Rustin P - Search Results

1

Limitations in a frataxin knockdown cell model for Friedreich ataxia in a high-throughput drug screen.

Calmels N, Seznec H, Villa P, Reutenauer L, Hibert M, Haiech J, Rustin P, Koenig M, Puccio H. Calmels N, et al. Among authors: rustin p. BMC Neurol. 2009 Aug 24;9:46. doi: 10.1186/1471-2377-9-46. BMC Neurol. 2009. PMID: 19703283 Free PMC article.

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. Seznec H, et al. Among authors: rustin p. Hum Mol Genet. 2004 May 15;13(10):1017-24. doi: 10.1093/hmg/ddh114. Epub 2004 Mar 17. Hum Mol Genet. 2004. PMID: 15028670

3

Friedreich ataxia mouse models with progressive cerebellar and sensory ataxia reveal autophagic neurodegeneration in dorsal root ganglia.

Simon D, Seznec H, Gansmuller A, Carelle N, Weber P, Metzger D, Rustin P, Koenig M, Puccio H. Simon D, et al. Among authors: rustin p. J Neurosci. 2004 Feb 25;24(8):1987-95. doi: 10.1523/JNEUROSCI.4549-03.2004. J Neurosci. 2004. PMID: 14985441 Free PMC article.

4

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. Puccio H, et al. Among authors: rustin p. Nat Genet. 2001 Feb;27(2):181-6. doi: 10.1038/84818. Nat Genet. 2001. PMID: 11175786

5

Disabled early recruitment of antioxidant defenses in Friedreich's ataxia.

Chantrel-Groussard K, Geromel V, Puccio H, Koenig M, Munnich A, Rötig A, Rustin P. Chantrel-Groussard K, et al. Among authors: rustin p. Hum Mol Genet. 2001 Sep 15;10(19):2061-7. doi: 10.1093/hmg/10.19.2061. Hum Mol Genet. 2001. PMID: 11590123

6

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. Rötig A, et al. Among authors: rustin p. Nat Genet. 1997 Oct;17(2):215-7. doi: 10.1038/ng1097-215. Nat Genet. 1997. PMID: 9326946

7

Deferiprone targets aconitase: implication for Friedreich's ataxia treatment.

Goncalves S, Paupe V, Dassa EP, Rustin P. Goncalves S, et al. Among authors: rustin p. BMC Neurol. 2008 Jun 16;8:20. doi: 10.1186/1471-2377-8-20. BMC Neurol. 2008. PMID: 18558000 Free PMC article.

8

Friedreich's ataxia: the vicious circle hypothesis revisited.

Bayot A, Santos R, Camadro JM, Rustin P. Bayot A, et al. Among authors: rustin p. BMC Med. 2011 Oct 11;9:112. doi: 10.1186/1741-7015-9-112. BMC Med. 2011. PMID: 21985033 Free PMC article.

9

ACO2 mutations: A novel phenotype associating severe optic atrophy and spastic paraplegia.

Marelli C, Hamel C, Quiles M, Carlander B, Larrieu L, Delettre C, Sarzi E, Chretien D, Rustin P, Koenig M, Guissart C. Marelli C, et al. Among authors: rustin p. Neurol Genet. 2018 Mar 20;4(2):e225. doi: 10.1212/NXG.0000000000000225. eCollection 2018 Apr. Neurol Genet. 2018. PMID: 29564393 Free PMC article. No abstract available.

10

Molecular insights into Friedreich's ataxia and antioxidant-based therapies.

Rötig A, Sidi D, Munnich A, Rustin P. Rötig A, et al. Among authors: rustin p. Trends Mol Med. 2002 May;8(5):221-4. doi: 10.1016/s1471-4914(02)02330-4. Trends Mol Med. 2002. PMID: 12067631 Review.

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