Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

72 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Exon skipping and translation in patients with frameshift deletions in the dystrophin gene.
Sherratt TG, Vulliamy T, Dubowitz V, Sewry CA, Strong PN. Sherratt TG, et al. Among authors: strong pn. Am J Hum Genet. 1993 Nov;53(5):1007-15. Am J Hum Genet. 1993. PMID: 8213828 Free PMC article.
Massive idiosyncratic exon skipping corrects the nonsense mutation in dystrophic mouse muscle and produces functional revertant fibers by clonal expansion.
Lu QL, Morris GE, Wilton SD, Ly T, Artem'yeva OV, Strong P, Partridge TA. Lu QL, et al. Among authors: strong p. J Cell Biol. 2000 Mar 6;148(5):985-96. doi: 10.1083/jcb.148.5.985. J Cell Biol. 2000. PMID: 10704448 Free PMC article.
Dystrophin and dystrophin-like proteins in muscle and brain of normal and mdx mice.
Clerk A, Muntoni F, Strong P. Clerk A, et al. Among authors: strong p. Biochem Soc Trans. 1990 Jun;18(3):388-9. doi: 10.1042/bst0180388. Biochem Soc Trans. 1990. PMID: 2197132 No abstract available.
Enhanced expression of recombinant dystrophin following intramuscular injection of Epstein-Barr virus (EBV)-based mini-chromosome vectors in mdx mice.
Tsukamoto H, Wells D, Brown S, Serpente P, Strong P, Drew J, Inui K, Okada S, Dickson G. Tsukamoto H, et al. Among authors: strong p. Gene Ther. 1999 Jul;6(7):1331-5. doi: 10.1038/sj.gt.3300944. Gene Ther. 1999. PMID: 10455444
Dystrophin immunoreactivity in normal and Duchenne human fetal neurons in culture.
Torelli S, Sogos V, Ennas MG, Muntoni F, Clerk A, Strong PN, Gremo F. Torelli S, et al. Among authors: strong pn. J Neurosci Res. 1992 May;32(1):116-25. doi: 10.1002/jnr.490320114. J Neurosci Res. 1992. PMID: 1378503
Dystrophin in frameshift deletion patients with Becker muscular dystrophy.
Gangopadhyay SB, Sherratt TG, Heckmatt JZ, Dubowitz V, Miller G, Shokeir M, Ray PN, Strong PN, Worton RG. Gangopadhyay SB, et al. Among authors: strong pn. Am J Hum Genet. 1992 Sep;51(3):562-70. Am J Hum Genet. 1992. PMID: 1496988 Free PMC article.
Genetic correction of dystrophin deficiency and skeletal muscle remodeling in adult MDX mouse via transplantation of retroviral producer cells.
Fassati A, Wells DJ, Sgro Serpente PA, Walsh FS, Brown SC, Strong PN, Dickson G. Fassati A, et al. Among authors: strong pn. J Clin Invest. 1997 Aug 1;100(3):620-8. doi: 10.1172/JCI119573. J Clin Invest. 1997. PMID: 9239410 Free PMC article.
Calmodulin-binding profiles for nebulin and dystrophin in human skeletal muscle.
Patel K, Strong PN, Dubowitz V, Dunn MJ. Patel K, et al. Among authors: strong pn. FEBS Lett. 1988 Jul 18;234(2):267-71. doi: 10.1016/0014-5793(88)80095-4. FEBS Lett. 1988. PMID: 3292289
Dystrophin and nebulin in the muscular dystrophies.
Patel K, Voit T, Dunn MJ, Strong PN, Dubowitz V. Patel K, et al. Among authors: strong pn. J Neurol Sci. 1988 Nov;87(2-3):315-26. doi: 10.1016/0022-510x(88)90256-0. J Neurol Sci. 1988. PMID: 3062133
Transcription of the dystrophin gene in Duchenne muscular dystrophy muscle.
Muntoni F, Strong PN. Muntoni F, et al. Among authors: strong pn. FEBS Lett. 1989 Jul 31;252(1-2):95-8. doi: 10.1016/0014-5793(89)80896-8. FEBS Lett. 1989. PMID: 2668030
72 results
Jump to page
Feedback