| 1 |
35052006 | Novel GNE Gene Variants Associated with Severe Congenital Thrombocytopenia and Platelet Sialylation Defect. | 2022 Jan 20 |
1 |
| 2 |
32053088 | Sialuria-Related Intellectual Disability in Children and Adolescent of Pakistan: Tenth Patient Described has a Novel Mutation in the GNE Gene. | 2020 |
1 |
| 3 |
32350996 | Multifaceted role of glycosylation in transfusion medicine, platelets, and red blood cells. | 2020 Jul |
1 |
| 4 |
31744945 | The Inherited Neuromuscular Disorder GNE Myopathy: Research to Patient Care. | 2019 Sep-Oct |
2 |
| 5 |
28505249 | Sialic acid deficiency is associated with oxidative stress leading to muscle atrophy and weakness in GNE myopathy. | 2017 Aug 15 |
1 |
| 6 |
27037841 | Aberrant O-GlcNAcylation disrupts GNE enzyme activity in GNE myopathy. | 2016 Jun |
1 |
| 7 |
18815882 | Biochemical characterization of human and murine isoforms of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE). | 2009 May |
2 |
| 8 |
19426133 | Regulation and pathophysiological implications of UDP-GlcNAc 2-epimerase/ManNAc kinase (GNE) as the key enzyme of sialic acid biosynthesis. | 2009 Jul |
2 |
| 9 |
17597614 | Prediction of three different isoforms of the human UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase. | 2007 Jul 10 |
2 |
| 10 |
17118363 | The collapsin response mediator protein 1 (CRMP-1) and the promyelocytic leukemia zinc finger protein (PLZF) bind to UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE), the key enzyme of sialic acid biosynthesis. | 2006 Dec 11 |
1 |
| 11 |
15498764 | Characterization of ligand binding to the bifunctional key enzyme in the sialic acid biosynthesis by NMR: I. Investigation of the UDP-GlcNAc 2-epimerase functionality. | 2004 Dec 31 |
1 |