-
1
-
-
0026624980
-
Diseases of the mitochondrial DNA
-
Wallace DC, (1992) Diseases of the mitochondrial DNA. Annu Rev Biochem 61: 1175-1212.
-
(1992)
Annu Rev Biochem
, vol.61
, pp. 1175-1212
-
-
Wallace, D.C.1
-
2
-
-
0028233947
-
Mitochondrial DNA mutations in diseases of energy metabolism
-
Wallace DC, (1994) Mitochondrial DNA mutations in diseases of energy metabolism. J Bioenerg Biomembr 26: 241-250.
-
(1994)
J Bioenerg Biomembr
, vol.26
, pp. 241-250
-
-
Wallace, D.C.1
-
3
-
-
58149328514
-
Batteries not included: diagnosis and management of mitochondrial disease
-
McFarland R, Turnbull DM, (2009) Batteries not included: diagnosis and management of mitochondrial disease. J Intern Med 265: 210-228.
-
(2009)
J Intern Med
, vol.265
, pp. 210-228
-
-
McFarland, R.1
Turnbull, D.M.2
-
4
-
-
23844558266
-
A mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicine
-
Wallace DC, (2005) A mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicine. Annu Rev Genet 39: 359-407.
-
(2005)
Annu Rev Genet
, vol.39
, pp. 359-407
-
-
Wallace, D.C.1
-
5
-
-
33846064419
-
-
Rimoin DL, Connor J.M., Pyeritz, R.E., Korf, B.R., editor. Philadelphis, PA: Churchill Livingstonr Elsevier, (Chapter 113)
-
Wallace DC, Lott MT, Procaccio V (2007) Mitochondrial genes in degenerative diseases, cancer and aging; Rimoin DL, Connor J.M., Pyeritz, R.E., Korf, B.R., editor. Philadelphis, PA: Churchill Livingstonr Elsevier. 194-298 (Chapter 113) p.
-
(2007)
Mitochondrial genes in degenerative diseases, cancer and aging
, pp. 194-298
-
-
Wallace, D.C.1
Lott, M.T.2
Procaccio, V.3
-
6
-
-
84859723840
-
The role of the mitochondrial genome in ageing and carcinogenesis
-
Czarnecka AM, Bartnik E, (2011) The role of the mitochondrial genome in ageing and carcinogenesis. J Aging Res 2011: 136435.
-
(2011)
J Aging Res
, vol.2011
, pp. 136435
-
-
Czarnecka, A.M.1
Bartnik, E.2
-
7
-
-
47749106479
-
Mitochondrial DNA polymorphism A4917G is independently associated with age-related macular degeneration
-
Canter JA, Olson LM, Spencer K, Schnetz-Boutaud N, Anderson B, et al. (2008) Mitochondrial DNA polymorphism A4917G is independently associated with age-related macular degeneration. PLoS ONE 3: e2091.
-
(2008)
PLoS ONE
, vol.3
-
-
Canter, J.A.1
Olson, L.M.2
Spencer, K.3
Schnetz-Boutaud, N.4
Anderson, B.5
-
8
-
-
34548612004
-
Mitochondrial DNA haplogroups and age-related maculopathy
-
Jones MM, Manwaring N, Wang JJ, Rochtchina E, Mitchell P, et al. (2007) Mitochondrial DNA haplogroups and age-related maculopathy. Arch Ophthalmol 125: 1235-1240.
-
(2007)
Arch Ophthalmol
, vol.125
, pp. 1235-1240
-
-
Jones, M.M.1
Manwaring, N.2
Wang, J.J.3
Rochtchina, E.4
Mitchell, P.5
-
9
-
-
66849130909
-
Mitochondrial DNA haplogroups associated with Age-related macular degeneration
-
Udar N, Atilano SR, Memarzadeh M, Boyer D, Chwa M, et al. (2009) Mitochondrial DNA haplogroups associated with Age-related macular degeneration. Invest Ophthalmol Vis Sci 50: 2966-2974.
-
(2009)
Invest Ophthalmol Vis Sci
, vol.50
, pp. 2966-2974
-
-
Udar, N.1
Atilano, S.R.2
Memarzadeh, M.3
Boyer, D.4
Chwa, M.5
-
10
-
-
65749108269
-
Mitochondrial DNA variants of respiratory complex I that uniquely characterize haplogroup T2 are associated with increased risk of age-related macular degeneration
-
SanGiovanni JP, Arking DE, Iyengar SK, Elashoff M, Clemons TE, et al. (2009) Mitochondrial DNA variants of respiratory complex I that uniquely characterize haplogroup T2 are associated with increased risk of age-related macular degeneration. PLoS One 4: e5508.
