Connection

ROY SILLITOE to Disease Models, Animal

This is a "connection" page, showing publications ROY SILLITOE has written about Disease Models, Animal.
Connection Strength

1.512
  1. Cerebellar nuclei cells produce distinct pathogenic spike signatures in mouse models of ataxia, dystonia, and tremor. Elife. 2024 Jul 29; 12.
    View in: PubMed
    Score: 0.402
  2. Cerebellar deep brain stimulation rescues Purkinje cell mitochondrial density in a genetic mouse model of cerebellar ataxia. Brain Res Bull. 2026 Jan; 234:111704.
    View in: PubMed
    Score: 0.111
  3. Olivocerebellar circuit development as a substrate for dystonia pathogenesis. Curr Top Dev Biol. 2026; 167:379-411.
    View in: PubMed
    Score: 0.111
  4. Cerebellar deep brain stimulation as a dual-function therapeutic for restoring movement and sleep in dystonic mice. Neurotherapeutics. 2024 10; 21(6):e00467.
    View in: PubMed
    Score: 0.102
  5. Purkinje cell dysfunction causes disrupted sleep in ataxic mice. Dis Model Mech. 2024 06 01; 17(6).
    View in: PubMed
    Score: 0.099
  6. Physiology of Dystonia: Animal Studies. Int Rev Neurobiol. 2023; 169:163-215.
    View in: PubMed
    Score: 0.092
  7. Deep Brain Stimulation of the Interposed Cerebellar Nuclei in a Conditional Genetic Mouse Model with Dystonia. Adv Neurobiol. 2023; 31:93-117.
    View in: PubMed
    Score: 0.090
  8. Neuromodulation of the cerebellum rescues movement in a mouse model of ataxia. Nat Commun. 2021 02 26; 12(1):1295.
    View in: PubMed
    Score: 0.079
  9. In vivo cerebellar circuit function is disrupted in an mdx mouse model of Duchenne muscular dystrophy. Dis Model Mech. 2019 12 09; 13(2).
    View in: PubMed
    Score: 0.073
  10. Persistent motor dysfunction despite homeostatic rescue of cerebellar morphogenesis in the Car8 waddles mutant mouse. Neural Dev. 2019 03 12; 14(1):6.
    View in: PubMed
    Score: 0.069
  11. Genetic silencing of olivocerebellar synapses causes dystonia-like behaviour in mice. Nat Commun. 2017 04 04; 8:14912.
    View in: PubMed
    Score: 0.061
  12. The pledge, the turn, and the prestige of transient cerebellar alterations in SCA6. J Physiol. 2017 02 01; 595(3):607-608.
    View in: PubMed
    Score: 0.060
  13. Cerebellar dysfunction in a mouse model of childhood-onset manganese-induced dystonia parkinsonism. Neurobiol Dis. 2025 11; 216:107115.
    View in: PubMed
    Score: 0.027
  14. Coenzyme Q headgroup intermediates can ameliorate a mitochondrial encephalopathy. Nature. 2025 09; 645(8080):466-474.
    View in: PubMed
    Score: 0.027
  15. Thalamic deep brain stimulation improves movement in a cerebellar model of lesion-based status dystonicus. Neurotherapeutics. 2025 Mar; 22(2):e00543.
    View in: PubMed
    Score: 0.026
  16. 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.
    View in: PubMed
    Score: 0.023
  17. Deleting Mecp2 from the cerebellum rather than its neuronal subtypes causes a delay in motor learning in mice. Elife. 2021 01 26; 10.
    View in: PubMed
    Score: 0.020
  18. Loss of cerebellar function selectively affects intrinsic rhythmicity of eupneic breathing. Biol Open. 2020 04 13; 9(4).
    View in: PubMed
    Score: 0.019
  19. Extensive cryptic splicing upon loss of RBM17 and TDP43 in neurodegeneration models. Hum Mol Genet. 2016 12 01; 25(23):5083-5093.
    View in: PubMed
    Score: 0.015
  20. Patterned Purkinje cell degeneration in mouse models of Niemann-Pick type C disease. J Comp Neurol. 2003 Feb 10; 456(3):279-91.
    View in: PubMed
    Score: 0.006
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.