Works matching AU Healy, Eugene


Results: 63
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    Impaired expression of metallothioneins contributes to allergen-induced inflammation in patients with atopic dermatitis.

    Published in:
    Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-38588-1
    By:
    • Sirvent, Sofia;
    • Vallejo, Andres F.;
    • Corden, Emma;
    • Teo, Ying;
    • Davies, James;
    • Clayton, Kalum;
    • Seaby, Eleanor G.;
    • Lai, Chester;
    • Ennis, Sarah;
    • Alyami, Rfeef;
    • Douilhet, Gemma;
    • Dean, Lareb S. N.;
    • Loxham, Matthew;
    • Horswill, Sarah;
    • Healy, Eugene;
    • Roberts, Graham;
    • Hall, Nigel J.;
    • Friedmann, Peter S.;
    • Singh, Harinder;
    • Bennett, Clare L.
    Publication type:
    Article
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    P07 Mutagenicity of narrowband ultraviolet B.

    Published in:
    British Journal of Dermatology, 2024, v. 190, n. 6, p. e82, doi. 10.1093/bjd/ljae105.029
    By:
    • Fowler, Joanna;
    • Coltart, George;
    • Sood, Roshan;
    • Lai, Chester;
    • Nadarajah, Noeline;
    • Jones, Philip;
    • Healy, Eugene
    Publication type:
    Article
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    A systematic review and network meta‐analysis of topical pharmacological, oral pharmacological, physical and combined treatments for acne vulgaris.

    Published in:
    British Journal of Dermatology, 2022, v. 187, n. 5, p. 639, doi. 10.1111/bjd.21739
    By:
    • Mavranezouli, Ifigeneia;
    • Daly, Caitlin H.;
    • Welton, Nicky J.;
    • Deshpande, Shalmali;
    • Berg, Laura;
    • Bromham, Nathan;
    • Arnold, Stephanie;
    • Phillippo, David M.;
    • Wilcock, Jane;
    • Xu, Jingyuan;
    • Ravenscroft, Jane C.;
    • Wood, Damian;
    • Rafiq, Mohammed;
    • Fou, Linyun;
    • Dworzynski, Katharina;
    • Healy, Eugene
    Publication type:
    Article
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    Prognostic significance of allelic losses in primary melanoma.

    Published in:
    Oncogene, 1998, v. 16, n. 17, p. 2213, doi. 10.1038/sj.onc.1200203
    By:
    • Healy, Eugene;
    • Belgaid, Christine;
    • Takata, Minoru;
    • Harrison, David;
    • Wen Zhu, Ning;
    • Burd, D Andrew R;
    • Rigby, Howard S;
    • Matthews, John NS;
    • Rees, Jonathan L
    Publication type:
    Article
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    Neanderthal man’s MC1R plays fair.

    Published in:
    Pigment Cell & Melanoma Research, 2008, v. 21, n. 3, p. 340, doi. 10.1111/j.1755-148X.2008.00465.x
    By:
    • Healy, Eugene
    Publication type:
    Article
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    Genetic Studies of the Human Melanocortin-1 Receptor.

    Published in:
    Annals of the New York Academy of Sciences, 1999, v. 885, n. 1, p. 134, doi. 10.1111/j.1749-6632.1999.tb08670.x
    By:
    • REES, JONATHAN L.;
    • BIRCH-MACHIN, MARK;
    • FLANAGAN, NIAMH;
    • HEALY, EUGENE;
    • PHILLIPS, SION;
    • TODD, CAROLE
    Publication type:
    Article
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    In this Issue.

    Published in:
    1999
    By:
    • Healy, Eugene
    Publication type:
    Bibliography
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    Melanocortin 1 Receptor Variants in an Irish Population.

    Published in:
    Journal of Investigative Dermatology, 1998, v. 111, n. 1, p. 119, doi. 10.1046/j.1523-1747.1998.00252.x
    By:
    • Smith, Rachel;
    • Healy, Eugene;
    • Siddiqui, Shazia;
    • Flanagan, Niamh;
    • Steijlen, Peter M.;
    • Rosdahl, Inger;
    • Jacques, Jon P.;
    • Rogers, Sarah;
    • Turner, Richard;
    • Jackson, Ian J.;
    • Birch‐machin, Mark A.;
    • Rees, Jonathan L.
    Publication type:
    Article
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    Reply to Fuxench et al.

    Published in:
    Pediatric Allergy & Immunology, 2023, v. 34, n. 9, p. 1, doi. 10.1111/pai.14009
    By:
    • El‐Heis, Sarah;
    • Crozier, Sarah;
    • Harvey, Nicholas;
    • Healy, Eugene;
    • Godfrey, Keith M.
    Publication type:
    Article
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    Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca[sup 2+] pump.

    Published in:
    Human Molecular Genetics, 2000, v. 9, n. 7, p. 1131, doi. 10.1093/hmg/9.7.1131
    By:
    • Sudbrak, Ralf;
    • Brown, Joanna;
    • Dobson-Stone, Carol;
    • Carter, Simon;
    • Ramser, Juliane;
    • White, Jacqueline;
    • Healy, Eugene;
    • Dissanayake, Manel;
    • Larrègue, Marc;
    • Perrussel, Marc;
    • Lehrach, Hans;
    • Munro, Colin S.;
    • Strachan, Tom;
    • Burge, Susan;
    • Hovnanian, Alain;
    • Monaco, Anthony P.
    Publication type:
    Article
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    ATP2A2 mutations in Darier's disease: variant cutaneous phenotypes are associated with missense mutations, but neuropsychiatric features are independent of mutation class.

    Published in:
    Human Molecular Genetics, 1999, v. 8, n. 9, p. 1621, doi. 10.1093/hmg/8.9.1621
    By:
    • Ruiz-Perez, Victor L.;
    • Carter, Simon A.;
    • Healy, Eugene;
    • Todd, Carole;
    • Rees, Jonathan L.;
    • Steijlen, Peter M.;
    • Carmichael, Andrew J.;
    • Lewis, Helen M.;
    • Hohl, D.;
    • Itin, Peter;
    • Vahlquist, Anders;
    • Gobello, T.;
    • Mazzanti, C.;
    • Reggazini, R.;
    • Nagy, Gyula;
    • Munro, Colin S.;
    • Strachan, Tom
    Publication type:
    Article
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    Multiple Congenital Melanocytic Nevi and Neurocutaneous Melanosis Are Caused by Postzygotic Mutations in Codon 61 of NRAS.

    Published in:
    Journal of Investigative Dermatology, 2013, v. 133, n. 9, p. 2229, doi. 10.1038/jid.2013.70
    By:
    • Kinsler, Veronica A;
    • Thomas, Anna C;
    • Ishida, Miho;
    • Bulstrode, Neil W;
    • Loughlin, Sam;
    • Hing, Sandra;
    • Chalker, Jane;
    • McKenzie, Kathryn;
    • Abu-Amero, Sayeda;
    • Slater, Olga;
    • Chanudet, Estelle;
    • Palmer, Rodger;
    • Morrogh, Deborah;
    • Stanier, Philip;
    • Healy, Eugene;
    • Sebire, Neil J;
    • Moore, Gudrun E
    Publication type:
    Article
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