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Nature Genetics|November 1, 1993
Missing links: Weber-Cockayne keratin mutations implicate the L12 linker domain in effective cytoskeleton functionE L Rugg, S M Morley, F J Smith, et al.Nature Genetics|December 1, 1995
A mutation in the mucosal keratin K4 is associated with oral white sponge nevusE L Rugg, W H McLean, W E Allison, et al.The British Journal of Dermatology|September 6, 2000
A keratin 14 'knockout' mutation in recessive epidermolysis bullosa simplex resulting in less severe diseaseK Batta, E L Rugg, N J Wilson, et al.Laboratory Investigation; a Journal of Technical Methods and Pathology|November 25, 2000
K15 expression implies lateral differentiation within stratified epithelial basal cellsR M Porter, D P Lunny, P H Ogden, et al.Prenatal Diagnosis|May 23, 2000
DNA based prenatal testing for the skin blistering disorder epidermolysis bullosa simplexE L Rugg, D Baty, C S Shemanko, et al.Genes & Development|November 1, 1994
A functional "knockout" of human keratin 14E L Rugg, W H McLean, E B Lane, et al.The British Journal of Dermatology|August 2, 2003
Generation and characterization of epidermolysis bullosa simplex cell lines: scratch assays show faster migration with disruptive keratin mutationsS M Morley, M D'Alessandro, C Sexton, et al.Nature Genetics|March 1, 1995
Keratin 16 and keratin 17 mutations cause pachyonychia congenitaW H McLean, E L Rugg, D P Lunny, et al.The Journal of Investigative Dermatology|February 1, 1997
Missense mutations in keratin 17 cause either pachyonychia congenita type 2 or a phenotype resembling steatocystoma multiplexF J Smith, L D Corden, E L Rugg, et al.Journal of Cell Science|April 20, 2004
Human keratin 8 mutations that disturb filament assembly observed in inflammatory bowel disease patientsD W Owens, N J Wilson, A J M Hill, et al.Pageof 4