| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| S Mazdak Abulnaga, Zhen Yang, Aaron Carass, Kalyani Kansal, Bruno M Jedynak, Chiadi U Onyike, Sarah H Ying, Jerry L Princ. A toolbox to visually explore cerebellar shape changes in cerebellar disease and dysfunction. Proceedings of SPIE--the International Society for Optical Engineering. vol 9785. 2020-10-01. PMID:28479655. |
the toolbox takes as input landmark shape representations of subjects' cerebellar substructures. |
2020-10-01 |
2023-08-13 |
human |
| Jiawei Chen, Han Zhang, Dong Nie, Li Wang, Gang Li, Weili Lin, Dinggang She. Automatic Accurate Infant Cerebellar Tissue Segmentation with Densely Connected Convolutional Network. Machine learning in medical imaging. MLMI (Workshop). vol 11046. 2020-10-01. PMID:30381806. |
we tackle this challenge by proposing a densely connected convolutional network to learn robust feature representations of different cerebellar tissues towards automatic and accurate segmentation. |
2020-10-01 |
2023-08-13 |
human |
| Richard R Carrillo, Francisco Naveros, Eduardo Ros, Niceto R Luqu. A Metric for Evaluating Neural Input Representation in Supervised Learning Networks. Frontiers in neuroscience. vol 12. 2020-10-01. PMID:30618549. |
in this study we present an algorithm for evaluating quantitatively the level of compatibility/interference amongst a set of given cerebellar states according to their representation (granule-cell activation patterns) without the need for actually conducting simulations and network training. |
2020-10-01 |
2023-08-13 |
Not clear |
| Laurentiu S Popa, Timothy J Ebne. Cerebellum, Predictions and Errors. Frontiers in cellular neuroscience. vol 12. 2020-10-01. PMID:30697149. |
therefore, cerebellar representations bridge motor and non-motor domains and provide a better understanding of cerebellar function within the functional architecture of the brain. |
2020-10-01 |
2023-08-13 |
monkey |
| Zeynab Rezaee, Surbhi Kaura, Dhaval Solanki, Adyasha Dash, M V Padma Srivastava, Uttama Lahiri, Anirban Dutt. Deep Cerebellar Transcranial Direct Current Stimulation of the Dentate Nucleus to Facilitate Standing Balance in Chronic Stroke Survivors-A Pilot Study. Brain sciences. vol 10. issue 2. 2020-09-28. PMID:32050704. |
we hypothesized that cerebellar transcranial direct current stimulation (ctdcs) of the dentate nuclei and the lower-limb representations in the cerebellum can improve functional reach during standing balance in chronic (>6 months' post-stroke) stroke survivors. |
2020-09-28 |
2023-08-13 |
Not clear |
| Leonard Faul, Daniel Stjepanović, Joshua M Stivers, Gregory W Stewart, John L Graner, Rajendra A Morey, Kevin S LaBa. Proximal threats promote enhanced acquisition and persistence of reactive fear-learning circuits. Proceedings of the National Academy of Sciences of the United States of America. vol 117. issue 28. 2020-09-21. PMID:32601212. |
with an analysis of representational pattern similarity between the acquisition and extinction phases, we further demonstrate that proximal threats impaired extinction efficacy via persistent multivariate representations of conditioned learning in the cerebellum, which predicted susceptibility to later fear reinstatement. |
2020-09-21 |
2023-08-13 |
human |
| Jeremy D Schmahmann, Xavier Guell, Catherine J Stoodley, Mark A Halk. The Theory and Neuroscience of Cerebellar Cognition. Annual review of neuroscience. vol 42. 2020-09-10. PMID:30939101. |
the framework for cerebellar cognition stems from the identification of three cognitive representations in the posterior lobe, which are interconnected with cerebral association areas and distinct from the primary and secondary cerebellar sensorimotor representations linked with the spinal cord and cerebral motor areas. |
2020-09-10 |
2023-08-13 |
Not clear |
| Jeremy D Schmahmann, Xavier Guell, Catherine J Stoodley, Mark A Halk. The Theory and Neuroscience of Cerebellar Cognition. Annual review of neuroscience. vol 42. 2020-09-10. PMID:30939101. |
lesions of the anterior lobe primary sensorimotor representations produce dysmetria of movement, the cerebellar motor syndrome. |
2020-09-10 |
2023-08-13 |
Not clear |
| Isabelle Mackrous, Jerome Carriot, Mohsen Jamali, Kathleen E Culle. Cerebellar Prediction of the Dynamic Sensory Consequences of Gravity. Current biology : CB. vol 29. issue 16. 2020-08-03. PMID:31378613. |
here, we provide evidence that, although during passive movements, individual cerebellar output neurons encode representations of head motion and orientation relative to gravity, these gravity-driven responses are cancelled when head movement is a consequence of voluntary generated movement. |
2020-08-03 |
2023-08-13 |
Not clear |
| Samuel S McAfee, Yu Liu, Roy V Sillitoe, Detlef H Hec. Cerebellar Lobulus Simplex and Crus I Differentially Represent Phase and Phase Difference of Prefrontal Cortical and Hippocampal Oscillations. Cell reports. vol 27. issue 8. 2020-07-16. PMID:31116979. |
purkinje cells in cerebellar ls and crus i differentially represented specific phases and phase differences of mpfc and dca1 lfp oscillations in a frequency-specific manner, suggesting a site- and frequency-specific cerebellar representation of temporal aspects of neuronal oscillations in non-motor cerebral cortical areas. |
2020-07-16 |
2023-08-13 |
Not clear |
