-
1
-
-
33745675536
-
Mitochondrial abnormalities in patients with primary open-angle glaucoma
-
Abu-Amero KK, Morales J, Bosley TM (2006) Mitochondrial abnormalities in patients with primary open-angle glaucoma. Invest. Ophthalmol. Vis. Sci. 47, 2533-2541.
-
(2006)
Invest. Ophthalmol. Vis. Sci.
, vol.47
, pp. 2533-2541
-
-
Abu-Amero, K.K.1
Morales, J.2
Bosley, T.M.3
-
2
-
-
0026782895
-
Deleterious mitochondrial DNA mutations accumulate in aging human tissues
-
Arnheim N, Cortopassi G (1992) Deleterious mitochondrial DNA mutations accumulate in aging human tissues. Mutat. Res. 275, 157-167.
-
(1992)
Mutat. Res.
, vol.275
, pp. 157-167
-
-
Arnheim, N.1
Cortopassi, G.2
-
3
-
-
0030062175
-
Accumulation of mitochondrial DNA deletions in human retina during aging
-
Barreau E, Brossas JY, Courtois Y, Treton JA (1996) Accumulation of mitochondrial DNA deletions in human retina during aging. Invest. Ophthalmol. Vis. Sci. 37, 384.
-
(1996)
Invest. Ophthalmol. Vis. Sci.
, vol.37
, pp. 384
-
-
Barreau, E.1
Brossas, J.Y.2
Courtois, Y.3
Treton, J.A.4
-
4
-
-
25444474703
-
Mitochondria take center stage in aging and neurodegeneration
-
Beal MF (2005) Mitochondria take center stage in aging and neurodegeneration. Ann. Neurol. 58, 495-505.
-
(2005)
Ann. Neurol.
, vol.58
, pp. 495-505
-
-
Beal, M.F.1
-
5
-
-
1542359647
-
Ganglion cell contributions to the rat full-field electroretinogram
-
Bui BV, Fortune B (2004) Ganglion cell contributions to the rat full-field electroretinogram. J. Physiol. 555, 153-173.
-
(2004)
J. Physiol.
, vol.555
, pp. 153-173
-
-
Bui, B.V.1
Fortune, B.2
-
6
-
-
11144305010
-
The gradient of retinal functional changes during acute intraocular pressure elevation
-
Bui BV, Edmunds B, Cioffi GA, Fortune B (2005) The gradient of retinal functional changes during acute intraocular pressure elevation. Invest. Ophthalmol. Vis. Sci. 46, 202-213.
-
(2005)
Invest. Ophthalmol. Vis. Sci.
, vol.46
, pp. 202-213
-
-
Bui, B.V.1
Edmunds, B.2
Cioffi, G.A.3
Fortune, B.4
-
7
-
-
0025442474
-
In situ hybridization histochemistry of Ca2+/calmodulin-dependent protein kinase in developing rat brain
-
Burgin KE, Waxham MN, Rickling S, Westgate SA, Mobley WC, Kelly PT (1990) In situ hybridization histochemistry of Ca2+/calmodulin-dependent protein kinase in developing rat brain. J. Neurosci. 10, 1788-1798.
-
(1990)
J. Neurosci.
, vol.10
, pp. 1788-1798
-
-
Burgin, K.E.1
Waxham, M.N.2
Rickling, S.3
Westgate, S.A.4
Mobley, W.C.5
Kelly, P.T.6
-
8
-
-
25144514232
-
Somatic mitochondrial DNA mutations in single neurons and glia
-
Cantuti-Castelvetri I, Lin MT, Zheng K, Keller-McGandy CE, Betensky RA, Johns DR, Beal MF, Standaert DG, Simon DK (2005) Somatic mitochondrial DNA mutations in single neurons and glia. Neurobiol. Aging 26, 1343-1355.
-
(2005)
Neurobiol. Aging
, vol.26
, pp. 1343-1355
-
-
Cantuti-Castelvetri, I.1
Lin, M.T.2
Zheng, K.3
Keller-McGandy, C.E.4
Betensky, R.A.5
Johns, D.R.6
Beal, M.F.7
Standaert, D.G.8
Simon, D.K.9
-
10
-
-
65549119721
-
Life history of cones in the rhodopsin-mutant P23H-3 rat: evidence of long-term survival
-
Chrysostomou V, Stone J, Valter K (2009) Life history of cones in the rhodopsin-mutant P23H-3 rat: evidence of long-term survival. Invest. Ophthalmol. Vis. Sci. 50, 2407-2416.
