-
1
-
-
25144452879
-
Presbycusis
-
Gates GA, Mills JH. Presbycusis. Lancet 2005; 366:1111-1120.
-
(2005)
Lancet
, vol.366
, pp. 1111-1120
-
-
Gates, G.A.1
Mills, J.H.2
-
2
-
-
2942752118
-
Age-related hearing loss and its association with reactive oxygen species and mitochondrial DNA damage
-
Seidman MD, Ahmad N., Joshi D., Seidman J., Thawani S., Quirk WS. Age-related hearing loss and its association with reactive oxygen species and mitochondrial DNA damage. Acta Otolaryngol Suppl 2004; 552:16-24.
-
(2004)
Acta Otolaryngol Suppl
, vol.552
, pp. 16-24
-
-
Seidman, M.D.1
Ahmad, N.2
Joshi, D.3
Seidman, J.4
Thawani, S.5
Quirk, W.S.6
-
3
-
-
0141529803
-
Presbycusis: A human temporal bone study of individuals with flat audiometric patterns of hearing loss using a new method to quantify stria vascularis volume
-
Nelson EG, Hinojosa R. Presbycusis: a human temporal bone study of individuals with flat audiometric patterns of hearing loss using a new method to quantify stria vascularis volume. Laryngoscope 2003; 113:1672-1686.
-
(2003)
Laryngoscope
, vol.113
, pp. 1672-1686
-
-
Nelson, E.G.1
Hinojosa, R.2
-
4
-
-
33748344698
-
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. Presbycusis: a human temporal bone study of individuals with downward sloping audiometric patterns of hearing loss and review of the literature. Laryngoscope 2006; 116 (suppl 112) :1-12.
-
(2006)
Laryngoscope
, vol.116
, Issue.SUPPL. 112
, pp. 1-12
-
-
Nelson, E.G.1
Hinojosa, R.2
-
5
-
-
0030849125
-
Mitochondrial DNA deletions associated with aging and possibly presbycusis: A human archival temporal bone study
-
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; 18:449-453.
-
(1997)
Am J Otol
, vol.18
, pp. 449-453
-
-
Bai, U.1
Seidman, M.D.2
Hinojosa, R.3
Quirk, W.S.4
-
6
-
-
70350411987
-
Mitochondrial DNA deletion is a predisposing cause for sensorineural hearing loss
-
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; 108:580-584.
-
(1998)
Laryngoscope
, vol.108
, pp. 580-584
-
-
Ueda, N.1
Oshima, T.2
Ikeda, K.3
Abe, K.4
Aoki, M.5
Takasaka, T.6
-
7
-
-
1642267429
-
Correlation of cochlear blood supply with mitochondrial DNA common deletion in presbycusis
-
Dai P., Yang W., Jiang S., et al. Correlation of cochlear blood supply with mitochondrial DNA common deletion in presbycusis. Acta Otolaryngol 2004; 124:130-136.
-
(2004)
Acta Otolaryngol
, vol.124
, pp. 130-136
-
-
Dai, P.1
Yang, W.2
Jiang, S.3
-
8
-
-
52049105860
-
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. Laser microdissection of cochlear structures from celloidin embedded human temporal bone tissues and detection of the mitochondrial DNA common deletion using real time PCR. Hear Res 2008; 244:1-6.
-
(2008)
Hear Res
, vol.244
, pp. 1-6
-
-
Markaryan, A.1
Nelson, E.G.2
Tretiakova, M.3
Hinojosa, R.4
-
9
-
-
0028140454
-
Distribution of wild-type and common deletion forms of mtDNA in normal and respiration-deficient muscle fibers from patients with mitochondrial myopathy
-
Sciacco M., Bonilla E., Schon EA, DiMauro S., Moraes CT. Distribution of wild-type and common deletion forms of mtDNA in normal and respiration-deficient muscle fibers from patients with mitochondrial myopathy. Hum Mol Genet 1994; 3:13-19.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 13-19
-
-
Sciacco, M.1
Bonilla, E.2
Schon, E.A.3
DiMauro, S.4
Moraes, C.T.5
-
10
-
-
0037444769
-
Mitochondrial threshold effects
-
Rossignol R., Faustin B., Rocher C., Malgat M., Mazat J-P, Letellier T. Mitochondrial threshold effects. Biochem J 2003; 370:751-762.
