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The Journal of Allergy and Clinical Immunology|May 29, 2007
Filaggrin null mutations are associated with increased asthma severity in children and young adultsColin N A Palmer, Tahmina Ismail, Simon P Lee, et al.The Journal of Allergy and Clinical Immunology|March 4, 2008
Filaggrin null mutations and childhood atopic eczema: a population-based case-control studySara J Brown, Caroline L Relton, Haihui Liao, et al.The Journal of Investigative Dermatology|September 19, 2014
Mechanisms of chemical cooperative carcinogenesis by epidermal Langerhans cellsJulia M Lewis, Christina D Bürgler, Juliet A Fraser, et al.Investigative Ophthalmology & Visual Science|December 13, 2012
Allele-specific siRNA silencing for the common keratin 12 founder mutation in Meesmann epithelial corneal dystrophyEdwin H A Allen, Sarah D Atkinson, Haihui Liao, et al.The Journal of Allergy and Clinical Immunology|March 8, 2008
The burden of disease associated with filaggrin mutations: a population-based, longitudinal birth cohort studyJohn Henderson, Kate Northstone, Simon P Lee, et al.The Journal of Investigative Dermatology|July 1, 2006
Prevalent and rare mutations in the gene encoding filaggrin cause ichthyosis vulgaris and predispose individuals to atopic dermatitisAileen Sandilands, Gráinne M O'Regan, Haihui Liao, et al.Plos One|December 17, 2011
Development of allele-specific therapeutic siRNA in Meesmann epithelial corneal dystrophyHaihui Liao, Alan D Irvine, Caroline J Macewen, et al.The Journal of Allergy and Clinical Immunology|February 13, 2007
Unique mutations in the filaggrin gene in Japanese patients with ichthyosis vulgaris and atopic dermatitisToshifumi Nomura, Aileen Sandilands, Masashi Akiyama, et al.The Journal of Investigative Dermatology|September 23, 2006
Null mutations in the filaggrin gene (FLG) determine major susceptibility to early-onset atopic dermatitis that persists into adulthoodJonathan N W N Barker, Colin N A Palmer, Yiwei Zhao, et al.Journal of Dermatological Science|August 28, 2007
A spectrum of mutations in keratins K6a, K16 and K17 causing pachyonychia congenitaHaihui Liao, Jane M Sayers, Neil J Wilson, et al.Pageof 3