Autophagy in a mouse model of distal myopathy with rimmed vacuoles or hereditary inclusion body myopathy.
about
X-linked myopathy with excessive autophagy: a failure of self-eatingNon-specific accumulation of glycosphingolipids in GNE myopathyGanglioside GM3 levels are altered in a mouse model of HIBM: GM3 as a cellular marker of the disease.Autophagy activation reduces renal tubular injury induced by urinary proteins.UDP-GlcNAc 2-Epimerase/ManNAc Kinase (GNE): A Master Regulator of Sialic Acid Synthesis.Perspectives on distal myopathy with rimmed vacuoles or hereditary inclusion body myopathy: contributions from an animal model. Lack of sialic acid, a central determinant in sugar chains, causes myopathy?Aquaporin-4 expression in distal myopathy with rimmed vacuoles.A preclinical trial of sialic acid metabolites on distal myopathy with rimmed vacuoles/hereditary inclusion body myopathy, a sugar-deficient myopathy: a review.Rimmed vacuoles in Becker muscular dystrophy have similar features with inclusion myopathies.Autophagy-Lysosome Pathway in Renal Tubular Epithelial Cells Is Disrupted by Advanced Glycation End Products in Diabetic NephropathyDiagnosis and treatment of inflammatory myopathy: issues and management.Unfolded protein response and activated degradative pathways regulation in GNE myopathy.Hereditary inclusion-body myopathy: clues on pathogenesis and possible therapy.Rhein Inhibits Autophagy in Rat Renal Tubular Cells by Regulation of AMPK/mTOR Signaling.Diet-induced obesity impairs spermatogenesis: a potential role for autophagy.Animal models of inflammatory myopathy.New ALS-Related Genes Expand the Spectrum Paradigm of Amyotrophic Lateral Sclerosis.Sialic acid deficiency is associated with oxidative stress leading to muscle atrophy and weakness in GNE myopathy.Prophylactic treatment with sialic acid metabolites precludes the development of the myopathic phenotype in the DMRV-hIBM mouse model.Variable phenotypes of knockin mice carrying the M712T Gne mutation.GNE myopathy: from clinics and genetics to pathology and research strategies.Function and Mutations of the GNE Gene Leading to Distal Myopathy with Rimmed Vacuoles/Hereditary Inclusion-Body Myopathy, Animal Models, and Potential TreatmentMuscle weakness correlates with muscle atrophy and precedes the development of inclusion body or rimmed vacuoles in the mouse model of DMRV/hIBMAutophagy Mechanism, Regulation, Functions, and Disorders
P2860
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P2860
Autophagy in a mouse model of distal myopathy with rimmed vacuoles or hereditary inclusion body myopathy.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年学术文章
@wuu
2007年学术文章
@zh
2007年学术文章
@zh-cn
2007年学术文章
@zh-hans
2007年学术文章
@zh-my
2007年学术文章
@zh-sg
2007年學術文章
@yue
2007年學術文章
@zh-hant
name
Autophagy in a mouse model of ...... itary inclusion body myopathy.
@en
Autophagy in a mouse model of ...... itary inclusion body myopathy.
@nl
type
label
Autophagy in a mouse model of ...... itary inclusion body myopathy.
@en
Autophagy in a mouse model of ...... itary inclusion body myopathy.
@nl
prefLabel
Autophagy in a mouse model of ...... itary inclusion body myopathy.
@en
Autophagy in a mouse model of ...... itary inclusion body myopathy.
@nl
P2093
P356
P1433
P1476
Autophagy in a mouse model of ...... itary inclusion body myopathy.
@en
P2093
Ichizo Nishino
May Christine V Malicdan
Satoru Noguchi
P304
P356
10.4161/AUTO.4270
P577
2007-07-12T00:00:00Z