Laminin α2 deficiency and muscular dystrophy; genotype-phenotype correlation in mutant mice von Guo, L.T., Zhang, X.U., Kuang, W., Xu, H., Liu, L.A., Vilquin, J.-T., Miyagoe-Suzuki, Y., Takeda, S., Ruegg, M.A., Wewer, U.M., Engvall, E.

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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 Wor... von 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, Yurchenco, P.D, Urtizberea, J.A, Wewer, U.M, Guicheney, P

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To live or let die von P.H., Vachon, F., Loechel, H., Xu, U.M., Wewer, E., Engvall

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Exon organization of the mouse entactin gene corresponds to the structural domains of the polypeptide and has regional homology to the low-density lipoprotein receptor gene von Durkin, Marian E., Wewer, Ulla M., Chung, Albert E.

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Selective assembly of laminin variants by human carcinoma cells von Lan, F., Albrechtsen, R., Zhang, X., Wewer, U.M.

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Characterization of the human laminin β2 chain locus (LAMB2): linkage to a gene containing a nonprocessed, transcribed LAMB2-like pseudogene (LAMB2L) and to the gene encoding gluta... von Durkin, M.E., Jäger, A.C., Khurana, T.S., Nielsen, F.C., Albrechtsen, R., Wewer, U.M.

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