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Journal of Clinical Microbiology|December 10, 2003
Characterization of Salmonella enterica serotype newport isolated from humans and food animalsS Zhao, S Qaiyumi, S Friedman, et al.
The Journal of Investigative Dermatology|March 12, 2002
Novel and recurrent mutations in the genes encoding keratins K6a, K16 and K17 in 13 cases of pachyonychia congenitaA Terrinoni, F J Smith, B Didona, et al.
Dermatology (Basel, Switzerland)|May 31, 2002
Safety and efficacy of combined high-dose treatment with calcipotriol ointment and solution in patients with psoriasisP C M Van de Kerkhof, C Green, K J Hamberg, 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.
The British Journal of Dermatology|April 1, 1997
Treatment of psoriasis with intermittent short course cyclosporin (Neoral). A multicentre studyJ Berth-Jones, C A Henderson, C S Munro, et al.
Human Molecular Genetics|April 18, 2000
Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca(2+) pumpR Sudbrak, J Brown, C Dobson-Stone, et al.
The Journal of General Virology|January 7, 2020
Characterization of ranaviruses isolated from lumpfish Cyclopterus lumpus L. in the North Atlantic area: proposal for a new ranavirus species (European North Atlantic Ranavirus)Hannah E B Stagg, Sigríður Guðmundsdóttir, Niccolò Vendramin, et al.
American Journal of Human Genetics|July 9, 2013
Mutations in AQP5, encoding a water-channel protein, cause autosomal-dominant diffuse nonepidermolytic palmoplantar keratodermaDiana C Blaydon, Lisbet K Lind, Vincent Plagnol, et al.
Nature Genetics|March 18, 1999
Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier diseaseA Sakuntabhai, V Ruiz-Perez, S Carter, et al.
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