1 - 25 of 31 results for author:"Saudou F." in Literature citations
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| Huntington's disease knock-in male mice show specific anxiety-like behaviour and altered neuronal maturation. Orvoen S., Pla P., Gardier A.M., Saudou F., David D.J. Neurosci. Lett. 507:127-132(2012) · Mapped (2) |
| Modification of Mecp2 dosage alters axonal transport through the Huntingtin/Hap1 pathway. Roux J.C., Zala D., Panayotis N., Borges-Correia A., Saudou F., Villard L. Neurobiol. Dis. 45:786-795(2012) · Mapped (3) |
| Ciliogenesis is regulated by a huntingtin-HAP1-PCM1 pathway and is altered in Huntington disease. Keryer G., Pineda J.R., Liot G., Kim J., Dietrich P., Benstaali C., Smith K., Cordelieres F.P., Spassky N., Ferrante R.J. et al. J. Clin. Invest. 121:4372-4382(2011) · Mapped (17) |
| Huntingtin is required for mitotic spindle orientation and mammalian neurogenesis. Godin J.D., Colombo K., Molina-Calavita M., Keryer G., Zala D., Charrin B.C., Dietrich P., Volvert M.L., Guillemot F., Dragatsis I. et al. Neuron 67:392-406(2010) · Mapped (47) |
| pARIS-htt: an optimised expression platform to study huntingtin reveals functional domains required for vesicular trafficking. Pardo R., Molina-Calavita M., Poizat G., Keryer G., Humbert S., Saudou F. Mol Brain 3:17-17(2010) |
| Delivery of GABAARs to synapses is mediated by HAP1-KIF5 and disrupted by mutant huntingtin. Twelvetrees A.E., Yuen E.Y., Arancibia-Carcamo I.L., MacAskill A.F., Rostaing P., Lumb M.J., Humbert S., Triller A., Saudou F., Yan Z. et al. Neuron 65:53-65(2010) · Mapped (1) |
| Elongator - an emerging role in neurological disorders. Nguyen L., Humbert S., Saudou F., Chariot A. Trends Mol Med 16:1-6(2010) · Mapped (6) |
| Serotonin transporter oligomerization documented in RN46A cells and neurons by sensitized acceptor emission FRET and fluorescence lifetime imaging microscopy. Fjorback A.W., Pla P., Muller H.K., Wiborg O., Saudou F., Nyengaard J.R. Biochem. Biophys. Res. Commun. 380:724-728(2009) · Mapped (3) |
| 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. Hum. Mol. Genet. 17:3837-3846(2008) · Mapped (4) |
| Huntingtin phosphorylation acts as a molecular switch for anterograde/retrograde transport in neurons. Colin E., Zala D., Liot G., Rangone H., Borrell-Pages M., Li X.J., Saudou F., Humbert S. EMBO J. 27:2124-2134(2008) · Mapped (15) |
| Phosphorylation of huntingtin by cyclin-dependent kinase 5 is induced by DNA damage and regulates wild-type and mutant huntingtin toxicity in neurons. Anne S.L., Saudou F., Humbert S. J. Neurosci. 27:7318-7328(2007) · UniProtKB (2) · Mapped (4) |
| Cystamine and cysteamine increase brain levels of BDNF in Huntington disease via HSJ1b and transglutaminase. Borrell-Pages M., Canals J.M., Cordelieres F.P., Parker J.A., Pineda J.R., Grange G., Bryson E.A., Guillermier M., Hirsch E., Hantraye P. et al. J. Clin. Invest. 116:1410-1424(2006) · Mapped (25) |
| Involvement of mitochondrial complex II defects in neuronal death produced by N-terminus fragment of mutated huntingtin. Benchoua A., Trioulier Y., Zala D., Gaillard M.C., Lefort N., Dufour N., Saudou F., Elalouf J.M., Hirsch E., Hantraye P. et al. Mol. Biol. Cell 17:1652-1663(2006) · Mapped (4) |
| Akt is altered in an animal model of Huntington's disease and in patients. Colin E., Regulier E., Perrin V., Durr A., Brice A., Aebischer P., Deglon N., Humbert S., Saudou F. Eur. J. Neurosci. 21:1478-1488(2005) · Mapped (5) |
| Phosphorylation of arfaptin 2 at Ser260 by Akt Inhibits PolyQ-huntingtin-induced toxicity by rescuing proteasome impairment. Rangone H., Pardo R., Colin E., Girault J.A., Saudou F., Humbert S. J. Biol. Chem. 280:22021-22028(2005) · Mapped (13) |
| Huntington's disease: how does huntingtin, an anti-apoptotic protein, become toxic? Rangone H., Humbert S., Saudou F. Pathol. Biol. 52:338-342(2004) · Mapped (4) |
| Huntingtin controls neurotrophic support and survival of neurons by enhancing BDNF vesicular transport along microtubules. Gauthier L.R., Charrin B.C., Borrell-Pages M., Dompierre J.P., Rangone H., Cordelieres F.P., De Mey J., MacDonald M.E., Lessmann V., Humbert S. et al. Cell 118:127-138(2004) · Mapped (22) |
| The serum- and glucocorticoid-induced kinase SGK inhibits mutant huntingtin-induced toxicity by phosphorylating serine 421 of huntingtin. Rangone H., Poizat G., Troncoso J., Ross C.A., MacDonald M.E., Saudou F., Humbert S. Eur. J. Neurosci. 19:273-279(2004) · Mapped (5) |
| Cdc42-interacting protein 4 binds to huntingtin: neuropathologic and biological evidence for a role in Huntington's disease. Holbert S., Dedeoglu A., Humbert S., Saudou F., Ferrante R.J., Neri C. Proc. Natl. Acad. Sci. U.S.A. 100:2712-2717(2003) · UniProtKB (1) · Mapped (3) |
| The IGF-1/Akt pathway is neuroprotective in Huntington's disease and involves Huntingtin phosphorylation by Akt. Humbert S., Bryson E.A., Cordelieres F.P., Connors N.C., Datta S.R., Finkbeiner S., Greenberg M.E., Saudou F. Dev. Cell 2:831-837(2002) · Mapped (11) |
| Essential role of the fosB gene in molecular, cellular, and behavioral actions of chronic electroconvulsive seizures. Hiroi N., Marek G.J., Brown J.R., Ye H., Saudou F., Vaidya V.A., Duman R.S., Greenberg M.E., Nestler E.J. J. Neurosci. 18:6952-6962(1998) · Mapped (2) |
| Fos family members induce cell cycle entry by activating cyclin D1. Brown J.R., Nigh E., Lee R.J., Ye H., Thompson M.A., Saudou F., Pestell R.G., Greenberg M.E. Mol. Cell. Biol. 18:5609-5619(1998) · Mapped (5) |
| Absence of fenfluramine-induced anorexia and reduced c-Fos induction in the hypothalamus and central amygdaloid complex of serotonin 1B receptor knock-out mice. Lucas J.J., Yamamoto A., Scearce-Levie K., Saudou F., Hen R. J. Neurosci. 18:5537-5544(1998) · Mapped (2) |
| Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion. David G., Abbas N., Stevanin G., Duerr A., Yvert G., Cancel G., Weber C., Imbert G., Saudou F., Antoniou E. et al. Nat. Genet. 17:65-70(1997) · UniProtKB (1) |
| Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats. Imbert G., Saudou F., Yvert G., Devys D., Trottier Y., Garnier J.-M., Weber C., Mandel J.-L., Cancel G., Abbas N. et al. Nat. Genet. 14:285-291(1996) · UniProtKB (5) |