Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ghassan Y. Dally"'
Autor:
Geoff H. Werstuck, Joan E.B. Fox, Cameron Ackerley, Alan R. Stafford, Peter N. Ray, Dennis E. Bulman, Ghassan Y. Dally, Jeffrey I. Weitz, Richard C. Austin
Publikováno v:
Journal of Biological Chemistry. 277:47106-47113
Utrophin is a component of the platelet membrane cytoskeleton and participates in cytoskeletal reorganization (Earnest, J. P., Santos, G. F., Zuerbig, S., and Fox, J. E. B. (1995) J. Biol. Chem. 270, 27259–27265). Although platelets do not contain
Autor:
Richard G. Weleber, Daniel G. Green, Perry L. Howard, Verne M. Chapman, William R. Woodward, Sean M. Rash, Peter N. Ray, De-Ann M. Pillers, Michael R. Powers, Ghassan Y. Dally, Donald C. Hood
Publikováno v:
Molecular Genetics and Metabolism. 66:100-110
Duchenne and Becker muscular dystrophy patients have mutations in the dystrophin gene. Most show reduced b-wave amplitudes in the dark-adapted electroretinogram (ERG). We studied normal C57BL/6J mice and five X-linked muscular dystrophy strains with
Autor:
Perry L. Howard, Henry J. Klamut, Ghassan Y. Dally, Richard C. Austin, Ronald G. Worton, Stephanie D. Ditta, Peter N. Ray
Publikováno v:
Muscle & Nerve. 22:16-27
Duchenne muscular dystrophy is caused by mutations in the dystrophin gene, a complex gene that generates a family of distinct isoforms. In immature muscle cells, two dystrophin isoforms are expressed, Dp427 and Dp71. To characterize the function of D
Autor:
Richard G. Weleber, Alex Ho, Ghassan Y. Dally, Perry L. Howard, Peter N. Ray, De-Ann M. Pillers, Melanie H. Wong
Publikováno v:
Human Molecular Genetics. 7:1385-1391
The electroretinograms (ERGs) of patients with Duchenne muscular dystrophy and an allelic variant of the mdx mouse (mdxCv3) have been shown to be abnormal. Analysis of five allelic variants of the mdx mouse with mutations in the dystrophin gene has s
Autor:
Richard C, Austin, Joan E B, Fox, Geoff H, Werstuck, Alan R, Stafford, Dennis E, Bulman, Ghassan Y, Dally, Cameron A, Ackerley, Jeffrey I, Weitz, Peter N, Ray
Publikováno v:
The Journal of biological chemistry. 277(49)
Utrophin is a component of the platelet membrane cytoskeleton and participates in cytoskeletal reorganization (Earnest, J. P., Santos, G. F., Zuerbig, S., and Fox, J. E. B. (1995) J. Biol. Chem. 270, 27259-27265). Although platelets do not contain dy
Publikováno v:
Human molecular genetics. 5(10)
The dystrophin gene defective in Duchenne muscular dystrophy (DMD) is extreme in size and complexity with several promoters which direct expression of different isoforms in different tissues. In contrast with adult skeletal muscle which expresses 427