Lightowlers RN - Search Results

1

Mitochondrial DNA deletion in "identical" twin brothers.

Blakely EL, He L, Taylor RW, Chinnery PF, Lightowlers RN, Schaefer AM, Turnbull DM. Blakely EL, et al. Among authors: lightowlers rn. J Med Genet. 2004 Feb;41(2):e19. doi: 10.1136/jmg.2003.011296. J Med Genet. 2004. PMID: 14757869 Free PMC article. No abstract available.

2

Medium chain acyl-CoA dehydrogenase deficiency caused by a deletion of exons 11 and 12.

Morris AA, Taylor RW, Lightowlers RN, Aynsley-Green A, Bartlett K, Turnbull DM. Morris AA, et al. Among authors: lightowlers rn. Hum Mol Genet. 1995 Apr;4(4):747-9. doi: 10.1093/hmg/4.4.747. Hum Mol Genet. 1995. PMID: 7633427 No abstract available.

3

Gene therapy for mitochondrial DNA defects: is it possible?

Chrzanowska-Lightowlers ZM, Lightowlers RN, Turnbull DM. Chrzanowska-Lightowlers ZM, et al. Among authors: lightowlers rn. Gene Ther. 1995 Jul;2(5):311-6. Gene Ther. 1995. PMID: 7671106 Review.

4

An antisense oligodeoxynucleotide approach to investigate the function of the nuclear-encoded subunits of human cytochrome c oxidase.

Chrzanowska-Lightowlers ZM, Turnbull DM, Bindoff LA, Lightowlers RN. Chrzanowska-Lightowlers ZM, et al. Among authors: lightowlers rn. Biochem Biophys Res Commun. 1993 Oct 15;196(1):328-35. doi: 10.1006/bbrc.1993.2252. Biochem Biophys Res Commun. 1993. PMID: 8216308

5

A microtiter plate assay for cytochrome c oxidase in permeabilized whole cells.

Chrzanowska-Lightowlers ZM, Turnbull DM, Lightowlers RN. Chrzanowska-Lightowlers ZM, et al. Among authors: lightowlers rn. Anal Biochem. 1993 Oct;214(1):45-9. doi: 10.1006/abio.1993.1454. Anal Biochem. 1993. PMID: 8250253

6

Abnormal RNA processing associated with a novel tRNA mutation in mitochondrial DNA. A potential disease mechanism.

Bindoff LA, Howell N, Poulton J, McCullough DA, Morten KJ, Lightowlers RN, Turnbull DM, Weber K. Bindoff LA, et al. Among authors: lightowlers rn. J Biol Chem. 1993 Sep 15;268(26):19559-64. J Biol Chem. 1993. PMID: 8366098 Free article.

7

Selective inhibition of mutant human mitochondrial DNA replication in vitro by peptide nucleic acids.

Taylor RW, Chinnery PF, Turnbull DM, Lightowlers RN. Taylor RW, et al. Among authors: lightowlers rn. Nat Genet. 1997 Feb;15(2):212-5. doi: 10.1038/ng0297-212. Nat Genet. 1997. PMID: 9020853

8

Molecular analysis of cytochrome c oxidase deficiency in Leigh's syndrome.

Adams PL, Lightowlers RN, Turnbull DM. Adams PL, et al. Among authors: lightowlers rn. Ann Neurol. 1997 Feb;41(2):268-70. doi: 10.1002/ana.410410219. Ann Neurol. 1997. PMID: 9029077

9

A novel mitochondrial tRNA phenylalanine mutation presenting with acute rhabdomyolysis.

Chinnery PF, Johnson MA, Taylor RW, Lightowlers RN, Turnbull DM. Chinnery PF, et al. Among authors: lightowlers rn. Ann Neurol. 1997 Mar;41(3):408-10. doi: 10.1002/ana.410410319. Ann Neurol. 1997. PMID: 9066365

10

Reversal of a mitochondrial DNA defect in human skeletal muscle.

Clark KM, Bindoff LA, Lightowlers RN, Andrews RM, Griffiths PG, Johnson MA, Brierley EJ, Turnbull DM. Clark KM, et al. Among authors: lightowlers rn. Nat Genet. 1997 Jul;16(3):222-4. doi: 10.1038/ng0797-222. Nat Genet. 1997. PMID: 9207784 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

195 results

Search Page

Filters