-
1
-
-
0033965329
-
Higher sedentary energy expenditure in patients with Huntington's disease
-
Pratley, R.E., Salbe, A.D., Ravussin, E. and Caviness, J.N. (2000) Higher sedentary energy expenditure in patients with Huntington's disease. Ann. Neurol., 47, 64-70.
-
(2000)
Ann. Neurol.
, vol.47
, pp. 64-70
-
-
Pratley, R.E.1
Salbe, A.D.2
Ravussin, E.3
Caviness, J.N.4
-
2
-
-
41349100027
-
The metabolic profile of early Huntington's disease-a combined human and transgenic mouse study
-
Goodman, A.O., Murgatroyd, P.R., Medina-Gomez, G., Wood, N.I., Finer, N., Vidal-Puig, A.J., Morton, A.J. and Barker, R.A. (2008) The metabolic profile of early Huntington's disease-a combined human and transgenic mouse study. Exp. Neurol., 210, 691-698.
-
(2008)
Exp. Neurol.
, vol.210
, pp. 691-698
-
-
Goodman, A.O.1
Murgatroyd, P.R.2
Medina-Gomez, G.3
Wood, N.I.4
Finer, N.5
Vidal-Puig, A.J.6
Morton, A.J.7
Barker, R.A.8
-
3
-
-
0037069280
-
Weight loss in early stage of Huntington's disease
-
Djousse, L., Knowlton, B., Cupples, L.A., Marder, K., Shoulson, I. and Myers, R.H. (2002) Weight loss in early stage of Huntington's disease. Neurology, 59, 1325-1330.
-
(2002)
Neurology
, vol.59
, pp. 1325-1330
-
-
Djousse, L.1
Knowlton, B.2
Cupples, L.A.3
Marder, K.4
Shoulson, I.5
Myers, R.H.6
-
4
-
-
0032919205
-
Formation of polyglutamine inclusions in non-CNS tissue
-
Sathasivam, K., Hobbs, C., Turmaine, M., Mangiarini, L., Mahal, A., Bertaux, F., Wanker, E.E., Doherty, P., Davies, S.W. and Bates, G.P. (1999) Formation of polyglutamine inclusions in non-CNS tissue. Hum. Mol. Genet., 8, 813-822.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 813-822
-
-
Sathasivam, K.1
Hobbs, C.2
Turmaine, M.3
Mangiarini, L.4
Mahal, A.5
Bertaux, F.6
Wanker, E.E.7
Doherty, P.8
Davies, S.W.9
Bates, G.P.10
-
5
-
-
10844273236
-
Progressive abnormalities in skeletal muscle and neuromuscular junctions of transgenic mice expressing the Huntington's disease mutation
-
Ribchester, R.R., Thomson, D., Wood, N.I., Hinks, T., Gillingwater, T.H., Wishart, T.M., Court, F.A. and Morton, A.J. (2004) Progressive abnormalities in skeletal muscle and neuromuscular junctions of transgenic mice expressing the Huntington's disease mutation. Eur. J. Neurosci., 20, 3092-3114.
-
(2004)
Eur. J. Neurosci.
, vol.20
, pp. 3092-3114
-
-
Ribchester, R.R.1
Thomson, D.2
Wood, N.I.3
Hinks, T.4
Gillingwater, T.H.5
Wishart, T.M.6
Court, F.A.7
Morton, A.J.8
-
6
-
-
0026475301
-
Serial changes of cerebral glucose metabolism and caudate size in persons at risk for Huntington's disease
-
Grafton, S.T., Mazziotta, J.C., Pahl, J.J., St George-Hyslop, P., Haines, J.L., Gusella, J., Hoffman, J.M., Baxter, L.R. and Phelps, M.E. (1992) Serial changes of cerebral glucose metabolism and caudate size in persons at risk for Huntington's disease. Arch. Neurol., 49, 1161-1167.
-
(1992)
Arch. Neurol.
, vol.49
, pp. 1161-1167
-
-
Grafton, S.T.1
Mazziotta, J.C.2
Pahl, J.J.3
St George-Hyslop, P.4
Haines, J.L.5
Gusella, J.6
Hoffman, J.M.7
Baxter, L.R.8
Phelps, M.E.9
-
7
-
-
0035209380
-
Metabolic network abnormalities in early Huntington's disease: an [(18)F]FDG PET study
-
Feigin, A., Leenders, K.L., Moeller, J.R., Missimer, J., Kuenig, G., Spetsieris, P., Antonini, A. and Eidelberg, D. (2001) Metabolic network abnormalities in early Huntington's disease: an [(18)F]FDG PET study. J. Nucl. Med., 42, 1591-1595.