-
(2009)
Invest. Ophthalmol. Vis. Sci.
, vol.50
, pp. 2407-2416
-
-
Chrysostomou, V.1
Stone, J.2
Valter, K.3
-
11
-
-
0027017232
-
Mitochondrial DNA deletions in human brain: regional variability and increase with advanced age
-
Corral-Debrinski M, Horton T, Lott MT, Shoffner JM, Beal MF, Wallace DC (1992) Mitochondrial DNA deletions in human brain: regional variability and increase with advanced age. Nat. Genet. 2, 324-329.
-
(1992)
Nat. Genet.
, vol.2
, pp. 324-329
-
-
Corral-Debrinski, M.1
Horton, T.2
Lott, M.T.3
Shoffner, J.M.4
Beal, M.F.5
Wallace, D.C.6
-
12
-
-
0025674177
-
Detection of a specific mitochondrial DNA deletion in tissues of older humans
-
Cortopassi GA, Arnheim N (1990) Detection of a specific mitochondrial DNA deletion in tissues of older humans. Nucleic Acids Res. 18, 6927.
-
(1990)
Nucleic Acids Res.
, vol.18
, pp. 6927
-
-
Cortopassi, G.A.1
Arnheim, N.2
-
13
-
-
0026732706
-
A pattern of accumulation of a somatic deletion of mitochondrial DNA in aging human tissues
-
Cortopassi GA, Shibata D, Soong NW, Arnheim N (1992) A pattern of accumulation of a somatic deletion of mitochondrial DNA in aging human tissues. Proc. Natl. Acad. Sci. U S A 89, 7370-7374.
-
(1992)
Proc. Natl. Acad. Sci. U S A
, vol.89
, pp. 7370-7374
-
-
Cortopassi, G.A.1
Shibata, D.2
Soong, N.W.3
Arnheim, N.4
-
14
-
-
3242668604
-
Alzheimer's brains harbor somatic mtDNA control-region mutations that suppress mitochondrial transcription and replication
-
Coskun PE, Beal MF, Wallace DC (2004) Alzheimer's brains harbor somatic mtDNA control-region mutations that suppress mitochondrial transcription and replication. Proc. Natl. Acad. Sci. U S A 101, 10726-10731.
-
(2004)
Proc. Natl. Acad. Sci. U S A
, vol.101
, pp. 10726-10731
-
-
Coskun, P.E.1
Beal, M.F.2
Wallace, D.C.3
-
15
-
-
78049434938
-
Age-dependent cardiomyopathy in mitochondrial mutator mice is attenuated by overexpression of catalase targeted to mitochondria
-
Dai DF, Chen T, Wanagat J, Laflamme M, Marcinek DJ, Emond MJ, Ngo CP, Prolla TA, Rabinovitch PS (2010) Age-dependent cardiomyopathy in mitochondrial mutator mice is attenuated by overexpression of catalase targeted to mitochondria. Aging Cell 9, 536-544.
-
(2010)
Aging Cell
, vol.9
, pp. 536-544
-
-
Dai, D.F.1
Chen, T.2
Wanagat, J.3
Laflamme, M.4
Marcinek, D.J.5
Emond, M.J.6
Ngo, C.P.7
Prolla, T.A.8
Rabinovitch, P.S.9
-
16
-
-
72649100107
-
Point mutations are causing progeroid phenotypes in the mtDNA mutator mouse
-
Edgar D, Larsson NG, Trifunovic A (2009) Point mutations are causing progeroid phenotypes in the mtDNA mutator mouse. Cell Metab. 11, 1.
-
(2009)
Cell Metab.
, vol.11
, pp. 1
-
-
Edgar, D.1
Larsson, N.G.2
Trifunovic, A.3
-
17
-
-
72649099157
-
Response: point mutations are causing progeroid phenotypes in the mtDNA mutator mouse
-
Edgar D, Larsson NG, Trifunovic A (2010) Response: point mutations are causing progeroid phenotypes in the mtDNA mutator mouse. Cell Metab. 11, 93.
-
(2010)
Cell Metab.
, vol.11
, pp. 93
-
-
Edgar, D.1
Larsson, N.G.2
Trifunovic, A.3
-
18
-
-
34648817006
-
CaMKIIalphaB mediates a survival response in retinal ganglion cells subjected to a glutamate stimulus
-
Fan W, Li X, Cooper NG (2007) CaMKIIalphaB mediates a survival response in retinal ganglion cells subjected to a glutamate stimulus. Invest. Ophthalmol. Vis. Sci. 48, 3854-3863.
