213 Matching Annotations
  1. Nov 2016
    1. t(27) = 0.41, p<0.05;

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    2. : t(27) = 2.66, p<0.05)

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    3. t(27) = 5.31, p<0.01)

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    4. t(44) = 3.10, p<0.05;

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    5. vs. t(72) = 3.07, p<0.05)

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    6. t(27) = 3.12, p<0.05)

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    7. t(55) = 2.02, p<0.05)

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    18. t = 0.81,

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    19. t= 1.01,

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    20. t = 2.31,

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    21. References

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    22. Kendall et al., 2005)

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    23. Irino & Tada 2009)

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    24. Lee and Sherman, 2011)

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    25. Sherman and Guillery, 1998)

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    26. Groenewegen and Berendse, 1994;

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    27. Golding et al., 2002)

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    28. Popescu et al., 2007)

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    29. Pakhotin and Bracci, 2007)

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    30. Pawlak and Kerr, 2008)

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    31. Surmeier et al., 2007;

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    32. Calabresi et al., 2007;

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    33. Mahon et al., 2004;

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    34. Kreitzer and Malenka, 2007;

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    35. Kreitzer and Malenka, 2008)

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    36. Losonczy et al., 2008)

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    37. Plotkin et al., 2011)

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    38. Nanda et al., 2009)

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    39. Berndt et al., 2011)

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    40. Gunaydin et al., 2010)

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    41. Smeal et al., 2007)

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    42. Ding et al., 2010)

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    43. Kitai et al., 1976;

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    44. Ellender et al., 2011)

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    45. Groenewegen, 1988)

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    46. Herkenham, 1979;

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    47. Krettek and Price, 1977;

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    48. Boyden et al., 2005)

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    49. Smeal et al., 2008)

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    50. Ding et al., 2008;

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    51. Moss and Bolam, 2008;

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    52. Raju et al., 2006;

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    53. Fujiyama et al., 2006;

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    54. Lacey et al., 2005;

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    55. Sidibe and Smith, 1999)

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    56. Rudkin and Sadikot, 1999;

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    57. Lapper and Bolam, 1992;

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    58. Lacey et al., 2007)

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    59. Sadikot et al., 1992;

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    60. Xu et al., 1991;

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    61. Smith et al., 2009)

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    62. Castle et al., 2005;

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    63. Berendse and Groenewegen, 1990;

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    64. Macchi et al., 1984)

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    65. Doig et al., 2010)

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    66. Smith et al., 2004;

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    67. Buchwald et al., 1973;

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    68. Yin and Knowlton, 2006)

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    69. Grillner et al., 2005;

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    70. Graybiel et al., 1994;

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    71. Have you explained whether participants and personnel were blinded?

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    73. bstract

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    74. Van der Werf YD, Witter MP, Groenewegen HJ (2002) The intralaminar and midline nuclei of the thalamus. Anatomical and functional evidence for participation in processes of arousal and awareness. Brain Res Brain Res Rev 39:107-140.

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    75. Minamimoto T, Hori Y, Kimura M (2005) Complementary process to response bias in the centromedian nucleus of the thalamus. Science 308:1798-1801.

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    76. Matsumoto N, Minamimoto T, Graybiel AM, Kimura M (2001) Neurons in the thalamic CM-Pf complex supply striatal neurons with information about behaviorally significant sensory events. J Neurophysiol 85:960-976.

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    77. Kinomura S, Larsson J, Gulyas B, Roland PE (1996) Activation by attention of the human reticular formation and thalamic intralaminar nuclei. Science 271:512-515.

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    78. Irino, T; Tada, R (2009): Chemical and mineral compositions of sediments from ODP Site 127‐797. Geological Institute, University of Tokyo. http://dx.doi.org/10.1594/PANGAEA.726855

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    79. Yin HH, Knowlton BJ (2006) The role of the basal ganglia in habit formation. Nat Rev Neurosci 7:464-476.

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    80. Xu ZC, Wilson CJ, Emson PC (1991) Restoration of thalamostriatal projections in rat neostriatal grafts: an electron microscopic analysis. J Comp Neurol 303:22-34.

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    81. Surmeier DJ, Ding J, Day M, Wang Z, Shen W (2007) D1 and D2 dopamine-receptor modulation of striatal glutamatergic signaling in striatal medium spiny neurons. Trends Neurosci 30:228-235.

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    82. Smith Y, Raju D, Nanda B, Pare JF, Galvan A, Wichmann T (2009) The thalamostriatal systems: anatomical and functional organization in normal and parkinsonian states. Brain Res Bull 78:60-68.