-
(2001)
J. Nucl. Med.
, vol.42
, pp. 1591-1595
-
-
Feigin, A.1
Leenders, K.L.2
Moeller, J.R.3
Missimer, J.4
Kuenig, G.5
Spetsieris, P.6
Antonini, A.7
Eidelberg, D.8
-
8
-
-
12644252940
-
Striatal glucose metabolism and dopamine D2 receptor binding in asymptomatic gene carriers and patients with Huntington's disease
-
Antonini, A., Leenders, K.L., Spiegel, R., Meier, D., Vontobel, P., Weigell-Weber, M., Sanchez-Pernaute, R., de Yebenez, J.G., Boesiger, P., Weindl, A. et al. (1996) Striatal glucose metabolism and dopamine D2 receptor binding in asymptomatic gene carriers and patients with Huntington's disease. Brain, 119, 2085-2095.
-
(1996)
Brain
, vol.119
, pp. 2085-2095
-
-
Antonini, A.1
Leenders, K.L.2
Spiegel, R.3
Meier, D.4
Vontobel, P.5
Weigell-Weber, M.6
Sanchez-Pernaute, R.7
de Yebenez, J.G.8
Boesiger, P.9
Weindl, A.10
-
9
-
-
0027441163
-
Striatal glucose consumption in chorea-free subjects at risk of Huntington's disease
-
Kuwert, T., Lange, H.W., Boecker, H., Titz, H., Herzog, H., Aulich, A., Wang, B.C., Nayak, U. and Feinendegen, L.E. (1993) Striatal glucose consumption in chorea-free subjects at risk of Huntington's disease. J. Neurol., 241, 31-36.
-
(1993)
J. Neurol.
, vol.241
, pp. 31-36
-
-
Kuwert, T.1
Lange, H.W.2
Boecker, H.3
Titz, H.4
Herzog, H.5
Aulich, A.6
Wang, B.C.7
Nayak, U.8
Feinendegen, L.E.9
-
10
-
-
0027741301
-
Evidence for impairment of energy metabolism in vivo in Huntington's disease using localized 1H NMR spectroscopy
-
Jenkins, B.G., Koroshetz, W.J., Beal, M.F. and Rosen, B.R. (1993) Evidence for impairment of energy metabolism in vivo in Huntington's disease using localized 1H NMR spectroscopy. Neurology, 43, 2689-2695.
-
(1993)
Neurology
, vol.43
, pp. 2689-2695
-
-
Jenkins, B.G.1
Koroshetz, W.J.2
Beal, M.F.3
Rosen, B.R.4
-
11
-
-
0031044805
-
Energy metabolism defects in Huntington's disease and effects of coenzyme Q10
-
Koroshetz, W.J., Jenkins, B.G., Rosen, B.R. and Beal, M.F. (1997) Energy metabolism defects in Huntington's disease and effects of coenzyme Q10. Ann. Neurol., 41, 160-165.
-
(1997)
Ann. Neurol.
, vol.41
, pp. 160-165
-
-
Koroshetz, W.J.1
Jenkins, B.G.2
Rosen, B.R.3
Beal, M.F.4
-
12
-
-
0033914747
-
Abnormal in vivo skeletal muscle energy metabolism in Huntington's disease and dentatorubropallidoluysian atrophy
-
Lodi, R., Schapira, A.H., Manners, D., Styles, P., Wood, N.W., Taylor, D.J. and Warner, T.T. (2000) Abnormal in vivo skeletal muscle energy metabolism in Huntington's disease and dentatorubropallidoluysian atrophy. Ann. Neurol., 48, 72-76.
-
(2000)
Ann. Neurol.
, vol.48
, pp. 72-76
-
-
Lodi, R.1
Schapira, A.H.2
Manners, D.3
Styles, P.4
Wood, N.W.5
Taylor, D.J.6
Warner, T.T.7
-
13
-
-
22844440902
-
Mitochondrial impairment in patients and asymptomatic mutation carriers of Huntington's disease
-
Saft, C., Zange, J., Andrich, J., Muller, K., Lindenberg, K., Landwehrmeyer, B., Vorgerd, M., Kraus, P.H., Przuntek, H. and Schols, L. (2005) Mitochondrial impairment in patients and asymptomatic mutation carriers of Huntington's disease. Mov. Disord., 20, 674-679.
-
(2005)
Mov. Disord.
, vol.20
, pp. 674-679
-
-
Saft, C.1
Zange, J.2
Andrich, J.3
Muller, K.4
Lindenberg, K.5
Landwehrmeyer, B.6
Vorgerd, M.7
Kraus, P.H.8
Przuntek, H.9
Schols, L.10
-
14
-
-
0030919567
-
Oxidative damage and metabolic dysfunction in Huntington's disease: selective vulnerability of the basal ganglia
-
Browne, S.E., Bowling, A.C., MacGarvey, U., Baik, M.J., Berger, S.C., Muqit, M.M., Bird, E.D. and Beal, M.F. (1997) Oxidative damage and metabolic dysfunction in Huntington's disease: selective vulnerability of the basal ganglia. Ann. Neurol., 41, 646-653.
-
(1997)
Ann. Neurol.
