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Browsing publications by Dr Kathryn White

Newcastle AuthorsTitleYearFull text
Dr Carla Mellough
Dr Roman Bauer
Dr Joseph Collin
Dr Darin Zerti
Dr David Dolan
et al.
An integrated transcriptional analysis of the developing human retina2019
Majed Felemban
Dr Gerrit Hilgen
Dr Darin Zerti
Dr Nicola Hunt
Dr Dean Hallam
et al.
Decellularised extracellular matrix-derived peptides from neural retina and retinal pigment epithelium enhance the expression of synaptic markers and light responsiveness of human pluripotent stem cell derived retinal organoids2019
Dr Amy Vincent
Dr Kathryn White
Tracey Davey
Jonathan Phillips
Dr Conor Lawless
et al.
Quantiative 3D Mapping of The Human Skeletal Muscle Mitochondrial Network2019
Dr Carla Mellough
Dr Joseph Collin
Dr Rachel Queen
Dr Gerrit Hilgen
Dr Darin Zerti
et al.
Systematic Comparison of Retinal Organoid Differentiation from Human Pluripotent Stem Cells Reveals Stage Specific, Cell Line, and Methodological Differences2019
Sumaya Alkanderi
Dr Elisa Molinari
Veronica Sammut
Dr Simon Ramsbottom
Dr Shalabh Srivastava
et al.
ARL3 Mutations Cause Joubert Syndrome by Disrupting Ciliary Protein Composition2018
Erin Cocks
Professor Michael Taggart
Dr Claire Rind
Dr Kathryn White
A guide to analysis and reconstruction of serial block face scanning electron microscopy data2018
Adriana Buskin
Dr Lili Zhu
Dr Valeria Chichagova
Dr David Dolan
Dr Joseph Collin
et al.
Disrupted alternative splicing for genes implicated in splicing and ciliogenesis causes PRPF31 retinitis pigmentosa2018
Adriana Buskin
Dr Lili Zhu
Dr Valeria Chichagova
Dr David Dolan
Dr Gerrit Hilgen
et al.
Disrupted alternative splicing for genes implicated in splicing and ciliogenesis causes PRPF31 retinitis pigmentosa2018
Dr Amy Vincent
Hannah Rosa
Kamil Pabis
Dr Conor Lawless
Chun Chen
et al.
Subcellular origin of mitochondrial DNA deletions in human skeletal muscle2018
Dr Simon Ramsbottom
Dr Elisa Molinari
Dr Shalabh Srivastava
Sumaya Alkanderi
Laura Devlin
et al.
Targeted exon skipping of a CEP290 mutation rescues Joubert syndrome phenotypes in vitro and in a murine model2018
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