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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2008 1
2009 1
2010 1
2012 3
2013 3
2014 3
2015 3
2016 2
2017 1
2018 1
2019 4
2020 2
2021 6
2022 0
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28 results
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Page 1
WDR34, a candidate gene for non-syndromic rod-cone dystrophy.
Solaguren-Beascoa M, Bujakowska KM, Méjécase C, Emmenegger L, Orhan E, Neuillé M, Mohand-Saïd S, Condroyer C, Lancelot ME, Michiels C, Demontant V, Antonio A, Letexier M, Saraiva JP, Lonjou C, Carpentier W, Léveillard T, Pierce EA, Dollfus H, Sahel JA, Bhattacharya SS, Audo I, Zeitz C. Solaguren-Beascoa M, et al. Among authors: michiels c. Clin Genet. 2021 Feb;99(2):298-302. doi: 10.1111/cge.13872. Epub 2020 Nov 9. Clin Genet. 2021. PMID: 33124039 Free PMC article.
Identification and characterization of novel TRPM1 autoantibodies from serum of patients with melanoma-associated retinopathy.
Varin J, Reynolds MM, Bouzidi N, Tick S, Wohlschlegel J, Becquart O, Michiels C, Dereure O, Duvoisin RM, Morgans CW, Sahel JA, Samaran Q, Guillot B, Pulido JS, Audo I, Zeitz C. Varin J, et al. Among authors: michiels c. PLoS One. 2020 Apr 23;15(4):e0231750. doi: 10.1371/journal.pone.0231750. eCollection 2020. PLoS One. 2020. PMID: 32324760 Free PMC article.
Substantial restoration of night vision in adult mice with congenital stationary night blindness.
Varin J, Bouzidi N, Gauvain G, Joffrois C, Desrosiers M, Robert C, De Sousa Dias MM, Neuillé M, Michiels C, Nassisi M, Sahel JA, Picaud S, Audo I, Dalkara D, Zeitz C. Varin J, et al. Among authors: michiels c. Mol Ther Methods Clin Dev. 2021 May 21;22:15-25. doi: 10.1016/j.omtm.2021.05.008. eCollection 2021 Sep 10. Mol Ther Methods Clin Dev. 2021. PMID: 34401402 Free PMC article.
Generation of human induced pluripotent stem cell lines from a patient with ITM2B-related retinal dystrophy and a non mutated brother.
Wohlschlegel J, Letellier C, Liu B, Méjécase C, Slembrouck-Brec A, Condroyer C, Michiels C, Sahel JA, Reichman S, Zeitz C, Goureau O, Audo I. Wohlschlegel J, et al. Among authors: michiels c. Stem Cell Res. 2019 Dec;41:101625. doi: 10.1016/j.scr.2019.101625. Epub 2019 Nov 5. Stem Cell Res. 2019. PMID: 31731182 Free article.
Phenotype Analysis of Retinal Dystrophies in Light of the Underlying Genetic Defects: Application to Cone and Cone-Rod Dystrophies.
Boulanger-Scemama E, Mohand-Saïd S, El Shamieh S, Démontant V, Condroyer C, Antonio A, Michiels C, Boyard F, Saraiva JP, Letexier M, Sahel JA, Zeitz C, Audo I. Boulanger-Scemama E, et al. Among authors: michiels c. Int J Mol Sci. 2019 Sep 30;20(19):4854. doi: 10.3390/ijms20194854. Int J Mol Sci. 2019. PMID: 31574917 Free PMC article.
Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of CACNA1F-mediated inherited retinal disorders.
Zeitz C, Michiels C, Neuillé M, Friedburg C, Condroyer C, Boyard F, Antonio A, Bouzidi N, Milicevic D, Veaux R, Tourville A, Zoumba A, Seneina I, Foussard M, Andrieu C, N Preising M, Blanchard S, Saraiva JP, Mesrob L, Le Floch E, Jubin C, Meyer V, Blanché H, Boland A, Deleuze JF, Sharon D, Drumare I, Defoort-Dhellemmes S, De Baere E, Leroy BP, Zanlonghi X, Casteels I, de Ravel TJ, Balikova I, Koenekoop RK, Laffargue F, McLean R, Gottlob I, Bonneau D, Schorderet DF, L Munier F, McKibbin M, Prescott K, Pelletier V, Dollfus H, Perdomo-Trujillo Y, Faure C, Reiff C, Wissinger B, Meunier I, Kohl S, Banin E, Zrenner E, Jurklies B, Lorenz B, Sahel JA, Audo I. Zeitz C, et al. Among authors: michiels c. Hum Mutat. 2019 Jun;40(6):765-787. doi: 10.1002/humu.23735. Epub 2019 Mar 28. Hum Mutat. 2019. PMID: 30825406
Genotypic and phenotypic characterization of P23H line 1 rat model.
Orhan E, Dalkara D, Neuillé M, Lechauve C, Michiels C, Picaud S, Léveillard T, Sahel JA, Naash MI, Lavail MM, Zeitz C, Audo I. Orhan E, et al. Among authors: michiels c. PLoS One. 2015 May 26;10(5):e0127319. doi: 10.1371/journal.pone.0127319. eCollection 2015. PLoS One. 2015. PMID: 26009893 Free PMC article.
28 results