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Chapter 15 - Cerebellar Regulation of the Thalamus

from Section 6: - Motor Control

Published online by Cambridge University Press:  12 August 2022

Michael M. Halassa
Affiliation:
Massachusetts Institute of Technology
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Summary

The motor thalamus is a complex system made of several subnuclei that together play a pivotal role in the planning and execution of movement. Some subnuclei were considered to form the “classical motor thalamus” (ventroanterior, ventrolateral, and ventromedial nuclei), and other thalamic subnuclei (centrolateral, parafascicular, and centromedian nuclei) innervate sensorimotor cortical areas. The cerebellum innervates all motor thalamus nuclei, with axons from all four different cerebellar nuclei. Decades of neuroanatomical tracer experiments have revealed that the cerebellar nuclei axons form excitatory synapses in the thalamus, thus creating somototopically organized cerebello-thalamo-cortical networks. Electrophysiological data at the synaptic, cellular, and network levels reveal how the action-potential firing patterns of cerebellar and cerebral cortical inputs are integrated in the motor thalamus to synergistically drive its output. In the current chapter, we provide a review of the anatomical and electrophysiological data and share our opinion on how the cerebellum regulates the precise timing of thalamo-cortical activity. We conclude our chapter with a discussion of the role of the cerebello-thalamo-cortical tract in the pathophysiology and treatment of movement disorders, autism spectrum disorders, and epilepsy.

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The Thalamus , pp. 284 - 306
Publisher: Cambridge University Press
Print publication year: 2022

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References

Aeby, A, Liu, Y, De Tiège, X, Denolin, V, David, P, Balériaux, D, Kavec, M, Metens, T, Van Bogaert, P (2009) Maturation of thalamic radiations between 34 and 41 weeks’ gestation: a combined voxel-based study and probabilistic tractography with diffusion tensor imaging. AJNR Am J Neuroradiol 30:17801786.Google Scholar
Ahmed, A, Taylor, NRW (1959) The analysis of drug-induced tremor in mice. Brit J Pharmacol Chemother 14:350354. Available at: https://bpspubs.onlinelibrary.wiley.com/doi/abs/10.1111/j.1476-5381.1959.tb00255.x [Accessed March 8, 2021].CrossRefGoogle ScholarPubMed
Alcauter, S, Lin, W, Smith, JK, Short, SJ, Goldman, BD, Reznick, JS, Gilmore, JH, Gao, W (2014) Development of thalamocortical connectivity during infancy and its cognitive correlations. J Neurosci 34:90679075. Available at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4078084/ [Accessed March 6, 2021].CrossRefGoogle ScholarPubMed
Altman, J, Bayer, SA (1997) Development of the Cerebellar System: In Relation to Its Evolution, Structure, and Functions. Boca Raton, FL: CRC Press. Available at: https://books.google.com/books?id=WN1qAAAAMAAJ.Google Scholar
Anderson, ME, Turner, RS (1991) Activity of neurons in cerebellar-receiving and pallidal-receiving areas of the thalamus of the behaving monkey. J Neuorphysiol 66: 879893.CrossRefGoogle ScholarPubMed
Angaut, P, Cicirata, F (1990) Dentate control pathways of cortical motor activity. Anatomical and physiological studies in rat: comparative considerations. Arch Ital Biol 128:315330.Google Scholar
Angaut, P, Cicirata, F, Serapide, F (1985) Topographic organization of the cerebellothalamic projections in the rat. An autoradiographic study. Neuroscience 15:389401.Google Scholar
Antziferova, LI, YuI, Arshavsky, Orlovsky, GN, Pavlova, GA (1980) Activity of neurons of cerebellar nuclei during fictitious scratch reflex in the cat. I. Fastigial nucleus. Brain Res 200:239248. Available at: https://www.sciencedirect.com/science/article/pii/0006899380909166 [Accessed March 4, 2021].Google Scholar
Aoki, S, Smith, JB, Li, H, Yan, X, Igarashi, M, Coulon, P, Wickens, JR, Ruigrok, TJ, Jin, X (2019) An open cortico-basal ganglia loop allows limbic control over motor output via the nigrothalamic pathway. eLife 8:e49995.Google Scholar
Armstrong, DM, Edgley, SA (1984) Discharges of nucleus interpositus neurones during locomotion in the cat. J Physiol 351:411432.Google Scholar
Asanuma, C, Ohkawa, R, Stanfield, BB, Cowan, WM (1988) Observations on the development of certain ascending inputs to the thalamus in rats. I. Postnatal development. Brain Res 469:159170.Google Scholar
Auladell, C, Pérez-Sust, P, Supèr, H, Soriano, E (2000) The early development of thalamocortical and corticothalamic projections in the mouse. Anat Embryol (Berl) 201:169179.CrossRefGoogle ScholarPubMed
Aumann, TD, Horne, MK (1996) Ramification and termination of single axons in the cerebellothalamic pathway of the rat. J Comp Neurol 376:420430.Google Scholar
Aumann, TD, Rawson, JA, Finkelstein, DI, Horne, MK (1994) Projections from the lateral and interposed cerebellar nuclei to the thalamus of the rat: a light and electron microscopic study using single and double anterograde labelling. J Comp Neurol 349:165181.Google Scholar
Aumann, TD, Redman, SJ, Horne, MK (2000) Long-term potentiation across rat cerebello-thalamic synapses in vitro. Neurosci Lett 287:151155.CrossRefGoogle ScholarPubMed
Badura, A. et al. Normal cognitive and social development require posterior cerebellar activity. eLife 7, doi:10.7554/eLife.36401 (2018), PMC6195348.Google Scholar
Bava, A, Cicirata, F, Giuffrida, R, Licciardello, S, Panto, MR (1986) Electrophysiologic properties and nature of ventrolateral thalamic nucleus neurons reactive to converging inputs of paleo- and neocerebellar origin. Exp Neur 91:112.CrossRefGoogle ScholarPubMed
Bava, A, Cicirata, F, Licciardello, S, Pantò, MR (1980) [Organization of corticothalamic projections, arising from the sensorimotor cerebral areas, on neurons belonging to the diencephalic relay-nucleus of cerebello-cerebral pathway (n. ventralis lateralis, VL): an electrophysiological study]. Boll Soc Ital Biol Sper 56:17081714.Google Scholar
