-
1
-
-
84860218310
-
Global estimates of visual impairment: 2010
-
Pascolini D, Mariotti SP, (2012) Global estimates of visual impairment: 2010. Br J Ophthalmol 96: 614-8.
-
(2012)
Br J Ophthalmol
, vol.96
, pp. 614-618
-
-
Pascolini, D.1
Mariotti, S.P.2
-
3
-
-
14444283397
-
Identification of a gene that causes primary open angle glaucoma
-
Stone EM, Fingert JH, Alward WL, Nguyen TD, Polansky JR, et al. (1997) Identification of a gene that causes primary open angle glaucoma. Science 275: 668-70.
-
(1997)
Science
, vol.275
, pp. 668-670
-
-
Stone, E.M.1
Fingert, J.H.2
Alward, W.L.3
Nguyen, T.D.4
Polansky, J.R.5
-
4
-
-
18244385269
-
Adult-onset primary open-angle glaucoma caused by mutations in optineurin
-
Rezaie T, Child A, Hitchings R, Brice G, Miller L, et al. (2002) Adult-onset primary open-angle glaucoma caused by mutations in optineurin. Science 295: 1077-9.
-
(2002)
Science
, vol.295
, pp. 1077-1079
-
-
Rezaie, T.1
Child, A.2
Hitchings, R.3
Brice, G.4
Miller, L.5
-
5
-
-
20144382615
-
Identification of a novel adult-onset primary open-angle glaucoma (POAG) gene on 5q22.1
-
Monemi S, Spaeth G, DaSilva A, Popinchalk S, Ilitchev E, et al. (2005) Identification of a novel adult-onset primary open-angle glaucoma (POAG) gene on 5q22.1. Hum Mol Genet 14: 725-33.
-
(2005)
Hum Mol Genet
, vol.14
, pp. 725-733
-
-
Monemi, S.1
Spaeth, G.2
DaSilva, A.3
Popinchalk, S.4
Ilitchev, E.5
-
6
-
-
70350500461
-
Heterozygous NTF4 mutations impairing neurotrophin-4 signaling in patients with primary open-angle glaucoma
-
Pasutto F, Matsumoto T, Mardin CY, Sticht H, Brandstatter JH, et al. (2009) Heterozygous NTF4 mutations impairing neurotrophin-4 signaling in patients with primary open-angle glaucoma. Am J Hum Genet 85: 447-56.
-
(2009)
Am J Hum Genet
, vol.85
, pp. 447-456
-
-
Pasutto, F.1
Matsumoto, T.2
Mardin, C.Y.3
Sticht, H.4
Brandstatter, J.H.5
-
7
-
-
84863230410
-
Variants in ASB10 are associated with open-angle glaucoma
-
Pasutto F, Keller KE, Weisschuh N, Sticht H, Samples JR, et al. (2012) Variants in ASB10 are associated with open-angle glaucoma. Hum Mol Genet 21: 1336-49.
-
(2012)
Hum Mol Genet
, vol.21
, pp. 1336-1349
-
-
Pasutto, F.1
Keller, K.E.2
Weisschuh, N.3
Sticht, H.4
Samples, J.R.5
-
8
-
-
0035687286
-
Genetic modification of human trabecular meshwork with lentiviral vectors
-
Loewen N, Fautsch MP, Peretz M, Bahler CK, Cameron JD, et al. (2001) Genetic modification of human trabecular meshwork with lentiviral vectors. Hum Gene Ther 12: 2109-19.
-
(2001)
Hum Gene Ther
, vol.12
, pp. 2109-2119
-
-
Loewen, N.1
Fautsch, M.P.2
Peretz, M.3
Bahler, C.K.4
Cameron, J.D.5
-
9
-
-
0021853368
-
The resistance of the trabecular meshwork to aqueous humor outflow
-
Seiler T, Wollensak J, (1985) The resistance of the trabecular meshwork to aqueous humor outflow. Graefes Arch Clin Exp Ophthalmol 223: 88-91.
-
(1985)
Graefes Arch Clin Exp Ophthalmol
, vol.223
, pp. 88-91
-
-
Seiler, T.1
Wollensak, J.2
-
10
-
-
34848910727
-
Open-angle glaucoma - an epidemiologic overview
-
Leske MC, (2007) Open-angle glaucoma - an epidemiologic overview. Ophthalmic Epidemiol 14: 166-72.
-
(2007)
Ophthalmic Epidemiol
, vol.14
, pp. 166-172
-
-
Leske, M.C.1
-
11
-
-
80052788505
-
Mitochondrial dysfunction in glaucoma and emerging bioenergetic therapies
-
Lee S, Van Bergen NJ, Kong GY, Chrysostomou V, Waugh HS, et al. (2011) Mitochondrial dysfunction in glaucoma and emerging bioenergetic therapies. Exp Eye Res 93: 204-12.
-
(2011)
Exp Eye Res
, vol.93
, pp. 204-212
-
-
Lee, S.1
Van Bergen, N.J.2
Kong, G.Y.3
Chrysostomou, V.4
Waugh, H.S.5
-
12
-
-
0035933650
-
A metabotropic glutamate receptor antagonist, alpha-methyl-4-carboxyphenylglycine, attenuates immediate early gene mRNA expression following traumatic injury in cultured rat cortical glial cells
-
Katano H, Fujita K, Kato T, Asai K, Kawamura Y, et al. (2001) A metabotropic glutamate receptor antagonist, alpha-methyl-4-carboxyphenylglycine, attenuates immediate early gene mRNA expression following traumatic injury in cultured rat cortical glial cells. Neurosci Lett 306: 101-5.
