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Journal Abstract Search

548 related items for PubMed ID: 18492800

  • 1. Reduced SMN protein impairs maturation of the neuromuscular junctions in mouse models of spinal muscular atrophy.
    Kariya S, Park GH, Maeno-Hikichi Y, Leykekhman O, Lutz C, Arkovitz MS, Landmesser LT, Monani UR.
    Hum Mol Genet; 2008 Aug 15; 17(16):2552-69. PubMed ID: 18492800
    [Abstract] [Full Text] [Related]

  • 2. Selective vulnerability of motor neurons and dissociation of pre- and post-synaptic pathology at the neuromuscular junction in mouse models of spinal muscular atrophy.
    Murray LM, Comley LH, Thomson D, Parkinson N, Talbot K, Gillingwater TH.
    Hum Mol Genet; 2008 Apr 01; 17(7):949-62. PubMed ID: 18065780
    [Abstract] [Full Text] [Related]

  • 3. Reduced survival of motor neuron (SMN) protein in motor neuronal progenitors functions cell autonomously to cause spinal muscular atrophy in model mice expressing the human centromeric (SMN2) gene.
    Park GH, Maeno-Hikichi Y, Awano T, Landmesser LT, Monani UR.
    J Neurosci; 2010 Sep 08; 30(36):12005-19. PubMed ID: 20826664
    [Abstract] [Full Text] [Related]

  • 4. Motor transmission defects with sex differences in a new mouse model of mild spinal muscular atrophy.
    Deguise MO, De Repentigny Y, Tierney A, Beauvais A, Michaud J, Chehade L, Thabet M, Paul B, Reilly A, Gagnon S, Renaud JM, Kothary R.
    EBioMedicine; 2020 May 08; 55():102750. PubMed ID: 32339936
    [Abstract] [Full Text] [Related]

  • 5. Motor neuronal repletion of the NMJ organizer, Agrin, modulates the severity of the spinal muscular atrophy disease phenotype in model mice.
    Kim JK, Caine C, Awano T, Herbst R, Monani UR.
    Hum Mol Genet; 2017 Jul 01; 26(13):2377-2385. PubMed ID: 28379354
    [Abstract] [Full Text] [Related]

  • 6. Embryonic motor axon development in the severe SMA mouse.
    McGovern VL, Gavrilina TO, Beattie CE, Burghes AH.
    Hum Mol Genet; 2008 Sep 15; 17(18):2900-9. PubMed ID: 18603534
    [Abstract] [Full Text] [Related]

  • 7. SMNDelta7, the major product of the centromeric survival motor neuron (SMN2) gene, extends survival in mice with spinal muscular atrophy and associates with full-length SMN.
    Le TT, Pham LT, Butchbach ME, Zhang HL, Monani UR, Coovert DD, Gavrilina TO, Xing L, Bassell GJ, Burghes AH.
    Hum Mol Genet; 2005 Mar 15; 14(6):845-57. PubMed ID: 15703193
    [Abstract] [Full Text] [Related]

  • 8. The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn(-/-) mice and results in a mouse with spinal muscular atrophy.
    Monani UR, Sendtner M, Coovert DD, Parsons DW, Andreassi C, Le TT, Jablonka S, Schrank B, Rossoll W, Prior TW, Morris GE, Burghes AH.
    Hum Mol Genet; 2000 Feb 12; 9(3):333-9. PubMed ID: 10655541
    [Abstract] [Full Text] [Related]

  • 9. Understanding motoneurone development explains spinal muscular atrophy.
    Vrbová G.
    Arch Ital Biol; 2007 Nov 12; 145(3-4):325-35. PubMed ID: 18075125
    [No Abstract] [Full Text] [Related]

  • 10. A critical smn threshold in mice dictates onset of an intermediate spinal muscular atrophy phenotype associated with a distinct neuromuscular junction pathology.
    Bowerman M, Murray LM, Beauvais A, Pinheiro B, Kothary R.
    Neuromuscul Disord; 2012 Mar 12; 22(3):263-76. PubMed ID: 22071333
    [Abstract] [Full Text] [Related]

  • 11. Hydroxyurea enhances SMN2 gene expression in spinal muscular atrophy cells.
    Grzeschik SM, Ganta M, Prior TW, Heavlin WD, Wang CH.
    Ann Neurol; 2005 Aug 12; 58(2):194-202. PubMed ID: 16049920
    [Abstract] [Full Text] [Related]

  • 12. Neuronal SMN expression corrects spinal muscular atrophy in severe SMA mice while muscle-specific SMN expression has no phenotypic effect.
    Gavrilina TO, McGovern VL, Workman E, Crawford TO, Gogliotti RG, DiDonato CJ, Monani UR, Morris GE, Burghes AH.
    Hum Mol Genet; 2008 Apr 15; 17(8):1063-75. PubMed ID: 18178576
    [Abstract] [Full Text] [Related]

  • 13. Survival motor neuron protein in motor neurons determines synaptic integrity in spinal muscular atrophy.
    Martinez TL, Kong L, Wang X, Osborne MA, Crowder ME, Van Meerbeke JP, Xu X, Davis C, Wooley J, Goldhamer DJ, Lutz CM, Rich MM, Sumner CJ.
    J Neurosci; 2012 Jun 20; 32(25):8703-15. PubMed ID: 22723710
    [Abstract] [Full Text] [Related]

  • 14. Therapeutics development for spinal muscular atrophy.
    Sumner CJ.
    NeuroRx; 2006 Apr 20; 3(2):235-45. PubMed ID: 16554261
    [Abstract] [Full Text] [Related]

  • 15. 5-(N-ethyl-N-isopropyl)-amiloride enhances SMN2 exon 7 inclusion and protein expression in spinal muscular atrophy cells.
    Yuo CY, Lin HH, Chang YS, Yang WK, Chang JG.
    Ann Neurol; 2008 Jan 20; 63(1):26-34. PubMed ID: 17924536
    [Abstract] [Full Text] [Related]

  • 16. Restoration of SMN function: delivery of a trans-splicing RNA re-directs SMN2 pre-mRNA splicing.
    Coady TH, Shababi M, Tullis GE, Lorson CL.
    Mol Ther; 2007 Aug 20; 15(8):1471-8. PubMed ID: 17551501
    [Abstract] [Full Text] [Related]

  • 17. Fishing for a mechanism: using zebrafish to understand spinal muscular atrophy.
    Beattie CE, Carrel TL, McWhorter ML.
    J Child Neurol; 2007 Aug 20; 22(8):995-1003. PubMed ID: 17761655
    [Abstract] [Full Text] [Related]

  • 18. Other forms of survival motor neuron protein and spinal muscular atrophy: an opinion.
    Burghes HM.
    Neuromuscul Disord; 2008 Jan 20; 18(1):82-3. PubMed ID: 18365339
    [No Abstract] [Full Text] [Related]

  • 19. Neuromuscular defects in a Drosophila survival motor neuron gene mutant.
    Chan YB, Miguel-Aliaga I, Franks C, Thomas N, Trülzsch B, Sattelle DB, Davies KE, van den Heuvel M.
    Hum Mol Genet; 2003 Jun 15; 12(12):1367-76. PubMed ID: 12783845
    [Abstract] [Full Text] [Related]

  • 20. Spinal muscular atrophy: the RNP connection.
    Eggert C, Chari A, Laggerbauer B, Fischer U.
    Trends Mol Med; 2006 Mar 15; 12(3):113-21. PubMed ID: 16473550
    [Abstract] [Full Text] [Related]

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