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Expression of IL-18 in human keratinocytes.
Companjen AR, Prens E, Mee JB, Groves RW. Companjen AR, et al. Among authors: mee jb. J Invest Dermatol. 2000 Mar;114(3):598-9. doi: 10.1046/j.1523-1747.2000.02003.x. J Invest Dermatol. 2000. PMID: 10777359 Free article. No abstract available.
Loss-of-function FERMT1 mutations in kindler syndrome implicate a role for fermitin family homolog-1 in integrin activation.
Lai-Cheong JE, Parsons M, Tanaka A, Ussar S, South AP, Gomathy S, Mee JB, Barbaroux JB, Techanukul T, Almaani N, Clements SE, Hart IR, McGrath JA. Lai-Cheong JE, et al. Among authors: mee jb. Am J Pathol. 2009 Oct;175(4):1431-41. doi: 10.2353/ajpath.2009.081154. Epub 2009 Sep 17. Am J Pathol. 2009. PMID: 19762710 Free PMC article.
A homozygous nonsense mutation within the dystonin gene coding for the coiled-coil domain of the epithelial isoform of BPAG1 underlies a new subtype of autosomal recessive epidermolysis bullosa simplex.
Groves RW, Liu L, Dopping-Hepenstal PJ, Markus HS, Lovell PA, Ozoemena L, Lai-Cheong JE, Gawler J, Owaribe K, Hashimoto T, Mellerio JE, Mee JB, McGrath JA. Groves RW, et al. Among authors: mee jb. J Invest Dermatol. 2010 Jun;130(6):1551-7. doi: 10.1038/jid.2010.19. Epub 2010 Feb 18. J Invest Dermatol. 2010. PMID: 20164846 Free article.
30 results