-
(2007)
Invest. Ophthalmol. Vis. Sci.
, vol.48
, pp. 3854-3863
-
-
Fan, W.1
Li, X.2
Cooper, N.G.3
-
19
-
-
3042526498
-
Selective ganglion cell functional loss in rats with experimental glaucoma
-
Fortune B, Bui BV, Morrison JC, Johnson EC, Dong J, Cepurna WO, Jia L, Barber S, Cioffi GA (2004) Selective ganglion cell functional loss in rats with experimental glaucoma. Invest. Ophthalmol. Vis. Sci. 45, 1854-1862.
-
(2004)
Invest. Ophthalmol. Vis. Sci.
, vol.45
, pp. 1854-1862
-
-
Fortune, B.1
Bui, B.V.2
Morrison, J.C.3
Johnson, E.C.4
Dong, J.5
Cepurna, W.O.6
Jia, L.7
Barber, S.8
Cioffi, G.A.9
-
20
-
-
33644635644
-
DNA polymerase gamma in mitochondrial DNA replication and repair
-
Graziewicz MA, Longley MJ, Copeland WC (2006) DNA polymerase gamma in mitochondrial DNA replication and repair. Chem. Rev. 106, 383-405.
-
(2006)
Chem. Rev.
, vol.106
, pp. 383-405
-
-
Graziewicz, M.A.1
Longley, M.J.2
Copeland, W.C.3
-
21
-
-
0021891869
-
The mitochondrial electron transport and oxidative phosphorylation system
-
Hatefi Y (1985) The mitochondrial electron transport and oxidative phosphorylation system. Annu. Rev. Biochem. 54, 1015-1069.
-
(1985)
Annu. Rev. Biochem.
, vol.54
, pp. 1015-1069
-
-
Hatefi, Y.1
-
24
-
-
33745713884
-
Phenotypic spectrum associated with mutations of the mitochondrial polymerase gamma gene
-
Horvath R, Hudson G, Ferrari G, Fütterer N, Ahola S, Lamantea E, Prokisch H, Lochmüller H, McFarland R, Ramesh V, Klopstock T, Freisinger P, Salvi F, Mayr JA, Santer R, Tesarova M, Zeman J, Udd B, Taylor RW, Turnbull D, Hanna M, Fialho D, Suomalainen A, Zeviani M, Chinnery PF (2006) Phenotypic spectrum associated with mutations of the mitochondrial polymerase gamma gene. Brain: J Neurol. 129, 1674-1684.
-
(2006)
Brain: J Neurol.
, vol.129
, pp. 1674-1684
-
-
Horvath, R.1
Hudson, G.2
Ferrari, G.3
Fütterer, N.4
Ahola, S.5
Lamantea, E.6
Prokisch, H.7
Lochmüller, H.8
McFarland, R.9
Ramesh, V.10
Klopstock, T.11
Freisinger, P.12
Salvi, F.13
Mayr, J.A.14
Santer, R.15
Tesarova, M.16
Zeman, J.17
Udd, B.18
Taylor, R.W.19
Turnbull, D.20
Hanna, M.21
Fialho, D.22
Suomalainen, A.23
Zeviani, M.24
Chinnery, P.F.25
more..
-
25
-
-
0031968397
-
Essential iris atrophy, pigment dispersion, and glaucoma in DBA/2J mice
-
John SW, Smith RS, Savinova OV, Hawes NL, Chang B, Turnbull D, Davisson M, Roderick TH, Heckenlively JR (1998) Essential iris atrophy, pigment dispersion, and glaucoma in DBA/2J mice. Invest. Ophthalmol. Vis. Sci. 39, 951-962.
-
(1998)
Invest. Ophthalmol. Vis. Sci.
, vol.39
, pp. 951-962
-
-
John, S.W.1
Smith, R.S.2
Savinova, O.V.3
Hawes, N.L.4
Chang, B.5
Turnbull, D.6
Davisson, M.7
Roderick, T.H.8
Heckenlively, J.R.9
-
26
-
-
2342429459
-
DNA polymerase gamma, the mitochondrial replicase
-
Kaguni LS (2004) DNA polymerase gamma, the mitochondrial replicase. Annu. Rev. Biochem. 73, 293-320.
-
(2004)
Annu. Rev. Biochem.
