AAAAAA

   
Results: 1-5 |
Results: 5

Authors: Roth, W Deussing, J Botchkarev, VA Pauly-Evers, M Saftig, P Hafner, A Schmidt, P Schmahl, W Scherer, J Anton-Lamprecht, I Von Figura, K Paus, R Peters, C
Citation: W. Roth et al., Cathepsin L deficiency as molecular defect of furless: hyperproliferation of keratinocytes and pertubation of hair follicle cycling, FASEB J, 14(13), 2000, pp. 2075-2086

Authors: Mohrenschlager, M Rizzo, WB Kraus, CS Limbrock, J Cohen, M Anton-Lamprecht, I Abeck, D Ring, J
Citation: M. Mohrenschlager et al., Sjogren-Larsson syndrome, HAUTARZT, 51(4), 2000, pp. 250-255

Authors: Muller, FB Anton-Lamprecht, I Kuster, W Korge, BP
Citation: Fb. Muller et al., A premature stop codon mutation in the 2B helix termination peptide of keratin 5 in a German epidermolysis bullosa simplex Dowling-Meara case, J INVES DER, 112(6), 1999, pp. 988-990

Authors: Sorensen, CB Ladekjaer-Mikkelsen, AS Andresen, BS Brandrup, F Veien, NK Buus, SK Anton-Lamprecht, I Kruse, TA Jensen, PKA Eiberg, H Bolund, L Gregersen, N
Citation: Cb. Sorensen et al., Identification of novel and known mutations in the genes for keratin 5 and14 in Danish patients with epidermolysis bullosa simplex: Correlation between genotype and phenotype, J INVES DER, 112(2), 1999, pp. 184-190

Authors: Pigg, M Gedde-Dahl, T Cox, D Hausser, I Anton-Lamprecht, I Dahl, N
Citation: M. Pigg et al., Strong founder effect for a transglutaminase 1 gene mutation in lamellar ichthyosis and congenital ichthyosiform erythroderma from Norway, EUR J HUM G, 6(6), 1998, pp. 589-596
Risultati: 1-5 |