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Results:
1-6
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Results: 6
A nonsense mutation in MSX1 causes Witkop syndrome
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
Collagen XVIII/endostatin structure and functional role in angiogenesis
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
Secreted cathepsin L generates endostatin from collagen XVIII
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
Generation and degradation of human endostatin proteins by various proteinases
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
Allelic heterogeneity of alkaptonuria in Central Europe
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
Ocular ochronosis in alkaptonuria patients carrying mutations in the homogentisate 1,2-dioxygenase gene
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
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