Marian Seda
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 10 publications
Ciliopathy-Associated Missense Mutations in IFT140 are Tolerated by the Inherent Resilience of the IFT Machinery.
Journal: Molecular & cellular proteomics : MCP
Published: April 25, 2024
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
Structure and tethering mechanism of dynein-2 intermediate chains in intraflagellar transport.
Journal: The EMBO journal
Published: September 05, 2023
A CRISPR/Cas9-generated mutation in the zebrafish orthologue of PPP2R3B causes idiopathic scoliosis.
A CRISPR/Cas9-generated mutation in the zebrafish orthologue of PPP2R3B causes idiopathic scoliosis.
Journal: Scientific reports
Published: November 15, 2022
Diverse species-specific phenotypic consequences of loss of function sorting nexin 14 mutations.
Journal: Scientific reports
Published: November 15, 2019
Generating Mutant Renal Cell Lines Using CRISPR Technologies.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: November 09, 2019
An FDA-Approved Drug Screen for Compounds Influencing Craniofacial Skeletal Development and Craniosynostosis.
Journal: Molecular syndromology
Published: April 13, 2019
SNX14 mutations affect endoplasmic reticulum-associated neutral lipid metabolism in autosomal recessive spinocerebellar ataxia 20.
Journal: Human molecular genetics
Published: January 17, 2018
Showing 1-10 of 10
Last Updated: 09/26/2026