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Volumn 23, Issue 17, 2014, Pages 4510-4527

Progressive axonal transport and synaptic protein changes correlate with behavioral and neuropathological abnormalities in the heterozygous Q175 KI mouse model of Huntington's disease

Author keywords

[No Author keywords available]

Indexed keywords

4 AMINOBUTYRIC ACID; 5 HYDROXYINDOLEACETIC ACID; BETA TUBULIN; BRAIN DERIVED NEUROTROPHIC FACTOR; BRAIN DERIVED NEUROTROPHIC FACTOR RECEPTOR; DOPAMINE; DYNACTIN; DYNEIN ADENOSINE TRIPHOSPHATASE; HUNTINGTIN; KIF3A PROTEIN; N METHYL DEXTRO ASPARTIC ACID RECEPTOR 1; PHOSPHOPROTEIN DARPP 32; POSTSYNAPTIC DENSITY PROTEIN 95; RAB PROTEIN; SEROTONIN; SYNAPTOPHYSIN; SYNAPTOSOMAL ASSOCIATED PROTEIN 25; TRANSLOCASE OF OUTER MITOCHONDRIAL MEMBRANE 20; TYROSINE 3 MONOOXYGENASE; UNCLASSIFIED DRUG; AGENTS INTERACTING WITH TRANSMITTER, HORMONE OR DRUG RECEPTORS; SEROTONIN TRANSPORTER; SLC6A4 PROTEIN, MOUSE;

EID: 84905667224     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddu166     Document Type: Article
Times cited : (72)

References (84)
  • 1
    • 0033757718 scopus 로고    scopus 로고
    • Inactivation of Hdh in the brain and testis results in progressive neurodegeneration and sterility in mice
    • Dragatsis, I., Levine, M.S. and Zeitlin, S. (2000) Inactivation of Hdh in the brain and testis results in progressive neurodegeneration and sterility in mice. Nat. Genet., 26, 300-306.
    • (2000) Nat. Genet. , vol.26 , pp. 300-306
    • Dragatsis, I.1    Levine, M.S.2    Zeitlin, S.3
  • 2
    • 84860841192 scopus 로고    scopus 로고
    • Light and electron microscopic characterization of the evolution of cellular pathology in HdhQ92 Huntington's disease knock-in mice
    • Bayram-Weston, Z., Jones, L., Dunnett, S.B. and Brooks, S.P. (2012) Light and electron microscopic characterization of the evolution of cellular pathology in HdhQ92 Huntington's disease knock-in mice. Brain Res. Bull., 88, 171-181.
    • (2012) Brain Res. Bull. , vol.88 , pp. 171-181
    • Bayram-Weston, Z.1    Jones, L.2    Dunnett, S.B.3    Brooks, S.P.4
  • 3
    • 84860841633 scopus 로고    scopus 로고
    • Light and electron microscopic characterization of the evolution of cellular pathology in the Hdh(CAG)150 Huntington's disease knock-in mouse
    • Bayram-Weston, Z., Torres, E.M., Jones, L., Dunnett, S.B. and Brooks, S.P. (2012) Light and electron microscopic characterization of the evolution of cellular pathology in the Hdh(CAG)150 Huntington's disease knock-in mouse. Brain Res. Bull., 88, 189-198.
    • (2012) Brain Res. Bull. , vol.88 , pp. 189-198
    • Bayram-Weston, Z.1    Torres, E.M.2    Jones, L.3    Dunnett, S.B.4    Brooks, S.P.5
  • 4
    • 33847684865 scopus 로고    scopus 로고
    • The Hdh(Q150/Q150) knock-in mouse model of HD and the R6/2 exon 1 model develop comparable and widespread molecular phenotypes
    • Woodman, B., Butler, R., Landles, C., Lupton, M.K., Tse, J., Hockly, E., Moffitt, H., Sathasivam, K. and Bates, G.P. (2007) 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., 72, 83-97.
    • (2007) Brain Res. Bull. , 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
  • 6
    • 63849332293 scopus 로고    scopus 로고
    • Dynamic changes in presynaptic and axonal transport proteins combined with striatal neuroinflammation precede dopaminergic neuronal loss in a rat model of AAV alpha-synucleinopathy
    • Chung, C.Y., Koprich, J.B., Siddiqi, H. and Isacson, O. (2009) Dynamic changes in presynaptic and axonal transport proteins combined with striatal neuroinflammation precede dopaminergic neuronal loss in a rat model of AAV alpha-synucleinopathy. J. Neurosci., 29, 3365-3373.
