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Scientific Reports|May 23, 2020
Characterisation of mexiletine's translational therapeutic index for suppression of ischaemia-induced ventricular fibrillation in the rat isolated heartLouise M Hesketh, Catherine D E Wilder, Niraja N Ranadive, et al.
The Journal of Investigative Dermatology|December 18, 1998
Mutations in keratin K9 in kindreds with epidermolytic palmoplantar keratoderma and epidemiology in Northern IrelandS P Covello, A D Irvine, K E McKenna, et al.
Jac-Antimicrobial Resistance|July 5, 2021
Improving paediatric antimicrobial stewardship in hospital-based settings: why, where and how?E Tanner, A P S Munro, J Gray, et al.
Human Molecular Genetics|June 17, 1999
A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated familiesE Maestrini, B P Korge, J Ocaña-Sierra, 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 Journal of Investigative Dermatology|December 20, 2000
Mutant loricrin is not crosslinked into the cornified cell envelope but is translocated into the nucleus in loricrin keratodermaA Ishida-Yamamoto, H Kato, H Kiyama, et al.
The British Journal of Dermatology|October 10, 1998
Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2S P Covello, F J Smith, J H Sillevis Smitt, et al.
Genomics|November 15, 1994
Linkage analyses in British pedigrees suggest a single locus for Darier disease and narrow the location to the interval between D12S105 and D12S129S A Carter, S D Bryce, C S Munro, et al.
The British Journal of Dermatology|December 22, 1999
Novel proline substitution mutations in keratin 16 in two cases of pachyonychia congenita type 1F J Smith, M Del Monaco, P M Steijlen, et al.
The Journal of Investigative Dermatology|February 14, 2002
Hailey-Hailey disease: molecular and clinical characterization of novel mutations in the ATP2C1 geneCarol Dobson-Stone, Rebecca Fairclough, Eimear Dunne, et al.
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