Bava, A, Fadiga, E, Manzoni, T (1967) Lemniscal afferents and extracallosal mechanisms for interhemispheric transmission of somato-sensory evoked potentials. Electroencephalogr Clin Neurophysiol: Suppl 26:182187.Google Scholar
Bell, CC, Kawasaki, T (1972) Relations among climbing fiber responses of nearby Purkinje cells. J Neurophysiol 35:155169. Available at: https://journals.physiology.org/doi/abs/10.1152/jn.1972.35.2.155 [Accessed March 4, 2021].Google Scholar
Beloozerova, IN, Marlinski, V (2020) Contribution of the ventrolateral thalamus to the locomotion-related activity of motor cortex. J Neurophysiol 124:14801504.Google Scholar
Beversdorf, DQ, Manning, SE, Hillier, A, Anderson, SL, Nordgren, RE, Walters, SE, Nagaraja, HN, Cooley, WC, Gaelic, SE, Bauman, ML (2005) Timing of prenatal stressors and autism. J Autism Dev Disord 35:471478.Google Scholar
Blackshaw, S, Scholpp, S, Placzek, M, Ingraham, H, Simerly, R, Shimogori, T (2010) Molecular pathways controlling development of thalamus and hypothalamus: from neural specification to circuit formation. J Neurosci 30:1492514930. Available at: https://www.jneurosci.org/content/30/45/14925 [Accessed September 21, 2021].Google Scholar
Bodor, AL, Giber, K, Rovó, Z, Ulbert, I, Acsády, L (2008) Structural correlates of efficient GABAergic transmission in the basal ganglia-thalamus pathway. J Neurosci 28:30903102.CrossRefGoogle ScholarPubMed
Bohne, P, Schwarz, MK, Herlitze, S, Mark, MD (2019) A new projection from the deep cerebellar nuclei to the hippocampus via the ventrolateral and laterodorsal thalamus in mice. Front Neural Circuits 13:51.CrossRefGoogle Scholar
Bosch-Bouju, C, Hyland, BI, Parr-Brownlie, LC (2013) Motor thalamus integration of cortical, cerebellar and basal ganglia information: implications for normal and parkinsonian conditions. Front Comput Neurosci 7. Available at: https://www.frontiersin.org/articles/10.3389/fncom.2013.00163/full [Accessed March 4, 2021].Google Scholar
Brooks, VB, Thach, WT (1981). Cerebellar control of posture and movement. In: Handbook of Physiology, sec. I, vol. 2, part 2 (Brooks, VB, eds), pp 877946. Rockville, MD: American Physiological Society.Google Scholar
Brown, AM, White, JJ, van der Heijden, ME, Zhou, J, Lin, T, Sillitoe, RV (2020) Purkinje cell misfiring generates high-amplitude action tremors that are corrected by cerebellar deep brain stimulation. eLife 9:e51928.Google Scholar
Buee, J, Deniau, JM, Chevalier, G (1986) Nigral modulation of cerebello-thalamo-cortical transmission in the ventral medial thalamic nucleus. Exp Brain Res 65:241244.Google Scholar
Canto, CB, Onuki, Y, Bruinsma, B, Werf, YD, van der, Zeeuw, CID (2017) The sleeping cerebellum. Trends Neurosci 40:309323. Available at: https://www.cell.com/trends/neurosciences/abstract/S0166-2236(17)30030-9 [Accessed March 4, 2021].Google Scholar
Canto, CB, Witter, L, De Zeeuw, CI (2016) Whole-cell properties of cerebellar nuclei neurons in vivo. PloS One 11:e0165887.CrossRefGoogle ScholarPubMed
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 483:143153. Available at: https://onlinelibrary.wiley.com/doi/abs/10.1002/cne.20421 [Accessed March 3, 2021].Google Scholar
Chen, CH, Fremont, R, Arteaga-Bracho, EE, Khodakhah, K (2014) Short latency cerebellar modulation of the basal ganglia. Nat Neurosci 17:17671775.Google Scholar
Chevalier, G, Deniau, JM (1982) Inhibitory nigral influence on cerebellar evoked responses in the rat ventromedial thalamic nucleus. Exp Brain Res 48:369376.Google Scholar
Chkhenkeli, SA, Sramka, M, Lortkipanidze, GS, Rakviashvili, TN, Bregvadze, ES, Magalashvili, GE, Gagoshidze, TS, Chkhenkeli, IS (2004) Electrophysiological effects and clinical results of direct brain stimulation for intractable epilepsy. Clin Neurol Neurosurg 106:318329.CrossRefGoogle ScholarPubMed
Cicirata, F, Angaut, P, Cioni, M, Serapide, MF, Papale, A (1986) Functional organization of thalamic projections to the motor cortex. An anatomical and electrophysiological study in the rat. Neuroscience 19:8199.Google Scholar
Condé, H, Angaut, P (1970) An electrophysiological study of the cerebellar projections to the nucleus ventralis lateralis thalami in the cat. 2. Nucleus lateralis. Brain Res 20:107119.CrossRefGoogle Scholar
Courchesne, E, Redcay, E, Morgan, JT, Kennedy, DP (2005) Autism at the beginning: microstructural and growth abnormalities underlying the cognitive and behavioral phenotype of autism. Dev Psychopathol 17:577597.Google Scholar
Crooks, R, Mitchell, T, Thom, M (2000) Patterns of cerebellar atrophy in patients with chronic epilepsy: a quantitative neuropathological study. Epilepsy Res 41:6373.CrossRefGoogle ScholarPubMed
Cury, RG, Fraix, V, Castrioto, A, Fernández, MAP, Krack, P, Chabardes, S, Seigneuret, E, Alho, EJL, Benabid A-L, Moro E (2017) Thalamic deep brain stimulation for tremor in Parkinson disease, essential tremor, and dystonia. Neurology 89:14161423. Available at: https://n.neurology.org/content/89/13/1416 [Accessed March 5, 2021].Google Scholar
Dacre, J, Colligan, M, Clarke, T, Ammer, JJ, Schiemann, J, Chamosa-Pino, V, Claudi, F, Harston, JA, Eleftheriou, C, Pakan, JMP, Huang, C-C, Hantman, AW, Rochefort, NL, Duguid, I (2021) A cerebellar-thalamocortical pathway drives behavioral context-dependent movement initiation. Neuron 109:2326–2338.e8. Available at: https://linkinghub.elsevier.com/retrieve/pii/S0896627321003561 [Accessed September 22, 2021].Google Scholar
De Zeeuw, CI, Hoebeek, FE, Bosman, LW, Schonewille, M, Witter, L, Koekkoek, SK (2011) Spatiotemporal firing patterns in the cerebellum. Nat Rev Neurosci 12:327344.Google Scholar
Del Rio-Bermudez, C, Plumeau, AM, Sattler, NJ, Sokoloff, G, Blumberg, MS (2016) Spontaneous activity and functional connectivity in the developing cerebellorubral system. J Neurophysiol 116:13161327.Google Scholar