    • (2009) J. Neurosci. , vol.29 , pp. 3365-3373
    • Chung, C.Y.1    Koprich, J.B.2    Siddiqi, H.3    Isacson, O.4
  • 8
    • 0036403826 scopus 로고    scopus 로고
    • Pyramidal cell loss in motor cortices in Huntington's disease
    • Macdonald, V. and Halliday,G. (2002) Pyramidal cell loss in motor cortices in Huntington's disease. Neurobiol. Dis., 10, 378-386.
    • (2002) Neurobiol. Dis. , vol.10 , pp. 378-386
    • Macdonald, V.1    Halliday, G.2
  • 10
    • 0032987513 scopus 로고    scopus 로고
    • Axonal transport of N-terminal huntingtin suggests early pathology of corticostriatal projections in Huntington disease
    • Sapp, E., Penney, J., Young, A., Aronin, N., Vonsattel, J.P. and DiFiglia, M. (1999) Axonal transport of N-terminal huntingtin suggests early pathology of corticostriatal projections in Huntington disease. J. Neuropathol. Exp. Neurol., 58, 165-173.
    • (1999) J. Neuropathol. Exp. Neurol. , vol.58 , pp. 165-173
    • Sapp, E.1    Penney, J.2    Young, A.3    Aronin, N.4    Vonsattel, J.P.5    DiFiglia, M.6
  • 11
    • 84859609686 scopus 로고    scopus 로고
    • Huntington disease and the huntingtin protein
    • Zheng, Z. and Diamond, M.I. (2012) Huntington disease and the huntingtin protein. Prog. Mol. Biol. Transl. Sci., 107, 189-214.
    • (2012) Prog. Mol. Biol. Transl. Sci. , vol.107 , pp. 189-214
    • Zheng, Z.1    Diamond, M.I.2
  • 14
    • 4444303263 scopus 로고    scopus 로고
    • Generalized brain and skin proteasome inhibition in Huntington's disease
    • Seo, H., Sonntag, K.C. and Isacson, O. (2004) Generalized brain and skin proteasome inhibition in Huntington's disease. Ann. Neurol., 56, 319-328.
    • (2004) Ann. Neurol. , vol.56 , pp. 319-328
    • Seo, H.1    Sonntag, K.C.2    Isacson, O.3
  • 16
    • 84875443717 scopus 로고    scopus 로고
    • Axonal transport deficits and neurodegenerative diseases
    • Millecamps, S. and Julien, J.P. (2013) Axonal transport deficits and neurodegenerative diseases. Nat. Rev. Neurosci., 14, 161-176.
    • (2013) Nat. Rev. Neurosci. , vol.14 , pp. 161-176
    • Millecamps, S.1    Julien, J.P.2
  • 18
    • 0036500862 scopus 로고    scopus 로고
    • Perinuclear localization of huntingtin as a consequence of its binding to microtubules through an interaction with beta-tubulin: relevance to Huntington's disease
    • Hoffner, G., Kahlem, P. and Djian, P. (2002) Perinuclear localization of huntingtin as a consequence of its binding to microtubules through an interaction with beta-tubulin: relevance to Huntington's disease. J. Cell. Sci., 115, 941-948.
    • (2002) J. Cell. Sci. , vol.115 , pp. 941-948
    • Hoffner, G.1    Kahlem, P.2    Djian, P.3
  • 20
    • 0031867231 scopus 로고    scopus 로고
    • Wild-type and mutant huntingtins function in vesicle trafficking in the secretory and endocytic pathways
    • Velier, J., Kim, M., Schwarz, C., Kim, T.W., Sapp, E., Chase, K., Aronin, N. and DiFiglia, M. (1998) Wild-type and mutant huntingtins function in vesicle trafficking in the secretory and endocytic pathways. Exp. Neurol., 152, 34-40.
