E. Lane

发表

Stem Cells in Hair Follicles

C. A. Wilson, I. Leigh, B. Hughes, 1991 .

Generation and characterization of epidermolysis bullosa simplex cell lines: scratch assays show faster migration with disruptive keratin mutations

M. D'alessandro, D. Hohl, I. Leigh, 2003, The British journal of dermatology.

Clinical and pathological features of pachyonychia congenita.

E. Lane, S. Leachman, S. Florell, 2005, The journal of investigative dermatology. Symposium proceedings.

Human keratin 8 mutations that disturb filament assembly observed in inflammatory bowel disease patients

M. Parkes, J. Satsangi, D. Jewell, 2004, Journal of Cell Science.

A Novel Mutation in the Keratin 13 Gene Causing Oral White Sponge Nevus

G. Melino, A. Terrinoni, C. Munro, 2001, Journal of dental research.

A keratin 14 ‘knockout’ mutation in recessive epidermolysis bullosa simplex resulting in less severe disease

E. Lane, R. Eady, N. West, 2000, The British journal of dermatology.

DNA based prenatal testing for the skin blistering disorder epidermolysis bullosa simplex

E. Lane, R. Bergman, T. Falik-Zaccai, 2000, Prenatal diagnosis.

Laryngeal involvement in the Dowling–Meara variant of epidermolysis bullosa simplex with keratin mutations of severely disruptive potential

N. Hepburn, S. Keohane, E. B. Lane, 2000, The British journal of dermatology.

Novel and recurrent mutations in keratin 10 causing bullous congenital ichthyosiform erythroderma

I. Leigh, M. White, P. Bowden, 1999, Experimental dermatology.

Missing links: Weber–Cockayne keratin mutations implicate the L12 linker domain in effective cytoskeleton function

I. Leigh, H. Navsaria, M. Boxer, 1993, Nature Genetics.

Wide spectrum of filaggrin‐null mutations in atopic dermatitis highlights differences between Singaporean Chinese and European populations

M. Tang, J. Common, H. Cordell, 2011, The British journal of dermatology.

Plectin defects in epidermolysis bullosa simplex with muscular dystrophy

E. Lane, J. R. McMillan, M. Akiyama, 2007, Muscle & nerve.