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Volumn 1, Issue 2, 2012, Pages 221-241

Age-dependent resistance to excitotoxicity in Htt CAG140 mice and the effect of strain background

Author keywords

cell death; Excitotoxin; genetic background; Huntington's disease; inbred mouse strains; neurodegeneration; resistance

Indexed keywords

HUNTINGTIN; KAINIC ACID; QUINOLINIC ACID; HUNTINGTON PROTEIN, MOUSE; NERVE PROTEIN; NUCLEAR PROTEIN;

EID: 84892595897     PISSN: 18796397     EISSN: 18796400     Source Type: Journal    
DOI: 10.3233/JHD-129005     Document Type: Article
Times cited : (12)

References (64)
  • 1
    • 0025363346 scopus 로고
    • Excitotoxic injury of the neostriatum: A model for Huntington's disease
    • DiFiglia M. Excitotoxic injury of the neostriatum: A model for Huntington's disease. Trends Neurosci. 1990;13(7):286-9.
    • (1990) Trends Neurosci , vol.13 , Issue.7 , pp. 286-289
    • Difiglia, M.1
  • 2
    • 45149107487 scopus 로고    scopus 로고
    • Mechanisms of neurodegeneration in Huntington's disease
    • DOI 10.1111/j.1460-9568.2008.06310.x
    • Gil JM,RegoAC. Mechanisms of neurodegeneration in Huntington's disease. Eur J Neurosci. 2008;27(11):2803-20. (Pubitemid 351832229)
    • (2008) European Journal of Neuroscience , vol.27 , Issue.11 , pp. 2803-2820
    • Gil, J.M.1    Rego, A.C.2
  • 3
    • 65249104851 scopus 로고    scopus 로고
    • Molecular mechanisms of excitotoxicity and their relevance to pathogenesis of neurodegenerative diseases
    • Dong XX, Wang Y, Qin ZH. Molecular mechanisms of excitotoxicity and their relevance to pathogenesis of neurodegenerative diseases. Acta Pharmacol Sin. 2009;30(4):379-87.
    • (2009) Acta Pharmacol Sin , vol.30 , Issue.4 , pp. 379-387
    • Dong, X.X.1    Wang, Y.2    Qin, Z.H.3
  • 4
    • 0022446150 scopus 로고
    • Replication of the neurochemical characteristics of Huntington's disease by quinolinic acid
    • Beal MF, Kowall NW, Ellison DW, Mazurek MF, Swartz KJ, Martin JB. Replication of the neurochemical characteristics of Huntington's disease by quinolinic acid. Nature. 1986;321(6066):168-71. (Pubitemid 16022019)
    • (1986) Nature , vol.321 , Issue.6066 , pp. 168-171
    • Beal, M.F.1    Kowall, N.W.2    Ellison, D.W.3
  • 5
    • 0037075624 scopus 로고    scopus 로고
    • Increased sensitivity to N-methyl-D-aspartate receptor-mediated excitotoxicity in a mouse model of Huntington's disease
    • DOI 10.1016/S0896-6273(02)00615-3
    • Zeron MM, Hansson O, Chen N, Wellington CL, Leavitt BR, Brundin P, et al. Increased sensitivity to N-methyl-Daspartate receptor-mediated excitotoxicity in a mouse model of Huntington's disease. Neuron. 2002;33(6):849-60. (Pubitemid 34246352)
    • (2002) Neuron , vol.33 , Issue.6 , pp. 849-860
    • Zeron, M.M.1    Hansson, O.2    Chen, N.3    Wellington, C.L.4    Leavitt, B.R.5    Brundin, P.6    Hayden, M.R.7    Raymond, L.A.8
  • 7
    • 39149137852 scopus 로고    scopus 로고
    • Genes on distal chromosome 18 determine vulnerability to excitotoxic neurodegeneration following status epilepticus, but not striatal neurodegeneration induced by quinolinic acid
