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Browsing publications by Dr Eugene Healy

Newcastle AuthorsTitleYearFull text
Emeritus Professor Brian Diffey
Dr Eugene Healy
Mutation burden of narrowband ultraviolet B phototherapy (NB-UVB) in human skin: relevance to NB-UVB lifetime exposures and skin cancer surveillance2025
Dr Jing Xuan Lim
Grace Mallett
Dr David McDonald
Dr Gill Hulme
Dr Stephanie Laba
et al.		Programmed cell death-1 receptor-mediated regulation of Tbet+NK1.1- innate lymphoid cells within the tumor microenvironment2023
Dr Eugene Healy
Professor Sian Robinson
Faltering of prenatal growth precedes the development of atopic eczema in infancy: cohort study2018
Dr Sara Brown
Stacey Langan
Professor Nick Reynolds
Dr Eugene Healy
Identifying translational dermatology research priorities in the UK: results of an e-Delphi exercise2015
Emeritus Professor Brian Diffey
Dr Eugene Healy
Protection against UVR Involves MC1R-Mediated Non-Pigmentary and Pigmentary Mechanisms In Vivo2010
Dr Eugene Healy
Dr Amanda Ray
Dr Niamh Flanagan
Carole Todd
Professor Mark Birch-Machin
et al.		Evidence for variable selective pressures at MC1R2000
Simon Carter
Dr Eugene Healy
Professor Tom Strachan
Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca2+ pump2000
Dr Eugene Healy
Dr Amanda Ray
Professor John Matthews
Professor Mark Birch-Machin
Professor Jonathan Rees
Melanocortin-1-receptor gene and sun sensitivity in individuals without red hair2000
Dr Eugene Healy
Professor Jonathan Rees
Novel keratin 16 mutations and protein expression studies in pachyonychia congenita type 1 and focal palmoplantar keratoderma2000
Dr Niamh Flanagan
Dr Eugene Healy
Dr Amanda Ray
Carole Todd
Professor Mark Birch-Machin
et al.		Pleiotropic effects of the melanocortin 1 receptor (MC1R) gene on human pigmentation2000
Dr Eugene Healy
Professor Mark Birch-Machin
Professor Jonathan Rees
The Human Melanocortin1-Receptor Gene2000
Dr Victor Ruiz-Perez
Simon Carter
Dr Eugene Healy
Carole Todd
Professor Jonathan Rees
et al.		ATP2A2 mutations in Darier's disease: Variant cutaneous phenotypes are associated with missense mutations, but neuropsychiatric features are independent of mutation class1999
Dr Victor Ruiz-Perez
Simon Carter
Dr Eugene Healy
Professor Jonathan Rees
Professor Tom Strachan
Classical and variant Darier disease due to mutation in ATP2A21999
Dr Eugene Healy
Professor Mark Birch-Machin
Professor Jonathan Rees
Distinct mutations in human basic hair keratins 1 and 6 cause monilethrix: Implications for protein structure and clinical phenotype1999
Professor Jonathan Rees
Professor Mark Birch-Machin
Dr Niamh Flanagan
Dr Eugene Healy
Genetic studies of the human melanocortin-1 receptor1999
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