Quigley A - Search Results

1

In vivo and in vitro correction of the mdx dystrophin gene nonsense mutation by short-fragment homologous replacement.

Kapsa R, Quigley A, Lynch GS, Steeper K, Kornberg AJ, Gregorevic P, Austin L, Byrne E. Kapsa R, et al. Among authors: quigley a. Hum Gene Ther. 2001 Apr 10;12(6):629-42. doi: 10.1089/104303401300057324. Hum Gene Ther. 2001. PMID: 11426463

2

The polymerase chain reaction in the study of mitochondrial genetics.

Kapsa R, Siregar N, Quigley A, Ojaimi J, Katsabanis S, Sue C, Byrne E. Kapsa R, et al. Among authors: quigley a. J Biochem Biophys Methods. 1997 Dec 17;36(1):31-50. doi: 10.1016/s0165-022x(97)00044-4. J Biochem Biophys Methods. 1997. PMID: 9507371

3

Mitochondrial DNA in stroke and migraine with aura.

Ojaimi J, Katsabanis S, Bower S, Quigley A, Byrne E. Ojaimi J, et al. Among authors: quigley a. Cerebrovasc Dis. 1998 Mar-Apr;8(2):102-6. doi: 10.1159/000015826. Cerebrovasc Dis. 1998. PMID: 9548008 Clinical Trial.

4

mtDNA replicative potential remains constant during ageing: polymerase gamma activity does not correlate with age related cytochrome oxidase activity decline in platelets.

Kapsa RM, Quigley AF, Han TF, Jean-Francois MJ, Vaughan P, Byrne E. Kapsa RM, et al. Among authors: quigley af. Nucleic Acids Res. 1998 Oct 1;26(19):4365-73. doi: 10.1093/nar/26.19.4365. Nucleic Acids Res. 1998. PMID: 9742236 Free PMC article.

5

Detection of MELAS A3243G point mutation in muscle, blood and hair follicles.

Sue CM, Quigley A, Katsabanis S, Kapsa R, Crimmins DS, Byrne E, Morris JG. Sue CM, et al. Among authors: quigley a. J Neurol Sci. 1998 Nov 26;161(1):36-9. doi: 10.1016/s0022-510x(98)00179-8. J Neurol Sci. 1998. PMID: 9879679 Free article.

6

Mitochondrial respiratory chain activity in idiopathic dilated cardiomyopathy.

Quigley AF, Kapsa RM, Esmore D, Hale G, Byrne E. Quigley AF, et al. J Card Fail. 2000 Mar;6(1):47-55. doi: 10.1016/s1071-9164(00)00011-7. J Card Fail. 2000. PMID: 10746819

7

Targeted gene correction in the mdx mouse using short DNA fragments: towards application with bone marrow-derived cells for autologous remodeling of dystrophic muscle.

Kapsa RM, Quigley AF, Vadolas J, Steeper K, Ioannou PA, Byrne E, Kornberg AJ. Kapsa RM, et al. Among authors: quigley af. Gene Ther. 2002 Jun;9(11):695-9. doi: 10.1038/sj.gt.3301737. Gene Ther. 2002. PMID: 12032690

8

CD45 fraction bone marrow cells as potential delivery vehicles for genetically corrected dystrophin loci.

Kapsa RM, Wong SH, Bertoncello I, Quigley AF, Williams B, Sells K, Marotta R, Kita M, Simmons P, Byrne E, Kornberg AJ. Kapsa RM, et al. Among authors: quigley af. Neuromuscul Disord. 2002 Oct;12 Suppl 1:S61-6. doi: 10.1016/s0960-8966(02)00084-6. Neuromuscul Disord. 2002. PMID: 12206798

9

Diagnostic screening of mitochondrial DNA mutations in Australian adults 1990-2001.

Marotta R, Chin J, Quigley A, Katsabanis S, Kapsa R, Byrne E, Collins S. Marotta R, et al. Among authors: quigley a. Intern Med J. 2004 Jan-Feb;34(1-2):10-9. doi: 10.1111/j.1444-0903.2004.t01-3-.x. Intern Med J. 2004. PMID: 14748908

10

DNA electroporation in vivo targets mature fibres in dystrophic mdx muscle.

Wong SH, Lowes KN, Quigley AF, Marotta R, Kita M, Byrne E, Kornberg AJ, Cook MJ, Kapsa RM. Wong SH, et al. Among authors: quigley af. Neuromuscul Disord. 2005 Oct;15(9-10):630-41. doi: 10.1016/j.nmd.2005.04.008. Neuromuscul Disord. 2005. PMID: 16084723

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