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PUBMED FOR HANDHELDS

Journal Abstract Search


432 related items for PubMed ID: 16925593

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  • 2. Changes in the astrocytic aquaporin-4 and inwardly rectifying potassium channel expression in the brain of the amyotrophic lateral sclerosis SOD1(G93A) rat model.
    Bataveljić D, Nikolić L, Milosević M, Todorović N, Andjus PR.
    Glia; 2012 Dec; 60(12):1991-2003. PubMed ID: 22987392
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  • 5. Transgenic SOD1 G93A mice develop reduced GLT-1 in spinal cord without alterations in cerebrospinal fluid glutamate levels.
    Bendotti C, Tortarolo M, Suchak SK, Calvaresi N, Carvelli L, Bastone A, Rizzi M, Rattray M, Mennini T.
    J Neurochem; 2001 Nov; 79(4):737-46. PubMed ID: 11723166
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  • 7. Alterations in AQP4 expression and polarization in the course of motor neuron degeneration in SOD1G93A mice.
    Dai J, Lin W, Zheng M, Liu Q, He B, Luo C, Lu X, Pei Z, Su H, Yao X.
    Mol Med Rep; 2017 Aug; 16(2):1739-1746. PubMed ID: 28627708
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  • 8. 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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  • 10. 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
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  • 11. Adipose-derived Stem Cell Conditioned Media Extends Survival time of a mouse model of Amyotrophic Lateral Sclerosis.
    Fontanilla CV, Gu H, Liu Q, Zhu TZ, Zhou C, Johnstone BH, March KL, Pascuzzi RM, Farlow MR, Du Y.
    Sci Rep; 2015 Nov 20; 5():16953. PubMed ID: 26586020
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  • 12. Histological evidence of protein aggregation in mutant SOD1 transgenic mice and in amyotrophic lateral sclerosis neural tissues.
    Watanabe M, Dykes-Hoberg M, Culotta VC, Price DL, Wong PC, Rothstein JD.
    Neurobiol Dis; 2001 Dec 20; 8(6):933-41. PubMed ID: 11741389
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  • 13. Glycine receptor channels in spinal motoneurons are abnormal in a transgenic mouse model of amyotrophic lateral sclerosis.
    Chang Q, Martin LJ.
    J Neurosci; 2011 Feb 23; 31(8):2815-27. PubMed ID: 21414903
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  • 15. Differential distribution of Kir4.1 in spinal cord astrocytes suggests regional differences in K+ homeostasis.
    Olsen ML, Campbell SL, Sontheimer H.
    J Neurophysiol; 2007 Aug 23; 98(2):786-93. PubMed ID: 17581847
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  • 16. Selective loss of neurofilament expression in Cu/Zn superoxide dismutase (SOD1) linked amyotrophic lateral sclerosis.
    Menzies FM, Grierson AJ, Cookson MR, Heath PR, Tomkins J, Figlewicz DA, Ince PG, Shaw PJ.
    J Neurochem; 2002 Sep 23; 82(5):1118-28. PubMed ID: 12358759
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  • 17. 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 23; 70(3):321-9. PubMed ID: 21453731
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  • 18. Parvalbumin and calbindin D-28k immunoreactivity in transgenic mice with a G93A mutant SOD1 gene.
    Sasaki S, Warita H, Komori T, Murakami T, Abe K, Iwata M.
    Brain Res; 2006 Apr 14; 1083(1):196-203. PubMed ID: 16546142
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  • 19. Tardive decrease of astrocytic glutamate transporter protein in transgenic mice with ALS-linked mutant SOD1.
    Warita H, Manabe Y, Murakami T, Shiote M, Shiro Y, Hayashi T, Nagano I, Shoji M, Abe K.
    Neurol Res; 2002 Sep 14; 24(6):577-81. PubMed ID: 12238624
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  • 20. Chromogranin-mediated secretion of mutant superoxide dismutase proteins linked to amyotrophic lateral sclerosis.
    Urushitani M, Sik A, Sakurai T, Nukina N, Takahashi R, Julien JP.
    Nat Neurosci; 2006 Jan 14; 9(1):108-18. PubMed ID: 16369483
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