-
1
-
-
79959389010
-
AAA+ proteases: ATP-fueled machines of protein destruction
-
Sauer, R.T. and Baker, T.A. (2011) AAA+ proteases: ATP-fueled machines of protein destruction. Annu. Rev. Biochem., 80, 587-612.
-
(2011)
Annu. Rev. Biochem.
, vol.80
, pp. 587-612
-
-
Sauer, R.T.1
Baker, T.A.2
-
2
-
-
71749108967
-
Mitochondrial protein homeostasis: the cooperative roles of chaperones and proteases
-
Voos, W. (2009) Mitochondrial protein homeostasis: the cooperative roles of chaperones and proteases. Res. Microbiol., 160, 718-725.
-
(2009)
Res. Microbiol.
, vol.160
, pp. 718-725
-
-
Voos, W.1
-
3
-
-
84855195754
-
ClpXP, an ATP-powered unfolding and protein-degradation machine
-
Baker, T.A. and Sauer, R.T. (2012) ClpXP, an ATP-powered unfolding and protein-degradation machine. Biochim. Biophys. Acta., 1823, 15-28.
-
(2012)
Biochim. Biophys. Acta.
, vol.1823
, pp. 15-28
-
-
Baker, T.A.1
Sauer, R.T.2
-
4
-
-
0035122947
-
Molecular determinants of complex formation between Clp/Hsp100 ATPases and the ClpP peptidase
-
Kim, Y.I., Levchenko, I., Fraczkowska, K., Woodruff, R.V., Sauer, R.T. and Baker, T.A. (2001) Molecular determinants of complex formation between Clp/Hsp100 ATPases and the ClpP peptidase. Nat. Struct. Biol., 8, 230-233.
-
(2001)
Nat. Struct. Biol.
, vol.8
, pp. 230-233
-
-
Kim, Y.I.1
Levchenko, I.2
Fraczkowska, K.3
Woodruff, R.V.4
Sauer, R.T.5
Baker, T.A.6
-
5
-
-
34347232349
-
Distinctive types of ATP-dependent Clp proteases in cyanobacteria
-
Stanne, T.M., Pojidaeva, E., Andersson, F.I. and Clarke, A.K. (2007) Distinctive types of ATP-dependent Clp proteases in cyanobacteria. J. Biol. Chem., 282, 14394-14402.
-
(2007)
J. Biol. Chem.
, vol.282
, pp. 14394-14402
-
-
Stanne, T.M.1
Pojidaeva, E.2
Andersson, F.I.3
Clarke, A.K.4
-
6
-
-
1542283751
-
Role of the processing pore of the ClpX AAA+ ATPase in the recognition and engagement of specific protein substrates
-
Siddiqui, S.M., Sauer, R.T. and Baker, T.A. (2004) Role of the processing pore of the ClpX AAA+ ATPase in the recognition and engagement of specific protein substrates. Genes Dev., 18, 369-374.
-
(2004)
Genes Dev.
, vol.18
, pp. 369-374
-
-
Siddiqui, S.M.1
Sauer, R.T.2
Baker, T.A.3
-
7
-
-
33646021005
-
Proteomic profiling of ClpXP substrates after DNA damage reveals extensive instability within SOS regulon
-
Neher, S.B., Villen, J., Oakes, E.C., Bakalarski, C.E., Sauer, R.T., Gygi, S.P. and Baker, T.A. (2006) Proteomic profiling of ClpXP substrates after DNA damage reveals extensive instability within SOS regulon. Mol. Cell, 22, 193-204.
-
(2006)
Mol. Cell
, vol.22
, pp. 193-204
-
-
Neher, S.B.1
Villen, J.2
Oakes, E.C.3
Bakalarski, C.E.4
Sauer, R.T.5
Gygi, S.P.6
Baker, T.A.7
-
8
-
-
33750060718
-
Degradation of Escherichia coli RecN aggregates by ClpXP protease and its implications for DNA damage tolerance
-
Nagashima, K., Kubota, Y., Shibata, T., Sakaguchi, C., Shinagawa, H. and Hishida, T. (2006) Degradation of Escherichia coli RecN aggregates by ClpXP protease and its implications for DNA damage tolerance. J. Biol. Chem., 281, 30941-30946.
-
(2006)
J. Biol. Chem.
, vol.281
, pp. 30941-30946
-
-
Nagashima, K.1
Kubota, Y.2
Shibata, T.3
Sakaguchi, C.4
Shinagawa, H.5
Hishida, T.6
-
9
-
-
71749093772
-
Proteolysis of sigmaS (RpoS) and the general stress response in Escherichia coli
-
Hengge, R. (2009) Proteolysis of sigmaS (RpoS) and the general stress response in Escherichia coli. Res. Microbiol., 160, 667-676.
-
(2009)
Res. Microbiol.
, vol.160
, pp. 667-676
-
-
Hengge, R.1
-
10
-
-
4444377383
-
Modulating substrate choice: the SspB adaptor delivers a regulator of the extracytoplasmic-stress response to the AAA+ protease ClpXP for degradation
-
Flynn, J.M., Levchenko, I., Sauer, R.T. and Baker, T.A. (2004) Modulating substrate choice: the SspB adaptor delivers a regulator of the extracytoplasmic-stress response to the AAA+ protease ClpXP for degradation. Genes Dev., 18, 2292-2301.
-
(2004)
Genes Dev.
, vol.18
, pp. 2292-2301
-
-
Flynn, J.M.1
Levchenko, I.2
Sauer, R.T.3
Baker, T.A.4
-
11
-
-
0034876170
-
Rapid degradation of bacteriophage lambda O protein by ClpP/ClpX protease influences the lysis-versus-lysogenization decision of the phage under certain growth conditions of the host cells
-
Czyz, A., Zielke, R. and Wegrzyn, G. (2001) Rapid degradation of bacteriophage lambda O protein by ClpP/ClpX protease influences the lysis-versus-lysogenization decision of the phage under certain growth conditions of the host cells. Arch. Virol., 146, 1487-1498.
-
(2001)
Arch. Virol.
, vol.146
, pp. 1487-1498
-
-
Czyz, A.1
Zielke, R.2
Wegrzyn, G.3
-
12
-
-
0036385946
-
Derepression of bacteriophage mu transposition functions by truncated forms of the immunity repressor
-
O'Handley, D. and Nakai, H. (2002) Derepression of bacteriophage mu transposition functions by truncated forms of the immunity repressor. J. Mol. Biol., 322, 311-324.
-
(2002)
J. Mol. Biol.
, vol.322
, pp. 311-324
-
-
O'Handley, D.1
Nakai, H.2
-
13
-
-
0037009521
-
A mitochondrial specific stress response in mammalian cells
-
Zhao, Q., Wang, J., Levichkin, I.V., Stasinopoulos, S., Ryan, M.T. and Hoogenraad, N.J. (2002) A mitochondrial specific stress response in mammalian cells. EMBO J., 21, 4411-4419.
-
(2002)
EMBO J.
, vol.21
, pp. 4411-4419
-
-
Zhao, Q.1
Wang, J.2
Levichkin, I.V.3
Stasinopoulos, S.4
Ryan, M.T.5
Hoogenraad, N.J.6
-
14
-
-
0031831529
-
Stress induction of the Bacillus subtilis clpP gene encoding a homologue of the proteolytic component of the Clp protease and the involvement of ClpP and ClpX in stress tolerance
-
Gerth, U., Kruger, E., Derre, I., Msadek, T. and Hecker, M. (1998) Stress induction of the Bacillus subtilis clpP gene encoding a homologue of the proteolytic component of the Clp protease and the involvement of ClpP and ClpX in stress tolerance. Mol. Microbiol., 28, 787-802.
-
(1998)
Mol. Microbiol.
, vol.28
, pp. 787-802
-
-
Gerth, U.1
Kruger, E.2
Derre, I.3
Msadek, T.4
Hecker, M.5
-
15
-
-
0036095346
-
Characterization of chloroplast Clp proteins in arabidopsis: localization, tissue specificity and stress responses
-
Zheng, B., Halperin, T., Hruskova-Heidingsfeldova, O., Adam, Z. and Clarke, A.K. (2002) Characterization of chloroplast Clp proteins in arabidopsis: localization, tissue specificity and stress responses. Physiol. Plant, 114, 92-101.
-
(2002)
Physiol. Plant
, vol.114
, pp. 92-101
-
-
Zheng, B.1
Halperin, T.2
Hruskova-Heidingsfeldova, O.3
Adam, Z.4
Clarke, A.K.5
-
16
-
-
84879151902
-
HumanCLPP reverts the longevity phenotype of a fungal ClpP deletion strain
-
Fischer, F., Weil, A., Hamann,A. and Osiewacz, H.D. (2013)HumanCLPP reverts the longevity phenotype of a fungal ClpP deletion strain. Nat. Commun., 4, 1397.
-
(2013)
Nat. Commun.
, vol.4
, pp. 1397
-
-
Fischer, F.1
Weil, A.2
Hamann, A.3
Osiewacz, H.D.4
-
17
-
-
34848861368
-
Clpp mediates activation of a mitochondrial unfolded protein response in C elegans
-
Haynes, C.M., Petrova, K., Benedetti, C., Yang, Y. and Ron, D. (2007) Clpp mediates activation of a mitochondrial unfolded protein response in C elegans. Dev. Cell, 13, 467-480.
