Urea Cycle Disorder
About the Disease
Urea Cycle Disorder, also known as urea cycle disorders, inborn, is related to carbamoyl phosphate synthetase i deficiency, hyperammonemia due to and n-acetylglutamate synthase deficiency. An important gene associated with Urea Cycle Disorder is SLC25A13 (Solute Carrier Family 25 Member 13), and among its related pathways/superpathways are Metabolism and Regulation of expression of SLITs and ROBOs. The drugs 4-phenylbutyric acid and Protective Agents have been mentioned in the context of this disorder. Affiliated tissues include brain, liver and prefrontal cortex, and related phenotypes are no effect and no effect
Common Targets
G1610 | G1373 | G383 | P6058 | G35 | Chaperone (nonspecified subtype) | G162417 | Histone deacetylase (nonspecified subtype) | Pyruvate dehydrogenase kinase (nonspecified subtype) | G5009
The "Target / Biomarker Review Report" is a comprehensive and customizable review of hundreds up to thousends of related scientific research literature by AI technology, covering specific information about the Target(s) / Biomarker(s) of your choice related to Urea Cycle Disorder, including but not limited to:
• general information;
• protein structure and compound binding;
• protein biological mechanisms;
• its importance;
• the target screening and validation;
• expression level;
• disease relevance;
• drug resistance;
• related combination drugs;
• pharmacochemistry experiments;
• related patent analysis;
• advantages and risks of development, etc.
The report is helpful for project application, drug molecule design, research progress updates, publication of research papers, patent applications, etc. If you are interested to get a full version of this report, please feel free to contact us at BD@silexon.ai
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