, vol.73
, pp. 293-320
-
-
Kaguni, L.S.1
-
28
-
-
33745712834
-
Mice with neuron-specific accumulation of mitochondrial DNA mutations show mood disorder-like phenotypes
-
Kasahara T, Kubota M, Miyauchi T, Noda Y, Mouri A, Nabeshima T, Kato T (2006) Mice with neuron-specific accumulation of mitochondrial DNA mutations show mood disorder-like phenotypes. Mol. Psychiatry 11, 577-593.
-
(2006)
Mol. Psychiatry
, vol.11
, pp. 577-593
-
-
Kasahara, T.1
Kubota, M.2
Miyauchi, T.3
Noda, Y.4
Mouri, A.5
Nabeshima, T.6
Kato, T.7
-
29
-
-
34047095284
-
Mitochondrial DNA mutations and aging: a case closed?
-
Khrapko K, Vijg J (2007) Mitochondrial DNA mutations and aging: a case closed? Nat. Genet. 39, 445-446.
-
(2007)
Nat. Genet.
, vol.39
, pp. 445-446
-
-
Khrapko, K.1
Vijg, J.2
-
30
-
-
33744458966
-
Does premature aging of the mtDNA mutator mouse prove that mtDNA mutations are involved in natural aging?
-
Khrapko K, Kraytsberg Y, De Grey A, Vijg J, Schon EA (2006) Does premature aging of the mtDNA mutator mouse prove that mtDNA mutations are involved in natural aging? Aging cell 5, 279-282.
-
(2006)
Aging cell
, vol.5
, pp. 279-282
-
-
Khrapko, K.1
Kraytsberg, Y.2
De Grey, A.3
Vijg, J.4
Schon, E.A.5
-
31
-
-
73349130447
-
Functional changes in the retina during and after acute intraocular pressure elevation in mice
-
Kong YX, Crowston JG, Vingrys AJ, Trounce IA, Bui VB (2009) Functional changes in the retina during and after acute intraocular pressure elevation in mice. Invest. Ophthalmol. Vis. Sci. 50, 5732-5740.
-
(2009)
Invest. Ophthalmol. Vis. Sci.
, vol.50
, pp. 5732-5740
-
-
Kong, Y.X.1
Crowston, J.G.2
Vingrys, A.J.3
Trounce, I.A.4
Bui, V.B.5
-
32
-
-
67651177611
-
Do mtDNA deletions drive premature aging in mtDNA mutator mice?
-
Kraytsberg Y, Simon DK, Turnbull DM, Khrapko K (2009) Do mtDNA deletions drive premature aging in mtDNA mutator mice? Aging Cell 8, 502-506.
-
(2009)
Aging Cell
, vol.8
, pp. 502-506
-
-
Kraytsberg, Y.1
Simon, D.K.2
Turnbull, D.M.3
Khrapko, K.4
-
33
-
-
22344456832
-
Mitochondrial DNA mutations, oxidative stress, and apoptosis in mammalian aging
-
Kujoth GC, Hiona A, Pugh TD, Someya S, Panzer K, Wohlgemuth SE, Hofer T, Seo AY, Sullivan R, Jobling WA, Morrow JD, Van Remmen H, Sedivy JM, Yamasoba T, Tanokura M, Weindruch R, Leeuwenburgh C, Prolla TA (2005) Mitochondrial DNA mutations, oxidative stress, and apoptosis in mammalian aging. Science 309, 481-484.
-
(2005)
Science
, vol.309
, pp. 481-484
-
-
Kujoth, G.C.1
Hiona, A.2
Pugh, T.D.3
Someya, S.4
Panzer, K.5
Wohlgemuth, S.E.6
Hofer, T.7
Seo, A.Y.8
Sullivan, R.9
Jobling, W.A.10
Morrow, J.D.11
Van Remmen, H.12
Sedivy, J.M.13
Yamasoba, T.14
Tanokura, M.15
Weindruch, R.16
Leeuwenburgh, C.17
Prolla, T.A.18
-
34
-
-
0033621374
-
The mitochondrial p55 accessory subunit of human DNA polymerase gamma enhances DNA binding, promotes processive DNA synthesis, and confers N-ethylmaleimide resistance
-
Lim SE, Longley MJ, Copeland WC (1999) The mitochondrial p55 accessory subunit of human DNA polymerase gamma enhances DNA binding, promotes processive DNA synthesis, and confers N-ethylmaleimide resistance. J. Biol. Chem. 274, 38197-38203.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 38197-38203
-
-
Lim, S.E.1
Longley, M.J.2
Copeland, W.C.3
-
35
-
-
0034693090
-
Photoreceptor regulated expression of Ca(2+)/calmodulin-dependent protein kinase II in the mouse retina
-
Liu LO, Li G, McCall MA, Cooper NG (2000) Photoreceptor regulated expression of Ca(2+)/calmodulin-dependent protein kinase II in the mouse retina. Brain Res. Mol. Brain Res. 82, 150-166.