, vol.41
, pp. 646-653
-
-
Browne, S.E.1
Bowling, A.C.2
MacGarvey, U.3
Baik, M.J.4
Berger, S.C.5
Muqit, M.M.6
Bird, E.D.7
Beal, M.F.8
-
15
-
-
0029875381
-
Mitochondrial defect in Huntington's disease caudate nucleus
-
Gu, M., Gash, M.T., Mann, V.M., Javoy-Agid, F., Cooper, J.M. and Schapira, A.H. (1996) Mitochondrial defect in Huntington's disease caudate nucleus. Ann. Neurol., 39, 385-389.
-
(1996)
Ann. Neurol.
, vol.39
, pp. 385-389
-
-
Gu, M.1
Gash, M.T.2
Mann, V.M.3
Javoy-Agid, F.4
Cooper, J.M.5
Schapira, A.H.6
-
16
-
-
0032900574
-
Biochemical abnormalities and excitotoxicity in Huntington's disease brain
-
Tabrizi, S.J., Cleeter, M.W., Xuereb, J., Taanman, J.W., Cooper, J.M. and Schapira, A.H. (1999) Biochemical abnormalities and excitotoxicity in Huntington's disease brain. Ann. Neurol., 45, 25-32.
-
(1999)
Ann. Neurol.
, vol.45
, pp. 25-32
-
-
Tabrizi, S.J.1
Cleeter, M.W.2
Xuereb, J.3
Taanman, J.W.4
Cooper, J.M.5
Schapira, A.H.6
-
17
-
-
26444441008
-
HD CAG repeat implicates a dominant property of huntingtin in mitochondrial energy metabolism
-
Seong, I.S., Ivanova, E., Lee, J.M., Choo, Y.S., Fossale, E., Anderson, M., Gusella, J.F., Laramie, J.M., Myers, R.H., Lesort, M. et al. (2005) HD CAG repeat implicates a dominant property of huntingtin in mitochondrial energy metabolism. Hum. Mol. Genet., 14, 2871-2880.
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 2871-2880
-
-
Seong, I.S.1
Ivanova, E.2
Lee, J.M.3
Choo, Y.S.4
Fossale, E.5
Anderson, M.6
Gusella, J.F.7
Laramie, J.M.8
Myers, R.H.9
Lesort, M.10
-
18
-
-
24744444740
-
Mitochondrial respiration and ATP production are significantly impaired in striatal cells expressing mutant huntingtin
-
Milakovic, T. and Johnson, G.V. (2005) Mitochondrial respiration and ATP production are significantly impaired in striatal cells expressing mutant huntingtin. J. Biol. Chem., 280, 30773-30782.
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 30773-30782
-
-
Milakovic, T.1
Johnson, G.V.2
-
19
-
-
0027204154
-
Age-dependent striatal excitotoxic lesions produced by the endogenous mitochondrial inhibitor malonate
-
Beal, M.F., Brouillet, E., Jenkins, B., Henshaw, R., Rosen, B. and Hyman, B.T. (1993) Age-dependent striatal excitotoxic lesions produced by the endogenous mitochondrial inhibitor malonate. J. Neurochem., 61, 1147-1150.
-
(1993)
J. Neurochem.
, vol.61
, pp. 1147-1150
-
-
Beal, M.F.1
Brouillet, E.2
Jenkins, B.3
Henshaw, R.4
Rosen, B.5
Hyman, B.T.6
-
20
-
-
0029118136
-
Chronic mitochondrial energy impairment produces selective striatal degeneration and abnormal choreiform movements in primates
-
Brouillet, E., Hantraye, P., Ferrante, R.J., Dolan, R., Leroy-Willig, A., Kowall, N.W. and Beal, M.F. (1995) Chronic mitochondrial energy impairment produces selective striatal degeneration and abnormal choreiform movements in primates. Proc. Natl Acad. Sci. USA, 92, 7105-7109.
-
(1995)
Proc. Natl Acad. Sci. USA
, vol.92
, pp. 7105-7109
-
-
Brouillet, E.1
Hantraye, P.2
Ferrante, R.J.3
Dolan, R.4
Leroy-Willig, A.5
Kowall, N.W.6
Beal, M.F.7
-
21
-
-
0026357457
-
3-Nitropropionic acid-exogenous animal neurotoxin and possible human striatal toxin
-
Ludolph, A.C., He, F., Spencer, P.S., Hammerstad, J. and Sabri, M. (1991) 3-Nitropropionic acid-exogenous animal neurotoxin and possible human striatal toxin. Can J. Neurol. Sci., 18, 492-498.
-
(1991)
Can J. Neurol. Sci.
, vol.18
, pp. 492-498
-
-
Ludolph, A.C.1
He, F.2
Spencer, P.S.3
Hammerstad, J.4
Sabri, M.5
-
22
-
-
0027448161
-
Age-dependent vulnerability of the striatum to the mitochondrial toxin 3-nitropropionic acid
-
Brouillet, E., Jenkins, B.G., Hyman, B.T., Ferrante, R.J., Kowall, N.W., Srivastava, R., Roy, D.S., Rosen, B.R. and Beal, M.F. (1993) Age-dependent vulnerability of the striatum to the mitochondrial toxin 3-nitropropionic acid. J. Neurochem., 60, 356-359.