-
(2001)
Neurosci Lett
, vol.306
, pp. 101-105
-
-
Katano, H.1
Fujita, K.2
Kato, T.3
Asai, K.4
Kawamura, Y.5
-
13
-
-
0034738347
-
Oxidative stress protection and vulnerability in aging: putative nutritional implications for intervention
-
Joseph JA, Denisova NA, Bielinski D, Fisher DR, Shukitt-Hale B, (2000) Oxidative stress protection and vulnerability in aging: putative nutritional implications for intervention. Mech Ageing Dev 116: 141-53.
-
(2000)
Mech Ageing Dev
, vol.116
, pp. 141-153
-
-
Joseph, J.A.1
Denisova, N.A.2
Bielinski, D.3
Fisher, D.R.4
Shukitt-Hale, B.5
-
14
-
-
0026704066
-
An introduction to the free radical hypothesis in Parkinson's disease
-
Olanow CW, (1992) An introduction to the free radical hypothesis in Parkinson's disease. Ann Neurol 32Suppl: S2-9.
-
(1992)
Ann Neurol
, vol.32
-
-
Olanow, C.W.1
-
15
-
-
84871328016
-
Oxidative stress and mitochondrial dysfunction in glaucoma
-
Chrysostomou V, Rezania F, Trounce IA, Crowston JG, (2013) Oxidative stress and mitochondrial dysfunction in glaucoma. Curr Opin Pharmacol 13: 12-5.
-
(2013)
Curr Opin Pharmacol
, vol.13
, pp. 12-15
-
-
Chrysostomou, V.1
Rezania, F.2
Trounce, I.A.3
Crowston, J.G.4
-
16
-
-
84858006274
-
Mitochondrial dysfunction in glaucoma: understanding genetic influences
-
Lascaratos G, Garway-Heath DF, Willoughby CE, Chau KY, Schapira AH, (2012) Mitochondrial dysfunction in glaucoma: understanding genetic influences. Mitochondrion 12: 202-12.
-
(2012)
Mitochondrion
, vol.12
, pp. 202-212
-
-
Lascaratos, G.1
Garway-Heath, D.F.2
Willoughby, C.E.3
Chau, K.Y.4
Schapira, A.H.5
-
17
-
-
33846810059
-
Glaucomatous outflow pathway and oxidative stress
-
Sacca SC, Izzotti A, Rossi P, Traverso C, (2007) Glaucomatous outflow pathway and oxidative stress. Exp Eye Res 84: 389-99.
-
(2007)
Exp Eye Res
, vol.84
, pp. 389-399
-
-
Sacca, S.C.1
Izzotti, A.2
Rossi, P.3
Traverso, C.4
-
18
-
-
0026469073
-
Analyses of mitochondrial respiratory chain function and mitochondrial DNA deletion in human skeletal muscle: effect of ageing
-
Cooper JM, Mann VM, Schapira AH, (1992) Analyses of mitochondrial respiratory chain function and mitochondrial DNA deletion in human skeletal muscle: effect of ageing. J Neurol Sci 113: 91-8.
-
(1992)
J Neurol Sci
, vol.113
, pp. 91-98
-
-
Cooper, J.M.1
Mann, V.M.2
Schapira, A.H.3
-
19
-
-
0032845895
-
Mitochondrial respiratory chain activity in the human brain as a function of age
-
Ojaimi J, Masters CL, Opeskin K, McKelvie P, Byrne E, (1999) Mitochondrial respiratory chain activity in the human brain as a function of age. Mech Ageing Dev 111: 39-47.
-
(1999)
Mech Ageing Dev
, vol.111
, pp. 39-47
-
-
Ojaimi, J.1
Masters, C.L.2
Opeskin, K.3
McKelvie, P.4
Byrne, E.5
-
20
-
-
46349093995
-
Brain mitochondrial dysfunction in aging
-
Boveris A, Navarro A, (2008) Brain mitochondrial dysfunction in aging. IUBMB Life 60: 308-14.
-
(2008)
IUBMB Life
, vol.60
, pp. 308-314
-
-
Boveris, A.1
Navarro, A.2
-
21
-
-
33847059997
-
The mitochondrial energy transduction system and the aging process
-
Navarro A, Boveris A, (2007) The mitochondrial energy transduction system and the aging process. Am J Physiol Cell Physiol 292: C670-86.
-
(2007)
Am J Physiol Cell Physiol
, vol.292
-
-
Navarro, A.1
Boveris, A.2
-
22
-
-
84859421209
-
A mitochondrial etiology of Alzheimer and Parkinson disease
-
Coskun P, Wyrembak J, Schriner SE, Chen HW, Marciniack C, et al. (2012) A mitochondrial etiology of Alzheimer and Parkinson disease. Biochim Biophys Acta 1820: 553-64.
-
(2012)
Biochim Biophys Acta
, vol.1820
, pp. 553-564
-
-
Coskun, P.1
Wyrembak, J.2
Schriner, S.E.3
Chen, H.W.4
Marciniack, C.5
-
23
-
-
79959344446
-
Mitochondria as a therapeutic target for aging and neurodegenerative diseases
-
Reddy PH, Reddy TP, (2011) Mitochondria as a therapeutic target for aging and neurodegenerative diseases. Curr Alzheimer Res 8: 393-409.
-
(2011)
Curr Alzheimer Res
, vol.8
, pp. 393-409
-
-
Reddy, P.H.1
Reddy, T.P.2
-
24
-
-
84863245760
-
Defects in mitochondrial dynamics and metabolomic signatures of evolving energetic stress in mouse models of familial Alzheimer's disease
-
Trushina E, Nemutlu E, Zhang S, Christensen T, Camp J, et al. (2012) Defects in mitochondrial dynamics and metabolomic signatures of evolving energetic stress in mouse models of familial Alzheimer's disease. PLoS One 7: e32737.