-
(2000)
Brain Res. Mol. Brain Res.
, vol.82
, pp. 150-166
-
-
Liu, L.O.1
Li, G.2
McCall, M.A.3
Cooper, N.G.4
-
36
-
-
35748975164
-
Oxidative stress is an early event in hydrostatic pressure induced retinal ganglion cell damage
-
Liu Q, Ju WK, Crowston JG, Xie F, Perry G, Smith MA, Lindsey JD, Weinreb RN (2007) Oxidative stress is an early event in hydrostatic pressure induced retinal ganglion cell damage. Invest. Ophthalmol. Vis. Sci. 48, 4580-4589.
-
(2007)
Invest. Ophthalmol. Vis. Sci.
, vol.48
, pp. 4580-4589
-
-
Liu, Q.1
Ju, W.K.2
Crowston, J.G.3
Xie, F.4
Perry, G.5
Smith, M.A.6
Lindsey, J.D.7
Weinreb, R.N.8
-
37
-
-
0035914329
-
The fidelity of human DNA polymerase gamma with and without exonucleolytic proofreading and the p55 accessory subunit
-
Longley MJ, Nguyen D, Kunkel TA, Copeland WC (2001) The fidelity of human DNA polymerase gamma with and without exonucleolytic proofreading and the p55 accessory subunit. J. Biol. Chem. 276, 38555-38562.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 38555-38562
-
-
Longley, M.J.1
Nguyen, D.2
Kunkel, T.A.3
Copeland, W.C.4
-
38
-
-
71849104860
-
Protein measurement with the Folin phenol reagent
-
Lowry OH, Rosebrough NJ, Farr AL, Randall RJ (1951) Protein measurement with the Folin phenol reagent. J. Biol. Chem. 193, 265-275.
-
(1951)
J. Biol. Chem.
, vol.193
, pp. 265-275
-
-
Lowry, O.H.1
Rosebrough, N.J.2
Farr, A.L.3
Randall, R.J.4
-
39
-
-
41149175383
-
Near complete loss of retinal ganglion cells in the math5/brn3b double knockout elicits severe reductions of other cell types during retinal development
-
Moshiri A, Gonzalez E, Tagawa K, Maeda H, Wang M, Frishman LJ, Wang SW (2008) Near complete loss of retinal ganglion cells in the math5/brn3b double knockout elicits severe reductions of other cell types during retinal development. Dev. Biol. 316, 214-227.
-
(2008)
Dev. Biol.
, vol.316
, pp. 214-227
-
-
Moshiri, A.1
Gonzalez, E.2
Tagawa, K.3
Maeda, H.4
Wang, M.5
Frishman, L.J.6
Wang, S.W.7
-
40
-
-
0035283326
-
Oxidative stress is not an obligate mediator of disease provoked by mitochondrial DNA mutations
-
Mott JL, Zhang D, Stevens M, Chang S, Denniger G, Zassenhaus HP (2001) Oxidative stress is not an obligate mediator of disease provoked by mitochondrial DNA mutations. Mutat. Res. 474, 35-45.
-
(2001)
Mutat. Res.
, vol.474
, pp. 35-45
-
-
Mott, J.L.1
Zhang, D.2
Stevens, M.3
Chang, S.4
Denniger, G.5
Zassenhaus, H.P.6
-
41
-
-
68349101301
-
Brn3a as a marker of retinal ganglion cells: qualitative and quantitative time course studies in naive and optic nerve-injured retinas
-
Nadal-Nicolas FM, Jimenez-Lopez M, Sobrado-Calvo P, Nieto-Lopez L, Canovas-Martinez I, Salinas-Navarro M, Vidal-Sanz M, Agudo M (2009) Brn3a as a marker of retinal ganglion cells: qualitative and quantitative time course studies in naive and optic nerve-injured retinas. Invest. Ophthalmol. Vis. Sci. 50, 3860-3868.
