These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


387 related items for PubMed ID: 17387722

  • 1. Huntington's disease--like 2 is associated with CUG repeat-containing RNA foci.
    Rudnicki DD, Holmes SE, Lin MW, Thornton CA, Ross CA, Margolis RL.
    Ann Neurol; 2007 Mar; 61(3):272-82. PubMed ID: 17387722
    [Abstract] [Full Text] [Related]

  • 2. Myotonic dystrophy associated expanded CUG repeat muscleblind positive ribonuclear foci are not toxic to Drosophila.
    Houseley JM, Wang Z, Brock GJ, Soloway J, Artero R, Perez-Alonso M, O'Dell KM, Monckton DG.
    Hum Mol Genet; 2005 Mar 15; 14(6):873-83. PubMed ID: 15703191
    [Abstract] [Full Text] [Related]

  • 3. Colocalization of muscleblind with RNA foci is separable from mis-regulation of alternative splicing in myotonic dystrophy.
    Ho TH, Savkur RS, Poulos MG, Mancini MA, Swanson MS, Cooper TA.
    J Cell Sci; 2005 Jul 01; 118(Pt 13):2923-33. PubMed ID: 15961406
    [Abstract] [Full Text] [Related]

  • 4. MBNL1 and CUGBP1 modify expanded CUG-induced toxicity in a Drosophila model of myotonic dystrophy type 1.
    de Haro M, Al-Ramahi I, De Gouyon B, Ukani L, Rosa A, Faustino NA, Ashizawa T, Cooper TA, Botas J.
    Hum Mol Genet; 2006 Jul 01; 15(13):2138-45. PubMed ID: 16723374
    [Abstract] [Full Text] [Related]

  • 5. Myotonic dystrophy type 1 is associated with nuclear foci of mutant RNA, sequestration of muscleblind proteins and deregulated alternative splicing in neurons.
    Jiang H, Mankodi A, Swanson MS, Moxley RT, Thornton CA.
    Hum Mol Genet; 2004 Dec 15; 13(24):3079-88. PubMed ID: 15496431
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. Analysis of MTMR1 expression and correlation with muscle pathological features in juvenile/adult onset myotonic dystrophy type 1 (DM1) and in myotonic dystrophy type 2 (DM2).
    Santoro M, Modoni A, Masciullo M, Gidaro T, Broccolini A, Ricci E, Tonali PA, Silvestri G.
    Exp Mol Pathol; 2010 Oct 15; 89(2):158-68. PubMed ID: 20685272
    [Abstract] [Full Text] [Related]

  • 8. Nuclear RNA foci in the heart in myotonic dystrophy.
    Mankodi A, Lin X, Blaxall BC, Swanson MS, Thornton CA.
    Circ Res; 2005 Nov 25; 97(11):1152-5. PubMed ID: 16254211
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Aberrantly spliced alpha-dystrobrevin alters alpha-syntrophin binding in myotonic dystrophy type 1.
    Nakamori M, Kimura T, Kubota T, Matsumura T, Sumi H, Fujimura H, Takahashi MP, Sakoda S.
    Neurology; 2008 Feb 26; 70(9):677-85. PubMed ID: 18299519
    [Abstract] [Full Text] [Related]

  • 12. Length-dependent toxicity of untranslated CUG repeats on Caenorhabditis elegans.
    Chen KY, Pan H, Lin MJ, Li YY, Wang LC, Wu YC, Hsiao KM.
    Biochem Biophys Res Commun; 2007 Jan 19; 352(3):774-9. PubMed ID: 17150182
    [Abstract] [Full Text] [Related]

  • 13. Ribonuclear inclusions in skeletal muscle in myotonic dystrophy types 1 and 2.
    Mankodi A, Teng-Umnuay P, Krym M, Henderson D, Swanson M, Thornton CA.
    Ann Neurol; 2003 Dec 19; 54(6):760-8. PubMed ID: 14681885
    [Abstract] [Full Text] [Related]

  • 14. Aberrant regulation of insulin receptor alternative splicing is associated with insulin resistance in myotonic dystrophy.
    Savkur RS, Philips AV, Cooper TA.
    Nat Genet; 2001 Sep 19; 29(1):40-7. PubMed ID: 11528389
    [Abstract] [Full Text] [Related]

  • 15. Gain of RNA function in pathological cases: Focus on myotonic dystrophy.
    Klein AF, Gasnier E, Furling D.
    Biochimie; 2011 Nov 19; 93(11):2006-12. PubMed ID: 21763392
    [Abstract] [Full Text] [Related]

  • 16. Myotonic dystrophy expanded CUG repeats disturb the expression and phosphorylation of tau in PC12 cells.
    Hernández-Hernández O, Bermúdez-de-León M, Gómez P, Velázquez-Bernardino P, García-Sierra F, Cisneros B.
    J Neurosci Res; 2006 Sep 19; 84(4):841-51. PubMed ID: 16862553
    [Abstract] [Full Text] [Related]

  • 17. Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes.
    Stevanin G, Fujigasaki H, Lebre AS, Camuzat A, Jeannequin C, Dode C, Takahashi J, San C, Bellance R, Brice A, Durr A.
    Brain; 2003 Jul 19; 126(Pt 7):1599-603. PubMed ID: 12805114
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. RNA-mediated neuromuscular disorders.
    Ranum LP, Cooper TA.
    Annu Rev Neurosci; 2006 Jul 19; 29():259-77. PubMed ID: 16776586
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 20.