Connection

ROY SILLITOE to Disease Models, Animal

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

1.295
  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: 0.412
  2. Cerebellar deep brain stimulation as a dual-function therapeutic for restoring movement and sleep in dystonic mice. Neurotherapeutics. 2024 Oct; 21(6):e00467.
    View in: PubMed
    Score: 0.105
  3. Purkinje cell dysfunction causes disrupted sleep in ataxic mice. Dis Model Mech. 2024 Jun 01; 17(6).
    View in: PubMed
    Score: 0.102
  4. Physiology of Dystonia: Animal Studies. Int Rev Neurobiol. 2023; 169:163-215.
    View in: PubMed
    Score: 0.095
  5. 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: 0.092
  6. Neuromodulation of the cerebellum rescues movement in a mouse model of ataxia. Nat Commun. 2021 02 26; 12(1):1295.
    View in: PubMed
    Score: 0.081
  7. 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: 0.075
  8. 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: 0.071
  9. Genetic silencing of olivocerebellar synapses causes dystonia-like behaviour in mice. Nat Commun. 2017 04 04; 8:14912.
    View in: PubMed
    Score: 0.062
  10. 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: 0.061
  11. Coenzyme Q headgroup intermediates can ameliorate a mitochondrial encephalopathy. Nature. 2025 Sep; 645(8080):466-474.
    View in: PubMed
    Score: 0.028
  12. 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: 0.027
  13. 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: 0.024
  14. 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
  15. Loss of cerebellar function selectively affects intrinsic rhythmicity of eupneic breathing. Biol Open. 2020 04 13; 9(4).
    View in: PubMed
    Score: 0.019
  16. 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
  17. 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.