-
(2009)
Invest. Ophthalmol. Vis. Sci.
, vol.50
, pp. 3860-3868
-
-
Nadal-Nicolas, F.M.1
Jimenez-Lopez, M.2
Sobrado-Calvo, P.3
Nieto-Lopez, L.4
Canovas-Martinez, I.5
Salinas-Navarro, M.6
Vidal-Sanz, M.7
Agudo, M.8
-
43
-
-
35248837377
-
Somatic mtDNA mutations cause progressive hearing loss in the mouse
-
Niu X, Trifunovic A, Larsson NG, Canlon B (2007) Somatic mtDNA mutations cause progressive hearing loss in the mouse. Exp. Cell Res. 313, 3924-3934.
-
(2007)
Exp. Cell Res.
, vol.313
, pp. 3924-3934
-
-
Niu, X.1
Trifunovic, A.2
Larsson, N.G.3
Canlon, B.4
-
44
-
-
48249104648
-
Mitochondrial proteomics of the retinal pigment epithelium at progressive stages of age-related macular degeneration
-
Nordgaard CL, Karunadharma PP, Feng X, Olsen TW, Ferrington DA (2008) Mitochondrial proteomics of the retinal pigment epithelium at progressive stages of age-related macular degeneration. Invest. Ophthalmol. Vis. Sci. 49, 2848-2855.
-
(2008)
Invest. Ophthalmol. Vis. Sci.
, vol.49
, pp. 2848-2855
-
-
Nordgaard, C.L.1
Karunadharma, P.P.2
Feng, X.3
Olsen, T.W.4
Ferrington, D.A.5
-
45
-
-
0025159341
-
The effect of photocoagulation on the oxygenation and ultrastructure of avascular retina
-
Novack RL, Stefansson E, Hatchell DL (1990) The effect of photocoagulation on the oxygenation and ultrastructure of avascular retina. Exp. Eye Res. 50, 289-296.
-
(1990)
Exp. Eye Res.
, vol.50
, pp. 289-296
-
-
Novack, R.L.1
Stefansson, E.2
Hatchell, D.L.3
-
46
-
-
0028174349
-
Immunohistochemical localization of Ca2+/calmodulin-dependent protein kinase II in the rat retina
-
Ochiishi T, Terashima T, Sugiura H, Yamauchi T (1994) Immunohistochemical localization of Ca2+/calmodulin-dependent protein kinase II in the rat retina. Brain Res. 634, 257-265.
-
(1994)
Brain Res.
, vol.634
, pp. 257-265
-
-
Ochiishi, T.1
Terashima, T.2
Sugiura, H.3
Yamauchi, T.4
-
47
-
-
0038336001
-
Electrophysiological analysis of visual function in mutant mice
-
Peachey NS, Ball SL (2003) Electrophysiological analysis of visual function in mutant mice. Doc. Ophthalmol. 107, 13-36.
-
(2003)
Doc. Ophthalmol.
, vol.107
, pp. 13-36
-
-
Peachey, N.S.1
Ball, S.L.2
-
48
-
-
0036355070
-
Measuring oxidative mtDNA damage and repair using quantitative PCR
-
(WC Copeland, ed). Totowa: Humana Press Inc.
-
Santos JH, Mandavilli BS, Van Houten B (2002). Measuring oxidative mtDNA damage and repair using quantitative PCR. In Mitochondrial DNA: Methods and Protocols. (WC Copeland, ed). Totowa: Humana Press Inc., pp. 159-176.
-
(2002)
Mitochondrial DNA: Methods and Protocols
, pp. 159-176
-
-
Santos, J.H.1
Mandavilli, B.S.2
Van Houten, B.3
-
49
-
-
0037106295
-
The scotopic threshold response of the dark-adapted electroretinogram of the mouse
-
Saszik SM, Robson JG, Frishman LJ (2002) The scotopic threshold response of the dark-adapted electroretinogram of the mouse. J. Physiol. 543, 899-916.
-
(2002)
J. Physiol.
, vol.543
, pp. 899-916
-
-
Saszik, S.M.1
Robson, J.G.2
Frishman, L.J.3
-
50
-
-
0029840825
-
Regional heterogeneity of mtDNA heteroplasmy in parkinsonian brain
-
Schnopp NM, Kosel S, Egensperger R, Graeber MB (1996) Regional heterogeneity of mtDNA heteroplasmy in parkinsonian brain. Clin. Neuropathol. 15, 348-352.
