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Over ons Praktische zaken Waar vindt u ons ing. M. (Michel) Meijer

Publicaties

Brain macrophages acquire distinct transcriptomes in multiple sclerosis lesions and normal appearing white matter

Human Microglia Acquire a More Mature, Homeostatic Phenotype During the Transition of the First and Second Trimester of Gestation.

Elevated mutant dynorphin A causes Purkinje cell loss and motor dysfunction in spinocerebellar ataxia type 23

Erratum to: The L450P mutation in KCND3 brings spinocerebellar ataxia and Brugada syndrome closer together (vol 14, pg 257, 2013)

Functional Analysis Helps to Define KCNC3 Mutational Spectrum in Dutch Ataxia Cases

Spinocerebellar ataxia type 19/22 mutations alter heterocomplex Kv4.3 channel function and gating in a dominant manner

Priming of microglia in a DNA-repair deficient model of accelerated aging

Inhibition of CXCR3-mediated chemotaxis by the human chemokine receptor-like protein CCX-CKR

The L450P mutation in KCND3 brings spinocerebellar ataxia and Brugada syndrome closer together

Mutations in Potassium Channel KCND3 Cause Spinocerebellar Ataxia Type 19

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