-
(2009)
PLoS One
, vol.4
-
-
SanGiovanni, J.P.1
Arking, D.E.2
Iyengar, S.K.3
Elashoff, M.4
Clemons, T.E.5
-
11
-
-
65749119166
-
Mitochondrial DNA haplogroup T is associated with coronary artery disease and diabetic retinopathy: a case control study
-
Kofler B, Mueller EE, Eder W, Stanger O, Maier R, et al. (2009) Mitochondrial DNA haplogroup T is associated with coronary artery disease and diabetic retinopathy: a case control study. BMC Med Genet 10: 35.
-
(2009)
BMC Med Genet
, vol.10
, pp. 35
-
-
Kofler, B.1
Mueller, E.E.2
Eder, W.3
Stanger, O.4
Maier, R.5
-
12
-
-
77649312366
-
Mitochondrial haplogroup U is associated with a reduced risk to develop exfoliation glaucoma in the German population
-
Wolf C, Gramer E, Muller-Myhsok B, Pasutto F, Wissinger B, et al. (2010) Mitochondrial haplogroup U is associated with a reduced risk to develop exfoliation glaucoma in the German population. BMC Genet 11: 8.
-
(2010)
BMC Genet
, vol.11
, pp. 8
-
-
Wolf, C.1
Gramer, E.2
Muller-Myhsok, B.3
Pasutto, F.4
Wissinger, B.5
-
13
-
-
79952127786
-
Eurasian and Sub-Saharan African mitochondrial DNA haplogroup influences pseudoexfoliation glaucoma development in Saudi patients
-
Abu-Amero KK, Cabrera VM, Larruga JM, Osman EA, Gonzalez AM, et al. (2011) Eurasian and Sub-Saharan African mitochondrial DNA haplogroup influences pseudoexfoliation glaucoma development in Saudi patients. Mol Vis 17: 543-547.
-
(2011)
Mol Vis
, vol.17
, pp. 543-547
-
-
Abu-Amero, K.K.1
Cabrera, V.M.2
Larruga, J.M.3
Osman, E.A.4
Gonzalez, A.M.5
-
14
-
-
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: 1468-1472.
-
(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
-
15
-
-
79958814885
-
Mitochondrial complex 1 gene analysis in keratoconus
-
Pathak D, Nayak B, Singh M, Sharma N, Tandon R, et al. (2011) Mitochondrial complex 1 gene analysis in keratoconus. Mol Vis 17: 1514-1525.
-
(2011)
Mol Vis
, vol.17
, pp. 1514-1525
-
-
Pathak, D.1
Nayak, B.2
Singh, M.3
Sharma, N.4
Tandon, R.5
-
16
-
-
0032904495
-
mtDNA haplogroup J: a contributing factor of optic neuritis
-
Reynier P, Penisson-Besnier I, Moreau C, Savagner F, Vielle B, et al. (1999) mtDNA haplogroup J: a contributing factor of optic neuritis. Eur J Hum Genet 7: 404-406.
-
(1999)
Eur J Hum Genet
, vol.7
, pp. 404-406
-
-
Reynier, P.1
Penisson-Besnier, I.2
Moreau, C.3
Savagner, F.4
Vielle, B.5
-
17
-
-
17644435064
-
[Multiple sclerosis and Leber's hereditary optic neuropathy mitochondrial DNA mutations]
-
Penisson-Besnier I, Moreau C, Jacques C, Roger JC, Dubas F, et al. (2001) [Multiple sclerosis and Leber's hereditary optic neuropathy mitochondrial DNA mutations]. Rev Neurol (Paris) 157: 537-541.
-
(2001)
Rev Neurol (Paris)
, vol.157
, pp. 537-541
-
-
Penisson-Besnier, I.1
Moreau, C.2
Jacques, C.3
Roger, J.C.4
Dubas, F.5
-
18
-
-
0026753354
-
A mitochondrial DNA variant, identified in Leber hereditary optic neuropathy patients, which extends the amino acid sequence of cytochrome c oxidase subunit I
-
Brown MD, Yang CC, Trounce I, Torroni A, Lott MT, et al. (1992) A mitochondrial DNA variant, identified in Leber hereditary optic neuropathy patients, which extends the amino acid sequence of cytochrome c oxidase subunit I. Am J Hum Genet 51: 378-385.
-
(1992)
Am J Hum Genet
, vol.51
, pp. 378-385
-
-
Brown, M.D.1
Yang, C.C.2
Trounce, I.3
Torroni, A.4
Lott, M.T.5
-
19
-
-
84856899157
-
Mitochondrial haplogroups and control region polymorphisms in age-related macular degeneration: a case-control study
-
Mueller EE, Schaier E, Brunner SM, Eder W, Mayr JA, et al. (2012) Mitochondrial haplogroups and control region polymorphisms in age-related macular degeneration: a case-control study. PLoS ONE 7: e30874.
