References
- Shoffner JM, Lott MT, Voljavec AS, Soueidan SA, Costigan DA, Wallace DC. Spontaneous Kearns-Sayre/ chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy. Proc Natl Acad Sci U S A 1989; 86: 7952–6.
- Seidman MD, Bai U, Khan MJ, Murphy MJ, Quirk WS, Castora FL, et al. The association of mitochondrial DNA deletions and cochlear pathology: a molecular biologic tool. Laryngoscope 1996; 106: 777–83.
- Zhang X, Han D, Ding D, Dai P, Yang W, Jiang S, et al. Cochlear mitochondrial DNA3867bp deletion in aged mice. Chin Med J (Engl) 2002; 115: 1390–3.
- Seidman MD, Bai U, Khan MJ, Quirk WS. Mitochondrial DNA deletions associated with aging and presby-acusis. Arch Otolaryngol Head Neck Surg 1997; 123: 1039–45.
- Bai U, Seidman MD, Hinojosa R, Quirk WS. Mitochondrial DNA deletions associated with aging and possibly presbycusis: a human archival temporal bone study. Am J Otol 1997; 18: 449–53.
- Seidman MD, Khan MJ, Tang WX, Quirk WS. Influence of lecithin on mitochondrial DNA and age-related hearing loss. Otolaryngol Head Neck Surg 2002; 127: 138–44.
- Seidman MD. Effects of dietary restriction and antioxidants on presbyacusis. Laryngoscope 2000; 110: 727–38.
- Simpson TA, Smith RJH. Amplification of mitochondrial DNA from archival temporal bone specimens. Laryngoscope 1995; 105: 28–34.
- Dai P, Jiang SC, Yang WY. Extraction, amplification, recombination and sequencing of the mitochondrial DNA from celloidin embedded human temporal bone sections. Chin J Otorhinolaryngol 1998; 33: 206–9.
- Fischel-Ghodsian N, Bykhovskaya Y, Taylor K, Kahen T, Cantor R, Ehrenman K, et al. Temporal bone analysis of patients with presbycusis reveals high frequency of mitochondrial mutations. Hear Res 1997; 110: 147–54.
- Corral-Debrinski M, Stepien G, Shoffner JM, Lott MT, Kanter K, Wallace DC. Hypoxemia is associated with mitochondrial DNA damage and gene induction (implications for cardiac disease). JAMA 1991; 266: 1812–6.
- Merril CR, Zullo S, Ghanbari H, Herman MM, Klein-man JE, Bigelow LB, et al. Possible relationship between conditions associated with chronic hypoxia and brain mitochondrial DNA deletion. Arch Biochem Biophys 1996; 326: 172–7.
- Ueda N, Oshima T, Ikeda K, Abe K, Aoki M, Takasaka T. Mitochondrial DNA deletion is a predisposing cause for sensorineural hearing loss. Laryngoscope 1998; 108: 580–4.
- Zhang XX, Han DY, Ding DL, Dai P, Yang WY, Jiang SC, et al. Deletions are easily detectable in cochlear mitochondrial DNA of Cu/Zn superoxide dismutase gene knock out mice. Chin Med J (Engl) 2002; 115: 258 63.
- Seidman MD, Khan MJ, Bai U, Shirwany N, Quirk WS. Biologic activity of mitochondrial metabolites on aging and age-related hearing loss. Am J Otol 2000; 21: 161–7.