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    83. Smith Y, Raju DV, Pare JF, Sidibe M (2004) The thalamostriatal system: a highly specific network of the basal ganglia circuitry. Trends Neurosci 27:520-527.

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    84. Smeal RM, Gaspar RC, Keefe KA, Wilcox KS (2007) A rat brain slice preparation for characterizing both thalamostriatal and corticostriatal afferents. J Neurosci Methods 159:224-235.

      This reference is cited

    85. Smeal RM, Keefe KA, Wilcox KS (2008) Differences in excitatory transmission between thalamic and cortical afferents to single spiny efferent neurons of rat dorsal striatum. Eur J Neurosci 28:2041-2052.

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    86. Sidibe M, Smith Y (1999) Thalamic inputs to striatal interneurons in monkeys: synaptic organization and co-localization of calcium binding proteins. Neuroscience 89:1189-1208.

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    87. Sherman SM, Guillery RW (1998) On the actions that one nerve cell can have on another: distinguishing "drivers" from "modulators". Proc Natl Acad Sci U S A 95:7121-7126.

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    88. Sadikot AF, Parent A, Smith Y, Bolam JP (1992) Efferent connections of the centromedian and parafascicular thalamic nuclei in the squirrel monkey: a light and electron microscopic study of the thalamostriatal projection in relation to striatal heterogeneity. J Comp Neurol 320:228-242.

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    89. Rudkin TM, Sadikot AF (1999) Thalamic input to parvalbumin-immunoreactive GABAergic interneurons: organization in normal striatum and effect of neonatal decortication. Neuroscience 88:1165-1175.

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    90. Raju DV, Shah DJ, Wright TM, Hall RA, Smith Y (2006) Differential synaptology of vGluT2-containing thalamostriatal afferents between the patch and matrix compartments in rats. J Comp Neurol 499:231-243.

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    91. Popescu AT, Saghyan AA, Pare D (2007) NMDA-dependent facilitation of corticostriatal plasticity by the amygdala. Proc Natl Acad Sci U S A 104:341-346.

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    92. Plotkin JL, Day M, Surmeier DJ (2011) Synaptically driven state transitions in distal dendrites of striatal spiny neurons. Nat Neurosci 14:881-888.

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    93. Pawlak V, Kerr JN (2008) Dopamine receptor activation is required for corticostriatal spike-timing-dependent plasticity. J Neurosci 28:2435-2446.

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    94. Pakhotin P, Bracci E (2007) Cholinergic interneurons control the excitatory input to the striatum. J Neurosci 27:391-400.

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    95. Nanda B, Galvan A, Smith Y, Wichmann T (2009) Effects of stimulation of the centromedian nucleus of the thalamus on the activity of striatal cells in awake rhesus monkeys. Eur J Neurosci 29:588-598.

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    96. Moss J, Bolam JP (2008) A dopaminergic axon lattice in the striatum and its relationship with cortical and thalamic terminals. J Neurosci 28:11221-11230.

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    97. Mahon S, Deniau JM, Charpier S (2004) Corticostriatal plasticity: life after the depression. Trends Neurosci 27:460-467.

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    98. Macchi G, Bentivoglio M, Molinari M, Minciacchi D (1984) The thalamo-caudate versus thalamo-cortical projections as studied in the cat with fluorescent retrograde double labeling. Exp Brain Res 54:225-239.

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    99. Losonczy A, Makara JK, Magee JC (2008) Compartmentalized dendritic plasticity and input feature storage in neurons. Nature 452:436-441.

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    100. Lee CC, Sherman SM (2011) Drivers and modulators in the central auditory pathways. Front Neurosci 4:79.

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    101. Lapper SR, Bolam JP (1992) Input from the frontal cortex and the parafascicular nucleus to cholinergic interneurons in the dorsal striatum of the rat. Neuroscience 51:533-545.

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    102. Lacey CJ, Boyes J, Gerlach O, Chen L, Magill PJ, Bolam JP (2005) GABA(B) receptors at glutamatergic synapses in the rat striatum. Neuroscience 136:1083-1095.

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    103. Lacey CJ, Bolam JP, Magill PJ (2007) Novel and distinct operational principles of intralaminar thalamic neurons and their striatal projections. J Neurosci 27:4374-4384.

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    104. Krettek JE, Price JL (1977) The cortical projections of the mediodorsal nucleus and adjacent thalamic nuclei in the rat. J Comp Neurol 171:157-191.

