Sarcoglycan Isoforms in Skeletal Muscle*
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[1] H. Sweeney,et al. Muscle degeneration without mechanical injury in sarcoglycan deficiency. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[2] K. Campbell,et al. Biochemical Characterization of the Epithelial Dystroglycan Complex* , 1999, The Journal of Biological Chemistry.
[3] H. Hama,et al. Loss of the sarcoglycan complex and sarcospan leads to muscular dystrophy in beta-sarcoglycan-deficient mice. , 1999, Human molecular genetics.
[4] K. Campbell,et al. Disruption of the Sarcoglycan–Sarcospan Complex in Vascular Smooth Muscle A Novel Mechanism for Cardiomyopathy and Muscular Dystrophy , 1999, Cell.
[5] S. Carbonetto,et al. α-Dystroglycan Is a Laminin Receptor Involved in Extracellular Matrix Assembly on Myotubes and Muscle Cell Viability , 1999, The Journal of cell biology.
[6] S. Ohno,et al. The one-to-four rule and paralogues of sex-determining genes , 1999, Cellular and Molecular Life Sciences CMLS.
[7] P. Yurchenco,et al. Laminin Polymerization Induces a Receptor–Cytoskeleton Network , 1999, The Journal of cell biology.
[8] D. Biral,et al. Ecto-ATPase Activity of α-Sarcoglycan (Adhalin)* , 1999, The Journal of Biological Chemistry.
[9] C. Bönnemann. Limb-girdle muscular dystrophies: an overview. , 1999, Journal of child neurology.
[10] L. Kunkel,et al. Molecular Organization of Sarcoglycan Complex in Mouse Myotubes in Culture , 1998, The Journal of cell biology.
[11] K. Campbell,et al. Assembly of the Sarcoglycan Complex , 1998, The Journal of Biological Chemistry.
[12] K. Campbell,et al. A Role for Dystroglycan in Basement Membrane Assembly , 1998, Cell.
[13] John A. Faulkner,et al. Progressive Muscular Dystrophy in α-Sarcoglycan–deficient Mice , 1998, The Journal of cell biology.
[14] R. Wollmann,et al. γ-Sarcoglycan Deficiency Leads to Muscle Membrane Defects and Apoptosis Independent of Dystrophin , 1998, The Journal of cell biology.
[15] E. Engvall,et al. Merosin-deficient congenital muscular dystrophy. Partial genetic correction in two mouse models. , 1998, The Journal of clinical investigation.
[16] S. Noguchi,et al. From dystrophinopathy to sarcoglycanopathy: Evolution of a concept of muscular dystrophy , 1998, Muscle & nerve.
[17] L. Kunkel,et al. Human ϵ‐sarcoglycan is highly related to α‐sarcoglycan (adhalin), the limb girdle muscular dystrophy 2D gene 1 , 1998, FEBS letters.
[18] M. Shigekawa,et al. Bidirectional Signaling between Sarcoglycans and the Integrin Adhesion System in Cultured L6 Myocytes* , 1998, The Journal of Biological Chemistry.
[19] J. Sanes,et al. ε-Sarcoglycan, a Broadly Expressed Homologue of the Gene Mutated in Limb-Girdle Muscular Dystrophy 2D* , 1997, The Journal of Biological Chemistry.
[20] K. Campbell,et al. Sarcospan, the 25-kDa Transmembrane Component of the Dystrophin-Glycoprotein Complex* , 1997, The Journal of Biological Chemistry.
[21] Y. Murakami,et al. Both hypertrophic and dilated cardiomyopathies are caused by mutation of the same gene, delta-sarcoglycan, in hamster: an animal model of disrupted dystrophin-associated glycoprotein complex. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[22] K. Campbell,et al. Animal Models for Muscular Dystrophy Show Different Patterns of Sarcolemmal Disruption , 1997, The Journal of cell biology.
