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Loss of CRB2 in the mouse retina mimics human retinitis pigmentosa due to mutations in the CRB1 gene.
Alves CH, Sanz AS, Park B, Pellissier LP, Tanimoto N, Beck SC, Huber G, Murtaza M, Richard F, Sridevi Gurubaran I, Garcia Garrido M, Levelt CN, Rashbass P, Le Bivic A, Seeliger MW, Wijnholds J. Alves CH, et al. Among authors: pellissier lp. Hum Mol Genet. 2013 Jan 1;22(1):35-50. doi: 10.1093/hmg/dds398. Epub 2012 Sep 21. Hum Mol Genet. 2013. PMID: 23001562
Targeted ablation of Crb2 in photoreceptor cells induces retinitis pigmentosa.
Alves CH, Pellissier LP, Vos RM, Garcia Garrido M, Sothilingam V, Seide C, Beck SC, Klooster J, Furukawa T, Flannery JG, Verhaagen J, Seeliger MW, Wijnholds J. Alves CH, et al. Among authors: pellissier lp. Hum Mol Genet. 2014 Jul 1;23(13):3384-401. doi: 10.1093/hmg/ddu048. Epub 2014 Feb 2. Hum Mol Genet. 2014. PMID: 24493795 Free article.
CRB2 acts as a modifying factor of CRB1-related retinal dystrophies in mice.
Pellissier LP, Lundvig DM, Tanimoto N, Klooster J, Vos RM, Richard F, Sothilingam V, Garcia Garrido M, Le Bivic A, Seeliger MW, Wijnholds J. Pellissier LP, et al. Hum Mol Genet. 2014 Jul 15;23(14):3759-71. doi: 10.1093/hmg/ddu089. Epub 2014 Feb 23. Hum Mol Genet. 2014. PMID: 24565864
AAV Serotype Testing on Cultured Human Donor Retinal Explants.
Buck TM, Pellissier LP, Vos RM, van Dijk EHC, Boon CJF, Wijnholds J. Buck TM, et al. Among authors: pellissier lp. Methods Mol Biol. 2018;1715:275-288. doi: 10.1007/978-1-4939-7522-8_20. Methods Mol Biol. 2018. PMID: 29188521
36 results