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Expression of the E6 and E7 genes of human papillomavirus (HPV16) extends the life span of human myoblasts.
Lochm├╝ller H, Johns T, Shoubridge EA. Lochm├╝ller H, et al. Among authors: shoubridge ea. Exp Cell Res. 1999 Apr 10;248(1):186-93. doi: 10.1006/excr.1999.4407. Exp Cell Res. 1999. PMID: 10094825
Distribution and threshold expression of the tRNA(Lys) mutation in skeletal muscle of patients with myoclonic epilepsy and ragged-red fibers (MERRF).
Boulet L, Karpati G, Shoubridge EA. Boulet L, et al. Among authors: shoubridge ea. Am J Hum Genet. 1992 Dec;51(6):1187-200. Am J Hum Genet. 1992. PMID: 1334369 Free PMC article.
Deletion mutants are functionally dominant over wild-type mitochondrial genomes in skeletal muscle fiber segments in mitochondrial disease.
Shoubridge EA, Karpati G, Hastings KE. Shoubridge EA, et al. Cell. 1990 Jul 13;62(1):43-9. doi: 10.1016/0092-8674(90)90238-a. Cell. 1990. PMID: 2163769
Segregation of mitochondrial DNAs carrying a pathogenic point mutation (tRNA(leu3243)) in cybrid cells.
Shoubridge EA. Shoubridge EA. Biochem Biophys Res Commun. 1995 Aug 4;213(1):189-95. doi: 10.1006/bbrc.1995.2115. Biochem Biophys Res Commun. 1995. PMID: 7639735
Mitochondrial DNA diseases: histological and cellular studies.
Shoubridge EA. Shoubridge EA. J Bioenerg Biomembr. 1994 Jun;26(3):301-10. doi: 10.1007/BF00763101. J Bioenerg Biomembr. 1994. PMID: 8077183 Review.
Myoblast transfer in Duchenne muscular dystrophy.
Karpati G, Ajdukovic D, Arnold D, Gledhill RB, Guttmann R, Holland P, Koch PA, Shoubridge E, Spence D, Vanasse M, et al. Karpati G, et al. Ann Neurol. 1993 Jul;34(1):8-17. doi: 10.1002/ana.410340105. Ann Neurol. 1993. PMID: 8517684 Clinical Trial.
Characterization of the mitochondrial DNA abnormalities in the skeletal muscle of patients with inclusion body myositis.
Horvath R, Fu K, Johns T, Genge A, Karpati G, Shoubridge EA. Horvath R, et al. Among authors: shoubridge ea. J Neuropathol Exp Neurol. 1998 May;57(5):396-403. doi: 10.1097/00005072-199805000-00003. J Neuropathol Exp Neurol. 1998. PMID: 9596410
Gene shifting: a novel therapy for mitochondrial myopathy.
Taivassalo T, Fu K, Johns T, Arnold D, Karpati G, Shoubridge EA. Taivassalo T, et al. Among authors: shoubridge ea. Hum Mol Genet. 1999 Jun;8(6):1047-52. doi: 10.1093/hmg/8.6.1047. Hum Mol Genet. 1999. PMID: 10332036
Myophosphorylase gene transfer in McArdle's disease myoblasts in vitro.
Pari G, Crerar MM, Nalbantoglu J, Shoubridge E, Jani A, Tsujino S, Shanske S, DiMauro S, Howell JM, Karpati G. Pari G, et al. Neurology. 1999 Oct 12;53(6):1352-4. doi: 10.1212/wnl.53.6.1352. Neurology. 1999. PMID: 10522901
Expression and functional analysis of SURF1 in Leigh syndrome patients with cytochrome c oxidase deficiency.
Yao J, Shoubridge EA. Yao J, et al. Among authors: shoubridge ea. Hum Mol Genet. 1999 Dec;8(13):2541-9. doi: 10.1093/hmg/8.13.2541. Hum Mol Genet. 1999. PMID: 10556303
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