Publications by Dr Eugene Healy - ePrints

Browsing publications by Dr Eugene Healy.

Newcastle Authors	Title	Year
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 microenvironment	2023
Dr Eugene Healy Professor Sian Robinson	Faltering of prenatal growth precedes the development of atopic eczema in infancy: cohort study	2018
Dr Sara Brown Stacey Langan Professor Nick Reynolds Dr Eugene Healy	Identifying translational dermatology research priorities in the UK: results of an e-Delphi exercise	2015
Emeritus Professor Brian Diffey Dr Eugene Healy	Protection against UVR Involves MC1R-Mediated Non-Pigmentary and Pigmentary Mechanisms In Vivo	2010
Dr Eugene Healy Dr Amanda Ray Dr Niamh Flanagan Carole Todd Professor Mark Birch-Machin et al.	Evidence for variable selective pressures at MC1R	2000
Simon Carter Dr Eugene Healy Professor Tom Strachan	Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca2+ pump	2000
Dr Eugene Healy Dr Amanda Ray Professor John Matthews Professor Mark Birch-Machin Professor Jonathan Rees et al.	Melanocortin-1-receptor gene and sun sensitivity in individuals without red hair	2000
Dr Eugene Healy Professor Jonathan Rees	Novel keratin 16 mutations and protein expression studies in pachyonychia congenita type 1 and focal palmoplantar keratoderma	2000
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 pigmentation	2000
Dr Eugene Healy Professor Mark Birch-Machin Professor Jonathan Rees	The Human Melanocortin1-Receptor Gene	2000
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 class	1999
Dr Victor Ruiz-Perez Simon Carter Dr Eugene Healy Professor Jonathan Rees Professor Tom Strachan et al.	Classical and variant Darier disease due to mutation in ATP2A2	1999
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 phenotype	1999
Professor Jonathan Rees Professor Mark Birch-Machin Dr Niamh Flanagan Dr Eugene Healy	Genetic studies of the human melanocortin-1 receptor	1999
Professor Jonathan Rees Professor Mark Birch-Machin Dr Niamh Flanagan Dr Eugene Healy	Genetic studies of the human melanocortin-1 receptor	1999
Dr Niamh Flanagan Dr Eugene Healy Dr Amanda Ray Professor Mark Birch-Machin	Heterozygote mutants of the melanocortin 1 receptor show reduced tanning whilst homozyotes show red hair	1999
Dr Eugene Healy Professor Mark Birch-Machin Professor Jonathan Rees	Identification of novel mutations in basic hair keratins hHb1 and hHb6 in monilethrix: Implications for protein structure and clinical phenotype	1999
Dr Amanda Ray Dr Eugene Healy Carein Todd Dr Niamh Flanagan Professor Mark Birch-Machin et al.	Molecular genetic evidence for evolutionary selection of the red hair (MC1R) phenotype	1999
Dr Eugene Healy Professor Mark Birch-Machin Professor Jonathan Rees Catriona Munro	Point mutation in the helix termination peptide (HTP) of human type II hair keratin hHb6 causes monilethrix in five families	1999
Dr Eugene Healy Professor Mark Birch-Machin	Point mutations in the 1A domain (N114) of hair keratin hHb6 in monilethrix patients: A new hotspot for mutations?	1999
Dr Eugene Healy Professor Jonathan Rees	Rescue of pigmentation phenotype in ee mice transgenic for murine and human wild type melanocortin 1 receptor genes demonstrates that this receptor controls both interfollicular and follicular pigmentation	1999
Dr Eugene Healy Carole Todd Professor Mark Birch-Machin Professor Jonathan Rees	Skin type, melanoma, and melanocortin 1 receptor variants	1999
Emeritus Professor Drew Rowan Dr Eugene Healy	Somatic mutations in the Peutz-Jegners (LKB1/STKII) gene in sporadic malignant melanomas	1999