Deficiency of merosin in dystrophic dy mice and genetic linkage of laminin M chain gene to dy locus.
Open Access
- 1 May 1994
- journal article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 269 (19) , 13729-13732
- https://doi.org/10.1016/s0021-9258(17)36704-2
Abstract
No abstract availableKeywords
This publication has 32 references indexed in Scilit:
- Human laminin M chain (merosin): complete primary structure, chromosomal assignment, and expression of the M and A chain in human fetal tissuesThe Journal of cell biology, 1994
- Differential expression of dystrophin, utrophin and dystrophin‐associated proteins in peripheral nerveFEBS Letters, 1993
- Expression of the N‐terminal domain of dystrophin in E. coli and demonstration of binding to F‐actinFEBS Letters, 1992
- Binding sites involved in the interaction of actin with the N‐terminal region of dystrophinFEBS Letters, 1992
- Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrixNature, 1992
- Merosin promotes cell attachment and neurite outgrowth and ls a component of the neurite-promoting factor of RN22 schwannoma cellsExperimental Cell Research, 1992
- Structure and biological activity of basement membrane proteinsEuropean Journal of Biochemistry, 1989
- Normal basal laminas are realized on dystrophic Schwann cells in dystrophic in equilibrium shiverer chimera nerves.The Journal of cell biology, 1984
- Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications.Proceedings of the National Academy of Sciences, 1979
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970