Deniau, JM, Kita, H, Kitai, ST (1992) Patterns of termination of cerebellar and basal ganglia efferents in the rat thalamus. Strictly segregated and partly overlapping projections. Neurosci Lett 144:202206.Google Scholar
Deschênes, M, Bourassa, J, Parent, A (1996) Striatal and cortical projections of single neurons from the central lateral thalamic nucleus in the rat. Neuroscience 72:679687.Google Scholar
Diedrichsen, J, Maderwald, S, Küper, M, Thürling, M, Rabe, K, Gizewski, ER, Ladd, ME, Timmann, D (2011) Imaging the deep cerebellar nuclei: a probabilistic atlas and normalization procedure. NeuroImage 54:17861794. Available at: http://www.sciencedirect.com/science/article/pii/S1053811910013273 [Accessed October 30, 2020].Google Scholar
Dimitrova, A, Zeljko, D, Schwarze, F, Maschke, M, Gerwig, M, Frings, M, Beck, A, Aurich, V, Forsting, M, Timmann, D (2006) Probabilistic 3D MRI atlas of the human cerebellar dentate/interposed nuclei. NeuroImage 30:1225.Google Scholar
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 30:1461014618. Available at: https://www.jneurosci.org/content/30/44/14610 [Accessed March 3, 2021].CrossRefGoogle ScholarPubMed
Dum, RP, Strick, PL (2003) An unfolded map of the cerebellar dentate nucleus and its projections to the cerebral cortex. J Neurophysiol 89:634639. Available at: https://journals.physiology.org/doi/full/10.1152/jn.00626.2002 [Accessed October 31, 2020].Google Scholar
Dumas, DB, Gornati, SV, Adolfs, Y, Shimogori, T, Pasterkamp, RJ, Hoebeek, FE (2019) Anatomical development of the cerebellothalamic tract in embryonic mice. bioRxiv: 731968. Available at: https://www.biorxiv.org/content/10.1101/731968v1 [Accessed October 5, 2020].Google Scholar
Eelkman Rooda, OHJ, Kros, L, Faneyte, SJ, Holland, PJ, Gornati, SV, Poelman, HJ, Jansen, NA, Tolner, EA, van den Maagdenberg, AMJM, De Zeeuw, CI, Hoebeek, FE (2021) Single-pulse stimulation of cerebellar nuclei stops epileptic thalamic activity. Brain Stimul 14:861872. Available at: https://linkinghub.elsevier.com/retrieve/pii/S1935861X21001005 [Accessed July 14, 2021].Google Scholar
Elsen, GE, Juric-Sekhar, G, Daza, RAM, Hevner, RF (2013) Development of cerebellar nuclei. In: Handbook of the Cerebellum and Cerebellar Disorders (Manto, M, Schmahmann, JD, Rossi, F, Gruol, DL, Koibuchi, N, eds), pp 179205. Dordrecht: Springer Netherlands. Available at: https://doi.org/10.1007/978–94-007–1333-8_10 [Accessed October 29, 2020].Google Scholar
Elvsåshagen, T, Shadrin, A, Frei, O, van der Meer, D, Bahrami, S, Kumar, VJ, Smeland, O, Westlye, LT, Andreassen, OA, Kaufmann, T (2021) The genetic architecture of the human thalamus and its overlap with ten common brain disorders. Nat Commun 12:2909. Available at: https://www.nature.com/articles/s41467-021–23175-z [Accessed September 21, 2021].Google Scholar
Ernst, TM, Thürling, M, Müller, S, Kahl, F, Maderwald, S, Schlamann, M, Boele, H-J, Koekkoek, SKE, Diedrichsen, J, De Zeeuw, CI, Ladd, ME, Timmann, D (2017) Modulation of 7 T fMRI signal in the cerebellar cortex and nuclei during acquisition, extinction, and reacquisition of conditioned eyeblink responses. Hum Brain Mapp 38:39573974.Google Scholar
Evarts, EV, Thach, WT (1969) Motor mechanisms of the CNS: cerebrocerebellar interrelations. Annu Rev Physiol 31:451498.Google Scholar
Filion, M, Lamarre, Y, Cordeau, JP (1971) Neuronal discharges of the ventrolateral nucleus of the thalamus during sleep and wakefulness in the cat. II. Evoked activity. Exp Brain Res 12:499508.Google Scholar
Fink, AJ, Englund, C, Daza, RAM, Pham, D, Lau, C, Nivison, M, Kowalczyk, T, Hevner, RF (2006) Development of the deep cerebellar nuclei: transcription factors and cell migration from the rhombic lip. J Neurosci 26:30663076. Available at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6673970/ [Accessed October 30, 2020].Google Scholar
França, C, Ciampide Andrade, D, Jacobsen Teixeira, M, Galhardoni, R, Silva, V, Reis Barbosa, E, Gisbert Cury, R. (2018) Effects of cerebellar neuromodulation in movement disorders: a systematic review. Brain Stimul 11: 249260.Google Scholar
Fujita, H., Kodama, T. & du Lac, S. Modular output circuits of the fastigial nucleus for diverse motor and nonmotor functions of the cerebellar vermis. eLife 9, doi:10.7554/eLife.58613 (2020), PMC7438114.Google Scholar
Fulton, J (1929) Case of cerebellar tumor with seizures of head retraction described by Wurffbain in 1691. J Nerv Ment Dis 70:577583.Google Scholar
Gaidica, M, Hurst, A, Cyr, C, Leventhal, DK (2018) Distinct populations of motor thalamic neurons encode action initiation, action selection, and movement vigor. J Neurosci 38:65636573.Google Scholar
Gallay, MN, Jeanmonod, D, Liu, J, Morel, A (2008) Human pallidothalamic and cerebellothalamic tracts: anatomical basis for functional stereotactic neurosurgery. Brain Struct Funct 212:443463.CrossRefGoogle ScholarPubMed
Galvez, R, Greenough, WT (2005) Sequence of abnormal dendritic spine development in primary somatosensory cortex of a mouse model of the fragile X mental retardation syndrome. Am J Med Genet 135A:155160. Available at: https://onlinelibrary.wiley.com/doi/abs/10.1002/ajmg.a.30709 [Accessed July 31, 2019].Google Scholar
Gao, Z, Davis, C, Thomas, AM, Economo, MN, Abrego, AM, Svoboda, K, De Zeeuw, CI, Li, N (2018) A cortico-cerebellar loop for motor planning. Nature 563:113116.Google Scholar
Gardette, R, Debono, M, Dupont, JL, Crepel, F (1985) Electrophysiological studies on the postnatal development of intracerebellar nuclei neurons in rat cerebellar slices maintained in vitro. II. Membrane conductances. Brain Res 352:97106.Google Scholar
Garin, N, Escher, G (2001) The development of inhibitory synaptic specializations in the mouse deep cerebellar nuclei. Neuroscience 105:431441.Google Scholar