-
(2007)
Dev. Cell
, vol.13
, pp. 467-480
-
-
Haynes, C.M.1
Petrova, K.2
Benedetti, C.3
Yang, Y.4
Ron, D.5
-
18
-
-
76849100919
-
The matrix peptide exporter HAF-1 signals a mitochondrial UPR by activating the transcription factor ZC376.7 in C
-
Haynes, C.M., Yang, Y., Blais, S.P., Neubert, T.A. and Ron, D. (2010) The matrix peptide exporter HAF-1 signals a mitochondrial UPR by activating the transcription factor ZC376.7 in C. elegans. Mol. Cell, 37, 529-540.
-
(2010)
elegans. Mol. Cell
, vol.37
, pp. 529-540
-
-
Haynes, C.M.1
Yang, Y.2
Blais, S.P.3
Neubert, T.A.4
Ron, D.5
-
19
-
-
37849048003
-
Discovery of genes activated by the mitochondrial unfolded protein response (mtUPR) and cognate promoter elements
-
Aldridge, J.E., Horibe, T. and Hoogenraad, N.J. (2007) Discovery of genes activated by the mitochondrial unfolded protein response (mtUPR) and cognate promoter elements. PloS ONE, 2, e874.
-
(2007)
PloS ONE
, vol.2
-
-
Aldridge, J.E.1
Horibe, T.2
Hoogenraad, N.J.3
-
20
-
-
37849022851
-
Mitochondrial stress signaling: a pathway unfolds
-
Broadley, S.A. and Hartl, F.U. (2008) Mitochondrial stress signaling: a pathway unfolds. Trends Cell Biol., 18, 1-4.
-
(2008)
Trends Cell Biol.
, vol.18
, pp. 1-4
-
-
Broadley, S.A.1
Hartl, F.U.2
-
21
-
-
0037036431
-
Functional proteolytic complexes of the human mitochondrial ATP-dependent protease, hClpXP
-
Kang, S.G., Ortega, J., Singh, S.K., Wang, N., Huang, N.N., Steven, A.C. and Maurizi, M.R. (2002) Functional proteolytic complexes of the human mitochondrial ATP-dependent protease, hClpXP. J. Biol. Chem., 277, 21095-21102.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 21095-21102
-
-
Kang, S.G.1
Ortega, J.2
Singh, S.K.3
Wang, N.4
Huang, N.N.5
Steven, A.C.6
Maurizi, M.R.7
-
22
-
-
84875944287
-
Perrault syndrome is caused by recessive mutations in CLPP, encoding a mitochondrial ATP-dependent chambered protease
-
Jenkinson, E.M., Rehman, A.U., Walsh, T., Clayton-Smith, J., Lee, K., Morell, R.J., Drummond, M.C., Khan, S.N., Naeem, M.A., Rauf, B. et al. (2013) Perrault syndrome is caused by recessive mutations in CLPP, encoding a mitochondrial ATP-dependent chambered protease. Am. J. Hum. Genet., 92, 605-613.
-
(2013)
Am. J. Hum. Genet.
, vol.92
, pp. 605-613
-
-
Jenkinson, E.M.1
Rehman, A.U.2
Walsh, T.3
Clayton-Smith, J.4
Lee, K.5
Morell, R.J.6
Drummond, M.C.7
Khan, S.N.8
Naeem, M.A.9
Rauf, B.10
-
23
-
-
43049159563
-
Decreased expression of the mitochondrial matrix proteases Lon and clpP in cells from a patient with hereditary spastic paraplegia (SPG13)
-
Hansen, J., Corydon, T.J., Palmfeldt, J., Durr, A., Fontaine, B., Nielsen, M.N., Christensen, J.H., Gregersen, N. and Bross, P. (2008) Decreased expression of the mitochondrial matrix proteases Lon and clpP in cells from a patient with hereditary spastic paraplegia (SPG13). Neuroscience, 153, 474-482.
-
(2008)
Neuroscience
, vol.153
, pp. 474-482
-
-
Hansen, J.1
Corydon, T.J.2
Palmfeldt, J.3
Durr, A.4
Fontaine, B.5
Nielsen, M.N.6
Christensen, J.H.7
Gregersen, N.8
Bross, P.9
-
24
-
-
46149118689
-
The Hsp60-(p.V98I) mutation associated with hereditary spastic paraplegia SPG13 compromises chaperonin function both in vitro and in vivo
-
Bross, P., Naundrup, S., Hansen, J., Nielsen, M.N., Christensen, J.H., Kruhoffer, M., Palmfeldt, J., Corydon, T.J., Gregersen, N., Ang, D. et al. (2008) The Hsp60-(p.V98I) mutation associated with hereditary spastic paraplegia SPG13 compromises chaperonin function both in vitro and in vivo. J. Biol. Chem., 283, 15694-15700.
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 15694-15700
-
-
Bross, P.1
Naundrup, S.2
Hansen, J.3
Nielsen, M.N.4
Christensen, J.H.5
Kruhoffer, M.6
Palmfeldt, J.7
Corydon, T.J.8
Gregersen, N.9
Ang, D.10
-
25
-
-
58849111392
-
Frataxin deficiency causes upregulation of mitochondrial Lon and ClpP proteases and severe loss of mitochondrial Fe-S proteins
-
Guillon, B., Bulteau, A.L., Wattenhofer-Donze, M., Schmucker, S., Friguet, B., Puccio, H., Drapier, J.C. and Bouton, C. (2009) Frataxin deficiency causes upregulation of mitochondrial Lon and ClpP proteases and severe loss of mitochondrial Fe-S proteins. FEBS J., 276, 1036-1047.
-
(2009)
FEBS J.
, vol.276
, pp. 1036-1047
-
-
Guillon, B.1
Bulteau, A.L.2
Wattenhofer-Donze, M.3
Schmucker, S.4
Friguet, B.5
Puccio, H.6
Drapier, J.C.7
Bouton, C.8
-
26
-
-
71749119260
-
Emerging roles of mitochondrial proteases in neurodegeneration
-
Martinelli, P. and Rugarli, E.I. (2010) Emerging roles of mitochondrial proteases in neurodegeneration. Biochim. Biophys. Acta., 1797, 1-10.
-
(2010)
Biochim. Biophys. Acta.
, vol.1797
, pp. 1-10
-
-
Martinelli, P.1
Rugarli, E.I.2
-
27
-
-
84859428688
-
Mitochondrial processing peptidase regulates PINK1 processing, import and Parkin recruitment
-
Greene, A.W., Grenier, K., Aguileta, M.A., Muise, S., Farazifard, R., Haque, M.E., McBride, H.M., Park, D.S. and Fon, E.A. (2012) Mitochondrial processing peptidase regulates PINK1 processing, import and Parkin recruitment. EMBO Rep., 13, 378-385.
-
(2012)
EMBO Rep.
, vol.13
, pp. 378-385
-
-
Greene, A.W.1
Grenier, K.2
Aguileta, M.A.3
Muise, S.4
Farazifard, R.5
Haque, M.E.6
McBride, H.M.7
Park, D.S.8
Fon, E.A.9
-
28
-
-
25444498785
-
Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease
-
Strauss, K.M., Martins, L.M., Plun-Favreau, H., Marx, F.P., Kautzmann, S., Berg, D., Gasser, T., Wszolek, Z., Muller, T., Bornemann, A. et al. (2005) Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease. Hum. Mol. Genet., 14, 2099-2111.
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 2099-2111
-
-
Strauss, K.M.1
Martins, L.M.2
Plun-Favreau, H.3
Marx, F.P.4
Kautzmann, S.5
Berg, D.6
Gasser, T.7
Wszolek, Z.8
Muller, T.9
Bornemann, A.10
-
29
-
-
78649685455
-
Mitochondrialmembranepotential regulatesPINK1import and proteolytic destabilization by PARL
-
Jin, S.M., Lazarou, M., Wang, C., Kane, L.A., Narendra, D.P. and Youle, R.J. (2010) Mitochondrialmembranepotential regulatesPINK1import and proteolytic destabilization by PARL. J. Cell Biol., 191, 933-942.
-
(2010)
J. Cell Biol.
, vol.191
, pp. 933-942
-
-
Jin, S.M.1
Lazarou, M.2
Wang, C.3
Kane, L.A.4
Narendra, D.P.5
Youle, R.J.6
-
30
-
-
77950298030
-
Mutations in the mitochondrial protease geneAFG3L2 cause dominant hereditary ataxia SCA28
-
Di Bella, D., Lazzaro, F., Brusco, A., Plumari, M., Battaglia, G., Pastore, A., Finardi, A., Cagnoli, C., Tempia, F., Frontali, M. et al. (2010) Mutations in the mitochondrial protease geneAFG3L2 cause dominant hereditary ataxia SCA28. Nat. Genet., 42, 313-321.
-
(2010)
Nat. Genet.
