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1975
2025

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1975 1
1976 3
1977 1
1978 1
1979 1
1981 3
1982 1
1983 1
1985 4
1986 1
1988 3
1989 1
1994 1
1996 3
1998 2
1999 1
2000 1
2001 3
2002 5
2005 2
2006 2
2010 1
2013 2
2014 1
2016 2
2017 2
2018 1
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2025 0

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51 results

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Page 1
Manganese metabolism in humans.
Chen P, Bornhorst J, Aschner M. Chen P, et al. Front Biosci (Landmark Ed). 2018 Mar 1;23(9):1655-1679. doi: 10.2741/4665. Front Biosci (Landmark Ed). 2018. PMID: 29293455 Free article. Review.
Manganese (Mn) is an essential nutrient for intracellular activities; it functions as a cofactor for a variety of enzymes, including arginase, glutamine synthetase (GS), pyruvate carboxylase and Mn superoxide dismutase (Mn-SOD). Through these metalloproteins, Mn pla …
Manganese (Mn) is an essential nutrient for intracellular activities; it functions as a cofactor for a variety of enzymes, including arginas …
Pyruvate carboxylase.
Wallace JC, Jitrapakdee S, Chapman-Smith A. Wallace JC, et al. Int J Biochem Cell Biol. 1998 Jan;30(1):1-5. doi: 10.1016/s1357-2725(97)00147-7. Int J Biochem Cell Biol. 1998. PMID: 9597748 Review.
Pyruvate carboxylase [EC 6.4.1.1] is a member of the family of biotin-dependent carboxylases and is found widely among eukaryotic tissues and in many prokaryotic species. ...Diabetes and hyperthyroidism increase the level of expression of pyruvate carboxyl
Pyruvate carboxylase [EC 6.4.1.1] is a member of the family of biotin-dependent carboxylases and is found widely among eukaryo
Pyruvate carboxylase deficiency: mechanisms, mimics and anaplerosis.
Marin-Valencia I, Roe CR, Pascual JM. Marin-Valencia I, et al. Mol Genet Metab. 2010 Sep;101(1):9-17. doi: 10.1016/j.ymgme.2010.05.004. Epub 2010 Jun 9. Mol Genet Metab. 2010. PMID: 20598931 Review.
Pyruvate carboxylase (PC) is a regulated mitochondrial enzyme that catalyzes the conversion of pyruvate to oxaloacetate, a critical transition that replenishes citric acid cycle intermediates and facilitates other biosynthetic reactions that drive anabolism.
Pyruvate carboxylase (PC) is a regulated mitochondrial enzyme that catalyzes the conversion of pyruvate to oxaloacetate
Multiple carboxylase deficiency.
Nyhan WL. Nyhan WL. Int J Biochem. 1988;20(4):363-70. doi: 10.1016/0020-711x(88)90202-9. Int J Biochem. 1988. PMID: 3284772 Review.
1. The multiple carboxylase deficiencies are inborn errors in the metabolism of biotin in which there is defective activity of propionyl CoA carboxylase, 3-methylcrotonyl CoA carboxylase and pyruvate carboxylase. 2. ...
1. The multiple carboxylase deficiencies are inborn errors in the metabolism of biotin in which there is defective activity of propio …
Disorders of gluconeogenesis.
van den Berghe G. van den Berghe G. J Inherit Metab Dis. 1996;19(4):470-7. doi: 10.1007/BF01799108. J Inherit Metab Dis. 1996. PMID: 8884571 Review.
Gluconeogenesis, or the formation of glucose from mainly lactate/ pyruvate, glycerol and alanine, plays an essential role in the maintenance of normoglycaemia during fasting. Inborn deficiencies are known of each of the four enzymes of the glycolytic-gluconeogenic pathway …
Gluconeogenesis, or the formation of glucose from mainly lactate/ pyruvate, glycerol and alanine, plays an essential role in the main …
Mitochondrial myopathies.
DiMauro S, Bonilla E, Zeviani M, Nakagawa M, DeVivo DC. DiMauro S, et al. Ann Neurol. 1985 Jun;17(6):521-38. doi: 10.1002/ana.410170602. Ann Neurol. 1985. PMID: 3927817 Review.
[Pyruvate carboxylase deficiency].
Naito E. Naito E. Nihon Rinsho. 2002 Apr;60 Suppl 4:755-8. Nihon Rinsho. 2002. PMID: 12013992 Review. Japanese. No abstract available.
[Pyruvate carboxylase deficiency].
Naito E. Naito E. Ryoikibetsu Shokogun Shirizu. 1998;(18 Pt 1):345-7. Ryoikibetsu Shokogun Shirizu. 1998. PMID: 9590065 Review. Japanese. No abstract available.
Disorders of pyruvate metabolism.
De Meirleir L. De Meirleir L. Handb Clin Neurol. 2013;113:1667-73. doi: 10.1016/B978-0-444-59565-2.00034-4. Handb Clin Neurol. 2013. PMID: 23622387 Review.
Pyruvate dehydrogenase and pyruvate carboxylase deficiency are the most common disorders in pyruvate metabolism. ...Deficiencies in the other subunits have also been described, but in a smaller number of patients. Pyruvate carboxylase
Pyruvate dehydrogenase and pyruvate carboxylase deficiency are the most common disorders in pyruvate meta
Biotin.
McCormick DB. McCormick DB. Nutr Rev. 1975 Apr;33(4):97-102. doi: 10.1111/j.1753-4887.1975.tb07426.x. Nutr Rev. 1975. PMID: 236527 Review. No abstract available.
51 results