    • DOI 10.1016/j.nbd.2007.10.002, PII S0969996107002264
    • McLin JP, Thompson LM, Lusis AJ, Davis RC, Steward O. Genes on distal chromosome 18 determine vulnerability to excitotoxic neurodegeneration following status epilepticus, but not striatal neurodegeneration induced by quinolinic acid. Neurobiol Dis. 2008;29(3):391-9. (Pubitemid 351258349)
    • (2008) Neurobiology of Disease , vol.29 , Issue.3 , pp. 391-399
    • McLin, J.P.1    Thompson, L.M.2    Lusis, A.J.3    Davis, R.C.4    Steward, O.5
  • 9
    • 33750361629 scopus 로고    scopus 로고
    • Comparison of seizure phenotype and neurodegeneration induced by systemic kainic acid in inbred, outbred, and hybrid mouse strains
    • DOI 10.1111/j.1460-9568.2006.05111.x
    • McLin JP, Steward O. Comparison of seizure phenotype and neurodegeneration induced by systemic kainic acid in inbred, outbred, and hybrid mouse strains. Eur J Neurosci. 2006;24(8):2191-202. (Pubitemid 44622340)
    • (2006) European Journal of Neuroscience , vol.24 , Issue.8 , pp. 2191-2202
    • McLin, J.P.1    Steward, O.2
  • 10
    • 33750381007 scopus 로고    scopus 로고
    • Differential susceptibility to striatal neurodegeneration induced by quinolinic acid and kainate in inbred, outbred and hybrid mouse strains
    • DOI 10.1111/j.1460-9568.2006.05198.x
    • McLin JP, Thompson LM, Steward O. Differential susceptibility to striatal neurodegeneration induced by quinolinic acid and kainate in inbred, outbred and hybrid mouse strains. Eur J Neurosci. 2006;24(11):3134-40. (Pubitemid 44952645)
    • (2006) European Journal of Neuroscience , vol.24 , Issue.11 , pp. 3134-3140
    • McLin, J.P.1    Thompson, L.M.2    Steward, O.3
  • 11
    • 3843081736 scopus 로고    scopus 로고
    • Genetic control of sensitivity to hippocampal cell death induced by kainic acids: A quantitative trait loci analysis
    • DOI 10.1002/cne.20245
    • Schauwecker PE, Williams RW, Santos JB. Genetic control of sensitivity to hippocampal cell death induced by kainic acid: A quantitative trait loci analysis. J Comp Neurol. 2004;477(1):96-107. (Pubitemid 39038182)
    • (2004) Journal of Comparative Neurology , vol.477 , Issue.1 , pp. 96-107
    • Schauwecker, P.E.1    Williams, R.W.2    Santos, J.B.3
  • 13
    • 33750936733 scopus 로고    scopus 로고
    • Know thy mouse
    • DOI 10.1016/j.tig.2006.09.010, PII S0168952506003143
    • Taft RA, Davisson M, Wiles MV. Know thy mouse. Trends Genet. 2006;22(12):649-53. (Pubitemid 44738127)
    • (2006) Trends in Genetics , vol.22 , Issue.12 , pp. 649-653
    • Taft, R.A.1    Davisson, M.2    Wiles, M.V.3
  • 14
    • 46749157501 scopus 로고    scopus 로고
    • Full-length human mutant huntingtin with a stable polyglutamine repeat can elicit progressive and selective neuropathogenesis in BACHD mice
    • Gray M, Shirasaki DI, Cepeda C, Andre VM, Wilburn B, Lu XH, et al. Full-length human mutant huntingtin with a stable polyglutamine repeat can elicit progressive and selective neuropathogenesis in BACHD mice. J Neurosci. 2008;28(24):6182-95.
