679 related articles for article (PubMed ID: 11175786)
1. Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron deposits.
Puccio H; Simon D; Cossée M; Criqui-Filipe P; Tiziano F; Melki J; Hindelang C; Matyas R; Rustin P; Koenig M
Nat Genet; 2001 Feb; 27(2):181-6. PubMed ID: 11175786
[TBL] [Abstract][Full Text] [Related]
2. Idebenone delays the onset of cardiac functional alteration without correction of Fe-S enzymes deficit in a mouse model for Friedreich ataxia.
Seznec H; Simon D; Monassier L; Criqui-Filipe P; Gansmuller A; Rustin P; Koenig M; Puccio H
Hum Mol Genet; 2004 May; 13(10):1017-24. PubMed ID: 15028670
[TBL] [Abstract][Full Text] [Related]
3. Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia.
Rötig A; de Lonlay P; Chretien D; Foury F; Koenig M; Sidi D; Munnich A; Rustin P
Nat Genet; 1997 Oct; 17(2):215-7. PubMed ID: 9326946
[TBL] [Abstract][Full Text] [Related]
4. Conditional mouse models for Friedreich ataxia, a neurodegenerative disorder associating cardiomyopathy.
Puccio H
Handb Exp Pharmacol; 2007; (178):365-75. PubMed ID: 17203663
[TBL] [Abstract][Full Text] [Related]
5. Friedreich ataxia: the oxidative stress paradox.
Seznec H; Simon D; Bouton C; Reutenauer L; Hertzog A; Golik P; Procaccio V; Patel M; Drapier JC; Koenig M; Puccio H
Hum Mol Genet; 2005 Feb; 14(4):463-74. PubMed ID: 15615771
[TBL] [Abstract][Full Text] [Related]
6. Frataxin deficiency causes upregulation of mitochondrial Lon and ClpP proteases and severe loss of mitochondrial Fe-S proteins.
Guillon B; Bulteau AL; Wattenhofer-Donzé M; Schmucker S; Friguet B; Puccio H; Drapier JC; Bouton C
FEBS J; 2009 Feb; 276(4):1036-47. PubMed ID: 19154341
[TBL] [Abstract][Full Text] [Related]
7. Frataxin is essential for extramitochondrial Fe-S cluster proteins in mammalian tissues.
Martelli A; Wattenhofer-Donzé M; Schmucker S; Bouvet S; Reutenauer L; Puccio H
Hum Mol Genet; 2007 Nov; 16(22):2651-8. PubMed ID: 17597094
[TBL] [Abstract][Full Text] [Related]
8. Mitochondrial frataxin interacts with ISD11 of the NFS1/ISCU complex and multiple mitochondrial chaperones.
Shan Y; Napoli E; Cortopassi G
Hum Mol Genet; 2007 Apr; 16(8):929-41. PubMed ID: 17331979
[TBL] [Abstract][Full Text] [Related]
9. Inactivation of the Friedreich ataxia mouse gene leads to early embryonic lethality without iron accumulation.
Cossée M; Puccio H; Gansmuller A; Koutnikova H; Dierich A; LeMeur M; Fischbeck K; Dollé P; Koenig M
Hum Mol Genet; 2000 May; 9(8):1219-26. PubMed ID: 10767347
[TBL] [Abstract][Full Text] [Related]
10. Respiratory deficiency due to loss of mitochondrial DNA in yeast lacking the frataxin homologue.
Wilson RB; Roof DM
Nat Genet; 1997 Aug; 16(4):352-7. PubMed ID: 9241271
[TBL] [Abstract][Full Text] [Related]
11. Iron-sulfur protein maturation in human cells: evidence for a function of frataxin.
Stehling O; Elsässer HP; Brückel B; Mühlenhoff U; Lill R
Hum Mol Genet; 2004 Dec; 13(23):3007-15. PubMed ID: 15509595
[TBL] [Abstract][Full Text] [Related]
12. Frataxin overexpressing mice.
Miranda CJ; Santos MM; Ohshima K; Tessaro M; Sequeiros J; Pandolfo M
FEBS Lett; 2004 Aug; 572(1-3):281-8. PubMed ID: 15304363
[TBL] [Abstract][Full Text] [Related]
13. Studies of human, mouse and yeast homologues indicate a mitochondrial function for frataxin.
Koutnikova H; Campuzano V; Foury F; Dollé P; Cazzalini O; Koenig M
Nat Genet; 1997 Aug; 16(4):345-51. PubMed ID: 9241270
[TBL] [Abstract][Full Text] [Related]
14. PPAR gamma agonist leriglitazone improves frataxin-loss impairments in cellular and animal models of Friedreich Ataxia.
Rodríguez-Pascau L; Britti E; Calap-Quintana P; Dong YN; Vergara C; Delaspre F; Medina-Carbonero M; Tamarit J; Pallardó FV; Gonzalez-Cabo P; Ros J; Lynch DR; Martinell M; Pizcueta P
Neurobiol Dis; 2021 Jan; 148():105162. PubMed ID: 33171227
[TBL] [Abstract][Full Text] [Related]
15. Recent advances in the molecular pathogenesis of Friedreich ataxia.
Puccio H; Koenig M
Hum Mol Genet; 2000 Apr; 9(6):887-92. PubMed ID: 10767311
[TBL] [Abstract][Full Text] [Related]
16. The in vivo mitochondrial two-step maturation of human frataxin.
Schmucker S; Argentini M; Carelle-Calmels N; Martelli A; Puccio H
Hum Mol Genet; 2008 Nov; 17(22):3521-31. PubMed ID: 18725397
[TBL] [Abstract][Full Text] [Related]
17. Friedreich's ataxia: past, present and future.
Marmolino D
Brain Res Rev; 2011 Jun; 67(1-2):311-30. PubMed ID: 21550666
[TBL] [Abstract][Full Text] [Related]
18. Glutathione-dependent redox status of frataxin-deficient cells in a yeast model of Friedreich's ataxia.
Auchère F; Santos R; Planamente S; Lesuisse E; Camadro JM
Hum Mol Genet; 2008 Sep; 17(18):2790-802. PubMed ID: 18562474
[TBL] [Abstract][Full Text] [Related]
19. Frataxin shows developmentally regulated tissue-specific expression in the mouse embryo.
Jiralerspong S; Liu Y; Montermini L; Stifani S; Pandolfo M
Neurobiol Dis; 1997; 4(2):103-13. PubMed ID: 9331900
[TBL] [Abstract][Full Text] [Related]
20. Extra-mitochondrial localisation of frataxin and its association with IscU1 during enterocyte-like differentiation of the human colon adenocarcinoma cell line Caco-2.
Acquaviva F; De Biase I; Nezi L; Ruggiero G; Tatangelo F; Pisano C; Monticelli A; Garbi C; Acquaviva AM; Cocozza S
J Cell Sci; 2005 Sep; 118(Pt 17):3917-24. PubMed ID: 16091420
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
