E. B. Lane

发表

Keratin K6irs is specific to the inner root sheath of hair follicles in mice and humans

D. Lunny, R. Porter, F. Smith, 2001, The British journal of dermatology.

Stem Cells in Hair Follicles

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

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.

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

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

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.

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.

Monospecific monoclonal antibodies to keratin 1 carboxy terminal (synthetic peptide) and to keratin 10 as markers of epidermal differentiation

I. Leigh, P. Purkis, E. B. Lane, 1993, The British journal of 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.

Sequence of cDNA coding for human keratin 19.

P. Stasiak, E. B. Lane, 1987, Nucleic acids research.

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

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

Plectin defects in epidermolysis bullosa simplex with muscular dystrophy

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

Recessive epidermolysis bullosa simplex associated with plectin mutations: infantile respiratory complications in two unrelated cases

E. Lane, J. R. McMillan, J. Uitto, 1997, The British journal of dermatology.

Functional analysis of keratin components in the mouse hair follicle inner root sheath

R. Porter, N. Wilson, W. McLean, 2004, The British journal of dermatology.

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.

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

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

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.

Keratin 19: predicted amino acid sequence and broad tissue distribution suggest it evolved from keratinocyte keratins.

I. Leigh, P. Purkis, P. Stasiak, 1989, The Journal of investigative dermatology.

Steatocystoma multiplex, oligodontia and partial persistent primary dentition associated with a novel keratin 17 mutation

E. Lane, N. Burrows, N. Wilson, 2009, The British journal of dermatology.

Immunohistochemical localization of cytokeratins, smooth muscle actin and vimentin in human normal salivery glands and pleomorphic adenomas with particular reference to myoepithelial and basal cells

A. Draeger, T. Stigbrand, B. Sundström, 1991 .

A functional "knockout" of human keratin 14.

E. Lane, J. R. McMillan, I. Leigh, 1994, Genes & development.

(16) The cytokeratin profile of normal vulval epithelium and vulval lichen sclerosus

I. Leigh, S. Neill, E. B. Lane, 1990 .