-
1
-
-
0034701029
-
Human mitochondrial DNA polymerase holoenzyme: Reconstitution and characterization
-
DOI 10.1021/bi992104w
-
Johnson, A. A., Tsai, Y. C., Graves, S. W., and Johnson, K. A. (2000) Human mitochondrial DNA polymerase holoenzyme. Reconstitution and characterization. Biochemistry 39, 1702-1708 (Pubitemid 30108960)
-
(2000)
Biochemistry
, vol.39
, Issue.7
, pp. 1702-1708
-
-
Johnson, A.A.1
Tsai, Y.-C.2
Graves, S.W.3
Johnson, K.A.4
-
2
-
-
0035851098
-
Exonuclease proofreading by human mitochondrial DNA polymerase
-
Johnson, A. A., and Johnson, K. A. (2001) Exonuclease proofreading by human mitochondrial DNA polymerase. J. Biol. Chem. 276, 38097-38107
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 38097-38107
-
-
Johnson, A.A.1
Johnson, K.A.2
-
3
-
-
0034938364
-
Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria
-
DOI 10.1038/90058
-
Spelbrink, J. N., Li, F. Y., Tiranti, V., Nikali, K., Yuan, Q. P., Tariq, M., Wanrooij, S., Garrido, N., Comi, G., Morandi, L., Santoro, L., Toscano, A., Fabrizi, G. M., Somer, H., Croxen, R., Beeson, D., Poulton, J., Suomalainen, A., Jacobs, H. T., Zeviani, M., and Larsson, C. (2001) Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria, Nat. Genet. 28, 223-231 (Pubitemid 32626024)
-
(2001)
Nature Genetics
, vol.28
, Issue.3
, pp. 223-231
-
-
Spelbrink, J.N.1
Li, F.-Y.2
Tiranti, V.3
Nikali, K.4
Yuan, Q.-P.5
Tariq, M.6
Wanrooij, S.7
Garrido, N.8
Comi, G.9
Morandi, L.10
Santoro, L.11
Toscano, A.12
Fabrizi, G.-M.13
Somer, H.14
Croxen, R.15
Beeson, D.16
Poulton, J.17
Suomalainen, A.18
Jacobs, H.T.19
Zeviani, M.20
Larsson, C.21
more..
-
4
-
-
84896875816
-
Towards efficient reconstitution of the human mitochondrial DNA replication complex
-
Qian, Y., Ziehr, J. L., and Johnson, K. A. (2013) Towards efficient reconstitution of the human mitochondrial DNA replication complex. Biophys. J. 104, 74a
-
(2013)
Biophys. J.
, vol.104
-
-
Qian, Y.1
Ziehr, J.L.2
Johnson, K.A.3
-
5
-
-
3242739284
-
Reconstitution of a minimal mtDNA replisome in vitro
-
DOI 10.1038/sj.emboj.7600257
-
Korhonen, J. A., Pham, X. H., Pellegrini, M., and Falkenberg, M. (2004) Reconstitution of a minimal mtDNA replisome in vitro. EMBO J. 23, 2423-2429 (Pubitemid 38954849)
-
(2004)
EMBO Journal
, vol.23
, Issue.12
, pp. 2423-2429
-
-
Korhonen, J.A.1
Pham, X.H.2
Pellegrini, M.3
Falkenberg, M.4
-
6
-
-
78651369034
-
Mitochondrial DNA replication and disease. Insights from DNA polymerase γ mutations
-
Stumpf, J. D., and Copeland, W. C. (2011) Mitochondrial DNA replication and disease. Insights from DNA polymerase γ mutations. Cell. Mol. Life Sci. 68, 219-233
-
(2011)
Cell. Mol. Life Sci.
, vol.68
, pp. 219-233
-
-
Stumpf, J.D.1
Copeland, W.C.2
-
7
-
-
39649120348
-
Inherited mitochondrial diseases of DNA replication
-
Copeland, W. C. (2008) Inherited mitochondrial diseases of DNA replication. Annu. Rev. Med. 59, 131-146
-
(2008)
Annu. Rev. Med.
, vol.59
, pp. 131-146
-
-
Copeland, W.C.1
-
8
-
-
77958538173
-
Role of histidine 932 of the human mitochondrial DNA polymerase in nucleotide discrimination and inherited disease
-
Batabyal, D., McKenzie, J. L., and Johnson, K. A. (2010) Role of histidine 932 of the human mitochondrial DNA polymerase in nucleotide discrimination and inherited disease. J. Biol. Chem. 285, 34191-34201
-
(2010)
