Saudou F - Search Results

1

Modification of Mecp2 dosage alters axonal transport through the Huntingtin/Hap1 pathway.

Roux JC, Zala D, Panayotis N, Borges-Correia A, Saudou F, Villard L. Roux JC, et al. Among authors: saudou f. Neurobiol Dis. 2012 Feb;45(2):786-95. doi: 10.1016/j.nbd.2011.11.002. Epub 2011 Nov 15. Neurobiol Dis. 2012. PMID: 22127389

2

Involvement of mitochondrial complex II defects in neuronal death produced by N-terminus fragment of mutated huntingtin.

Benchoua A, Trioulier Y, Zala D, Gaillard MC, Lefort N, Dufour N, Saudou F, Elalouf JM, Hirsch E, Hantraye P, Déglon N, Brouillet E. Benchoua A, et al. Among authors: saudou f. Mol Biol Cell. 2006 Apr;17(4):1652-63. doi: 10.1091/mbc.e05-07-0607. Epub 2006 Feb 1. Mol Biol Cell. 2006. PMID: 16452635 Free PMC article.

3

Huntington's disease: from huntingtin function and dysfunction to therapeutic strategies.

Borrell-Pagès M, Zala D, Humbert S, Saudou F. Borrell-Pagès M, et al. Among authors: saudou f. Cell Mol Life Sci. 2006 Nov;63(22):2642-60. doi: 10.1007/s00018-006-6242-0. Cell Mol Life Sci. 2006. PMID: 17041811 Review.

4

Huntingtin phosphorylation acts as a molecular switch for anterograde/retrograde transport in neurons.

Colin E, Zala D, Liot G, Rangone H, Borrell-Pagès M, Li XJ, Saudou F, Humbert S. Colin E, et al. Among authors: saudou f. EMBO J. 2008 Aug 6;27(15):2124-34. doi: 10.1038/emboj.2008.133. Epub 2008 Jul 10. EMBO J. 2008. PMID: 18615096 Free PMC article.

5

Phosphorylation of mutant huntingtin at S421 restores anterograde and retrograde transport in neurons.

Zala D, Colin E, Rangone H, Liot G, Humbert S, Saudou F. Zala D, et al. Among authors: saudou f. Hum Mol Genet. 2008 Dec 15;17(24):3837-46. doi: 10.1093/hmg/ddn281. Epub 2008 Sep 4. Hum Mol Genet. 2008. PMID: 18772195

6

Genetic and pharmacological inhibition of calcineurin corrects the BDNF transport defect in Huntington's disease.

Pineda JR, Pardo R, Zala D, Yu H, Humbert S, Saudou F. Pineda JR, et al. Among authors: saudou f. Mol Brain. 2009 Oct 27;2:33. doi: 10.1186/1756-6606-2-33. Mol Brain. 2009. PMID: 19860865 Free PMC article.

7

Huntingtin is required for mitotic spindle orientation and mammalian neurogenesis.

Godin JD, Colombo K, Molina-Calavita M, Keryer G, Zala D, Charrin BC, Dietrich P, Volvert ML, Guillemot F, Dragatsis I, Bellaiche Y, Saudou F, Nguyen L, Humbert S. Godin JD, et al. Among authors: saudou f. Neuron. 2010 Aug 12;67(3):392-406. doi: 10.1016/j.neuron.2010.06.027. Neuron. 2010. PMID: 20696378 Free article.

8

Ciliogenesis is regulated by a huntingtin-HAP1-PCM1 pathway and is altered in Huntington disease.

Keryer G, Pineda JR, Liot G, Kim J, Dietrich P, Benstaali C, Smith K, Cordelières FP, Spassky N, Ferrante RJ, Dragatsis I, Saudou F. Keryer G, et al. Among authors: saudou f. J Clin Invest. 2011 Nov;121(11):4372-82. doi: 10.1172/JCI57552. Epub 2011 Oct 10. J Clin Invest. 2011. PMID: 21985783 Free PMC article.

9

[Unexpected link between Huntington disease and Rett syndrome].

Roux JC, Zala D, Panayotis N, Borges-Correia A, Saudou F, Villard L. Roux JC, et al. Among authors: saudou f. Med Sci (Paris). 2012 Jan;28(1):44-6. doi: 10.1051/medsci/2012281016. Epub 2012 Jan 27. Med Sci (Paris). 2012. PMID: 22289830 Free article. French. No abstract available.

10

Vesicular glycolysis provides on-board energy for fast axonal transport.

Zala D, Hinckelmann MV, Yu H, Lyra da Cunha MM, Liot G, Cordelières FP, Marco S, Saudou F. Zala D, et al. Among authors: saudou f. Cell. 2013 Jan 31;152(3):479-91. doi: 10.1016/j.cell.2012.12.029. Cell. 2013. PMID: 23374344 Free article.

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