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Persistent motor dysfunction despite homeostatic rescue of cerebellar morphogenesis in the Car8 waddles mutant mouse.

Neural development | 2019

Purkinje cells play a central role in establishing the cerebellar circuit. Accordingly, disrupting Purkinje cell development impairs cerebellar morphogenesis and motor function. In the Car8wdl mouse model of hereditary ataxia, severe motor deficits arise despite the cerebellum overcoming initial defects in size and morphology.

Pubmed ID: 30867000 RIS Download

Research resources used in this publication

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Associated grants

  • Agency: NINDS NIH HHS, United States
    Id: R01 NS100874
  • Agency: NICHD NIH HHS, United States
    Id: U54 HD083092
  • Agency: NINDS NIH HHS, United States
    Id: R01 NS089664

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B6.Cg-Tg(Npy-MAPT/Sapphire)1Rck/J (tool)

RRID:IMSR_JAX:008321

Mus musculus with name B6.Cg-Tg(Npy-MAPT/Sapphire)1Rck/J from IMSR.

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C57BLKS/J (tool)

RRID:IMSR_JAX:000662

Mus musculus with name C57BLKS/J from IMSR.

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