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Neuromuscular Disorders : NMD|December 1, 1996
Merosin/laminin-2 and muscular dystrophyU M Wewer, E EngvallNature Genetics|November 1, 1994
Murine muscular dystrophy caused by a mutation in the laminin alpha 2 (Lama2) geneH Xu, X R Wu, U M Wewer, et al.Laboratory Investigation; a Journal of Technical Methods and Pathology|March 1, 1992
Laminin A, B1, B2, S and M subunits in the postnatal rat liver development and after partial hepatectomyU M Wewer, E Engvall, M Paulsson, et al.The Journal of Biological Chemistry|June 27, 1998
Human ADAM 12 (meltrin alpha) is an active metalloproteaseF Loechel, B J Gilpin, E Engvall, et al.Proceedings of the National Academy of Sciences of the United States of America|June 7, 1994
Defective muscle basement membrane and lack of M-laminin in the dystrophic dy/dy mouseH Xu, P Christmas, X R Wu, et al.The Journal of Cell Biology|September 1, 1996
Merosin and laminin in myogenesis; specific requirement for merosin in myotube stability and survivalP H Vachon, F Loechel, H Xu, et al.The Journal of Biological Chemistry|May 2, 2000
Binding of ADAM12, a marker of skeletal muscle regeneration, to the muscle-specific actin-binding protein, alpha -actinin-2, is required for myoblast fusionM F Galliano, C Huet, J Frygelius, et al.The Journal of Biological Chemistry|February 7, 1998
A novel, secreted form of human ADAM 12 (meltrin alpha) provokes myogenesis in vivoB J Gilpin, F Loechel, M G Mattei, et al.Journal of Muscle Research and Cell Motility|August 25, 2001
Tetranectin in slow intra- and extrafusal chicken muscle fibersX Xu, B Gilpin, K Iba, et al.Pageof 22