Jackson IJ - Search Results

1

Mouse slc9a8 mutants exhibit retinal defects due to retinal pigmented epithelium dysfunction.

Jadeja S, Barnard AR, McKie L, Cross SH, White JK; Sanger Mouse Genetics Project; Robertson M, Budd PS, MacLaren RE, Jackson IJ. Jadeja S, et al. Among authors: jackson ij. Invest Ophthalmol Vis Sci. 2015 May;56(5):3015-26. doi: 10.1167/iovs.14-15735. Invest Ophthalmol Vis Sci. 2015. PMID: 25736793 Free PMC article.

2

Genotype-phenotype correlation of mouse pde6b mutations.

Hart AW, McKie L, Morgan JE, Gautier P, West K, Jackson IJ, Cross SH. Hart AW, et al. Among authors: jackson ij. Invest Ophthalmol Vis Sci. 2005 Sep;46(9):3443-50. doi: 10.1167/iovs.05-0254. Invest Ophthalmol Vis Sci. 2005. PMID: 16123450

3

Missense Mutations in the Human Nanophthalmos Gene TMEM98 Cause Retinal Defects in the Mouse.

Cross SH, Mckie L, Keighren M, West K, Thaung C, Davey T, Soares DC, Sanchez-Pulido L, Jackson IJ. Cross SH, et al. Among authors: jackson ij. Invest Ophthalmol Vis Sci. 2019 Jul 1;60(8):2875-2887. doi: 10.1167/iovs.18-25954. Invest Ophthalmol Vis Sci. 2019. PMID: 31266059 Free PMC article.

4

A CNS-specific hypomorphic Pdgfr-beta mutant model of diabetic retinopathy.

Jadeja S, Mort RL, Keighren M, Hart AW, Joynson R, Wells S, Potter PK, Jackson IJ. Jadeja S, et al. Among authors: jackson ij. Invest Ophthalmol Vis Sci. 2013 May 1;54(5):3569-78. doi: 10.1167/iovs.12-11125. Invest Ophthalmol Vis Sci. 2013. PMID: 23633653 Free PMC article.

5

Mouse Idh3a mutations cause retinal degeneration and reduced mitochondrial function.

Findlay AS, Carter RN, Starbuck B, McKie L, Nováková K, Budd PS, Keighren MA, Marsh JA, Cross SH, Simon MM, Potter PK, Morton NM, Jackson IJ. Findlay AS, et al. Among authors: jackson ij. Dis Model Mech. 2018 Dec 18;11(12):dmm036426. doi: 10.1242/dmm.036426. Dis Model Mech. 2018. PMID: 30478029 Free PMC article.

6

The nanophthalmos protein TMEM98 inhibits MYRF self-cleavage and is required for eye size specification.

Cross SH, Mckie L, Hurd TW, Riley S, Wills J, Barnard AR, Young F, MacLaren RE, Jackson IJ. Cross SH, et al. Among authors: jackson ij. PLoS Genet. 2020 Apr 1;16(4):e1008583. doi: 10.1371/journal.pgen.1008583. eCollection 2020 Apr. PLoS Genet. 2020. PMID: 32236127 Free PMC article.

7

Fam151b, the mouse homologue of C.elegans menorin gene, is essential for retinal function.

Findlay AS, McKie L, Keighren M, Clementson-Mobbs S, Sanchez-Pulido L, Wells S, Cross SH, Jackson IJ. Findlay AS, et al. Among authors: jackson ij. Sci Rep. 2020 Jan 16;10(1):437. doi: 10.1038/s41598-019-57398-4. Sci Rep. 2020. PMID: 31949211 Free PMC article.

8

Cardiac malformations and midline skeletal defects in mice lacking filamin A.

Hart AW, Morgan JE, Schneider J, West K, McKie L, Bhattacharya S, Jackson IJ, Cross SH. Hart AW, et al. Among authors: jackson ij. Hum Mol Genet. 2006 Aug 15;15(16):2457-67. doi: 10.1093/hmg/ddl168. Epub 2006 Jul 6. Hum Mol Genet. 2006. PMID: 16825286

9

Diphthamide modification of eEF2 requires a J-domain protein and is essential for normal development.

Webb TR, Cross SH, McKie L, Edgar R, Vizor L, Harrison J, Peters J, Jackson IJ. Webb TR, et al. Among authors: jackson ij. J Cell Sci. 2008 Oct 1;121(Pt 19):3140-5. doi: 10.1242/jcs.035550. Epub 2008 Sep 2. J Cell Sci. 2008. PMID: 18765564 Free PMC article.

10

The Opdc missense mutation of Pax2 has a milder than loss-of-function phenotype.

Cross SH, McKie L, West K, Coghill EL, Favor J, Bhattacharya S, Brown SD, Jackson IJ. Cross SH, et al. Among authors: jackson ij. Hum Mol Genet. 2011 Jan 15;20(2):223-34. doi: 10.1093/hmg/ddq457. Epub 2010 Oct 13. Hum Mol Genet. 2011. PMID: 20943750 Free PMC article.

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