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「Neurobiol Dis[Journal]」の検索結果

4504件中 41件~60件表示    検索結果をPubMedで見る PubMedで見る

Pathogenesis of SCA3 and implications for other polyglutamine diseases.

Environmental enrichment prevents Aβ oligomer-induced synaptic dysfunction through mirna-132 and hdac3 signaling pathways.

Cardiorespiratory depression from brainstem seizure activity in freely moving rats.

Targeting the cannabinoid receptor CB2 in a mouse model of l-dopa induced dyskinesia.

Cerebrospinal fluid neurogranin in an inducible mouse model of neurodegeneration: A translatable marker of synaptic degeneration.

Optimizing intracellular antibodies (intrabodies/nanobodies) to treat neurodegenerative disorders.

Functional screening of GATOR1 complex variants reveals a role for mTORC1 deregulation in FCD and focal epilepsy.

Glucocerebrosidase activity, cathepsin D and monomeric α-synuclein interactions in a stem cell derived neuronal model of a PD associated GBA1 mutation.

FAAH inhibition as a preventive treatment for migraine: A pre-clinical study.

Active immunization with tau epitope in a mouse model of tauopathy induced strong antibody response together with improvement in short memory and pSer396-tau pathology.

Pathological high frequency oscillations associate with increased GABA synaptic activity in pediatric epilepsy surgery patients.

Exercise, diet and stress as modulators of gut microbiota: Implications for neurodegenerative diseases.

Neural connectivity predicts spreading of alpha-synuclein pathology in fibril-injected mouse models: Involvement of retrograde and anterograde axonal propagation.

Stress granule mediated protein aggregation and underlying gene defects in the FTD-ALS spectrum.

LRRK2 inhibition prevents endolysosomal deficits seen in human Parkinson's disease.

Decreased number of striatal cholinergic interneurons and motor deficits in dopamine receptor 2-expressing-cell-specific Dyt1 conditional knockout mice.

Loss of huntingtin function slows synaptic vesicle endocytosis in striatal neurons from the htt mouse model of Huntington's disease.

The C-terminal domain of LRRK2 with the G2019S mutation is sufficient to produce neurodegeneration of dopaminergic neurons in vivo.

Hypothalamic orexin and mechanistic target of rapamycin activation mediate sleep dysfunction in a mouse model of tuberous sclerosis complex.

Coding and non-coding transcriptome of mesial temporal lobe epilepsy: Critical role of small non-coding RNAs.

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