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GNE gene
Known as:
GLCNE
, Uae1
, glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase
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National Institutes of Health
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Aberrant O‐GlcNAcylation disrupts GNE enzyme activity in GNE myopathy
Dorit Bennmann
,
Wenke Weidemann
,
A. Thate
,
Denise Kreuzmann
,
R. Horstkorte
The FEBS Journal
2016
Corpus ID: 44754198
UDP‐N‐acetylglucosamine 2‐epimerase/N‐acetylmannosamine kinase (GNE) is the key enzyme for the biosynthesis of sialic acids…
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2013
2013
Novel GNE mutations in autosomal recessive hereditary inclusion body myopathy patients.
Daniel No
,
Y. Valles-Ayoub
,
+8 authors
D. Darvish
Genetic Testing and Molecular Biomarkers
2013
Corpus ID: 22299443
Hereditary Inclusion Body Myopathy (HIBM, IBM2, MIM:600737) is an autosomal recessive adult onset progressive muscle wasting…
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2011
2011
GNE Is Involved in the Early Development of Skeletal and Cardiac Muscle
Irit Milman Krentsis
,
I. Sela
,
+4 authors
S. Mitrani-Rosenbaum
PLoS ONE
2011
Corpus ID: 1516944
UDP-N-acetylglucosamine 2 epimerase/N-acetylmannosamime kinase (GNE) is a bifunctional enzyme which catalyzes the two key…
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2010
2010
Hereditary inclusion body myopathy: single patient response to GNE gene Lipoplex therapy
G. Nemunaitis
,
P. Maples
,
+11 authors
J. Nemunaitis
Journal of Gene Medicine
2010
Corpus ID: 10737897
Hereditary inclusion body myopathy (HIBM) is an autosomal recessive adult onset myopathy. It is characterized by mutations of the…
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2009
2009
Safety and in vivo Expression of a GNE-Transgene: A Novel Treatment Approach for Hereditary Inclusion Body Myopathy-2
A. Phadke
,
C. Jay
,
+10 authors
J. Nemunaitis
Gene Regulation and Systems Biology
2009
Corpus ID: 31577537
Hereditary inclusion body myopathy-2 (HIBM2) is an adult-onset, muscular disease caused by mutations in the GNE gene. HIBM2…
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2008
2008
The key enzyme of sialic acid biosynthesis (GNE) promotes neurite outgrowth of PC12 cells
M. Kontou
,
Wenke Weidemann
,
C. Bauer
,
W. Reutter
,
R. Horstkorte
NeuroReport
2008
Corpus ID: 44679641
Axonal outgrowth is a prerequisite for the development of the most complex organ, the brain. It depends partially on the…
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Review
2003
Review
2003
Magnesium may help patients with recessive hereditary inclusion body myopathy, a pathological review.
D. Darvish
Medical Hypotheses
2003
Corpus ID: 22365691
Review
2002
Review
2002
Four novel mutations associated with autosomal recessive inclusion body myopathy (MIM: 600737).
D. Darvish
,
P. Vahedifar
,
Y. Huo
Molecular Genetics and Metabolism
2002
Corpus ID: 32574973
Highly Cited
2002
Highly Cited
2002
A novel extinction screen in Arabidopsis thaliana identifies mutant plants defective in early microsporangial development.
A. Sorensen
,
F. Guerineau
,
C. Canales-Holzeis
,
H. Dickinson
,
R. Scott
The Plant Journal
2002
Corpus ID: 19983238
Few Arabidopsis mutants defective in early male or female germline development have been reported. A novel extinction screen has…
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1967
1967
Dynamics of Water in Crystal Hydrates
I. Berthold
,
A. Weiss
1967
Corpus ID: 3458166
The crystal structure of Na2S2O6·2 H2O has been refined by means of single crystal X-ray intensity data. The structure of the…
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