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817 related items for PubMed ID: 29961886
21. Plastin 3 is upregulated in iPSC-derived motoneurons from asymptomatic SMN1-deleted individuals. Heesen L, Peitz M, Torres-Benito L, Hölker I, Hupperich K, Dobrindt K, Jungverdorben J, Ritzenhofen S, Weykopf B, Eckert D, Hosseini-Barkooie SM, Storbeck M, Fusaki N, Lonigro R, Heller R, Kye MJ, Brüstle O, Wirth B. Cell Mol Life Sci; 2016 May; 73(10):2089-104. PubMed ID: 26573968 [Abstract] [Full Text] [Related]
25. 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]
26. Loganin possesses neuroprotective properties, restores SMN protein and activates protein synthesis positive regulator Akt/mTOR in experimental models of spinal muscular atrophy. Tseng YT, Chen CS, Jong YJ, Chang FR, Lo YC. Pharmacol Res; 2016 Sep 01; 111():58-75. PubMed ID: 27241020 [Abstract] [Full Text] [Related]
27. AAV9-Stathmin1 gene delivery improves disease phenotype in an intermediate mouse model of spinal muscular atrophy. Villalón E, Kline RA, Smith CE, Lorson ZC, Osman EY, O'Day S, Murray LM, Lorson CL. Hum Mol Genet; 2019 Nov 15; 28(22):3742-3754. PubMed ID: 31363739 [Abstract] [Full Text] [Related]
28. Dual SMN inducing therapies can rescue survival and motor unit function in symptomatic ∆7SMA mice. Kray KM, McGovern VL, Chugh D, Arnold WD, Burghes AHM. Neurobiol Dis; 2021 Nov 15; 159():105488. PubMed ID: 34425216 [Abstract] [Full Text] [Related]
29. 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 [Abstract] [Full Text] [Related]
30. Tissue-specific models of spinal muscular atrophy confirm a critical role of SMN in motor neurons from embryonic to adult stages. Laird AS, Mackovski N, Rinkwitz S, Becker TS, Giacomotto J. Hum Mol Genet; 2016 May 01; 25(9):1728-38. PubMed ID: 26908606 [Abstract] [Full Text] [Related]
35. 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]
36. Nusinersen ameliorates motor function and prevents motoneuron Cajal body disassembly and abnormal poly(A) RNA distribution in a SMA mouse model. Berciano MT, Puente-Bedia A, Medina-Samamé A, Rodríguez-Rey JC, Calderó J, Lafarga M, Tapia O. Sci Rep; 2020 Jul 01; 10(1):10738. PubMed ID: 32612161 [Abstract] [Full Text] [Related]
38. Plastin 3 is a protective modifier of autosomal recessive spinal muscular atrophy. Oprea GE, Kröber S, McWhorter ML, Rossoll W, Müller S, Krawczak M, Bassell GJ, Beattie CE, Wirth B. Science; 2008 Apr 25; 320(5875):524-7. PubMed ID: 18440926 [Abstract] [Full Text] [Related]
39. A large animal model of spinal muscular atrophy and correction of phenotype. Duque SI, Arnold WD, Odermatt P, Li X, Porensky PN, Schmelzer L, Meyer K, Kolb SJ, Schümperli D, Kaspar BK, Burghes AH. Ann Neurol; 2015 Mar 25; 77(3):399-414. PubMed ID: 25516063 [Abstract] [Full Text] [Related]
40. PLS3 Overexpression Delays Ataxia in Chp1 Mutant Mice. Janzen E, Wolff L, Mendoza-Ferreira N, Hupperich K, Delle Vedove A, Hosseinibarkooie S, Kye MJ, Wirth B. Front Neurosci; 2019 Mar 25; 13():993. PubMed ID: 31607845 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]