N-Acetylneuraminic Acid

glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase ; Mus musculus







30 Article(s)
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1 34511508 Visualizing Muscle Sialic Acid Expression in the GNED207VTgGne-/- Cmah-/- Model of GNE Myopathy: A Comparison of Dietary and Gene Therapy Approaches. 2022 3
2 34224569 Uridine diphosphate-N-acetylglucosamine-2-epimerase/N-acetylmannosamine kinase deletion in mice leads to lethal intracerebral hemorrhage during embryonic development. 2021 Dec 18 2
3 32087947 Reduced sialylation triggers homeostatic synapse and neuronal loss in middle-aged mice. 2020 Apr 1
4 32439590 Long noncoding RNA Gm20319, acting as competing endogenous RNA, regulated GNE expression by sponging miR-7240-5p to involve in deoxynivalenol-induced liver damage in vitro. 2020 Jul 2
5 31073169 Galactosyl carbohydrate residues on hematopoietic stem/progenitor cells are essential for homing and engraftment to the bone marrow. 2019 May 9 1
6 28232658 [Therapeutic development for GNE myopathy.] 2017 3
7 28641925 Safety, pharmacokinetics and sialic acid production after oral administration of N-acetylmannosamine (ManNAc) to subjects with GNE myopathy. 2017 Sep 1
8 25850639 In vivo stimulation of early peripheral axon regeneration by N-propionylmannosamine in the presence of polysialyltransferase ST8SIA2. 2015 Sep 2
9 26329152 [Sialic Acid Replacement Therapy for Distal Myopathy with Rimmed Vacuoles]. 2015 Sep 1
10 25062695 Sialyllactose ameliorates myopathic phenotypes in symptomatic GNE myopathy model mice. 2014 Oct 2
11 23266873 Murine isoforms of UDP-GlcNAc 2-epimerase/ManNAc kinase: Secondary structures, expression profiles, and response to ManNAc therapy. 2013 Aug 1
12 24129184 The key enzyme of the sialic acid metabolism is involved in embryoid body formation and expression of marker genes of germ layer formation. 2013 Oct 14 1
13 24349002 Sialylation and muscle performance: sialic acid is a marker of muscle ageing. 2013 1
14 22157763 Peracetylated N-acetylmannosamine, a synthetic sugar molecule, efficiently rescues muscle phenotype and biochemical defects in mouse model of sialic acid-deficient myopathy. 2012 Jan 20 1
15 22253810 Glycoprotein hyposialylation gives rise to a nephrotic-like syndrome that is prevented by sialic acid administration in GNE V572L point-mutant mice. 2012 1
16 23122659 Oral monosaccharide therapies to reverse renal and muscle hyposialylation in a mouse model of GNE myopathy. 2012 Dec 3
17 21731727 GNE is involved in the early development of skeletal and cardiac muscle. 2011 1
18 19797319 Lessons from GNE-deficient embryonic stem cells: sialic acid biosynthesis is involved in proliferation and gene expression. 2010 Jan 2
19 20383336 Ganglioside GM3 levels are altered in a mouse model of HIBM: GM3 as a cellular marker of the disease. 2010 Apr 7 1
20 20548120 [Animal model of distal myopathy with rimmed vacuoles/hereditary inclusion body myopathy and preclinical trial with sugar compounds]. 2010 Jun 3
21 19426133 Regulation and pathophysiological implications of UDP-GlcNAc 2-epimerase/ManNAc kinase (GNE) as the key enzyme of sialic acid biosynthesis. 2009 Jul 1
22 19448634 Prophylactic treatment with sialic acid metabolites precludes the development of the myopathic phenotype in the DMRV-hIBM mouse model. 2009 Jun 1
23 20030229 [Development of therapy for distal myopathy with rimmed vacuoles]. 2009 Nov 1
24 18628337 Muscle weakness correlates with muscle atrophy and precedes the development of inclusion body or rimmed vacuoles in the mouse model of DMRV/hIBM. 2008 Sep 17 2
25 17164266 A Gne knockout mouse expressing human V572L mutation develops features similar to distal myopathy with rimmed vacuoles or hereditary inclusion body myopathy. 2007 Jan 15 1
26 17235685 Reduced sialylation status in UDP-N-acetylglucosamine-2-epimerase/N-acetylmannosamine kinase (GNE)-deficient mice. 2007 Apr 2
27 17471014 Autophagy in a mouse model of distal myopathy with rimmed vacuoles or hereditary inclusion body myopathy. 2007 Jul-Aug 1
28 17549251 Sizing up sialic acid in glomerular disease. 2007 Jun 1
29 17549255 Mutation in the key enzyme of sialic acid biosynthesis causes severe glomerular proteinuria and is rescued by N-acetylmannosamine. 2007 Jun 1
30 17704511 A Gne knockout mouse expressing human GNE D176V mutation develops features similar to distal myopathy with rimmed vacuoles or hereditary inclusion body myopathy. 2007 Nov 15 1