Lafora disease fibroblasts exemplify the molecular interdependence between thioredoxin 1 and the proteasome in mammalian cells.
about
Oxidative stress and mitochondrial dysfunction across broad-ranging pathologies: toward mitochondria-targeted clinical strategies.Increased oxidative stress and impaired antioxidant response in Lafora disease.Control of Trx1 redox state modulates protection against methyl methanesulfonate-induced DNA damage via stabilization of p21.Methylglyoxal-induced AMPK activation leads to autophagic degradation of thioredoxin 1 and glyoxalase 2 in HT22 nerve cells.Methylglyoxal, the foe and friend of glyoxalase and Trx/TrxR systems in HT22 nerve cells.Inflammation in Lafora Disease: Evolution with Disease Progression in Laforin and Malin Knock-out Mouse Models.
P2860
Lafora disease fibroblasts exemplify the molecular interdependence between thioredoxin 1 and the proteasome in mammalian cells.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
2013年论文
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2013年论文
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name
Lafora disease fibroblasts exe ...... proteasome in mammalian cells.
@en
Lafora disease fibroblasts exe ...... proteasome in mammalian cells.
@nl
type
label
Lafora disease fibroblasts exe ...... proteasome in mammalian cells.
@en
Lafora disease fibroblasts exe ...... proteasome in mammalian cells.
@nl
prefLabel
Lafora disease fibroblasts exe ...... proteasome in mammalian cells.
@en
Lafora disease fibroblasts exe ...... proteasome in mammalian cells.
@nl
P2093
P50
P1476
Lafora disease fibroblasts exe ...... proteasome in mammalian cells
@en
P2093
Carmen Aguado
Erwin Knecht
Federico V Pallardó
Jelena Markovic
Sonia Priego
P304
P356
10.1016/J.FREERADBIOMED.2013.07.001
P577
2013-07-09T00:00:00Z