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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2001 | 1 |
2002 | 1 |
2004 | 1 |
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2006 | 1 |
2008 | 1 |
2014 | 1 |
2015 | 1 |
2024 | 0 |
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Page 1
Genetically engineered mouse models of neurodegenerative diseases.
Nat Neurosci. 2002 Jul;5(7):633-9. doi: 10.1038/nn0702-633.
Nat Neurosci. 2002.
PMID: 12085093
Review.
Genetically engineered models relevant to neurodegenerative disorders: their value for understanding disease mechanisms and designing/testing experimental therapeutics.
Wong PC, Cai H, Borchelt DR, Price DL.
Wong PC, et al.
J Mol Neurosci. 2001 Oct;17(2):233-57. doi: 10.1385/JMN:17:2:233.
J Mol Neurosci. 2001.
PMID: 11816796
Review.
Item in Clipboard
Low dietary protein content alleviates motor symptoms in mice with mutant dynactin/dynein-mediated neurodegeneration.
Wiesner D, Sinniger J, Henriques A, Dieterlé S, Müller HP, Rasche V, Ferger B, Dirrig-Grosch S, Soylu-Kucharz R, Petersén A, Walther P, Linkus B, Kassubek J, Wong PC, Ludolph AC, Dupuis L.
Wiesner D, et al.
Hum Mol Genet. 2015 Apr 15;24(8):2228-40. doi: 10.1093/hmg/ddu741. Epub 2014 Dec 30.
Hum Mol Genet. 2015.
PMID: 25552654
Free PMC article.
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Motor neuron disease occurring in a mutant dynactin mouse model is characterized by defects in vesicular trafficking.
Laird FM, Farah MH, Ackerley S, Hoke A, Maragakis N, Rothstein JD, Griffin J, Price DL, Martin LJ, Wong PC.
Laird FM, et al.
J Neurosci. 2008 Feb 27;28(9):1997-2005. doi: 10.1523/JNEUROSCI.4231-07.2008.
J Neurosci. 2008.
PMID: 18305234
Free PMC article.
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Amyotrophic lateral sclerosis 2-deficiency leads to neuronal degeneration in amyotrophic lateral sclerosis through altered AMPA receptor trafficking.
Lai C, Xie C, McCormack SG, Chiang HC, Michalak MK, Lin X, Chandran J, Shim H, Shimoji M, Cookson MR, Huganir RL, Rothstein JD, Price DL, Wong PC, Martin LJ, Zhu JJ, Cai H.
Lai C, et al.
J Neurosci. 2006 Nov 8;26(45):11798-806. doi: 10.1523/JNEUROSCI.2084-06.2006.
J Neurosci. 2006.
PMID: 17093100
Free PMC article.
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Toxicity of familial ALS-linked SOD1 mutants from selective recruitment to spinal mitochondria.
Liu J, Lillo C, Jonsson PA, Vande Velde C, Ward CM, Miller TM, Subramaniam JR, Rothstein JD, Marklund S, Andersen PM, Brännström T, Gredal O, Wong PC, Williams DS, Cleveland DW.
Liu J, et al.
Neuron. 2004 Jul 8;43(1):5-17. doi: 10.1016/j.neuron.2004.06.016.
Neuron. 2004.
PMID: 15233913
Free article.
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Loss of ALS2 function is insufficient to trigger motor neuron degeneration in knock-out mice but predisposes neurons to oxidative stress.
Cai H, Lin X, Xie C, Laird FM, Lai C, Wen H, Chiang HC, Shim H, Farah MH, Hoke A, Price DL, Wong PC.
Cai H, et al.
J Neurosci. 2005 Aug 17;25(33):7567-74. doi: 10.1523/JNEUROSCI.1645-05.2005.
J Neurosci. 2005.
PMID: 16107644
Free PMC article.
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