UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE) binds to alpha-actinin 1: novel pathways in skeletal muscle?
about
Insights into muscle degeneration from heritable inclusion body myopathiesGNE is involved in the early development of skeletal and cardiac muscleHereditary inclusion body myopathy: a decade of progressNon-specific accumulation of glycosphingolipids in GNE myopathyThe proteomic profile of hereditary inclusion body myopathyHereditary inclusion-body myopathy with sparing of the quadriceps: the many tiles of an incomplete puzzleGanglioside GM3 levels are altered in a mouse model of HIBM: GM3 as a cellular marker of the disease.Effects of altered sialic acid biosynthesis on N-linked glycan branching and cell surface interactionsUDP-GlcNAc 2-Epimerase/ManNAc Kinase (GNE): A Master Regulator of Sialic Acid Synthesis.Metabolic flux increases glycoprotein sialylation: implications for cell adhesion and cancer metastasis.Substantial deficiency of free sialic acid in muscles of patients with GNE myopathy and in a mouse modelThe hereditary inclusion body myopathy enigma and its future therapy.Beyond glycosylation: sialic acid precursors act as signaling molecules and are involved in cellular control of differentiation of PC12 cells.Regulation and pathophysiological implications of UDP-GlcNAc 2-epimerase/ManNAc kinase (GNE) as the key enzyme of sialic acid biosynthesis.Hereditary Inclusion Body Myopathy (HIBM2)The Interaction of UDP-N-Acetylglucosamine 2-Epimerase/N-Acetylmannosamine Kinase (GNE) and Alpha-Actinin 2 Is Altered in GNE Myopathy M743T Mutant.Mutation in GNE Downregulates Peroxiredoxin IV Altering ER Redox Homeostasis.GNE Myopathy and Cell Apoptosis: A Comparative Mutation Analysis.Role of IGF-1R in ameliorating apoptosis of GNE deficient cells.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 TreatmentFighting the Cause of Alzheimer's and GNE Myopathy
P2860
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P2860
UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE) binds to alpha-actinin 1: novel pathways in skeletal muscle?
description
2008 nî lūn-bûn
@nan
2008 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
UDP-N-acetylglucosamine 2-epim ...... l pathways in skeletal muscle?
@ast
UDP-N-acetylglucosamine 2-epim ...... l pathways in skeletal muscle?
@en
type
label
UDP-N-acetylglucosamine 2-epim ...... l pathways in skeletal muscle?
@ast
UDP-N-acetylglucosamine 2-epim ...... l pathways in skeletal muscle?
@en
prefLabel
UDP-N-acetylglucosamine 2-epim ...... l pathways in skeletal muscle?
@ast
UDP-N-acetylglucosamine 2-epim ...... l pathways in skeletal muscle?
@en
P2093
P2860
P1433
P1476
UDP-N-acetylglucosamine 2-epim ...... l pathways in skeletal muscle?
@en
P2093
Daniel G MacArthur
Kathryn N North
Michal Becker-Cohen
Sabine Krause
Shira Amsili
Stella Mitrani-Rosenbaum
Stephan Hinderlich
P2860
P356
10.1371/JOURNAL.PONE.0002477
P407
P577
2008-06-18T00:00:00Z