    • (2008) J Neurosci , vol.28 , Issue.24 , pp. 6182-6195
    • Gray, M.1    Shirasaki, D.I.2    Cepeda, C.3    Andre, V.M.4    Wilburn, B.5    Lu, X.H.6
  • 15
    • 34548161707 scopus 로고    scopus 로고
    • Longitudinal evaluation of the Hdh(CAG)150 knock-in murine model of Huntington's disease
    • DOI 10.1523/JNEUROSCI.1830-07.2007
    • Heng MY, Tallaksen-Greene SJ, Detloff PJ, Albin RL. Longitudinal evaluation of the Hdh(CAG)150 knockin murine model of Huntington's disease. J Neurosci. 2007;27(34):8989-98. (Pubitemid 47312064)
    • (2007) Journal of Neuroscience , vol.27 , Issue.34 , pp. 8989-8998
    • Heng, M.Y.1    Tallaksen-Greene, S.J.2    Detloff, P.J.3    Albin, R.L.4
  • 18
    • 0041691176 scopus 로고    scopus 로고
    • Time course of early motor and neuropathological anomalies in a knock-in mouse model of Huntington's disease with 140 CAG repeats
    • DOI 10.1002/cne.10776
    • Menalled LB, Sison JD, Dragatsis I, Zeitlin S, Chesselet MF. Time course of early motor and neuropathological anomalies in a knock-in mouse model of Huntington's disease with 140 CAG repeats. J Comp Neurol. 2003;465(1):11-26. (Pubitemid 37075677)
    • (2003) Journal of Comparative Neurology , vol.465 , Issue.1 , pp. 11-26
    • Menalled, L.B.1    Sison, J.D.2    Dragatsis, I.3    Zeitlin, S.4    Chesselet, M.-F.5
  • 21
    • 33847684865 scopus 로고    scopus 로고
    • The HdhQ150/Q150 knock-in mouse model of HD and the R6/2 exon 1 model develop comparable and widespread molecular phenotypes
    • DOI 10.1016/j.brainresbull.2006.11.004, PII S0361923006003522
    • Woodman B, Butler R, Landles C, Lupton MK, Tse J, Hockly E, et al. The Hdh(Q150/Q150) knock-in mouse model of HD and the R6/2 exon 1 model develop comparable and widespread molecular phenotypes. Brain Res Bull. 2007;72(2-3):83-97. (Pubitemid 46367466)
    • (2007) Brain Research Bulletin , vol.72 , pp. 83-97
    • Woodman, B.1    Butler, R.2    Landles, C.3    Lupton, M.K.4    Tse, J.5    Hockly, E.6    Moffitt, H.7    Sathasivam, K.8    Bates, G.P.9
  • 23
    • 54549087605 scopus 로고    scopus 로고
    • Extensive early motor and non-motor behavioral deficits are followed by striatal neuronal loss in knock-in Huntington's disease mice
    • Hickey MA, Kosmalska A, Enayati J, Cohen R, Zeitlin S, Levine MS, et al. Extensive early motor and non-motor behavioral deficits are followed by striatal neuronal loss in knock-in Huntington's disease mice. Neuroscience. 2008;157(1):280-95.
