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EC Number Disease PubMed ID Title of Publication Category Confidence Level
Display the word mapDisplay the reaction diagram Show all sequences 1.21.1.1Goiter 443737 [Quantitative aspects of iodine metabolism in one case of congenital iodotyrosine deiodinase defect (author's transl)] unassigned 0
Display the word mapDisplay the reaction diagram Show all sequences 1.21.1.1Hypothyroidism 443737 [Quantitative aspects of iodine metabolism in one case of congenital iodotyrosine deiodinase defect (author's transl)] unassigned 0
Display the word mapDisplay the reaction diagram Show all sequences 1.21.1.1Thyroid Diseases 5913151 Iodotyrosine deiodinase isozymes in the normal and in thyroid diseases. ongoing research
unassigned
2
0
Display the word mapDisplay the reaction diagram Show all sequences 1.21.1.1Graves Disease 17322488 Characterisation of DEHAL1 expression in thyroid pathologies. causal interaction
diagnostic usage
unassigned
3
1
0
Display the word mapDisplay the reaction diagram Show all sequences 1.21.1.1Thyroid Cancer, Papillary 17322488 Characterisation of DEHAL1 expression in thyroid pathologies. causal interaction
diagnostic usage
unassigned
3
1
0
Display the word mapDisplay the reaction diagram Show all sequences 1.21.1.1Thyroid Carcinoma, Anaplastic 17322488 Characterisation of DEHAL1 expression in thyroid pathologies. causal interaction
diagnostic usage
unassigned
3
1
0
Display the word mapDisplay the reaction diagram Show all sequences 1.21.1.1Thyroid Neoplasms 17322488 Characterisation of DEHAL1 expression in thyroid pathologies. causal interaction
diagnostic usage
unassigned
3
1
0
Display the word mapDisplay the reaction diagram Show all sequences 1.21.1.1Thyroid Nodule 17322488 Characterisation of DEHAL1 expression in thyroid pathologies. causal interaction
diagnostic usage
unassigned
3
1
0
Display the word mapDisplay the reaction diagram Show all sequences 1.21.1.1Thyrotoxicosis 17322488 Characterisation of DEHAL1 expression in thyroid pathologies. causal interaction
diagnostic usage
unassigned
3
1
0
Display the word mapDisplay the reaction diagram Show all sequences 1.21.1.1Congenital Hypothyroidism 18434651 Mutations in the iodotyrosine deiodinase gene and hypothyroidism. causal interaction
unassigned
4
0
Results 1 - 10 of 25 > >>