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Results 1 - 10 of 180 > >>
EC Number Disease PubMed ID Title of Publication Category Confidence Level
Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.32Alopecia 32901930 Novel small-insertion mutation in the LIPH gene in a patient with autosomal recessive woolly hair/hypotrichosis. causal interaction
unassigned
3
0
Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.32Carcinoma, Hepatocellular 9049257 Growth-inhibitory activity and downregulation of the class II tumor-suppressor gene H-rev107 in tumor cell lines and experimental tumors. causal interaction
ongoing research
therapeutic application
unassigned
2
4
1
0
Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.32Graves Disease 34166709 Phosphatidylserine-specific phospholipase A1: A friend or the devil in disguise. causal interaction
diagnostic usage
therapeutic application
unassigned
4
4
1
0
Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.32Hypersensitivity 12403934 Individual hymenoptera venom compounds induce upregulation of the basophil activation marker ectonucleotide pyrophosphatase/phosphodiesterase 3 (CD203c) in sensitized patients. causal interaction
therapeutic application
unassigned
1
1
0
Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.32Hypersensitivity 32784438 A Role of Newly Found Auxiliary Site in Phospholipase A1 from Thai Banded Tiger Wasp (Vespa affinis) in Its Enzymatic Enhancement: In Silico Homology Modeling and Molecular Dynamics Insights. causal interaction
unassigned
1
0
Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.32Paraplegia 27216551 A novel frameshift mutation of DDHD1 in a Japanese patient with autosomal recessive spastic paraplegia. causal interaction
unassigned
3
0
Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.32Paraplegia 33600578 Ddhd1 knockout mouse as a model of locomotive and physiological abnormality in familial spastic paraplegia. causal interaction
unassigned
1
0
Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.32Spastic Paraplegia, Hereditary 25178427 Inborn errors of metabolism in the biosynthesis and remodelling of phospholipids. causal interaction
unassigned
2
0
Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.32Spastic Paraplegia, Hereditary 26944165 Mitochondrial dysfunction in hereditary spastic paraparesis with mutations in DDHD1/SPG28. causal interaction
unassigned
2
0
Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.32Hypersensitivity 20359368 Recombinant phospholipase A1 (Ves v 1) from yellow jacket venom for improved diagnosis of hymenoptera venom hypersensitivity. causal interaction
diagnostic usage
therapeutic application
unassigned
1
2
3
0
Results 1 - 10 of 180 > >>