    • (2008) Neuroscience , vol.157 , Issue.1 , pp. 280-295
    • Hickey, M.A.1    Kosmalska, A.2    Enayati, J.3    Cohen, R.4    Zeitlin, S.5    Levine, M.S.6
  • 24
    • 26844498655 scopus 로고    scopus 로고
    • The use of the R6 transgenic mouse models of Huntington' s disease in attempts to develop novel therapeutic strategies
    • DOI 10.1602/neurorx.2.3.447
    • Li JY, Popovic N, Brundin P. The use of the R6 transgenic mouse models of Huntington's disease in attempts to develop novel therapeutic strategies. NeuroRx. 2005;2(3):447-64. (Pubitemid 41444878)
    • (2005) NeuroRx , vol.2 , Issue.3 , pp. 447-464
    • Li, J.Y.1    Popovic, N.2    Brundin, P.3
  • 25
    • 33847663446 scopus 로고    scopus 로고
    • Selective degeneration in YAC mouse models of Huntington disease
    • DOI 10.1016/j.brainresbull.2006.10.018, PII S0361923006003212
    • Van Raamsdonk JM, Warby SC, Hayden MR. Selective degeneration in YAC mouse models of Huntington disease. Brain Res Bull. 2007;72(2-3):124-31. (Pubitemid 46367458)
    • (2007) Brain Research Bulletin , vol.72 , Issue.2-3 SPEC. ISS. , pp. 124-131
    • Van Raamsdonk, J.M.1    Warby, S.C.2    Hayden, M.R.3
  • 26
    • 33947286031 scopus 로고    scopus 로고
    • Phenotypic abnormalities in the YAC128 mouse model of Huntington disease are penetrant on multiple genetic backgrounds and modulated by strain
    • DOI 10.1016/j.nbd.2006.12.010, PII S0969996106003238
    • Van Raamsdonk JM, Metzler M, Slow E, Pearson J, Schwab C, Carroll J, et al. Phenotypic abnormalities in the YAC128 mouse model of Huntington disease are penetrant on multiple genetic backgrounds and modulated by strain. Neurobiol Dis. 2007;26(1):189-200. (Pubitemid 46436497)
    • (2007) Neurobiology of Disease , vol.26 , Issue.1 , pp. 189-200
    • Van Raamsdonk, J.M.1    Metzler, M.2    Slow, E.3    Pearson, J.4    Schwab, C.5    Carroll, J.6    Graham, R.K.7    Leavitt, B.R.8    Hayden, M.R.9
  • 27
    • 84862610758 scopus 로고    scopus 로고
    • Genetic background modulates behavioral impairments in R6/2 mice and suggests a role for dominant genetic modifiers in Huntington's disease pathogenesis
    • Cowin RM, Bui N, Graham D, Green JR, Yuva-Paylor LA, Weiss A, et al. Genetic background modulates behavioral impairments in R6/2 mice and suggests a role for dominant genetic modifiers in Huntington's disease pathogenesis. Mamm Genome. 2012;23(5-6):367-77.
    • (2012) Mamm Genome , vol.23 , Issue.5-6 , pp. 367-377
    • Cowin, R.M.1    Bui, N.2    Graham, D.3    Green, J.R.4    Yuva-Paylor, L.A.5    Weiss, A.6
  • 28
    • 1542346231 scopus 로고    scopus 로고
    • Regulation of proteins affecting NMDA receptor-induced excitotoxicity in a Huntington's mouse model
    • DOI 10.1093/brain/awh058
    • Jarabek BR, Yasuda RP, Wolfe BB. Regulation of proteins affecting NMDA receptor-induced excitotoxicity in a Huntington's mouse model. Brain. 2004;127(Pt 3):505-16. (Pubitemid 38295468)
    • (2004) Brain , vol.127 , Issue.3 , pp. 505-516
    • Jarabek, B.R.1    Yasuda, R.P.2    Wolfe, B.B.3
  • 30
    • 0036254430 scopus 로고    scopus 로고
    • Maintenance of susceptibility to neurodegeneration following intrastriatal injections of quinolinic acid in a new transgenic mouse model of Huntington's disease
    • DOI 10.1006/exnr.2002.7885
    • Petersen A, Chase K, Puschban Z, DiFiglia M, Brundin P, Aronin N. Maintenance of susceptibility to neurodegeneration following intrastriatal injections of quinolinic acid in a new transgenic mouse model of Huntington's disease. Exp Neurol. 2002;175(1):297-300. (Pubitemid 34507930)
    • (2002) Experimental Neurology , vol.175 , Issue.1 , pp. 297-300
    • Petersen, A.1    Chase, K.2    Puschban, Z.3    DiFiglia, M.4    Brundin, P.5    Aronin, N.6
  • 32
    • 0035783462 scopus 로고    scopus 로고
    • Resistance to NMDA toxicity correlates with appearance of nuclear inclusions, behavioural deficits and changes in calcium homeostasis in mice transgenic for exon 1 of the huntington gene
    • DOI 10.1046/j.0953-816X.2001.01767.x
    • Hansson O, Guatteo E, Mercuri NB, Bernardi G, Li XJ, Castilho RF, et al. Resistance to NMDA toxicity correlates with appearance of nuclear inclusions, behavioural deficits and changes in calcium homeostasis in mice transgenic for exon 1 of the huntington gene. Eur J Neurosci. 2001;14(9): 1492-504. (Pubitemid 35463716)
    • (2001) European Journal of Neuroscience , vol.14 , Issue.9 , pp. 1492-1504
    • Hansson, O.1    Guatteo, E.2    Mercuri, N.B.3    Bernardi, G.4    Li, X.-J.5    Castilho, R.F.6    Brundin, P.7
  • 33
    • 60849093185 scopus 로고    scopus 로고
    • Differential susceptibility to excitotoxic stress in YAC128 mouse models of Huntington disease between initiation and progression of disease
    • Graham RK, Pouladi MA, Joshi P, Lu G, Deng Y, Wu NP, et al. Differential susceptibility to excitotoxic stress in YAC128 mouse models of Huntington disease between initiation and progression of disease. J Neurosci. 2009;29(7):2193-204.
