Taylor RW - Search Results

1

Clinical features of the pathogenic m.5540G>A mitochondrial transfer RNA tryptophan gene mutation.

Ng YS, Hardy SA, Shrier V, Quaghebeur G, Mole DR, Daniels MJ, Downes SM, Freebody J, Fratter C, Hofer M, Nemeth AH, Poulton J, Taylor RW. Ng YS, et al. Among authors: taylor rw. Neuromuscul Disord. 2016 Oct;26(10):702-705. doi: 10.1016/j.nmd.2016.08.009. Epub 2016 Aug 17. Neuromuscul Disord. 2016. PMID: 27618137 Free PMC article.

2

MELAS associated with a mutation in the valine transfer RNA gene of mitochondrial DNA.

Taylor RW, Chinnery PF, Haldane F, Morris AA, Bindoff LA, Wilson J, Turnbull DM. Taylor RW, et al. Ann Neurol. 1996 Sep;40(3):459-62. doi: 10.1002/ana.410400318. Ann Neurol. 1996. PMID: 8797538

3

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: taylor rw. Ann Neurol. 1997 Mar;41(3):408-10. doi: 10.1002/ana.410410319. Ann Neurol. 1997. PMID: 9066365

4

Treatment of mitochondrial disease.

Taylor RW, Chinnery PF, Clark KM, Lightowlers RN, Turnbull DM. Taylor RW, et al. J Bioenerg Biomembr. 1997 Apr;29(2):195-205. doi: 10.1023/a:1022646215643. J Bioenerg Biomembr. 1997. PMID: 9239544 Review.

5

A novel mitochondrial tRNA isoleucine gene mutation causing chronic progressive external ophthalmoplegia.

Chinnery PF, Johnson MA, Taylor RW, Durward WF, Turnbull DM. Chinnery PF, et al. Among authors: taylor rw. Neurology. 1997 Oct;49(4):1166-8. doi: 10.1212/wnl.49.4.1166. Neurology. 1997. PMID: 9339712

6

The epidemiology of pathogenic mitochondrial DNA mutations.

Chinnery PF, Johnson MA, Wardell TM, Singh-Kler R, Hayes C, Brown DT, Taylor RW, Bindoff LA, Turnbull DM. Chinnery PF, et al. Among authors: taylor rw. Ann Neurol. 2000 Aug;48(2):188-93. Ann Neurol. 2000. PMID: 10939569

7

In-vitro genetic modification of mitochondrial function.

Taylor RW, Chinnery PF, Turnbull DM, Lightowlers RN. Taylor RW, et al. Hum Reprod. 2000 Jul;15 Suppl 2:79-85. doi: 10.1093/humrep/15.suppl_2.79. Hum Reprod. 2000. PMID: 11041515 Review.

8

Progressive mitochondrial disease resulting from a novel missense mutation in the mitochondrial DNA ND3 gene.

Taylor RW, Singh-Kler R, Hayes CM, Smith PE, Turnbull DM. Taylor RW, et al. Ann Neurol. 2001 Jul;50(1):104-7. doi: 10.1002/ana.1084. Ann Neurol. 2001. PMID: 11456298

9

The mitochondrial genome and mitochondrial muscle disorders.

Schaefer AM, Taylor RW, Turnbull DM. Schaefer AM, et al. Among authors: taylor rw. Curr Opin Pharmacol. 2001 Jun;1(3):288-93. doi: 10.1016/s1471-4892(01)00051-0. Curr Opin Pharmacol. 2001. PMID: 11712753 Review.

10

Multiple neonatal deaths due to a homoplasmic mitochondrial DNA mutation.

McFarland R, Clark KM, Morris AA, Taylor RW, Macphail S, Lightowlers RN, Turnbull DM. McFarland R, et al. Among authors: taylor rw. Nat Genet. 2002 Feb;30(2):145-6. doi: 10.1038/ng819. Epub 2002 Jan 22. Nat Genet. 2002. PMID: 11799391

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