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Pubmed for Handhelds

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Journal Abstract Search

548 related items for PubMed ID: 18492800

  • 21.
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  • 22. Molecular and functional analysis of intragenic SMN1 mutations in patients with spinal muscular atrophy.
    Sun Y, Grimmler M, Schwarzer V, Schoenen F, Fischer U, Wirth B.
    Hum Mutat; 2005 Jan; 25(1):64-71. PubMed ID: 15580564
    [Abstract] [Full Text] [Related]

  • 23. Activation of Muscle-Specific Kinase (MuSK) Reduces Neuromuscular Defects in the Delta7 Mouse Model of Spinal Muscular Atrophy (SMA).
    Feng Z, Lam S, Tenn ES, Ghosh AS, Cantor S, Zhang W, Yen PF, Chen KS, Burden S, Paushkin S, Ayalon G, Ko CP.
    Int J Mol Sci; 2021 Jul 27; 22(15):. PubMed ID: 34360794
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  • 26. The benzamide M344, a novel histone deacetylase inhibitor, significantly increases SMN2 RNA/protein levels in spinal muscular atrophy cells.
    Riessland M, Brichta L, Hahnen E, Wirth B.
    Hum Genet; 2006 Aug 27; 120(1):101-10. PubMed ID: 16724231
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  • 28. Molecular and cellular basis of spinal muscular atrophy.
    Jablonka S, Sendtner M.
    Amyotroph Lateral Scler Other Motor Neuron Disord; 2003 Sep 27; 4(3):144-9. PubMed ID: 13129800
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  • 30. Animal models of spinal muscular atrophy.
    Schmid A, DiDonato CJ.
    J Child Neurol; 2007 Aug 27; 22(8):1004-12. PubMed ID: 17761656
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  • 31.
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  • 32. Neurotransmitter release in motor nerve terminals of a mouse model of mild spinal muscular atrophy.
    Ruiz R, Tabares L.
    J Anat; 2014 Jan 27; 224(1):74-84. PubMed ID: 23489475
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  • 33. Stat5 constitutive activation rescues defects in spinal muscular atrophy.
    Ting CH, Lin CW, Wen SL, Hsieh-Li HM, Li H.
    Hum Mol Genet; 2007 Mar 01; 16(5):499-514. PubMed ID: 17220171
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  • 34.
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  • 35. The neuroprotective factor Wld(s) fails to mitigate distal axonal and neuromuscular junction (NMJ) defects in mouse models of spinal muscular atrophy.
    Kariya S, Mauricio R, Dai Y, Monani UR.
    Neurosci Lett; 2009 Jan 16; 449(3):246-51. PubMed ID: 19010394
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  • 36. Refined characterization of the expression and stability of the SMN gene products.
    Vitte J, Fassier C, Tiziano FD, Dalard C, Soave S, Roblot N, Brahe C, Saugier-Veber P, Bonnefont JP, Melki J.
    Am J Pathol; 2007 Oct 16; 171(4):1269-80. PubMed ID: 17717146
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  • 37. Neuromuscular defects and breathing disorders in a new mouse model of spinal muscular atrophy.
    Michaud M, Arnoux T, Bielli S, Durand E, Rotrou Y, Jablonka S, Robert F, Giraudon-Paoli M, Riessland M, Mattei MG, Andriambeloson E, Wirth B, Sendtner M, Gallego J, Pruss RM, Bordet T.
    Neurobiol Dis; 2010 Apr 16; 38(1):125-35. PubMed ID: 20085811
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  • 38. Distinct and overlapping alterations in motor and sensory neurons in a mouse model of spinal muscular atrophy.
    Jablonka S, Karle K, Sandner B, Andreassi C, von Au K, Sendtner M.
    Hum Mol Genet; 2006 Feb 01; 15(3):511-8. PubMed ID: 16396995
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  • 39. A role for complexes of survival of motor neurons (SMN) protein with gemins and profilin in neurite-like cytoplasmic extensions of cultured nerve cells.
    Sharma A, Lambrechts A, Hao le T, Le TT, Sewry CA, Ampe C, Burghes AH, Morris GE.
    Exp Cell Res; 2005 Sep 10; 309(1):185-97. PubMed ID: 15975577
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  • 40. In vitro and in cellulo evidences for association of the survival of motor neuron complex with the fragile X mental retardation protein.
    Piazzon N, Rage F, Schlotter F, Moine H, Branlant C, Massenet S.
    J Biol Chem; 2008 Feb 29; 283(9):5598-610. PubMed ID: 18093976
    [Abstract] [Full Text] [Related]

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