    • (2009) J Neurosci , vol.29 , Issue.7 , pp. 2193-2204
    • Graham, R.K.1    Pouladi, M.A.2    Joshi, P.3    Lu, G.4    Deng, Y.5    Wu, N.P.6
  • 36
    • 0034714392 scopus 로고    scopus 로고
    • Fluoro-Jade B: A high affinity fluorescent marker for the localization of neuronal degeneration
    • Schmued LC, Hopkins KJ. Fluoro-Jade B: A high affinity fluorescent marker for the localization of neuronal degeneration. Brain Res. 2000;874(2):123-30.
    • (2000) Brain Res , vol.874 , Issue.2 , pp. 123-130
    • Schmued, L.C.1    Hopkins, K.J.2
  • 37
    • 82955237522 scopus 로고    scopus 로고
    • Potent and selective antisense oligonucleotides targeting single-nucleotide polymorphisms in the Huntington disease gene/allele-specific silencing of mutant huntingtin
    • Carroll JB, Warby SC, Southwell AL, Doty CN, Greenlee S, Skotte N, et al. Potent and selective antisense oligonucleotides targeting single-nucleotide polymorphisms in the Huntington disease gene/allele-specific silencing of mutant huntingtin. Mol Ther. 2011;19(12):2178-85.
    • (2011) Mol Ther , vol.19 , Issue.12 , pp. 2178-2185
    • Carroll, J.B.1    Warby, S.C.2    Southwell, A.L.3    Doty, C.N.4    Greenlee, S.5    Skotte, N.6
  • 39
    • 0032879437 scopus 로고    scopus 로고
    • Membrane filter assay for detection of amyloid-like polyglutamine- containing protein aggregates
    • DOI 10.1016/S0076-6879(99)09026-6
    • Wanker EE, Scherzinger E, Heiser V, Sittler A, Eickhoff H, Lehrach H. Membrane filter assay for detection of amyloidlike polyglutamine-containing protein aggregates. Methods Enzymol. 1999;309:375-86. (Pubitemid 29446461)
    • (1999) Methods in Enzymology , vol.309 , pp. 375-386
    • Wanker, E.E.1    Scherzinger, E.2    Heiser, V.3    Sittler, A.4    Eickhoff, H.5    Lehrach, H.6
  • 41
    • 45949099949 scopus 로고    scopus 로고
    • VEGF receptor antagonist Cyclo-VEGI reduces inflammatory reactivity and vascular leakiness and is neuroprotective against acute excitotoxic striatal insult
    • Ryu JK, McLarnon JG. VEGF receptor antagonist Cyclo-VEGI reduces inflammatory reactivity and vascular leakiness and is neuroprotective against acute excitotoxic striatal insult. J Neuroinflammation. 2008;5:18.
