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The EMBO Journal|January 1, 1989
Purification of axonin-1, a protein that is secreted from axons during neurogenesisM A Ruegg, E T Stoeckli, T B Kuhn, et al.The European Journal of Neuroscience|October 24, 1998
A minigene of neural agrin encoding the laminin-binding and acetylcholine receptor-aggregating domains is sufficient to induce postsynaptic differentiation in muscle fibresT Meier, P A Marangi, J Moll, et al.European Journal of Biochemistry|March 15, 1989
Identification of proteins secreted from axons of embryonic dorsal-root-ganglia neuronsE T Stoeckli, P F Lemkin, T B Kuhn, et al.The EMBO Journal|February 28, 1998
Electron microscopic structure of agrin and mapping of its binding site in laminin-1A J Denzer, T Schulthess, C Fauser, et al.Nature|September 21, 2001
An agrin minigene rescues dystrophic symptoms in a mouse model for congenital muscular dystrophyJ Moll, P Barzaghi, S Lin, et al.Neuron|April 1, 1992
The agrin gene codes for a family of basal lamina proteins that differ in function and distributionM A Ruegg, K W Tsim, S E Horton, et al.Current Opinion in Cell Biology|October 1, 1992
Agrin isoforms and their role in synaptogenesisU J McMahan, S E Horton, M J Werle, et al.The EMBO Journal|December 3, 1999
Interaction of agrin with laminin requires a coiled-coil conformation of the agrin-binding site within the laminin gamma1 chainR A Kammerer, T Schulthess, R Landwehr, et al.The Journal of Biological Chemistry|September 20, 1996
Dystroglycan is a dual receptor for agrin and laminin-2 in Schwann cell membraneH Yamada, A J Denzer, H Hori, et al.Neuromuscular Disorders : NMD|March 1, 2003
Laminin alpha2 deficiency and muscular dystrophy; genotype-phenotype correlation in mutant miceL T Guo, X U Zhang, W Kuang, et al.Pageof 4