-
(2012)
PLoS ONE
, vol.7
-
-
Mueller, E.E.1
Schaier, E.2
Brunner, S.M.3
Eder, W.4
Mayr, J.A.5
-
20
-
-
27744468403
-
Proteomics of organelles and large cellular structures
-
Yates JR 3rd, Gilchrist A, Howell KE, Bergeron JJ, (2005) Proteomics of organelles and large cellular structures. Nat Rev Mol Cell Biol 6: 702-714.
-
(2005)
Nat Rev Mol Cell Biol
, vol.6
, pp. 702-714
-
-
Yates 3rd, J.R.1
Gilchrist, A.2
Howell, K.E.3
Bergeron, J.J.4
-
21
-
-
20444483650
-
Nuclear gene expression changes due to mitochondrial dysfunction in ARPE-19 cells: implications for age-related macular degeneration
-
Miceli MV, Jazwinski SM, (2005) Nuclear gene expression changes due to mitochondrial dysfunction in ARPE-19 cells: implications for age-related macular degeneration. Invest Ophthalmol Vis Sci 46: 1765-1773.
-
(2005)
Invest Ophthalmol Vis Sci
, vol.46
, pp. 1765-1773
-
-
Miceli, M.V.1
Jazwinski, S.M.2
-
23
-
-
77951256226
-
Mitochondrial haplogroup H correlates with ATP levels and age at onset in Huntington disease
-
Arning L, Haghikia A, Taherzadeh-Fard E, Saft C, Andrich J, et al. (2010) Mitochondrial haplogroup H correlates with ATP levels and age at onset in Huntington disease. J Mol Med (Berl) 88: 431-436.
-
(2010)
J Mol Med (Berl)
, vol.88
, pp. 431-436
-
-
Arning, L.1
Haghikia, A.2
Taherzadeh-Fard, E.3
Saft, C.4
Andrich, J.5
-
24
-
-
0347356538
-
Effects of purifying and adaptive selection on regional variation in human mtDNA
-
Ruiz-Pesini E, Mishmar D, Brandon M, Procaccio V, Wallace DC, (2004) Effects of purifying and adaptive selection on regional variation in human mtDNA. Science 303: 223-226.
-
(2004)
Science
, vol.303
, pp. 223-226
-
-
Ruiz-Pesini, E.1
Mishmar, D.2
Brandon, M.3
Procaccio, V.4
Wallace, D.C.5
-
25
-
-
84857353838
-
Global DNA methylation levels are modulated by mitochondrial DNA variants
-
Bellizzi D, D'Aquila P, Giordano M, Montesanto A, Passarino G, (2012) Global DNA methylation levels are modulated by mitochondrial DNA variants. Epigenomics 4: 17-27.
-
(2012)
Epigenomics
, vol.4
, pp. 17-27
-
-
Bellizzi, D.1
D'Aquila, P.2
Giordano, M.3
Montesanto, A.4
Passarino, G.5
-
26
-
-
60249093506
-
Human mitochondrial variants influence on oxygen consumption
-
Marcuello A, Martinez-Redondo D, Dahmani Y, Casajus JA, Ruiz-Pesini E, et al. (2009) Human mitochondrial variants influence on oxygen consumption. Mitochondrion 9: 27-30.
-
(2009)
Mitochondrion
, vol.9
, pp. 27-30
-
-
Marcuello, A.1
Martinez-Redondo, D.2
Dahmani, Y.3
Casajus, J.A.4
Ruiz-Pesini, E.5
-
27
-
-
70249132505
-
Steady exercise removes VO(2max) difference between mitochondrial genomic variants
-
Marcuello A, Martinez-Redondo D, Dahmani Y, Terreros JL, Aragones T, et al. (2009) Steady exercise removes VO(2max) difference between mitochondrial genomic variants. Mitochondrion 9: 326-330.
-
(2009)
Mitochondrion
, vol.9
, pp. 326-330
-
-
Marcuello, A.1
Martinez-Redondo, D.2
Dahmani, Y.3
Terreros, J.L.4
Aragones, T.5
-
28
-
-
76049103005
-
Human mitochondrial haplogroup H: the highest VO2max consumer-is it a paradox?
-
Martinez-Redondo D, Marcuello A, Casajus JA, Ara I, Dahmani Y, et al. (2010) Human mitochondrial haplogroup H: the highest VO2max consumer-is it a paradox? Mitochondrion 10: 102-107.
-
(2010)
Mitochondrion
, vol.10
, pp. 102-107
-
-
Martinez-Redondo, D.1
Marcuello, A.2
Casajus, J.A.3
Ara, I.4
Dahmani, Y.5
-
29
-
-
0032851615
-
Mitochondrial DNA inherited variants are associated with successful aging and longevity in humans
-
De Benedictis G, Rose G, Carrieri G, De Luca M, Falcone E, et al. (1999) Mitochondrial DNA inherited variants are associated with successful aging and longevity in humans. Faseb J 13: 1532-1536.