J. Biol. Chem.
, vol.285
, pp. 34191-34201
-
-
Batabyal, D.1
McKenzie, J.L.2
Johnson, K.A.3
-
9
-
-
79960481596
-
Effect of the Y955C mutation on mitochondrial DNA polymerase nucleotide incorporation efficiency and fidelity
-
Estep, P. A., and Johnson, K. A. (2011) Effect of the Y955C mutation on mitochondrial DNA polymerase nucleotide incorporation efficiency and fidelity. Biochemistry 50, 6376-6386
-
(2011)
Biochemistry
, vol.50
, pp. 6376-6386
-
-
Estep, P.A.1
Johnson, K.A.2
-
10
-
-
82755197808
-
Biochemical analysis of the G517V POLG variant reveals wild-type like activity
-
Kasiviswanathan, R., and Copeland, W. C. (2011) Biochemical analysis of the G517V POLG variant reveals wild-type like activity. Mitochondrion 11, 929-934
-
(2011)
Mitochondrion
, vol.11
, pp. 929-934
-
-
Kasiviswanathan, R.1
Copeland, W.C.2
-
11
-
-
79952034603
-
Sequence-specific stalling of DNA polymerase γ and the effects of mutations causing progressive ophthalmoplegia
-
Atanassova, N., Fusté, J. M., Wanrooij, S., Macao, B., Goffart, S., Bäckström, S., Farge, G., Khvorostov, I., Larsson, N. G., Spelbrink, J. N., and Falkenberg, M. (2011) Sequence-specific stalling of DNA polymerase γ and the effects of mutations causing progressive ophthalmoplegia. Hum. Mol. Genet. 20, 1212-1223
-
(2011)
Hum. Mol. Genet.
, vol.20
, pp. 1212-1223
-
-
Atanassova, N.1
Fusté, J.M.2
Wanrooij, S.3
Macao, B.4
Goffart, S.5
Bäckström, S.6
Farge, G.7
Khvorostov, I.8
Larsson, N.G.9
Spelbrink, J.N.10
Falkenberg, M.11
-
12
-
-
3543039417
-
Structure-function defects of human mitochondrial DNA polymerase in autosomal dominant progressive external ophthalmoplegia
-
DOI 10.1038/nsmb805
-
Graziewicz, M. A., Longley, M. J., Bienstock, R. J., Zeviani, M., and Copeland, W. C. (2004) Structure-function defects of human mitochondrial DNA polymerase in autosomal dominant progressive external ophthalmoplegia. Nat. Struct. Mol. Biol. 11, 770-776 (Pubitemid 39014503)
-
(2004)
Nature Structural and Molecular Biology
, vol.11
, Issue.8
, pp. 770-776
-
-
Graziewicz, M.A.1
Longley, M.J.2
Bienstock, R.J.3
Zeviani, M.4
Copeland, W.C.5
-
13
-
-
80955158521
-
Mitochondrial DNA polymerase γ mutations. An ever expanding molecular and clinical spectrum
-
Tang, S., Wang, J., Lee, N. C., Milone, M., Halberg, M. C., Schmitt, E. S., Craigen, W. J., Zhang, W., and Wong, L. J. (2011) Mitochondrial DNA polymerase γ mutations. An ever expanding molecular and clinical spectrum. J. Med. Genet. 48, 669-681
-
(2011)
J. Med. Genet.
, vol.48
, pp. 669-681
-
-
Tang, S.1
Wang, J.2
Lee, N.C.3
Milone, M.4
Halberg, M.C.5
Schmitt, E.S.6
Craigen, W.J.7
Zhang, W.8
Wong, L.J.9
-
14
-
-
70349807756
-
Structural insight into processive human mitochondrial DNA synthesis and disease-related polymerase mutations
-
Lee, Y. S., Kennedy, W. D., and Yin, Y. W. (2009) Structural insight into processive human mitochondrial DNA synthesis and disease-related polymerase mutations. Cell 139, 312-324
-
(2009)
Cell
, vol.139
, pp. 312-324
-
-
Lee, Y.S.1
Kennedy, W.D.2
Yin, Y.W.3
-
15
-
-
4444276204
-
POLG mutations in sporadic mitochondrial disorders with multiple mtDNA deletions
-
Di Fonzo, A., Bordoni, A., Crimi, M., Sara, G., Del Bo, R., Bresolin, N., and Comi, G. P. (2003) POLG mutations in sporadic mitochondrial disorders with multiple mtDNA deletions. Hum. Mutat. 22, 498-499
-
(2003)
Hum. Mutat.
, vol.22
, pp. 498-499
-
-
Di Fonzo, A.1
Bordoni, A.2
Crimi, M.3
Sara, G.4
Del Bo, R.5
Bresolin, N.6
Comi, G.P.7
-
16
-
-
0034943967
-
Mutation of POLG is associated with progressive external opthalmoplegia characterized by mtDNA deletions
-
Van Goethem, G., Dermaut, B., Lofgren, A., Martin, J. J., and Van Broeckhoven, C. (2001) Mutation of POLG is associated with progressive external opthalmoplegia characterized by mtDNA deletions. Nat. Genet. 28, 2
-
(2001)
Nat. Genet.
