Ulla M. Wewer

Ulla M. Wewer

Professor

  • BRIC Administration

    Ole Maaløes Vej 5

    2200 København N.

    Phone: +4535327051Mobile: +4528757051

Publication year:
All
1 - 10 out of 10Page size: 10
  1. 1998
  2. Published

    Laminin alpha2 chain-deficient congenital muscular dystrophy: variable epitope expression in severe and mild cases

    Cohn, R. D., Herrmann, R., Sorokin, L., Wewer, Ulla M. & Voit, T., 1 Jul 1998, In: Neurology. 51, 1, p. 94-100 7 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  3. Published

    Congenital myasthenic syndromes in two kinships with end-plate acetylcholine receptor and utrophin deficiency

    Sieb, J. P., Dörfler, P., Tzartos, S., Wewer, Ulla M., Rüegg, M. A., Meyer, D., Baumann, I., Lindemuth, R., Jakschik, J. & Ries, F., 1 Jan 1998, In: Neurology. 50, 1, p. 54-61 8 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  4. Published

    A novel, secreted form of human ADAM 12 (meltrin alpha) provokes myogenesis in vivo.

    Gilpin, B. J., Loechel, F., Mattei, M. G., Engvall, E., Albrechtsen, Reidar & Wewer, Ulla M., 1998, In: Journal of Biological Chemistry. 273, 1, p. 157-66 9 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  5. Published

    Congenital myastenic syndromes in two kinships with endplate acetylcholine receptor and utropin deficiency

    Sieb, J. P., Dörfler, P., Tzartos, S., Wewer, Ulla M., Rüegg, M. A., Meyer, D., Baumann, I. & Lindemuth, R., 1998, In: Neurology. 50, p. 54-61

    Research output: Contribution to journal › Journal article › Research › peer-review

  6. Published

    Evaluation of Lama5 as a candidate for the mouse ragged (Ra) mutation.

    Durkin, M. E., Albrechtsen, Reidar, Chambers, D. M., Abbott, C. M. & Wewer, Ulla M., 1998, In: Biochemical and Biophysical Research Communications. 250, 1, p. 125-30 5 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  7. Published

    Genetic correction of merosin deficiency in the dy2J mouse model of congenital muscular dystrophy. Partial genetic correction in two models

    Kuang, W., Xu, H., Vachon, P. H., Liu, L., Loechel, F., Wewer, Ulla M. & Engvall, E., 1998, In: Journal of Clinical Investigation. 102, p. 844-852

    Research output: Contribution to journal › Journal article › Research › peer-review

  8. Published

    Human ADAM 12 (meltrin alpha) is an active metalloprotease.

    Loechel, F., Gilpin, B. J., Engvall, E., Albrechtsen, Reidar & Wewer, Ulla M., 1998, In: Journal of Biological Chemistry. 273, 27, p. 16993-7 4 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  9. Published

    Laminin alpha2 chain-deficient muscular dystrophy: variable epitope expression in severe and mild cases

    Cohn, R. D., Herrmann, R. J., Sorokin, L., Wewer, Ulla M. & Voit, T., 1998, In: Neurology. 51, p. 94-100

    Research output: Contribution to journal › Journal article › Research › peer-review

  10. Published

    Merosin-deficient congenital muscular dystrophy. Partial genetic correction in two mouse models

    Kuang, W., Xu, H., Vachon, P. H., Liu, L., Loechel, F., Wewer, Ulla M. & Engvall, E., 1998, In: Journal of Clinical Investigation. 102, 4, p. 844-52 9 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  11. Published

    Tetranectin is a novel marker for myogenesis during embryonic development, muscle regeneration, and muscle cell differentiation in vitro.

    Wewer, Ulla M., Iba, K., Durkin, M. E., Nielsen, F. C., Loechel, F., Gilpin, B. J., Kuang, W., Engvall, E. & Albrechtsen, Reidar, 1998, In: Developmental Biology. 200, 2, p. 247-59 12 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

ID: 914939