490 related articles for article (PubMed ID: 29348607)
21. Isolated mitochondrial complex I deficiency: explorative data analysis of patient cell parameters.
Blanchet L; Buydens MC; Smeitink JA; Willems PH; Koopman WJ
Curr Pharm Des; 2011 Dec; 17(36):4023-33. PubMed ID: 22188452
[TBL] [Abstract][Full Text] [Related]
22. Bcl-x
Pfeiffer A; Schneider J; Bueno D; Dolga A; Voss TD; Lewerenz J; Wüllner V; Methner A
Free Radic Biol Med; 2017 Nov; 112():350-359. PubMed ID: 28807815
[TBL] [Abstract][Full Text] [Related]
23. Deficiency in mitochondrial complex I activity due to Ndufs6 gene trap insertion induces renal disease.
Forbes JM; Ke BX; Nguyen TV; Henstridge DC; Penfold SA; Laskowski A; Sourris KC; Groschner LN; Cooper ME; Thorburn DR; Coughlan MT
Antioxid Redox Signal; 2013 Aug; 19(4):331-43. PubMed ID: 23320803
[TBL] [Abstract][Full Text] [Related]
24. TAT-MTS-MCM fusion proteins reduce MMA levels and improve mitochondrial activity and liver function in MCM-deficient cells.
Erlich-Hadad T; Hadad R; Feldman A; Greif H; Lictenstein M; Lorberboum-Galski H
J Cell Mol Med; 2018 Mar; 22(3):1601-1613. PubMed ID: 29265583
[TBL] [Abstract][Full Text] [Related]
25. Lifetime exercise intolerance with lactic acidosis as key manifestation of novel compound heterozygous ACAD9 mutations causing complex I deficiency.
Schrank B; Schoser B; Klopstock T; Schneiderat P; Horvath R; Abicht A; Holinski-Feder E; Augustis S
Neuromuscul Disord; 2017 May; 27(5):473-476. PubMed ID: 28279569
[TBL] [Abstract][Full Text] [Related]
26. Mechanism underlying the antioxidant activity of taurine: prevention of mitochondrial oxidant production.
Jong CJ; Azuma J; Schaffer S
Amino Acids; 2012 Jun; 42(6):2223-32. PubMed ID: 21691752
[TBL] [Abstract][Full Text] [Related]
27. Coenzyme Q deficiency triggers mitochondria degradation by mitophagy.
Rodríguez-Hernández A; Cordero MD; Salviati L; Artuch R; Pineda M; Briones P; Gómez Izquierdo L; Cotán D; Navas P; Sánchez-Alcázar JA
Autophagy; 2009 Jan; 5(1):19-32. PubMed ID: 19115482
[TBL] [Abstract][Full Text] [Related]
28. Screening for active small molecules in mitochondrial complex I deficient patient's fibroblasts, reveals AICAR as the most beneficial compound.
Golubitzky A; Dan P; Weissman S; Link G; Wikstrom JD; Saada A
PLoS One; 2011; 6(10):e26883. PubMed ID: 22046392
[TBL] [Abstract][Full Text] [Related]
29. N-acetylcysteine and vitamin E rescue animal longevity and cellular oxidative stress in pre-clinical models of mitochondrial complex I disease.
Polyak E; Ostrovsky J; Peng M; Dingley SD; Tsukikawa M; Kwon YJ; McCormack SE; Bennett M; Xiao R; Seiler C; Zhang Z; Falk MJ
Mol Genet Metab; 2018 Apr; 123(4):449-462. PubMed ID: 29526616
[TBL] [Abstract][Full Text] [Related]
30. High incidence and variable clinical outcome of cardiac hypertrophy due to ACAD9 mutations in childhood.
Collet M; Assouline Z; Bonnet D; Rio M; Iserin F; Sidi D; Goldenberg A; Lardennois C; Metodiev MD; Haberberger B; Haack T; Munnich A; Prokisch H; Rötig A
Eur J Hum Genet; 2016 Aug; 24(8):1112-6. PubMed ID: 26669660
[TBL] [Abstract][Full Text] [Related]
31. Calcium signalling-dependent mitochondrial dysfunction and bioenergetics regulation in respiratory chain Complex II deficiency.