, vol.28
, pp. 2
-
-
Van Goethem, G.1
Dermaut, B.2
Lofgren, A.3
Martin, J.J.4
Van Broeckhoven, C.5
-
17
-
-
84874513478
-
Mutations in human DNA polymerase γ confer unique mechanisms of catalytic deficiency that mirror the disease severity in mitochondrial disorder patients
-
Sohl, C. D., Kasiviswanathan, R., Copeland, W. C., and Anderson, K. S. (2013) Mutations in human DNA polymerase γ confer unique mechanisms of catalytic deficiency that mirror the disease severity in mitochondrial disorder patients. Hum. Mol. Genet. 22, 1074-1085
-
(2013)
Hum. Mol. Genet.
, vol.22
, pp. 1074-1085
-
-
Sohl, C.D.1
Kasiviswanathan, R.2
Copeland, W.C.3
Anderson, K.S.4
-
18
-
-
0033365008
-
Yeast as a model for human mtDNA replication
-
Shadel, G. S. (1999) Yeast as a model for human mtDNA replication. Am. J. Hum. Genet. 65, 1230-1237
-
(1999)
Am. J. Hum. Genet.
, vol.65
, pp. 1230-1237
-
-
Shadel, G.S.1
-
19
-
-
0036468956
-
Yeast mitochondrial biogenesis: A model system for humans?
-
DOI 10.1016/S1367-5931(01)00276-9
-
Foury, F., and Kucej, M. (2002) Yeast mitochondrial biogenesis. A model system for humans? Curr. Opin. Chem. Biol. 6, 106-111 (Pubitemid 34122045)
-
(2002)
Current Opinion in Chemical Biology
, vol.6
, Issue.1
, pp. 106-111
-
-
Foury, F.1
Kucej, M.2
-
20
-
-
0036699060
-
Systematic screen for human disease genes in yeast
-
DOI 10.1038/ng929
-
Steinmetz, L. M., Scharfe, C., Deutschbauer, A. M., Mokranjac, D., Herman, Z. S., Jones, T., Chu, A. M., Giaever, G., Prokisch, H., Oefner, P. J., and Davis, R. W. (2002) Systematic screen for human disease genes in yeast. Nat. Genet. 31, 400-404 (Pubitemid 35154450)
-
(2002)
Nature Genetics
, vol.31
, Issue.4
, pp. 400-404
-
-
Steinmetz, L.M.1
Scharfe, C.2
Deutschbauer, A.M.3
Mokranjac, D.4
Herman, Z.S.5
Jones, T.6
Chu, A.M.7
Giaever, G.8
Prokisch, H.9
Oefner, P.J.10
Davis, R.W.11
-
21
-
-
78349257393
-
Mitochondrial diseases and the role of the yeast models
-
Rinaldi, T., Dallabona, C., Ferrero, I., Frontali, L., and Bolotin-Fukuhara, M. (2010) Mitochondrial diseases and the role of the yeast models. FEMS Yeast Res. 10, 1006-1022
-
(2010)
FEMS Yeast Res.
, vol.10
, pp. 1006-1022
-
-
Rinaldi, T.1
Dallabona, C.2
Ferrero, I.3
Frontali, L.4
Bolotin-Fukuhara, M.5
-
22
-
-
31444454598
-
Bacteriophage origins of mitochondrial replication and transcription proteins
-
DOI 10.1016/j.tig.2005.11.007, PII S0168952505003367
-
Shutt, T. E., and Gray, M. W. (2006) Bacteriophage origins of mitochondrial replication and transcription proteins, Trends Genet. 22, 90-95 (Pubitemid 43152027)
-
(2006)
Trends in Genetics
, vol.22
, Issue.2
, pp. 90-95
-
-
Shutt, T.E.1
Gray, M.W.2
-
23
-
-
31144476302
-
Mitochondrial and nuclear DNA defects in Saccharomyces cerevisiae with mutations in DNA polymerase γ associated with progressive external ophthalmoplegia
-
DOI 10.1093/hmg/ddi454
-
Stuart, G. R., Santos, J. H., Strand, M. K., Van Houten, B., and Copeland, W. C. (2006) Mitochondrial and nuclear DNA defects in Saccharomyces cerevisiae with mutations in DNA polymerase γ associated with progressive external ophthalmoplegia. Hum. Mol. Genet. 15, 363-374 (Pubitemid 43125990)
-
(2006)
Human Molecular Genetics
, vol.15
, Issue.2
, pp. 363-374
-
-
Stuart, G.R.1
Santos, J.H.2
Strand, M.K.3
Van Houten, B.4
Copeland, W.C.5
-
24
-
-
37049033589
-
Mitochondrial DNA defects in Saccharomyces cerevisiae caused by functional interactions between DNA polymerase gamma mutations associated with disease in human
-
DOI 10.1016/j.bbadis.2007.10.002, PII S0925443907001937
-
Baruffini, E., Ferrero, I., and Foury, F. (2007) Mitochondrial DNA defects in Saccharomyces cerevisiae caused by functional interactions between DNA polymerase γ mutations associated with disease in human. Biochim. Biophys. Acta 1772, 1225-1235 (Pubitemid 350245440)
-
(2007)
Biochimica et Biophysica Acta - Molecular Basis of Disease
, vol.1772
, Issue.11-12
, pp. 1225-1235
-
-
Baruffini, E.1
Ferrero, I.2
Foury, F.3
-
25
-
-
77953499335
-
mip1 containing mutations associated with mitochondrial disease causes mutagenesis and depletion of mtDNA in Saccharomyces cerevisiae
-
Stumpf, J. D., Bailey, C. M., Spell, D., Stillwagon, M., Anderson, K. S., and Copeland, W. C. (2010) mip1 containing mutations associated with mitochondrial disease causes mutagenesis and depletion of mtDNA in Saccharomyces cerevisiae. Hum. Mol. Genet. 19, 2123-2133
-
(2010)
Hum. Mol. Genet.
