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Page 1
Crumbs homologue 1 in polarity and blindness.
Meuleman J, van de Pavert SA, Wijnholds J. Meuleman J, et al. Among authors: wijnholds j. Biochem Soc Trans. 2004 Nov;32(Pt 5):828-30. doi: 10.1042/BST0320828. Biochem Soc Trans. 2004. PMID: 15494026 Review.
MPP5 recruits MPP4 to the CRB1 complex in photoreceptors.
Kantardzhieva A, Gosens I, Alexeeva S, Punte IM, Versteeg I, Krieger E, Neefjes-Mol CA, den Hollander AI, Letteboer SJ, Klooster J, Cremers FP, Roepman R, Wijnholds J. Kantardzhieva A, et al. Among authors: wijnholds j. Invest Ophthalmol Vis Sci. 2005 Jun;46(6):2192-201. doi: 10.1167/iovs.04-1417. Invest Ophthalmol Vis Sci. 2005. PMID: 15914641
A single amino acid substitution (Cys249Trp) in Crb1 causes retinal degeneration and deregulates expression of pituitary tumor transforming gene Pttg1.
van de Pavert SA, Meuleman J, Malysheva A, Aartsen WM, Versteeg I, Tonagel F, Kamphuis W, McCabe CJ, Seeliger MW, Wijnholds J. van de Pavert SA, et al. Among authors: wijnholds j. J Neurosci. 2007 Jan 17;27(3):564-73. doi: 10.1523/JNEUROSCI.3496-06.2007. J Neurosci. 2007. PMID: 17234588 Free PMC article.
Crb1 is a determinant of retinal apical Müller glia cell features.
van de Pavert SA, Sanz AS, Aartsen WM, Vos RM, Versteeg I, Beck SC, Klooster J, Seeliger MW, Wijnholds J. van de Pavert SA, et al. Among authors: wijnholds j. Glia. 2007 Nov 1;55(14):1486-97. doi: 10.1002/glia.20561. Glia. 2007. PMID: 17705196
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: wijnholds j. 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
109 results