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The American Journal of Physiology|August 13, 1999
Blood glucose patterns and appetite in time-blinded humans: carbohydrate versus fatK J Melanson, M S Westerterp-Plantenga, W H Saris, et al.American Journal of Ophthalmology|December 28, 1999
A novel mutation in the helix termination motif of keratin K12 in a US family with Meesmann corneal dystrophyC M Coleman, S Hannush, S P Covello, et al.Pediatric Rheumatology Online Journal|October 21, 2016
"Sometimes I feel like a pharmacist": identity and medication use among adolescents with juvenile arthritisJ E McDonagh, K L Shaw, J Prescott, et al.Experimental Eye Research|January 25, 2000
Molecular genetics of Meesmann's corneal dystrophy: ancestral and novel mutations in keratin 12 (K12) and complete sequence of the human KRT12 geneL D Corden, O Swensson, B Swensson, et al.The British Journal of Dermatology|November 13, 2001
Keratin K6irs is specific to the inner root sheath of hair follicles in mice and humansR M Porter, L D Corden, D P Lunny, et al.Clinical and Experimental Dermatology|January 24, 2021
Identification of clinically useful predictive genetic variants in pachyonychia congenitaL Samuelov, O Sarig, N Adir, et al.The Journal of Investigative Dermatology|May 12, 2001
Novel keratin 17 mutations in pachyonychia congenita type 2F J Smith, C M Coleman, N M Bayoumy, et al.The British Journal of Dermatology|May 8, 1999
Ichthyosis bullosa of Siemens: report of a family with evidence of a keratin 2e mutation, and a review of the literatureT Basarab, F J Smith, V M Jolliffe, et al.The Journal of Clinical Investigation|November 15, 1996
A homozygous nonsense mutation in the PLEC1 gene in patients with epidermolysis bullosa simplex with muscular dystrophyS Chavanas, L Pulkkinen, Y Gache, et al.The Journal of Investigative Dermatology|June 9, 2000
A mutation in the V1 domain of K16 is responsible for unilateral palmoplantar verrucous nevusA Terrinoni, P Puddu, B Didona, et al.Pageof 10