-
(1996)
Clin. Neuropathol.
, vol.15
, pp. 348-352
-
-
Schnopp, N.M.1
Kosel, S.2
Egensperger, R.3
Graeber, M.B.4
-
51
-
-
10744231633
-
Somatic mitochondrial DNA mutations in cortex and substantia nigra in aging and Parkinson's disease
-
Simon DK, Lin MT (2004) Somatic mitochondrial DNA mutations in cortex and substantia nigra in aging and Parkinson's disease. Neurobiol. Aging 25, 71-81.
-
(2004)
Neurobiol. Aging
, vol.25
, pp. 71-81
-
-
Simon, D.K.1
Lin, M.T.2
-
52
-
-
0026471872
-
Accumulation of deletions in human mitochondrial DNA during normal aging: analysis by quantitative PCR
-
Simonetti S, Chen X, DiMauro S, Schon EA (1992) Accumulation of deletions in human mitochondrial DNA during normal aging: analysis by quantitative PCR. Biochim. Biophys. Acta 1180, 113-122.
-
(1992)
Biochim. Biophys. Acta
, vol.1180
, pp. 113-122
-
-
Simonetti, S.1
Chen, X.2
DiMauro, S.3
Schon, E.A.4
-
53
-
-
29144458899
-
Somatic mtDNA mutations cause aging phenotypes without affecting reactive oxygen species production
-
Trifunovic A, Hansson A, Wredenberg A, Rovio AT, Dufour E, Khvorostov I, Spelbrink JN, Wibom R, Jacobs HT, Larsson NG (2005) Somatic mtDNA mutations cause aging phenotypes without affecting reactive oxygen species production. Proc. Natl. Acad. Sci. U S A 102, 17993-17998.
-
(2005)
Proc. Natl. Acad. Sci. U S A
, vol.102
, pp. 17993-17998
-
-
Trifunovic, A.1
Hansson, A.2
Wredenberg, A.3
Rovio, A.T.4
Dufour, E.5
Khvorostov, I.6
Spelbrink, J.N.7
Wibom, R.8
Jacobs, H.T.9
Larsson, N.G.10
-
54
-
-
0029964226
-
Assessment of mitochondrial oxidative phosphorylation in patient muscle biopsies, lymphoblasts, and transmitochondrial cell lines
-
Trounce IA, Kim YL, Jun AS, Wallace DC (1996) Assessment of mitochondrial oxidative phosphorylation in patient muscle biopsies, lymphoblasts, and transmitochondrial cell lines. Methods Enzymol. 264, 484-509.
-
(1996)
Methods Enzymol.
, vol.264
, pp. 484-509
-
-
Trounce, I.A.1
Kim, Y.L.2
Jun, A.S.3
Wallace, D.C.4
-
55
-
-
34047116291
-
Mitochondrial point mutations do not limit the natural lifespan of mice
-
Vermulst M, Bielas J, Kujoth G, Ladiges W, Rabinovitch P, Prolla T, Loeb L (2007) Mitochondrial point mutations do not limit the natural lifespan of mice. Nat. Genet. 39, 540-543.
-
(2007)
Nat. Genet.
, vol.39
, pp. 540-543
-
-
Vermulst, M.1
Bielas, J.2
Kujoth, G.3
Ladiges, W.4
Rabinovitch, P.5
Prolla, T.6
Loeb, L.7
-
56
-
-
70450121949
-
On mitochondria, mutations, and methodology
-
Vermulst M, Wanagat J, Loeb LA (2009) On mitochondria, mutations, and methodology. Cell Metab. 10, 437.
-
(2009)
Cell Metab.
, vol.10
, pp. 437
-
-
Vermulst, M.1
Wanagat, J.2
Loeb, L.A.3
-
57
-
-
0033525773
-
Mitochondrial diseases in man and mouse
-
Wallace DC (1999) Mitochondrial diseases in man and mouse. Science 283, 1482-1488.
-
(1999)
Science
, vol.283
, pp. 1482-1488
-
-
Wallace, D.C.1
-
58
-
-
77956926306
-
Age-related increase in mitochondrial DNA damage and loss of DNA repair capacity in the neural retina
-
Wang AL, Lukas TJ, Yuan M, Neufeld AH (2010) Age-related increase in mitochondrial DNA damage and loss of DNA repair capacity in the neural retina. Neurobiol. Aging 31, 2002-2010.