    • (1998) Exp. Neurol. , vol.152 , pp. 34-40
    • Velier, J.1    Kim, M.2    Schwarz, C.3    Kim, T.W.4    Sapp, E.5    Chase, K.6    Aronin, N.7    DiFiglia, M.8
  • 24
    • 1542267796 scopus 로고    scopus 로고
    • Cytoplasmic aggregates trap polyglutamine-containing proteins and block axonal transport in a Drosophila model of Huntington's disease
    • Lee, W.C., Yoshihara, M. and Littleton, J.T. (2004) Cytoplasmic aggregates trap polyglutamine-containing proteins and block axonal transport in a Drosophila model of Huntington's disease. Proc. Natl. Acad. Sci. USA, 101, 3224-3229.
    • (2004) Proc. Natl. Acad. Sci. USA , vol.101 , pp. 3224-3229
    • Lee, W.C.1    Yoshihara, M.2    Littleton, J.T.3
  • 26
    • 0035503511 scopus 로고    scopus 로고
    • Huntingtin aggregate-associated axonal degeneration is an early pathological event in Huntington's disease mice
    • Li, H., Li, S.H., Yu, Z.X., Shelbourne, P. and Li, X.J. (2001) Huntingtin aggregate-associated axonal degeneration is an early pathological event in Huntington's disease mice. J. Neurosci., 21, 8473-8481.
    • (2001) J. Neurosci. , vol.21 , pp. 8473-8481
    • Li, H.1    Li, S.H.2    Yu, Z.X.3    Shelbourne, P.4    Li, X.J.5
  • 27
    • 34047175919 scopus 로고    scopus 로고
    • Histone deacetylase 6 inhibition compensates for the transport deficit in Huntington's disease by increasing tubulin acetylation
    • Dompierre, J.P., Godin, J.D., Charrin, B.C., Cordelieres, F.P., King, S.J., Humbert, S. and Saudou, F. (2007) Histone deacetylase 6 inhibition compensates for the transport deficit in Huntington's disease by increasing tubulin acetylation. J. Neurosci., 27, 3571-3583.
    • (2007) J. Neurosci. , vol.27 , pp. 3571-3583
    • Dompierre, J.P.1    Godin, J.D.2    Charrin, B.C.3    Cordelieres, F.P.4    King, S.J.5    Humbert, S.6    Saudou, F.7
  • 30
    • 34047130812 scopus 로고    scopus 로고
    • Role of brain-derived neurotrophic factor in Huntington's disease
    • Zuccato, C. and Cattaneo, E. (2007) Role of brain-derived neurotrophic factor in Huntington's disease. Prog. Neurobiol., 81, 294-330.
    • (2007) Prog. Neurobiol. , vol.81 , pp. 294-330
    • Zuccato, C.1    Cattaneo, E.2
  • 32
    • 84875509193 scopus 로고    scopus 로고
    • Mutant Huntingtin alters retrograde transport of TrkB receptors in striatal dendrites
    • Liot, G., Zala, D., Pla, P., Mottet, G., Piel, M. and Saudou, F. (2013) Mutant Huntingtin alters retrograde transport of TrkB receptors in striatal dendrites. J. Neurosci., 33, 6298-6309.
    • (2013) J. Neurosci. , vol.33 , pp. 6298-6309
    • Liot, G.1    Zala, D.2    Pla, P.3    Mottet, G.4    Piel, M.5    Saudou, F.6
  • 33
    • 84864628471 scopus 로고    scopus 로고
    • Induced pluripotent stem cells from patients with Huntington's disease show CAG-repeat-expansion-associated phenotypes
    • HD-iPSC-Consortium
    • HD-iPSC-Consortium (2012) Induced pluripotent stem cells from patients with Huntington's disease show CAG-repeat-expansion-associated phenotypes. Cell Stem Cell, 11, 264-278.
    • (2012) Cell Stem Cell , vol.11 , pp. 264-278
  • 35
    • 76049093950 scopus 로고    scopus 로고
    • Functional enhancement and protection of dopaminergic terminals by RAB3B overexpression
    • Chung, C.Y., Koprich, J.B., Hallett, P.J. and Isacson, O. (2009) Functional enhancement and protection of dopaminergic terminals by RAB3B overexpression. Proc. Natl. Acad. Sci. USA, 106, 22474-22479.
