W. McLean

Calpain 12 Function Revealed through the Study of an Atypical Case of Autosomal Recessive Congenital Ichthyosis.

O. Sarig, G. Ast, N. Shomron, 2016, The Journal of investigative dermatology.

Unique and recurrent mutations in the filaggrin gene in Singaporean Chinese patients with ichthyosis vulgaris.

E. Lane, W. McLean, Huijia Chen, 2008, The Journal of investigative dermatology.

Specific filaggrin mutations cause ichthyosis vulgaris and are significantly associated with atopic dermatitis in Japan.

M. Akiyama, H. Shimizu, C. Palmer, 2008, The Journal of investigative dermatology.

De novo occurrence of the filaggrin mutation p.R501X with prevalent mutation c.3321delA in a Japanese family with ichthyosis vulgaris complicated by atopic dermatitis.

W. McLean, T. Hashimoto, B. Ohyama, 2008, The Journal of investigative dermatology.

Filaggrin genotype does not determine the skin's threshold to UV-induced erythema

A. Dinkova-Kostova, R. Dawe, S. Maccallum, 2016, The Journal of allergy and clinical immunology.

Filaggrin breakdown products determine corneocyte conformation in patients with atopic dermatitis

S. Kežić, A. Irvine, M. McAleer, 2015, The Journal of allergy and clinical immunology.

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

S. Weiland, N. Klopp, T. Illig, 2008, The Journal of allergy and clinical immunology.