, vol.19
, pp. 2123-2133
-
-
Stumpf, J.D.1
Bailey, C.M.2
Spell, D.3
Stillwagon, M.4
Anderson, K.S.5
Copeland, W.C.6
-
26
-
-
77956123004
-
A cluster of pathogenic mutations in the 3′-5′ exonuclease domain of DNA polymerase γ defines a novel module coupling DNA synthesis and degradation
-
Szczepanowska, K., and Foury, F. (2010) A cluster of pathogenic mutations in the 3′-5′ exonuclease domain of DNA polymerase γ defines a novel module coupling DNA synthesis and degradation. Hum. Mol. Genet. 19, 3516-3529
-
(2010)
Hum. Mol. Genet.
, vol.19
, pp. 3516-3529
-
-
Szczepanowska, K.1
Foury, F.2
-
27
-
-
78649984326
-
Predicting the contribution of novel POLG mutations to human disease through analysis in yeast model
-
Baruffini, E., Horvath, R., Dallabona, C., Czermin, B., Lamantea, E., Bindoff, L., Invernizzi, F., Ferrero, I., Zeviani, M., and Lodi, T. (2011) Predicting the contribution of novel POLG mutations to human disease through analysis in yeast model. Mitochondrion 11, 182-190
-
(2011)
Mitochondrion
, vol.11
, pp. 182-190
-
-
Baruffini, E.1
Horvath, R.2
Dallabona, C.3
Czermin, B.4
Lamantea, E.5
Bindoff, L.6
Invernizzi, F.7
Ferrero, I.8
Zeviani, M.9
Lodi, T.10
-
28
-
-
16544382212
-
Mutation in AAC2, equivalent to human adPEO-associated ANT1 mutations, lead to defective oxidative phosphorylation in Saccharomyces cerevisiae and affect mitochondrial DNA stability
-
DOI 10.1093/hmg/ddh108
-
Fontanesi, F., Palmieri, L., Scarcia, P., Lodi, T., Donnini, C., Limongelli, A., Tiranti, V., Zeviani, M., Ferrero, I., and Viola, A. M. (2004) Mutations in AAC2, equivalent to human adPEO-associated ANT1 mutations, lead to defective oxidative phosphorylation in Saccharomyces cerevisiae and affect mitochondrial DNA stability. Hum. Mol. Genet. 13, 923-934 (Pubitemid 38628428)
-
(2004)
Human Molecular Genetics
, vol.13
, Issue.9
, pp. 923-934
-
-
Fontanesi, F.1
Palmieri, L.2
Scarcia, P.3
Lodi, T.4
Donnini, C.5
Limongelli, A.6
Tiranti, V.7
Zeviani, M.8
Ferrero, I.9
Viola, A.M.10
-
29
-
-
78650008112
-
Yeast mitochondrial DNA polymerase is a highly processive single-subunit enzyme
-
Viikov, K., Väljamäe, P., and Sedman, J. (2011) Yeast mitochondrial DNA polymerase is a highly processive single-subunit enzyme. Mitochondrion 11, 119-126
-
(2011)
Mitochondrion
, vol.11
, pp. 119-126
-
-
Viikov, K.1
Väljamäe, P.2
Sedman, J.3
-
30
-
-
77957346278
-
Late-onset ptosis and myopathy in a patient with a heterozygous insertion in POLG2
-
Walter, M. C., Czermin, B., Muller-Ziermann, S., Bulst, S., Stewart, J. D., Hudson, G., Schneiderat, P., Abicht, A., Holinski-Feder, E., Lochmüller, H., Chinnery, P. F., Klopstock, T., and Horvath, R. (2010) Late-onset ptosis and myopathy in a patient with a heterozygous insertion in POLG2. J. Neurol. 257, 1517-1523
-
(2010)