    • (2009) Proc. Natl. Acad. Sci. USA , vol.106 , pp. 22474-22479
    • Chung, C.Y.1    Koprich, J.B.2    Hallett, P.J.3    Isacson, O.4
  • 36
    • 79959294945 scopus 로고    scopus 로고
    • Rab GTPases, membrane trafficking and diseases
    • Li, G. (2011) Rab GTPases, membrane trafficking and diseases. Curr. Drug Targets, 12, 1188-1193.
    • (2011) Curr. Drug Targets , vol.12 , pp. 1188-1193
    • Li, G.1
  • 38
    • 20444408739 scopus 로고    scopus 로고
    • Altered distribution of striatal activity-dependent synaptic plasticity in the 3-nitropropionic acid model of Huntington's disease
    • Dalbem, A., Silveira, C.V., Pedroso, M.F., Breda, R.V., Werne Baes, C.V., Bartmann, A.P. and da Costa, J.C. (2005) Altered distribution of striatal activity-dependent synaptic plasticity in the 3-nitropropionic acid model of Huntington's disease. Brain Res., 1047, 148-158.
    • (2005) Brain Res , vol.1047 , pp. 148-158
    • Dalbem, A.1    Silveira, C.V.2    Pedroso, M.F.3    Breda, R.V.4    Werne Baes, C.V.5    Bartmann, A.P.6    da Costa, J.C.7
  • 39
    • 26944493771 scopus 로고    scopus 로고
    • A similar impairment in CA3 mossy fibre LTP in the R6/2 mouse model of Huntington's disease and in the complexin II knockout mouse
    • Gibson, H.E., Reim, K., Brose, N., Morton, A.J. and Jones, S. (2005) A similar impairment in CA3 mossy fibre LTP in the R6/2 mouse model of Huntington's disease and in the complexin II knockout mouse. Eur. J. Neurosci., 22, 1701-1712.
    • (2005) Eur. J. Neurosci. , vol.22 , pp. 1701-1712
    • Gibson, H.E.1    Reim, K.2    Brose, N.3    Morton, A.J.4    Jones, S.5
  • 40
    • 34249026735 scopus 로고    scopus 로고
    • Dopamine-dependent long term potentiation in the dorsal striatum is reduced in the R6/2 mouse model of Huntington's disease
    • Kung, V.W., Hassam, R., Morton, A.J. and Jones, S. (2007) Dopamine-dependent long term potentiation in the dorsal striatum is reduced in the R6/2 mouse model of Huntington's disease. Neuroscience, 146, 1571-1580.
    • (2007) Neuroscience , vol.146 , pp. 1571-1580
    • Kung, V.W.1    Hassam, R.2    Morton, A.J.3    Jones, S.4
  • 41
    • 37449011119 scopus 로고    scopus 로고
    • Corticostriatal synaptic function in mouse models of Huntington's disease: early effects of huntingtin repeat length and protein load
    • Milnerwood, A.J. and Raymond, L.A. (2007) Corticostriatal synaptic function in mouse models of Huntington's disease: early effects of huntingtin repeat length and protein load. J. Physiol., 585, 817-831.
    • (2007) J. Physiol. , vol.585 , pp. 817-831
    • Milnerwood, A.J.1    Raymond, L.A.2
  • 42
    • 0032897760 scopus 로고    scopus 로고
    • Impaired synaptic plasticity in mice carrying the Huntington's disease mutation
    • Usdin, M.T., Shelbourne, P.F., Myers, R.M. and Madison, D.V. (1999) Impaired synaptic plasticity in mice carrying the Huntington's disease mutation. Hum. Mol. Genet., 8, 839-846.
    • (1999) Hum. Mol. Genet. , vol.8 , pp. 839-846
    • Usdin, M.T.1    Shelbourne, P.F.2    Myers, R.M.3    Madison, D.V.4
  • 44
    • 84860837080 scopus 로고    scopus 로고
    • Light and electron microscopic characterization of the evolution of cellular pathology in the R6/1 Huntington's disease transgenic mice
    • Bayram-Weston, Z., Jones, L., Dunnett, S.B. and Brooks, S.P. (2012) Light and electron microscopic characterization of the evolution of cellular pathology in the R6/1 Huntington's disease transgenic mice. Brain. Res. Bull., 88, 104-112.