Gauck, V, Jaeger, D (2000) The control of rate and timing of spikes in the deep cerebellar nuclei by inhibition. J Neurosci 20:30063016.Google Scholar
Glenn, LL, Steriade, M (1982) Discharge rate and excitability of cortically projecting intralaminar thalamic neurons during waking and sleep states. J Neurosci 2:13871404. Available at: https://www.jneurosci.org/content/2/10/1387 [Accessed March 4, 2021].Google Scholar
Goffinet, AM (1983) The embryonic development of the cerebellum in normal and reeler mutant mice. Anat Embryol 168:7386. Available at: https://doi.org/10.1007/BF00305400 [Accessed October 30, 2020].Google Scholar
Gornati, SV, Schäfer, CB, Eelkman Rooda, OHJ, Nigg, AL, De Zeeuw, CI, Hoebeek, FE (2018) Differentiating cerebellar impact on thalamic nuclei. Cell Rep 23:26902704.Google Scholar
Graber, KD, Fisher, RS (2012) Deep brain stimulation for epilepsy: animal models. In: Jasper’s Basic Mechanisms of the Epilepsies, 4th ed. (Noebels, JL, Avoli, M, Rogawski, MA, Olsen, RW, Delgado-Escueta, AV, eds). Bethesda, MD: National Center for Biotechnology Information. Available at: http://www.ncbi.nlm.nih.gov/books/NBK98160/ [Accessed March 1, 2021].Google Scholar
Green, MJ, Wingate, RJ (2014) Developmental origins of diversity in cerebellar output nuclei. Neural Dev 9:1. Available at: https://doi.org/10.1186/1749-8104-9-1 [Accessed October 27, 2020].Google Scholar
Hara, S, Kaneyama, T, Inamata, Y, Onodera, R, Shirasaki, R (2016) Interstitial branch formation within the red nucleus by deep cerebellar nuclei-derived commissural axons during target recognition. J Comp Neurol 524:9991014.Google Scholar
Hashimoto, T, Tayama, M, Murakawa, K, Yoshimoto, T, Miyazaki, M, Harada, M, Kuroda, Y (1995) Development of the brainstem and cerebellum in autistic patients. J Autism Dev Disord 25:118.Google Scholar
Hassler, E (1950) [Penicillin therapy of scarlet fever]. Kinderarztl Prax 18:132136.Google Scholar
Hayaran, A, Wadhwa, S, Bijlani, V (1992) Cytoarchitectural development of the human dentate nucleus: a Golgi study. Dev Neurosci 14:181194.Google Scholar
Heck, DH (2015) The Neural Codes of the Cerebellum, 1st ed. Academic Press.Google Scholar
Hendry, SHC, Jones, EG, Graham, J (1979) Thalamic relay nuclei for cerebellar and certain related fiber systems in the cat. J Compe Neurol 185:679713. Available at: https://onlinelibrary.wiley.com/doi/abs/10.1002/cne.901850406 [Accessed March 3, 2021].Google Scholar
Hensch, TK (2004) Critical period regulation. Annu Rev Neurosci 27:549579.Google Scholar
Hintzen, A, Pelzer, EA, Tittgemeyer, M (2018) Thalamic interactions of cerebellum and basal ganglia. Brain Struct Funct 223:569587.Google Scholar
Hoebeek, FE, Stahl, JS, van Alphen, AM, Schonewille, M, Luo, C, Rutteman, M, van den Maagdenberg, AM, Molenaar, PC, Goossens, HH, Frens, MA, De Zeeuw, CI (2005) Increased noise level of Purkinje cell activities minimizes impact of their modulation during sensorimotor control. Neuron 45:953965.Google Scholar
Hoerder-Suabedissen, A, Molnár, Z (2015) Development, evolution and pathology of neocortical subplate neurons. Nat Rev Neurosci 16:133146.Google Scholar
Hoover, JE, Strick, PL (1999) The organization of cerebellar and basal ganglia outputs to primary motor cortex as revealed by retrograde transneuronal transport of herpes simplex virus type 1. J Neurosci 19:14461463. Available at: http://www.jneurosci.org/lookup/doi/10.1523/JNEUROSCI.19–04-01446.1999 [Accessed October 28, 2020].Google Scholar
Hortensius, LM, Dijkshoorn, ABC, Ecury-Goossen, GM, Steggerda, SJ, Hoebeek, FE, Benders, MJNL, Dudink, J (2018) Neurodevelopmental consequences of preterm isolated cerebellar hemorrhage: a systematic review. Pediatrics 142:e20180609.Google Scholar
Houck, BD, Person, AL (2015) Cerebellar premotor output neurons collateralize to innervate the cerebellar cortex. J Comp Neurol 523:22542271.Google Scholar
Hutsler, JJ, Zhang, H (2010) Increased dendritic spine densities on cortical projection neurons in autism spectrum disorders. Brain Res 1309:8394. Available at: http://linkinghub.elsevier.com/retrieve/pii/S0006899309023117 [Accessed December 7, 2018].Google Scholar
Ilyas, A, Pizarro, D, Romeo, AK, Riley, KO, Pati, S (2019) The centromedian nucleus: anatomy, physiology, and clinical implications. J Clin Neurosci 63:17. Available at: https://www.jocn-journal.com/article/S0967-5868(19)30016-5/abstract [Accessed February 15, 2021].Google Scholar
Ito, M (2002) Historical review of the significance of the cerebellum and the role of Purkinje cells in motor learning. Ann NY Acad Sci 978:273288.Google Scholar
Jackson, J. (1871) Case of tumor of the middle lobe of the cerebellum: rigidity in cerebellar attitude—occasional tetanus-like seizures. Brit Med J ii:528.Google Scholar
Jackson, J. (1906) Case of tumour of the middle lobe of the cerebellum. Brain, Volume 29, Issue 4, March 1907, Pages 425–440, https://doi.org/10.1093/brain/29.4.425.Google Scholar
Jahnsen, H, Llinás, R (1984) Voltage-dependent burst-to-tonic switching of thalamic cell activity: an in vitro study. Arch Ital Biol 122:7382.Google Scholar
Jörntell, H, Ekerot, CF (1999) Topographical organization of projections to cat motor cortex from nucleus interpositus anterior and forelimb skin. J Physiol 514 (Pt 2):551566.Google Scholar
Kelly, E, et al. (2020) Regulation of autism-relevant behaviors by cerebellar-prefrontal cortical circuits. Nat Neurosci 23:11021110.Google Scholar
Kelly, RM, Strick, PL (2003) Cerebellar loops with motor cortex and prefrontal cortex of a nonhuman primate. J Neurosci 23:84328444.Google Scholar
Kostović, I, Goldman-Rakic, PS (1983) Transient cholinesterase staining in the mediodorsal nucleus of the thalamus and its connections in the developing human and monkey brain. J Comp Neurol 219:431447.Google Scholar
Kostović, I, Judas, M (2002) Correlation between the sequential ingrowth of afferents and transient patterns of cortical lamination in preterm infants. Anat Rec 267:16.Google Scholar
