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Journal Abstract Search

397 related items for PubMed ID: 27170316

  • 21. Neurodevelopmental consequences of Smn depletion in a mouse model of spinal muscular atrophy.
    Liu H, Shafey D, Moores JN, Kothary R.
    J Neurosci Res; 2010 Jan; 88(1):111-22. PubMed ID: 19642194
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  • 22. Astrocyte-produced miR-146a as a mediator of motor neuron loss in spinal muscular atrophy.
    Sison SL, Patitucci TN, Seminary ER, Villalon E, Lorson CL, Ebert AD.
    Hum Mol Genet; 2017 Sep 01; 26(17):3409-3420. PubMed ID: 28637335
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  • 23. Spinal muscular atrophy: antisense oligonucleotide therapy opens the door to an integrated therapeutic landscape.
    Wood MJA, Talbot K, Bowerman M.
    Hum Mol Genet; 2017 Oct 01; 26(R2):R151-R159. PubMed ID: 28977438
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  • 25. Low levels of Survival Motor Neuron protein are sufficient for normal muscle function in the SMNΔ7 mouse model of SMA.
    Iyer CC, McGovern VL, Murray JD, Gombash SE, Zaworski PG, Foust KD, Janssen PM, Burghes AH.
    Hum Mol Genet; 2015 Nov 01; 24(21):6160-73. PubMed ID: 26276812
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  • 26. The water extract of Liuwei dihuang possesses multi-protective properties on neurons and muscle tissue against deficiency of survival motor neuron protein.
    Tseng YT, Jong YJ, Liang WF, Chang FR, Lo YC.
    Phytomedicine; 2017 Oct 15; 34():97-105. PubMed ID: 28899515
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  • 30. Depletion of SMN protein in mesenchymal progenitors impairs the development of bone and neuromuscular junction in spinal muscular atrophy.
    Hann SH, Kim SY, Kim YL, Jo YW, Kang JS, Park H, Choi SY, Kong YY.
    Elife; 2024 Feb 06; 12():. PubMed ID: 38318851
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  • 31. The Biochemistry of Survival Motor Neuron Protein Is Paving the Way to Novel Therapies for Spinal Muscle Atrophy.
    Lomonte P, Baklouti F, Binda O.
    Biochemistry; 2020 Apr 14; 59(14):1391-1397. PubMed ID: 32227847
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  • 33. Central and peripheral defects in motor units of the diaphragm of spinal muscular atrophy mice.
    Neve A, Trüb J, Saxena S, Schümperli D.
    Mol Cell Neurosci; 2016 Jan 14; 70():30-41. PubMed ID: 26621405
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  • 36. Temporal requirement for high SMN expression in SMA mice.
    Le TT, McGovern VL, Alwine IE, Wang X, Massoni-Laporte A, Rich MM, Burghes AH.
    Hum Mol Genet; 2011 Sep 15; 20(18):3578-91. PubMed ID: 21672919
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  • 37. CHP1 reduction ameliorates spinal muscular atrophy pathology by restoring calcineurin activity and endocytosis.
    Janzen E, Mendoza-Ferreira N, Hosseinibarkooie S, Schneider S, Hupperich K, Tschanz T, Grysko V, Riessland M, Hammerschmidt M, Rigo F, Bennett CF, Kye MJ, Torres-Benito L, Wirth B.
    Brain; 2018 Aug 01; 141(8):2343-2361. PubMed ID: 29961886
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  • 39. Development and characterization of an SMN2-based intermediate mouse model of Spinal Muscular Atrophy.
    Cobb MS, Rose FF, Rindt H, Glascock JJ, Shababi M, Miller MR, Osman EY, Yen PF, Garcia ML, Martin BR, Wetz MJ, Mazzasette C, Feng Z, Ko CP, Lorson CL.
    Hum Mol Genet; 2013 May 01; 22(9):1843-55. PubMed ID: 23390132
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  • 40. A novel zebrafish model for intermediate type spinal muscular atrophy demonstrates importance of Smn for maintenance of mature motor neurons.
    Tay SH, Ellieyana EN, Le Y, Sarusie MV, Grimm C, Ohmer J, Mathuru AS, Fischer U, Winkler C.
    Hum Mol Genet; 2021 Nov 30; 30(24):2488-2502. PubMed ID: 34302176
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