-
(1999)
Faseb J
, vol.13
, pp. 1532-1536
-
-
De Benedictis, G.1
Rose, G.2
Carrieri, G.3
De Luca, M.4
Falcone, E.5
-
30
-
-
0037209210
-
Mitochondrial DNA polymorphisms associated with longevity in a Finnish population
-
Niemi AK, Hervonen A, Hurme M, Karhunen PJ, Jylha M, et al. (2003) Mitochondrial DNA polymorphisms associated with longevity in a Finnish population. Hum Genet 112: 29-33.
-
(2003)
Hum Genet
, vol.112
, pp. 29-33
-
-
Niemi, A.K.1
Hervonen, A.2
Hurme, M.3
Karhunen, P.J.4
Jylha, M.5
-
31
-
-
0034973482
-
Mitochondrial DNA polymorphism: its role in longevity of the Irish population
-
Ross OA, McCormack R, Curran MD, Duguid RA, Barnett YA, et al. (2001) Mitochondrial DNA polymorphism: its role in longevity of the Irish population. Exp Gerontol 36: 1161-1178.
-
(2001)
Exp Gerontol
, vol.36
, pp. 1161-1178
-
-
Ross, O.A.1
McCormack, R.2
Curran, M.D.3
Duguid, R.A.4
Barnett, Y.A.5
-
32
-
-
77955364142
-
Unmasking the causes of multifactorial disorders: OXPHOS differences between mitochondrial haplogroups
-
Gomez-Duran A, Pacheu-Grau D, Lopez-Gallardo E, Diez-Sanchez C, Montoya J, et al. (2010) Unmasking the causes of multifactorial disorders: OXPHOS differences between mitochondrial haplogroups. Hum Mol Genet 19: 3343-3353.
-
(2010)
Hum Mol Genet
, vol.19
, pp. 3343-3353
-
-
Gomez-Duran, A.1
Pacheu-Grau, D.2
Lopez-Gallardo, E.3
Diez-Sanchez, C.4
Montoya, J.5
-
33
-
-
67149136517
-
Ancient mtDNA genetic variants modulate mtDNA transcription and replication
-
Suissa S, Wang Z, Poole J, Wittkopp S, Feder J, et al. (2009) Ancient mtDNA genetic variants modulate mtDNA transcription and replication. PLoS Genet 5: e1000474.
-
(2009)
PLoS Genet
, vol.5
-
-
Suissa, S.1
Wang, Z.2
Poole, J.3
Wittkopp, S.4
Feder, J.5
-
34
-
-
44949185645
-
Resistance of mtDNA-depleted cells to apoptosis
-
Ferraresi R, Troiano L, Pinti M, Roat E, Lugli E, et al. (2008) Resistance of mtDNA-depleted cells to apoptosis. Cytometry A 73: 528-537.
-
(2008)
Cytometry A
, vol.73
, pp. 528-537
-
-
Ferraresi, R.1
Troiano, L.2
Pinti, M.3
Roat, E.4
Lugli, E.5
-
35
-
-
9244238708
-
Common and cell type-specific responses of human cells to mitochondrial dysfunction
-
Miceli MV, Jazwinski SM, (2005) Common and cell type-specific responses of human cells to mitochondrial dysfunction. Exp Cell Res 302: 270-280.
-
(2005)
Exp Cell Res
, vol.302
, pp. 270-280
-
-
Miceli, M.V.1
Jazwinski, S.M.2
-
36
-
-
84866422138
-
The retrograde response: When mitochondrial quality control is not enough
-
Jazwinski SM, (2012) The retrograde response: When mitochondrial quality control is not enough. Biochim Biophys Acta.
-
(2012)
Biochim Biophys Acta
-
-
Jazwinski, S.M.1
-
37
-
-
84866409979
-
The yeast retrograde response as a model of intracellular signaling of mitochondrial dysfunction
-
Jazwinski SM, Kriete A, (2012) The yeast retrograde response as a model of intracellular signaling of mitochondrial dysfunction. Front Physiol 3: 139.
-
(2012)
Front Physiol
, vol.3
, pp. 139
-
-
Jazwinski, S.M.1
Kriete, A.2
-
38
-
-
17244379811
-
Complement factor H polymorphism and age-related macular degeneration
-
Edwards AO, Ritter R 3rd, Abel KJ, Manning A, Panhuysen C, et al. (2005) Complement factor H polymorphism and age-related macular degeneration. Science 308: 421-424.
-
(2005)
Science
, vol.308
, pp. 421-424
-
-
Edwards, A.O.1
Ritter 3rd, R.2
Abel, K.J.3
Manning, A.4
Panhuysen, C.5
-
39
-
-
20244380171
-
Complement factor H polymorphism in age-related macular degeneration
-
Klein RJ, Zeiss C, Chew EY, Tsai JY, Sackler RS, et al. (2005) Complement factor H polymorphism in age-related macular degeneration. Science 308: 385-389.