Kostović, I, Kostović-Srzentić, M, Benjak, V, Jovanov-Milošević, N, Radoš, M (2014) Developmental dynamics of radial vulnerability in the cerebral compartments in preterm infants and neonates. Front Neurol 5: 139. Available at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4114264/ [Accessed March 6, 2021].Google Scholar
Kostović, I, Rakic, P (1984) Development of prestriate visual projections in the monkey and human fetal cerebrum revealed by transient cholinesterase staining. J Neurosci 4:2542. Available at: https://www.jneurosci.org/content/4/1/25 [Accessed March 6, 2021].CrossRefGoogle ScholarPubMed
Krook-Magnuson, E, Szabo, GG, Armstrong, C, Oijala, M, Soltesz, I (2014) Cerebellar directed optogenetic intervention inhibits spontaneous hippocampal seizures in a mouse model of temporal lobe epilepsy.eNeuro 1. Available at: https://www.eneuro.org/content/1/1/ENEURO.0005-14.2014 [Accessed February 26, 2021].Google Scholar
Kros, L, Eelkman Rooda, OHJ, De Zeeuw, CI, Hoebeek, FE (2015) Controlling cerebellar output to treat refractory epilepsy. Trends Neurosci 38:787799. Available at: http://www.sciencedirect.com/science/article/pii/S016622361500226X [Accessed January 28, 2021].Google Scholar
Krsnik, Ž, Majić, V, Vasung, L, Huang, H, Kostović, I (2017) Growth of thalamocortical fibers to the somatosensory cortex in the human fetal brain. Front Neurosci 11. Available at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5406414/ [Accessed March 6, 2021].Google Scholar
Kuramoto, E, Furuta, T, Nakamura, KC, Unzai, T, Hioki, H, Kaneko, T (2009) Two types of thalamocortical projections from the motor thalamic nuclei of the rat: a single neuron-tracing study using viral vectors. Cereb Cortex 19:20652077.CrossRefGoogle Scholar
Kuramoto, E, Ohno, S, Furuta, T, Unzai, T, Tanaka, YR, Hioki, H, Kaneko, T (2015) Ventral medial nucleus neurons send thalamocortical afferents more widely and more preferentially to layer 1 than neurons of the ventral anterior-ventral lateral nuclear complex in the rat. Cereb Cortex 25:221235.Google Scholar
Lang, EJ, Sugihara, I, Llinas, R (2006) Olivocerebellar modulation of motor cortex ability to generate vibrissal movements in rat. J Physiol 571:101120.Google Scholar
Larsell, O (1935) The development and morphology of the cerebellum in the opossum. Part I. Early development. J Comp Neurol 63:6594.Google Scholar
Leto, K, et al. (2016) Consensus paper: cerebellar development. Cerebellum 15:789828. Available at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4846577/ [Accessed October 30, 2020].Google Scholar
Limperopoulos, C, Bassan, H, Gauvreau, K, Robertson, RL, Sullivan, NR, Benson, CB, Avery, L, Stewart, J, Soul, JS, Ringer, SA, Volpe, JJ, duPlessis, AJ (2007) Does cerebellar injury in premature infants contribute to the high prevalence of long-term cognitive, learning, and behavioral disability in survivors? Pediatrics 120:584593.Google Scholar
Limperopoulos, C, Chilingaryan, G, Sullivan, N, Guizard, N, Robertson, RL, du Plessis, AJ (2014) Injury to the premature cerebellum: outcome is related to remote cortical development. Cereb Cortex 24:728736.Google Scholar
Llinás, R, Jahnsen, H (1982) Electrophysiology of mammalian thalamic neurones in vitro. Nature 297:406408.Google Scholar
Llinás, R, Sasaki, K (1989) The functional organization of the olivo-cerebellar system as examined by multiple Purkinje cell recordings. Eur J Neurosci 1:587602.Google Scholar
Llinás, R, Volkind, RA (1973) The olivo-cerebellar system: functional properties as revealed by harmaline-induced tremor. Exp Brain Res 18:6987. Available at: https://doi.org/10.1007/BF00236557 [Accessed March 8, 2021].Google Scholar
Lopez-Bendito, G, Molnar, Z (2003) Thalamocortical development: how are we going to get there? Nat Rev Neurosci 4:276289.Google Scholar
Machold, R, Fishell, G (2005) Math1 is expressed in temporally discrete pools of cerebellar rhombic-lip neural progenitors. Neuron 48:1724.Google Scholar
MacLeod, NK, James, TA (1984) Regulation of cerebello-cortical transmission in the rat ventromedial thalamic nucleus. Exp Brain Res 55:535552.Google Scholar
Maejima, T, Wollenweber, P, Teusner, LUC, Noebels, JL, Herlitze, S, Mark, MD (2013) Postnatal loss of P/Q-type channels confined to rhombic-lip-derived neurons alters synaptic transmission at the parallel fiber to Purkinje cell synapse and replicates genomic Cacna1a mutation phenotype of ataxia and seizures in mice. J Neurosci 33:51625174.Google Scholar
Marin-Padilla, M (1970) Prenatal and early postnatal ontogenesis of the human motor cortex: a golgi study. II. The basket-pyramidal system. Brain Res 23:185191.Google Scholar
Mark, MD, Maejima, T, Kuckelsberg, D, Yoo, JW, Hyde, RA, Shah, V, Gutierrez, D, Moreno, RL, Kruse, W, Noebels, JL, Herlitze, S (2011a) Delayed postnatal loss of P/Q-type calcium channels recapitulates the absence epilepsy, dyskinesia, and ataxia phenotypes of genomic Cacna1a mutations. J Neurosci 31:43114326.Google Scholar
Marlinski, V, Nilaweera, WU, Zelenin, PV, Sirota, MG, Beloozerova, IN (2011) Signals from the ventrolateral thalamus to the motor cortex during locomotion. J Neurophysiol 107:455472. Available at: https://journals.physiology.org/doi/full/10.1152/jn.01113.2010 [Accessed March 4, 2021].Google Scholar
Marsden, JF, Werhahn, KJ, Ashby, P, Rothwell, J, Noachtar, S, Brown, P (2000) Organization of cortical activities related to movement in humans. J Neurosci 20:23072314.Google Scholar
Martin, GF, Cabana, T, Hazlett, JC, Ho, R, Waltzer, R (1987) Development of brainstem and cerebellar projections to the diencephalon with notes on thalamocortical projections: studies in the North American opossum. J Comp Neurol 260:186200.Google Scholar
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 85:960976. Available at: https://journals.physiology.org/doi/full/10.1152/jn.2001.85.2.960 [Accessed February 15, 2021].Google Scholar