, vol.42
, pp. 313-321
-
-
Di Bella, D.1
Lazzaro, F.2
Brusco, A.3
Plumari, M.4
Battaglia, G.5
Pastore, A.6
Finardi, A.7
Cagnoli, C.8
Tempia, F.9
Frontali, M.10
-
31
-
-
78751600248
-
Missense mutations in the AFG3L2 proteolytic domain account for approximately 1.5% of European autosomal dominant cerebellar ataxias
-
Cagnoli, C., Stevanin, G., Brussino, A., Barberis, M., Mancini, C., Margolis, R.L., Holmes, S.E., Nobili, M., Forlani, S., Padovan, S. et al. (2010) Missense mutations in the AFG3L2 proteolytic domain account for approximately 1.5% of European autosomal dominant cerebellar ataxias. Hum. Mutat., 31, 1117-1124.
-
(2010)
Hum. Mutat.
, vol.31
, pp. 1117-1124
-
-
Cagnoli, C.1
Stevanin, G.2
Brussino, A.3
Barberis, M.4
Mancini, C.5
Margolis, R.L.6
Holmes, S.E.7
Nobili, M.8
Forlani, S.9
Padovan, S.10
-
32
-
-
80055087830
-
Whole-exome sequencing identifies homozygous AFG3L2 mutations in a spastic ataxia-neuropathy syndrome linked to mitochondrial m-AAA proteases
-
Pierson, T.M., Adams, D., Bonn, F., Martinelli, P., Cherukuri, P.F., Teer, J.K., Hansen, N.F. and Cruz, P., Mullikin For The Nisc Comparative Sequencing Program, J.C., Blakesley, R.W. et al. (2011) Whole-exome sequencing identifies homozygous AFG3L2 mutations in a spastic ataxia-neuropathy syndrome linked to mitochondrial m-AAA proteases. PLoS Genet., 7, e1002325.
-
(2011)
PLoS Genet.
, vol.7
-
-
Pierson, T.M.1
Adams, D.2
Bonn, F.3
Martinelli, P.4
Cherukuri, P.F.5
Teer, J.K.6
Hansen, N.F.7
Cruz, P.8
Mullikin For The Nisc Comparative Sequencing Program, J.C.9
Blakesley, R.W.10
-
33
-
-
26844484821
-
The m-AAA protease defective in hereditary spastic paraplegia controls ribosome assembly in mitochondria
-
Nolden, M., Ehses, S., Koppen, M., Bernacchia, A., Rugarli, E.I. and Langer, T. (2005) The m-AAA protease defective in hereditary spastic paraplegia controls ribosome assembly in mitochondria. Cell, 123, 277-289.
-
(2005)
Cell
, vol.123
, pp. 277-289
-
-
Nolden, M.1
Ehses, S.2
Koppen, M.3
Bernacchia, A.4
Rugarli, E.I.5
Langer, T.6
-
34
-
-
0033772264
-
OPA1, Encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28
-
Alexander, C., Votruba, M., Pesch, U.E., Thiselton, D.L., Mayer, S., Moore, A., Rodriguez, M., Kellner, U., Leo-Kottler, B., Auburger, G. et al. (2000) OPA1, Encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28. Nat. Genet., 26, 211-215.
-
(2000)
Nat. Genet.
, vol.26
, pp. 211-215
-
-
Alexander, C.1
Votruba, M.2
Pesch, U.E.3
Thiselton, D.L.4
Mayer, S.5
Moore, A.6
Rodriguez, M.7
Kellner, U.8
Leo-Kottler, B.9
Auburger, G.10
-
35
-
-
84862884156
-
Mitochondrial quality control: an integrated network of pathways
-
Fischer, F., Hamann, A. and Osiewacz, H.D. (2012) Mitochondrial quality control: an integrated network of pathways. Trends Biochem. Sci., 37, 284-292.
-
(2012)
Trends Biochem. Sci.
, vol.37
, pp. 284-292
-
-
Fischer, F.1
Hamann, A.2
Osiewacz, H.D.3
-
36
-
-
79955664111
-
Mitochondrial protein quality control during biogenesis and aging
-
Baker, B.M. and Haynes, C.M. (2011) Mitochondrial protein quality control during biogenesis and aging. Trends Biochem. Sci., 36, 254-261.
-
(2011)
Trends Biochem. Sci.
, vol.36
, pp. 254-261
-
-
Baker, B.M.1
Haynes, C.M.2
-
37
-
-
38549101188
-
Quality control of mitochondria: protection against neurodegeneration and ageing
-
Tatsuta, T. and Langer, T. (2008) Quality control of mitochondria: protection against neurodegeneration and ageing. EMBO J., 27, 306-314.
-
(2008)
EMBO J.
, vol.27
, pp. 306-314
-
-
Tatsuta, T.1
Langer, T.2
-
38
-
-
0035202150
-
Animal models for respiratory chain disease
-
Larsson, N.G. and Rustin, P. (2001) Animal models for respiratory chain disease. Trends Mol. Med., 7, 578-581.
-
(2001)
Trends Mol. Med.
, vol.7
, pp. 578-581
-
-
Larsson, N.G.1
Rustin, P.2
-
39
-
-
0034119712
-
Characterization of mouse Clpp protease cDNA, gene, and protein
-
Andresen, B.S., Corydon, T.J., Wilsbech, M., Bross, P., Schroeder, L.D., Hindkjaer, T.F., Bolund, L. and Gregersen, N. (2000) Characterization of mouse Clpp protease cDNA, gene, and protein. Mamm. Genome, 11, 275-280.
-
(2000)
Mamm. Genome
, vol.11
, pp. 275-280
-
-
Andresen, B.S.1
Corydon, T.J.2
Wilsbech, M.3
Bross, P.4
Schroeder, L.D.5
Hindkjaer, T.F.6
Bolund, L.7
Gregersen, N.8
-
40
-
-
0033523120
-
Molecular cloning and characterization of a mouse homolog of bacterial ClpX, a novel mammalian class II member of the Hsp100/Clp chaperone family
-
Santagata, S., Bhattacharyya, D., Wang, F.H., Singha, N., Hodtsev, A. and Spanopoulou, E. (1999) Molecular cloning and characterization of a mouse homolog of bacterial ClpX, a novel mammalian class II member of the Hsp100/Clp chaperone family. J. Biol. Chem., 274, 16311-16319.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 16311-16319
-
-
Santagata, S.1
Bhattacharyya, D.2
Wang, F.H.3
Singha, N.4
Hodtsev, A.5
Spanopoulou, E.6
-
41
-
-
46349103594
-
A mitochondrial protein compendium elucidates complex I disease biology
-
Pagliarini, D.J., Calvo, S.E., Chang, B., Sheth, S.A., Vafai, S.B., Ong, S.E., Walford, G.A., Sugiana, C., Boneh, A., Chen, W.K. et al. (2008) A mitochondrial protein compendium elucidates complex I disease biology. Cell, 134, 112-123.
-
(2008)
Cell
, vol.134
, pp. 112-123
-
-
Pagliarini, D.J.1
Calvo, S.E.2
Chang, B.3
Sheth, S.A.4
Vafai, S.B.5
Ong, S.E.6
Walford, G.A.7
Sugiana, C.8
Boneh, A.9
Chen, W.K.10
-
42
-
-
0033808682
-
Human and mouse mitochondrial orthologs of bacterial ClpX
-
Corydon, T.J., Wilsbech, M., Jespersgaard, C., Andresen, B.S., Borglum, A.D., Pedersen, S., Bolund, L., Gregersen, N. and Bross, P. (2000) Human and mouse mitochondrial orthologs of bacterial ClpX.Mamm.Genome, 11, 899-905.
-
(2000)
Mamm.Genome
, vol.11
, pp. 899-905
-
-
Corydon, T.J.1
Wilsbech, M.2
Jespersgaard, C.3
Andresen, B.S.4
Borglum, A.D.5
Pedersen, S.6
Bolund, L.7
Gregersen, N.8
Bross, P.9
-
43
-
-
79953791495
-
Primary follicular dystrophy with scarring dermatitis in C57BL/6 mouse substrains resembles central centrifugal cicatricial alopecia in humans
-
Sundberg, J.P., Taylor, D., Lorch, G., Miller, J., Silva, K.A., Sundberg, B.A., Roopenian, D., Sperling, L., Ong, D., King, L.E. et al. (2010) Primary follicular dystrophy with scarring dermatitis in C57BL/6 mouse substrains resembles central centrifugal cicatricial alopecia in humans. Vet. Pathol., 48, 513-524.
-
(2010)
Vet. Pathol.
, vol.48
, pp. 513-524
-
-
Sundberg, J.P.1
Taylor, D.2
Lorch, G.3
Miller, J.4
Silva, K.A.5
Sundberg, B.A.6
Roopenian, D.7
Sperling, L.8
Ong, D.9
King, L.E.10
-
45
-
-
33847130937
-
A retrospective study of idiopathic ulcerative dermatitis in mice with a C57BL/6 background
-
Kastenmayer, R.J., Fain, M.A. and Perdue, K.A. (2006) A retrospective study of idiopathic ulcerative dermatitis in mice with a C57BL/6 background. J. Am. Assoc. Lab. Anim. Sci., 45, 8-12.
-
(2006)
J. Am. Assoc. Lab. Anim. Sci.
, vol.45
, pp. 8-12
-
-
Kastenmayer, R.J.1
Fain, M.A.2
Perdue, K.A.3
-
46
-
-
3042764752
-
Perrault syndrome: evidence for progressive nervous system involvement
-
Fiumara, A., Sorge, G., Toscano, A., Parano, E., Pavone, L. and Opitz, J.M. (2004) Perrault syndrome: evidence for progressive nervous system involvement. Am. J. Med. Genet. A, 128A, 246-249.
