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Hydrogen–deuterium exchange in vivo to measure turnover of an ALS-associated mutant SOD1 protein in spinal cord of mice

Mutations of cytosolic Cu/Zn superoxide dismutase 1 (SOD1) in humans and overexpression of mutant human SOD1 genes in transgenic mice are associated with the motor neuron degenerative condition known as amyotrophic lateral sclerosis (ALS; Lou Gehrig's disease). Gain-of-function toxicity from th...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
मुख्य लेखकों: Farr, George W, Ying, Zheng, Fenton, Wayne A, Horwich, Arthur L
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: Wiley Subscription Services, Inc., A Wiley Company 2011
विषय:
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC3218362/
https://ncbi.nlm.nih.gov/pubmed/21780215
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/pro.700
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