    • (2012) Brain. Res. Bull. , vol.88 , pp. 104-112
    • Bayram-Weston, Z.1    Jones, L.2    Dunnett, S.B.3    Brooks, S.P.4
  • 45
    • 84860836853 scopus 로고    scopus 로고
    • Light and electron microscopic characterization of the evolution of cellular pathology in YAC128 Huntington's disease transgenic mice
    • Bayram-Weston, Z., Jones, L., Dunnett, S.B. and Brooks, S.P. (2012) Light and electron microscopic characterization of the evolution of cellular pathology in YAC128 Huntington's disease transgenic mice. Brain. Res. Bull., 88, 137-147.
    • (2012) Brain. Res. Bull. , vol.88 , pp. 137-147
    • Bayram-Weston, Z.1    Jones, L.2    Dunnett, S.B.3    Brooks, S.P.4
  • 46
    • 84866421220 scopus 로고    scopus 로고
    • Characterization of a rat model of Huntington's disease based on targeted expression of mutant huntingtin in the forebrain using adeno-associated viral vectors
    • Gabery, S., Sajjad, M.U., Hult, S., Soylu, R., Kirik, D. and Petersen, A. (2012) Characterization of a rat model of Huntington's disease based on targeted expression of mutant huntingtin in the forebrain using adeno-associated viral vectors. Eur. J. Neurosci., 36, 2789-2800.
    • (2012) Eur. J. Neurosci. , vol.36 , pp. 2789-2800
    • Gabery, S.1    Sajjad, M.U.2    Hult, S.3    Soylu, R.4    Kirik, D.5    Petersen, A.6
  • 47
    • 84879032355 scopus 로고    scopus 로고
    • Predictors of phenotypic progression and disease onset in premanifest and early-stage Huntington's disease in the TRACK-HD study: analysis of 36-month observational data
    • Tabrizi, S.J., Scahill, R.I., Owen, G., Durr, A., Leavitt, B.R., Roos, R.A., Borowsky, B., Landwehrmeyer, B., Frost, C., Johnson, H. et al. (2013) Predictors of phenotypic progression and disease onset in premanifest and early-stage Huntington's disease in the TRACK-HD study: analysis of 36-month observational data. Lancet Neurol., 12, 637-649.
    • (2013) Lancet Neurol , vol.12 , pp. 637-649
    • Tabrizi, S.J.1    Scahill, R.I.2    Owen, G.3    Durr, A.4    Leavitt, B.R.5    Roos, R.A.6    Borowsky, B.7    Landwehrmeyer, B.8    Frost, C.9    Johnson, H.10
  • 50
    • 80052533413 scopus 로고    scopus 로고
    • Genetics and neuropathology of Huntington's disease
    • Reiner, A., Dragatsis, I. and Dietrich, P. (2011) Genetics and neuropathology of Huntington's disease. Int. Rev. Neurobiol., 98, 325-372.
    • (2011) Int. Rev. Neurobiol. , vol.98 , pp. 325-372
    • Reiner, A.1    Dragatsis, I.2    Dietrich, P.3
  • 52
    • 0031856524 scopus 로고    scopus 로고
    • Apoptosis of retrogradely degenerating neurons occurs in association with the accumulation of perikaryal mitochondria and oxidativedamageto the nucleus
    • Al-Abdulla, N.A. and Martin, L.J. (1998) Apoptosis of retrogradely degenerating neurons occurs in association with the accumulation of perikaryal mitochondria and oxidativedamageto the nucleus.Am.J. Pathol., 153, 447-456.
    • (1998) Am. J. Pathol. , vol.153 , pp. 447-456
    • Al-Abdulla, N.A.1    Martin, L.J.2
  • 53
    • 84884134047 scopus 로고    scopus 로고
    • Loss of corticostriatal and thalamostriatal synaptic terminals precedes striatal projection neuron pathology in heterozygous Q140 Huntington's disease mice
    • Deng, Y.P., Wong, T., Bricker-Anthony, C., Deng, B. and Reiner, A. (2013) Loss of corticostriatal and thalamostriatal synaptic terminals precedes striatal projection neuron pathology in heterozygous Q140 Huntington's disease mice. Neurobiol. Dis., 60, 89-107.