-
(2012)
PLoS One
, vol.7
-
-
Trushina, E.1
Nemutlu, E.2
Zhang, S.3
Christensen, T.4
Camp, J.5
-
25
-
-
84864150600
-
Mitochondrial dysfunction in Parkinson's disease: molecular mechanisms and pathophysiological consequences
-
Exner N, Lutz AK, Haass C, Winklhofer KF, (2012) Mitochondrial dysfunction in Parkinson's disease: molecular mechanisms and pathophysiological consequences. EMBO J 31: 3038-62.
-
(2012)
EMBO J
, vol.31
, pp. 3038-3062
-
-
Exner, N.1
Lutz, A.K.2
Haass, C.3
Winklhofer, K.F.4
-
26
-
-
0344413426
-
Mitochondrial fission in apoptosis, neurodegeneration and aging
-
Bossy-Wetzel E, Barsoum MJ, Godzik A, Schwarzenbacher R, Lipton SA, (2003) Mitochondrial fission in apoptosis, neurodegeneration and aging. Curr Opin Cell Biol 15: 706-16.
-
(2003)
Curr Opin Cell Biol
, vol.15
, pp. 706-716
-
-
Bossy-Wetzel, E.1
Barsoum, M.J.2
Godzik, A.3
Schwarzenbacher, R.4
Lipton, S.A.5
-
27
-
-
45749117188
-
Mitochondrial fragmentation in neurodegeneration
-
Knott AB, Perkins G, Schwarzenbacher R, Bossy-Wetzel E, (2008) Mitochondrial fragmentation in neurodegeneration. Nat Rev Neurosci 9: 505-18.
-
(2008)
Nat Rev Neurosci
, vol.9
, pp. 505-518
-
-
Knott, A.B.1
Perkins, G.2
Schwarzenbacher, R.3
Bossy-Wetzel, E.4
-
28
-
-
34250202543
-
Degenerative and apoptotic events at retinal and optic nerve level after experimental induction of ocular hypertension
-
Calandrella N, Scarsella G, Pescosolido N, Risuleo G, (2007) Degenerative and apoptotic events at retinal and optic nerve level after experimental induction of ocular hypertension. Mol Cell Biochem 301: 155-63.
-
(2007)
Mol Cell Biochem
, vol.301
, pp. 155-163
-
-
Calandrella, N.1
Scarsella, G.2
Pescosolido, N.3
Risuleo, G.4
-
29
-
-
78649997080
-
Modulation of mitochondria in the axon and soma of retinal ganglion cells in a rat glaucoma model
-
Munemasa Y, Kitaoka Y, Kuribayashi J, Ueno S, (2010) Modulation of mitochondria in the axon and soma of retinal ganglion cells in a rat glaucoma model. J Neurochem 115: 1508-19.
-
(2010)
J Neurochem
, vol.115
, pp. 1508-1519
-
-
Munemasa, Y.1
Kitaoka, Y.2
Kuribayashi, J.3
Ueno, S.4
-
30
-
-
34250164631
-
Elevated hydrostatic pressure triggers mitochondrial fission and decreases cellular ATP in differentiated RGC-5 cells
-
Ju WK, Liu Q, Kim KY, Crowston JG, Lindsey JD, et al. (2007) Elevated hydrostatic pressure triggers mitochondrial fission and decreases cellular ATP in differentiated RGC-5 cells. Invest Ophthalmol Vis Sci 48: 2145-51.
-
(2007)
Invest Ophthalmol Vis Sci
, vol.48
, pp. 2145-2151
-
-
Ju, W.K.1
Liu, Q.2
Kim, K.Y.3
Crowston, J.G.4
Lindsey, J.D.5
-
31
-
-
58149338891
-
Elevated hydrostatic pressure triggers release of OPA1 and cytochrome C, and induces apoptotic cell death in differentiated RGC-5 cells
-
Ju WK, Kim KY, Lindsey JD, Angert M, Patel A, et al. (2009) Elevated hydrostatic pressure triggers release of OPA1 and cytochrome C, and induces apoptotic cell death in differentiated RGC-5 cells. Mol Vis 15: 120-34.
-
(2009)
Mol Vis
, vol.15
, pp. 120-134
-
-
Ju, W.K.1
Kim, K.Y.2
Lindsey, J.D.3
Angert, M.4
Patel, A.5
-
32
-
-
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: 2533-41.
-
(2006)
Invest Ophthalmol Vis Sci
, vol.47
, pp. 2533-2541
-
-
Abu-Amero, K.K.1
Morales, J.2
Bosley, T.M.3
-
33
-
-
45549087104
-
Mitochondrial complex I defect induces ROS release and degeneration in trabecular meshwork cells of POAG patients: protection by antioxidants
-
He Y, Leung KW, Zhang YH, Duan S, Zhong XF, et al. (2008) Mitochondrial complex I defect induces ROS release and degeneration in trabecular meshwork cells of POAG patients: protection by antioxidants. Invest Ophthalmol Vis Sci 49: 1447-58.
-
(2008)
Invest Ophthalmol Vis Sci
, vol.49
, pp. 1447-1458
-
-
He, Y.1
Leung, K.W.2
Zhang, Y.H.3
Duan, S.4
Zhong, X.F.5
-
34
-
-
77953645397
-
Mitochondrial damage in the trabecular meshwork of patients with glaucoma
-
Izzotti A, Sacca SC, Longobardi M, Cartiglia C, (2010) Mitochondrial damage in the trabecular meshwork of patients with glaucoma. Arch Ophthalmol 128: 724-30.
-
(2010)
Arch Ophthalmol
, vol.128
, pp. 724-730
-
-
Izzotti, A.1
Sacca, S.C.2
Longobardi, M.3
Cartiglia, C.4
-
35
-
-
33845496314
-
The OPA1 gene polymorphism is associated with normal tension and high tension glaucoma
-
Mabuchi F, Tang S, Kashiwagi K, Yamagata Z, Iijima H, et al. (2007) The OPA1 gene polymorphism is associated with normal tension and high tension glaucoma. Am J Ophthalmol 143: 125-130.
