Early whole-body mutant huntingtin lowering averts changes in proteins and lipids important for synapse function and white matter maintenance in the LacQ140 mouse model-Reference-Cited by-同舟云学术

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Early whole-body mutant huntingtin lowering averts changes in proteins and lipids important for synapse function and white matter maintenance in the LacQ140 mouse model

Published:2023-10 Issue: Volume:187 Page:106313
ISSN:0969-9961
Container-title:Neurobiology of Disease
language:en
Short-container-title:Neurobiology of Disease

Author:

Shing Kai,Sapp Ellen,Boudi Adel,Liu Sophia,Seeley Connor,Marchionini Deanna,DiFiglia Marian,Kegel-Gleason Kimberly B.

Funder

National Institutes of Health

CHDI Foundation

Publisher

Elsevier BV

Subject

Neurology

Reference154 articles.

1. Novel proteomic changes in brain mitochondria provide insights into mitochondrial dysfunction in mouse models of Huntington’s disease;Agrawal;Mitochondrion,2019

2. FA2H-dependent fatty acid 2-hydroxylation in postnatal mouse brain;Alderson;J. Lipid Res.,2006

3. A divalent siRNA chemical scaffold for potent and sustained modulation of gene expression throughout the central nervous system;Alterman;Nat. Biotechnol.,2019

4. Intrinsic mutant HTT-mediated defects in oligodendroglia cause myelination deficits and behavioral abnormalities in Huntington disease;Bardile;Proc. Natl. Acad. Sci. U. S. A.,2019

5. Huntingtin and the Synapse;Barron;Front. Cell. Neurosci.,2021

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Exploring the thermodynamics of protein aggregation: an insight to Huntington's disease therapeutics;Neuroscience and Behavioral Physiology;2024-08-27

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