    • (2013) Neurobiol. Dis. , vol.60 , pp. 89-107
    • Deng, Y.P.1    Wong, T.2    Bricker-Anthony, C.3    Deng, B.4    Reiner, A.5
  • 55
    • 0033560924 scopus 로고    scopus 로고
    • Characterization of progressive motor deficits in mice transgenic for the human Huntington's disease mutation
    • Carter, R.J., Lione, L.A., Humby, T., Mangiarini, L., Mahal, A., Bates, G.P., Dunnett, S.B. and Morton, A.J. (1999) Characterization of progressive motor deficits in mice transgenic for the human Huntington's disease mutation. J. Neurosci., 19, 3248-3257.
    • (1999) J. Neurosci. , vol.19 , pp. 3248-3257
    • Carter, R.J.1    Lione, L.A.2    Humby, T.3    Mangiarini, L.4    Mahal, A.5    Bates, G.P.6    Dunnett, S.B.7    Morton, A.J.8
  • 56
    • 0035180327 scopus 로고    scopus 로고
    • Altered striatal amino acid neurotransmitter release monitored using microdialysis in R6/1 Huntington transgenic mice
    • Nicniocaill, B., Haraldsson, B., Hansson, O., O'Connor, W.T. and Brundin, P. (2001) Altered striatal amino acid neurotransmitter release monitored using microdialysis in R6/1 Huntington transgenic mice. Eur. J. Neurosci., 13, 206-210.
    • (2001) Eur. J. Neurosci. , vol.13 , pp. 206-210
    • Nicniocaill, B.1    Haraldsson, B.2    Hansson, O.3    O'Connor, W.T.4    Brundin, P.5
  • 57
    • 84880851601 scopus 로고    scopus 로고
    • The Q175 mouse model of Huntington's disease shows gene dosage- and age-related decline in circadian rhythms of activity and sleep
    • Loh, D.H., Kudo, T., Truong, D., Wu, Y. and Colwell, C.S. (2013) The Q175 mouse model of Huntington's disease shows gene dosage- and age-related decline in circadian rhythms of activity and sleep. PLoS One, 8, e69993.
    • (2013) PLoS One , vol.8
    • Loh, D.H.1    Kudo, T.2    Truong, D.3    Wu, Y.4    Colwell, C.S.5
  • 58
    • 84875381701 scopus 로고    scopus 로고
    • Circadian and sleep disorder in Huntington's disease
    • Morton, A.J. (2013) Circadian and sleep disorder in Huntington's disease. Exp. Neurol., 243, 34-44.
    • (2013) Exp. Neurol. , vol.243 , pp. 34-44
    • Morton, A.J.1
  • 59
    • 81255160494 scopus 로고    scopus 로고
    • Altered balance of activity in the striatal direct and indirect pathways in mouse models of Huntington's disease
    • Andre, V.M., Fisher, Y.E. and Levine, M.S. (2011) Altered balance of activity in the striatal direct and indirect pathways in mouse models of Huntington's disease. Front. Syst. Neurosci., 5, 46.
    • (2011) Front. Syst. Neurosci. , vol.5 , pp. 46
    • Andre, V.M.1    Fisher, Y.E.2    Levine, M.S.3
  • 60
    • 80055002896 scopus 로고    scopus 로고
    • In vivo dopamine efflux is decreased in striatum of both fragment (R6/2) and full-Length (YAC128) transgenic mouse models of Huntington's disease
    • Callahan, J.W. and Abercrombie, E.D. (2011) In vivo dopamine efflux is decreased in striatum of both fragment (R6/2) and full-Length (YAC128) transgenic mouse models of Huntington's disease. Front. Syst. Neurosci., 5, 61.
    • (2011) Front. Syst. Neurosci. , vol.5 , pp. 61
    • Callahan, J.W.1    Abercrombie, E.D.2
  • 61
    • 0029984570 scopus 로고    scopus 로고
    • Nucleocytoplasmic transport
    • Gorlich, D. and Mattaj, I.W. (1996) Nucleocytoplasmic transport. Science, 271, 1513-1518.
    • (1996) Science , vol.271 , pp. 1513-1518
    • Gorlich, D.1    Mattaj, I.W.2
  • 62
    • 84855499458 scopus 로고    scopus 로고
    • Huntington's disease: molecular basis of neurodegeneration
    • Rubinsztein, D.C. and Carmichael, J. (2003) Huntington's disease: molecular basis of neurodegeneration. Expert. Rev. Mol. Med., 5, 1-21.
