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<< < Results 11 - 20 of 38 > >>
EC Number Disease PubMed ID Title of Publication Category Confidence Level
Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.106Congenital, Hereditary, and Neonatal Diseases and Abnormalities 30619475 Mono-ADP-Ribosylhydrolase MACROD2 Is Dispensable for Murine Responses to Metabolic and Genotoxic Insults. causal interaction
ongoing research
therapeutic application
unassigned
3
2
1
0
Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.106Fatty Liver 25975270 Loss of the Mono-ADP-ribosyltransferase, Tiparp, Increases Sensitivity to Dioxin-induced Steatohepatitis and Lethality. causal interaction
ongoing research
therapeutic application
unassigned
1
1
2
0
Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.106Graves Disease 27304844 Association of Polymorphisms in MACRO Domain Containing 2 With Thyroid-Associated Orbitopathy. causal interaction
unassigned
4
0
Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.106Insulin Resistance 30343302 High Genetic Risk Scores of ASIC2, MACROD2, CHRM3, and C2orf83 Genetic Variants Associated with Polycystic Ovary Syndrome Impair Insulin Sensitivity and Interact with Energy Intake in Korean Women. diagnostic usage
unassigned
3
0
Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.106Intellectual Disability 30619475 Mono-ADP-Ribosylhydrolase MACROD2 Is Dispensable for Murine Responses to Metabolic and Genotoxic Insults. causal interaction
ongoing research
therapeutic application
unassigned
3
2
1
0
Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.106Intellectual Disability 31055587 Intragenic Deletion in MACROD2: A Family with Complex Phenotypes Including Microcephaly, Intellectual Disability, Polydactyly, Renal and Pancreatic Malformations. diagnostic usage
unassigned
3
0
Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.106Microcephaly 31055587 Intragenic Deletion in MACROD2: A Family with Complex Phenotypes Including Microcephaly, Intellectual Disability, Polydactyly, Renal and Pancreatic Malformations. diagnostic usage
unassigned
3
0
Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.106Neoplasm Metastasis 25422431 MACROD2 overexpression mediates estrogen independent growth and tamoxifen resistance in breast cancers. causal interaction
diagnostic usage
ongoing research
therapeutic application
4
4
2
1
Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.106Neoplasm Metastasis 32257385 MACROD2 deficiency promotes hepatocellular carcinoma growth and metastasis by activating GSK-3?/?-catenin signaling. causal interaction
diagnostic usage
ongoing research
unassigned
4
4
1
0
Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.106Neoplasms 23805207 Two Distinct Categories of Focal Deletions in Cancer Genomes. ongoing research
therapeutic application
unassigned
2
1
0
<< < Results 11 - 20 of 38 > >>