J. Neurol.
, vol.257
, pp. 1517-1523
-
-
Walter, M.C.1
Czermin, B.2
Muller-Ziermann, S.3
Bulst, S.4
Stewart, J.D.5
Hudson, G.6
Schneiderat, P.7
Abicht, A.8
Holinski-Feder, E.9
Lochmüller, H.10
Chinnery, P.F.11
Klopstock, T.12
Horvath, R.13
-
31
-
-
38349038411
-
Progressive external ophthalmoplegia and vision and hearing loss in a patient with mutations in POLG2 and OPA1
-
Ferraris, S., Clark, S., Garelli, E., Davidzon, G., Moore, S. A., Kardon, R. H., Bienstock, R. J., Longley, M. J., Mancuso, M., Gutiérrez Ríos, P., Hirano, M., Copeland, W. C., and DiMauro, S. (2008) Progressive external ophthalmoplegia and vision and hearing loss in a patient with mutations in POLG2 and OPA1. Arch. Neurol. 65, 125-131
-
(2008)
Arch. Neurol.
, vol.65
, pp. 125-131
-
-
Ferraris, S.1
Clark, S.2
Garelli, E.3
Davidzon, G.4
Moore, S.A.5
Kardon, R.H.6
Bienstock, R.J.7
Longley, M.J.8
Mancuso, M.9
Gutiérrez Ríos, P.10
Hirano, M.11
Copeland, W.C.12
DiMauro, S.13
-
32
-
-
71149100270
-
Assessing pathogenicity of MLH1 variants by co-expression of human MLH1 and PMS2 genes in yeast
-
Vogelsang, M., Comino, A., Zupanec, N., Hudler, P., and Komel, R. (2009) Assessing pathogenicity of MLH1 variants by co-expression of human MLH1 and PMS2 genes in yeast. BMC Cancer 9, 382
-
(2009)
BMC Cancer
, vol.9
, pp. 382
-
-
Vogelsang, M.1
Comino, A.2
Zupanec, N.3
Hudler, P.4
Komel, R.5
-
33
-
-
46549089111
-
Protein folding diseases and neurodegeneration. Lessons learned from yeast
-
Winderickx, J., Delay, C., De Vos, A., Klinger, H., Pellens, K., Vanhelmont, T., Van Leuven, F., and Zabrocki, P. (2008) Protein folding diseases and neurodegeneration. Lessons learned from yeast. Biochim. Biophys. Acta. 1783, 1381-1395
-
(2008)
Biochim. Biophys. Acta.
, vol.1783
, pp. 1381-1395
-
-
Winderickx, J.1
Delay, C.2
De Vos, A.3
Klinger, H.4
Pellens, K.5
Vanhelmont, T.6
Van Leuven, F.7
Zabrocki, P.8
-
34
-
-
84889561956
-
Contemporary, yeast-based approaches to understanding human genetic variation
-
Dunham, M. J., and Fowler, D. M. (2013) Contemporary, yeast-based approaches to understanding human genetic variation. Curr. Opin. Genet. Dev. 23, 658-664
-
(2013)
Curr. Opin. Genet. Dev.
, vol.23
, pp. 658-664
-
-
Dunham, M.J.1
Fowler, D.M.2
-
35
-
-
84880910987
-
The benefits of humanized yeast models to study Parkinson's disease
-
Franssens, V., Bynens, T., Van den Brande, J., Vandermeeren, K., Verduyckt, M., and Winderickx, J. (2013) The benefits of humanized yeast models to study Parkinson's disease. Oxid. Med. Cell. Longev. 2013, 760629
-
(2013)
Oxid. Med. Cell. Longev.
, vol.2013
, pp. 760629
-
-
Franssens, V.1
Bynens, T.2
Van Den Brande, J.3
Vandermeeren, K.4
Verduyckt, M.5
Winderickx, J.6
-
36
-
-
0025978949
-
Getting started with yeast
-
Sherman, F. (1991) Getting started with yeast. Methods Enzymol. 194, 3-21
-
(1991)
Methods Enzymol.
