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Page 1
DNA repair in the degenerating mouse retina.
Menu dit Huart L, Lorentz O, Goureau O, Léveillard T, Sahel JA. Menu dit Huart L, et al. Among authors: goureau o. Mol Cell Neurosci. 2004 Jul;26(3):441-9. doi: 10.1016/j.mcn.2004.04.002. Mol Cell Neurosci. 2004. PMID: 15234348
Foveal damage in habitual poppers users.
Audo I, El Sanharawi M, Vignal-Clermont C, Villa A, Morin A, Conrath J, Fompeydie D, Sahel JA, Gocho-Nakashima K, Goureau O, Paques M. Audo I, et al. Among authors: goureau o. Arch Ophthalmol. 2011 Jun;129(6):703-8. doi: 10.1001/archophthalmol.2011.6. Epub 2011 Feb 14. Arch Ophthalmol. 2011. PMID: 21320953
A regulatory domain is required for Foxn4 activity during retinogenesis.
Lelièvre EC, Benayoun BA, Mahieu L, Roger JE, Sahel JA, Sennlaub F, Veitia RA, Goureau O, Guillonneau X. Lelièvre EC, et al. Among authors: goureau o. J Mol Neurosci. 2012 Feb;46(2):315-23. doi: 10.1007/s12031-011-9585-4. Epub 2011 Jun 24. J Mol Neurosci. 2012. PMID: 21701787 Free PMC article.
Ptf1a/Rbpj complex inhibits ganglion cell fate and drives the specification of all horizontal cell subtypes in the chick retina.
Lelièvre EC, Lek M, Boije H, Houille-Vernes L, Brajeul V, Slembrouck A, Roger JE, Sahel JA, Matter JM, Sennlaub F, Hallböök F, Goureau O, Guillonneau X. Lelièvre EC, et al. Among authors: goureau o. Dev Biol. 2011 Oct 15;358(2):296-308. doi: 10.1016/j.ydbio.2011.07.033. Epub 2011 Jul 31. Dev Biol. 2011. PMID: 21839069 Free article.
The familial dementia gene revisited: a missense mutation revealed by whole-exome sequencing identifies ITM2B as a candidate gene underlying a novel autosomal dominant retinal dystrophy in a large family.
Audo I, Bujakowska K, Orhan E, El Shamieh S, Sennlaub F, Guillonneau X, Antonio A, Michiels C, Lancelot ME, Letexier M, Saraiva JP, Nguyen H, Luu TD, Léveillard T, Poch O, Dollfus H, Paques M, Goureau O, Mohand-Saïd S, Bhattacharya SS, Sahel JA, Zeitz C. Audo I, et al. Among authors: goureau o. Hum Mol Genet. 2014 Jan 15;23(2):491-501. doi: 10.1093/hmg/ddt439. Epub 2013 Sep 10. Hum Mol Genet. 2014. PMID: 24026677
107 results