[23] E. Engvall,et al. Mouse adhalin: primary structure and expression during late stages of muscle differentiation in vitro. , 1997, Biochemical and biophysical research communications.
[24] K. Campbell,et al. Muscular dystrophies and the dystrophin-glycoprotein complex. , 1997, Current opinion in neurology.
[25] Y. Hayashizaki,et al. Identification of the Syrian hamster cardiomyopathy gene. , 1997, Human Molecular Genetics.
[26] S. Carbonetto,et al. Laminin-induced Clustering of Dystroglycan on Embryonic Muscle Cells: Comparison with Agrin-induced Clustering , 1997, The Journal of cell biology.
[27] K. Bushby. Towards the classification of the autosomal recessive limb-girdle muscular dystrophies , 1996, Neuromuscular Disorders.
[28] M. Passos-Bueno,et al. Autosomal recessive limbgirdle muscular dystrophy, LGMD2F, is caused by a mutation in the δ–sarcoglycan gene , 1996, Nature Genetics.
[29] G. Viglietto,et al. Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein. , 1996, Human molecular genetics.
[30] L. Kunkel,et al. Mutations in the Dystrophin-Associated Protein γ-Sarcoglycan in Chromosome 13 Muscular Dystrophy , 1995, Science.
[31] L. Kunkel,et al. β–sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex , 1995, Nature Genetics.
[32] A. Nishikawa,et al. Visualization of dystrophic muscle fibers in mdx mouse by vital staining with Evans blue: evidence of apoptosis in dystrophin-deficient muscle. , 1995, Journal of biochemistry.
[33] S. Noguchi,et al. Dystrophin-associated proteins in muscular dystrophy. , 1995, Human molecular genetics.
[34] K. Campbell. Three muscular dystrophies: Loss of cytoskeleton-extracellular matrix linkage , 1995, Cell.
[35] J. Beckmann,et al. Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy , 1994, Cell.
[36] H. Yamamoto,et al. Dissociation of the complex of dystrophin and its associated proteins into several unique groups by n-octyl beta-D-glucoside. , 1994, European journal of biochemistry.
[37] A. E. Oakeley,et al. C2C12 cells: biophysical, biochemical, and immunocytochemical properties. , 1994, The American journal of physiology.
[38] O. Ibraghimov-Beskrovnaya,et al. Primary structure and muscle-specific expression of the 50-kDa dystrophin-associated glycoprotein (adhalin). , 1993, The Journal of biological chemistry.
[39] J. Ervasti,et al. A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin , 1993, The Journal of cell biology.
[40] H. Sweeney,et al. Dystrophin protects the sarcolemma from stresses developed during muscle contraction. , 1993, Proceedings of the National Academy of Sciences of the United States of America.
[41] K. Campbell,et al. Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy , 1992, Nature.
[42] O. Ibraghimov-Beskrovnaya,et al. Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix , 1992, Nature.
[43] J. Ervasti,et al. Dystrophin-glycoprotein complex is highly enriched in isolated skeletal muscle sarcolemma , 1991, The Journal of cell biology.
[44] T. Yagi,et al. Homologous recombination at c-fyn locus of mouse embryonic stem cells with use of diphtheria toxin A-fragment gene in negative selection. , 1990, Proceedings of the National Academy of Sciences of the United States of America.
[45] E. Ozawa,et al. Glycoprotein complex anchoring dystrophin to sarcolemma. , 1990, Journal of biochemistry.
[46] L. Kunkel,et al. Subcellular fractionation of dystrophin to the triads of skeletal muscle , 1987, Nature.
[47] H. Blau,et al. Developmental progression of myosin gene expression in cultured muscle cells , 1986, Cell.
[48] M. O'Sullivan,et al. Comparison of two methods of preparing enzyme-antibody conjugates: application of these conjugates for enzyme immunoassay. , 1979, Analytical biochemistry.
[49] D. Yaffe,et al. Serial passaging and differentiation of myogenic cells isolated from dystrophic mouse muscle , 1977, Nature.