, vol.194
, pp. 3-21
-
-
Sherman, F.1
-
37
-
-
0020213475
-
Homothallic switching of yeast mating type cassettes is initiated by a double-stranded cut in the MAT locus
-
Strathern, J. N., Klar, A. J., Hicks, J. B., Abraham, J. A., Ivy, J. M., Nasmyth, K. A., and McGill, C. (1982) Homothallic switching of yeast mating type cassettes is initiated by a double-stranded cut in the MAT locus. Cell 31, 183-192
-
(1982)
Cell
, vol.31
, pp. 183-192
-
-
Strathern, J.N.1
Klar, A.J.2
Hicks, J.B.3
Abraham, J.A.4
Ivy, J.M.5
Nasmyth, K.A.6
McGill, C.7
-
38
-
-
33745225170
-
The delitto perfetto approach to in vivo site-directed mutagenesis and chromosome rearrangements with synthetic oligonucleotides in yeast
-
Storici, F., and Resnick, M. A. (2006) The delitto perfetto approach to in vivo site-directed mutagenesis and chromosome rearrangements with synthetic oligonucleotides in yeast. Methods Enzymol. 409, 329-345
-
(2006)
Methods Enzymol.
, vol.409
, pp. 329-345
-
-
Storici, F.1
Resnick, M.A.2
-
39
-
-
76249088524
-
Genome-wide deletion mutant analysis reveals genes required for respiratory growth, mitochondrial genome maintenance, and mitochondrial protein synthesis in Saccharomyces cerevisiae
-
Merz, S., and Westermann, B. (2009) Genome-wide deletion mutant analysis reveals genes required for respiratory growth, mitochondrial genome maintenance, and mitochondrial protein synthesis in Saccharomyces cerevisiae. Genome Biol. 10, R95
-
(2009)
Genome Biol.
, vol.10
-
-
Merz, S.1
Westermann, B.2
-
40
-
-
34548727395
-
The chronological life span of Saccharomyces cerevisiae
-
DOI 10.1385/1-59745-361-7:89, Biological Aging: Methods and Protocols
-
Fabrizio, P., and Longo, V. D. (2007) The chronological life span of Saccharomyces cerevisiae. Methods Mol. Biol. 371, 89-95 (Pubitemid 350183420)
-
(2007)
Methods in Molecular Biology
, vol.371
, pp. 89-95
-
-
Fabrizio, P.1
Longo, V.D.2
-
41
-
-
74049134918
-
Each monomer of the dimeric accessory protein for human mitochondrial DNA polymerase has a distinct role in conferring processivity
-
Lee, Y. S., Lee, S., Demeler, B., Molineux, I. J., Johnson, K. A., and Yin, Y. W. (2010) Each monomer of the dimeric accessory protein for human mitochondrial DNA polymerase has a distinct role in conferring processivity. J. Biol. Chem. 285, 1490-1499
-
(2010)
J. Biol. Chem.
, vol.285
, pp. 1490-1499
-
-
Lee, Y.S.1
Lee, S.2
Demeler, B.3
Molineux, I.J.4
Johnson, K.A.5
Yin, Y.W.6
-
42
-
-
35748959603
-
Analysis of Rev1p and Pol ζ in mitochondrial mutagenesis suggests an alternative pathway of damage tolerance
-
DOI 10.1016/j.dnarep.2007.06.005, PII S1568786407002194
-
Kalifa, L., and Sia, E. A. (2007) Analysis of Rev1p and Pol ζ in mitochondrial mutagenesis suggests an alternative pathway of damage tolerance. DNA Repair 6, 1732-1739 (Pubitemid 350052725)
-
(2007)
DNA Repair
, vol.6
, Issue.12
, pp. 1732-1739
-
-
Kalifa, L.1
Sia, E.A.2
-
43
-
-
84555195856
-
Autophagy, mitochondria and oxidative stress. Cross-talk and redox signalling
-
Lee, J., Giordano, S., and Zhang, J. (2012) Autophagy, mitochondria and oxidative stress. Cross-talk and redox signalling. Biochem. J. 441, 523-540
-
(2012)
Biochem. J.
