Sally H. Cross
Edinburgh, SCT EH42XU, United Kingdom
Last Updated: 09/26/2026
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Found 10 publications
Genetic background modifies vulnerability to glaucoma-related phenotypes in Lmx1b mutant mice.
Journal: Disease models & mechanisms
Published: August 11, 2020
Fam151b, the mouse homologue of C.elegans menorin gene, is essential for retinal function.
Journal: Scientific reports
Published: September 03, 2019
Missense Mutations in the Human Nanophthalmos Gene TMEM98 Cause Retinal Defects in the Mouse.
Journal: Investigative ophthalmology & visual science
Published: July 03, 2019
Mouse Idh3a mutations cause retinal degeneration and reduced mitochondrial function.
Journal: Disease models & mechanisms
Published: July 09, 2018
Novel gene function revealed by mouse mutagenesis screens for models of age-related disease.
Journal: Nature communications
Published: February 29, 2016
The goya mouse mutant reveals distinct newly identified roles for MAP3K1 in the development and survival of cochlear sensory hair cells.
Journal: Disease models & mechanisms
Published: September 04, 2015
Mouse slc9a8 mutants exhibit retinal defects due to retinal pigmented epithelium dysfunction.
Journal: Investigative ophthalmology & visual science
Published: March 05, 2015
Normal X-inactivation mosaicism in corneas of heterozygous FlnaDilp2/+ female mice--a model of human filamin A (FLNA) diseases.
Journal: BMC research notes
Published: November 03, 2011
Showing 1-10 of 10
Last Updated: 09/26/2026