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

158 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Nuclear genetic control of mitochondrial DNA segregation.
Battersby BJ, Loredo-Osti JC, Shoubridge EA. Battersby BJ, et al. Among authors: shoubridge ea. Nat Genet. 2003 Feb;33(2):183-6. doi: 10.1038/ng1073. Epub 2003 Jan 21. Nat Genet. 2003. PMID: 12539044
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.
Mitochondrial dysfunction in multiple symmetrical lipomatosis.
Berkovic SF, Andermann F, Shoubridge EA, Carpenter S, Robitaille Y, Andermann E, Melmed C, Karpati G. Berkovic SF, et al. Among authors: shoubridge ea. Ann Neurol. 1991 May;29(5):566-9. doi: 10.1002/ana.410290519. Ann Neurol. 1991. PMID: 1650162
Correlative multidisciplinary approach to the study of mitochondrial encephalomyopathies.
Karpati G, Arnold D, Matthews P, Carpenter S, Andermann F, Shoubridge E. Karpati G, et al. Among authors: shoubridge e. Rev Neurol (Paris). 1991;147(6-7):455-61. Rev Neurol (Paris). 1991. PMID: 1962050 Review.
In vivo muscle magnetic resonance spectroscopy in the clinical investigation of mitochondrial disease.
Matthews PM, Allaire C, Shoubridge EA, Karpati G, Carpenter S, Arnold DL. Matthews PM, et al. Among authors: shoubridge ea. Neurology. 1991 Jan;41(1):114-20. doi: 10.1212/wnl.41.1.114. Neurology. 1991. PMID: 1985275
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
Familial myopathy with conspicuous depletion of mitochondria in muscle fibers: a morphologically distinct disease.
Genge A, Karpati G, Arnold D, Shoubridge EA, Carpenter S. Genge A, et al. Among authors: shoubridge ea. Neuromuscul Disord. 1995 Mar;5(2):139-44. doi: 10.1016/0960-8966(94)00039-c. Neuromuscul Disord. 1995. PMID: 7767093
Late-onset mitochondrial myopathy.
Johnston W, Karpati G, Carpenter S, Arnold D, Shoubridge EA. Johnston W, et al. Among authors: shoubridge ea. Ann Neurol. 1995 Jan;37(1):16-23. doi: 10.1002/ana.410370106. Ann Neurol. 1995. PMID: 7818252
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.
158 results
Jump to page