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Results 1 - 10 of 120 > >>
EC Number Disease PubMed ID Title of Publication Category Confidence Level
Display the word mapDisplay the reaction diagram Show all sequences 3.4.24.84Colorectal Neoplasms 27729169 Mutational and expressional alterations of ZMPSTE24, DNA damage response-related gene, in gastric and colorectal cancers. causal interaction
diagnostic usage
ongoing research
unassigned
2
3
4
0
Display the word mapDisplay the reaction diagram Show all sequences 3.4.24.84Laminopathies 16297189 Homozygous and compound heterozygous mutations in ZMPSTE24 cause the laminopathy restrictive dermopathy. causal interaction
unassigned
3
0
Display the word mapDisplay the reaction diagram Show all sequences 3.4.24.84Laminopathies 16364671 Laminopathies: multisystem dystrophy syndromes. causal interaction
unassigned
3
0
Display the word mapDisplay the reaction diagram Show all sequences 3.4.24.84Laminopathies 19645629 LMNA, ZMPSTE24, and LBR are not mutated in scleroderma. causal interaction
unassigned
1
0
Display the word mapDisplay the reaction diagram Show all sequences 3.4.24.84Laminopathies 20074077 HIV protease inhibitors inhibit FACE1/ZMPSTE24: a mechanism for acquired lipodystrophy in patients on highly active antiretroviral therapy? causal interaction
therapeutic application
unassigned
4
4
0
Display the word mapDisplay the reaction diagram Show all sequences 3.4.24.84Laminopathies 27120622 A Heterozygous ZMPSTE24 Mutation Associated with Severe Metabolic Syndrome, Ectopic Fat Accumulation, and Dilated Cardiomyopathy. causal interaction
ongoing research
therapeutic application
unassigned
4
1
1
0
Display the word mapDisplay the reaction diagram Show all sequences 3.4.24.84Laminopathies 33590450 Lonafarnib: First Approval. causal interaction
therapeutic application
unassigned
2
4
0
Display the word mapDisplay the reaction diagram Show all sequences 3.4.24.84Lipodystrophy 26602028 A novel homozygous LMNA mutation (p.Met540Ile) causes mandibuloacral dysplasia type A. causal interaction
unassigned
3
0
Display the word mapDisplay the reaction diagram Show all sequences 3.4.24.84Progeria 19851476 Genomic Instability and DNA Damage Responses in Progeria Arising from Defective Maturation of Prelamin A. causal interaction
unassigned
4
0
Display the word mapDisplay the reaction diagram Show all sequences 3.4.24.84Progeria 20458013 Prelamin A acts to accelerate smooth muscle cell senescence and is a novel biomarker of human vascular aging. causal interaction
unassigned
4
0
Results 1 - 10 of 120 > >>