakpoint identified in a balanced de novo translocation t(7;9)(p14.1;q31.3) disrupts the A-kinase (PRKA) anchor protein 2 gene (AKAP2) on chromosome 9 in a patient with Kallmann syndrome and bone anomalies.
    Panza E, Gimelli G, Passalacqua M, Cohen A, Gimelli S, Giglio S, Ghezzi C, Sparatore B, Heye B, Zuffardi O, Rugarli E, Meitinger T, Romeo G, Ravazzolo R, Seri M.
    Int J Mol Med; 2007 Mar 04; 19(3):429-35. PubMed ID: 17273791
    [Abstract] [Full Text] [Related]

  • 17. claudin-18, a novel downstream target gene for the T/EBP/NKX2.1 homeodomain transcription factor, encodes lung- and stomach-specific isoforms through alternative splicing.
    Niimi T, Nagashima K, Ward JM, Minoo P, Zimonjic DB, Popescu NC, Kimura S.
    Mol Cell Biol; 2001 Nov 04; 21(21):7380-90. PubMed ID: 11585919
    [Abstract] [Full Text] [Related]

  • 18. Identification and characterization of rat Dact1 and Dact2 genes in silico.
    Katoh M, Katoh M.
    Int J Mol Med; 2005 Jun 04; 15(6):1045-9. PubMed ID: 15870912
    [Abstract] [Full Text] [Related]

  • 19. Identification and characterization of human DIAPH3 gene in silico.
    Katoh M, Katoh M.
    Int J Mol Med; 2004 Mar 04; 13(3):473-8. PubMed ID: 14767582
    [Abstract] [Full Text] [Related]

  • 20. Identification and characterization of JMJD2 family genes in silico.
    Katoh M, Katoh M.
    Int J Oncol; 2004 Jun 04; 24(6):1623-8. PubMed ID: 15138608
    [Abstract] [Full Text] [Related]

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