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GNE gene

Known as: GLCNE, Uae1, glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase 
National Institutes of Health

Papers overview

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2016
2016
UDP‐N‐acetylglucosamine 2‐epimerase/N‐acetylmannosamine kinase (GNE) is the key enzyme for the biosynthesis of sialic acids… 
2013
2013
Hereditary Inclusion Body Myopathy (HIBM, IBM2, MIM:600737) is an autosomal recessive adult onset progressive muscle wasting… 
2011
2011
UDP-N-acetylglucosamine 2 epimerase/N-acetylmannosamime kinase (GNE) is a bifunctional enzyme which catalyzes the two key… 
2010
2010
Hereditary inclusion body myopathy (HIBM) is an autosomal recessive adult onset myopathy. It is characterized by mutations of the… 
2009
2009
Hereditary inclusion body myopathy-2 (HIBM2) is an adult-onset, muscular disease caused by mutations in the GNE gene. HIBM2… 
2008
2008
Axonal outgrowth is a prerequisite for the development of the most complex organ, the brain. It depends partially on the… 
Highly Cited
2002
Highly Cited
2002
Few Arabidopsis mutants defective in early male or female germline development have been reported. A novel extinction screen has… 
1967
1967
The crystal structure of Na2S2O6·2 H2O has been refined by means of single crystal X-ray intensity data. The structure of the…