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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2009 | 1 |
2010 | 4 |
2011 | 2 |
2024 | 0 |
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7 results
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Page 1
Altered zinc transport disrupts mitochondrial protein processing/import in fragile X-associated tremor/ataxia syndrome.
Hum Mol Genet. 2011 Aug 1;20(15):3079-92. doi: 10.1093/hmg/ddr211. Epub 2011 May 10.
Hum Mol Genet. 2011.
PMID: 21558427
Free PMC article.
Molecular pathogenesis of fragile X-associated tremor/ataxia syndrome.
Raske C, Hagerman PJ.
Raske C, et al.
J Investig Med. 2009 Dec;57(8):825-9. doi: 10.2310/JIM.0b013e3181be329a.
J Investig Med. 2009.
PMID: 19794313
Free PMC article.
Review.
Item in Clipboard
Evidence of mitochondrial dysfunction in fragile X-associated tremor/ataxia syndrome.
Ross-Inta C, Omanska-Klusek A, Wong S, Barrow C, Garcia-Arocena D, Iwahashi C, Berry-Kravis E, Hagerman RJ, Hagerman PJ, Giulivi C.
Ross-Inta C, et al.
Biochem J. 2010 Aug 1;429(3):545-52. doi: 10.1042/BJ20091960.
Biochem J. 2010.
PMID: 20513237
Free PMC article.
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Temporal ordering deficits in female CGG KI mice heterozygous for the fragile X premutation.
Hunsaker MR, Goodrich-Hunsaker NJ, Willemsen R, Berman RF.
Hunsaker MR, et al.
Behav Brain Res. 2010 Dec 1;213(2):263-8. doi: 10.1016/j.bbr.2010.05.010. Epub 2010 May 15.
Behav Brain Res. 2010.
PMID: 20478339
Free PMC article.
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Murine hippocampal neurons expressing Fmr1 gene premutations show early developmental deficits and late degeneration.
Chen Y, Tassone F, Berman RF, Hagerman PJ, Hagerman RJ, Willemsen R, Pessah IN.
Chen Y, et al.
Hum Mol Genet. 2010 Jan 1;19(1):196-208. doi: 10.1093/hmg/ddp479.
Hum Mol Genet. 2010.
PMID: 19846466
Free PMC article.
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Mitochondrial dysfunction in NnaD mutant flies and Purkinje cell degeneration mice reveals a role for Nna proteins in neuronal bioenergetics.
Chakrabarti L, Zahra R, Jackson SM, Kazemi-Esfarjani P, Sopher BL, Mason AG, Toneff T, Ryu S, Shaffer S, Kansy JW, Eng J, Merrihew G, MacCoss MJ, Murphy A, Goodlett DR, Hook V, Bennett CL, Pallanck LJ, La Spada AR.
Chakrabarti L, et al.
Neuron. 2010 Jun 24;66(6):835-47. doi: 10.1016/j.neuron.2010.05.024.
Neuron. 2010.
PMID: 20620870
Free PMC article.
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Spinocerebellar ataxia type 7 cerebellar disease requires the coordinated action of mutant ataxin-7 in neurons and glia, and displays non-cell-autonomous bergmann glia degeneration.
Furrer SA, Mohanachandran MS, Waldherr SM, Chang C, Damian VA, Sopher BL, Garden GA, La Spada AR.
Furrer SA, et al.
J Neurosci. 2011 Nov 9;31(45):16269-78. doi: 10.1523/JNEUROSCI.4000-11.2011.
J Neurosci. 2011.
PMID: 22072678
Free PMC article.
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