Ian Coldicott
School of Medicine and Population Health
Research Technician
    
         i.coldicott@sheffield.ac.uk
    
        
+44 114 222 2273
          
        
      
    
  
  
+44 114 222 2273
      Sheffield Institute for Translational Neuroscience (SITraN)
  
Full contact details
         Ian Coldicott
School of Medicine and Population Health
Sheffield Institute for Translational Neuroscience (SITraN)
385a Glossop Road
Sheffield
S10 2HQ
          
      
  
School of Medicine and Population Health
Sheffield Institute for Translational Neuroscience (SITraN)
385a Glossop Road
Sheffield
S10 2HQ
- Publications
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Journal articles
- . Disease Models & Mechanisms, 18(2).
 - . Life Science Alliance, 8(2).
 - . EMBO Molecular Medicine, 16(11), 2882-2917.
 - . Brain Communications, 5(1).
 - . Acta Neuropathologica, 144(3), 437-464.
 - . Muscle and Nerve, 66(3), 362-369.
 - . Human Molecular Genetics, 31(16), 2693-2710.
 - . ACS Chemical Neuroscience, 12(10), 1768-1776.
 - . Brain, 1-20.
 - . Molecular Therapy : Nucleic Acids, 12, 75-88.
 - . Molecular Therapy - Methods and Clinical Development, 9, 81-89.
 - . Scientific Reports, 7.
 - . Nature Neuroscience, 20(9), 1225-1235.
 - . Disease Models and Mechanisms.
 - . Molecular Therapy — Methods & Clinical Development, 2016(3).
 
Conference proceedings
- AAV9-mediated gene replacement therapy for spastic paraplegia 47. Human Gene Therapy, Vol. 35(3-4) (pp A181-A182). Brussels, Belgium, 24 October 2023 - 24 October 2023.
 - Gene-based therapeutics for C9ALS/FTD. HUMAN GENE THERAPY, Vol. 33(23-24) (pp A91-A91)
 - Gene Replacement Therapy for Spastic Paraplegia 47. HUMAN GENE THERAPY, Vol. 33(23-24) (pp A26-A27)
 - Use of FACs to isolate targeted neurons for transcriptomic analysis. NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, Vol. 46 (pp 47-47)
 - Gene editing as a potential therapeutic approach for ALS/FTD-associated with expanded C9ORF72. HUMAN GENE THERAPY, Vol. 30(8) (pp A22-A22)
 - Development of an AAV9-mediated gene therapy for hereditary spastic paraplegia 47. HUMAN GENE THERAPY, Vol. 30(8) (pp A18-A18)
 - Adipose derived stem cells for cell therapy of motor neuron disease (MND). HUMAN GENE THERAPY, Vol. 30(8) (pp A16-A16)
 - AAV-mediated gene editing as a potential therapeutic approach for C9ORF72-linked ALS/FTD. HUMAN GENE THERAPY, Vol. 30(11) (pp A96-A96)
 - . Human Gene Therapy, Vol. 27(7) (pp A12-A12). University College London Institute of Child Health
 - Experimental modelling of ALS by AAV-mediated in vivo modulation of the C9ORF72 gene. HUMAN GENE THERAPY, Vol. 27(7) (pp A16-A16)