-
(1993)
J. Neurochem.
, vol.60
, pp. 356-359
-
-
Brouillet, E.1
Jenkins, B.G.2
Hyman, B.T.3
Ferrante, R.J.4
Kowall, N.W.5
Srivastava, R.6
Roy, D.S.7
Rosen, B.R.8
Beal, M.F.9
-
23
-
-
40849147435
-
N-terminal mutant huntingtin associates with mitochondria and impairs mitochondrial trafficking
-
Orr, A.L., Li, S., Wang, C.E., Li, H., Wang, J., Rong, J., Xu, X., Mastroberardino, P.G., Greenamyre, J.T. and Li, X.J. (2008) N-terminal mutant huntingtin associates with mitochondria and impairs mitochondrial trafficking. J. Neurosci., 28, 2783-2792.
-
(2008)
J. Neurosci.
, vol.28
, pp. 2783-2792
-
-
Orr, A.L.1
Li, S.2
Wang, C.E.3
Li, H.4
Wang, J.5
Rong, J.6
Xu, X.7
Mastroberardino, P.G.8
Greenamyre, J.T.9
Li, X.J.10
-
24
-
-
67349247037
-
Mitochondrial structural and functional dynamics in Huntington's disease
-
Reddy, P.H., Mao, P. and Manczak, M. (2009) Mitochondrial structural and functional dynamics in Huntington's disease. Brain. Res. Rev., 61, 33-48.
-
(2009)
Brain. Res. Rev.
, vol.61
, pp. 33-48
-
-
Reddy, P.H.1
Mao, P.2
Manczak, M.3
-
25
-
-
3543141113
-
Mutant huntingtin directly increases susceptibility of mitochondria to the calcium-induced permeability transition and cytochrome c release
-
Choo, Y.S., Johnson, G.V., MacDonald, M., Detloff, P.J. and Lesort, M. (2004) Mutant huntingtin directly increases susceptibility of mitochondria to the calcium-induced permeability transition and cytochrome c release. Hum. Mol. Genet., 13, 1407-1420.
-
(2004)
Hum. Mol. Genet.
, vol.13
, pp. 1407-1420
-
-
Choo, Y.S.1
Johnson, G.V.2
MacDonald, M.3
Detloff, P.J.4
Lesort, M.5
-
26
-
-
0036327065
-
Early mitochondrial calcium defects in Huntington's disease are a direct effect of polyglutamines
-
Panov, A.V., Gutekunst, C.A., Leavitt, B.R., Hayden, M.R., Burke, J.R., Strittmatter, W.J. and Greenamyre, J.T. (2002) Early mitochondrial calcium defects in Huntington's disease are a direct effect of polyglutamines. Nat. Neurosci., 5, 731-736.
-
(2002)
Nat. Neurosci.
, vol.5
, pp. 731-736
-
-
Panov, A.V.1
Gutekunst, C.A.2
Leavitt, B.R.3
Hayden, M.R.4
Burke, J.R.5
Strittmatter, W.J.6
Greenamyre, J.T.7
-
27
-
-
33846540080
-
The first 17 amino acids of Huntingtin modulate its sub-cellular localization, aggregation and effects on calcium homeostasis
-
Rockabrand, E., Slepko, N., Pantalone, A., Nukala, V.N., Kazantsev, A., Marsh, J.L., Sullivan, P.G., Steffan, J.S., Sensi, S.L. and Thompson, L.M. (2007) The first 17 amino acids of Huntingtin modulate its sub-cellular localization, aggregation and effects on calcium homeostasis. Hum. Mol. Genet., 16, 61-77.
-
(2007)
Hum. Mol. Genet.
, vol.16
, pp. 61-77
-
-
Rockabrand, E.1
Slepko, N.2
Pantalone, A.3
Nukala, V.N.4
Kazantsev, A.5
Marsh, J.L.6
Sullivan, P.G.7
Steffan, J.S.8
Sensi, S.L.9
Thompson, L.M.10
-
28
-
-
35348877164
-
Transcriptional signatures in Huntington's disease
-
Cha, J.H. (2007) Transcriptional signatures in Huntington's disease. Prog. Neurobiol., 83, 228-248.
-
(2007)
Prog. Neurobiol.
, vol.83
, pp. 228-248
-
-
Cha, J.H.1
-
29
-
-
0037408279
-
Transcriptional abnormalities in Huntington disease
-
Sugars, K.L. and Rubinsztein, D.C. (2003) Transcriptional abnormalities in Huntington disease. Trends Genet., 19, 233-238.
-
(2003)
Trends Genet.
, vol.19
, pp. 233-238
-
-
Sugars, K.L.1
Rubinsztein, D.C.2
-
30
-
-
0037150687
-
Sp1 and TAFII130 transcriptional activity disrupted in early Huntington's disease
-
Dunah, A.W., Jeong, H., Griffin, A., Kim, Y.M., Standaert, D.G., Hersch, S.M., Mouradian, M.M., Young, A.B., Tanese, N. and Krainc, D. (2002) Sp1 and TAFII130 transcriptional activity disrupted in early Huntington's disease. Science, 296, 2238-2243.
