Kapsa RM - Search Results

1

Developmental genetics of deleted mtDNA in mitochondrial oculomyopathy.

Marzuki S, Berkovic SF, Saifuddin Noer A, Kapsa RM, Kalnins RM, Byrne E, Sasmono T, Sudoyo H. Marzuki S, et al. Among authors: kapsa rm. J Neurol Sci. 1997 Feb 12;145(2):155-62. doi: 10.1016/s0022-510x(96)00241-9. J Neurol Sci. 1997. PMID: 9094043

2

A novel mtDNA deletion in an infant with Pearson syndrome.

Kapsa R, Thompson GN, Thorburn DR, Dahl HH, Marzuki S, Byrne E, Blok RB. Kapsa R, et al. J Inherit Metab Dis. 1994;17(5):521-6. doi: 10.1007/BF00711584. J Inherit Metab Dis. 1994. PMID: 7837757

3

Mitochondrial DNA polymorphism in disease: a possible contributor to respiratory dysfunction.

Lertrit P, Kapsa RM, Jean-Francois MJ, Thyagarajan D, Noer AS, Marzuki S, Byrne E. Lertrit P, et al. Among authors: kapsa rm. Hum Mol Genet. 1994 Nov;3(11):1973-81. doi: 10.1093/hmg/3.11.1973. Hum Mol Genet. 1994. PMID: 7874114

4

Rapid and noninvasive screening of patients with mitochondrial myopathy.

Kotsimbos N, Jean-Francois MJ, Huizing M, Kapsa RM, Lertrit P, Siregar NC, Marzuki S, Sue C, Byrne E. Kotsimbos N, et al. Among authors: kapsa rm. Hum Mutat. 1994;4(2):132-5. doi: 10.1002/humu.1380040207. Hum Mutat. 1994. PMID: 7981717

5

Mitochondrial DNA polymorphism in substantia nigra.

Kapsa RM, Jean-Francois MJ, Lertrit P, Weng S, Siregar N, Ojaimi J, Donnan G, Masters C, Byrne E. Kapsa RM, et al. J Neurol Sci. 1996 Dec;144(1-2):204-11. doi: 10.1016/s0022-510x(96)00247-x. J Neurol Sci. 1996. PMID: 8994125

6

Significance of mitochondrial DNA deletions in myotonic dystrophy.

Thyagarajan D, Byrne E, Noer S, Lertrit P, Utthanophol P, Kapsa R, Marzuki S. Thyagarajan D, et al. Acta Neurol Scand. 1993 Jan;87(1):32-6. doi: 10.1111/j.1600-0404.1993.tb04071.x. Acta Neurol Scand. 1993. PMID: 8093820

7

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. 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.

8

A tRNA(Lys) mutation in the mtDNA is the causal genetic lesion underlying myoclonic epilepsy and ragged-red fiber (MERRF) syndrome.

Noer AS, Sudoyo H, Lertrit P, Thyagarajan D, Utthanaphol P, Kapsa R, Byrne E, Marzuki S. Noer AS, et al. Am J Hum Genet. 1991 Oct;49(4):715-22. Am J Hum Genet. 1991. PMID: 1910259 Free PMC article.

9

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. 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

10

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. 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.

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