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    105. Kreitzer AC, Malenka RC (2008) Striatal plasticity and basal ganglia circuit function. Neuron 60:543-554.

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    106. Kreitzer AC, Malenka RC (2007) Endocannabinoid-mediated rescue of striatal LTD and motor deficits in Parkinson's disease models. Nature 445:643-647.

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    107. Kitai ST, Kocsis JD, Preston RJ, Sugimori M (1976) Monosynaptic inputs to caudate neurons identified by intracellular injection of horseradish peroxidase. Brain Res 109:601-606.

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    108. Herkenham M (1979) The afferent and efferent connections of the ventromedial thalamic nucleus in the rat. J Comp Neurol 183:487-517.

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    109. Gunaydin LA, Yizhar O, Berndt A, Sohal VS, Deisseroth K, Hegemann P (2010) Ultrafast optogenetic control. Nat Neurosci 13:387-392.

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    110. Groenewegen HJ, Berendse HW (1994) The specificity of the 'nonspecific' midline and intralaminar thalamic nuclei. Trends Neurosci 17:52-57.

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    111. Groenewegen HJ (1988) Organization of the afferent connections of the mediodorsal thalamic nucleus in the rat, related to the mediodorsal-prefrontal topography. Neuroscience 24:379-431.

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    112. Grillner S, Hellgren J, Menard A, Saitoh K, Wikstrom MA (2005) Mechanisms for selection of basic motor programs--roles for the striatum and pallidum. Trends Neurosci 28:364-370.

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    113. Graybiel AM, Aosaki T, Flaherty AW, Kimura M (1994) The basal ganglia and adaptive motor control. Science 265:1826-1831.

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    114. Golding NL, Staff NP, Spruston N (2002) Dendritic spikes as a mechanism for cooperative long-term potentiation. Nature 418:326-331.

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    115. Fujiyama F, Unzai T, Nakamura K, Nomura S, Kaneko T (2006) Difference in organization of corticostriatal and thalamostriatal synapses between patch and matrix compartments of rat neostriatum. Eur J Neurosci 24:2813-2824.

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    116. Ellender TJ, Huerta-Ocampo I, Deisseroth K, Capogna M, Bolam JP (2011) Differential modulation of excitatory and inhibitory striatal synaptic transmission by histamine. J Neurosci 31:15340-15351.

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    117. Doig NM, Moss J, Bolam JP (2010) Cortical and thalamic innervation of direct and indirect pathway medium-sized spiny neurons in mouse striatum. J Neurosci 30:14610-14618.

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    118. Ding JB, Guzman JN, Peterson JD, Goldberg JA, Surmeier DJ (2010) Thalamic gating of corticostriatal signaling by cholinergic interneurons. Neuron 67:294-307.

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    119. Ding J, Peterson JD, Surmeier DJ (2008) Corticostriatal and thalamostriatal synapses have distinctive properties. J Neurosci 28:6483-6492.

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    120. Castle M, Aymerich MS, Sanchez-Escobar C, Gonzalo N, Obeso JA, Lanciego JL (2005) Thalamic innervation of the direct and indirect basal ganglia pathways in the rat: Ipsi- and contralateral projections. J Comp Neurol 483:143-153.

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    121. Calabresi P, Picconi B, Tozzi A, Di Filippo M (2007) Dopamine-mediated regulation of corticostriatal synaptic plasticity. Trends Neurosci 30:211-219.

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    122. Buchwald NA, Price DD, Vernon L, Hull CD (1973) Caudate intracellular response to thalamic and cortical inputs. Exp Neurol 38:311-323.

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    123. Boyden ES, Zhang F, Bamberg E, Nagel G, Deisseroth K (2005) Millisecond-timescale, genetically targeted optical control of neural activity. Nat Neurosci 8:1263-1268.

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    124. Berndt A, Schoenenberger P, Mattis J, Tye KM, Deisseroth K, Hegemann P, Oertner TG (2011) High-efficiency channelrhodopsins for fast neuronal stimulation at low light levels. Proc Natl Acad Sci U S A.

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    125. Berendse HW, Groenewegen HJ (1990) Organization of the thalamostriatal projections in the rat, with special emphasis on the ventral striatum. J Comp Neurol 299:187-228.

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    126. Have you included a word count?

    127. Did you receive ethical approval for this study?

    128. This analysis revealed that the response to CL axon stimulation was consistently larger in amplitude than the response to Pf for both direct and indirect pathway MSNs (direct pathway: t(27) = 1.98, p<0.05).