-
(2005)
Science
, vol.308
, pp. 385-389
-
-
Klein, R.J.1
Zeiss, C.2
Chew, E.Y.3
Tsai, J.Y.4
Sackler, R.S.5
-
40
-
-
20244388812
-
Complement factor H variant increases the risk of age-related macular degeneration
-
Haines JL, Hauser MA, Schmidt S, Scott WK, Olson LM, et al. (2005) Complement factor H variant increases the risk of age-related macular degeneration. Science 308: 419-421.
-
(2005)
Science
, vol.308
, pp. 419-421
-
-
Haines, J.L.1
Hauser, M.A.2
Schmidt, S.3
Scott, W.K.4
Olson, L.M.5
-
41
-
-
23944475451
-
Candidate gene analysis suggests a role for fatty acid biosynthesis and regulation of the complement system in the etiology of age-related maculopathy
-
Conley YP, Thalamuthu A, Jakobsdottir J, Weeks DE, Mah T, et al. (2005) Candidate gene analysis suggests a role for fatty acid biosynthesis and regulation of the complement system in the etiology of age-related maculopathy. Hum Mol Genet 14: 1991-2002.
-
(2005)
Hum Mol Genet
, vol.14
, pp. 1991-2002
-
-
Conley, Y.P.1
Thalamuthu, A.2
Jakobsdottir, J.3
Weeks, D.E.4
Mah, T.5
-
42
-
-
34347244210
-
Complement factor H polymorphism in age-related macular degeneration
-
Narayanan R, Butani V, Boyer DS, Atilano SR, Resende GP, et al. (2007) Complement factor H polymorphism in age-related macular degeneration. Ophthalmology 114: 1327-1331.
-
(2007)
Ophthalmology
, vol.114
, pp. 1327-1331
-
-
Narayanan, R.1
Butani, V.2
Boyer, D.S.3
Atilano, S.R.4
Resende, G.P.5
-
43
-
-
33745728418
-
No association between complement factor H gene polymorphism and exudative age-related macular degeneration in Japanese
-
Gotoh N, Yamada R, Hiratani H, Renault V, Kuroiwa S, et al. (2006) No association between complement factor H gene polymorphism and exudative age-related macular degeneration in Japanese. Hum Genet 120: 139-143.
-
(2006)
Hum Genet
, vol.120
, pp. 139-143
-
-
Gotoh, N.1
Yamada, R.2
Hiratani, H.3
Renault, V.4
Kuroiwa, S.5
-
44
-
-
33748357958
-
Ethnic variation in AMD-associated complement factor H polymorphism p.Tyr402His
-
Grassi MA, Fingert JH, Scheetz TE, Roos BR, Ritch R, et al. (2006) Ethnic variation in AMD-associated complement factor H polymorphism p.Tyr402His. Hum Mutat 27: 921-925.
-
(2006)
Hum Mutat
, vol.27
, pp. 921-925
-
-
Grassi, M.A.1
Fingert, J.H.2
Scheetz, T.E.3
Roos, B.R.4
Ritch, R.5
-
45
-
-
33644676878
-
Complement factor H polymorphisms in Japanese population with age-related macular degeneration
-
Okamoto H, Umeda S, Obazawa M, Minami M, Noda T, et al. (2006) Complement factor H polymorphisms in Japanese population with age-related macular degeneration. Mol Vis 12: 156-158.
-
(2006)
Mol Vis
, vol.12
, pp. 156-158
-
-
Okamoto, H.1
Umeda, S.2
Obazawa, M.3
Minami, M.4
Noda, T.5
-
46
-
-
36749004311
-
Complement factor H deficiency in aged mice causes retinal abnormalities and visual dysfunction
-
Coffey PJ, Gias C, McDermott CJ, Lundh P, Pickering MC, et al. (2007) Complement factor H deficiency in aged mice causes retinal abnormalities and visual dysfunction. Proc Natl Acad Sci U S A 104: 16651-16656.
-
(2007)
Proc Natl Acad Sci U S A
, vol.104
, pp. 16651-16656
-
-
Coffey, P.J.1
Gias, C.2
McDermott, C.J.3
Lundh, P.4
Pickering, M.C.5
-
47
-
-
80053904386
-
Complement factor H binds malondialdehyde epitopes and protects from oxidative stress
-
Weismann D, Hartvigsen K, Lauer N, Bennett KL, Scholl HP, et al. (2011) Complement factor H binds malondialdehyde epitopes and protects from oxidative stress. Nature 478: 76-81.
