Movement-related inputs to intermediate cerebellum of the monkey.
By P. L. V. Kan, A. Gibson, J. Houk. 1993
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
- R. Silver
- N. A. Cayco-Gajic
- Guy O. Billings
- Nicolas Schweighofer
- A. Lorincz
- E. Cesana
- Eugenio Piasini
- Carl-Fredrik Ekerot
Citations in the corpus
- Unsupervised learning of granule cell sparse codes enhances cerebellar adaptive control. (2001, background): “Furthermore, the threshold of the GO is adjusted so that the cell has a background ®ring rate of about 20 spikes/s, in accordance with experimental results.(53) The learning algorithms proposed are plausible and well supported by existing data.”
- Granule Cell Ascending Axon Excitatory Synapses onto Golgi Cells Implement a Potent Feedback Circuit in the Cerebellar Granular Layer (2013, background): “…firing is modulated by sensory inputs (Vos et al., 1999a; Holtzman et al., 2006; Barmack and Yakhnitsa, 2008; Xu and Edgley, 2010), sensorimotor activity (Edgley and Lidierth, 1987; van Kan et al., 1993; Prsa et al., 2009; Heine et al., 2010), and cortical up- and down-states (Ros et al., 2009).”
- Consensus Paper: Roles of the Cerebellum in Motor Control—The Diversity of Ideas on Cerebellar Involvement in Movement (2011, background): “that in nonhuman primates, visual [240–244] and kinesthetic [245–247] inputs reach the cerebellum, either”
- Cerebellar Golgi cells in the rat: receptive fields and timing of responses to facial stimulation (1999, methodology): “…ranges reported by others for Golgi cells in anaesthetized rodents (Schulman & Bloom, 1981), awake rabbits (Atkins et al., 1997), anaesthetized (Van Kan et al., 1993), decerebrate (Eccles et al., 1966b) or awake cats (Edgley & Lidierth, 1987), or awake primates (Miles et al., 1980; Van Kan et…”
- Properties of Somatosensory Synaptic Integration in Cerebellar Granule Cells In Vivo (2006, background): “Also, proprioceptive mossy fibers of the LRN (Clendenin et al., 1974) and the P-CCT (Cooke et al., 1971) can fire at 1 kHz under appropriate peripheral activation, but activation under behavior seems to consist in much more moderate firing rates (50 – 300 Hz) (van Kan et al., 1993).”
- NMDA receptors with incomplete Mg2+ block enable low-frequency transmission through the cerebellar cortex (2012, background): “In contrast, continuous variables encoded as lower frequency rate-coded MF firing (van Kan et al., 1993; Arenz et al., 2008; Prsa et al., 2009; Sawtell, 2010) are integrated by GCs.”
- Shunting inhibition modulates neuronal gain during synaptic excitation. (2003, methodology): “An analogous shift was observed with tonic current excitation (gain changed by 4% cles et al., 1967), which fire irregularly in vivo (van Kan et al., 1993), and evoke predominantly AMPA receptor- 2%, p 0.17; offset changed from 11 4 pA to 35 2 pA, p 0.01, n 4; data not shown) as previouslymediated…”
- Synaptic and cellular properties of the feed-forward inhibitory circuit within the input layer of the cerebellar cortex (2008, unknown): “We next examined AP precision during trains of MF activity, because some sensory inputs are sustained (van Kan et al., 1993).”