-
(2003)
Biochem J
, vol.370
, pp. 751-762
-
-
Rossignol, R.1
Faustin, B.2
Rocher, C.3
Malgat, M.4
Mazat, J.-P.5
Letellier, T.6
-
11
-
-
0025674177
-
Detection of a specific mitochondrial DNA deletion in tissues of older humans
-
Cortopassi GA, Arnheim N. Detection of a specific mitochondrial DNA deletion in tissues of older humans. Nucleic Acids Res 1990; 18:6927-6933.
-
(1990)
Nucleic Acids Res
, vol.18
, pp. 6927-6933
-
-
Cortopassi, G.A.1
Arnheim, N.2
-
13
-
-
33646375711
-
High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease
-
Bender A., Krishnan KJ, Morris CM, et al. High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease. Nat Genet 2006; 38:515-517.
-
(2006)
Nat Genet
, vol.38
, pp. 515-517
-
-
Bender, A.1
Krishnan, K.J.2
Morris, C.M.3
-
14
-
-
33646351299
-
Mitochondrial deletions are abundant and cause functional impairment in aged human substantia nigra neurons
-
Kraytsberg Y., Kudryavtseva E., McKee AC, Geula C., Kowall NW, Khrapko K. Mitochondrial deletions are abundant and cause functional impairment in aged human substantia nigra neurons. Nat Genet 2006; 38:518-520.
-
(2006)
Nat Genet
, vol.38
, pp. 518-520
-
-
Kraytsberg, Y.1
Kudryavtseva, E.2
McKee, A.C.3
Geula, C.4
Kowall, N.W.5
Khrapko, K.6
-
15
-
-
0030745117
-
Temporal bone analysis of patients with presbycusis reveals high frequency of mitochondrial mutations
-
Fischel-Ghodsian N., Bykhovskaya Y., Taylor K., et al. Temporal bone analysis of patients with presbycusis reveals high frequency of mitochondrial mutations. Hear Res 1997; 110:147-154.
-
(1997)
Hear Res
, vol.110
, pp. 147-154
-
-
Fischel-Ghodsian, N.1
Bykhovskaya, Y.2
Taylor, K.3
-
17
-
-
40649104716
-
Detection of mitochondrial DNA deletions in the cochlea and its structural elements from archival human temporal bone tissue
-
Markaryan A., Nelson EG, Hinojosa R. Detection of mitochondrial DNA deletions in the cochlea and its structural elements from archival human temporal bone tissue. Mutat Res 2008; 640:38-45.
-
(2008)
Mutat Res
, vol.640
, pp. 38-45
-
-
Markaryan, A.1
Nelson, E.G.2
Hinojosa, R.3
-
18
-
-
0024208299
-
The developing and senescent inner ear: Selected topics and models
-
Cohen GM, Park JC. The developing and senescent inner ear: selected topics and models. Crit Rev Neurobiol 1988; 4:179-199.
-
(1988)
Crit Rev Neurobiol
, vol.4
, pp. 179-199
-
-
Cohen, G.M.1
Park, J.C.2
-
19
-
-
34548253352
-
The role of mitochondrial DNA large deletion for the development of presbycusis in Fischer 344 rats
-
Yin S., Yu Z., Sockalingam R., Bance M., Sun G., Wang J. The role of mitochondrial DNA large deletion for the development of presbycusis in Fischer 344 rats. Neurobiol Dis 2007; 27:370-377.
-
(2007)
Neurobiol Dis
, vol.27
, pp. 370-377
-
-
Yin, S.1
Yu, Z.2
Sockalingam, R.3
Bance, M.4
Sun, G.5
Wang, J.6
-
20
-
-
2642580016
-
Premature ageing in mice expressing defective mitochondrial DNA polymerase
-
Trifunovic A., Wredenberg A., Falkenberg M., et al. Premature ageing in mice expressing defective mitochondrial DNA polymerase. Nature 2004; 429:417-423.
-
(2004)
Nature
, vol.429
, pp. 417-423
-
-
Trifunovic, A.1
Wredenberg, A.2
Falkenberg, M.3
-
21
-
-
22344456832
-
Mitochondria DNA mutations, oxidative stress, and apoptosis in mammalian aging
-
Kujoth GC, Hiona A., Pugh TD, et al. Mitochondria DNA mutations, oxidative stress, and apoptosis in mammalian aging. Science 2005; 309:481-484.
-
(2005)
Science
, vol.309
, pp. 481-484
-
-
Kujoth, G.C.1
Hiona, A.2
Pugh, T.D.3
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