-
(2007)
Am J Ophthalmol
, vol.143
, pp. 125-130
-
-
Mabuchi, F.1
Tang, S.2
Kashiwagi, K.3
Yamagata, Z.4
Iijima, H.5
-
36
-
-
70349328234
-
Evaluation of nine candidate genes in patients with normal tension glaucoma: a case control study
-
Wolf C, Gramer E, Muller-Myhsok B, Pasutto F, Reinthal E, et al. (2009) Evaluation of nine candidate genes in patients with normal tension glaucoma: a case control study. BMC Med Genet 10: 91.
-
(2009)
BMC Med Genet
, vol.10
, pp. 91
-
-
Wolf, C.1
Gramer, E.2
Muller-Myhsok, B.3
Pasutto, F.4
Reinthal, E.5
-
37
-
-
84863316262
-
Comprehensive analysis of myocilin variants in east Indian POAG patients
-
Banerjee D, Bhattacharjee A, Ponda A, Sen A, Ray K, (2012) Comprehensive analysis of myocilin variants in east Indian POAG patients. Mol Vis 18: 1548-57.
-
(2012)
Mol Vis
, vol.18
, pp. 1548-1557
-
-
Banerjee, D.1
Bhattacharjee, A.2
Ponda, A.3
Sen, A.4
Ray, K.5
-
38
-
-
26244440242
-
Evaluation of Optineurin as a candidate gene in Indian patients with primary open angle glaucoma
-
Mukhopadhyay A, Komatireddy S, Acharya M, Bhattacharjee A, Mandal AK, et al. (2005) Evaluation of Optineurin as a candidate gene in Indian patients with primary open angle glaucoma. Mol Vis 11: 792-7.
-
(2005)
Mol Vis
, vol.11
, pp. 792-797
-
-
Mukhopadhyay, A.1
Komatireddy, S.2
Acharya, M.3
Bhattacharjee, A.4
Mandal, A.K.5
-
39
-
-
83055178366
-
WDR36 variants in East Indian primary open-angle glaucoma patients
-
Mookherjee S, Chakraborty S, Vishal M, Banerjee D, Sen A, et al. (2011) WDR36 variants in East Indian primary open-angle glaucoma patients. Mol Vis 17: 2618-27.
-
(2011)
Mol Vis
, vol.17
, pp. 2618-2627
-
-
Mookherjee, S.1
Chakraborty, S.2
Vishal, M.3
Banerjee, D.4
Sen, A.5
-
40
-
-
33645860816
-
Primary role of CYP1B1 in Indian juvenile-onset POAG patients
-
Acharya M, Mookherjee S, Bhattacharjee A, Bandyopadhyay AK, Daulat Thakur SK, et al. (2006) Primary role of CYP1B1 in Indian juvenile-onset POAG patients. Mol Vis 12: 399-404.
-
(2006)
Mol Vis
, vol.12
, pp. 399-404
-
-
Acharya, M.1
Mookherjee, S.2
Bhattacharjee, A.3
Bandyopadhyay, A.K.4
Daulat Thakur, S.K.5
-
41
-
-
34248139646
-
Evaluation of the OPTC gene in primary open angle glaucoma: functional significance of a silent change
-
Acharya M, Mookherjee S, Bhattacharjee A, Thakur SK, Bandyopadhyay AK, et al. (2007) Evaluation of the OPTC gene in primary open angle glaucoma: functional significance of a silent change. BMC Mol Biol 8: 21.
-
(2007)
BMC Mol Biol
, vol.8
, pp. 21
-
-
Acharya, M.1
Mookherjee, S.2
Bhattacharjee, A.3
Thakur, S.K.4
Bandyopadhyay, A.K.5
-
42
-
-
44149120064
-
Leu432Val polymorphism in CYP1B1 as a susceptible factor towards predisposition to primary open-angle glaucoma
-
Bhattacharjee A, Banerjee D, Mookherjee S, Acharya M, Banerjee A, et al. (2008) Leu432Val polymorphism in CYP1B1 as a susceptible factor towards predisposition to primary open-angle glaucoma. Mol Vis 14: 841-50.
-
(2008)
Mol Vis
, vol.14
, pp. 841-850
-
-
Bhattacharjee, A.1
Banerjee, D.2
Mookherjee, S.3
Acharya, M.4
Banerjee, A.5
-
43
-
-
44149107150
-
Genetic landscape of the people of India: a canvas for disease gene exploration
-
Indian Genome Variation Consortium
-
Indian Genome Variation Consortium, (2008) Genetic landscape of the people of India: a canvas for disease gene exploration. J Genet 87: 3-20.
-
(2008)
J Genet
, vol.87
, pp. 3-20
-
-
-
45
-
-
33846094306
-
An enhanced MITOMAP with a global mtDNA mutational phylogeny
-
Ruiz-Pesini E, Lott MT, Procaccio V, Poole JC, Brandon MC, et al. (2007) An enhanced MITOMAP with a global mtDNA mutational phylogeny. Nucleic Acids Res 35: D823-8.
-
(2007)
Nucleic Acids Res
, vol.35
-
-
Ruiz-Pesini, E.1
Lott, M.T.2
Procaccio, V.3
Poole, J.C.4
Brandon, M.C.5
-
46
-
-
0016491430
-
On the number of segregating sites in genetical models without recombination
-
Watterson G, (1975) On the number of segregating sites in genetical models without recombination. Theor Popul Biol. Apr 7: 256-76.
-
(1975)
Theor Popul Biol Apr
, vol.7
, pp. 256-276
-
-
Watterson, G.1
-
47
-
-
84870267223
-
The generalisation of student's problems when several different population variances are involved
-
Welch BL, (1947) The generalisation of student's problems when several different population variances are involved. Biometrika 34: 28-35.
