Smith FJ - Search Results

1

Prevalent and rare mutations in the gene encoding filaggrin in Japanese patients with ichthyosis vulgaris and atopic dermatitis.

Nomura T, Akiyama M, Sandilands A, Nemoto-Hasebe I, Sakai K, Nagasaki A, Palmer CN, Smith FJ, McLean WH, Shimizu H. Nomura T, et al. Among authors: smith fj. J Invest Dermatol. 2009 May;129(5):1302-5. doi: 10.1038/jid.2008.372. Epub 2008 Nov 27. J Invest Dermatol. 2009. PMID: 19037238 Free article. No abstract available.

2

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: smith fj. 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.

3

Unique mutations in the filaggrin gene in Japanese patients with ichthyosis vulgaris and atopic dermatitis.

Nomura T, Sandilands A, Akiyama M, Liao H, Evans AT, Sakai K, Ota M, Sugiura H, Yamamoto K, Sato H, Palmer CN, Smith FJ, McLean WH, Shimizu H. Nomura T, et al. Among authors: smith fj. J Allergy Clin Immunol. 2007 Feb;119(2):434-40. doi: 10.1016/j.jaci.2006.12.646. J Allergy Clin Immunol. 2007. PMID: 17291859

4

Filaggrin's fuller figure: a glimpse into the genetic architecture of atopic dermatitis.

Sandilands A, Smith FJ, Irvine AD, McLean WH. Sandilands A, et al. Among authors: smith fj. J Invest Dermatol. 2007 Jun;127(6):1282-4. doi: 10.1038/sj.jid.5700876. J Invest Dermatol. 2007. PMID: 17502856 Free article. Review.

5

Heterozygous null alleles in filaggrin contribute to clinical dry skin in young adults and the elderly.

Sergeant A, Campbell LE, Hull PR, Porter M, Palmer CN, Smith FJ, McLean WH, Munro CS. Sergeant A, et al. Among authors: smith fj. J Invest Dermatol. 2009 Apr;129(4):1042-5. doi: 10.1038/jid.2008.324. Epub 2008 Nov 6. J Invest Dermatol. 2009. PMID: 18987673 Free article. No abstract available.

6

Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema.

Sandilands A, Terron-Kwiatkowski A, Hull PR, O'Regan GM, Clayton TH, Watson RM, Carrick T, Evans AT, Liao H, Zhao Y, Campbell LE, Schmuth M, Gruber R, Janecke AR, Elias PM, van Steensel MA, Nagtzaam I, van Geel M, Steijlen PM, Munro CS, Bradley DG, Palmer CN, Smith FJ, McLean WH, Irvine AD. Sandilands A, et al. Among authors: smith fj. Nat Genet. 2007 May;39(5):650-4. doi: 10.1038/ng2020. Epub 2007 Apr 8. Nat Genet. 2007. PMID: 17417636

7

Filaggrin mutations are genetic modifying factors exacerbating X-linked ichthyosis.

Liao H, Waters AJ, Goudie DR, Aitken DA, Graham G, Smith FJ, Lewis-Jones S, McLean WH. Liao H, et al. Among authors: smith fj. J Invest Dermatol. 2007 Dec;127(12):2795-8. doi: 10.1038/sj.jid.5700971. Epub 2007 Jul 26. J Invest Dermatol. 2007. PMID: 17657246 Free article.

8

A novel connexin 30 mutation in Clouston syndrome.

Smith FJ, Morley SM, McLean WH. Smith FJ, et al. J Invest Dermatol. 2002 Mar;118(3):530-2. doi: 10.1046/j.0022-202x.2001.01689.x. J Invest Dermatol. 2002. PMID: 11874494 Free article.

9

Novel mechanism of revertant mosaicism in Dowling-Meara epidermolysis bullosa simplex.

Smith FJ, Morley SM, McLean WH. Smith FJ, et al. J Invest Dermatol. 2004 Jan;122(1):73-7. doi: 10.1046/j.0022-202X.2003.22129.x. J Invest Dermatol. 2004. PMID: 14962092 Free article.

10

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. Nat Genet. 2006 Mar;38(3):337-42. doi: 10.1038/ng1743. Epub 2006 Jan 29. Nat Genet. 2006. PMID: 16444271

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