Daniel S. Osborn
St George's University Of London
London, ENG, United Kingdom
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 12 publications
Autosomal recessive cardiomyopathy and sudden cardiac death associated with variants in MYL3.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: May 04, 2020
A Technique for Studying Glomerular Filtration Integrity in the Zebrafish Pronephros.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: November 09, 2019
Fgf-driven Tbx protein activities directly induce myf5 and myod to initiate zebrafish myogenesis.
Journal: Development (Cambridge, England)
Published: September 13, 2019
Cardiomyopathy with lethal arrhythmias associated with inactivation of KLHL24.
Journal: Human molecular genetics
Published: December 30, 2018
Bi-allelic variants in RNF170 are associated with hereditary spastic paraplegia.
Journal: Nature communications
Published: September 06, 2018
Synaptotagmin 5 regulates Ca2+-dependent Weibel-Palade body exocytosis in human endothelial cells.
Journal: Journal of cell science
Published: July 23, 2018
Bi-allelic mutations in MYL1 cause a severe congenital myopathy.
Journal: Human molecular genetics
Published: March 14, 2018
Mutations in INPP5K Cause a Form of Congenital Muscular Dystrophy Overlapping Marinesco-Sjögren Syndrome and Dystroglycanopathy.
Journal: American journal of human genetics
Published: October 17, 2016
Zebrafish: a vertebrate tool for studying basal body biogenesis, structure, and function.
Journal: Cilia
Published: January 20, 2016
Evaluation of zebrafish kidney function using a fluorescent clearance assay.
Journal: Journal of visualized experiments : JoVE
Published: March 06, 2015
Heat shock induces rapid resorption of primary cilia.
Journal: Journal of cell science
Published: June 22, 2012
Showing 1-12 of 12
Last Updated: 09/26/2026