    • (2008) J Neuroinflammation , vol.5 , pp. 18
    • Ryu, J.K.1    McLarnon, J.G.2
  • 43
    • 80053031331 scopus 로고    scopus 로고
    • Forebrain striatal-specific expression of mutant huntingtin protein in vivo induces cell-autonomous age-dependent alterations in sensitivity to excitotoxicity and mitochondrial function
    • Kim SH, Thomas CA, Andre VM, Cummings DM, Cepeda C, Levine MS, et al. Forebrain striatal-specific expression of mutant huntingtin protein in vivo induces cell-autonomous age-dependent alterations in sensitivity to excitotoxicity and mitochondrial function. ASN Neuro. 2011;3(3):e00060.
    • (2011) ASN Neuro , vol.3 , Issue.3
    • Kim, S.H.1    Thomas, C.A.2    Andre, V.M.3    Cummings, D.M.4    Cepeda, C.5    Levine, M.S.6
  • 44
    • 0026536514 scopus 로고
    • Pattern of neuronal death in the rat hippocampus after status epilepticus. Relationship to calcium binding protein content and ischemic vulnerability
    • Freund TF, Ylinen A, Miettinen R, Pitkanen A, Lahtinen H, Baimbridge KG, et al. Pattern of neuronal death in the rat hippocampus after status epilepticus. Relationship to calcium binding protein content and ischemic vulnerability. Brain Res Bull. 1992;28(1):27-38.
    • (1992) Brain Res Bull , vol.28 , Issue.1 , pp. 27-38
    • Freund, T.F.1    Ylinen, A.2    Miettinen, R.3    Pitkanen, A.4    Lahtinen, H.5    Baimbridge, K.G.6
  • 45
    • 7244236320 scopus 로고    scopus 로고
    • Inclusion body formation reduces levels of mutant huntingtin and the risk of neuronal death
    • DOI 10.1038/nature02998
    • Arrasate M, Mitra S, Schweitzer ES, Segal MR, Finkbeiner S. Inclusion body formation reduces levels of mutant huntingtin and the risk of neuronal death. Nature. 2004;431(7010):805-10. (Pubitemid 39434070)
    • (2004) Nature , vol.431 , Issue.7010 , pp. 805-810
    • Arrasate, M.1    Mitra, S.2    Schweitzer, E.S.3    Segal, M.R.4    Finkbeiner, S.5
  • 47
    • 0003999762 scopus 로고
    • Mouse genetics concepts and applications
    • Oxford, University Press
    • Silver LM. Mouse Genetics Concepts and Applications. In Concepts and Applications. Oxford, University Press; 1995.
    • (1995) Concepts and Applications
    • Silver, L.M.1
  • 49
    • 33846576161 scopus 로고    scopus 로고
    • Wild-type huntingtin ameliorates striatal neuronal atrophy but does not prevent other abnormalities in the YAC128 mouse model of Huntington disease
    • Van Raamsdonk JM, Pearson J, Murphy Z, Hayden MR, Leavitt BR. Wild-type huntingtin ameliorates striatal neuronal atrophy but does not prevent other abnormalities in the YAC128 mouse model of Huntington disease. BMCNeurosci. 2006;7:80.
    • (2006) BMCNeurosci , vol.7 , pp. 80
    • Van Raamsdonk, J.M.1    Pearson, J.2    Murphy, Z.3    Hayden, M.R.4    Leavitt, B.R.5
  • 50
    • 78650811716 scopus 로고    scopus 로고
    • Formation and toxicity of soluble polyglutamine oligomers in living cells
    • Lajoie P, Snapp EL. Formation and toxicity of soluble polyglutamine oligomers in living cells. PLoS One. 2010;5(12):e15245.
    • (2010) PLoS One , vol.5 , Issue.12
    • Lajoie, P.1    Snapp, E.L.2
  • 51
    • 84860879196 scopus 로고    scopus 로고
    • Identification of novel potentially toxic oligomers formed in vitro from mammalian-derived expanded huntingtin exon-1 protein
    • Nucifora LG, Burke KA, Feng X, Arbez N, Zhu S, Miller J, et al. Identification of novel potentially toxic oligomers formed in vitro from mammalian-derived expanded huntingtin exon-1 protein. J Biol Chem. 2012;287(19):16017-28.