-
(2004)
Am. J. Med. Genet. A
, vol.128 A
, pp. 246-249
-
-
Fiumara, A.1
Sorge, G.2
Toscano, A.3
Parano, E.4
Pavone, L.5
Opitz, J.M.6
-
47
-
-
0023737599
-
The Perrault syndrome: clinical report and review
-
Nishi, Y., Hamamoto, K., Kajiyama, M. and Kawamura, I. (1988) The Perrault syndrome: clinical report and review. Am. J. Med. Genet., 31, 623-629.
-
(1988)
Am. J. Med. Genet.
, vol.31
, pp. 623-629
-
-
Nishi, Y.1
Hamamoto, K.2
Kajiyama, M.3
Kawamura, I.4
-
48
-
-
0020071940
-
Morphogenesis of the mitochondrial alterations in muscle diseases
-
Shah, A.J., Sahgal, V., Muschler, G., Subramani, V. and Singh, H. (1982) Morphogenesis of the mitochondrial alterations in muscle diseases. J. Neurol. Sci., 55, 25-37.
-
(1982)
J. Neurol. Sci.
, vol.55
, pp. 25-37
-
-
Shah, A.J.1
Sahgal, V.2
Muschler, G.3
Subramani, V.4
Singh, H.5
-
49
-
-
0018619968
-
The Perrault syndrome: autosomal recessive ovarian dysgenesis with facultative, non-sex-limited sensorineural deafness
-
Pallister, P.D. and Opitz, J.M. (1979) The Perrault syndrome: autosomal recessive ovarian dysgenesis with facultative, non-sex-limited sensorineural deafness. Am. J. Med. Genet., 4, 239-246.
-
(1979)
Am. J. Med. Genet.
, vol.4
, pp. 239-246
-
-
Pallister, P.D.1
Opitz, J.M.2
-
50
-
-
0028325310
-
Deafness, sensory neuropathy, and ovarian dysgenesis: a new syndrome or a broader spectrum of Perrault syndrome?
-
Linssen, W.H., Van den Bent, M.J., Brunner, H.G. and Poels, P.J. (1994) Deafness, sensory neuropathy, and ovarian dysgenesis: a new syndrome or a broader spectrum of Perrault syndrome? Am. J. Med. Genet., 51, 81-82.
-
(1994)
Am. J. Med. Genet.
, vol.51
, pp. 81-82
-
-
Linssen, W.H.1
Van den Bent, M.J.2
Brunner, H.G.3
Poels, P.J.4
-
51
-
-
66749163493
-
Parkinson phenotype in aged PINK1-deficient mice is accompanied by progressive mitochondrial dysfunction in absence of neurodegeneration
-
Gispert, S., Ricciardi, F., Kurz, A., Azizov, M., Hoepken, H.H., Becker, D., Voos, W., Leuner, K., Muller, W.E., Kudin, A.P. et al. (2009) Parkinson phenotype in aged PINK1-deficient mice is accompanied by progressive mitochondrial dysfunction in absence of neurodegeneration. PloS ONE, 4, e5777.
-
(2009)
PloS ONE
, vol.4
-
-
Gispert, S.1
Ricciardi, F.2
Kurz, A.3
Azizov, M.4
Hoepken, H.H.5
Becker, D.6
Voos, W.7
Leuner, K.8
Muller, W.E.9
Kudin, A.P.10
-
52
-
-
80052275825
-
Mitochondria in innate immunity
-
Arnoult, D., Soares, F., Tattoli, I. and Girardin, S.E. (2011) Mitochondria in innate immunity. EMBO Rep., 12, 901-910.
-
(2011)
EMBO Rep.
, vol.12
, pp. 901-910
-
-
Arnoult, D.1
Soares, F.2
Tattoli, I.3
Girardin, S.E.4
-
53
-
-
77952885088
-
The role of mitochondria in the mammalian antiviral defense system
-
Scott, I. (2010) The role of mitochondria in the mammalian antiviral defense system. Mitochondrion, 10, 316-320.
-
(2010)
Mitochondrion
, vol.10
, pp. 316-320
-
-
Scott, I.1
-
54
-
-
77953153023
-
The mitochondrion-a Trojan horse that kicks off inflammation?
-
Manfredi, A.A. and Rovere-Querini, P. (2010) The mitochondrion-a Trojan horse that kicks off inflammation? N. Engl. J. Med., 362, 2132-2134.
-
(2010)
N. Engl. J. Med.
, vol.362
, pp. 2132-2134
-
-
Manfredi, A.A.1
Rovere-Querini, P.2
-
55
-
-
77950275298
-
Circulating mitochondrial DAMPs cause inflammatory responses to injury
-
Zhang, Q., Raoof, M., Chen, Y., Sumi, Y., Sursal, T., Junger, W., Brohi, K., Itagaki, K. and Hauser, C.J. (2010) Circulating mitochondrial DAMPs cause inflammatory responses to injury. Nature, 464, 104-107.
-
(2010)
Nature
, vol.464
, pp. 104-107
-
-
Zhang, Q.1
Raoof, M.2
Chen, Y.3
Sumi, Y.4
Sursal, T.5
Junger, W.6
Brohi, K.7
Itagaki, K.8
Hauser, C.J.9
-
56
-
-
84865305875
-
Maintenance of mitochondrial genome distribution by mitochondrial AAA+ protein ClpX
-
Kasashima, K., Sumitani, M. and Endo, H. (2012) Maintenance of mitochondrial genome distribution by mitochondrial AAA+ protein ClpX. Exp. Cell Res., 318, 2335-2343.
-
(2012)
Exp. Cell Res.
, vol.318
, pp. 2335-2343
-
-
Kasashima, K.1
Sumitani, M.2
Endo, H.3
-
57
-
-
77953507107
-
Mitochondrial DNA mutations in disease and aging
-
Wallace, D.C. (2010) Mitochondrial DNA mutations in disease and aging. Environ. Mol. Mutagen., 51, 440-450.
-
(2010)
Environ. Mol. Mutagen.
, vol.51
, pp. 440-450
-
-
Wallace, D.C.1
-
58
-
-
84867417361
-
Bioenergetic origins of complexity and disease
-
Wallace, D.C. (2011) Bioenergetic origins of complexity and disease. Cold Spring Harb. Symp. Quant. Biol., 76, 1-16.
-
(2011)
Cold Spring Harb. Symp. Quant. Biol.
, vol.76
, pp. 1-16
-
-
Wallace, D.C.1
-
59
-
-
84868136478
-
Opa3, a novel regulator of mitochondrial function, controls thermogenesis and abdominal fat mass in a mouse model for Costeff syndrome
-
Wells, T., Davies, J.R., Guschina, I.A., Ball, D.J., Davies, J.S., Davies, V.J., Evans, B.A. and Votruba, M. (2012) Opa3, a novel regulator of mitochondrial function, controls thermogenesis and abdominal fat mass in a mouse model for Costeff syndrome. Hum. Mol. Genet., 21, 4836-4844.
-
(2012)
Hum. Mol. Genet.
, vol.21
, pp. 4836-4844
-
-
Wells, T.1
Davies, J.R.2
Guschina, I.A.3
Ball, D.J.4
Davies, J.S.5
Davies, V.J.6
Evans, B.A.7
Votruba, M.8
-
60
-
-
84862001736
-
Proteomic and metabolomic analyses of mitochondrial complex I-deficient mouse model generated by spontaneous B2 short interspersed nuclear element (SINE) insertion intoNADHdehydrogenase (ubiquinone) Fe-S protein 4 (Ndufs4) gene
-
Leong, D.W., Komen, J.C., Hewitt, C.A., Arnaud, E., McKenzie, M., Phipson, B., Bahlo, M., Laskowski, A., Kinkel, S.A., Davey, G.M. et al. (2012) Proteomic and metabolomic analyses of mitochondrial complex I-deficient mouse model generated by spontaneous B2 short interspersed nuclear element (SINE) insertion intoNADHdehydrogenase (ubiquinone) Fe-S protein 4 (Ndufs4) gene. J. Biol. Chem., 287, 20652-20663.
-
(2012)
J. Biol. Chem.
, vol.287
, pp. 20652-20663
-
-
Leong, D.W.1
Komen, J.C.2
Hewitt, C.A.3
Arnaud, E.4
McKenzie, M.5
Phipson, B.6
Bahlo, M.7
Laskowski, A.8
Kinkel, S.A.9
Davey, G.M.10
-
61
-
-
84861168127
-
Exercise early in life in rats born small does not normalize reductions in skeletal muscle PGC-1alpha in adulthood
-
Laker, R.C., Wlodek, M.E., Wadley, G.D., Gallo, L.A., Meikle, P.J. and McConell, G.K. (2012) Exercise early in life in rats born small does not normalize reductions in skeletal muscle PGC-1alpha in adulthood. Am. J. Physiol. Endocrinol. Metab., 302, E1221-E1230.
-
(2012)
Am. J. Physiol. Endocrinol. Metab.
