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Results 1 - 10 of 38 > >>
EC Number Disease PubMed ID Title of Publication Category Confidence Level
Display the word mapDisplay the reaction diagram Show all sequences 3.4.22.43Myasthenia Gravis 12925692 Cathepsin V is involved in the degradation of invariant chain in human thymus and is overexpressed in myasthenia gravis. causal interaction
diagnostic usage
unassigned
3
1
0
Display the word mapDisplay the reaction diagram Show all sequences 3.4.22.43Keratoconus 15728537 Increased levels of catalase and cathepsin V/L2 but decreased TIMP-1 in keratoconus corneas: evidence that oxidative stress plays a role in this disorder. causal interaction
diagnostic usage
ongoing research
therapeutic application
4
2
4
1
Display the word mapDisplay the reaction diagram Show all sequences 3.4.22.43Arthritis 17869649 Polymorphisms in the cathepsin L2 (CTSL2) gene show association with type 1 diabetes and early-onset myasthenia gravis. causal interaction
diagnostic usage
ongoing research
therapeutic application
3
3
4
1
Display the word mapDisplay the reaction diagram Show all sequences 3.4.22.43Arthritis, Juvenile 17869649 Polymorphisms in the cathepsin L2 (CTSL2) gene show association with type 1 diabetes and early-onset myasthenia gravis. causal interaction
diagnostic usage
ongoing research
therapeutic application
3
3
4
1
Display the word mapDisplay the reaction diagram Show all sequences 3.4.22.43Arthritis, Rheumatoid 17869649 Polymorphisms in the cathepsin L2 (CTSL2) gene show association with type 1 diabetes and early-onset myasthenia gravis. causal interaction
diagnostic usage
ongoing research
therapeutic application
3
3
4
1
Display the word mapDisplay the reaction diagram Show all sequences 3.4.22.43Autoimmune Diseases 17869649 Polymorphisms in the cathepsin L2 (CTSL2) gene show association with type 1 diabetes and early-onset myasthenia gravis. causal interaction
diagnostic usage
ongoing research
therapeutic application
3
3
4
1
Display the word mapDisplay the reaction diagram Show all sequences 3.4.22.43Alopecia 17934903 Evaluation of the CTSL2 Gene as a Candidate Gene For Alopecia X in Pomeranians and Keeshonden. causal interaction
diagnostic usage
ongoing research
therapeutic application
1
1
2
1
Display the word mapDisplay the reaction diagram Show all sequences 3.4.22.43Dermatitis, Atopic 19438477 The cystatin M / E-controlled pathway of skin barrier formation: expression of its key components in psoriasis and atopic dermatitis. causal interaction
diagnostic usage
therapeutic application
unassigned
3
4
1
0
Display the word mapDisplay the reaction diagram Show all sequences 3.4.22.43Psoriasis 19438477 The cystatin M / E-controlled pathway of skin barrier formation: expression of its key components in psoriasis and atopic dermatitis. causal interaction
diagnostic usage
therapeutic application
unassigned
3
4
1
0
Display the word mapDisplay the reaction diagram Show all sequences 3.4.22.43Atherosclerosis 20578711 Solution phase synthesis of a combinatorial library of chalcones and flavones as potent cathepsin V inhibitors. causal interaction
therapeutic application
unassigned
4
4
0
Results 1 - 10 of 38 > >>