Bowden PE - Search Results

1

Photosensitive Smith-Lemli-Opitz syndrome is not caused by a single gene mutation: analysis of the gene encoding 7-dehydrocholesterol reductase in five U.K. families.

Anstey AV, Azurdia RM, Rhodes LE, Pearse AD, Bowden PE. Anstey AV, et al. Among authors: bowden pe. Br J Dermatol. 2005 Oct;153(4):774-9. doi: 10.1111/j.1365-2133.2005.06761.x. Br J Dermatol. 2005. PMID: 16181459

2

Epidermolysis bullosa simplex due to KRT5 mutations: mutation-related differences in cellular fragility and the protective effects of trimethylamine N-oxide in cultured primary keratinocytes.

Chamcheu JC, Virtanen M, Navsaria H, Bowden PE, Vahlquist A, Törmä H. Chamcheu JC, et al. Among authors: bowden pe. Br J Dermatol. 2010 May;162(5):980-9. doi: 10.1111/j.1365-2133.2009.09615.x. Epub 2010 Feb 1. Br J Dermatol. 2010. PMID: 20128788

3

A new keratin 2e mutation in ichthyosis bullosa of Siemens.

Jones DO, Watts C, Mills C, Sharpe G, Marks R, Bowden PE. Jones DO, et al. Among authors: bowden pe. J Invest Dermatol. 1997 Mar;108(3):354-6. doi: 10.1111/1523-1747.ep12286487. J Invest Dermatol. 1997. PMID: 9036938 Free article.

4

Utilization of a cryptic noncanonical donor splice site in the KRT14 gene causes a mild form of epidermolysis bullosa simplex.

Han S, Cooper DN, Bowden PE. Han S, et al. Among authors: bowden pe. Br J Dermatol. 2006 Jul;155(1):201-3. doi: 10.1111/j.1365-2133.2006.07269.x. Br J Dermatol. 2006. PMID: 16792776 No abstract available.

5

Splice site and deletion mutations in keratin (KRT1 and KRT10) genes: unusual phenotypic alterations in Scandinavian patients with epidermolytic hyperkeratosis.

Virtanen M, Smith SK, Gedde-Dahl T Jr, Vahlquist A, Bowden PE. Virtanen M, et al. Among authors: bowden pe. J Invest Dermatol. 2003 Nov;121(5):1013-20. doi: 10.1046/j.1523-1747.2003.12534.x. J Invest Dermatol. 2003. PMID: 14708600 Free article.

6

Two different mutations in the same codon of a type II hair keratin (hHb6) in patients with monilethrix.

Pearce EG, Smith SK, Lanigan SW, Bowden PE. Pearce EG, et al. Among authors: bowden pe. J Invest Dermatol. 1999 Dec;113(6):1123-7. doi: 10.1046/j.1523-1747.1999.00777.x. J Invest Dermatol. 1999. PMID: 10594761 Free article.

7

Mutations in a keratin 6 isomer (K6c) cause a type of focal palmoplantar keratoderma.

Bowden PE. Bowden PE. J Invest Dermatol. 2010 Feb;130(2):336-8. doi: 10.1038/jid.2009.395. J Invest Dermatol. 2010. PMID: 20081885 Free article.

8

Numerous keratinocyte subtypes involved in wound re-epithelialization.

Patel GK, Wilson CH, Harding KG, Finlay AY, Bowden PE. Patel GK, et al. Among authors: bowden pe. J Invest Dermatol. 2006 Feb;126(2):497-502. doi: 10.1038/sj.jid.5700101. J Invest Dermatol. 2006. PMID: 16374449 Free article.

9

Peeling skin syndrome: genetic defects in late terminal differentiation of the epidermis.

Bowden PE. Bowden PE. J Invest Dermatol. 2011 Mar;131(3):561-4. doi: 10.1038/jid.2010.434. J Invest Dermatol. 2011. PMID: 21307953 Free article.

10

A mutation (N177S) in the structurally conserved helix initiation peptide motif of keratin 5 causes a mild EBS phenotype.

Liovic M, Bowden PE, Marks R, Komel R. Liovic M, et al. Among authors: bowden pe. Exp Dermatol. 2004 May;13(5):332-4. doi: 10.1111/j.0906-6705.2004.00171.x. Exp Dermatol. 2004. PMID: 15140024

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