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Robust Genetic Analysis of the X-Linked Anophthalmic (Ie) Mouse.
Hernandez-Moran BA, Papanastasiou AS, Parry D, Meynert A, Gautier P, Grimes G, Adams IR, Trejo-Reveles V, Bengani H, Keighren M, Jackson IJ, Adams DJ, FitzPatrick DR, Rainger J. Hernandez-Moran BA, et al. Among authors: keighren m. Genes (Basel). 2022 Oct 5;13(10):1797. doi: 10.3390/genes13101797. Genes (Basel). 2022. PMID: 36292683 Free PMC article.
A trans-acting protein effect causes severe eye malformation in the Mp mouse.
Rainger J, Keighren M, Keene DR, Charbonneau NL, Rainger JK, Fisher M, Mella S, Huang JT, Rose L, van't Hof R, Sakai LY, Jackson IJ, Fitzpatrick DR. Rainger J, et al. Among authors: keighren m. PLoS Genet. 2013;9(12):e1003998. doi: 10.1371/journal.pgen.1003998. Epub 2013 Dec 12. PLoS Genet. 2013. PMID: 24348270 Free PMC article.
A dominant-negative mutation of mouse Lmx1b causes glaucoma and is semi-lethal via LDB1-mediated dimerization [corrected].
Cross SH, Macalinao DG, McKie L, Rose L, Kearney AL, Rainger J, Thaung C, Keighren M, Jadeja S, West K, Kneeland SC, Smith RS, Howell GR, Young F, Robertson M, van T' Hof R, John SW, Jackson IJ. Cross SH, et al. Among authors: keighren m. PLoS Genet. 2014 May 8;10(5):e1004359. doi: 10.1371/journal.pgen.1004359. eCollection 2014 May. PLoS Genet. 2014. PMID: 24809698 Free PMC article.
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: keighren m. 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.
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: keighren ma. Dis Model Mech. 2018 Dec 18;11(12):dmm036426. doi: 10.1242/dmm.036426. Dis Model Mech. 2018. PMID: 30478029 Free PMC article.
Genetically engineered multicistronic allele of Pmel yielding highly specific CreERT2-mediated recombination in the melanocyte lineage.
Wilkinson EL, Brennan LC, Harrison OJ, Crane-Smith Z, Gautier P, Keighren MA, Budd P, Swaminathan K, Machesky LM, Allinson SL, Jackson IJ, Mort RL. Wilkinson EL, et al. Among authors: keighren ma. Pigment Cell Melanoma Res. 2023 Jan;36(1):71-77. doi: 10.1111/pcmr.13076. Epub 2022 Dec 19. Pigment Cell Melanoma Res. 2023. PMID: 36412082 Free PMC article.
44 results