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EC Number
Disease
PubMed ID
Title of Publication
Category
Confidence Level
Myasthenic Syndromes, Congenital
A 3'-UTR mutation creates a microRNA target site in the GFPT1 gene of patients with congenital myasthenic syndrome.
unassigned
0
Myasthenic Syndromes, Congenital
A 3'-UTR mutation creates a microRNA target site in the GFPT1 gene of patients with congenital myasthenic syndrome.
therapeutic application
1
Myasthenic Syndromes, Congenital
A 3'-UTR mutation creates a microRNA target site in the GFPT1 gene of patients with congenital myasthenic syndrome.
causal interaction
2
Hyperglycemia
A Genetic Model to Study Increased Hexosamine Biosynthetic Flux.
unassigned
0
Hyperglycemia
A Genetic Model to Study Increased Hexosamine Biosynthetic Flux.
therapeutic application
2
Hyperglycemia
A Genetic Model to Study Increased Hexosamine Biosynthetic Flux.
causal interaction
2
Insulin Resistance
A Genetic Model to Study Increased Hexosamine Biosynthetic Flux.
therapeutic application
2
Insulin Resistance
A Genetic Model to Study Increased Hexosamine Biosynthetic Flux.
unassigned
0
Insulin Resistance
A Genetic Model to Study Increased Hexosamine Biosynthetic Flux.
causal interaction
2
Insulin Resistance
Activation of the hexosamine signaling pathway in adipose tissue results in decreased serum adiponectin and skeletal muscle insulin resistance.
unassigned
0
Results 1 - 10 of 220 > >>