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Journal Abstract Search

750 related items for PubMed ID: 23969236

  • 1. Genetic ablation of phospholipase C delta 1 increases survival in SOD1(G93A) mice.
    Staats KA, Van Helleputte L, Jones AR, Bento-Abreu A, Van Hoecke A, Shatunov A, Simpson CL, Lemmens R, Jaspers T, Fukami K, Nakamura Y, Brown RH, Van Damme P, Liston A, Robberecht W, Al-Chalabi A, Van Den Bosch L.
    Neurobiol Dis; 2013 Dec; 60():11-7. PubMed ID: 23969236
    [Abstract] [Full Text] [Related]

  • 2. Overexpression of human mutated G93A SOD1 changes dynamics of the ER mitochondria calcium cycle specifically in mouse embryonic motor neurons.
    Lautenschläger J, Prell T, Ruhmer J, Weidemann L, Witte OW, Grosskreutz J.
    Exp Neurol; 2013 Sep; 247():91-100. PubMed ID: 23578819
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  • 3. Neuroprotective effects of the Sigma-1 receptor (S1R) agonist PRE-084, in a mouse model of motor neuron disease not linked to SOD1 mutation.
    Peviani M, Salvaneschi E, Bontempi L, Petese A, Manzo A, Rossi D, Salmona M, Collina S, Bigini P, Curti D.
    Neurobiol Dis; 2014 Feb; 62():218-32. PubMed ID: 24141020
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  • 4. Overexpression of Abeta is associated with acceleration of onset of motor impairment and superoxide dismutase 1 aggregation in an amyotrophic lateral sclerosis mouse model.
    Li QX, Mok SS, Laughton KM, McLean CA, Volitakis I, Cherny RA, Cheung NS, White AR, Masters CL.
    Aging Cell; 2006 Apr; 5(2):153-65. PubMed ID: 16626394
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  • 5. Knocking down metabotropic glutamate receptor 1 improves survival and disease progression in the SOD1(G93A) mouse model of amyotrophic lateral sclerosis.
    Milanese M, Giribaldi F, Melone M, Bonifacino T, Musante I, Carminati E, Rossi PI, Vergani L, Voci A, Conti F, Puliti A, Bonanno G.
    Neurobiol Dis; 2014 Apr; 64():48-59. PubMed ID: 24361555
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  • 6. Loss of glial fibrillary acidic protein marginally accelerates disease progression in a SOD1(H46R) transgenic mouse model of ALS.
    Yoshii Y, Otomo A, Pan L, Ohtsuka M, Hadano S.
    Neurosci Res; 2011 Jul; 70(3):321-9. PubMed ID: 21453731
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  • 7. GAB(A) receptors present higher affinity and modified subunit composition in spinal motor neurons from a genetic model of amyotrophic lateral sclerosis.
    Carunchio I, Mollinari C, Pieri M, Merlo D, Zona C.
    Eur J Neurosci; 2008 Oct; 28(7):1275-85. PubMed ID: 18973555
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  • 8. Trehalose decreases mutant SOD1 expression and alleviates motor deficiency in early but not end-stage amyotrophic lateral sclerosis in a SOD1-G93A mouse model.
    Li Y, Guo Y, Wang X, Yu X, Duan W, Hong K, Wang J, Han H, Li C.
    Neuroscience; 2015 Jul 09; 298():12-25. PubMed ID: 25841320
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  • 9. Altered distribution and levels of cathepsinD and cystatins in amyotrophic lateral sclerosis transgenic mice: possible roles in motor neuron survival.
    Wootz H, Weber E, Korhonen L, Lindholm D.
    Neuroscience; 2006 Dec 01; 143(2):419-30. PubMed ID: 16973300
    [Abstract] [Full Text] [Related]

  • 10. Amyloid precursor protein (APP) contributes to pathology in the SOD1(G93A) mouse model of amyotrophic lateral sclerosis.
    Bryson JB, Hobbs C, Parsons MJ, Bosch KD, Pandraud A, Walsh FS, Doherty P, Greensmith L.
    Hum Mol Genet; 2012 Sep 01; 21(17):3871-82. PubMed ID: 22678056
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  • 12. Ablation of P2X7 receptor exacerbates gliosis and motoneuron death in the SOD1-G93A mouse model of amyotrophic lateral sclerosis.
    Apolloni S, Amadio S, Montilli C, Volonté C, D'Ambrosi N.
    Hum Mol Genet; 2013 Oct 15; 22(20):4102-16. PubMed ID: 23736299
    [Abstract] [Full Text] [Related]

  • 13. In-vivo genetic ablation of metabotropic glutamate receptor type 5 slows down disease progression in the SOD1G93A mouse model of amyotrophic lateral sclerosis.
    Bonifacino T, Provenzano F, Gallia E, Ravera S, Torazza C, Bossi S, Ferrando S, Puliti A, Van Den Bosch L, Bonanno G, Milanese M.
    Neurobiol Dis; 2019 Sep 15; 129():79-92. PubMed ID: 31102766
    [Abstract] [Full Text] [Related]

  • 14. Neuronal overexpression of IP₃ receptor 2 is detrimental in mutant SOD1 mice.
    Staats KA, Bogaert E, Hersmus N, Jaspers T, Luyten T, Bultynck G, Parys JB, Hisatsune C, Mikoshiba K, Van Damme P, Robberecht W, Van Den Bosch L.
    Biochem Biophys Res Commun; 2012 Dec 14; 429(3-4):210-3. PubMed ID: 23131553
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  • 17. Over-expression of Hsp27 does not influence disease in the mutant SOD1(G93A) mouse model of amyotrophic lateral sclerosis.
    Krishnan J, Vannuvel K, Andries M, Waelkens E, Robberecht W, Van Den Bosch L.
    J Neurochem; 2008 Sep 14; 106(5):2170-83. PubMed ID: 18624915
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  • 18. Mislocalization of TDP-43 in the G93A mutant SOD1 transgenic mouse model of ALS.
    Shan X, Vocadlo D, Krieger C.
    Neurosci Lett; 2009 Jul 17; 458(2):70-4. PubMed ID: 19379791
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  • 19. Guanabenz delays the onset of disease symptoms, extends lifespan, improves motor performance and attenuates motor neuron loss in the SOD1 G93A mouse model of amyotrophic lateral sclerosis.
    Jiang HQ, Ren M, Jiang HZ, Wang J, Zhang J, Yin X, Wang SY, Qi Y, Wang XD, Feng HL.
    Neuroscience; 2014 Sep 26; 277():132-8. PubMed ID: 24699224
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