Margaret A. Keighren
Edinburgh, SCT, United Kingdom
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 24 publications
A Dominant Mutation in Gαs-Protein Increases Hair Pigmentation.
Journal: Pigment cell & melanoma research
Published: April 19, 2025
Robust Genetic Analysis of the X-Linked Anophthalmic (Ie) Mouse.
Journal: Genes
Published: August 05, 2022
Genetically engineered multicistronic allele of Pmel yielding highly specific CreERT2-mediated recombination in the melanocyte lineage.
Journal: Pigment cell & melanoma research
Published: July 15, 2022
A WDR35-dependent coat protein complex transports ciliary membrane cargo vesicles to cilia.
Journal: eLife
Published: April 26, 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
Missense Mutations in the Human Nanophthalmos Gene TMEM98 Cause Retinal Defects in the Mouse.
Journal: Investigative ophthalmology & visual science
Published: July 03, 2019
Re-evaluation of the causes of variation among mouse aggregation chimaeras.
Journal: Biology open
Published: May 31, 2019
Mouse Idh3a mutations cause retinal degeneration and reduced mitochondrial function.
Journal: Disease models & mechanisms
Published: July 09, 2018
A Cell/Cilia Cycle Biosensor for Single-Cell Kinetics Reveals Persistence of Cilia after G1/S Transition Is a General Property in Cells and Mice.
Journal: Developmental cell
Published: March 22, 2018
Selection against BALB/c strain cells in mouse chimaeras.
Journal: Biology open
Published: January 14, 2018
ZMYND10 functions in a chaperone relay during axonemal dynein assembly.
Journal: eLife
Published: December 15, 2017
Last Updated: 09/26/2026