-
(1947)
Biometrika
, vol.34
, pp. 28-35
-
-
Welch, B.L.1
-
48
-
-
0001595204
-
Tables for estimating the goodness of fit of empirical distributions
-
Smirnov N, (1948) Tables for estimating the goodness of fit of empirical distributions. Annals of Mathematical Statistics 19: 279.
-
(1948)
Annals of Mathematical Statistics
, vol.19
, pp. 279
-
-
Smirnov, N.1
-
49
-
-
0001869771
-
Sulla determinazione empirica di una legge di distribuzione. G
-
Kolmogorov A, (1933) Sulla determinazione empirica di una legge di distribuzione. G. Inst. Ital. Attuari 4: 83.
-
(1933)
Inst. Ital Attuari
, vol.4
, pp. 83
-
-
Kolmogorov, A.1
-
50
-
-
65149104318
-
The diversity present in 5140 human mitochondrial genomes
-
Pereira L, Freitas F, Fernandes V, Pereira JB, Costa MD, et al. (2009) The diversity present in 5140 human mitochondrial genomes. Am J Hum Genet 84: 628-40.
-
(2009)
Am J Hum Genet
, vol.84
, pp. 628-640
-
-
Pereira, L.1
Freitas, F.2
Fernandes, V.3
Pereira, J.B.4
Costa, M.D.5
-
51
-
-
0034619822
-
Mitochondrial genome variation and the origin of modern humans
-
Ingman M, Kaessmann H, Paabo S, Gyllensten U, (2000) Mitochondrial genome variation and the origin of modern humans. Nature 408: 708-13.
-
(2000)
Nature
, vol.408
, pp. 708-713
-
-
Ingman, M.1
Kaessmann, H.2
Paabo, S.3
Gyllensten, U.4
-
52
-
-
77951890443
-
Molecular complexity of primary open angle glaucoma: current concepts
-
Ray K, Mookherjee S, (2009) Molecular complexity of primary open angle glaucoma: current concepts. J Genet 88: 451-67.
-
(2009)
J Genet
, vol.88
, pp. 451-467
-
-
Ray, K.1
Mookherjee, S.2
-
53
-
-
84881118024
-
Normal Tension Glaucoma - a Sick Eye in a Sick Body
-
Leung D (2009) Normal Tension Glaucoma- a Sick Eye in a Sick Body. The Hong Kong Medical Diary 12.
-
(2009)
The Hong Kong Medical Diary
, vol.12
-
-
Leung, D.1
-
54
-
-
33746329868
-
Energy converting NADH:quinone oxidoreductase (complex I)
-
Brandt U, (2006) Energy converting NADH:quinone oxidoreductase (complex I). Annu Rev Biochem 75: 69-92.
-
(2006)
Annu Rev Biochem
, vol.75
, pp. 69-92
-
-
Brandt, U.1
-
55
-
-
0034456720
-
Mitochondrial production of hydrogen peroxide regulation by nitric oxide and the role of ubisemiquinone
-
Boveris A, Cadenas E, (2000) Mitochondrial production of hydrogen peroxide regulation by nitric oxide and the role of ubisemiquinone. IUBMB Life 50: 245-50.
-
(2000)
IUBMB Life
, vol.50
, pp. 245-250
-
-
Boveris, A.1
Cadenas, E.2
-
56
-
-
0018776894
-
Hydroperoxide metabolism in mammalian organs
-
Chance B, Sies H, Boveris A, (1979) Hydroperoxide metabolism in mammalian organs. Physiol Rev 59: 527-605.
-
(1979)
Physiol Rev
, vol.59
, pp. 527-605
-
-
Chance, B.1
Sies, H.2
Boveris, A.3
-
57
-
-
0142150051
-
Mitochondrial formation of reactive oxygen species
-
Turrens JF, (2003) Mitochondrial formation of reactive oxygen species. J Physiol 552: 335-44.
-
(2003)
J Physiol
, vol.552
, pp. 335-344
-
-
Turrens, J.F.1
-
58
-
-
0015882341
-
The mitochondrial generation of hydrogen peroxide. General properties and effect of hyperbaric oxygen
-
Boveris A, Chance B, (1973) The mitochondrial generation of hydrogen peroxide. General properties and effect of hyperbaric oxygen. Biochem J 134: 707-16.
-
(1973)
Biochem J
, vol.134
, pp. 707-716
-
-
Boveris, A.1
Chance, B.2
-
59
-
-
14644386835
-
Characterization of the membrane domain subunit NuoJ (ND6) of the NADH-quinone oxidoreductase from Escherichia coli by chromosomal DNA manipulation
-
Kao MC, Di Bernardo S, Nakamaru-Ogiso E, Miyoshi H, Matsuno-Yagi A, et al. (2005) Characterization of the membrane domain subunit NuoJ (ND6) of the NADH-quinone oxidoreductase from Escherichia coli by chromosomal DNA manipulation. Biochemistry 44: 3562-71.
-
(2005)
Biochemistry
, vol.44
, pp. 3562-3571
-
-
Kao, M.C.1
Di Bernardo, S.2
Nakamaru-Ogiso, E.3
Miyoshi, H.4
Matsuno-Yagi, A.5
-
60
-
-
0036304765
-
Impact of mutations affecting ND mitochondria-encoded subunits on the activity and assembly of complex I in Chlamydomonas. Implication for the structural organization of the enzyme
-
Cardol P, Matagne RF, Remacle C, (2002) Impact of mutations affecting ND mitochondria-encoded subunits on the activity and assembly of complex I in Chlamydomonas. Implication for the structural organization of the enzyme. J Mol Biol 319: 1211-21.
