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Results: 1-6 |
Results: 6

Authors: Jumlongras, D Bei, M Stimson, JM Wang, WF DePalma, SR Seidman, CE Felbor, U Maas, R Seidman, JG Olsen, BR
Citation: D. Jumlongras et al., A nonsense mutation in MSX1 causes Witkop syndrome, AM J HU GEN, 69(1), 2001, pp. 67-74

Authors: Zatterstrom, UK Felbor, U Fukai, N Olsen, BR
Citation: Uk. Zatterstrom et al., Collagen XVIII/endostatin structure and functional role in angiogenesis, CELL STRUCT, 25(2), 2000, pp. 97-101

Authors: Felbor, U Dreier, L Bryant, RAR Ploegh, HL Olsen, BR Mothes, W
Citation: U. Felbor et al., Secreted cathepsin L generates endostatin from collagen XVIII, EMBO J, 19(6), 2000, pp. 1187-1194

Authors: Ferreras, M Felbor, U Lenhard, T Olsen, BR Delaisse, JM
Citation: M. Ferreras et al., Generation and degradation of human endostatin proteins by various proteinases, FEBS LETTER, 486(3), 2000, pp. 247-251

Authors: Muller, CR Fregin, A Srsen, S Srsnova, K Halliger-Keller, B Felbor, U Seemanova, E Kress, W
Citation: Cr. Muller et al., Allelic heterogeneity of alkaptonuria in Central Europe, EUR J HUM G, 7(6), 1999, pp. 645-651

Authors: Felbor, U Mutsch, Y Grehn, F Muller, CR Kress, W
Citation: U. Felbor et al., Ocular ochronosis in alkaptonuria patients carrying mutations in the homogentisate 1,2-dioxygenase gene, BR J OPHTH, 83(6), 1999, pp. 680-683
Risultati: 1-6 |