These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
157 related articles for article (PubMed ID: 7994642)
1. [Mitochondrial DNA mutations in patients with myocardial diseases]. Li YY; Xu J; Zhang JN Zhonghua Yi Xue Za Zhi; 1994 Jun; 74(6):345-8, 350. PubMed ID: 7994642 [TBL] [Abstract][Full Text] [Related]
2. Whole mitochondrial genome amplification reveals basal level multiple deletions in mtDNA of patients with dilated cardiomyopathy. Li YY; Hengstenberg C; Maisch B Biochem Biophys Res Commun; 1995 May; 210(1):211-8. PubMed ID: 7741744 [TBL] [Abstract][Full Text] [Related]
3. Novel point mutations in the mitochondrial DNA detected in patients with dilated cardiomyopathy by screening the whole mitochondrial genome. Ruppert V; Nolte D; Aschenbrenner T; Pankuweit S; Funck R; Maisch B Biochem Biophys Res Commun; 2004 May; 318(2):535-43. PubMed ID: 15120634 [TBL] [Abstract][Full Text] [Related]
4. The complete sequence of mtDNA genes in idiopathic dilated cardiomyopathy shows novel missense and tRNA mutations. Marin-Garcia J; Goldenthal MJ; Ananthakrishnan R; Pierpont ME J Card Fail; 2000 Dec; 6(4):321-9. PubMed ID: 11145757 [TBL] [Abstract][Full Text] [Related]
5. Specific mitochondrial DNA deletions in idiopathic dilated cardiomyopathy. Marin-Garcia J; Goldenthal MJ; Ananthakrishnan R; Pierpont ME; Fricker FJ; Lipshultz SE; Perez-Atayde A Cardiovasc Res; 1996 Feb; 31(2):306-13. PubMed ID: 8730408 [TBL] [Abstract][Full Text] [Related]
6. Point mutations in mitochondrial DNA of patients with dilated cardiomyopathy. Li YY; Maisch B; Rose ML; Hengstenberg C J Mol Cell Cardiol; 1997 Oct; 29(10):2699-709. PubMed ID: 9344764 [TBL] [Abstract][Full Text] [Related]
7. Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathy. Arbustini E; Diegoli M; Fasani R; Grasso M; Morbini P; Banchieri N; Bellini O; Dal Bello B; Pilotto A; Magrini G; Campana C; Fortina P; Gavazzi A; Narula J; ViganĂ² M Am J Pathol; 1998 Nov; 153(5):1501-10. PubMed ID: 9811342 [TBL] [Abstract][Full Text] [Related]
8. Differential occurrence of mutations in mitochondrial DNA of human skeletal muscle during aging. Zhang C; Liu VW; Addessi CL; Sheffield DA; Linnane AW; Nagley P Hum Mutat; 1998; 11(5):360-71. PubMed ID: 9600454 [TBL] [Abstract][Full Text] [Related]
9. [Mitochondrial DNA mutations in patients with chronic progressive external ophthalmoplegia and Kearns-Sayre syndrome]. Wang ZX; Yuan Y; Gao F; Qi Y; Shen DG; Chen QT Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Aug; 20(4):273-8. PubMed ID: 12903032 [TBL] [Abstract][Full Text] [Related]
10. Accumulation of deletions in MtDNA during tissue aging: analysis by long PCR. Reynier P; Malthiery Y Biochem Biophys Res Commun; 1995 Dec; 217(1):59-67. PubMed ID: 8526940 [TBL] [Abstract][Full Text] [Related]
11. [Mutation analysis of mitochondrial DNA of children with Rett syndrome]. Tang J; Qi Y; Bao X Zhonghua Yi Xue Za Zhi; 1996 Sep; 76(9):684-7. PubMed ID: 9275552 [TBL] [Abstract][Full Text] [Related]
12. [The mitochondrial DNA mutation in spinocerebellar ataxia type 3]. Wang J; Luo M; Yuan Z; Yang X; Li G Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Dec; 25(6):667-9. PubMed ID: 19065528 [TBL] [Abstract][Full Text] [Related]
13. Characterization of retinal and blood mitochondrial DNA from age-related macular degeneration patients. Kenney MC; Atilano SR; Boyer D; Chwa M; Chak G; Chinichian S; Coskun P; Wallace DC; Nesburn AB; Udar NS Invest Ophthalmol Vis Sci; 2010 Aug; 51(8):4289-97. PubMed ID: 20357205 [TBL] [Abstract][Full Text] [Related]
14. Age-dependent 6kb deletion in human liver mitochondrial DNA. Yen TC; Pang CY; Hsieh RH; Su CH; King KL; Wei YH Biochem Int; 1992 Mar; 26(3):457-68. PubMed ID: 1627156 [TBL] [Abstract][Full Text] [Related]
15. Fragmentation of human heart mitochondrial DNA associated with premature aging. Katsumata K; Hayakawa M; Tanaka M; Sugiyama S; Ozawa T Biochem Biophys Res Commun; 1994 Jul; 202(1):102-10. PubMed ID: 8037701 [TBL] [Abstract][Full Text] [Related]
17. The frequency of point mutations in mitochondrial DNA is elevated in the Alzheimer's brain. Chang SW; Zhang D; Chung HD; Zassenhaus HP Biochem Biophys Res Commun; 2000 Jun; 273(1):203-8. PubMed ID: 10873587 [TBL] [Abstract][Full Text] [Related]
19. Independent occurrence of somatic mutations in mitochondrial DNA of human skin from subjects of various ages. Liu VW; Zhang C; Pang CY; Lee HC; Lu CY; Wei YH; Nagley P Hum Mutat; 1998; 11(3):191-6. PubMed ID: 9521419 [TBL] [Abstract][Full Text] [Related]
20. Surveyor Nuclease: a new strategy for a rapid identification of heteroplasmic mitochondrial DNA mutations in patients with respiratory chain defects. Bannwarth S; Procaccio V; Paquis-Flucklinger V Hum Mutat; 2005 Jun; 25(6):575-82. PubMed ID: 15880407 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]