Ulla M. Wewer

Professor

Globe Administration
Øster Voldgade 5-7
1350 København K
- ullaw@sund.ku.dk
Telefon: +4535327051Mobil: +4528757051

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2001
Udgivet
Tetranectin in slow intra- and extrafusal chicken muscle fibers.
Xu, X., Gilpin, B., Iba, K., Maier, A., Engvall, E., Albrechtsen, Reidar & Wewer, Ulla M., 2001, I: Journal of Muscle Research and Cell Motility. 22, 2, s. 121-32 11 s.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
2000
Udgivet
Binding of ADAM12, a marker for skeletal muscle regeneration, to the muscle-specific actin-binding protein, alfa-actinin-2, is required for myoblast fusion.
Galliano, H., Frygelius, J., Polgren, A. & Wewer, Ulla M., 2000, I: Journal of Biological Chemistry. 275, s. 13933-13999
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Udgivet
Binding of ADAM12, a marker of skeletal muscle regeneration, to the muscle-specific actin-binding protein, alpha -actinin-2, is required for myoblast fusion
Galliano, M. F., Huet, C., Frygelius, J., Polgren, A., Wewer, Ulla M. & Engvall, E., 5 maj 2000, I: Journal of Biological Chemistry. 275, 18, s. 13933-9 7 s.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Udgivet
Trafficking of human ADAM 12-L: retention in the trans-Golgi network.
Hougaard, S., Loechel, F., Xu, X., Tajima, R., Albrechtsen, Reidar & Wewer, Ulla M., 2000, I: Biochemical and Biophysical Research Communications. 275, 2, s. 261-7 6 s.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Udgivet
The cysteine-rich domain of human ADAM 12 supports cell adhesion through syndecans and triggers signaling events that lead to beta1 integrin-dependent cell spreading.
Iba, K., Albrechtsen, Reidar, Gilpin, B., Frohlich, C., Loechel, F., Zolkiewska, A., Ishiguro, K., Kojima, T., Liu, W., Langford, J. K., Sanderson, R. D., Brakebusch, Cord Herbert, Fässler, R. & Wewer, Ulla M., 2000, I: Journal of Cell Biology. 149, 5, s. 1143-56 13 s.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Udgivet
ADAM 12-S cleaves IGFBP-3 and IGFBP-5 and is inhibited by TIMP-3.
Loechel, F., Fox, J. W., Murphy, G., Albrechtsen, Reidar & Wewer, Ulla M., 2000, I: Biochemical and Biophysical Research Communications. 278, 3, s. 511-5 4 s.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Udgivet
H19 RNA binds four molecules of insulin-like growth factor II mRNA-binding protein
Runge, S., Nielsen, Finn Cilius, Nielsen, J., Andersen, J. L., Wewer, Ulla M. & Christiansen, Jan, 2000, I: Journal of Biological Chemistry. 275, 38, s. 29562-9 8 s.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Udgivet
ADAM 12, a disintegrin metalloprotease, interacts with insulin-like growth factor-binding protein-3
Shi, Z., Xu, W., Loechel, F., Wewer, Ulla M. & Murphy, L., 2000, I: Journal of Biological Chemistry. 275, 24, s. 18574-18580
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Udgivet
Celle-matrix-interaktioner ved cancer
Wewer, Ulla M., 2000, I: Ugeskrift for læger. 162, 36, s. 4783-5 3 s.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
1999
Udgivet
Characterization of the human laminin beta2 chain locus (LAMB2): linkage to a gene containing a nonprocessed, transcribed LAMB2-like pseudogene (LAMB2L) and to the gene encoding glutaminyl tRNA synthetase (QARS).
Durkin, M. E., Jäger, A. C., Khurana, T. S., Nielsen, F. C., Albrechtsen, Reidar & Wewer, Ulla M., 1999, I: Cytogenetic and Genome Research. 84, 3-4, s. 173-8 5 s.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Udgivet
Cysteine-rich domain of human ADAM 12 (meltrin alpha) supports tumor cell adhesion.
Iba, K., Albrechtsen, Reidar, Gilpin, B. J., Loechel, F. & Wewer, Ulla M., 1999, I: American Journal of Pathology. 154, 5, s. 1489-501 12 s.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Udgivet
Regulation of human ADAM 12 protease by the prodomain. Evidence for a functional cysteine switch.
Loechel, F., Overgaard, M. T., Oxvig, C., Albrechtsen, Reidar & Wewer, Ulla M., 1999, I: Journal of Biological Chemistry. 274, 19, s. 13427-33 6 s.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Udgivet
A family of insulin-like growth factor II mRNA-binding proteins represses translation in late development
Nielsen, J., Christiansen, Jan, Lykke-Andersen, J., Johnsen, A. H., Wewer, Ulla M. & Nielsen, Finn Cilius, 1999, I: Molecular and Cellular Biology. 19, 2, s. 1262-1270 9 s.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
1998
Udgivet
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, I: Neurology. 51, 1, s. 94-100 7 s.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Udgivet
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, I: Neurology. 51, s. 94-100
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Udgivet
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, I: Biochemical and Biophysical Research Communications. 250, 1, s. 125-30 5 s.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Udgivet
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, I: Journal of Biological Chemistry. 273, 1, s. 157-66 9 s.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Udgivet
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, I: Journal of Clinical Investigation. 102, 4, s. 844-52 9 s.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Udgivet
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, I: Journal of Clinical Investigation. 102, s. 844-852
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Udgivet
Human ADAM 12 (meltrin alpha) is an active metalloprotease.
Loechel, F., Gilpin, B. J., Engvall, E., Albrechtsen, Reidar & Wewer, Ulla M., 1998, I: Journal of Biological Chemistry. 273, 27, s. 16993-7 4 s.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Udgivet
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, I: Neurology. 50, 1, s. 54-61 8 s.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Udgivet
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, I: Neurology. 50, s. 54-61
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Udgivet
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, I: Developmental Biology. 200, 2, s. 247-59 12 s.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
1997
Udgivet
Changes of laminin beta 2 chain expression in congenital muscular dystrophy
Cohn, R. D., Herrmann, R., Wewer, Ulla M. & Voit, T., 1 sep. 1997, I: Neuromuscular Disorders. 7, 6-7, s. 373-8 6 s.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Udgivet
Changes in laminin ß2 chain expression in congenital muscular dystrophy
Cohn, R. D., Herremann, R., Wewer, Ulla M. & Voit, T., 1997, I: Neuromuscular Disorders. 7, s. 373-374
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