| Daniel M van Es, Wietske van der Zwaag, Tomas Knape. Topographic Maps of Visual Space in the Human Cerebellum. Current biology : CB. vol 29. issue 10. 2020-06-15. PMID:31080082. |
within sensorimotor areas of the cerebellum, functional organization is characterized by ipsilateral representations of the body [6]. |
2020-06-15 |
2023-08-13 |
human |
| Reiko Ashida, Nadia L Cerminara, Richard J Edwards, Richard Apps, Jonathan C W Brook. Sensorimotor, language, and working memory representation within the human cerebellum. Human brain mapping. vol 40. issue 16. 2020-04-14. PMID:31361075. |
sensorimotor, language, and working memory representation within the human cerebellum. |
2020-04-14 |
2023-08-13 |
human |
| Reiko Ashida, Nadia L Cerminara, Richard J Edwards, Richard Apps, Jonathan C W Brook. Sensorimotor, language, and working memory representation within the human cerebellum. Human brain mapping. vol 40. issue 16. 2020-04-14. PMID:31361075. |
sensorimotor localisation was uniform across individuals, but the representation of cognitive tasks was more variable, highlighting the importance of individual scans for mapping higher order functions within the cerebellum. |
2020-04-14 |
2023-08-13 |
human |
| Lucas Villalta Santos, Jamile Benite Palma Lopes, Natália Almeida Carvalho Duarte, Manuela Galli, Luanda André Collange Grecco, Claudia Santos Oliveir. Effect of Anodic tDCS Over Motor Cortex Versus Cerebellum in Cerebral Palsy: A Study Protocol. Pediatric physical therapy : the official publication of the Section on Pediatrics of the American Physical Therapy Association. vol 31. issue 3. 2019-12-19. PMID:31135599. |
to compare the clinical and functional effects of treadmill training combined with anodic transcranial direct current stimulation (atdcs) on the primary motor cortex (cz), specifically on the area of motor cortex representation of the lower limbs, and on the cerebellum (cb) in children with spastic cerebral palsy (cp). |
2019-12-19 |
2023-08-13 |
Not clear |
| Emma D Wilson, Sean R Anderson, Paul Dean, John Porril. Sensorimotor maps can be dynamically calibrated using an adaptive-filter model of the cerebellum. PLoS computational biology. vol 15. issue 7. 2019-12-19. PMID:31295248. |
map calibration would be a significant new role for the cerebellum given the ubiquity of map representations in the brain, but how it could perform such a task is unclear. |
2019-12-19 |
2023-08-13 |
Not clear |
| Antonio Artés-Rodriguez, Anibal R. Figueiras-Vidal, Francisco J. González-Serran. Fourier analysis of the generalized CMAC neural network. Neural networks : the official journal of the International Neural Network Society. vol 11. issue 3. 2019-11-20. PMID:12662817. |
the cerebellar model articulation controller (cmac) is a simple and fast neural network: these characteristics have extended its successful applications, while the analysis of its representation capabilities, as for many other neural networks, did not follow a similar development.in this article we discover the close parallelism between the representation of a function by a generalized cmac (gcmac) and nyquist sampling theory: discussing the role of different parameters and components of the network according to this similarity. |
2019-11-20 |
2023-08-12 |
Not clear |
| Ann K Shinn, Youkyung S Roh, Caitlin T Ravichandran, Justin T Baker, Dost Öngür, Bruce M Cohe. Aberrant cerebellar connectivity in bipolar disorder with psychosis. Biological psychiatry. Cognitive neuroscience and neuroimaging. vol 2. issue 5. 2019-11-20. PMID:28730183. |
however, no studies have investigated the topographic representations of resting state cerebellar networks in bipolar disorder, specifically their functional connectivity to cerebral cortical networks. |
2019-11-20 |
2023-08-13 |
Not clear |
| Sheeba Arnold Anteraper, Xavier Guell, Anila D'Mello, Neha Joshi, Susan Whitfield-Gabrieli, Gagan Josh. Disrupted Cerebrocerebellar Intrinsic Functional Connectivity in Young Adults with High-Functioning Autism Spectrum Disorder: A Data-Driven, Whole-Brain, High-Temporal Resolution Functional Magnetic Resonance Imaging Study. Brain connectivity. vol 9. issue 1. 2019-08-29. PMID:29896995. |
mvpa revealed two clusters (crus i/ii and lobule ix) of abnormal connectivity in the cerebellum that are consistent with the notion of a triple representation of nonmotor processing in the cerebellum. |
2019-08-29 |
2023-08-13 |
Not clear |
| Elizabeth Fleming, Court Hul. Serotonin regulates dynamics of cerebellar granule cell activity by modulating tonic inhibition. Journal of neurophysiology. vol 121. issue 1. 2019-08-22. PMID:30281395. |
this circuit mechanism reduces the probability of granule cell spiking without altering spike timing, thus suppressing cerebellar input without altering its temporal representation in the granule cell layer. |
2019-08-22 |
2023-08-13 |
rat |
| Julie Marie Lefort, Jean Vincent, Lucille Tallot, Frédéric Jarlier, Chris Innocentius De Zeeuw, Laure Rondi-Reig, Christelle Rochefor. Impaired cerebellar Purkinje cell potentiation generates unstable spatial map orientation and inaccurate navigation. Nature communications. vol 10. issue 1. 2019-07-01. PMID:31113954. |
cerebellar activity supported by pkc-dependent long-term depression in purkinje cells (pcs) is involved in the stabilization of self-motion based hippocampal representation, but the existence of cerebellar processes underlying integration of allocentric cues remains unclear. |
2019-07-01 |
2023-08-13 |
mouse |