-
(2010)
Neurobiol. Aging
, vol.31
, pp. 2002-2010
-
-
Wang, A.L.1
Lukas, T.J.2
Yuan, M.3
Neufeld, A.H.4
-
59
-
-
0032436502
-
Oxidative damage and mutation to mitochondrial DNA and age-dependent decline of mitochondrial respiratory function
-
Wei YH, Lu CY, Lee HC, Pang CY, Ma YS (1998) Oxidative damage and mutation to mitochondrial DNA and age-dependent decline of mitochondrial respiratory function. Ann. N Y Acad. Sci. 854, 155-170.
-
(1998)
Ann. N Y Acad. Sci.
, vol.854
, pp. 155-170
-
-
Wei, Y.H.1
Lu, C.Y.2
Lee, H.C.3
Pang, C.Y.4
Ma, Y.S.5
-
60
-
-
38349156704
-
Rodent electroretinography: methods for extraction and interpretation of rod and cone responses
-
Weymouth AE, Vingrys AJ (2008) Rodent electroretinography: methods for extraction and interpretation of rod and cone responses. Prog. Retin. Eye Res. 27, 1-44.
-
(2008)
Prog. Retin. Eye Res.
, vol.27
, pp. 1-44
-
-
Weymouth, A.E.1
Vingrys, A.J.2
-
61
-
-
0037144234
-
Developmentally regulated expression of CaMKII and iGluRs in the rat retina
-
Xue J, Li G, Bharucha E, Cooper NG (2002) Developmentally regulated expression of CaMKII and iGluRs in the rat retina. Brain Res. Dev. Brain Res. 138, 61-70.
-
(2002)
Brain Res. Dev. Brain Res.
, vol.138
, pp. 61-70
-
-
Xue, J.1
Li, G.2
Bharucha, E.3
Cooper, N.G.4
-
62
-
-
0034667349
-
Construction of transgenic mice with tissue-specific acceleration of mitochondrial DNA mutagenesis
-
Zhang D, Mott JL, Chang SW, Denniger G, Feng Z, Zassenhaus HP (2000) Construction of transgenic mice with tissue-specific acceleration of mitochondrial DNA mutagenesis. Genomics 69, 151-161.
-
(2000)
Genomics
, vol.69
, pp. 151-161
-
-
Zhang, D.1
Mott, J.L.2
Chang, S.W.3
Denniger, G.4
Feng, Z.5
Zassenhaus, H.P.6
-
63
-
-
0037214525
-
Mitochondrial DNA mutations activate the mitochondrial apoptotic pathway and cause dilated cardiomyopathy
-
Zhang D, Mott JL, Farrar P, Ryerse JS, Chang SW, Stevens M, Denniger G, Zassenhaus HP (2003) Mitochondrial DNA mutations activate the mitochondrial apoptotic pathway and cause dilated cardiomyopathy. Cardiovasc. Res. 57, 147-157.
-
(2003)
Cardiovasc. Res.
, vol.57
, pp. 147-157
-
-
Zhang, D.1
Mott, J.L.2
Farrar, P.3
Ryerse, J.S.4
Chang, S.W.5
Stevens, M.6
Denniger, G.7
Zassenhaus, H.P.8
-
64
-
-
15044364839
-
Gene expression profile in dilated cardiomyopathy caused by elevated frequencies of mitochondrial DNA mutations in the mouse heart
-
Zhang D, Ezekiel UR, Chang SW, Zassenhaus HP (2005a) Gene expression profile in dilated cardiomyopathy caused by elevated frequencies of mitochondrial DNA mutations in the mouse heart. Cardiovasc Pathol 14, 61-69.
-
(2005)
Cardiovasc Pathol
, vol.14
, pp. 61-69
-
-
Zhang, D.1
Ezekiel, U.R.2
Chang, S.W.3
Zassenhaus, H.P.4
-
65
-
-
18044379574
-
Mitochondrial DNA mutations activate programmed cell survival in the mouse heart
-
Zhang D, Mott JL, Chang SW, Stevens M, Mikolajczak P, Zassenhaus HP (2005b) Mitochondrial DNA mutations activate programmed cell survival in the mouse heart. Am. J. Physiol. Heart Circ. Physiol. 288, H2476-H2483.
-
(2005)
Am. J. Physiol. Heart Circ. Physiol.
, vol.288
-
-
Zhang, D.1
Mott, J.L.2
Chang, S.W.3
Stevens, M.4
Mikolajczak, P.5
Zassenhaus, H.P.6
|