-
(2002)
J Mol Biol
, vol.319
, pp. 1211-1221
-
-
Cardol, P.1
Matagne, R.F.2
Remacle, C.3
-
61
-
-
0033028388
-
Biochemical features of mtDNA 14484 (ND6/M64V) point mutation associated with Leber's hereditary optic neuropathy
-
Carelli V, Ghelli A, Bucchi L, Montagna P, De Negri A, et al. (1999) Biochemical features of mtDNA 14484 (ND6/M64V) point mutation associated with Leber's hereditary optic neuropathy. Ann Neurol 45: 320-8.
-
(1999)
Ann Neurol
, vol.45
, pp. 320-328
-
-
Carelli, V.1
Ghelli, A.2
Bucchi, L.3
Montagna, P.4
De Negri, A.5
-
62
-
-
0026531040
-
Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy
-
Brown MD, Voljavec AS, Lott MT, Torroni A, Yang CC, et al. (1992) Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy. Genetics 130: 163-73.
-
(1992)
Genetics
, vol.130
, pp. 163-173
-
-
Brown, M.D.1
Voljavec, A.S.2
Lott, M.T.3
Torroni, A.4
Yang, C.C.5
-
63
-
-
0024242545
-
Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy
-
Wallace DC, Singh G, Lott MT, Hodge JA, Schurr TG, et al. (1988) Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy. Science 242: 1427-30.
-
(1988)
Science
, vol.242
, pp. 1427-1430
-
-
Wallace, D.C.1
Singh, G.2
Lott, M.T.3
Hodge, J.A.4
Schurr, T.G.5
-
64
-
-
14844312924
-
Novel mitochondrial DNA ND5 mutation in a patient with clinical features of MELAS and MERRF
-
Naini AB, Lu J, Kaufmann P, Bernstein RA, Mancuso M, et al. (2005) Novel mitochondrial DNA ND5 mutation in a patient with clinical features of MELAS and MERRF. Arch Neurol 62: 473-6.
-
(2005)
Arch Neurol
, vol.62
, pp. 473-476
-
-
Naini, A.B.1
Lu, J.2
Kaufmann, P.3
Bernstein, R.A.4
Mancuso, M.5
-
65
-
-
67349197091
-
Identification of novel mutations in five patients with mitochondrial encephalomyopathy
-
Valente L, Piga D, Lamantea E, Carrara F, Uziel G, et al. (2009) Identification of novel mutations in five patients with mitochondrial encephalomyopathy. Biochim Biophys Acta 1787: 491-501.
-
(2009)
Biochim Biophys Acta
, vol.1787
, pp. 491-501
-
-
Valente, L.1
Piga, D.2
Lamantea, E.3
Carrara, F.4
Uziel, G.5
-
66
-
-
33745028132
-
The role of mitochondria in inherited neurodegenerative diseases
-
Kwong JQ, Beal MF, Manfredi G, (2006) The role of mitochondria in inherited neurodegenerative diseases. J Neurochem 97: 1659-75.
-
(2006)
J Neurochem
, vol.97
, pp. 1659-1675
-
-
Kwong, J.Q.1
Beal, M.F.2
Manfredi, G.3
-
67
-
-
0036138997
-
Complex I and Parkinson's disease
-
Greenamyre JT, Sherer TB, Betarbet R, Panov AV, (2001) Complex I and Parkinson's disease. IUBMB Life 52: 135-41.
-
(2001)
IUBMB Life
, vol.52
, pp. 135-141
-
-
Greenamyre, J.T.1
Sherer, T.B.2
Betarbet, R.3
Panov, A.V.4
-
68
-
-
33646948530
-
Parkinson's disease brain mitochondrial complex I has oxidatively damaged subunits and is functionally impaired and misassembled
-
Keeney PM, Xie J, Capaldi RA, Bennett JP Jr, (2006) Parkinson's disease brain mitochondrial complex I has oxidatively damaged subunits and is functionally impaired and misassembled. J Neurosci 26: 5256-64.
-
(2006)
J Neurosci
, vol.26
, pp. 5256-5264
-
-
Keeney, P.M.1
Xie, J.2
Capaldi, R.A.3
Bennett Jr., J.P.4
-
69
-
-
0031916812
-
Complex I defect in muscle from patients with Huntington's disease
-
Arenas J, Campos Y, Ribacoba R, Martin MA, Rubio JC, et al. (1998) Complex I defect in muscle from patients with Huntington's disease. Ann Neurol 43: 397-400.
-
(1998)
Ann Neurol
, vol.43
, pp. 397-400
-
-
Arenas, J.1
Campos, Y.2
Ribacoba, R.3
Martin, M.A.4
Rubio, J.C.5
-
70
-
-
0035990290
-
Primary and secondary defects of the mitochondrial respiratory chain
-
Schapira AH, (2002) Primary and secondary defects of the mitochondrial respiratory chain. J Inherit Metab Dis 25: 207-14.
-
(2002)
J Inherit Metab Dis
, vol.25
, pp. 207-214
-
-
Schapira, A.H.1
-
71
-
-
79955646829
-
Brain mitochondrial dysfunction in aging, neurodegeneration, and Parkinson's disease
-
Navarro A, Boveris A (2010) Brain mitochondrial dysfunction in aging, neurodegeneration, and Parkinson's disease. Front Aging Neurosci 2.
-
(2010)
Front Aging Neurosci
, vol.2
-
-
Navarro, A.1
Boveris, A.2
-
72
-
-
15944396616
-
Mitochondrial encephalomyopathies: an update
-
DiMauro S, Hirano M, (2005) Mitochondrial encephalomyopathies: an update. Neuromuscul Disord 15: 276-86.