    • (2003) Expert. Rev. Mol. Med. , vol.5 , pp. 1-21
    • Rubinsztein, D.C.1    Carmichael, J.2
  • 66
    • 33646759268 scopus 로고    scopus 로고
    • Kinesin-1 and Dynein are the primary motors for fast transport of mitochondria in Drosophila motor axons
    • Pilling, A.D., Horiuchi, D., Lively,C.M. and Saxton,W.M.(2006) Kinesin-1 and Dynein are the primary motors for fast transport of mitochondria in Drosophila motor axons. Mol. Biol. Cell, 17, 2057-2068.
    • (2006) Mol. Biol. Cell , vol.17 , pp. 2057-2068
    • Pilling, A.D.1    Horiuchi, D.2    Lively, C.M.3    Saxton, W.M.4
  • 67
    • 79955641945 scopus 로고    scopus 로고
    • Cytoplasmic dynein in neurodegeneration
    • Eschbach, J. and Dupuis, L. (2011) Cytoplasmic dynein in neurodegeneration. Pharmacol. Ther., 130, 348-363.
    • (2011) Pharmacol. Ther. , vol.130 , pp. 348-363
    • Eschbach, J.1    Dupuis, L.2
  • 70
    • 84877905808 scopus 로고    scopus 로고
    • Systemic delivery of recombinant brain derived neurotrophic factor (BDNF) in the R6/2 mouse model of Huntington's disease
    • Giampa, C., Montagna, E., Dato, C., Melone, M.A., Bernardi, G. and Fusco, F.R. (2013) Systemic delivery of recombinant brain derived neurotrophic factor (BDNF) in the R6/2 mouse model of Huntington's disease. PLoS One, 8, e64037.
    • (2013) PLoS One , vol.8
    • Giampa, C.1    Montagna, E.2    Dato, C.3    Melone, M.A.4    Bernardi, G.5    Fusco, F.R.6
  • 71
    • 84872681227 scopus 로고    scopus 로고
    • Relationship between BDNF expression in major striatal afferents, striatum morphology and motor behavior in the R6/2 mouse model of Huntington's disease
    • Samadi, P., Boutet, A., Rymar, V.V., Rawal, K., Maheux, J., Kvann, J.C., Tomaszewski, M., Beaubien, F., Cloutier, J.F., Levesque, D. et al. (2013) Relationship between BDNF expression in major striatal afferents, striatum morphology and motor behavior in the R6/2 mouse model of Huntington's disease. Genes Brain Behav., 12, 108-124.
    • (2013) Genes Brain Behav , vol.12 , pp. 108-124
    • Samadi, P.1    Boutet, A.2    Rymar, V.V.3    Rawal, K.4    Maheux, J.5    Kvann, J.C.6    Tomaszewski, M.7    Beaubien, F.8    Cloutier, J.F.9    Levesque, D.10
  • 72
    • 65449167971 scopus 로고    scopus 로고
    • Short-term striatal gene expression responses to brain-derived neurotrophic factor are dependent on MEK and ERK activation
    • Gokce, O., Runne, H., Kuhn, A. and Luthi-Carter, R. (2009) Short-term striatal gene expression responses to brain-derived neurotrophic factor are dependent on MEK and ERK activation. PLoS One, 4, e5292.
    • (2009) PLoS One , vol.4
    • Gokce, O.1    Runne, H.2    Kuhn, A.3    Luthi-Carter, R.4
  • 73
    • 84878227058 scopus 로고    scopus 로고
    • BDNF-based synaptic repair as a disease-modifying strategy for neurodegenerative diseases
    • Lu, B., Nagappan, G., Guan, X., Nathan, P.J. and Wren, P. (2013) BDNF-based synaptic repair as a disease-modifying strategy for neurodegenerative diseases. Nat. Rev. Neurosci., 14, 401-416.
    • (2013) Nat. Rev. Neurosci. , vol.14 , pp. 401-416
    • Lu, B.1    Nagappan, G.2    Guan, X.3    Nathan, P.J.4    Wren, P.5
  • 74
    • 84881148047 scopus 로고    scopus 로고
    • Dendritic spine instability leads to progressive neocortical spine loss in a mouse model of Huntington's disease
    • Murmu, R.P., Li, W., Holtmaat, A. and Li, J.Y. (2013) Dendritic spine instability leads to progressive neocortical spine loss in a mouse model of Huntington's disease. J. Neurosci., 33, 12997-13009.