Mbaya E; Oulès B; Caspersen C; Tacine R; Massinet H; Pennuto M; Chrétien D; Munnich A; Rötig A; Rizzuto R; Rutter GA; Paterlini-Bréchot P; Chami M
Cell Death Differ; 2010 Dec; 17(12):1855-66. PubMed ID: 20489732
[TBL] [Abstract][Full Text] [Related]
32. The mitochondrial respiratory chain is a modulator of apoptosis.
Kwong JQ; Henning MS; Starkov AA; Manfredi G
J Cell Biol; 2007 Dec; 179(6):1163-77. PubMed ID: 18086914
[TBL] [Abstract][Full Text] [Related]
33. Assembly defects induce oxidative stress in inherited mitochondrial complex I deficiency.
Leman G; Gueguen N; Desquiret-Dumas V; Kane MS; Wettervald C; Chupin S; Chevrollier A; Lebre AS; Bonnefont JP; Barth M; Amati-Bonneau P; Verny C; Henrion D; Bonneau D; Reynier P; Procaccio V
Int J Biochem Cell Biol; 2015 Aug; 65():91-103. PubMed ID: 26024641
[TBL] [Abstract][Full Text] [Related]
34. Assembly defects of multiple respiratory chain complexes in a child with cardiac hypertrophy associated with a novel ACAD9 mutation.
Fragaki K; Chaussenot A; Boutron A; Bannwarth S; Rouzier C; Chabrol B; Paquis-Flucklinger V
Mol Genet Metab; 2017 Jul; 121(3):224-226. PubMed ID: 28529009
[TBL] [Abstract][Full Text] [Related]
35. Mammalian mitochondrial complex I: biogenesis, regulation, and reactive oxygen species generation.
Koopman WJ; Nijtmans LG; Dieteren CE; Roestenberg P; Valsecchi F; Smeitink JA; Willems PH
Antioxid Redox Signal; 2010 Jun; 12(12):1431-70. PubMed ID: 19803744
[TBL] [Abstract][Full Text] [Related]
36. Impaired Cellular Bioenergetics Causes Mitochondrial Calcium Handling Defects in MT-ND5 Mutant Cybrids.
McKenzie M; Duchen MR
PLoS One; 2016; 11(4):e0154371. PubMed ID: 27110715
[TBL] [Abstract][Full Text] [Related]
37. Leigh syndrome associated with mitochondrial complex I deficiency due to novel mutations In NDUFV1 and NDUFS2.
Marin SE; Mesterman R; Robinson B; Rodenburg RJ; Smeitink J; Tarnopolsky MA
Gene; 2013 Mar; 516(1):162-7. PubMed ID: 23266820
[TBL] [Abstract][Full Text] [Related]
38. Disruption of mitochondrial electron transport chain function potentiates the pro-apoptotic effects of MAPK inhibition.
Trotta AP; Gelles JD; Serasinghe MN; Loi P; Arbiser JL; Chipuk JE
J Biol Chem; 2017 Jul; 292(28):11727-11739. PubMed ID: 28546431
[TBL] [Abstract][Full Text] [Related]
39. Treatment of human cells derived from MERRF syndrome by peptide-mediated mitochondrial delivery.
Chang JC; Liu KH; Chuang CS; Su HL; Wei YH; Kuo SJ; Liu CS
Cytotherapy; 2013 Dec; 15(12):1580-96. PubMed ID: 24199594
[TBL] [Abstract][Full Text] [Related]
40. Novel mutations in the NDUFS1 gene cause low residual activities in human complex I deficiencies.
Hoefs SJ; Skjeldal OH; Rodenburg RJ; Nedregaard B; van Kaauwen EP; Spiekerkötter U; von Kleist-Retzow JC; Smeitink JA; Nijtmans LG; van den Heuvel LP
Mol Genet Metab; 2010 Jul; 100(3):251-6. PubMed ID: 20382551
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