, vol.302
-
-
Laker, R.C.1
Wlodek, M.E.2
Wadley, G.D.3
Gallo, L.A.4
Meikle, P.J.5
McConell, G.K.6
-
62
-
-
79958718704
-
Mitochondrial superoxide anion (O(2)(-)) inducible 'mev-1' animal models for aging research
-
Ishii, T., Miyazawa, M., Hartman, P.S. and Ishii, N. (2011) Mitochondrial superoxide anion (O(2)(-)) inducible 'mev-1' animal models for aging research. BMB Rep., 44, 298-305.
-
(2011)
BMB Rep.
, vol.44
, pp. 298-305
-
-
Ishii, T.1
Miyazawa, M.2
Hartman, P.S.3
Ishii, N.4
-
63
-
-
79251499574
-
The GRACILE mutation introduced into Bcs1l causes postnatal complex III deficiency: a viable mouse model for mitochondrial hepatopathy
-
Leveen, P., Kotarsky, H., Morgelin, M., Karikoski, R., Elmer, E. and Fellman, V. (2011) The GRACILE mutation introduced into Bcs1l causes postnatal complex III deficiency: a viable mouse model for mitochondrial hepatopathy. Hepatology, 53, 437-447.
-
(2011)
Hepatology
, vol.53
, pp. 437-447
-
-
Leveen, P.1
Kotarsky, H.2
Morgelin, M.3
Karikoski, R.4
Elmer, E.5
Fellman, V.6
-
64
-
-
77956797735
-
Mitochondrial dysfunction and reduced prostaglandin synthesis in skeletal muscle of Group VIB Ca2+-independent phospholipase A2gamma-deficient mice
-
Yoda, E., Hachisu, K., Taketomi, Y., Yoshida, K., Nakamura, M., Ikeda, K., Taguchi, R., Nakatani, Y., Kuwata, H., Murakami, M. et al. (2010) Mitochondrial dysfunction and reduced prostaglandin synthesis in skeletal muscle of Group VIB Ca2+-independent phospholipase A2gamma-deficient mice. J. Lipid Res., 51, 3003-3015.
-
(2010)
J. Lipid Res.
, vol.51
, pp. 3003-3015
-
-
Yoda, E.1
Hachisu, K.2
Taketomi, Y.3
Yoshida, K.4
Nakamura, M.5
Ikeda, K.6
Taguchi, R.7
Nakatani, Y.8
Kuwata, H.9
Murakami, M.10
-
65
-
-
48049104077
-
Progressive loss of mitochondrial DNA in thymidine kinase 2-deficient mice
-
Zhou, X., Solaroli, N., Bjerke, M., Stewart, J.B., Rozell, B., Johansson,M. and Karlsson, A. (2008) Progressive loss of mitochondrial DNA in thymidine kinase 2-deficient mice. Hum. Mol. Genet., 17, 2329-2335.
-
(2008)
Hum. Mol. Genet.
, vol.17
, pp. 2329-2335
-
-
Zhou, X.1
Solaroli, N.2
Bjerke, M.3
Stewart, J.B.4
Rozell, B.5
Johansson, M.6
Karlsson, A.7
-
66
-
-
59649125006
-
Disruption of Supv3L1 damages the skin and causes sarcopenia, loss of fat, and death
-
Paul, E., Cronan, R., Weston, P.J., Boekelheide, K., Sedivy, J.M., Lee, S.Y., Wiest, D.L., Resnick, M.B. and Klysik, J.E. (2009) Disruption of Supv3L1 damages the skin and causes sarcopenia, loss of fat, and death. Mamm. Genome, 20, 92-108.
-
(2009)
Mamm. Genome
, vol.20
, pp. 92-108
-
-
Paul, E.1
Cronan, R.2
Weston, P.J.3
Boekelheide, K.4
Sedivy, J.M.5
Lee, S.Y.6
Wiest, D.L.7
Resnick, M.B.8
Klysik, J.E.9
-
67
-
-
33746509655
-
Role of human mitochondrial Nfs1 in cytosolic iron-sulfur protein biogenesis and iron regulation
-
Biederbick, A., Stehling, O., Rosser, R., Niggemeyer, B., Nakai, Y., Elsasser, H.P. and Lill, R. (2006) Role of human mitochondrial Nfs1 in cytosolic iron-sulfur protein biogenesis and iron regulation. Mol. Cell Biol., 26, 5675-5687.
-
(2006)
Mol. Cell Biol.
, vol.26
, pp. 5675-5687
-
-
Biederbick, A.1
Stehling, O.2
Rosser, R.3
Niggemeyer, B.4
Nakai, Y.5
Elsasser, H.P.6
Lill, R.7
-
68
-
-
0034956656
-
Mousemodels for mitochondrial disease.Am
-
Wallace, D.C. (2001)Mousemodels for mitochondrial disease.Am. J. Med. Genet., 106, 71-93.
-
(2001)
J. Med. Genet.
, vol.106
, pp. 71-93
-
-
Wallace, D.C.1
-
69
-
-
0035887747
-
Strain-dependent high-level expression of a transgene for manganese superoxide dismutase is associated with growth retardation and decreased fertility
-
Raineri, I., Carlson, E.J., Gacayan, R., Carra, S., Oberley, T.D., Huang, T.T. and Epstein, C.J. (2001) Strain-dependent high-level expression of a transgene for manganese superoxide dismutase is associated with growth retardation and decreased fertility. Free Radic. Biol. Med., 31, 1018-1030.
-
(2001)
Free Radic. Biol. Med.
, vol.31
, pp. 1018-1030
-
-
Raineri, I.1
Carlson, E.J.2
Gacayan, R.3
Carra, S.4
Oberley, T.D.5
Huang, T.T.6
Epstein, C.J.7
-
70
-
-
0034987233
-
Lack of mitochondrial trifunctional protein in mice causes neonatal hypoglycemia and sudden death
-
Ibdah, J.A., Paul, H., Zhao, Y., Binford, S., Salleng, K., Cline, M., Matern, D., Bennett, M.J., Rinaldo, P. and Strauss, A.W. (2001) Lack of mitochondrial trifunctional protein in mice causes neonatal hypoglycemia and sudden death. J. Clin. Invest., 107, 1403-1409.
-
(2001)
J. Clin. Invest.
, vol.107
, pp. 1403-1409
-
-
Ibdah, J.A.1
Paul, H.2
Zhao, Y.3
Binford, S.4
Salleng, K.5
Cline, M.6
Matern, D.7
Bennett, M.J.8
Rinaldo, P.9
Strauss, A.W.10
-
71
-
-
0033806989
-
gamma-glutamyltranspeptidase-deficient knockout mice as a model to study the relationship between glutathione status, mitochondrial function, and cellular function
-
Will, Y., Fischer, K.A., Horton, R.A., Kaetzel, R.S., Brown, M.K., Hedstrom, O., Lieberman, M.W. and Reed, D.J. (2000) gamma-glutamyltranspeptidase-deficient knockout mice as a model to study the relationship between glutathione status, mitochondrial function, and cellular function. Hepatology, 32, 740-749.
-
(2000)
Hepatology
, vol.32
, pp. 740-749
-
-
Will, Y.1
Fischer, K.A.2
Horton, R.A.3
Kaetzel, R.S.4
Brown, M.K.5
Hedstrom, O.6
Lieberman, M.W.7
Reed, D.J.8
-
72
-
-
0034062554
-
Mitochondrial oxidative stress in mice lacking the glutathione peroxidase-1 gene
-
Esposito, L.A., Kokoszka, J.E., Waymire, K.G., Cottrell, B., MacGregor, G.R. and Wallace, D.C. (2000) Mitochondrial oxidative stress in mice lacking the glutathione peroxidase-1 gene. Free Radic. Biol. Med., 28, 754-766.
-
(2000)
Free Radic. Biol. Med.
, vol.28
, pp. 754-766
-
-
Esposito, L.A.1
Kokoszka, J.E.2
Waymire, K.G.3
Cottrell, B.4
MacGregor, G.R.5
Wallace, D.C.6
-
73
-
-
0034687797
-
Maternal germ-line transmission of mutant mtDNAs from embryonic stem cell-derived chimeric mice
-
Sligh, J.E., Levy, S.E., Waymire, K.G., Allard, P., Dillehay, D.L., Nusinowitz, S., Heckenlively, J.R., MacGregor, G.R. and Wallace, D.C. (2000) Maternal germ-line transmission of mutant mtDNAs from embryonic stem cell-derived chimeric mice. Proc. Natl Acad. Sci.USA, 97, 14461-14466.
-
(2000)
Proc. Natl Acad. Sci.USA
, vol.97
, pp. 14461-14466
-
-
Sligh, J.E.1
Levy, S.E.2
Waymire, K.G.3
Allard, P.4
Dillehay, D.L.5
Nusinowitz, S.6
Heckenlively, J.R.7
MacGregor, G.R.8
Wallace, D.C.9
-
74
-
-
0032568790
-
Targeted disruption of mouse conventional kinesin heavy chain, kif5B, results in abnormal perinuclear clustering of mitochondria
-
Tanaka, Y., Kanai, Y., Okada, Y., Nonaka, S., Takeda, S., Harada, A. and Hirokawa, N. (1998) Targeted disruption of mouse conventional kinesin heavy chain, kif5B, results in abnormal perinuclear clustering of mitochondria. Cell, 93, 1147-1158.