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ID: 914939

Forskning

Ulla M. Wewer

Globe Administration

Tetranectin in slow intra- and extrafusal chicken muscle fibers.

Binding of ADAM12, a marker for skeletal muscle regeneration, to the muscle-specific actin-binding protein, alfa-actinin-2, is required for myoblast fusion.

Binding of ADAM12, a marker of skeletal muscle regeneration, to the muscle-specific actin-binding protein, alpha -actinin-2, is required for myoblast fusion

Trafficking of human ADAM 12-L: retention in the trans-Golgi network.

The cysteine-rich domain of human ADAM 12 supports cell adhesion through syndecans and triggers signaling events that lead to beta1 integrin-dependent cell spreading.

ADAM 12-S cleaves IGFBP-3 and IGFBP-5 and is inhibited by TIMP-3.

H19 RNA binds four molecules of insulin-like growth factor II mRNA-binding protein

ADAM 12, a disintegrin metalloprotease, interacts with insulin-like growth factor-binding protein-3

Celle-matrix-interaktioner ved cancer

Characterization of the human laminin beta2 chain locus (LAMB2): linkage to a gene containing a nonprocessed, transcribed LAMB2-like pseudogene (LAMB2L) and to the gene encoding glutaminyl tRNA synthetase (QARS).

Cysteine-rich domain of human ADAM 12 (meltrin alpha) supports tumor cell adhesion.

Regulation of human ADAM 12 protease by the prodomain. Evidence for a functional cysteine switch.

A family of insulin-like growth factor II mRNA-binding proteins represses translation in late development

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

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

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

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

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

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

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

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

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

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

Changes of laminin beta 2 chain expression in congenital muscular dystrophy

Changes in laminin ß2 chain expression in congenital muscular dystrophy

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The Phosphorylation and Distribution of Cortactin Downstream of Integrin α9β1 Affects Cancer Cell Behaviour