Lisa Mckie
Edinburgh, SCT, United Kingdom
Last Updated: 09/26/2026
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Found 21 publications
A Dominant Mutation in Gαs-Protein Increases Hair Pigmentation.
Journal: Pigment cell & melanoma research
Published: April 19, 2025
A progeria syndrome links DNA hypermethylation to age-related pathology.
Journal: Nature genetics
Published: April 07, 2025
Autophagy disruption and mitochondrial stress precede photoreceptor necroptosis in multiple mouse models of inherited retinal disorders.
Journal: Nature communications
Published: July 29, 2024
Ciliopathy patient variants reveal organelle-specific functions for TUBB4B in axonemal microtubules.
Ciliopathy patient variants reveal organelle-specific functions for TUBB4B in axonemal microtubules.
Journal: Science (New York, N.Y.)
Published: April 25, 2024
Ciliary tip actin dynamics regulate photoreceptor outer segment integrity.
Journal: Nature communications
Published: June 05, 2023
The Dct-/- Mouse Model to Unravel Retinogenesis Misregulation in Patients with Albinism.
Journal: Genes
Published: May 25, 2022
Monoallelic variants resulting in substitutions of MAB21L1 Arg51 Cause Aniridia and microphthalmia.
Journal: PloS one
Published: April 21, 2022
Centriolar satellites expedite mother centriole remodeling to promote ciliogenesis.
Journal: eLife
Published: April 06, 2022
A mouse model of brittle cornea syndrome caused by mutation in Zfp469.
Journal: Disease models & mechanisms
Published: June 18, 2021
Dopachrome tautomerase variants in patients with oculocutaneous albinism.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: June 26, 2020
Fam151b, the mouse homologue of C.elegans menorin gene, is essential for retinal function.
Journal: Scientific reports
Published: September 03, 2019
Last Updated: 09/26/2026