McCrory, PR, Bladin, PF, Berkovic, SF (1999) The cerebellar seizures of Hughlings Jackson. Neurology 52:1888–1888. Available at: https://n.neurology.org/content/52/9/1888 [Accessed February 27, 2021].Google Scholar
Mihajlovic, P, Zecevic, N (1986) Development of the human dentate nucleus. Hum Neurobiol 5:189197.Google Scholar
Minamimoto, T, Kimura, M (2002) Participation of the thalamic CM-Pf complex in attentional orienting. J Neurophysiol 87:30903101. Available at: https://journals.physiology.org/doi/full/10.1152/jn.2002.87.6.3090 [Accessed February 15, 2021].Google Scholar
Miterko, LN et al. (2019) Consensus paper: experimental neurostimulation of the cerebellum. Cerebellum 18:10641097. Available at: https://doi.org/10.1007/s12311-019-01041-5 [Accessed March 8, 2021].Google Scholar
Molnár, Z, Knott, GW, Blakemore, C, Saunders, NR (1998) Development of thalamocortical projections in the South American gray short-tailed opossum (Monodelphis domestica). J Comp Neurol 398:491514.Google Scholar
Moruzzi, G, Montanari, L, Rossi, CA, Rabbi, A, Jacoli, G (1950) [Active ultrafilterable fraction of corticotropic hormone with low nitrogen content]. Bollettino della Societa italiana di biologia sperimentale 26:15671569.Google Scholar
Muthuraman, M, Koirala, N, Ciolac, D, Pintea, B, Glaser, M, Groppa, S, Tamás, G, Groppa, S (2018) Deep brain stimulation and L-DOPA therapy: concepts of action and clinical applications in Parkinson’s disease. Front Neurol 9:711.Google Scholar
Najac, M, Raman, IM (2015) Integration of Purkinje cell inhibition by cerebellar nucleo-olivary neurons. J Neurosci 35:544549.Google Scholar
Nakamura, KC, Sharott, A, Magill, PJ (2014) Temporal coupling with cortex distinguishes spontaneous neuronal activities in identified basal ganglia-recipient and cerebellar-recipient zones of the motor thalamus. Cereb Cortex 24:8197.Google Scholar
Nashef, A, Mitelman, R, Harel, R, Joshua, M, Prut, Y (2021) Area-specific thalamocortical synchronization underlies the transition from motor planning to execution. Proc Natl Acad Sci USA 118. Available at: https://www.pnas.org/content/118/6/e2012658118 [Accessed March 4, 2021].Google Scholar
Ozden, I., Dombeck, D. A., Hoogland, T. M., Tank, D. W. & Wang, S. S. Widespread state-dependent shifts in cerebellar activity in locomoting mice. PLoS One 7, e42650, doi:10.1371/journal.pone.0042650 (2012), PMC3411825.Google Scholar
Palmen, SJMC, van Engeland, H, Hof, PR, Schmitz, C (2004) Neuropathological findings in autism. Brain 127:25722583.CrossRefGoogle ScholarPubMed
Parent, M, Parent, A (2005) Single-axon tracing and three-dimensional reconstruction of centre median-parafascicular thalamic neurons in primates. J Comp Neurol 481:127144.Google Scholar
Passamonti, L, Novellino, F, Cerasa, A, Chiriaco, C, Rocca, F, Matina, MS, Fera, F, Quattrone, A (2011) Altered cortical-cerebellar circuits during verbal working memory in essential tremor. Brain: J Neurol 134:22742286.Google Scholar
Paxinos, G, Watson, C (1986) The Rat Brain in Stereotaxic Coordinates. New York: Academic Press.Google Scholar
Pedrosa, DJ, Auth, M, Pauls, KAM, Runge, M, Maarouf, M, Fink, GR, Timmermann, L (2014) Verbal fluency in essential tremor patients: the effects of deep brain stimulation. Brain Stimul 7:359364. Available at: https://www.brainstimjrnl.com/article/S1935-861X(14)00110-7/abstract [Accessed March 5, 2021].Google Scholar
Person, AL, Raman, IM (2011) Purkinje neuron synchrony elicits time-locked spiking in the cerebellar nuclei. Nature 481:502505.Google Scholar
Phillips, JW, Schulmann, A, Hara, E, Winnubst, J, Liu, C, Valakh, V, Wang, L, Shields, BC, Korff, W, Chandrashekar, J, Lemire, AL, Mensh, B, Dudman, JT, Nelson, SB, Hantman, AW (2019) A repeated molecular architecture across thalamic pathways. Nat Neurosci 22:1925–1935.Google Scholar
Pierce, ET (1975) Histogenesis of the deep cerebellar nuclei in the mouse: an autoradiographic study. Brain Res 95:503518. Available at: http://www.sciencedirect.com/science/article/pii/0006899375901249 [Accessed October 30, 2020].Google Scholar
Pieterman, K, Batalle, D, Dudink, J, Tournier, J-D, Hughes, EJ, Barnett, M, Benders, MJ, Edwards, AD, Hoebeek, FE, Counsell, SJ (2017) Cerebello-cerebral connectivity in the developing brain. Brain Struct Funct 222:16251634.Google Scholar
Pisano, TJ, Dhanerawala, ZM, Kislin, M, Bakshinskaya, D, Engel, EA, Hansen, EJ, Hoag, AT, Lee, J, Oude, NL de, Venkataraju, KU, Verpeut, JL, Hoebeek, FE, Richardson, BD, Boele, H-J, Wang, SS-H (2021) Homologous organization of cerebellar pathways to sensory, motor, and associative forebrain. Cell Rep 36. Available at: https://www.cell.com/cell-reports/abstract/S2211-1247(21)01170-0 [Accessed September 21, 2021].Google Scholar
Proville, RD, Spolidoro, M, Guyon, N, Dugué, GP, Selimi, F, Isope, P, Popa, D, Léna, C (2014) Cerebellum involvement in cortical sensorimotor circuits for the control of voluntary movements. Nat Neurosci 17:12331239.Google Scholar
Puertas-Martín, V, Villarejo-Galende, A, Fernández-Guinea, S, Romero, JP, Louis, ED, Benito-León, J (2016) A comparison study of cognitive and neuropsychiatric features of essential tremor and Parkinson’s disease. Tremor Other Hyperkinet Mov 6:431. Available at: http://tremorjournal.org/article/10.5334/tohm.288/ [Accessed November 1, 2020].Google Scholar
Purpura, DP, Scarff, T, McMurtry, JG. (1965) Intracellular study of internuclear inhibition in ventrolateral thalamic neurons. J Neuorphysiol 28: 487496.Google Scholar
Reh, RK, Dias, BG, Nelson, CA, Kaufer, D, Werker, JF, Kolb, B, Levine, JD, Hensch, TK (2020) Critical period regulation across multiple timescales. Proc Natl Acad Sci USA 117:23242–23251.Google Scholar
Rispal-Padel, L, Harnois, C, Troiani, D (1987) Converging cerebellofugal inputs to the thalamus. I. Mapping of monosynaptic field potentials in the ventrolateral nucleus of the thalamus. Exp Brain Res 68:4758.Google Scholar
