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EC Number Disease PubMed ID Title of Publication Category Confidence Level
Show all pathways known for 2.9.1.2Display the word mapDisplay the reaction diagram Show all sequences 2.9.1.2Hepatitis, Autoimmune 28690845 Diagnostic autoantibodies for autoimmune liver diseases. causal interaction
unassigned
1
0
Show all pathways known for 2.9.1.2Display the word mapDisplay the reaction diagram Show all sequences 2.9.1.2Infections 26975431 Selenoproteins of African trypanosomes are dispensable for parasite survival in a mammalian host. ongoing research
therapeutic application
unassigned
3
1
0
Show all pathways known for 2.9.1.2Display the word mapDisplay the reaction diagram Show all sequences 2.9.1.2Infections 28810614 Evolution of correlation between Helicobacter pylori infection and autoimmune liver disease. diagnostic usage
unassigned
2
0
Show all pathways known for 2.9.1.2Display the word mapDisplay the reaction diagram Show all sequences 2.9.1.2Liver Cirrhosis, Biliary 11360449 [Presence of SLA/LP autoantibodies in patients with primary biliary cirrhosis as a marker for secondary autoimmune hepatitis (overlap syndrome)] causal interaction
diagnostic usage
unassigned
1
4
0
Show all pathways known for 2.9.1.2Display the word mapDisplay the reaction diagram Show all sequences 2.9.1.2Liver Cirrhosis, Biliary 17456317 [The significance of anti-soluble liver antigen/liver-pancreas in diagnosing and typing autoimmune hepatitis] diagnostic usage
unassigned
1
0
Show all pathways known for 2.9.1.2Display the word mapDisplay the reaction diagram Show all sequences 2.9.1.2Liver Diseases 11826415 Fine specificity of autoantibodies to soluble liver antigen and liver/pancreas. causal interaction
diagnostic usage
unassigned
4
4
0
Show all pathways known for 2.9.1.2Display the word mapDisplay the reaction diagram Show all sequences 2.9.1.2Microcephaly 29464431 A SEPSECS mutation in a 23-year-old woman with microcephaly and progressive cerebellar ataxia. causal interaction
ongoing research
unassigned
2
1
0
Show all pathways known for 2.9.1.2Display the word mapDisplay the reaction diagram Show all sequences 2.9.1.2Neurodegenerative Diseases 29709707 Consequences of mutations and inborn errors of selenoprotein biosynthesis and functions. causal interaction
unassigned
4
0
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