Superoxide dismutase-1 and other proteins in inclusions from transgenic amyotrophic lateral sclerosis model mice.
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Distinct changes in synaptic protein composition at neuromuscular junctions of extraocular muscles versus limb muscles of ALS donors.Protein Homeostasis in Amyotrophic Lateral Sclerosis: Therapeutic Opportunities?Spinal motor neuron protein supersaturation patterns are associated with inclusion body formation in ALS.Na+/K+-ATPase is present in scrapie-associated fibrils, modulates PrP misfolding in vitro and links PrP function and dysfunction.Glial nuclear aggregates of superoxide dismutase-1 are regularly present in patients with amyotrophic lateral sclerosis.Proteins that bind to misfolded mutant superoxide dismutase-1 in spinal cords from transgenic amyotrophic lateral sclerosis (ALS) model mice.Downregulation of VAPB expression in motor neurons derived from induced pluripotent stem cells of ALS8 patients.Elevated fecal peptidase D at onset of colitis in Galphai2-/- mice, a mouse model of IBDWidespread aggregation of mutant VAPB associated with ALS does not cause motor neuron degeneration or modulate mutant SOD1 aggregation and toxicity in mice.The small heat shock proteins αB-crystallin and Hsp27 suppress SOD1 aggregation in vitro.The SODyssey: superoxide dismutases from biochemistry, through proteomics, to oxidative stress, aging and nutraceuticals.Stress signaling from the endoplasmic reticulum: A central player in the pathogenesis of amyotrophic lateral sclerosis.The unfolded protein response in models of human mutant G93A amyotrophic lateral sclerosis.Characterization of Wnt/β-catenin and BMP/Smad signaling pathways in an in vitro model of amyotrophic lateral sclerosis.Spinal inhibitory interneuron pathology follows motor neuron degeneration independent of glial mutant superoxide dismutase 1 expression in SOD1-ALS mice.Expression of wild-type human superoxide dismutase-1 in mice causes amyotrophic lateral sclerosis.Amyotrophic lateral sclerosisMisfolded SOD1 pathology in sporadic Amyotrophic Lateral Sclerosis
P2860
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P2860
Superoxide dismutase-1 and other proteins in inclusions from transgenic amyotrophic lateral sclerosis model mice.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年学术文章
@wuu
2010年学术文章
@zh
2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
@zh-sg
2010年學術文章
@yue
2010年學術文章
@zh-hant
name
Superoxide dismutase-1 and oth ...... lateral sclerosis model mice.
@en
Superoxide dismutase-1 and oth ...... lateral sclerosis model mice.
@nl
type
label
Superoxide dismutase-1 and oth ...... lateral sclerosis model mice.
@en
Superoxide dismutase-1 and oth ...... lateral sclerosis model mice.
@nl
prefLabel
Superoxide dismutase-1 and oth ...... lateral sclerosis model mice.
@en
Superoxide dismutase-1 and oth ...... lateral sclerosis model mice.
@nl
P2093
P2860
P1476
Superoxide dismutase-1 and oth ...... lateral sclerosis model mice.
@en
P2093
Daniel Bergemalm
Gunnar Wingsle
Karin Forsberg
Karin S Graffmo
Stefan L Marklund
Thomas Brännström
Vaibhav Srivastava
P2860
P304
P356
10.1111/J.1471-4159.2010.06753.X
P407
P577
2010-04-19T00:00:00Z