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Items: 1 to 20 of 33

1.

Tricarboxylic acid cycle dysfunction as a cause of human diseases and tumor formation.

Brière JJ, Favier J, Gimenez-Roqueplo AP, Rustin P.

Am J Physiol Cell Physiol. 2006 Dec;291(6):C1114-20. Epub 2006 Jun 7. Review.

2.

Disorders of pyruvate metabolism and the tricarboxylic acid cycle.

Pithukpakorn M.

Mol Genet Metab. 2005 Aug;85(4):243-6. Review. No abstract available.

PMID:
16156009
3.

A role for mitochondrial enzymes in inherited neoplasia and beyond.

Eng C, Kiuru M, Fernandez MJ, Aaltonen LA.

Nat Rev Cancer. 2003 Mar;3(3):193-202. Review.

PMID:
12612654
4.

Succinate dehydrogenase and fumarate hydratase: linking mitochondrial dysfunction and cancer.

King A, Selak MA, Gottlieb E.

Oncogene. 2006 Aug 7;25(34):4675-82. Review.

PMID:
16892081
5.

Biochemical assays for mitochondrial activity: assays of TCA cycle enzymes and PDHc.

Reisch AS, Elpeleg O.

Methods Cell Biol. 2007;80:199-222. Review. No abstract available.

PMID:
17445696
6.

Inborn and acquired metabolic defects in cancer.

Frezza C, Pollard PJ, Gottlieb E.

J Mol Med (Berl). 2011 Mar;89(3):213-20. doi: 10.1007/s00109-011-0728-4. Epub 2011 Feb 8. Review.

7.

The TCA cycle and tumorigenesis: the examples of fumarate hydratase and succinate dehydrogenase.

Pollard PJ, Wortham NC, Tomlinson IP.

Ann Med. 2003;35(8):632-9. Review.

PMID:
14708972
8.

Mitochondrial dysfunctions in cancer: genetic defects and oncogenic signaling impinging on TCA cycle activity.

Desideri E, Vegliante R, Ciriolo MR.

Cancer Lett. 2015 Jan 28;356(2 Pt A):217-23. doi: 10.1016/j.canlet.2014.02.023. Epub 2014 Mar 12. Review.

PMID:
24614286
9.

Revisiting the TCA cycle: signaling to tumor formation.

Raimundo N, Baysal BE, Shadel GS.

Trends Mol Med. 2011 Nov;17(11):641-9. doi: 10.1016/j.molmed.2011.06.001. Epub 2011 Jul 20. Review.

10.

Enzyme-enzyme interactions as modulators of the metabolic flux through the citric acid cycle.

Beeckmans S, Kanarek L.

Biochem Soc Symp. 1987;54:163-172. Review.

PMID:
3332992
11.

Molecular genetics of yeast TCA cycle isozymes.

McAlister-Henn L, Small WC.

Prog Nucleic Acid Res Mol Biol. 1997;57:317-39. Review. No abstract available.

PMID:
9175438
12.

Biologic lessons from mutations in the Kreb's cycle enzyme, fumarate hydratase.

McGrath JA.

J Invest Dermatol. 2003 Oct;121(4):vii. Review. No abstract available.

13.

Succinate dehydrogenase and human diseases: new insights into a well-known enzyme.

Rustin P, Munnich A, Rötig A.

Eur J Hum Genet. 2002 May;10(5):289-91. Review.

14.

Metabolic adaptation of Pseudomonas pseudoalcaligenes CECT5344 to cyanide: role of malate-quinone oxidoreductases, aconitase and fumarase isoenzymes.

Igeño MI, Becerra G, Guijo MI, Merchán F, Blasco R.

Biochem Soc Trans. 2011 Dec;39(6):1849-53. doi: 10.1042/BST20110714. Review.

PMID:
22103538
15.

Succinate dehydrogenase deficiency in human.

Brière JJ, Favier J, El Ghouzzi V, Djouadi F, Bénit P, Gimenez AP, Rustin P.

Cell Mol Life Sci. 2005 Oct;62(19-20):2317-24. Review.

PMID:
16143825
16.

Defects of pyruvate metabolism and the Krebs cycle.

De Meirleir L.

J Child Neurol. 2002 Dec;17 Suppl 3:3S26-33; discussion 3S33-4. Review.

PMID:
12597053
17.

Inborn errors of the Krebs cycle: a group of unusual mitochondrial diseases in human.

Rustin P, Bourgeron T, Parfait B, Chretien D, Munnich A, Rötig A.

Biochim Biophys Acta. 1997 Aug 22;1361(2):185-97. Review.

18.

[Fumarase deficiency].

Miyabayashi S.

Nihon Rinsho. 2002 Apr;60 Suppl 4:759-62. Review. Japanese. No abstract available.

PMID:
12013993
19.

Unsuspected task for an old team: succinate, fumarate and other Krebs cycle acids in metabolic remodeling.

Bénit P, Letouzé E, Rak M, Aubry L, Burnichon N, Favier J, Gimenez-Roqueplo AP, Rustin P.

Biochim Biophys Acta. 2014 Aug;1837(8):1330-7. doi: 10.1016/j.bbabio.2014.03.013. Epub 2014 Mar 31. Review.

20.

Genetically-defined metabolic reprogramming in cancer.

Mullen AR, DeBerardinis RJ.

Trends Endocrinol Metab. 2012 Nov;23(11):552-9. doi: 10.1016/j.tem.2012.06.009. Epub 2012 Jul 31. Review.

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