Ian Coldicott

Department of Neuroscience

Research Technician

i.coldicott@sheffield.ac.uk
+44 114 222 2273

Full contact details

Ian Coldicott
Department of Neuroscience
Sheffield Institute for Translational Neuroscience (SITraN)
385a Glossop Road
Sheffield
S10 2HQ
Publications

Journal articles

Conference proceedings papers

  • Georgiou E, Coldicott I, Varcianna A & Heath PR (2020) Use of FACs to isolate targeted neurons for transcriptomic analysis. NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, Vol. 46 (pp 47-47) RIS download Bibtex download
  • Alves-Cruzeiro JM, Karyka E, Bauer C, Coldicott I, Simon S, Hautbergue GM, Webster C, Myszczynska M, Higginbottom A, Ferraiuolo L & Azzouz M (2019) Gene editing as a potential therapeutic approach for ALS/FTD-associated with expanded C9ORF72. HUMAN GENE THERAPY, Vol. 30(8) (pp A22-A22) RIS download Bibtex download
  • Scarrott JM, Coldicott I, Davies A, Hirst J, Karyka E, Bauer C & Azzouz M (2019) Development of an AAV9-mediated gene therapy for hereditary spastic paraplegia 47. HUMAN GENE THERAPY, Vol. 30(8) (pp A18-A18) RIS download Bibtex download
  • Ciervo Y, Coldicott I, Myszczynska M, Stopford M, Allen C, Grierson A, Xu J, Ferraiuolo L, Ning K, Shaw PJ & Mead RJ (2019) Adipose derived stem cells for cell therapy of motor neuron disease (MND). HUMAN GENE THERAPY, Vol. 30(8) (pp A16-A16) RIS download Bibtex download
  • Alves-Cruzeiro J, Karyka E, Bauer C, Coldicott I, Hautbergue G, Webster C, Castelli L, Simon S, Myszczynska M, Ferraiuolo L & Azzouz M (2019) AAV-mediated gene editing as a potential therapeutic approach for C9ORF72-linked ALS/FTD. HUMAN GENE THERAPY, Vol. 30(11) (pp A96-A96) RIS download Bibtex download
  • Iannitti T, Scarrot JM, Coldicott IRP, Kaspar BK, Ferraiuolo L, Shaw PJ & Azzouz M (2016) Gene Therapy for Familial ALS Using AAV9 Mediated Silencing of Mutant SOD1. HUMAN GENE THERAPY, Vol. 27(7) (pp A12-A12) View this article in WRRO RIS download Bibtex download
  • Herranz-Martin S, Lewis KE, Coldicott I, Chandran JS, Lukashchuk V, Iannitti T, Shaw PJ & Azzouz M (2016) Experimental modelling of ALS by AAV-mediated in vivo modulation of the C9ORF72 gene. HUMAN GENE THERAPY, Vol. 27(7) (pp A16-A16) RIS download Bibtex download
  • Lukashchuk V, Lewis K, Coldicott I, Grierson A & Azzouz M (2016) AAV9-mediated central nervous system-targeted gene delivery via cisterna magna route in mice. HUMAN GENE THERAPY, Vol. 27(7) (pp A11-A11) View this article in WRRO RIS download Bibtex download