-
(1998)
Cell
, vol.93
, pp. 1147-1158
-
-
Tanaka, Y.1
Kanai, Y.2
Okada, Y.3
Nonaka, S.4
Takeda, S.5
Harada, A.6
Hirokawa, N.7
-
75
-
-
0031930319
-
Mitochondrial transcription factor A is necessary for mtDNA maintenance and embryogenesis in mice
-
Larsson, N.G., Wang, J., Wilhelmsson, H., Oldfors, A., Rustin, P., Lewandoski, M., Barsh, G.S. and Clayton, D.A. (1998) Mitochondrial transcription factor A is necessary for mtDNA maintenance and embryogenesis in mice. Nat. Genet., 18, 231-236.
-
(1998)
Nat. Genet.
, vol.18
, pp. 231-236
-
-
Larsson, N.G.1
Wang, J.2
Wilhelmsson, H.3
Oldfors, A.4
Rustin, P.5
Lewandoski, M.6
Barsh, G.S.7
Clayton, D.A.8
-
76
-
-
0035914399
-
Immotile sperm and infertility in mice lacking mitochondrial voltage-dependent anion channel type 3
-
Sampson, M.J., Decker, W.K., Beaudet, A.L., Ruitenbeek, W., Armstrong, D., Hicks, M.J. and Craigen, W.J. (2001) Immotile sperm and infertility in mice lacking mitochondrial voltage-dependent anion channel type 3. J. Biol. Chem., 276, 39206-39212.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 39206-39212
-
-
Sampson, M.J.1
Decker, W.K.2
Beaudet, A.L.3
Ruitenbeek, W.4
Armstrong, D.5
Hicks, M.J.6
Craigen, W.J.7
-
77
-
-
77951243014
-
Neurologic dysfunction and male infertility in Drosophila porin mutants: a new model for mitochondrial dysfunction and disease
-
Graham, B.H., Li, Z., Alesii, E.P., Versteken, P., Lee, C., Wang, J. and Craigen, W.J. (2010) Neurologic dysfunction and male infertility in Drosophila porin mutants: a new model for mitochondrial dysfunction and disease. J. Biol. Chem., 285, 11143-11153.
-
(2010)
J. Biol. Chem.
, vol.285
, pp. 11143-11153
-
-
Graham, B.H.1
Li, Z.2
Alesii, E.P.3
Versteken, P.4
Lee, C.5
Wang, J.6
Craigen, W.J.7
-
78
-
-
0036314771
-
Testis-specific cytochrome c-null mice produce functional sperm but undergo early testicular atrophy
-
Narisawa, S., Hecht, N.B., Goldberg, E., Boatright, K.M., Reed, J.C. and Millan, J.L. (2002) Testis-specific cytochrome c-null mice produce functional sperm but undergo early testicular atrophy. Mol. Cell Biol., 22, 5554-5562.
-
(2002)
Mol. Cell Biol.
, vol.22
, pp. 5554-5562
-
-
Narisawa, S.1
Hecht, N.B.2
Goldberg, E.3
Boatright, K.M.4
Reed, J.C.5
Millan, J.L.6
-
79
-
-
70450257662
-
Depletion of selenoprotein GPx4 in spermatocytes causes male infertility in mice
-
Imai, H., Hakkaku, N., Iwamoto, R., Suzuki, J., Suzuki, T., Tajima, Y., Konishi, K., Minami, S., Ichinose, S., Ishizaka, K. et al. (2009) Depletion of selenoprotein GPx4 in spermatocytes causes male infertility in mice. J. Biol. Chem., 284, 32522-32532.
-
(2009)
J. Biol. Chem.
, vol.284
, pp. 32522-32532
-
-
Imai, H.1
Hakkaku, N.2
Iwamoto, R.3
Suzuki, J.4
Suzuki, T.5
Tajima, Y.6
Konishi, K.7
Minami, S.8
Ichinose, S.9
Ishizaka, K.10
-
80
-
-
70349326728
-
Mitochondrial glutathione peroxidase 4 disruption causes male infertility
-
Schneider, M., Forster, H., Boersma, A., Seiler, A., Wehnes, H., Sinowatz, F., Neumuller, C., Deutsch, M.J., Walch, A., Hrabe de Angelis, M. et al. (2009) Mitochondrial glutathione peroxidase 4 disruption causes male infertility. FASEB J., 23, 3233-3242.
-
(2009)
FASEB J.
, vol.23
, pp. 3233-3242
-
-
Schneider, M.1
Forster, H.2
Boersma, A.3
Seiler, A.4
Wehnes, H.5
Sinowatz, F.6
Neumuller, C.7
Deutsch, M.J.8
Walch, A.9
Hrabe de Angelis, M.10
-
81
-
-
71449113005
-
Short form glutathione peroxidase 4 is the essential isoform required for survival and somatic mitochondrial functions
-
Liang, H., Yoo, S.E., Na, R., Walter, C.A., Richardson, A. and Ran, Q. (2009) Short form glutathione peroxidase 4 is the essential isoform required for survival and somatic mitochondrial functions. J. Biol. Chem., 284, 30836-30844.
-
(2009)
J. Biol. Chem.
, vol.284
, pp. 30836-30844
-
-
Liang, H.1
Yoo, S.E.2
Na, R.3
Walter, C.A.4
Richardson, A.5
Ran, Q.6
-
82
-
-
0031440879
-
Developmentally regulated mitochondrial fusion mediated by a conserved, novel, predicted GTPase
-
Hales, K.G. and Fuller, M.T. (1997) Developmentally regulated mitochondrial fusion mediated by a conserved, novel, predicted GTPase. Cell, 90, 121-129.
-
(1997)
Cell
, vol.90
, pp. 121-129
-
-
Hales, K.G.1
Fuller, M.T.2
-
83
-
-
33750059763
-
Mitochondria-related male infertility
-
Nakada, K., Sato, A., Yoshida, K., Morita, T., Tanaka, H., Inoue, S., Yonekawa, H. and Hayashi, J. (2006) Mitochondria-related male infertility. Proc. Natl Acad. Sci. USA, 103, 15148-15153.
-
(2006)
Proc. Natl Acad. Sci. USA
, vol.103
, pp. 15148-15153
-
-
Nakada, K.1
Sato, A.2
Yoshida, K.3
Morita, T.4
Tanaka, H.5
Inoue, S.6
Yonekawa, H.7
Hayashi, J.8
-
84
-
-
41549167023
-
A mutation in the inner mitochondrial membrane peptidase 2-like gene (Immp2l) affects mitochondrial function and impairs fertility in mice
-
Lu, B., Poirier, C., Gaspar, T., Gratzke, C., Harrison, W., Busija, D., Matzuk, M.M., Andersson, K.E., Overbeek, P.A. and Bishop, C.E. (2008) A mutation in the inner mitochondrial membrane peptidase 2-like gene (Immp2l) affects mitochondrial function and impairs fertility in mice. Biol. Reprod., 78, 601-610.
-
(2008)
Biol. Reprod.
, vol.78
, pp. 601-610
-
-
Lu, B.1
Poirier, C.2
Gaspar, T.3
Gratzke, C.4
Harrison, W.5
Busija, D.6
Matzuk, M.M.7
Andersson, K.E.8
Overbeek, P.A.9
Bishop, C.E.10
-
85
-
-
79960327664
-
Mitochondrial peptidaseIMMP2Lmutation causes early onset of age-associated disorders and impairs adult stem cell self-renewal
-
George, S.K., Jiao, Y., Bishop, C.E. and Lu, B. (2011) Mitochondrial peptidaseIMMP2Lmutation causes early onset of age-associated disorders and impairs adult stem cell self-renewal. Aging Cell, 10, 584-594.
-
(2011)
Aging Cell
, vol.10
, pp. 584-594
-
-
George, S.K.1
Jiao, Y.2
Bishop, C.E.3
Lu, B.4
-
86
-
-
79955634426
-
Mutations in mitochondrial histidyl tRNA synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndrome
-
Pierce, S.B., Chisholm, K.M., Lynch, E.D., Lee, M.K., Walsh, T., Opitz, J.M., Li, W., Klevit, R.E. and King, M.C. (2011) Mutations in mitochondrial histidyl tRNA synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndrome. Proc. Natl Acad. Sci. USA, 108, 6543-6548.
-
(2011)
Proc. Natl Acad. Sci. USA
, vol.108
, pp. 6543-6548
-
-
Pierce, S.B.1
Chisholm, K.M.2
Lynch, E.D.3
Lee, M.K.4
Walsh, T.5
Opitz, J.M.6
Li, W.7
Klevit, R.E.8
King, M.C.9
-
87
-
-
77955574455
-
Mutations in the DBP-deficiency protein HSD17B4 cause ovarian dysgenesis, hearing loss, and ataxia of Perrault Syndrome
-
Pierce, S.B., Walsh, T., Chisholm, K.M., Lee, M.K., Thornton, A.M., Fiumara, A., Opitz, J.M., Levy-Lahad, E., Klevit, R.E. and King, M.C. (2010) Mutations in the DBP-deficiency protein HSD17B4 cause ovarian dysgenesis, hearing loss, and ataxia of Perrault Syndrome. Am. J. Hum. Genet., 87, 282-288.
-
(2010)
Am. J. Hum. Genet.
