ROY SILLITOE to Disease Models, Animal
This is a "connection" page, showing publications ROY SILLITOE has written about Disease Models, Animal.
Connection Strength
1.295
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Cerebellar nuclei cells produce distinct pathogenic spike signatures in mouse models of ataxia, dystonia, and tremor. Elife. 2024 Jul 29; 12.
Score: 0.412
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Cerebellar deep brain stimulation as a dual-function therapeutic for restoring movement and sleep in dystonic mice. Neurotherapeutics. 2024 Oct; 21(6):e00467.
Score: 0.105
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Purkinje cell dysfunction causes disrupted sleep in ataxic mice. Dis Model Mech. 2024 Jun 01; 17(6).
Score: 0.102
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Physiology of Dystonia: Animal Studies. Int Rev Neurobiol. 2023; 169:163-215.
Score: 0.095
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Deep Brain Stimulation of the Interposed Cerebellar Nuclei in a Conditional Genetic Mouse Model with Dystonia. Adv Neurobiol. 2023; 31:93-117.
Score: 0.092
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Neuromodulation of the cerebellum rescues movement in a mouse model of ataxia. Nat Commun. 2021 02 26; 12(1):1295.
Score: 0.081
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In vivo cerebellar circuit function is disrupted in an mdx mouse model of Duchenne muscular dystrophy. Dis Model Mech. 2019 12 09; 13(2).
Score: 0.075
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Persistent motor dysfunction despite homeostatic rescue of cerebellar morphogenesis in the Car8 waddles mutant mouse. Neural Dev. 2019 03 12; 14(1):6.
Score: 0.071
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Genetic silencing of olivocerebellar synapses causes dystonia-like behaviour in mice. Nat Commun. 2017 04 04; 8:14912.
Score: 0.062
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The pledge, the turn, and the prestige of transient cerebellar alterations in SCA6. J Physiol. 2017 02 01; 595(3):607-608.
Score: 0.061
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Coenzyme Q headgroup intermediates can ameliorate a mitochondrial encephalopathy. Nature. 2025 Sep; 645(8080):466-474.
Score: 0.028
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Thalamic deep brain stimulation improves movement in a cerebellar model of lesion-based status dystonicus. Neurotherapeutics. 2025 Mar; 22(2):e00543.
Score: 0.027
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Abnormal dysbindin expression in cerebellar mossy fiber synapses in the mdx mouse model of Duchenne muscular dystrophy. J Neurosci. 2003 Jul 23; 23(16):6576-85.
Score: 0.024
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Deleting Mecp2 from the cerebellum rather than its neuronal subtypes causes a delay in motor learning in mice. Elife. 2021 01 26; 10.
Score: 0.020
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Loss of cerebellar function selectively affects intrinsic rhythmicity of eupneic breathing. Biol Open. 2020 04 13; 9(4).
Score: 0.019
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Extensive cryptic splicing upon loss of RBM17 and TDP43 in neurodegeneration models. Hum Mol Genet. 2016 12 01; 25(23):5083-5093.
Score: 0.015
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Patterned Purkinje cell degeneration in mouse models of Niemann-Pick type C disease. J Comp Neurol. 2003 Feb 10; 456(3):279-91.
Score: 0.006