Ulla M. Wewer
Professor
Globe Administration
Øster Voldgade 5-7
1350 København K
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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, , 1 Sep 2003, In: Neuromuscular Disorders. 13, 7-8, p. 579-88 10 p.Research output: Contribution to journal › Journal article › Research › peer-review
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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 journal › Journal article › Research › peer-review
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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 journal › Journal article › Research › peer-review
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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 journal › Journal article › Research › peer-review
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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. 1045-1053Research output: Contribution to journal › Journal article › Research
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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. 2467-2479Research output: Contribution to journal › Journal article › Research › peer-review
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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 journal › Journal article › Research › peer-review
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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. 207-215Research output: Contribution to journal › Journal article › Research
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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 journal › Journal article › Research › peer-review
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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 journal › Journal article › Research › peer-review
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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 journal › Journal article › Research › peer-review
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The new frontier in muscular dystrophy: Booster genes.
Engvall, E. & Wewer, Ulla M., 2003, In: The FASEB Journal. 17, p. 1579-1584Research output: Contribution to journal › Journal article › Research
ID: 914939
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The Phosphorylation and Distribution of Cortactin Downstream of Integrin α9β1 Affects Cancer Cell Behaviour
Research output: Contribution to journal › Journal article › Research › peer-review
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