-
(2002)
Science
, vol.296
, pp. 2238-2243
-
-
Dunah, A.W.1
Jeong, H.2
Griffin, A.3
Kim, Y.M.4
Standaert, D.G.5
Hersch, S.M.6
Mouradian, M.M.7
Young, A.B.8
Tanese, N.9
Krainc, D.10
-
31
-
-
0035937523
-
Interference by huntingtin and atrophin-1 with cbp-mediated transcription leading to cellular toxicity
-
Nucifora, F.C. Jr, Sasaki, M., Peters, M.F., Huang, H., Cooper, J.K., Yamada, M., Takahashi, H., Tsuji, S., Troncoso, J., Dawson, V.L. et al. (2001) Interference by huntingtin and atrophin-1 with cbp-mediated transcription leading to cellular toxicity. Science, 291, 2423-2428.
-
(2001)
Science
, vol.291
, pp. 2423-2428
-
-
Nucifora F.C., Jr.1
Sasaki, M.2
Peters, M.F.3
Huang, H.4
Cooper, J.K.5
Yamada, M.6
Takahashi, H.7
Tsuji, S.8
Troncoso, J.9
Dawson, V.L.10
-
32
-
-
12944263711
-
The Huntington's disease protein interacts with p53 and CREB-binding protein and represses transcription
-
Steffan, J.S., Kazantsev, A., Spasic-Boskovic, O., Greenwald, M., Zhu, Y.Z., Gohler, H., Wanker, E.E., Bates, G.P., Housman, D.E. and Thompson, L.M. (2000) The Huntington's disease protein interacts with p53 and CREB-binding protein and represses transcription. Proc. Natl Acad. Sci. USA, 97, 6763-6768.
-
(2000)
Proc. Natl Acad. Sci. USA
, vol.97
, pp. 6763-6768
-
-
Steffan, J.S.1
Kazantsev, A.2
Spasic-Boskovic, O.3
Greenwald, M.4
Zhu, Y.Z.5
Gohler, H.6
Wanker, E.E.7
Bates, G.P.8
Housman, D.E.9
Thompson, L.M.10
-
33
-
-
21144446106
-
PGC-1alpha deficiency causes multi-system energy metabolic derangements: muscle dysfunction, abnormal weight control and hepatic steatosis
-
Leone, T.C., Lehman, J.J., Finck, B.N., Schaeffer, P.J., Wende, A.R., Boudina, S., Courtois, M., Wozniak, D.F., Sambandam, N., Bernal-Mizrachi, C. et al. (2005) PGC-1alpha deficiency causes multi-system energy metabolic derangements: muscle dysfunction, abnormal weight control and hepatic steatosis. PLoS. Biol., 3, e101.
-
(2005)
PLoS. Biol.
, vol.3
-
-
Leone, T.C.1
Lehman, J.J.2
Finck, B.N.3
Schaeffer, P.J.4
Wende, A.R.5
Boudina, S.6
Courtois, M.7
Wozniak, D.F.8
Sambandam, N.9
Bernal-Mizrachi, C.10
-
34
-
-
5344252327
-
Defects in adaptive energy metabolism with CNS-linked hyperactivity in PGC-1alpha null mice
-
Lin, J., Wu, P.H., Tarr, P.T., Lindenberg, K.S., St-Pierre, J., Zhang, C.Y., Mootha, V.K., Jager, S., Vianna, C.R., Reznick, R.M. et al. (2004) Defects in adaptive energy metabolism with CNS-linked hyperactivity in PGC-1alpha null mice. Cell, 119, 121-135.
-
(2004)
Cell
, vol.119
, pp. 121-135
-
-
Lin, J.1
Wu, P.H.2
Tarr, P.T.3
Lindenberg, K.S.4
St-Pierre, J.5
Zhang, C.Y.6
Mootha, V.K.7
Jager, S.8
Vianna, C.R.9
Reznick, R.M.10
-
35
-
-
0037326196
-
Peroxisome proliferator-activated receptor-gamma coactivator 1 alpha (PGC-1 alpha): transcriptional coactivator and metabolic regulator
-
Puigserver, P. and Spiegelman, B.M. (2003) Peroxisome proliferator-activated receptor-gamma coactivator 1 alpha (PGC-1 alpha): transcriptional coactivator and metabolic regulator. Endocr. Rev., 24, 78-90.
-
(2003)
Endocr. Rev.
, vol.24
, pp. 78-90
-
-
Puigserver, P.1
Spiegelman, B.M.2
-
36
-
-
0032549811
-
A cold-inducible coactivator of nuclear receptors linked to adaptive thermogenesis
-
Puigserver, P., Wu, Z., Park, C.W., Graves, R., Wright, M. and Spiegelman, B.M. (1998) A cold-inducible coactivator of nuclear receptors linked to adaptive thermogenesis. Cell, 92, 829-839.
