Leigh IM - Search Results

1

Genomic organization and fine mapping of the keratin 2e gene (KRT2E): K2e V1 domain polymorphism and novel mutations in ichthyosis bullosa of Siemens.

Smith FJ, Maingi C, Covello SP, Higgins C, Schmidt M, Lane EB, Uitto J, Leigh IM, McLean WH. Smith FJ, et al. Among authors: leigh im. J Invest Dermatol. 1998 Nov;111(5):817-21. doi: 10.1046/j.1523-1747.1998.00371.x. J Invest Dermatol. 1998. PMID: 9804344 Free article.

2

Ichthyosis bullosa of Siemens--a disease involving keratin 2e.

McLean WH, Morley SM, Lane EB, Eady RA, Griffiths WA, Paige DG, Harper JI, Higgins C, Leigh IM. McLean WH, et al. Among authors: leigh im. J Invest Dermatol. 1994 Sep;103(3):277-81. doi: 10.1111/1523-1747.ep12394307. J Invest Dermatol. 1994. PMID: 7521371 Free article.

3

Ultrastructural changes resulting from keratin-9 gene mutations in two families with epidermolytic palmoplantar keratoderma.

Navsaria HA, Swensson O, Ratnavel RC, Shamsher M, McLean WH, Lane EB, Griffiths D, Eady RA, Leigh IM. Navsaria HA, et al. Among authors: leigh im. J Invest Dermatol. 1995 Mar;104(3):425-9. doi: 10.1111/1523-1747.ep12666011. J Invest Dermatol. 1995. PMID: 7532198 Free article.

4

Altered laminin 5 expression due to mutations in the gene encoding the beta 3 chain (LAMB3) in generalized atrophic benign epidermolysis bullosa.

McGrath JA, Pulkkinen L, Christiano AM, Leigh IM, Eady RA, Uitto J. McGrath JA, et al. Among authors: leigh im. J Invest Dermatol. 1995 Apr;104(4):467-74. doi: 10.1111/1523-1747.ep12605904. J Invest Dermatol. 1995. PMID: 7706760 Free article.

5

Keratin 14-null cells as a model to test the efficacy of gene therapy approaches in epithelial cells.

D'Alessandro M, Coats SE, Jonkmann MF, Leigh IM, Lane EB. D'Alessandro M, et al. Among authors: leigh im. J Invest Dermatol. 2011 Jul;131(7):1412-9. doi: 10.1038/jid.2011.19. Epub 2011 Feb 17. J Invest Dermatol. 2011. PMID: 21326298 Free article.

6

Keratin expression in basal cell carcinomas.

Markey AC, Lane EB, Macdonald DM, Leigh IM. Markey AC, et al. Among authors: leigh im. Br J Dermatol. 1992 Feb;126(2):154-60. doi: 10.1111/j.1365-2133.1992.tb07813.x. Br J Dermatol. 1992. PMID: 1371396

7

Selective involvement of keratins K1 and K10 in the cytoskeletal abnormality of epidermolytic hyperkeratosis (bullous congenital ichthyosiform erythroderma).

Ishida-Yamamoto A, McGrath JA, Judge MR, Leigh IM, Lane EB, Eady RA. Ishida-Yamamoto A, et al. Among authors: leigh im. J Invest Dermatol. 1992 Jul;99(1):19-26. doi: 10.1111/1523-1747.ep12611391. J Invest Dermatol. 1992. PMID: 1376754 Free article.

8

Epidermolysis bullosa simplex (Dowling-Meara type) is a genetic disease characterized by an abnormal keratin-filament network involving keratins K5 and K14.

Ishida-Yamamoto A, McGrath JA, Chapman SJ, Leigh IM, Lane EB, Eady RA. Ishida-Yamamoto A, et al. Among authors: leigh im. J Invest Dermatol. 1991 Dec;97(6):959-68. doi: 10.1111/1523-1747.ep12491885. J Invest Dermatol. 1991. PMID: 1721080 Free article.

9

Mutations in the genes for epidermal keratins in epidermolysis bullosa and epidermolytic hyperkeratosis.

Leigh IM, Lane EB. Leigh IM, et al. Arch Dermatol. 1993 Dec;129(12):1571-7. Arch Dermatol. 1993. PMID: 7504434 Review.

10

Mutations in the rod 1A domain of keratins 1 and 10 in bullous congenital ichthyosiform erythroderma (BCIE).

McLean WH, Eady RA, Dopping-Hepenstal PJ, McMillan JR, Leigh IM, Navsaria HA, Higgins C, Harper JI, Paige DG, Morley SM, et al. McLean WH, et al. Among authors: leigh im. J Invest Dermatol. 1994 Jan;102(1):24-30. doi: 10.1111/1523-1747.ep12371726. J Invest Dermatol. 1994. PMID: 7507152 Free article.

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