, vol.441
, pp. 523-540
-
-
Lee, J.1
Giordano, S.2
Zhang, J.3
-
44
-
-
0025806764
-
Intracellular heterogeneity in mitochondrial membrane potentials revealed by a J-aggregate-forming lipophilic cation JC-1
-
Smiley, S. T., Reers, M., Mottola-Hartshorn, C., Lin, M., Chen, A., Smith, T. W., Steele, G. D., Jr., and Chen, L. B. (1991) Intracellular heterogeneity in mitochondrial membrane potentials revealed by a J-aggregate-forming lipophilic cation JC-1. Proc. Natl. Acad. Sci. U.S.A. 88, 3671-3675 (Pubitemid 21916685)
-
(1991)
Proceedings of the National Academy of Sciences of the United States of America
, vol.88
, Issue.9
, pp. 3671-3675
-
-
Smiley, S.T.1
Reers, M.2
Mottola-Hartshorn, C.3
Lin, M.4
Chen, A.5
Smith, T.W.6
Steele Jr., G.D.7
Chen, L.B.8
-
45
-
-
84863524526
-
Replicative and chronological aging in Saccharomyces cerevisiae
-
Longo, V. D., Shadel, G. S., Kaeberlein, M., and Kennedy, B. (2012) Replicative and chronological aging in Saccharomyces cerevisiae. Cell Metabolism 16, 18-31
-
(2012)
Cell Metabolism
, vol.16
, pp. 18-31
-
-
Longo, V.D.1
Shadel, G.S.2
Kaeberlein, M.3
Kennedy, B.4
-
46
-
-
0026059948
-
PIF1: A DNA helicase in yeast mitochondria
-
Lahaye, A., Stahl, H., Thines-Sempoux, D., and Foury, F. (1991) Pif-1. A DNA helicase in yeast mitochondria. EMBO J. 10, 997-1007 (Pubitemid 21905559)
-
(1991)
EMBO Journal
, vol.10
, Issue.4
, pp. 997-1007
-
-
Lahaye, A.1
Stahl, H.2
Thines-Sempoux, D.3
Foury, F.4
-
47
-
-
21644437636
-
Hmi1p from Saccharomyces cerevisiae mitochondria is a structure-specific DNA helicase
-
DOI 10.1074/jbc.M500354200
-
Kuusk, S., Sedman, T., Jõers, P., and Sedman, J. (2005) Hmi1p from Saccharomyces cerevisiae mitochondria is a structure-specific DNA helicase. J. Biol. Chem. 280, 24322-24329 (Pubitemid 40934514)
-
(2005)
Journal of Biological Chemistry
, vol.280
, Issue.26
, pp. 24322-24329
-
-
Kuusk, S.1
Sedman, T.2
Joers, P.3
Sedman, J.4
-
48
-
-
33646375711
-
High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease
-
Bender, A., Krishnan, K. J., Morris, C. M., Taylor, G. A., Reeve, A. K., Perry, R. H., Jaros, E., Hersheson, J. S., Betts, J., Klopstock, T., Taylor, R. W., and Turnbull, D. M. (2006) High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease. Nat. Genet. 38, 515-517
-
(2006)
Nat. Genet.
, vol.38
, pp. 515-517
-
-
Bender, A.1
Krishnan, K.J.2
Morris, C.M.3
Taylor, G.A.4
Reeve, A.K.5
Perry, R.H.6
Jaros, E.7
Hersheson, J.S.8
Betts, J.9
Klopstock, T.10
Taylor, R.W.11
Turnbull, D.M.12
-
49
-
-
0035957323
-
Muscle-specific mutations accumulate with aging in critical human mtDNA control sites for replication
-
DOI 10.1073/pnas.061013598
-
Wang, Y., Michikawa, Y., Mallidis, C., Bai, Y., Woodhouse, L., Yarasheski, K. E., Miller, C. A., Askanas, V., Engel, W. K., Bhasin, S., and Attardi, G. (2001) Muscle-specific mutations accumulate with aging in critical human mtDNA control sites for replication. Proc. Natl. Acad. Sci. U.S.A. 98, 4022-4027 (Pubitemid 32249891)
-
(2001)
Proceedings of the National Academy of Sciences of the United States of America
, vol.98
, Issue.7
, pp. 4022-4027
-
-
Wang, Y.1
Michikawa, Y.2
Mallidis, C.3
Bai, Y.4
Woodhouse, L.5
Yarasheski, K.E.6
Miller, C.A.7
Askanas, V.8
Engel, W.K.9
Bhasin, S.10
Attardi, G.11
-
50
-
-
2642580016
-
Premature ageing in mice expressing defective mitochondrial DNA polymerase
-
DOI 10.1038/nature02517
-
Trifunovic, A., Wredenberg, A., Falkenberg, M., Spelbrink, J. N., Rovio, A. T., Bruder, C. E., Bohlooly-Y, M., Gidlöf, S., Oldfors, A., Wibom, R., Törnell, J., Jacobs, H. T., and Larsson, N. G. (2004) Premature ageing in mice expressing defective mitochondrial DNA polymerase. Nature 429, 417-423 (Pubitemid 38715133)
-
(2004)
Nature
, vol.429
, Issue.6990
, pp. 417-423
-
-
Trifunovic, A.1
Wredenberg, A.2
Falkenberg, M.3
Spelbrink, J.N.4
Rovio, A.T.5
