Staff profile
Overview
https://internal.durham.ac.uk/images/profiles/1080/Jo_200pixelssquare.jpg
Miss Joanne Louise Robson
Experimental Officer (Bioimaging)
Human Genetics BSc

Affiliation | Room number | Telephone |
---|---|---|
Experimental Officer (Bioimaging) in the Department of Biosciences | 137 | +44 (0) 191 33 41333 |
Publications
Journal Article
- Finnegan, Sorcha, Robson, Joanne, Scaife, Caitriona, McAllister, Catherine, Pennington, Stephen R., Gibson, David S. & Rooney, Madeleine E. (2014). Synovial membrane protein expression differs between juvenile idiopathic arthritis subtypes in early disease. Arthritis Research & Therapy 16: R8.
- Brown, AP, Kroon, JTM Topping, JF, Robson, JL, Simon, WJ & Slabas, AR (2011). Components of Complex Lipid Biosynthetic Pathways in Developing Castor (Ricinus communis) Seeds Identified by MudPIT Analysis of Enriched Endoplasmic Reticulum. Journal of Proteome Research 10(8): 3565-3577.
- Foster, C.R., Robson, J.L., Simon, J.W., Twigg, J., Cruikshank, D., Wilson, R.G. & Hutchison, C.J. (2011). The role of Lamin A in cytoskeleton organization in colorectal cancer cells: a proteomic investigation. Nucleus 2(5): 434.
- Sorcha Finnegan Joanne Robson Paul M. Hocking Manir Ali, Chris F. Inglehearn Alan Stitt & William J. Curry. (2010). Proteomic profiling of the retinal dysplasia and degeneration chick retina. Molecular Vision 16: 7-17.
- Finnegan, Sorcha, Robson, Joanne L., Wylie, Mildred, Healy, Adrienne, Stitt, Alan W. & Curry, William J. (2008). Protein expression profiling during chick retinal maturation: a proteomics-based approach. Proteome Science 6(1): 34.
- Rowland, J.G., Robson, J.L., Simon, J.W., Leung, H.Y. & Slabas, A.R. (2007). Evaluation of an in vitro model of androgen ablation and identification of the androgen responsive proteome in LNCaP cells. Proteomics 7(1): 47-63.
- Tompson, W.J. Victor L. Ruiz-Perez. Helen J. Blair Stephanie Barton Victoria Navarro Joanne L Robson Michael J Wright & Judith A Goodship (2007). Sequencing EVC and EVC2 identifies mutations in two-thirds of Ellis-van Creveld syndrome patients. Human Genetics 120(5): 663-670.