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Ryan O´Shaughnessy

 

Dr. Ryan O´Shaughnessy

Senior Research Associate in Skin Biology
Immunobiology
UCL Institute of Child Health
30 Guilford Street
London WC1N 1EH
UK

phone: +44 (0)207 905 2182
r.oshaughnessy@ich.ucl.ac.uk


Research focus

  • The molecular mechanisms of barrier acquisition during development

  • Mechanisms of barrier disruption in skin disease (Eczema and Lamellar Ichthyosis), and viral infection (HPV)




Important publications

  • Ben Jackson, Stuart J. Brown, Ariel A. Avilion, Katherine Sully, O'Shaughnessy RFL, Mark Murphy, Maria Ambrus, Michael L. Cleary, Carolyn Byrne. TALE homeodomain proteins regulate body site-specific epidermal terminal differentiation and skin barrier. J Cell Sci 2011; 124:1681-1690

  • O'Shaughnessy RFL, Choudhary I and Harper JI. Interleukin-1 alpha blockade prevents hyperkeratosis in an in vitro model of lamellar ichthyosis -Human Molecular Genetics 2010; 19(13): 2594-2605

  • Byrne CR, Avilion AA, O'Shaughnessy RFL, Welti JC and Hardman MJ. Whole-Mount Assays for Gene Induction and Barrier Formation in the Developing Epidermis - Methods in Molecular Biology 2010; 585 (271-86)

  • O'Shaughnessy RFL, Welti JC, Byrne C, AKT-Dependent PP2A activity is required for epidermal barrier formation during late embryonic development. Development 2009. Sep, 136: 3423-3431

  • O'Shaughnessy RFL, Akgul B, Pfister H, Harwood C and Byrne CR. Cutaneous human papillomaviruses downregulate Akt1 while Akt2 upregulation and activation associates with tumours. Cancer Res. 2007 Sep 1; 67(17):1-9

  • O'Shaughnessy RFL, Welti JC, Cooke JC, Avilion AA, Monks B, Birnbaum MJ, Byrne C. AKT-dependent HspB1 (Hsp27) Activity in Epidermal Differentiation. J Biol Chem. 2007 Jun 8;282(23):17297-305

  • O'Shaughnessy RFL, Christiano AM. Inherited disorders of the skin in human and mouse: from development to differentiation. Int J Dev Biol. 2004;48(2-3):171-9

  • Jahoda CA, Kljuic A, O'Shaughnessy RFL, Crossley N, Whitehouse CJ, Robinson M, Reynolds AJ et al.,. The lanceolate hair rat phenotype results from a missense mutation in a calcium coordinating site of the desmoglein 4 gene. Genomics. 2004 May;83(5):747-56

  • Kljuic A, Bazzi H, Sundberg JP, Martinez-Mir A, O'Shaughnessy RFL, Mahoney MG et al.,. Desmoglein 4 in hair follicle differentiation and epidermal adhesion: evidence from inherited hypotrichosis and acquired pemphigus vulgaris. Cell. 2003 Apr 18;113(2):249-60

 

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