-
(1998)
Cell
, vol.92
, pp. 829-839
-
-
Puigserver, P.1
Wu, Z.2
Park, C.W.3
Graves, R.4
Wright, M.5
Spiegelman, B.M.6
-
37
-
-
24144463983
-
Metabolic control through the PGC-1 family of transcription coactivators
-
Lin, J., Handschin, C. and Spiegelman, B.M. (2005) Metabolic control through the PGC-1 family of transcription coactivators. Cell. Metab., 1, 361-370.
-
(2005)
Cell. Metab.
, vol.1
, pp. 361-370
-
-
Lin, J.1
Handschin, C.2
Spiegelman, B.M.3
-
38
-
-
1542373685
-
Transcriptional regulatory circuits controlling mitochondrial biogenesis and function
-
Kelly, D.P. and Scarpulla, R.C. (2004) Transcriptional regulatory circuits controlling mitochondrial biogenesis and function. Genes Dev., 18, 357-368.
-
(2004)
Genes Dev.
, vol.18
, pp. 357-368
-
-
Kelly, D.P.1
Scarpulla, R.C.2
-
39
-
-
69249084890
-
PGC-1{alpha} and PGC-1{beta} regulate mitochondrial density in neurons
-
Wareski, P., Vaarmann, A., Choubey, V., Safiulina, D., Liiv, J., Kuum, M. and Kaasik, A. (2009) PGC-1{alpha} and PGC-1{beta} regulate mitochondrial density in neurons. J. Biol. Chem., 284, 21379-21385.
-
(2009)
J. Biol. Chem.
, vol.284
, pp. 21379-21385
-
-
Wareski, P.1
Vaarmann, A.2
Choubey, V.3
Safiulina, D.4
Liiv, J.5
Kuum, M.6
Kaasik, A.7
-
40
-
-
33845399894
-
Resveratrol improves mitochondrial function and protects against metabolic disease by activating SIRT1 and PGC-1alpha
-
Lagouge, M., Argmann, C., Gerhart-Hines, Z., Meziane, H., Lerin, C., Daussin, F., Messadeq, N., Milne, J., Lambert, P., Elliott, P. et al. (2006) Resveratrol improves mitochondrial function and protects against metabolic disease by activating SIRT1 and PGC-1alpha. Cell, 127, 1109-1122.
-
(2006)
Cell
, vol.127
, pp. 1109-1122
-
-
Lagouge, M.1
Argmann, C.2
Gerhart-Hines, Z.3
Meziane, H.4
Lerin, C.5
Daussin, F.6
Messadeq, N.7
Milne, J.8
Lambert, P.9
Elliott, P.10
-
41
-
-
33751072349
-
Resveratrol improves health and survival of mice on a high-calorie diet
-
Baur, J.A., Pearson, K.J., Price, N.L., Jamieson, H.A., Lerin, C., Kalra, A., Prabhu, V.V., Allard, J.S., Lopez-Lluch, G., Lewis, K. et al. (2006) Resveratrol improves health and survival of mice on a high-calorie diet. Nature, 444, 337-342.
-
(2006)
Nature
, vol.444
, pp. 337-342
-
-
Baur, J.A.1
Pearson, K.J.2
Price, N.L.3
Jamieson, H.A.4
Lerin, C.5
Kalra, A.6
Prabhu, V.V.7
Allard, J.S.8
Lopez-Lluch, G.9
Lewis, K.10
-
42
-
-
48349144852
-
Resveratrol delays age-related deterioration and mimics transcriptional aspects of dietary restriction without extending life span
-
Pearson, K.J., Baur, J.A., Lewis, K.N., Peshkin, L., Price, N.L., Labinskyy, N., Swindell, W.R., Kamara, D., Minor, R.K., Perez, E. et al. (2008) Resveratrol delays age-related deterioration and mimics transcriptional aspects of dietary restriction without extending life span. Cell Metab., 8, 157-168.
-
(2008)
Cell Metab.
, vol.8
, pp. 157-168
-
-
Pearson, K.J.1
Baur, J.A.2
Lewis, K.N.3
Peshkin, L.4
Price, N.L.5
Labinskyy, N.6
Swindell, W.R.7
Kamara, D.8
Minor, R.K.9
Perez, E.10
-
43
-
-
33749042331
-
Transcriptional repression of PGC-1alpha by mutant huntingtin leads to mitochondrial dysfunction and neurodegeneration
-
Cui, L., Jeong, H., Borovecki, F., Parkhurst, C.N., Tanese, N. and Krainc, D. (2006) Transcriptional repression of PGC-1alpha by mutant huntingtin leads to mitochondrial dysfunction and neurodegeneration. Cell, 127, 59-69.
