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Human Molecular Genetics|July 27, 2007
Humanized MC1R transgenic mice reveal human specific receptor functionIan J Jackson, Peter S Budd, Margaret Keighren, et al.Nature Communications|April 29, 2025
Autophagy disruption and mitochondrial stress precede photoreceptor necroptosis in multiple mouse models of inherited retinal disordersFay Newton, Mihail Halachev, Linda Nguyen, et al.Investigative Ophthalmology & Visual Science|August 27, 2005
Genotype-phenotype correlation of mouse pde6b mutationsAlan W Hart, Lisa McKie, Joanne E Morgan, et al.Journal of Cell Science|September 4, 2008
Diphthamide modification of eEF2 requires a J-domain protein and is essential for normal developmentTom R Webb, Sally H Cross, Lisa McKie, et al.Neuropharmacology|July 15, 2009
GABAergic amacrine cells and visual function are reduced in PAC1 transgenic miceBing Lang, Lei Zhao, Li Cai, et al.Disease Models & Mechanisms|August 9, 2021
A mouse model of brittle cornea syndrome caused by mutation in Zfp469Chloe M Stanton, Amy S Findlay, Camilla Drake, et al.Human Molecular Genetics|July 11, 2006
Cardiac malformations and midline skeletal defects in mice lacking filamin AAlan W Hart, Joanne E Morgan, Jürgen Schneider, et al.Human Molecular Genetics|October 15, 2010
The Opdc missense mutation of Pax2 has a milder than loss-of-function phenotypeSally H Cross, Lisa McKie, Katrine West, et al.BMC Research Notes|February 29, 2012
Normal X-inactivation mosaicism in corneas of heterozygous FlnaDilp2/+ female mice--a model of human filamin A (FLNA) diseasesPanagiotis Douvaras, Weijia Liu, Richard L Mort, et al.Scientific Reports|January 18, 2020
Fam151b, the mouse homologue of C.elegans menorin gene, is essential for retinal functionAmy S Findlay, Lisa McKie, Margaret Keighren, et al.Pageof 4