Rispal-Padel, L, Latreille, J (1974) The organization of projections from the cerebellar nuclei to the contralateral motor cortex in the cat. Exp Brain Res 19:3660.Google Scholar
Rispal-Padel, L, Massion, J, Grangetto, A (1973) Relations between the ventrolateral thalamic nucleus and motor cortex and their possible role in the central organization of motor control. Brain Res 60:120.Google Scholar
Rowland, NC, Jaeger, D (2008) Responses to tactile stimulation in deep cerebellar nucleus neurons result from recurrent activation in multiple pathways. J Neurophysiol 99:704717.CrossRefGoogle ScholarPubMed
Ruigrok, TJH (2011) Ins and outs of cerebellar modules. Cerebellum 10:464474.CrossRefGoogle ScholarPubMed
Sakai, ST (2013) Cerebellar thalamic and thalamocortical projections. In: Handbook of the Cerebellum and Cerebellar Disorders (Manto, M, Schmahmann, JD, Rossi, F, Gruol, DL, Koibuchi, N, eds), pp 529547. Dordrecht: Springer Netherlands. Available at: https://doi.org/10.1007/978-94-007-1333-8_24 [Accessed September 20, 2021].Google Scholar
Sakata, H, Ishijima, T, Toyoda, Y (1966) Single unit studies on ventrolateral nucleus of the thalamus in cat: its relation to the cerebellum, motor cortex and basal ganglia. Jpn J Physiol 16:4260.Google Scholar
Sakayori, N, Kato, S, Sugawara, M, Setogawa, S, Fukushima, H, Ishikawa, R, Kida, S, Kobayashi, K (2019) Motor skills mediated through cerebellothalamic tracts projecting to the central lateral nucleus. Mol Brain 12:13. Available at: https://molecularbrain.biomedcentral.com/articles/10.1186/s13041-019-0431-x [Accessed October 5, 2020].Google Scholar
Sarnaik, R, Raman, IM (2018) Control of voluntary and optogenetically perturbed locomotion by spike rate and timing of neurons of the mouse cerebellar nuclei. eLife 7:e29546.Google Scholar
Sasaki, K, Kawaguchi, S, Matsuda, Y, Mizuno, N (1972a) Electrophysiological studies on cerebello-cerebral projections in the cat. Exp Brain Res 16:7588.Google Scholar
Sasaki, K, Matsuda, Y, Kawaguchi, S, Mizuno, N (1972b) On the cerebello-thalamo-cerebral pathway for the parietal cortex. Exp Brain Res 16:89103.Google Scholar
Sawyer, SF, Young, SJ, Groves, PM (1989) Quantitative Golgi study of anatomically identified subdivisions of motor thalamus in the rat. J Comp Neurol 286:127.CrossRefGoogle ScholarPubMed
Sawyer, SF, Young, SJ, Groves, PM, Tepper, JM (1994) Cerebellar-responsive neurons in the thalamic ventroanterior-ventrolateral complex of rats: in vivo electrophysiology. Neuroscience 63:711724.Google Scholar
Schäfer, CB, Gao, Z, Zeeuw, CID, Hoebeek, FE (2021) Temporal dynamics of the cerebello-cortical convergence in ventro-lateral motor thalamus. J Physiol 599:20552073. Available at: https://physoc.onlinelibrary.wiley.com/doi/abs/10.1113/JP280455 [Accessed March 4, 2021].Google Scholar
Schäfer, CB, Hoebeek, FE (2018) Convergence of primary sensory cortex and cerebellar nuclei pathways in the whisker system. Neuroscience 368:229239.Google Scholar
Serra, C, Guida, L, Staartjes, VE, Krayenbühl, N, Türe, U (2019) Historical controversies about the thalamus: from etymology to function. Neurosurg Focus 47:E13.Google Scholar
Shinoda, Y, Kano, M, Futami, T (1985) Synaptic organization of the cerebello-thalamo-cerebral pathway in the cat. I. Projection of individual cerebellar nuclei to single pyramidal tract neurons in areas 4 and 6. Neurosci Res 2:133156.Google Scholar
Shinoda, Y, Yamazaki, M, Futami, T (1982) Convergent inputs from the dentate and the interpositus nuclei to pyramidal tract neurons in the motor cortex. Neurosci Lett 34:111115.Google Scholar
Snider, RS, Magoun, HW (1949) Facilitation produced by cerebellar stimulation. J Neurophysiol 12:335345.Google Scholar
Šramka, M, Chkhenkeli, SA (1990) Clinical experience in intraoperational determination of brain inhibitory structures and application of implanted neurostimulators in epilepsy. Stereotact Funct Neurosurg 54:5659. Available at: https://www.karger.com/Article/FullText/100190 [Accessed March 1, 2021].Google Scholar
Steriade, M, Dossi, RC, Nunez, A (1991) Network modulation of a slow intrinsic oscillation of cat thalamocortical neurons implicated in sleep delta waves: cortically induced synchronization and brainstem cholinergic suppression. J Neurosci 11:32003217. Available at: https://www.jneurosci.org/content/11/10/3200 [Accessed March 4, 2021].Google Scholar
Steriade, M, McCormick, DA, Sejnowski, TJ (1993) Thalamocortical oscillations in the sleeping and aroused brain. Science 262:679685. Available at: https://science.sciencemag.org/content/262/5134/679 [Accessed March 4, 2021].Google Scholar
Stoodley, CJ (2012) The cerebellum and cognition: evidence from functional imaging studies. Cerebellum 11:352365.Google Scholar
Stoodley, CJ (2014) Distinct regions of the cerebellum show gray matter decreases in autism, ADHD, and developmental dyslexia. Front Syst Neurosci 8:92.Google Scholar
Stoodley, CJ, D’Mello, AM, Ellegood, J, Jakkamsetti, V, Liu, P, Nebel, MB, Gibson, JM, Kelly, E, Meng, F, Cano, CA, Pascual, JM, Mostofsky, SH, Lerch, JP, Tsai, PT (2017) Altered cerebellar connectivity in autism and cerebellar-mediated rescue of autism-related behaviors in mice. Nat Neurosci 20:17441751.Google Scholar
Stoodley, CJ, Limperopoulos, C (2016) Structure-function relationships in the developing cerebellum: Evidence from early-life cerebellar injury and neurodevelopmental disorders. Semin Fetal Neonatal Med 21:356364.Google Scholar
Stoodley, CJ, Valera, EM, Schmahmann, JD (2012) Functional topography of the cerebellum for motor and cognitive tasks: an fMRI study. NeuroImage 59:15601570.Google Scholar
Streng, ML, Krook-Magnuson, E (2020) The cerebellum and epilepsy. Epilepsy Behav: 106909. Available at: https://www.sciencedirect.com/science/article/pii/S1525505019311667 [Accessed February 26, 2021].Google Scholar