-
(2005)
Neuromuscul Disord
, vol.15
, pp. 276-286
-
-
DiMauro, S.1
Hirano, M.2
-
73
-
-
78649496491
-
The membrane subunit NuoL(ND5) is involved in the indirect proton pumping mechanism of Escherichia coli complex I
-
Nakamaru-Ogiso E, Kao MC, Chen H, Sinha SC, Yagi T, et al. (2010) The membrane subunit NuoL(ND5) is involved in the indirect proton pumping mechanism of Escherichia coli complex I. J Biol Chem. 285: 39070-8.
-
(2010)
J Biol Chem
, vol.285
, pp. 39070-39078
-
-
Nakamaru-Ogiso, E.1
Kao, M.C.2
Chen, H.3
Sinha, S.C.4
Yagi, T.5
-
74
-
-
34248394788
-
Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease
-
Blok MJ, Spruijt L, de Coo IF, Schoonderwoerd K, Hendrickx A, et al. (2007) Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease. J Med Genet 44: e74.
-
(2007)
J Med Genet
, vol.44
-
-
Blok, M.J.1
Spruijt, L.2
de Coo, I.F.3
Schoonderwoerd, K.4
Hendrickx, A.5
-
75
-
-
0033768121
-
A novel mitochondrial 12SrRNA point mutation in parkinsonism, deafness, and neuropathy
-
Thyagarajan D, Bressman S, Bruno C, Przedborski S, Shanske S, et al. (2000) A novel mitochondrial 12SrRNA point mutation in parkinsonism, deafness, and neuropathy. Ann Neurol 48: 730-6.
-
(2000)
Ann Neurol
, vol.48
, pp. 730-736
-
-
Thyagarajan, D.1
Bressman, S.2
Bruno, C.3
Przedborski, S.4
Shanske, S.5
-
76
-
-
11844282722
-
Mutations of mitochondrial 12S rRNA in gastric carcinoma and their significance
-
Han CB, Ma JM, Xin Y, Mao XY, Zhao YJ, et al. (2005) Mutations of mitochondrial 12S rRNA in gastric carcinoma and their significance. World J Gastroenterol 11: 31-5.
-
(2005)
World J Gastroenterol
, vol.11
, pp. 31-35
-
-
Han, C.B.1
Ma, J.M.2
Xin, Y.3
Mao, X.Y.4
Zhao, Y.J.5
-
77
-
-
79251600222
-
Mitochondrial 12S rRNA mutations associated with aminoglycoside ototoxicity
-
Guan MX, (2011) Mitochondrial 12S rRNA mutations associated with aminoglycoside ototoxicity. Mitochondrion 11: 237-45.
-
(2011)
Mitochondrion
, vol.11
, pp. 237-245
-
-
Guan, M.X.1
-
78
-
-
77952821177
-
Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing loss
-
Lu J, Li Z, Zhu Y, Yang A, Li R, et al. (2010) Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing loss. Mitochondrion 10: 380-90.
-
(2010)
Mitochondrion
, vol.10
, pp. 380-390
-
-
Lu, J.1
Li, Z.2
Zhu, Y.3
Yang, A.4
Li, R.5
-
79
-
-
20044362198
-
Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss
-
Zhao H, Young WY, Yan Q, Li R, Cao J, et al. (2005) Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss. Nucleic Acids Res 33: 1132-9.
-
(2005)
Nucleic Acids Res
, vol.33
, pp. 1132-1139
-
-
Zhao, H.1
Young, W.Y.2
Yan, Q.3
Li, R.4
Cao, J.5
-
80
-
-
0014429801
-
Misreading of ribonucleic acid code words induced by aminoglycoside antibiotics. The effect of drug concentration
-
Davies J, Davis BD, (1968) Misreading of ribonucleic acid code words induced by aminoglycoside antibiotics. The effect of drug concentration. J Biol Chem 243: 3312-6.
-
(1968)
J Biol Chem
, vol.243
, pp. 3312-3316
-
-
Davies, J.1
Davis, B.D.2
-
81
-
-
0025733603
-
Ribosomal RNA and translation
-
Noller HF, (1991) Ribosomal RNA and translation. Annu Rev Biochem 60: 191-227.
-
(1991)
Annu Rev Biochem
, vol.60
, pp. 191-227
-
-
Noller, H.F.1
-
82
-
-
20044371983
-
Proteomics reveal Cochlin deposits associated with glaucomatous trabecular meshwork
-
Bhattacharya SK, Rockwood EJ, Smith SD, Bonilha VL, Crabb JS, et al. (2005) Proteomics reveal Cochlin deposits associated with glaucomatous trabecular meshwork. J Biol Chem 280: 6080-4.
-
(2005)
J Biol Chem
, vol.280
, pp. 6080-6084
-
-
Bhattacharya, S.K.1
Rockwood, E.J.2
Smith, S.D.3
Bonilha, V.L.4
Crabb, J.S.5
-
84
-
-
35848929710
-
Import of nuclear DNA-encoded RNAs into mitochondria and mitochondrial translation
-
Tarassov I, Kamenski P, Kolesnikova O, Karicheva O, Martin RP, et al. (2007) Import of nuclear DNA-encoded RNAs into mitochondria and mitochondrial translation. Cell Cycle 6: 2473-7.
-
(2007)
Cell Cycle
, vol.6
, pp. 2473-2477
-
-
Tarassov, I.1
Kamenski, P.2
Kolesnikova, O.3
Karicheva, O.4
Martin, R.P.5
-
85
-
-
7444244924
-
Assigning pathogenicity to mitochondrial tRNA mutations: when "definitely maybe" is not good enough
-
McFarland R, Elson JL, Taylor RW, Howell N, Turnbull DM, (2004) Assigning pathogenicity to mitochondrial tRNA mutations: when "definitely maybe" is not good enough. Trends Genet 20: 591-6.
-
(2004)
Trends Genet
, vol.20
, pp. 591-596
-
-
McFarland, R.1
Elson, J.L.2
Taylor, R.W.3
Howell, N.4
Turnbull, D.M.5
-
86
-
-
70350707763
-
Pathogenic mitochondrial tRNA mutations-which mutations are inherited and why?
