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22 in total

1. Mitochondrial Citrate Transporter-dependent Metabolic Signature in the 22q11.2 Deletion Syndrome.

Authors: Eleonora Napoli; Flora Tassone; Sarah Wong; Kathleen Angkustsiri; Tony J Simon; Gyu Song; Cecilia Giulivi
Journal: J Biol Chem Date: 2015-07-28 Impact factor: 5.157

2. SIRT3 deacetylates and increases pyruvate dehydrogenase activity in cancer cells.

Authors: Ozkan Ozden; Seong-Hoon Park; Brett A Wagner; Ha Yong Song; Yueming Zhu; Athanassios Vassilopoulos; Barbara Jung; Garry R Buettner; David Gius
Journal: Free Radic Biol Med Date: 2014-08-22 Impact factor: 7.376

Review 3. Lactic acidosis in sepsis: a commentary.

Authors: G Gutierrez; M E Wulf
Journal: Intensive Care Med Date: 1996-01 Impact factor: 17.440

4. The X-chromosomal NDUFA1 gene of complex I in mitochondrial encephalomyopathies: tissue expression and mutation detection.

Authors: J Loeffen; R Smeets; J Smeitink; W Ruitenbeek; A Janssen; E Mariman; R Sengers; F Trijbels; L van den Heuvel
Journal: J Inherit Metab Dis Date: 1998-06 Impact factor: 4.982

5. Detection of mitochondrial defects by laser fluorimetry.

Authors: W S Kunz; K Winkler; A V Kuznetsov; H Lins; E Kirches; C W Wallesch
Journal: Mol Cell Biochem Date: 1997-09 Impact factor: 3.396

6. A genomewide linkage-disequilibrium scan localizes the Saguenay-Lac-Saint-Jean cytochrome oxidase deficiency to 2p16.

Authors: N Lee; M J Daly; T Delmonte; E S Lander; F Xu; T J Hudson; G A Mitchell; C C Morin; B H Robinson; J D Rioux
Journal: Am J Hum Genet Date: 2001-01-10 Impact factor: 11.025

Review 7. Disorders of pyruvate carboxylase and the pyruvate dehydrogenase complex.

Authors: B H Robinson; N MacKay; K Chun; M Ling
Journal: J Inherit Metab Dis Date: 1996 Impact factor: 4.982

8. Excessive formation of hydroxyl radicals and aldehydic lipid peroxidation products in cultured skin fibroblasts from patients with complex I deficiency.

Authors: X Luo; S Pitkänen; S Kassovska-Bratinova; B H Robinson; D C Lehotay
Journal: J Clin Invest Date: 1997-06-15 Impact factor: 14.808

9. Nuclear DNA origin of mitochondrial complex I deficiency in fatal infantile lactic acidosis evidenced by transnuclear complementation of cultured fibroblasts.

Authors: V Procaccio; B Mousson; R Beugnot; H Duborjal; F Feillet; G Putet; I Pignot-Paintrand; A Lombès; R De Coo; H Smeets; J Lunardi; J P Issartel
Journal: J Clin Invest Date: 1999-07 Impact factor: 14.808

Review 10. Mitochondrial disorders: prevalence, myths and advances.

Authors: D R Thorburn
Journal: J Inherit Metab Dis Date: 2004 Impact factor: 4.982