    • (2013) J. Neurosci. , vol.33 , pp. 12997-13009
    • Murmu, R.P.1    Li, W.2    Holtmaat, A.3    Li, J.Y.4
  • 75
    • 84884292211 scopus 로고    scopus 로고
    • Dysregulation of synaptic proteins, dendritic spine abnormalities and pathological plasticity of synapses as experience-dependent mediators of cognitive and psychiatric symptoms in Huntington's disease
    • Nithianantharajah, J. and Hannan, A.J. (2012) Dysregulation of synaptic proteins, dendritic spine abnormalities and pathological plasticity of synapses as experience-dependent mediators of cognitive and psychiatric symptoms in Huntington's disease. Neuroscience, 251, 66-74.
    • (2012) Neuroscience , vol.251 , pp. 66-74
    • Nithianantharajah, J.1    Hannan, A.J.2
  • 76
    • 20044377268 scopus 로고    scopus 로고
    • Early changes in Huntington's disease patient brains involve alterations in cytoskeletal and synaptic elements
    • DiProspero, N.A., Chen, E.Y., Charles, V., Plomann, M., Kordower, J.H. and Tagle, D.A. (2004) Early changes in Huntington's disease patient brains involve alterations in cytoskeletal and synaptic elements. J. Neurocytol., 33, 517-533.
    • (2004) J. Neurocytol. , vol.33 , pp. 517-533
    • DiProspero, N.A.1    Chen, E.Y.2    Charles, V.3    Plomann, M.4    Kordower, J.H.5    Tagle, D.A.6
  • 77
    • 84888419468 scopus 로고    scopus 로고
    • Reduced tonic inhibition in striatal output neurons from Huntington mice due to loss of astrocytic GABA release through GAT-3
    • Wojtowicz, A.M., Dvorzhak, A., Semtner, M. and Grantyn, R. (2013) Reduced tonic inhibition in striatal output neurons from Huntington mice due to loss of astrocytic GABA release through GAT-3. Front. Neural Circuits, 7, 188.
    • (2013) Front. Neural Circuits , vol.7 , pp. 188
    • Wojtowicz, A.M.1    Dvorzhak, A.2    Semtner, M.3    Grantyn, R.4
  • 81
    • 36348948083 scopus 로고    scopus 로고
    • Drosophila huntingtin-interacting protein 14 is a presynaptic protein required for photoreceptor synaptic transmission and expression of the palmitoylated proteins synaptosome-associated protein 25 and cysteine string protein
    • Stowers, R.S. and Isacoff, E.Y. (2007) Drosophila huntingtin-interacting protein 14 is a presynaptic protein required for photoreceptor synaptic transmission and expression of the palmitoylated proteins synaptosome-associated protein 25 and cysteine string protein. J. Neurosci., 27, 12874-12883.
    • (2007) J. Neurosci. , vol.27 , pp. 12874-12883
    • Stowers, R.S.1    Isacoff, E.Y.2
  • 83
    • 84864912383 scopus 로고    scopus 로고
    • Schizandrin, an antioxidant lignan from Schisandra chinensis, ameliorates Abeta1-42-induced memory impairment in mice
    • Hu, D., Cao, Y., He, R., Han, N., Liu, Z., Miao, L. and Yin, J. (2012) Schizandrin, an antioxidant lignan from Schisandra chinensis, ameliorates Abeta1-42-induced memory impairment in mice. Oxid. Med. Cell Longev., 2012, 721721.
    • (2012) Oxid. Med. Cell Longev. , vol.2012 , pp. 721721
    • Hu, D.1    Cao, Y.2    He, R.3    Han, N.4    Liu, Z.5    Miao, L.6    Yin, J.7
  • 84
    • 33947621993 scopus 로고    scopus 로고
    • Assessing nest building in mice
    • Deacon, R.M. (2006) Assessing nest building in mice. Nat. Protoc., 1, 1117-1119.
    • (2006) Nat. Protoc. , vol.1 , pp. 1117-1119
    • Deacon, R.M.1


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