Irvine AD - Search Results

1

Filaggrin mutations, atopic eczema, hay fever, and asthma in children.

Weidinger S, O'Sullivan M, Illig T, Baurecht H, Depner M, Rodriguez E, Ruether A, Klopp N, Vogelberg C, Weiland SK, McLean WH, von Mutius E, Irvine AD, Kabesch M. Weidinger S, et al. Among authors: irvine ad. J Allergy Clin Immunol. 2008 May;121(5):1203-1209.e1. doi: 10.1016/j.jaci.2008.02.014. Epub 2008 Apr 8. J Allergy Clin Immunol. 2008. PMID: 18396323

2

Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophy.

Irvine AD, Corden LD, Swensson O, Swensson B, Moore JE, Frazer DG, Smith FJ, Knowlton RG, Christophers E, Rochels R, Uitto J, McLean WH. Irvine AD, et al. Nat Genet. 1997 Jun;16(2):184-7. doi: 10.1038/ng0697-184. Nat Genet. 1997. PMID: 9171831

3

A mutation detection strategy for the human keratin 6A gene and novel missense mutations in two cases of pachyonychia congenita type 1.

Smith FJ, McKenna KE, Irvine AD, Bingham EA, Coleman CM, Uitto J, McLean WH. Smith FJ, et al. Among authors: irvine ad. Exp Dermatol. 1999 Apr;8(2):109-14. doi: 10.1111/j.1600-0625.1999.tb00356.x. Exp Dermatol. 1999. PMID: 10232400

4

Human keratin diseases: the increasing spectrum of disease and subtlety of the phenotype-genotype correlation.

Irvine AD, McLean WH. Irvine AD, et al. Br J Dermatol. 1999 May;140(5):815-28. doi: 10.1046/j.1365-2133.1999.02810.x. Br J Dermatol. 1999. PMID: 10354017 Review.

5

A novel mutation in the 2B domain of keratin 2e causing ichthyosis bullosa of Siemens.

Irvine AD, Smith FJ, Shum KW, Williams HC, McLean WH. Irvine AD, et al. Clin Exp Dermatol. 2000 Nov;25(8):648-51. doi: 10.1046/j.1365-2230.2000.00728.x. Clin Exp Dermatol. 2000. PMID: 11167982

6

Two cases of primarily palmoplantar keratoderma associated with novel mutations in keratin 1.

Terron-Kwiatkowski A, Paller AS, Compton J, Atherton DJ, McLean WH, Irvine AD. Terron-Kwiatkowski A, et al. Among authors: irvine ad. J Invest Dermatol. 2002 Oct;119(4):966-71. doi: 10.1046/j.1523-1747.2002.00186.x. J Invest Dermatol. 2002. PMID: 12406346 Free article.

7

Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris.

Smith FJ, Irvine AD, Terron-Kwiatkowski A, Sandilands A, Campbell LE, Zhao Y, Liao H, Evans AT, Goudie DR, Lewis-Jones S, Arseculeratne G, Munro CS, Sergeant A, O'Regan G, Bale SJ, Compton JG, DiGiovanna JJ, Presland RB, Fleckman P, McLean WH. Smith FJ, et al. Among authors: irvine ad. Nat Genet. 2006 Mar;38(3):337-42. doi: 10.1038/ng1743. Epub 2006 Jan 29. Nat Genet. 2006. PMID: 16444271

8

Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis.

Palmer CN, Irvine AD, Terron-Kwiatkowski A, Zhao Y, Liao H, Lee SP, Goudie DR, Sandilands A, Campbell LE, Smith FJ, O'Regan GM, Watson RM, Cecil JE, Bale SJ, Compton JG, DiGiovanna JJ, Fleckman P, Lewis-Jones S, Arseculeratne G, Sergeant A, Munro CS, El Houate B, McElreavey K, Halkjaer LB, Bisgaard H, Mukhopadhyay S, McLean WH. Palmer CN, et al. Among authors: irvine ad. Nat Genet. 2006 Apr;38(4):441-6. doi: 10.1038/ng1767. Epub 2006 Mar 19. Nat Genet. 2006. PMID: 16550169

9

Breaking the (un)sound barrier: filaggrin is a major gene for atopic dermatitis.

Irvine AD, McLean WH. Irvine AD, et al. J Invest Dermatol. 2006 Jun;126(6):1200-2. doi: 10.1038/sj.jid.5700365. J Invest Dermatol. 2006. PMID: 16702964 Free article.

10

Prevalent and rare mutations in the gene encoding filaggrin cause ichthyosis vulgaris and predispose individuals to atopic dermatitis.

Sandilands A, O'Regan GM, Liao H, Zhao Y, Terron-Kwiatkowski A, Watson RM, Cassidy AJ, Goudie DR, Smith FJ, McLean WH, Irvine AD. Sandilands A, et al. Among authors: irvine ad. J Invest Dermatol. 2006 Aug;126(8):1770-5. doi: 10.1038/sj.jid.5700459. Epub 2006 Jun 29. J Invest Dermatol. 2006. PMID: 16810297 Free article.

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