Ulla M. Wewer

Ulla M. Wewer

Professor


  1. 2003
  2. Published

    Compensation for dystrophin-deficiency: ADAM12 overexpression in skeletal muscle results in increased alpha 7 integrin, utrophin and associated glycoproteins

    Moghadaszadeh, B., Albrechtsen, Reidar, Guo, L. T., Zaik, M., Kawaguchi, N., Borup, R. H., Kronqvist, P., Schroder, H. D., Davies, K. E., Voit, T., Nielsen, Finn Cilius, Engvall, E. & Wewer, Ulla M., 1 Oct 2003, In: Human Molecular Genetics. 12, 19, p. 2467-79 13 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Published

    114th ENMC International Workshop on Congenital Muscular Dystrophy (CMD) 17-19 January 2003, Naarden, The Netherlands: (8th Workshop of the International Consortium on CMD; 3rd Workshop of the MYO-CLUSTER project GENRE)

    Muntoni, F., Valero de Bernabe, B., Bittner, R., Blake, D., van Bokhoven, H., Brockington, M., Brown, S., Bushby, K., Campbell, K. P., Fiszman, M., Gruenewald, S., Merlini, L., Quijano-Roy, S., Romero, N., Sabatelli, P., Sewry, C. A., Straub, V., Talim, B., Topaloglu, H., Voit, T. & 4 others, Yurchenco, P. D., Urtizberea, J. A., Wewer, Ulla M. & Guicheney, P., 1 Sep 2003, In: Neuromuscular Disorders. 13, 7-8, p. 579-88 10 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Published

    The new frontier in muscular dystrophy research: booster genes

    Engvall, E. & Wewer, Ulla M., 1 Sep 2003, In: F A S E B Journal. 17, 12, p. 1579-84 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. Published

    ADAM12 in human liver cancers: TGF-beta-regulated expression in stellate cells is associated with matrix remodeling

    Le Pabic, H., Bonnier, D., Wewer, Ulla M., Coutand, A., Musso, O., Baffet, G., Clément, B. & Théret, N., 1 May 2003, In: Hepatology. 37, 5, p. 1056-66 11 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  6. Published

    Selenoprotein N: an endoplasmic reticulum glycoprotein with an early developmental expression pattern

    Petit, N., Lescure, A., Rederstorff, M., Krol, A., Moghadaszadeh, B., Wewer, Ulla M. & Guicheney, P., 1 May 2003, In: Human Molecular Genetics. 12, 9, p. 1045-53 9 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  7. Published

    Laminin alpha2 deficiency and muscular dystrophy; genotype-phenotype correlation in mutant mice

    Guo, L. T., Zhang, X. U., Kuang, W., Xu, H., Liu, L. A., Vilquin, J., Miyagoe-Suzuki, Y., Takeda, S., Ruegg, M. A., Wewer, Ulla M. & Engvall, E., 1 Mar 2003, In: Neuromuscular Disorders. 13, 3, p. 207-15 9 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  8. Published

    ADAM12 induces actin cytoskeleton and extracellular matrix reorganization during early adipocyte differentiation by regulating beta1 integrin function.

    Kawaguchi, N., Sundberg, C., Kveiborg, Marie, Moghadaszadeh, B., Asmar, M., Dietrich, N., Thodeti, C. K., Nielsen, F. C., Möller, P., Mercurio, A. M., Albrechtsen, Reidar & Wewer, Ulla M., 2003, In: Journal of Cell Science. 116, Pt 19, p. 3893-904 11 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  9. Published

    ADAM12: a novel first-trimester maternal serum marker for Down syndrome.

    Laigaard, J., Sørensen, T., Fröhlich, C., Pedersen, B. N., Christiansen, M., Schiøtt, K., Uldbjerg, N., Albrechtsen, Reidar, Clausen, H. V., Ottesen, B. & Wewer, Ulla M., 2003, In: Prenatal Diagnosis. 23, 13, p. 1086-91 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  10. Published

    An endoplasmic reticulum glycoprotein with an early development expression pattern.

    Petit, N., Lescure, A., Rederstorff, M., Krol, A., Moghadas Zadeh, S. B., Wewer, Ulla M. & Guicheney, P., 2003, In: Human Molecular Genetics. 12, p. 1045-1053

    Research output: Contribution to journalJournal articleResearch

  11. Published

    Compensation for dystrophin-deficiency: ADAM12 overexpression in skeletal muscle results in increased alfa7 integrin, utrophin, and associated glycoproteins.

    Moghadas Zadeh, S. B., Albrechtsen, Reidar, Guo, L. T., Zaik, M., Kawaguchi, N., Borup, R. H., Kronqvist, P. E., Schröder, H. D., Davies, K. E., Voit, T., Nielsen, F. C., Engvall, E. & Wewer, Ulla M., 2003, In: Human Molecular Genetics. 12, p. 2467-2479

    Research output: Contribution to journalJournal articleResearchpeer-review

  12. Published

    Laminin afra2 deficiency and muscular dystrophy: genotype-phenotype correlation in mutant mice.

    Guo, L. T., Zhang, X. U., Kang, W., Xu, H., Liu, L. A., Miyagoe-Suzuki, Y., Takeda, S., Ruegg, M., Wewer, Ulla M. & Engvall, E., 2003, In: Neuromuscular Disorders. 13, p. 207-215

    Research output: Contribution to journalJournal articleResearch

  13. Published

    The new frontier in muscular dystrophy: Booster genes.

    Engvall, E. & Wewer, Ulla M., 2003, In: The FASEB Journal. 17, p. 1579-1584

    Research output: Contribution to journalJournal articleResearch

ID: 914939