Bruder, C.E.6
Bohlooly-Y, M.7
Gldlof, S.8
Oldfors, A.9
Wibom, R.10
Tornell, J.11
Jacobs, H.T.12
Larsson, N.-G.13
-
51
-
-
22344456832
-
Medicine: Mitochondrial DNA mutations, oxidative stress, and apoptosis in mammalian aging
-
DOI 10.1126/science.1112125
-
Kujoth, G. C., Hiona, A., Pugh, T. D., Someya, S., Panzer, K., Wohlgemuth, S. E., Hofer, T., Seo, A. Y., Sullivan, R., Jobling, W. A., Morrow, J. D., Van Remmen, H., Sedivy, J. M., Yamasoba, T., Tanokura, M., Weindruch, R., Leeuwenburgh, C., and Prolla, T. A. (2005) Mitochondrial DNA mutations, oxidative stress, and apoptosis in mammalian aging. Science 309, 481-484 (Pubitemid 40994689)
-
(2005)
Science
, vol.309
, Issue.5733
, pp. 481-484
-
-
Kujoth, C.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
-
52
-
-
9444282110
-
Genomic analysis of stationary-phase and exit in Saccharomyces cerevisiae: Gene expression and identification of novel essential genes
-
DOI 10.1091/mbc.E03-11-0856
-
Martinez, M. J., Roy, S., Archuletta, A. B., Wentzell, P. D., Santa Anna-Arriola, S. S., Rodriguez, A. L., Aragon, A. D., Quiñones, G. A., Allen, C., and Werner-Washburne, M. (2004) Genomic analysis of stationary-phase and exit in Saccharomyces cerevisiae. Gene expression and identification of novel essential genes. Mol. Biol. Cell 15, 5295-5305 (Pubitemid 39564725)
-
(2004)
Molecular Biology of the Cell
, vol.15
, Issue.12
, pp. 5295-5305
-
-
Martinez, M.J.1
Roy, S.2
Archuletta, A.B.3
Wentzell, P.D.4
Santa A.-Arriola, S.5
Rodriguez, A.L.6
Aragon, A.D.7
Quinones, G.A.8
Allen, C.9
Werner-Washburne, M.10
-
53
-
-
76149087433
-
A novel POLG gene mutation in 4 children with Alpers-like hepatocerebral syndromes
-
Kurt, B., Jaeken, J., Van Hove, J., Lagae, L., Löfgren, A., Everman, D. B., Jayakar, P., Naini, A., Wierenga, K. J., Van Goethem, G., Copeland, W. C., and DiMauro, S. (2010) A novel POLG gene mutation in 4 children with Alpers-like hepatocerebral syndromes. Arch. Neurol. 67, 239-244
-
(2010)
Arch. Neurol.
, vol.67
, pp. 239-244
-
-
Kurt, B.1
Jaeken, J.2
Van Hove, J.3
Lagae, L.4
Löfgren, A.5
Everman, D.B.6
Jayakar, P.7
Naini, A.8
Wierenga, K.J.9
Van Goethem, G.10
Copeland, W.C.11
DiMauro, S.12
-
54
-
-
0036743518
-
A mutation in the ATP2 gene abrogates the age asymmetry between mother and daughter cells of the yeast Saccharomyces cerevisiae
-
Lai, C. Y., Jaruga, E., Borghouts, C., and Jazwinski, S. M. (2002) A mutation in the ATP2 gene abrogates the age asymmetry between mother and daughter cells of the yeast Saccharomyces cerevisiae. Genetics 162, 73-87
-
(2002)
Genetics
, vol.162
, pp. 73-87
-
-
Lai, C.Y.1
Jaruga, E.2
Borghouts, C.3
Jazwinski, S.M.4
-
55
-
-
2942672611
-
Twinkle and POLG defects enhance age-dependent accumulation of mutations in the control region of mtDNA
-
DOI 10.1093/nar/gkh634
-
Wanrooij, S., Luoma, P., van Goethem, G., van Broeckhoven, C., Suomalainen, A., and Spelbrink, J. N. (2004) Twinkle and POLG defects enhance age-dependent accumulation of mutations in the control region of mtDNA. Nucleic Acids Res. 32, 3053-3064 (Pubitemid 39022996)
-
(2004)
Nucleic Acids Research
, vol.32
, Issue.10
, pp. 3053-3064
-
-
Wanrooij, S.1
Luoma, P.2
Van Goethem, G.3
Van Broeckhoven, C.4
Suomalainen, A.5
Spelbrink, J.N.6
-
56
-
-
17144419321
-
Low frequency of mtDNA point mutations in patients with PEO associated with POLG1 mutations
-
Kollberg, G., Jansson, M., Pérez-Bercoff, A., Melberg, A., Lindberg, C., Holme, E., Moslemi, A. R., and Oldfors, A. (2005) Low frequency of mtDNA point mutations in patients with PEO associated with POLG1 mutations. Eur. J. Hum. Genet. 13, 463-469
-
(2005)
Eur. J. Hum. Genet.
, vol.13
, pp. 463-469
-
-
Kollberg, G.1
Jansson, M.2
Pérez-Bercoff, A.3
Melberg, A.4
Lindberg, C.5
Holme, E.6
Moslemi, A.R.7
Oldfors, A.8
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