, vol.87
, pp. 282-288
-
-
Pierce, S.B.1
Walsh, T.2
Chisholm, K.M.3
Lee, M.K.4
Thornton, A.M.5
Fiumara, A.6
Opitz, J.M.7
Levy-Lahad, E.8
Klevit, R.E.9
King, M.C.10
-
88
-
-
78751642516
-
The mitochondrial connection in auditory neuropathy
-
Cacace, A.T. and Pinheiro, J.M. (2011) The mitochondrial connection in auditory neuropathy. Audiol. Neurootol., 16, 398-413.
-
(2011)
Audiol. Neurootol.
, vol.16
, pp. 398-413
-
-
Cacace, A.T.1
Pinheiro, J.M.2
-
89
-
-
84868504132
-
A mutation in PNPT1, encoding mitochondrial-RNA-import protein PNPase, causes hereditary hearing loss
-
von Ameln, S., Wang, G., Boulouiz, R., Rutherford, M.A., Smith, G.M., Li, Y., Pogoda, H.M., Nurnberg, G., Stiller, B., Volk, A.E. et al. (2012) A mutation in PNPT1, encoding mitochondrial-RNA-import protein PNPase, causes hereditary hearing loss. Am. J. Hum. Genet., 91, 919-927.
-
(2012)
Am. J. Hum. Genet.
, vol.91
, pp. 919-927
-
-
von Ameln, S.1
Wang, G.2
Boulouiz, R.3
Rutherford, M.A.4
Smith, G.M.5
Li, Y.6
Pogoda, H.M.7
Nurnberg, G.8
Stiller, B.9
Volk, A.E.10
-
90
-
-
0033659701
-
Regulation of mitochondrial DNA copy number during spermatogenesis
-
Rantanen, A. and Larsson, N.G. (2000) Regulation of mitochondrial DNA copy number during spermatogenesis. Hum. Reprod., 15(Suppl. 2), 86-91.
-
(2000)
Hum. Reprod.
, vol.15
, Issue.SUPPL. 2
, pp. 86-91
-
-
Rantanen, A.1
Larsson, N.G.2
-
91
-
-
77950862565
-
Is the mitochondrial cloud the selection machinery for preferentially transmitting wild-type mtDNA between generations? Rewinding Muller's ratchet efficiently
-
Zhou, R.R., Wang, B., Wang, J., Schatten,H. and Zhang, Y.Z. (2010) Is the mitochondrial cloud the selection machinery for preferentially transmitting wild-type mtDNA between generations? Rewinding Muller's ratchet efficiently. Curr. Genet., 56, 101-107.
-
(2010)
Curr. Genet.
, vol.56
, pp. 101-107
-
-
Zhou, R.R.1
Wang, B.2
Wang, J.3
Schatten, H.4
Zhang, Y.Z.5
-
92
-
-
77954035632
-
Mitochondrial DNA depletion syndromes-many genes, common mechanisms
-
Suomalainen, A. and Isohanni, P. (2010) Mitochondrial DNA depletion syndromes-many genes, common mechanisms. Neuromuscul. Disord., 20, 429-437.
-
(2010)
Neuromuscul. Disord.
, vol.20
, pp. 429-437
-
-
Suomalainen, A.1
Isohanni, P.2
-
93
-
-
25144446275
-
Control of bacteriophage mu lysogenic repression
-
Ranquet, C., Toussaint, A., de Jong, H., Maenhaut-Michel, G. and Geiselmann, J. (2005) Control of bacteriophage mu lysogenic repression. J. Mol. Biol., 353, 186-195.
-
(2005)
J. Mol. Biol.
, vol.353
, pp. 186-195
-
-
Ranquet, C.1
Toussaint, A.2
de Jong, H.3
Maenhaut-Michel, G.4
Geiselmann, J.5
-
94
-
-
84855564138
-
New insights into Staphylococcus aureus stress tolerance and virulence regulation from an analysis of the role of the ClpP protease in the strains Newman, COL, and SA564
-
Frees, D., Andersen, J.H., Hemmingsen, L., Koskenniemi, K., Baek, K.T., Muhammed, M.K., Gudeta, D.D., Nyman, T.A., Sukura, A., Varmanen, P. et al. (2012) New insights into Staphylococcus aureus stress tolerance and virulence regulation from an analysis of the role of the ClpP protease in the strains Newman, COL, and SA564. J. Proteome Res., 11, 95-108.
-
(2012)
J. Proteome Res.
, vol.11
, pp. 95-108
-
-
Frees, D.1
Andersen, J.H.2
Hemmingsen, L.3
Koskenniemi, K.4
Baek, K.T.5
Muhammed, M.K.6
Gudeta, D.D.7
Nyman, T.A.8
Sukura, A.9
Varmanen, P.10
-
95
-
-
84859164670
-
Immune and non-immune functions of the immunoproteasome
-
Angeles, A., Fung, G. and Luo, H. (2012) Immune and non-immune functions of the immunoproteasome. Front. Biosci., 17, 1904-1916.
-
(2012)
Front. Biosci.
, vol.17
, pp. 1904-1916
-
-
Angeles, A.1
Fung, G.2
Luo, H.3
-
96
-
-
79953791495
-
Primary follicular dystrophy with scarring dermatitis in C57BL/6 mouse substrains resembles central centrifugal cicatricial alopecia in humans
-
Sundberg, J.P., Taylor, D., Lorch, G., Miller, J., Silva, K.A., Sundberg, B.A., Roopenian, D., Sperling, L., Ong, D., King, L.E. et al. (2011) Primary follicular dystrophy with scarring dermatitis in C57BL/6 mouse substrains resembles central centrifugal cicatricial alopecia in humans. Vet. Pathol., 48, 513-524.
-
(2011)
Vet. Pathol.
, vol.48
, pp. 513-524
-
-
Sundberg, J.P.1
Taylor, D.2
Lorch, G.3
Miller, J.4
Silva, K.A.5
Sundberg, B.A.6
Roopenian, D.7
Sperling, L.8
Ong, D.9
King, L.E.10
-
97
-
-
0032475958
-
Import into mitochondria, folding and retrograde movement of fumarase in yeast
-
Knox, C., Sass, E., Neupert, W. and Pines, O. (1998) Import into mitochondria, folding and retrograde movement of fumarase in yeast. J. Biol. Chem., 273, 25587-25593.
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 25587-25593
-
-
Knox, C.1
Sass, E.2
Neupert, W.3
Pines, O.4
-
98
-
-
79951642032
-
Autophagy proteins regulate innate immune responses by inhibiting the release of mitochondrial DNA mediated by the NALP3 inflammasome
-
Nakahira, K., Haspel, J.A., Rathinam, V.A., Lee, S.J., Dolinay, T., Lam, H.C., Englert, J.A., Rabinovitch, M., Cernadas, M., Kim, H.P. et al. (2011) Autophagy proteins regulate innate immune responses by inhibiting the release of mitochondrial DNA mediated by the NALP3 inflammasome. Nat. Immunol., 12, 222-230.
-
(2011)
Nat. Immunol.
, vol.12
, pp. 222-230
-
-
Nakahira, K.1
Haspel, J.A.2
Rathinam, V.A.3
Lee, S.J.4
Dolinay, T.5
Lam, H.C.6
Englert, J.A.7
Rabinovitch, M.8
Cernadas, M.9
Kim, H.P.10
-
99
-
-
70149096023
-
SCID Dogs: similar transplant potential but distinct intra-uterine growth defects and premature replicative senescence compared with SCID mice
-
Meek, K., Jutkowitz, A., Allen, L., Glover, J., Convery, E., Massa, A., Mullaney, T., Stanley, B., Rosenstein, D., Bailey, S.M. et al. (2009) SCID Dogs: similar transplant potential but distinct intra-uterine growth defects and premature replicative senescence compared with SCID mice. J. Immunol., 183, 2529-2536.
-
(2009)
J. Immunol.
, vol.183
, pp. 2529-2536
-
-
Meek, K.1
Jutkowitz, A.2
Allen, L.3
Glover, J.4
Convery, E.5
Massa, A.6
Mullaney, T.7
Stanley, B.8
Rosenstein, D.9
Bailey, S.M.10
-
100
-
-
34247478549
-
Interleukin 10 regulates inflammatory cytokine synthesis to protect against lipopolysaccharide-induced abortion and fetal growth restriction in mice
-
Robertson, S.A., Care, A.S. and Skinner, R.J. (2007) Interleukin 10 regulates inflammatory cytokine synthesis to protect against lipopolysaccharide-induced abortion and fetal growth restriction in mice. Biol. Reprod., 76, 738-748.
-
(2007)
Biol. Reprod.
, vol.76
, pp. 738-748
-
-
Robertson, S.A.1
Care, A.S.2
Skinner, R.J.3
-
101
-
-
0031775861
-
Infection with cytotoxic T-lymphocyte escape mutants results in increased mortality and growth retardation in mice infected with a neurotropic coronavirus
-
Pewe, L., Xue, S. and Perlman, S. (1998) Infection with cytotoxic T-lymphocyte escape mutants results in increased mortality and growth retardation in mice infected with a neurotropic coronavirus. J. Virol., 72, 5912-5918.