-
(2011)
Nature
, vol.478
, pp. 76-81
-
-
Weismann, D.1
Hartvigsen, K.2
Lauer, N.3
Bennett, K.L.4
Scholl, H.P.5
-
48
-
-
34547764305
-
Complement C3 variant and the risk of age-related macular degeneration
-
Yates JR, Sepp T, Matharu BK, Khan JC, Thurlby DA, et al. (2007) Complement C3 variant and the risk of age-related macular degeneration. N Engl J Med 357: 553-561.
-
(2007)
N Engl J Med
, vol.357
, pp. 553-561
-
-
Yates, J.R.1
Sepp, T.2
Matharu, B.K.3
Khan, J.C.4
Thurlby, D.A.5
-
49
-
-
34748819371
-
Variation in complement factor 3 is associated with risk of age-related macular degeneration
-
Maller JB, Fagerness JA, Reynolds RC, Neale BM, Daly MJ, et al. (2007) Variation in complement factor 3 is associated with risk of age-related macular degeneration. Nat Genet 39: 1200-1201.
-
(2007)
Nat Genet
, vol.39
, pp. 1200-1201
-
-
Maller, J.B.1
Fagerness, J.A.2
Reynolds, R.C.3
Neale, B.M.4
Daly, M.J.5
-
50
-
-
69249221570
-
Multilocus analysis of age-related macular degeneration
-
Bergeron-Sawitzke J, Gold B, Olsh A, Schlotterbeck S, Lemon K, et al. (2009) Multilocus analysis of age-related macular degeneration. Eur J Hum Genet 17: 1190-1199.
-
(2009)
Eur J Hum Genet
, vol.17
, pp. 1190-1199
-
-
Bergeron-Sawitzke, J.1
Gold, B.2
Olsh, A.3
Schlotterbeck, S.4
Lemon, K.5
-
51
-
-
34247147197
-
Estimation of systemic complement C3 activity in age-related macular degeneration
-
Sivaprasad S, Adewoyin T, Bailey TA, Dandekar SS, Jenkins S, et al. (2007) Estimation of systemic complement C3 activity in age-related macular degeneration. Arch Ophthalmol 125: 515-519.
-
(2007)
Arch Ophthalmol
, vol.125
, pp. 515-519
-
-
Sivaprasad, S.1
Adewoyin, T.2
Bailey, T.A.3
Dandekar, S.S.4
Jenkins, S.5
-
52
-
-
0035699547
-
Complement activation and inflammatory processes in Drusen formation and age related macular degeneration
-
Johnson LV, Leitner WP, Staples MK, Anderson DH, (2001) Complement activation and inflammatory processes in Drusen formation and age related macular degeneration. Exp Eye Res 73: 887-896.
-
(2001)
Exp Eye Res
, vol.73
, pp. 887-896
-
-
Johnson, L.V.1
Leitner, W.P.2
Staples, M.K.3
Anderson, D.H.4
-
53
-
-
11144258543
-
Drusen proteome analysis: an approach to the etiology of age-related macular degeneration
-
Crabb JW, Miyagi M, Gu X, Shadrach K, West KA, et al. (2002) Drusen proteome analysis: an approach to the etiology of age-related macular degeneration. Proc Natl Acad Sci U S A 99: 14682-14687.
-
(2002)
Proc Natl Acad Sci U S A
, vol.99
, pp. 14682-14687
-
-
Crabb, J.W.1
Miyagi, M.2
Gu, X.3
Shadrach, K.4
West, K.A.5
-
54
-
-
79952106968
-
Retinal pigment epithelial cells upregulate expression of complement factors after co-culture with activated T cells
-
Juel HB, Kaestel C, Folkersen L, Faber C, Heegaard NH, et al. (2011) Retinal pigment epithelial cells upregulate expression of complement factors after co-culture with activated T cells. Exp Eye Res 92: 180-188.
-
(2011)
Exp Eye Res
, vol.92
, pp. 180-188
-
-
Juel, H.B.1
Kaestel, C.2
Folkersen, L.3
Faber, C.4
Heegaard, N.H.5
-
55
-
-
67650547973
-
Oxidative stress renders retinal pigment epithelial cells susceptible to complement-mediated injury
-
Thurman JM, Renner B, Kunchithapautham K, Ferreira VP, Pangburn MK, et al. (2009) Oxidative stress renders retinal pigment epithelial cells susceptible to complement-mediated injury. J Biol Chem 284: 16939-16947.
-
(2009)
J Biol Chem
, vol.284
, pp. 16939-16947
-
-
Thurman, J.M.1
Renner, B.2
Kunchithapautham, K.3
Ferreira, V.P.4
Pangburn, M.K.5
-
56
-
-
34848894584
-
The R345W mutation in EFEMP1 is pathogenic and causes AMD-like deposits in mice
-
Fu L, Garland D, Yang Z, Shukla D, Rajendran A, et al. (2007) The R345W mutation in EFEMP1 is pathogenic and causes AMD-like deposits in mice. Hum Mol Genet 16: 2411-2422.