-
Elson JL, Swalwell H, Blakely EL, McFarland R, Taylor RW, et al. (2009) Pathogenic mitochondrial tRNA mutations-which mutations are inherited and why? Hum Mutat 30: E984-92.
-
(2009)
Hum Mutat
, vol.30
-
-
Elson, J.L.1
Swalwell, H.2
Blakely, E.L.3
McFarland, R.4
Taylor, R.W.5
-
87
-
-
38949120469
-
Human mitochondrial transfer RNAs: role of pathogenic mutation in disease
-
Scaglia F, Wong LJ, (2008) Human mitochondrial transfer RNAs: role of pathogenic mutation in disease. Muscle Nerve 37: 150-71.
-
(2008)
Muscle Nerve
, vol.37
, pp. 150-171
-
-
Scaglia, F.1
Wong, L.J.2
-
88
-
-
34447530916
-
Mitochondrial tRNA mutations: clinical and functional perturbations
-
Zifa E, Giannouli S, Theotokis P, Stamatis C, Mamuris Z, et al. (2007) Mitochondrial tRNA mutations: clinical and functional perturbations. RNA Biol 4: 38-66.
-
(2007)
RNA Biol
, vol.4
, pp. 38-66
-
-
Zifa, E.1
Giannouli, S.2
Theotokis, P.3
Stamatis, C.4
Mamuris, Z.5
-
89
-
-
0036487274
-
Molecular investigations on tRNAs involved in human mitochondrial disorders
-
Florentz C, (2002) Molecular investigations on tRNAs involved in human mitochondrial disorders. Biosci Rep 22: 81-98.
-
(2002)
Biosci Rep
, vol.22
, pp. 81-98
-
-
Florentz, C.1
-
90
-
-
10644284714
-
An evolutionary perspective on pathogenic mtDNA mutations: haplogroup associations of clinical disorders
-
Herrnstadt C, Howell N, (2004) An evolutionary perspective on pathogenic mtDNA mutations: haplogroup associations of clinical disorders. Mitochondrion 4: 791-8.
-
(2004)
Mitochondrion
, vol.4
, pp. 791-798
-
-
Herrnstadt, C.1
Howell, N.2
-
91
-
-
33645305982
-
The role of mitochondrial haplogroups in primary open angle glaucoma
-
Andrews R, Ressiniotis T, Turnbull DM, Birch M, Keers S, et al. (2006) The role of mitochondrial haplogroups in primary open angle glaucoma. Br J Ophthalmol 90: 488-90.
-
(2006)
Br J Ophthalmol
, vol.90
, pp. 488-490
-
-
Andrews, R.1
Ressiniotis, T.2
Turnbull, D.M.3
Birch, M.4
Keers, S.5
-
92
-
-
41749115741
-
The role of mitochondrial haplogroups in glaucoma: a study in an Arab population
-
Abu-Amero KK, Morales J, Bosley TM, Mohamed GH, Cabrera VM, (2008) The role of mitochondrial haplogroups in glaucoma: a study in an Arab population. Mol Vis 14: 518-22.
-
(2008)
Mol Vis
, vol.14
, pp. 518-522
-
-
Abu-Amero, K.K.1
Morales, J.2
Bosley, T.M.3
Mohamed, G.H.4
Cabrera, V.M.5
-
93
-
-
79959248615
-
Mitochondrial DNA lineages of African origin confer susceptibility to primary open-angle glaucoma in Saudi patients
-
Abu-Amero KK, Gonzalez AM, Osman EA, Larruga JM, Cabrera VM, et al. (2011) Mitochondrial DNA lineages of African origin confer susceptibility to primary open-angle glaucoma in Saudi patients. Mol Vis 17: 1468-72.
-
(2011)
Mol Vis
, vol.17
, pp. 1468-1472
-
-
Abu-Amero, K.K.1
Gonzalez, A.M.2
Osman, E.A.3
Larruga, J.M.4
Cabrera, V.M.5
-
94
-
-
0037547014
-
Primary open-angle glaucoma in blacks: a review
-
Racette L, Wilson MR, Zangwill LM, Weinreb RN, Sample PA, (2003) Primary open-angle glaucoma in blacks: a review. Surv Ophthalmol 48: 295-313.
-
(2003)
Surv Ophthalmol
, vol.48
, pp. 295-313
-
-
Racette, L.1
Wilson, M.R.2
Zangwill, L.M.3
Weinreb, R.N.4
Sample, P.A.5
-
95
-
-
0027496766
-
Immunohistochemical monitoring of the effect of a synthetic fibronectin-like peptide (Arg-Gly-Asp) on the age-related changes in the isolated human corneoscleral tissue of glaucomatous eyes
-
Babizhayev MA, Brodskaya MW, (1993) Immunohistochemical monitoring of the effect of a synthetic fibronectin-like peptide (Arg-Gly-Asp) on the age-related changes in the isolated human corneoscleral tissue of glaucomatous eyes. Mechanisms of Ageing & Development 72: 1-12.
-
(1993)
Mechanisms of Ageing & Development
, vol.72
, pp. 1-12
-
-
Babizhayev, M.A.1
Brodskaya, M.W.2
-
96
-
-
79959467651
-
Dynamics of mitochondrial heteroplasmy in three families investigated via a repeatable re-sequencing study
-
Goto H, Dickins B, Afgan E, Paul IM, Taylor J, et al. (2011) Dynamics of mitochondrial heteroplasmy in three families investigated via a repeatable re-sequencing study. Genome Biol 12: R59.
-
(2011)
Genome Biol
, vol.12
-
-
Goto, H.1
Dickins, B.2
Afgan, E.3
Paul, I.M.4
Taylor, J.5
|