Emma Peskett
UCL Great Ormond Street Institute Of Child Health
London, ENG, United Kingdom
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 14 publications
Affinity Purification of Intraflagellar Transport (IFT) Proteins in Mice Using Endogenous Streptavidin/FLAG Tags.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: October 19, 2023
Diverse species-specific phenotypic consequences of loss of function sorting nexin 14 mutations.
Journal: Scientific reports
Published: November 15, 2019
Disruption of FOXF2 as a Likely Cause of Absent Uvula in an Egyptian Family.
Journal: Journal of dental research
Published: March 28, 2019
Overexpression of Fgfr2c causes craniofacial bone hypoplasia and ameliorates craniosynostosis in the Crouzon mouse.
Journal: Disease models & mechanisms
Published: May 04, 2018
SNX14 mutations affect endoplasmic reticulum-associated neutral lipid metabolism in autosomal recessive spinocerebellar ataxia 20.
Journal: Human molecular genetics
Published: January 17, 2018
Mice with endogenous TDP-43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis.
Journal: The EMBO journal
Published: November 20, 2017
Genetic Analyses in Small-for-Gestational-Age Newborns.
Journal: The Journal of clinical endocrinology and metabolism
Published: August 18, 2017
Analysis of the Fgfr2C342Y mouse model shows condensation defects due to misregulation of Sox9 expression in prechondrocytic mesenchyme.
Journal: Biology open
Published: January 11, 2017
Investigation of the Annexin A5 M2 haplotype in 500 white European couples who have experienced recurrent spontaneous abortion.
Journal: Reproductive biomedicine online
Published: December 16, 2014
Last Updated: 09/26/2026