Disruption of either the Nfkb1 or the Bcl3 gene inhibits skeletal muscle atrophy.
about
A novel ubiquitin-binding protein ZNF216 functioning in muscle atrophyPC4/Tis7/IFRD1 stimulates skeletal muscle regeneration and is involved in myoblast differentiation as a regulator of MyoD and NF-kappaBEffects of dietary curcumin or N-acetylcysteine on NF-kappaB activity and contractile performance in ambulatory and unloaded murine soleusCellular and molecular mechanisms of muscle atrophyLongevity and skeletal muscle mass: the role of IGF signalling, the sirtuins, dietary restriction and protein intakeOxygen consumption and usage during physical exercise: the balance between oxidative stress and ROS-dependent adaptive signalingTumor necrosis factor-α regulates distinct molecular pathways and gene networks in cultured skeletal muscle cellsREDD1 is a major target of testosterone action in preventing dexamethasone-induced muscle lossp38 MAPK links oxidative stress to autophagy-related gene expression in cachectic muscle wasting.The Systemic Effect of Burn Injury and Trauma on Muscle and Bone Mass and Composition.NF-kappaB mediates the transcription of mouse calsarcin-1 gene, but not calsarcin-2, in C2C12 cellsDynamic resolution of functionally related gene sets in response to acute heat stressRole of proteasomes in disease.Limb immobilization induces a coordinate down-regulation of mitochondrial and other metabolic pathways in men and womenGenomic profiling of messenger RNAs and microRNAs reveals potential mechanisms of TWEAK-induced skeletal muscle wasting in miceThe mERG1a channel modulates skeletal muscle MuRF1, but not MAFbx, expression.The TWEAK-Fn14 system is a critical regulator of denervation-induced skeletal muscle atrophy in mice.Oxidative stress, molecular inflammation and sarcopeniaThe proteasome inhibitor MG132 reduces immobilization-induced skeletal muscle atrophy in miceTWEAK causes myotube atrophy through coordinated activation of ubiquitin-proteasome system, autophagy, and caspases.TNF-related weak inducer of apoptosis (TWEAK) is a potent skeletal muscle-wasting cytokineCharacterization of GLPG0492, a selective androgen receptor modulator, in a mouse model of hindlimb immobilizationNF-κB activity in muscle from obese and type 2 diabetic subjects under basal and exercise-stimulated conditions.Identification of genes that elicit disuse muscle atrophy via the transcription factors p50 and Bcl-3.The ChIP-seq-defined networks of Bcl-3 gene binding support its required role in skeletal muscle atrophy.Nuclear factor-kappa B signaling in skeletal muscle atrophy.Bcl3 interacts cooperatively with peroxisome proliferator-activated receptor gamma (PPARgamma) coactivator 1alpha to coactivate nuclear receptors estrogen-related receptor alpha and PPARalphaInhibition of IkappaB kinase alpha (IKKα) or IKKbeta (IKKβ) plus forkhead box O (Foxo) abolishes skeletal muscle atrophy.Neurofibromin (Nf1) is required for skeletal muscle developmentC26 cancer-induced muscle wasting is IKKβ-dependent and NF-kappaB-independent.Expression of NF-kappaB and IkappaB proteins in skeletal muscle of gastric cancer patients.Central nervous system inflammation induces muscle atrophy via activation of the hypothalamic-pituitary-adrenal axis.The TWEAK-Fn14 system: breaking the silence of cytokine-induced skeletal muscle wasting.Interplay of IKK/NF-kappaB signaling in macrophages and myofibers promotes muscle degeneration in Duchenne muscular dystrophy.NF-κB in Aging and DiseaseMolecular events and signalling pathways involved in skeletal muscle disuse-induced atrophy and the impact of countermeasures.NO production results in suspension-induced muscle atrophy through dislocation of neuronal NOS.RNA-Seq Profiling of Intact and Enucleated Oocyte SCNT Embryos Reveals the Role of Pig Oocyte Nucleus in Somatic Reprogramming.Lack of NF-kappaB1 (p105/p50) attenuates unloading-induced downregulation of PPARalpha and PPARalpha-regulated gene expression in rodent heart.Transcriptome profile of rat genes in injured spinal cord at different stages by RNA-sequencing.
P2860
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P2860
Disruption of either the Nfkb1 or the Bcl3 gene inhibits skeletal muscle atrophy.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年学术文章
@wuu
2004年学术文章
@zh-cn
2004年学术文章
@zh-hans
2004年学术文章
@zh-my
2004年学术文章
@zh-sg
2004年學術文章
@yue
2004年學術文章
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2004年學術文章
@zh-hant
name
Disruption of either the Nfkb1 or the Bcl3 gene inhibits skeletal muscle atrophy.
@en
Disruption of either the Nfkb1 or the Bcl3 gene inhibits skeletal muscle atrophy.
@nl
type
label
Disruption of either the Nfkb1 or the Bcl3 gene inhibits skeletal muscle atrophy.
@en
Disruption of either the Nfkb1 or the Bcl3 gene inhibits skeletal muscle atrophy.
@nl
prefLabel
Disruption of either the Nfkb1 or the Bcl3 gene inhibits skeletal muscle atrophy.
@en
Disruption of either the Nfkb1 or the Bcl3 gene inhibits skeletal muscle atrophy.
@nl
P2860
P356
P1476
Disruption of either the Nfkb1 or the Bcl3 gene inhibits skeletal muscle atrophy.
@en
P2093
R Bridge Hunter
Susan C Kandarian
P2860
P304
P356
10.1172/JCI21696
P407
P577
2004-11-01T00:00:00Z