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Cited by 725

The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.

R EGULATION OF E NZYMES OF THE U REA C YCLE AND A RGININE M ETABOLISM

Morris, Sidney M.·2002·Annual Review of Nutrition

Abstract

▪ Abstract The urea cycle is comprised of five enzymes but also requires other enzymes and mitochondrial amino acid transporters to function fully. The complete urea cycle is expressed in liver and to a small degree also in enterocytes. However, highly regulated expression of several enzymes present in the urea cycle occurs also in many other tissues, where these enzymes are involved in synthesis of nitric oxide, polyamines, proline and glutamate. Glucagon, insulin, and glucocorticoids are major regulators of the expression of urea cycle enzymes in liver. In contrast, the “urea cycle” enzymes in nonhepatic cells are regulated by a wide range of pro- and antiinflammatory cytokines and other agents. Regulation of these enzymes is largely transcriptional in virtually all cell types. This review emphasizes recent information regarding roles and regulation of urea cycle and arginine metabolic enzymes in liver and other cell types.

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Metadata

Authors
Morris, S. M.
Venue
Annual Review of Nutrition
Published
2002-07
Volume
22
Issue
1
Pages
87-105
ISSN
  • 0199-9885 (ISSN-L)
  • 1545-4312
OpenAlex
W2109163588
Cited by
725
References
3
FWCI
1.57
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: R EGULATION OF E NZYMES OF THE U REA C YCLE AND A RGININE M ETABOLISM. https://app.cochat.ai/papers/10.1146/annurev.nutr.22.110801.140547
The paper
Morris, S. M. (2002). R EGULATION OF E NZYMES OF THE U REA C YCLE AND A RGININE M ETABOLISM. Annual Review of Nutrition. https://doi.org/10.1146/annurev.nutr.22.110801.140547

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.