-
(1998)
J. Virol.
, vol.72
, pp. 5912-5918
-
-
Pewe, L.1
Xue, S.2
Perlman, S.3
-
102
-
-
53549114498
-
Large-scale gene trapping in C57BL/6N mouse embryonic stem cells
-
Hansen, G.M., Markesich, D.C., Burnett, M.B., Zhu, Q., Dionne, K.M., Richter, L.J., Finnell, R.H., Sands, A.T., Zambrowicz, B.P. and Abuin, A. (2008) Large-scale gene trapping in C57BL/6N mouse embryonic stem cells. Genome Res., 18, 1670-1679.
-
(2008)
Genome Res.
, vol.18
, pp. 1670-1679
-
-
Hansen, G.M.1
Markesich, D.C.2
Burnett, M.B.3
Zhu, Q.4
Dionne, K.M.5
Richter, L.J.6
Finnell, R.H.7
Sands, A.T.8
Zambrowicz, B.P.9
Abuin, A.10
-
103
-
-
0035710746
-
Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method
-
Livak, K.J. and Schmittgen, T.D. (2001) Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. Methods, 25, 402-408.
-
(2001)
Methods
, vol.25
, pp. 402-408
-
-
Livak, K.J.1
Schmittgen, T.D.2
-
104
-
-
33845976357
-
Proteolytic processing of OPA1 links mitochondrial dysfunction to alterations in mitochondrial morphology
-
Duvezin-Caubet, S., Jagasia, R., Wagener, J., Hofmann, S., Trifunovic, A., Hansson, A., Chomyn, A., Bauer, M.F., Attardi, G., Larsson, N.G. et al. (2006) Proteolytic processing of OPA1 links mitochondrial dysfunction to alterations in mitochondrial morphology. J. Biol. Chem., 281, 37972-37979.
-
(2006)
J. Biol. Chem.
, vol.281
, pp. 37972-37979
-
-
Duvezin-Caubet, S.1
Jagasia, R.2
Wagener, J.3
Hofmann, S.4
Trifunovic, A.5
Hansson, A.6
Chomyn, A.7
Bauer, M.F.8
Attardi, G.9
Larsson, N.G.10
-
105
-
-
28744458859
-
Bioconductor: open software development for computational biology and bioinformatics
-
Gentleman, R.C., Carey, V.J., Bates, D.M., Bolstad, B., Dettling, M., Dudoit, S., Ellis, B., Gautier, L., Ge, Y., Gentry, J. et al. (2004) Bioconductor: open software development for computational biology and bioinformatics. Genome Biol., 5, R80.
-
(2004)
Genome Biol.
, vol.5
-
-
Gentleman, R.C.1
Carey, V.J.2
Bates, D.M.3
Bolstad, B.4
Dettling, M.5
Dudoit, S.6
Ellis, B.7
Gautier, L.8
Ge, Y.9
Gentry, J.10
-
106
-
-
12344280017
-
Summaries of Affymetrix GeneChip probe level data
-
Irizarry, R.A., Bolstad, B.M., Collin, F., Cope, L.M., Hobbs, B. and Speed, T.P. (2003) Summaries of Affymetrix GeneChip probe level data. Nucleic Acids Res., 31, e15.
-
(2003)
Nucleic Acids Res.
, vol.31
-
-
Irizarry, R.A.1
Bolstad, B.M.2
Collin, F.3
Cope, L.M.4
Hobbs, B.5
Speed, T.P.6
-
107
-
-
4544341015
-
Linear models and empirical bayes methods for assessing differential expression in microarray experiments
-
Article3
-
Smyth, G.K. (2004) Linear models and empirical bayes methods for assessing differential expression in microarray experiments. Stat. Appl. Genet. Mol. Biol., 3, Article3.
-
(2004)
Stat. Appl. Genet. Mol. Biol.
, vol.3
-
-
Smyth, G.K.1
-
108
-
-
0001677717
-
Controlling the false discovery rate: a practical and powerful approach to multiple testing
-
Benjamini, Y. and Hochberg, Y. (1995) Controlling the false discovery rate: a practical and powerful approach to multiple testing. J. Royal Stat. Soc. Ser. B, 57, 289-300.
-
(1995)
J. Royal Stat. Soc. Ser. B
, vol.57
, pp. 289-300
-
-
Benjamini, Y.1
Hochberg, Y.2
-
109
-
-
67349168463
-
DNA Extraction procedures meaningfully influence qPCR-based mtDNA copy number determination
-
Guo, W., Jiang, L., Bhasin, S., Khan, S.M. and Swerdlow, R.H. (2009) DNA Extraction procedures meaningfully influence qPCR-based mtDNA copy number determination. Mitochondrion, 9, 261-265.
-
(2009)
Mitochondrion
, vol.9
, pp. 261-265
-
-
Guo, W.1
Jiang, L.2
Bhasin, S.3
Khan, S.M.4
Swerdlow, R.H.5
-
110
-
-
0032698126
-
Impaired learning and motor behavior in heterozygous Pafah1b1 (Lis1) mutant mice
-
Paylor, R., Hirotsune, S., Gambello, M.J., Yuva-Paylor, L., Crawley, J.N. and Wynshaw-Boris, A. (1999) Impaired learning and motor behavior in heterozygous Pafah1b1 (Lis1) mutant mice. Learn. Mem., 6, 521-537.
-
(1999)
Learn. Mem.
, vol.6
, pp. 521-537
-
-
Paylor, R.1
Hirotsune, S.2
Gambello, M.J.3
Yuva-Paylor, L.4
Crawley, J.N.5
Wynshaw-Boris, A.6
-
111
-
-
33747630469
-
K+-independent actions of diazoxide question the role of inner membrane KATP channels in mitochondrial cytoprotective signaling
-
Dröse, S., Brandt, U. and Hanley, P.J. (2006) K+-independent actions of diazoxide question the role of inner membrane KATP channels in mitochondrial cytoprotective signaling. J. Biol. Chem., 281, 23733-23739.
-
(2006)
J. Biol. Chem.
, vol.281
, pp. 23733-23739
-
-
Dröse, S.1
Brandt, U.2
Hanley, P.J.3
-
112
-
-
69249211284
-
Mitochondrial dysfunction: an early event in Alzheimer pathology accumulates with age in AD transgenic mice
-
Hauptmann, S., Scherping, I., Drose, S., Brandt, U., Schulz, K.L., Jendrach, M., Leuner, K., Eckert, A. and Muller, W.E. (2009) Mitochondrial dysfunction: an early event in Alzheimer pathology accumulates with age in AD transgenic mice. Neurobiol. Aging, 30, 1574-1586.
-
(2009)
Neurobiol. Aging
, vol.30
, pp. 1574-1586
-
-
Hauptmann, S.1
Scherping, I.2
Drose, S.3
Brandt, U.4
Schulz, K.L.5
Jendrach, M.6
Leuner, K.7
Eckert, A.8
Muller, W.E.9
-
113
-
-
67650240465
-
Mitochondrial Pathways and Respiratory Control
-
(ed), 1st edn.OROBOROSMiPNet Publications, Innsbruck, Austria
-
Gnaiger, E. (2007) Mitochondrial Pathways and Respiratory Control. In Erich Gnaiger (ed), 1st edn.OROBOROSMiPNet Publications, Innsbruck, Austria, pp. 1-95.
-
(2007)
Erich Gnaiger
, pp. 1-95
-
-
Gnaiger, E.1
-
114
-
-
33750378958
-
Blue native PAGE
-
Wittig, I., Braun, H.P. and Schagger, H. (2006) Blue native PAGE. Nat. Protoc., 1, 418-428.
-
(2006)
Nat. Protoc.
, vol.1
, pp. 418-428
-
-
Wittig, I.1
Braun, H.P.2
Schagger, H.3
-
115
-
-
0030853263
-
Quantification of muscle mitochondrial oxidative phosphorylation enzymes via histochemical staining of blue native polyacrylamide gels
-
Zerbetto, E., Vergani, L. and Dabbeni-Sala, F. (1997) Quantification of muscle mitochondrial oxidative phosphorylation enzymes via histochemical staining of blue native polyacrylamide gels. Electrophoresis, 18, 2059-2064.
-
(1997)
Electrophoresis
, vol.18
, pp. 2059-2064
-
-
Zerbetto, E.1
Vergani, L.2
Dabbeni-Sala, F.3
-
116
-
-
36348941768
-
Functional assays in high-resolution clear native gels to quantify mitochondrial complexes in human biopsies and cell lines
-
Wittig, I., Carrozzo, R., Santorelli, F.M. and Schagger, H. (2007) Functional assays in high-resolution clear native gels to quantify mitochondrial complexes in human biopsies and cell lines. Electrophoresis, 28, 3811-3820.
-
(2007)
Electrophoresis
, vol.28
, pp. 3811-3820
-
-
Wittig, I.1
Carrozzo, R.2
Santorelli, F.M.3
Schagger, H.4
-
117
-
-
79251515158
-
SPICE: exploration and analysis of post-cytometric complex multivariate datasets
-
Roederer, M., Nozzi, J.L. and Nason, M.C. (2011) SPICE: exploration and analysis of post-cytometric complex multivariate datasets. Cytometry A, 79, 167-174.
-
(2011)
Cytometry A
, vol.79
, pp. 167-174
-
-
Roederer, M.1
Nozzi, J.L.2
Nason, M.C.3
|