230 related articles for article (PubMed ID: 15126306)
1. Quantitative PCR analysis of mitochondrial DNA content in patients with mitochondrial disease.
Bai RK; Perng CL; Hsu CH; Wong LJ
Ann N Y Acad Sci; 2004 Apr; 1011():304-9. PubMed ID: 15126306
[TBL] [Abstract][Full Text] [Related]
2. Quantitative evaluation of the mitochondrial DNA depletion syndrome.
Dimmock D; Tang LY; Schmitt ES; Wong LJ
Clin Chem; 2010 Jul; 56(7):1119-27. PubMed ID: 20448188
[TBL] [Abstract][Full Text] [Related]
3. Quantification of mitochondrial DNA deletion, depletion, and overreplication: application to diagnosis.
Chabi B; Mousson de Camaret B; Duborjal H; Issartel JP; Stepien G
Clin Chem; 2003 Aug; 49(8):1309-17. PubMed ID: 12881447
[TBL] [Abstract][Full Text] [Related]
4. Simultaneous detection and quantification of mitochondrial DNA deletion(s), depletion, and over-replication in patients with mitochondrial disease.
Bai RK; Wong LJ
J Mol Diagn; 2005 Nov; 7(5):613-22. PubMed ID: 16258160
[TBL] [Abstract][Full Text] [Related]
5. Comprehensive molecular diagnosis of mitochondrial disorders: qualitative and quantitative approach.
Wong LJ
Ann N Y Acad Sci; 2004 Apr; 1011():246-58. PubMed ID: 15126301
[TBL] [Abstract][Full Text] [Related]
6. Molecular and clinical characterization of the myopathic form of mitochondrial DNA depletion syndrome caused by mutations in the thymidine kinase (TK2) gene.
Chanprasert S; Wang J; Weng SW; Enns GM; Boué DR; Wong BL; Mendell JR; Perry DA; Sahenk Z; Craigen WJ; Alcala FJ; Pascual JM; Melancon S; Zhang VW; Scaglia F; Wong LJ
Mol Genet Metab; 2013; 110(1-2):153-61. PubMed ID: 23932787
[TBL] [Abstract][Full Text] [Related]
7. Loss of the antioxidant enzyme CuZnSOD (Sod1) mimics an age-related increase in absolute mitochondrial DNA copy number in the skeletal muscle.
Masser DR; Clark NW; Van Remmen H; Freeman WM
Age (Dordr); 2016 Aug; 38(4):323-333. PubMed ID: 27444179
[TBL] [Abstract][Full Text] [Related]
8. Platelets, a typical source of error in real-time PCR quantification of mitochondrial DNA content in human peripheral blood cells.
Banas B; Kost BP; Goebel FD
Eur J Med Res; 2004 Aug; 9(8):371-7. PubMed ID: 15337626
[TBL] [Abstract][Full Text] [Related]
9. Mitochondrial DNA depletion syndrome: new descriptions and the use of citrate synthase as a helpful tool to better characterise the patients.
Navarro-Sastre A; Tort F; Garcia-Villoria J; Pons MR; Nascimento A; Colomer J; Campistol J; Yoldi ME; López-Gallardo E; Montoya J; Unceta M; Martinez MJ; Briones P; Ribes A
Mol Genet Metab; 2012 Nov; 107(3):409-15. PubMed ID: 22980518
[TBL] [Abstract][Full Text] [Related]
10. qPCR-based mitochondrial DNA quantification: influence of template DNA fragmentation on accuracy.
Jackson CB; Gallati S; Schaller A
Biochem Biophys Res Commun; 2012 Jul; 423(3):441-7. PubMed ID: 22683632
[TBL] [Abstract][Full Text] [Related]
11. Liver mtDNA content increases during development: a comparison of methods and the importance of age- and tissue-specific controls for the diagnosis of mtDNA depletion.
Morten KJ; Ashley N; Wijburg F; Hadzic N; Parr J; Jayawant S; Adams S; Bindoff L; Bakker HD; Mieli-Vergani G; Zeviani M; Poulton J
Mitochondrion; 2007 Dec; 7(6):386-95. PubMed ID: 17981517
[TBL] [Abstract][Full Text] [Related]
12. Precise determination of mitochondrial DNA copy number in human skeletal and cardiac muscle by a PCR-based assay: lack of change of copy number with age.
Miller FJ; Rosenfeldt FL; Zhang C; Linnane AW; Nagley P
Nucleic Acids Res; 2003 Jun; 31(11):e61. PubMed ID: 12771225
[TBL] [Abstract][Full Text] [Related]
13. Real-time quantitative PCR analysis of mitochondrial DNA content.
Venegas V; Wang J; Dimmock D; Wong LJ
Curr Protoc Hum Genet; 2011 Jan; Chapter 19():Unit 19.7.. PubMed ID: 21234878
[TBL] [Abstract][Full Text] [Related]
14. Mitochondrial DNA depletion is a prevalent cause of multiple respiratory chain deficiency in childhood.
Sarzi E; Bourdon A; Chrétien D; Zarhrate M; Corcos J; Slama A; Cormier-Daire V; de Lonlay P; Munnich A; Rötig A
J Pediatr; 2007 May; 150(5):531-4, 534.e1-6. PubMed ID: 17452231
[TBL] [Abstract][Full Text] [Related]
15. Fatal infantile lactic acidosis and a novel homozygous mutation in the SUCLG1 gene: a mitochondrial DNA depletion disorder.
Randolph LM; Jackson HA; Wang J; Shimada H; Sanchez-Lara PA; Wong DA; Wong LJ; Boles RG
Mol Genet Metab; 2011 Feb; 102(2):149-52. PubMed ID: 21093335
[TBL] [Abstract][Full Text] [Related]
16. The clinical diagnosis of POLG disease and other mitochondrial DNA depletion disorders.
Cohen BH; Naviaux RK
Methods; 2010 Aug; 51(4):364-73. PubMed ID: 20558295
[TBL] [Abstract][Full Text] [Related]
17. Clonally expanded mitochondrial DNA mutations in epileptic individuals with mutated DNA polymerase gamma.
Zsurka G; Baron M; Stewart JD; Kornblum C; Bös M; Sassen R; Taylor RW; Elger CE; Chinnery PF; Kunz WS
J Neuropathol Exp Neurol; 2008 Sep; 67(9):857-66. PubMed ID: 18716558
[TBL] [Abstract][Full Text] [Related]
18. Depletion of the other genome-mitochondrial DNA depletion syndromes in humans.
Elpeleg O; Mandel H; Saada A
J Mol Med (Berl); 2002 Jul; 80(7):389-96. PubMed ID: 12110944
[TBL] [Abstract][Full Text] [Related]
19. Mitochondrial DNA mutations: an overview of clinical and molecular aspects.
Craigen WJ
Methods Mol Biol; 2012; 837():3-15. PubMed ID: 22215537
[TBL] [Abstract][Full Text] [Related]
20. Detection and analysis of mitochondrial DNA deletions by whole genome PCR.
Tengan CH; Moraes CT
Biochem Mol Med; 1996 Jun; 58(1):130-4. PubMed ID: 8809354
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
