R01 EY016501/EY/NEI NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2002	1
2008	1
2010	6
2011	4
2012	5
2013	3
2014	2
2015	4
2016	4
2017	3
2018	1
2020	1
2024	0

1

Disruption in murine Eml1 perturbs retinal lamination during early development.

Collin GB, Won J, Krebs MP, Hicks WJ, Charette JR, Naggert JK, Nishina PM. Collin GB, et al. Sci Rep. 2020 Mar 27;10(1):5647. doi: 10.1038/s41598-020-62373-5. Sci Rep. 2020. PMID: 32221352 Free PMC article.

2

An FRMD4B variant suppresses dysplastic photoreceptor lesions in models of enhanced S-cone syndrome and of Nrl deficiency.

Kong Y, Zhao L, Charette JR, Hicks WL, Stone L, Nishina PM, Naggert JK. Kong Y, et al. Hum Mol Genet. 2018 Oct 1;27(19):3340-3352. doi: 10.1093/hmg/ddy238. Hum Mol Genet. 2018. PMID: 29947801 Free PMC article.

3

Using Vascular Landmarks to Orient 3D Optical Coherence Tomography Images of the Mouse Eye.

Krebs MP. Krebs MP. Curr Protoc Mouse Biol. 2017 Sep 8;7(3):176-190. doi: 10.1002/cpmo.32. Curr Protoc Mouse Biol. 2017. PMID: 28884793 Free PMC article.

4

Mouse models of human ocular disease for translational research.

Krebs MP, Collin GB, Hicks WL, Yu M, Charette JR, Shi LY, Wang J, Naggert JK, Peachey NS, Nishina PM. Krebs MP, et al. PLoS One. 2017 Aug 31;12(8):e0183837. doi: 10.1371/journal.pone.0183837. eCollection 2017. PLoS One. 2017. PMID: 28859131 Free PMC article.

5

A mutagenesis-derived Lrp5 mouse mutant with abnormal retinal vasculature and low bone mineral density.

Charette JR, Earp SE, Bell BA, Ackert-Bicknell CL, Godfrey DA, Rao S, Anand-Apte B, Nishina PM, Peachey NS. Charette JR, et al. Mol Vis. 2017 Mar 18;23:140-148. eCollection 2017. Mol Vis. 2017. PMID: 28356706 Free PMC article.

6

Mouse Models of NMNAT1-Leber Congenital Amaurosis (LCA9) Recapitulate Key Features of the Human Disease.

Greenwald SH, Charette JR, Staniszewska M, Shi LY, Brown SDM, Stone L, Liu Q, Hicks WL, Collin GB, Bowl MR, Krebs MP, Nishina PM, Pierce EA. Greenwald SH, et al. Am J Pathol. 2016 Jul;186(7):1925-1938. doi: 10.1016/j.ajpath.2016.03.013. Epub 2016 May 18. Am J Pathol. 2016. PMID: 27207593 Free PMC article.

7

Retinal Pigment Epithelium Atrophy 1 (rpea1): A New Mouse Model With Retinal Detachment Caused by a Disruption of Protein Kinase C, θ.

Ji X, Liu Y, Hurd R, Wang J, Fitzmaurice B, Nishina PM, Chang B. Ji X, et al. Invest Ophthalmol Vis Sci. 2016 Mar;57(3):877-88. doi: 10.1167/iovs.15-17495. Invest Ophthalmol Vis Sci. 2016. PMID: 26978024 Free PMC article.

8

Mutations in CTNNA1 cause butterfly-shaped pigment dystrophy and perturbed retinal pigment epithelium integrity.

Saksens NT, Krebs MP, Schoenmaker-Koller FE, Hicks W, Yu M, Shi L, Rowe L, Collin GB, Charette JR, Letteboer SJ, Neveling K, van Moorsel TW, Abu-Ltaif S, De Baere E, Walraedt S, Banfi S, Simonelli F, Cremers FP, Boon CJ, Roepman R, Leroy BP, Peachey NS, Hoyng CB, Nishina PM, den Hollander AI. Saksens NT, et al. Nat Genet. 2016 Feb;48(2):144-51. doi: 10.1038/ng.3474. Epub 2015 Dec 21. Nat Genet. 2016. PMID: 26691986 Free PMC article.

9

Elevation of 20-carbon long chain bases due to a mutation in serine palmitoyltransferase small subunit b results in neurodegeneration.

Zhao L, Spassieva S, Gable K, Gupta SD, Shi LY, Wang J, Bielawski J, Hicks WL, Krebs MP, Naggert J, Hannun YA, Dunn TM, Nishina PM. Zhao L, et al. Proc Natl Acad Sci U S A. 2015 Oct 20;112(42):12962-7. doi: 10.1073/pnas.1516733112. Epub 2015 Oct 5. Proc Natl Acad Sci U S A. 2015. PMID: 26438849 Free PMC article.

10

A Chemical Mutagenesis Screen Identifies Mouse Models with ERG Defects.

Charette JR, Samuels IS, Yu M, Stone L, Hicks W, Shi LY, Krebs MP, Naggert JK, Nishina PM, Peachey NS. Charette JR, et al. Adv Exp Med Biol. 2016;854:177-83. doi: 10.1007/978-3-319-17121-0_24. Adv Exp Med Biol. 2016. PMID: 26427409 Free PMC article.

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