-
(2007)
Hum Mol Genet
, vol.16
, pp. 2411-2422
-
-
Fu, L.1
Garland, D.2
Yang, Z.3
Shukla, D.4
Rajendran, A.5
-
57
-
-
0036792087
-
Aberrant accumulation of EFEMP1 underlies drusen formation in Malattia Leventinese and age-related macular degeneration
-
Marmorstein LY, Munier FL, Arsenijevic Y, Schorderet DF, McLaughlin PJ, et al. (2002) Aberrant accumulation of EFEMP1 underlies drusen formation in Malattia Leventinese and age-related macular degeneration. Proc Natl Acad Sci U S A 99: 13067-13072.
-
(2002)
Proc Natl Acad Sci U S A
, vol.99
, pp. 13067-13072
-
-
Marmorstein, L.Y.1
Munier, F.L.2
Arsenijevic, Y.3
Schorderet, D.F.4
McLaughlin, P.J.5
-
58
-
-
79952814062
-
EFEMP1 expression promotes angiogenesis and accelerates the growth of cervical cancer in vivo
-
Song EL, Hou YP, Yu SP, Chen SG, Huang JT, et al. (2011) EFEMP1 expression promotes angiogenesis and accelerates the growth of cervical cancer in vivo. Gynecol Oncol 121: 174-180.
-
(2011)
Gynecol Oncol
, vol.121
, pp. 174-180
-
-
Song, E.L.1
Hou, Y.P.2
Yu, S.P.3
Chen, S.G.4
Huang, J.T.5
-
59
-
-
77951938614
-
The expression of EFEMP1 in cervical carcinoma and its relationship with prognosis
-
En-lin S, Sheng-guo C, Hua-qiao W, (2010) The expression of EFEMP1 in cervical carcinoma and its relationship with prognosis. Gynecol Oncol 117: 417-422.
-
(2010)
Gynecol Oncol
, vol.117
, pp. 417-422
-
-
En-lin, S.1
Sheng-guo, C.2
Hua-qiao, W.3
-
60
-
-
44649155930
-
Variants in the 10q26 gene cluster (LOC387715 and HTRA1) exhibit enhanced risk of age-related macular degeneration along with CFH in Indian patients
-
Kaur I, Katta S, Hussain A, Hussain N, Mathai A, et al. (2008) Variants in the 10q26 gene cluster (LOC387715 and HTRA1) exhibit enhanced risk of age-related macular degeneration along with CFH in Indian patients. Invest Ophthalmol Vis Sci 49: 1771-1776.
-
(2008)
Invest Ophthalmol Vis Sci
, vol.49
, pp. 1771-1776
-
-
Kaur, I.1
Katta, S.2
Hussain, A.3
Hussain, N.4
Mathai, A.5
-
61
-
-
36049042661
-
A variant of mitochondrial protein LOC387715/ARMS2, not HTRA1, is strongly associated with age-related macular degeneration
-
Kanda A, Chen W, Othman M, Branham KE, Brooks M, et al. (2007) A variant of mitochondrial protein LOC387715/ARMS2, not HTRA1, is strongly associated with age-related macular degeneration. Proc Natl Acad Sci U S A 104: 16227-16232.
-
(2007)
Proc Natl Acad Sci U S A
, vol.104
, pp. 16227-16232
-
-
Kanda, A.1
Chen, W.2
Othman, M.3
Branham, K.E.4
Brooks, M.5
-
62
-
-
67649998898
-
Localization of age-related macular degeneration-associated ARMS2 in cytosol, not mitochondria
-
Wang G, Spencer KL, Court BL, Olson LM, Scott WK, et al. (2009) Localization of age-related macular degeneration-associated ARMS2 in cytosol, not mitochondria. Invest Ophthalmol Vis Sci 50: 3084-3090.
-
(2009)
Invest Ophthalmol Vis Sci
, vol.50
, pp. 3084-3090
-
-
Wang, G.1
Spencer, K.L.2
Court, B.L.3
Olson, L.M.4
Scott, W.K.5
-
63
-
-
66149142821
-
Mitochondrial DNA variability modulates mRNA and intra-mitochondrial protein levels of HSP60 and HSP75: experimental evidence from cybrid lines
-
Bellizzi D, Taverna D, D'Aquila P, De Blasi S, De Benedictis G, (2009) Mitochondrial DNA variability modulates mRNA and intra-mitochondrial protein levels of HSP60 and HSP75: experimental evidence from cybrid lines. Cell Stress Chaperones 14: 265-271.
