7
results
for author:"Haasemann M."
in Literature Citations
| Molecular modelling of the Norrie disease protein predicts a cystine knot growth factor tertiary structure. Meitinger T., Meindl A., Bork P., Rost B., Sander C., Haasemann M., Murken J. Nat. Genet. 5:376-380(1993) · UniProtKB (1) |
| Complete DNA sequence of yeast chromosome XI. Dujon B., Alexandraki D., Andre B., Ansorge W., Baladron V., Ballesta J.P.G., Banrevi A., Bolle P.-A., Bolotin-Fukuhara M., Bossier P. et al. Nature 369:371-378(1994) · UniProtKB (1,168) |
| S-type lectins occur also in invertebrates: high conservation of the carbohydrate recognition domain in the lectin genes from the marine sponge Geodia cydonium. Pfeifer K., Haasemann M., Gamulin V., Bretting H., Fahrenholz F., Muller W.E. Glycobiology 3:179-184(1993) · UniProtKB (2) |
| Rat tyrosine kinase inhibitor shows sequence similarity to human alpha 2-HS glycoprotein and bovine fetuin. Haasemann M., Nawratil P., Mueller-Esterl W. Biochem. J. 274:899-902(1991) · UniProtKB (1) |
| The complete DNA sequence of yeast chromosome III. Oliver S.G., van der Aart Q.J.M., Agostoni-Carbone M.L., Aigle M., Alberghina L., Alexandraki D., Antoine G., Anwar R., Ballesta J.P.G., Benit P. et al. Nature 357:38-46(1992) · UniProtKB (1,006) |
| The nucleotide and partial amino acid sequences of rat fetuin. Identity with the natural tyrosine kinase inhibitor of the rat insulin receptor. Rauth G., Poeschke O., Fink E., Eulitz M., Tippmer S., Kellerer M., Haering H., Nawratil P., Haasemann M., Jahnen-Dechent W. et al. Eur. J. Biochem. 204:523-529(1992) · UniProtKB (1) |
| Norrie disease is caused by mutations in an extracellular protein resembling C-terminal globular domain of mucins. Meindl A., Berger W., Meitinger T., van de Pol D., Achatz H., Dorner C., Haasemann M., Hellebrand H., Gal A., Cremers F.P.M. et al. Nat. Genet. 2:139-143(1992) · UniProtKB (1) |
