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Morphological and Functional Correlates of Synaptic Pathology in the Cathepsin D Knock-Out Mouse Model of Congenital Neuronal Ceroid-Lipofuscinosis

Mutations in the cathepsin D (CTSD) gene cause an aggressive neurodegenerative disease (congenital neuronal ceroid lipofuscinosis) that leads to early death. Recent evidence suggests that presynaptic abnormalities play a major role in the pathogenesis of CTSD deficiencies. To identify the early even...

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Bibliografske podrobnosti
Main Authors: Koch, Sabine, Molchanova, Svetlana M., Wright, Ann K, Edwards, Andrew, Cooper, Jon D., Taira, Tomi, Gillingwater, Thomas H., Tyynelä, Jaana
Format: Artigo
Jezik:Inglês
Izdano: 2011
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC3242052/
https://ncbi.nlm.nih.gov/pubmed/22082660
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/NEN.0b013e318238fc28
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