-
(2009)
Cell Stress Chaperones
, vol.14
, pp. 265-271
-
-
Bellizzi, D.1
Taverna, D.2
D'Aquila, P.3
De Blasi, S.4
De Benedictis, G.5
-
64
-
-
33746158952
-
Gene expression of cytokines and cytokine receptors is modulated by the common variability of the mitochondrial DNA in cybrid cell lines
-
Bellizzi D, Cavalcante P, Taverna D, Rose G, Passarino G, et al. (2006) Gene expression of cytokines and cytokine receptors is modulated by the common variability of the mitochondrial DNA in cybrid cell lines. Genes Cells 11: 883-891.
-
(2006)
Genes Cells
, vol.11
, pp. 883-891
-
-
Bellizzi, D.1
Cavalcante, P.2
Taverna, D.3
Rose, G.4
Passarino, G.5
-
65
-
-
84856082982
-
Mitochondrial-nuclear DNA interactions contribute to the regulation of nuclear transcript levels as part of the inter-organelle communication system
-
Rodley CD, Grand RS, Gehlen LR, Greyling G, Jones MB, et al. (2012) Mitochondrial-nuclear DNA interactions contribute to the regulation of nuclear transcript levels as part of the inter-organelle communication system. PLoS ONE 7: e30943.
-
(2012)
PLoS ONE
, vol.7
-
-
Rodley, C.D.1
Grand, R.S.2
Gehlen, L.R.3
Greyling, G.4
Jones, M.B.5
-
66
-
-
0028815440
-
Defective myosin VIIA gene responsible for Usher syndrome type 1B
-
Weil D, Blanchard S, Kaplan J, Guilford P, Gibson F, et al. (1995) Defective myosin VIIA gene responsible for Usher syndrome type 1B. Nature 374: 60-61.
-
(1995)
Nature
, vol.374
, pp. 60-61
-
-
Weil, D.1
Blanchard, S.2
Kaplan, J.3
Guilford, P.4
Gibson, F.5
-
67
-
-
0028787263
-
Expression in cochlea and retina of myosin VIIa, the gene product defective in Usher syndrome type 1B
-
Hasson T, Heintzelman MB, Santos-Sacchi J, Corey DP, Mooseker MS, (1995) Expression in cochlea and retina of myosin VIIa, the gene product defective in Usher syndrome type 1B. Proc Natl Acad Sci U S A 92: 9815-9819.
-
(1995)
Proc Natl Acad Sci U S A
, vol.92
, pp. 9815-9819
-
-
Hasson, T.1
Heintzelman, M.B.2
Santos-Sacchi, J.3
Corey, D.P.4
Mooseker, M.S.5
-
68
-
-
9244233852
-
Human myosin VIIA responsible for the Usher 1B syndrome: a predicted membrane-associated motor protein expressed in developing sensory epithelia
-
Weil D, Levy G, Sahly I, Levi-Acobas F, Blanchard S, et al. (1996) Human myosin VIIA responsible for the Usher 1B syndrome: a predicted membrane-associated motor protein expressed in developing sensory epithelia. Proc Natl Acad Sci U S A 93: 3232-3237.
-
(1996)
Proc Natl Acad Sci U S A
, vol.93
, pp. 3232-3237
-
-
Weil, D.1
Levy, G.2
Sahly, I.3
Levi-Acobas, F.4
Blanchard, S.5
-
69
-
-
0032085412
-
Mutant myosin VIIa causes defective melanosome distribution in the RPE of shaker-1 mice
-
Liu X, Ondek B, Williams DS, (1998) Mutant myosin VIIa causes defective melanosome distribution in the RPE of shaker-1 mice. Nat Genet 19: 117-118.
-
(1998)
Nat Genet
, vol.19
, pp. 117-118
-
-
Liu, X.1
Ondek, B.2
Williams, D.S.3
-
70
-
-
81455161607
-
Mitochondrial DNA (mtDNA) haplogroups and serum levels of anti-oxidant enzymes in patients with osteoarthritis
-
Fernandez-Moreno M, Soto-Hermida A, Pertega S, Oreiro N, Fernandez-Lopez C, et al. (2011) Mitochondrial DNA (mtDNA) haplogroups and serum levels of anti-oxidant enzymes in patients with osteoarthritis. BMC Musculoskelet Disord 12: 264.
-
(2011)
BMC Musculoskelet Disord
, vol.12
, pp. 264
-
-
Fernandez-Moreno, M.1
Soto-Hermida, A.2
Pertega, S.3
Oreiro, N.4
Fernandez-Lopez, C.5
-
71
-
-
84866416300
-
Mitochondrial haplogroups define two phenotypes of osteoarthritis
-
Fernandez-Moreno M, Soto-Hermida A, Oreiro N, Pertega S, Fenandez-Lopez C, et al. (2012) Mitochondrial haplogroups define two phenotypes of osteoarthritis. Front Physiol 3: 129.
-
(2012)
Front Physiol
, vol.3
, pp. 129
-
-
Fernandez-Moreno, M.1
Soto-Hermida, A.2
Oreiro, N.3
Pertega, S.4
Fenandez-Lopez, C.5
|