381 related articles for article (PubMed ID: 18242646)
1. Detection of mitochondrial DNA deletions in the cochlea and its structural elements from archival human temporal bone tissue.
Markaryan A; Nelson EG; Hinojosa R
Mutat Res; 2008 Apr; 640(1-2):38-45. PubMed ID: 18242646
[TBL] [Abstract][Full Text] [Related]
2. Age-dependent respiratory function decline and DNA deletions in human muscle mitochondria.
Hsieh RH; Hou JH; Hsu HS; Wei YH
Biochem Mol Biol Int; 1994 Apr; 32(6):1009-22. PubMed ID: 8061617
[TBL] [Abstract][Full Text] [Related]
3. Contribution of common deletion to total deletion burden in mitochondrial DNA from inner ear of d-galactose-induced aging rats.
Zhong Y; Hu YJ; Yang Y; Peng W; Sun Y; Chen B; Huang X; Kong WJ
Mutat Res; 2011 Jul; 712(1-2):11-9. PubMed ID: 21473872
[TBL] [Abstract][Full Text] [Related]
4. Mitochondrial DNA deletions associated with aging and possibly presbycusis: a human archival temporal bone study.
Bai U; Seidman MD; Hinojosa R; Quirk WS
Am J Otol; 1997 Jul; 18(4):449-53. PubMed ID: 9233484
[TBL] [Abstract][Full Text] [Related]
5. [Effects of mtDNA deletion associated with abnormal expression in rat cochlear with presbycusis].
Wu H; Du B; Wang P; Niu C; Jin X
Zhonghua Er Bi Yan Hou Ke Za Zhi; 2002 Jun; 37(3):191-3. PubMed ID: 12772321
[TBL] [Abstract][Full Text] [Related]
6. [Mitochondrial DNA4568 deletions in guinea-pig associated with presbycusis].
Wei XM; Yang Y; Liang CY; Zheng Z
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Dec; 23(6):673-6. PubMed ID: 17160952
[TBL] [Abstract][Full Text] [Related]
7. Presbycusis: a human temporal bone study of individuals with downward sloping audiometric patterns of hearing loss and review of the literature.
Nelson EG; Hinojosa R
Laryngoscope; 2006 Sep; 116(9 Pt 3 Suppl 112):1-12. PubMed ID: 16946668
[TBL] [Abstract][Full Text] [Related]
8. Role of mitochondrial dysfunction and mitochondrial DNA mutations in age-related hearing loss.
Yamasoba T; Someya S; Yamada C; Weindruch R; Prolla TA; Tanokura M
Hear Res; 2007 Apr; 226(1-2):185-93. PubMed ID: 16870370
[TBL] [Abstract][Full Text] [Related]
9. Effects of dietary restriction and antioxidants on presbyacusis.
Seidman MD
Laryngoscope; 2000 May; 110(5 Pt 1):727-38. PubMed ID: 10807352
[TBL] [Abstract][Full Text] [Related]
10. Cochlear mitochondrial DNA3867bp deletion in aged mice.
Zhang X; Han D; Ding D; Dai P; Yang W; Jiang S; Salvi RJ
Chin Med J (Engl); 2002 Sep; 115(9):1390-3. PubMed ID: 12411120
[TBL] [Abstract][Full Text] [Related]
11. Major arc mitochondrial DNA deletions in cytochrome c oxidase-deficient human cochlear spiral ganglion cells.
Markaryan A; Nelson EG; Hinojosa R
Acta Otolaryngol; 2010 Jul; 130(7):780-7. PubMed ID: 20085441
[TBL] [Abstract][Full Text] [Related]
12. [Mitochondrial DNA4977 deletions associated with human presbycusis].
Han W; Han D; Jiang S
Zhonghua Er Bi Yan Hou Ke Za Zhi; 2000 Dec; 35(6):416-9. PubMed ID: 12768749
[TBL] [Abstract][Full Text] [Related]
13. Technical report: laser microdissection of cochlear structures from celloidin embedded human temporal bone tissues and detection of the mitochondrial DNA common deletion using real time PCR.
Markaryan A; Nelson EG; Tretiakova M; Hinojosa R
Hear Res; 2008 Oct; 244(1-2):1-6. PubMed ID: 18706496
[TBL] [Abstract][Full Text] [Related]
14. Quantification of the mitochondrial DNA common deletion in presbycusis.
Markaryan A; Nelson EG; Hinojosa R
Laryngoscope; 2009 Jun; 119(6):1184-9. PubMed ID: 19358252
[TBL] [Abstract][Full Text] [Related]
15. Human skin mitochondrial DNA deletions associated with light exposure.
Pang CY; Lee HC; Yang JH; Wei YH
Arch Biochem Biophys; 1994 Aug; 312(2):534-8. PubMed ID: 8037468
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Quantitative cellular level analysis of mitochondrial DNA 3243A > G mutations in individual tissues from the archival temporal bones of a MELAS patient.
Koda H; Kimura Y; Ishige I; Eishi Y; Iino Y; Kitamura K
Acta Otolaryngol; 2010 Mar; 130(3):344-50. PubMed ID: 19685357
[TBL] [Abstract][Full Text] [Related]
18. Mitochondrial gene mutation: the ageing process and degenerative diseases.
Linnane AW; Baumer A; Maxwell RJ; Preston H; Zhang CF; Marzuki S
Biochem Int; 1990 Dec; 22(6):1067-76. PubMed ID: 1965280
[TBL] [Abstract][Full Text] [Related]
19. Decreased cytochrome-c oxidase activity and lack of age-related accumulation of mitochondrial DNA deletions in the brains of schizophrenics.
Cavelier L; Jazin EE; Eriksson I; Prince J; Båve U; Oreland L; Gyllensten U
Genomics; 1995 Sep; 29(1):217-24. PubMed ID: 8530074
[TBL] [Abstract][Full Text] [Related]
20. Mitochondrial abnormalities in inclusion-body myositis.
Oldfors A; Moslemi AR; Jonasson L; Ohlsson M; Kollberg G; Lindberg C
Neurology; 2006 Jan; 66(2 Suppl 1):S49-55. PubMed ID: 16432145
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]