-
(2006)
Cell
, vol.127
, pp. 59-69
-
-
Cui, L.1
Jeong, H.2
Borovecki, F.3
Parkhurst, C.N.4
Tanese, N.5
Krainc, D.6
-
44
-
-
33750437278
-
Thermoregulatory and metabolic defects in Huntington's disease transgenic mice implicate PGC-1alpha in Huntington's disease neurodegeneration
-
Weydt, P., Pineda, V.V., Torrence, A.E., Libby, R.T., Satterfield, T.F., Lazarowski, E.R., Gilbert, M.L., Morton, G.J., Bammler, T.K., Strand, A.D. et al. (2006) Thermoregulatory and metabolic defects in Huntington's disease transgenic mice implicate PGC-1alpha in Huntington's disease neurodegeneration. Cell Metab., 4, 349-362.
-
(2006)
Cell Metab.
, vol.4
, pp. 349-362
-
-
Weydt, P.1
Pineda, V.V.2
Torrence, A.E.3
Libby, R.T.4
Satterfield, T.F.5
Lazarowski, E.R.6
Gilbert, M.L.7
Morton, G.J.8
Bammler, T.K.9
Strand, A.D.10
-
45
-
-
67650061723
-
Impaired PGC-1alpha function in muscle in Huntington's disease
-
Chaturvedi, R.K., Adhihetty, P., Shukla, S., Hennessy, T., Calingasan, N., Yang, L., Starkov, A., Kiaei, M., Cannella, M., Sassone, J. et al. (2009) Impaired PGC-1alpha function in muscle in Huntington's disease. Hum. Mol. Genet., 18, 3048-3065.
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 3048-3065
-
-
Chaturvedi, R.K.1
Adhihetty, P.2
Shukla, S.3
Hennessy, T.4
Calingasan, N.5
Yang, L.6
Starkov, A.7
Kiaei, M.8
Cannella, M.9
Sassone, J.10
-
46
-
-
61849093278
-
Adipose tissue dysfunction tracks disease progression in two Huntington's disease mouse models
-
Phan, J., Hickey, M.A., Zhang, P., Chesselet, M.F. and Reue, K. (2009) Adipose tissue dysfunction tracks disease progression in two Huntington's disease mouse models. Hum. Mol. Genet., 18, 1006-1016.
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 1006-1016
-
-
Phan, J.1
Hickey, M.A.2
Zhang, P.3
Chesselet, M.F.4
Reue, K.5
-
47
-
-
71549143207
-
Balance between synaptic versus extrasynaptic NMDA receptor activity influences inclusions and neurotoxicity of mutant huntingtin
-
Okamoto, S., Pouladi, M.A., Talantova, M., Yao, D., Xia, P., Ehrnhoefer, D.E., Zaidi, R., Clemente, A., Kaul, M., Graham, R.K. et al. (2009) Balance between synaptic versus extrasynaptic NMDA receptor activity influences inclusions and neurotoxicity of mutant huntingtin. Nat. Med., 15, 1407-1413.
-
(2009)
Nat. Med.
, vol.15
, pp. 1407-1413
-
-
Okamoto, S.1
Pouladi, M.A.2
Talantova, M.3
Yao, D.4
Xia, P.5
Ehrnhoefer, D.E.6
Zaidi, R.7
Clemente, A.8
Kaul, M.9
Graham, R.K.10
-
48
-
-
72949093579
-
Slowed progression in models of Huntington disease by adipose stem cell transplantation
-
Lee, S.T., Chu, K., Jung, K.H., Im, W.S., Park, J.E., Lim, H.C., Won, C.H., Shin, S.H., Lee, S.K., Kim, M. et al. (2009) Slowed progression in models of Huntington disease by adipose stem cell transplantation. Ann. Neurol., 66, 671-681.
-
(2009)
Ann. Neurol.
, vol.66
, pp. 671-681
-
-
Lee, S.T.1
Chu, K.2
Jung, K.H.3
Im, W.S.4
Park, J.E.5
Lim, H.C.6
Won, C.H.7
Shin, S.H.8
Lee, S.K.9
Kim, M.10
-
49
-
-
0037058977
-
AMP kinase is required for mitochondrial biogenesis in skeletal muscle in response to chronic energy deprivation
-
Zong, H., Ren, J.M., Young, L.H., Pypaert, M., Mu, J., Birnbaum, M.J. and Shulman, G.I. (2002) AMP kinase is required for mitochondrial biogenesis in skeletal muscle in response to chronic energy deprivation. Proc. Natl Acad. Sci. USA, 99, 15983-15987.
-
(2002)
Proc. Natl Acad. Sci. USA
, vol.99
, pp. 15983-15987
-
-
Zong, H.1
Ren, J.M.2
Young, L.H.3
Pypaert, M.4
Mu, J.5
Birnbaum, M.J.6
Shulman, G.I.7
-
50
-
-
33846580517
-
Aging-associated reductions in AMP-activated protein kinase activity and mitochondrial biogenesis
-
Reznick, R.M., Zong, H., Li, J., Morino, K., Moore, I.K., Yu, H.J., Liu, Z.X., Dong, J., Mustard, K.J., Hawley, S.A. et al. (2007) Aging-associated reductions in AMP-activated protein kinase activity and mitochondrial biogenesis. Cell Metab., 5, 151-156.