    • (2012) J Biol Chem , vol.287 , Issue.19 , pp. 16017-16028
    • Nucifora, L.G.1    Burke, K.A.2    Feng, X.3    Arbez, N.4    Zhu, S.5    Miller, J.6
  • 52
    • 39449105711 scopus 로고    scopus 로고
    • Mutant huntingtin can paradoxically protect neurons from death
    • DOI 10.1038/sj.cdd.4402261, PII 4402261
    • Zuchner T, Brundin P. Mutant huntingtin can paradoxically protect neurons from death. Cell Death Differ. 2008;15(3):435-42. (Pubitemid 351267294)
    • (2008) Cell Death and Differentiation , vol.15 , Issue.3 , pp. 435-442
    • Zuchner, T.1    Brundin, P.2
  • 53
    • 84860838242 scopus 로고    scopus 로고
    • Comparative analysis of pathology and behavioural phenotypes in mouse models of Huntington's disease
    • Brooks SP, Jones L, Dunnett SB. Comparative analysis of pathology and behavioural phenotypes in mouse models of Huntington's disease. Brain Res Bull. 2012;88(2-3):81-93.
    • (2012) Brain Res Bull , vol.88 , Issue.2-3 , pp. 81-93
    • Brooks, S.P.1    Jones, L.2    Dunnett, S.B.3
  • 55
    • 81355160169 scopus 로고    scopus 로고
    • Identifying polyglutamine protein species in situ that best predict neurodegeneration
    • Miller J, Arrasate M, Brooks E, Libeu CP, Legleiter J, Hatters D, et al. Identifying polyglutamine protein species in situ that best predict neurodegeneration. Nat Chem Biol. 2011;7(12): 925-34.
    • (2011) Nat Chem Biol , vol.7 , Issue.12 , pp. 925-934
    • Miller, J.1    Arrasate, M.2    Brooks, E.3    Libeu, C.P.4    Legleiter, J.5    Hatters, D.6
  • 56
    • 77956240426 scopus 로고    scopus 로고
    • Alterations in striatal synaptic transmission are consistent across genetic mouse models of Huntington's disease
    • Cummings DM, Cepeda C, Levine MS. Alterations in striatal synaptic transmission are consistent across genetic mouse models of Huntington's disease. ASN Neuro. 2010;2(3):e00036.
    • (2010) ASN Neuro , vol.2 , Issue.3
    • Cummings, D.M.1    Cepeda, C.2    Levine, M.S.3
  • 57
    • 69049091946 scopus 로고    scopus 로고
    • Alterations in cortical excitation and inhibition in genetic mouse models of Huntington's disease
    • Cummings DM, Andre VM, Uzgil BO, Gee SM, Fisher YE, Cepeda C, et al. Alterations in cortical excitation and inhibition in genetic mouse models of Huntington's disease. J Neurosci. 2009;29(33):10371-86.
    • (2009) J Neurosci , vol.29 , Issue.33 , pp. 10371-10386
    • Cummings, D.M.1    Andre, V.M.2    Uzgil, B.O.3    Gee, S.M.4    Fisher, Y.E.5    Cepeda, C.6
  • 58
    • 61449148438 scopus 로고    scopus 로고
    • Age-dependent alterations of corticostriatal activity in the YAC128 mouse model of Huntington disease
    • Joshi PR, Wu NP, Andre VM, Cummings DM, Cepeda C, Joyce JA, et al. Age-dependent alterations of corticostriatal activity in the YAC128 mouse model of Huntington disease. J Neurosci. 2009;29(8):2414-27.