Takahashi, E, Hayashi, E, Schmahmann, JD, Grant, PE (2014) Development of cerebellar connectivity in human fetal brains revealed by high angular resolution diffusion tractography. NeuroImage 96:326333.Google Scholar
Tang, G, Gudsnuk, K, Kuo, S-H, Cotrina, ML, Rosoklija, G, Sosunov, A, Sonders, MS, Kanter, E, Castagna, C, Yamamoto, A, Yue, Z, Arancio, O, Peterson, BS, Champagne, F, Dwork, AJ, Goldman, J, Sulzer, D (2014) Loss of mTOR-dependent macroautophagy causes autistic-like synaptic pruning deficits. Neuron 83:11311143. Available at: https://linkinghub.elsevier.com/retrieve/pii/S0896627314006515 [Accessed June 27, 2019].Google Scholar
Ten Brinke, MM, Heiney, SA, Wang, X, Proietti-Onori, M, Boele, H-J, Bakermans, J, Medina, JF, Gao, Z, De Zeeuw, CI (2017) Dynamic modulation of activity in cerebellar nuclei neurons during pavlovian eyeblink conditioning in mice. eLife 6:e28132.Google Scholar
Teune, TM, van der Burg, J, van der Moer, J, Voogd, J, Ruigrok, TJ (2000) Topography of cerebellar nuclear projections to the brain stem in the rat. Prog Brain Res 124:141172.Google Scholar
Tlamsa, AP, Brumberg, JC (2010) Organization and morphology of thalamocortical neurons of mouse ventral lateral thalamus. Somatosens Mot Res 27:3443.Google Scholar
Tracey, DJ, Asanuma, C, Jones, EG, Porter, R (1980) Thalamic relay to motor cortex: afferent pathways from brain stem, cerebellum, and spinal cord in monkeys. J Neurophysiol 44:532554. Available at: https://journals.physiology.org/doi/abs/10.1152/jn.1980.44.3.532 [Accessed March 3, 2021].Google Scholar
Tsai, PT, Hull, C, Chu, Y, Greene-Colozzi, E, Sadowski, AR, Leech, JM, Steinberg, J, Crawley, JN, Regehr, WG, Sahin, M (2012) Autistic-like behaviour and cerebellar dysfunction in Purkinje cell Tsc1 mutant mice. Nature 488:647651.Google Scholar
Ueki, A (1983) The mode of nigro-thalamic transmission investigated with intracellular recording in the cat. Exp Brain Res 49:116124.Google Scholar
Uno, M, Yoshida, M, Hirota, I (1970) The mode of cerebello-thalamic relay transmission investigated with intracellular recording from cells of the ventrolateral nucleus of cat’s thalamus. Exp Brain Res 10:121139.Google Scholar
Uusisaari, M, De Schutter, E (2011) The mysterious microcircuitry of the cerebellar nuclei. J Physiol 589:34413457.Google Scholar
Vitek, JL, Ashe, J, DeLong, MR, Alexander, GE (1994) Physiologic properties and somatotopic organization of the primate motor thalamus. J Neurophysiol 71:14981513. Available at: https://journals.physiology.org/doi/abs/10.1152/jn.1994.71.4.1498 [Accessed October 28, 2020].Google Scholar
Volpe, JJ (2009) Cerebellum of the premature infant: rapidly developing, vulnerable, clinically important. J Child Neurol 24:10851104.Google Scholar
Voogd, J, van Baarsen, K (2014) The horseshoe-shaped commissure of Wernekinck or the decussation of the brachium conjunctivum methodological changes in the 1840s. Cerebellum 13:113120.Google Scholar
Walter, JT, Alvina, K, Womack, MD, Chevez, C, Khodakhah, K (2006) Decreases in the precision of Purkinje cell pacemaking cause cerebellar dysfunction and ataxia. Nat Neurosci 9:389397.Google Scholar
Wang, C-C, Shyu, B-C (2004) Differential projections from the mediodorsal and centrolateral thalamic nuclei to the frontal cortex in rats. Brain Res 995:226235. Available at: https://www.sciencedirect.com/science/article/pii/S000689930303840X [Accessed March 3, 2021].Google Scholar
Wang, D, Smith-Bell, CA, Burhans, LB, O’Dell, DE, Bell, RW, Schreurs, BG (2018) Changes in membrane properties of rat deep cerebellar nuclear projection neurons during acquisition of eyeblink conditioning. Proc Natl Acad Sci USA 115:E9419E9428. Available at: http://www.pnas.org/lookup/doi/10.1073/pnas.1808539115 [Accessed September 22, 2021].Google Scholar
Wang, M, Li, H, Takumi, T, Qiu, Z, Xu, X, Yu, X, Bian, W-J (2017) Distinct defects in spine formation or pruning in two gene duplication mouse models of autism. Neurosci Bull 33:143152. Available at: http://link.springer.com/10.1007/s12264-017-0111-8 [Accessed June 27, 2019].Google Scholar
Wang, SS-H, Kloth, AD, Badura, A (2014) The cerebellum, sensitive periods, and autism. Neuron 83:518532. Available at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4135479/ [Accessed October 31, 2020].Google Scholar
Wang, VY, Rose, MF, Zoghbi, HY (2005) Math1 expression redefines the rhombic lip derivatives and reveals novel lineages within the brainstem and cerebellum. Neuron 48:3143.Google Scholar
Watson, TC, Obiang, P, Torres-Herraez, A, Watilliaux, A, Coulon, P, Rochefort, C, Rondi-Reig, L (2019) Anatomical and physiological foundations of cerebello-hippocampal interaction. eLife 8.Google Scholar
Wu, Y, Raman, IM (2017) Facilitation of mossy fibre-driven spiking in the cerebellar nuclei by the synchrony of inhibition. J Physiol 595:52455264.Google Scholar
Yamaguchi, K, Goto, N, Yamamoto, TY (1989) Development of human cerebellar nuclei. Morphometric study. Acta Anat (Basel) 136:6168.Google Scholar
Yamamoto, T, Hassler, R, Huber, C, Wagner, A, Sasaki, K (1983) Electrophysiologic studies on the pallido- and cerebellothalamic projections in squirrel monkeys (Saimiri sciureus). Exp Brain Res 51:7787.Google Scholar
Yamamoto, T, Noda, T, Miyata, M, Nishimura, Y (1984) Electrophysiological and morphological studies on thalamic neurons receiving entopedunculo- and cerebello-thalamic projections in the cat. Brain Res 301:231242.Google Scholar
Yarden‐Rabinowitz, Y, Yarom, Y (2017) In vivo analysis of synaptic activity in cerebellar nuclei neurons unravels the efficacy of excitatory inputs. J Physiol 595:59455963. Available at: https://physoc.onlinelibrary.wiley.com/doi/abs/10.1113/JP274115 [Accessed March 7, 2021].Google Scholar
Yuge, K, Kataoka, A, Yoshida, AC, Itoh, D, Aggarwal, M, Mori, S, Blackshaw, S, Shimogori, T (2011) Region-specific gene expression in early postnatal mouse thalamus. J Comp Neurol 519:544561.Google Scholar

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