      It's often good practice to accompany every p value with a confidence interval, or another measure of precision.

    129. Secondly, the cortical response recovers more quickly than the thalamic response after both 10 Hz and 20 Hz stimulation (ratio of response to first pulse: 10 Hz; cortical 0.87 ± 0.05, vs. thalamic 0.57 ± 0.05, 20 Hz; cortical, 0.90 ± 0.12 vs. t(72) = 3.07, p<0.05).

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    130. We found that the paired-pulse ratio (PPR) for afferents from CL are facilitating (t(55) = 2.02, p<0.05), whereas those from Pf are depressing (t(27) = 3.12, p<0.05).

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    131. We found that CL synapses are dominated by AMPA receptor-mediated currents, whereas Pf synapses are dominated by NMDA receptor-mediated currents (t(27) = 5.31, p<0.01).

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    132. Furthermore, the analysis revealed that the response to CL axon stimulation was larger in amplitude on direct pathway neurons (direct pathway: t(27) = 1.99, p<0.05; Table 1).

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    133. Cortical synapses exhibit an NMDA/AMPA ratio in between those of CL and Pf synapses and dominated by NMDA receptor-mediated currents (mean NMDA/AMPA ratio for cortical: t(27) = 2.66, p<0.05).

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    134. However, the same protocol applied to CL synapses did not lead to any change in the amplitude of evoked EPSPs (t(27) = 0.41, p<0.05; Figure 5A).

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    135. The average amplitude of response following CL axon stimulation was 66.3 ± 13.5 pA (stim strength; 450 mW; n = 16), whereas those following Pf axon stimulation were significantly smaller at 30.7 ± 4.1 pA (stim strength: 980 mW; t = 0.81, p<0.05).

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    136. The Pf response is significantly depressing following both the 10 and 20 Hz trains and the rate of recovery was the least of all three responses (t(44) = 3.10, p<0.05; Figure 3B).

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    137. Whereas all responses depress eventually, only the responses of CL inputs are facilitating for the first few spikes during both 10 and 20 Hz stimulation CL (t(72) = 1.73, p<0.05;

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    138. We found that the EPSC properties for CL and Pf synapses using this stimulation strength are remarkably similar, with some small differences in that CL EPSCs were larger in amplitude (t = 2.31, p<0.05) and Pf EPSCs slightly longer in duration (t= 1.01, p=0.02).

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    139. Figure 1A,

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    144. Acknowledgements and funding

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    145. t = 2.31,

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    147. Have you included a participant flow diagram? This is generally highly recommended for randomised trials.

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    149. Introduction

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    151. t(72) = 1.73, p<0.05;

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    152. : t(27) = 1.99, p<0.05;

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    153. : t(27) = 1.98, p<0.05)

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    154. bstract

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    155. This looks like an institutional email address

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    157. Figure 4: NMDA / AMPA receptor ratio at CL, Pf and cortical synapses on MSNs Postsynaptic excitatory currents were recorded from MSN held at +40 mV to reveal both AMPA receptor and NMDA receptor-mediated currents or just AMPA receptor-mediated currents in the presence of d-AP5. Each excitatory input has a distinct ratio of currents mediated by either receptor type. CL synapses on MSNs exhibit predominant AMPA receptor-mediated currents. Pf synapses on MSNs exhibit predominant NMDA receptor-mediated currents. Cortical inputs similarly exhibit predominant NMDA receptor-mediated expression, but to a lesser degree than Pf. The histogram shows the mean (± SEM) NMDA/AMPA receptor ratio for each synapse. Sourced from some citation

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    158. Figure 5: Long term plasticity at Pf, but not CL, synapses

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    159. Figure 3: Dynamic properties of CL, Pf and cortical synapses on MSNs

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    160. Figure 2: The majority of MSNs receive both thalamic and cortical input

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    161. 1: Localized transfection of thalamic neurons in the central lateral or parafascicular thalamic nucleus

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    162. Data Access

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    171. bstract

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    172. 32%

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    173. 30%

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    176. P. Bolam

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    177. P. Kossilo*

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    178. J. Harwood*

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    179. T. Ellender,

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    180. Abbreviated title

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    186. Discussion

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    187. bstract

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    188. p<0.05;

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    189. p<0.05)

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    190. p<0.01)

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    191. p<0.05;

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    192. p<0.05)

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    193. p<0.05;

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    194. p<0.05)

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    195. p<0.05)

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    196. p<0.05;

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    197. p<0.05)

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    198. p<0.05)

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    199. p<0.05)

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