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[Hereditary blistering disorders].
Has C, Kern JS, Bruckner-Tuderman L. Has C, et al. Among authors: kern js. Hautarzt. 2004 Oct;55(10):920, 922-30. doi: 10.1007/s00105-004-0798-0. Hautarzt. 2004. PMID: 15340710 Review. German.
A hypomorphic mouse model of dystrophic epidermolysis bullosa reveals mechanisms of disease and response to fibroblast therapy.
Fritsch A, Loeckermann S, Kern JS, Braun A, Bösl MR, Bley TA, Schumann H, von Elverfeldt D, Paul D, Erlacher M, Berens von Rautenfeld D, Hausser I, Fässler R, Bruckner-Tuderman L. Fritsch A, et al. Among authors: kern js. J Clin Invest. 2008 May;118(5):1669-79. doi: 10.1172/JCI34292. J Clin Invest. 2008. PMID: 18382769 Free PMC article.
Forty-two novel COL7A1 mutations and the role of a frequent single nucleotide polymorphism in the MMP1 promoter in modulation of disease severity in a large European dystrophic epidermolysis bullosa cohort.
Kern JS, Grüninger G, Imsak R, Müller ML, Schumann H, Kiritsi D, Emmert S, Borozdin W, Kohlhase J, Bruckner-Tuderman L, Has C. Kern JS, et al. Br J Dermatol. 2009 Nov;161(5):1089-97. doi: 10.1111/j.1365-2133.2009.09333.x. Epub 2009 Jun 5. Br J Dermatol. 2009. PMID: 19681861
110 results