    • (2009) J Neurosci , vol.29 , Issue.8 , pp. 2414-2427
    • Joshi, P.R.1    Wu, N.P.2    Andre, V.M.3    Cummings, D.M.4    Cepeda, C.5    Joyce, J.A.6
  • 59
    • 74549181538 scopus 로고    scopus 로고
    • Early increase in extrasynaptic NMDA receptor signaling and expression contributes to phenotype onset in Huntington's disease mice
    • Milnerwood AJ, Gladding CM, Pouladi MA, Kaufman AM, Hines RM, Boyd JD, et al. Early increase in extrasynaptic NMDA receptor signaling and expression contributes to phenotype onset in Huntington's disease mice. Neuron. 2010;65(2):178-90.
    • (2010) Neuron , vol.65 , Issue.2 , pp. 178-190
    • Milnerwood, A.J.1    Gladding, C.M.2    Pouladi, M.A.3    Kaufman, A.M.4    Hines, R.M.5    Boyd, J.D.6
  • 60
    • 77958192164 scopus 로고    scopus 로고
    • Early synaptic pathophysiology in neurodegeneration: Insights from Huntington's disease
    • Milnerwood AJ, Raymond LA. Early synaptic pathophysiology in neurodegeneration: Insights from Huntington's disease. Trends Neurosci. 2010;33(11):513-23.
    • (2010) Trends Neurosci , vol.33 , Issue.11 , pp. 513-523
    • Milnerwood, A.J.1    Raymond, L.A.2
  • 61
    • 4544293517 scopus 로고    scopus 로고
    • Huntingtin and its role in neuronal degeneration
    • Li SH, Li XJ. Huntingtin and its role in neuronal degeneration. Neuroscientist. 2004;10(5):467-75.
    • (2004) Neuroscientist , vol.10 , Issue.5 , pp. 467-475
    • Li, S.H.1    Li, X.J.2
  • 62
    • 79958054247 scopus 로고    scopus 로고
    • Striatal-enriched protein tyrosine phosphatase expression and activity in Huntington's disease: A STEP in the resistance to excitotoxicity
    • Saavedra A, Giralt A, Rue L, Xifro X, Xu J, Ortega Z, et al. Striatal-enriched protein tyrosine phosphatase expression and activity in Huntington's disease: A STEP in the resistance to excitotoxicity. J Neurosci. 2011;31(22):8150-62.
    • (2011) J Neurosci , vol.31 , Issue.22 , pp. 8150-8162
    • Saavedra, A.1    Giralt, A.2    Rue, L.3    Xifro, X.4    Xu, J.5    Ortega, Z.6
  • 63
    • 33947320461 scopus 로고    scopus 로고
    • Status epilepticus-induced somatostatinergic hilar interneuron degeneration is regulated by striatal enriched protein tyrosine phosphatase
    • DOI 10.1523/JNEUROSCI.4913-06.2007
    • Choi YS, Lin SL, Lee B, Kurup P, Cho HY, Naegele JR, et al. Status epilepticus-induced somatostatinergic hilar interneuron degeneration is regulated by striatal enriched protein tyrosine phosphatase. J Neurosci. 2007;27(11):2999-3009. (Pubitemid 46438970)
    • (2007) Journal of Neuroscience , vol.27 , Issue.11 , pp. 2999-3009
    • Choi, Y.-S.1    Lin, S.L.2    Lee, B.3    Kurup, P.4    Cho, H.-Y.5    Naegele, J.R.6    Lombroso, P.J.7    Obrietan, K.8
  • 64
    • 84865465570 scopus 로고    scopus 로고
    • Kainic acid-induced neuronal degeneration in hippocampal pyramidal neurons is driven by both intrinsic and extrinsic factors: Analysis of fvb/n?c57bl/6 chimeras
    • Liu L, Hamre KM, Goldowitz D. Kainic Acid-Induced Neuronal Degeneration in Hippocampal Pyramidal Neurons Is Driven by Both Intrinsic and Extrinsic Factors: Analysis of FVB/N?C57BL/6 Chimeras. J Neurosci. 2012;32(35):12093-101.
    • (2012) J Neurosci , vol.32 , Issue.35 , pp. 12093-12101
    • Liu, L.1    Hamre, K.M.2    Goldowitz, D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.