-
(2007)
Cell Metab.
, vol.5
, pp. 151-156
-
-
Reznick, R.M.1
Zong, H.2
Li, J.3
Morino, K.4
Moore, I.K.5
Yu, H.J.6
Liu, Z.X.7
Dong, J.8
Mustard, K.J.9
Hawley, S.A.10
-
51
-
-
66849084057
-
Muscle-specific differences in the response of mitochondrial proteins to beta-GPA feeding: an evaluation of potential mechanisms
-
Williams, D.B., Sutherland, L.N., Bomhof, M.R., Basaraba, S.A., Thrush, A.B., Dyck, D.J., Field, C.J. and Wright, D.C. (2009) Muscle-specific differences in the response of mitochondrial proteins to beta-GPA feeding: an evaluation of potential mechanisms. Am. J. Physiol. Endocrinol. Metab., 296, E1400-E1408.
-
(2009)
Am. J. Physiol. Endocrinol. Metab.
, vol.296
-
-
Williams, D.B.1
Sutherland, L.N.2
Bomhof, M.R.3
Basaraba, S.A.4
Thrush, A.B.5
Dyck, D.J.6
Field, C.J.7
Wright, D.C.8
-
52
-
-
34547545892
-
AMP-activated protein kinase (AMPK) action in skeletal muscle via direct phosphorylation of PGC-1alpha
-
Jager, S., Handschin, C., St-Pierre, J. and Spiegelman, B.M. (2007) AMP-activated protein kinase (AMPK) action in skeletal muscle via direct phosphorylation of PGC-1alpha. Proc. Natl Acad. Sci. USA, 104, 12017-12022.
-
(2007)
Proc. Natl Acad. Sci. USA
, vol.104
, pp. 12017-12022
-
-
Jager, S.1
Handschin, C.2
St-Pierre, J.3
Spiegelman, B.M.4
-
53
-
-
4344636957
-
Nuclear-targeting of mutant huntingtin fragments produces Huntington's disease-like phenotypes in transgenic mice
-
Schilling, G., Savonenko, A.V., Klevytska, A., Morton, J.L., Tucker, S.M., Poirier, M., Gale, A., Chan, N., Gonzales, V., Slunt, H.H. et al. (2004) Nuclear-targeting of mutant huntingtin fragments produces Huntington's disease-like phenotypes in transgenic mice. Hum. Mol. Genet., 13, 1599-1610.
-
(2004)
Hum. Mol. Genet.
, vol.13
, pp. 1599-1610
-
-
Schilling, G.1
Savonenko, A.V.2
Klevytska, A.3
Morton, J.L.4
Tucker, S.M.5
Poirier, M.6
Gale, A.7
Chan, N.8
Gonzales, V.9
Slunt, H.H.10
-
54
-
-
0015972081
-
Experimental depletion of creatine and phosphocreatine from skeletal muscle
-
Fitch, C.D., Jellinek, M. and Mueller, E.J. (1974) Experimental depletion of creatine and phosphocreatine from skeletal muscle. J. Biol. Chem., 249, 1060-1063.
-
(1974)
J. Biol. Chem.
, vol.249
, pp. 1060-1063
-
-
Fitch, C.D.1
Jellinek, M.2
Mueller, E.J.3
-
55
-
-
0022375423
-
Biochemical adaptation in the skeletal muscle of rats depleted of creatine with the substrate analogue beta-guanidinopropionic acid
-
Shoubridge, E.A., Challiss, R.A., Hayes, D.J. and Radda, G.K. (1985) Biochemical adaptation in the skeletal muscle of rats depleted of creatine with the substrate analogue beta-guanidinopropionic acid. Biochem. J., 232, 125-131.
-
(1985)
Biochem. J.
, vol.232
, pp. 125-131
-
-
Shoubridge, E.A.1
Challiss, R.A.2
Hayes, D.J.3
Radda, G.K.4
-
56
-
-
0037101835
-
Dysregulation of gene expression in the R6/2 model of polyglutamine disease: parallel changes in muscle and brain
-
Luthi-Carter, R., Hanson, S.A., Strand, A.D., Bergstrom, D.A., Chun, W., Peters, N.L., Woods, A.M., Chan, E.Y., Kooperberg, C., Krainc, D. et al. (2002) Dysregulation of gene expression in the R6/2 model of polyglutamine disease: parallel changes in muscle and brain. Hum. Mol. Genet., 11, 1911-1926.
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 1911-1926
-
-
Luthi-Carter, R.1
Hanson, S.A.2
Strand, A.D.3
Bergstrom, D.A.4
Chun, W.5
Peters, N.L.6
Woods, A.M.7
Chan, E.Y.8
Kooperberg, C.9
Krainc, D.10
-
57
-
-
77949472152
-
Mitochondrial DNA background modifies the bioenergetics of NARP/MILS ATP6 mutant cells
-
D'Aurelio, M., Vives-Bauza, C., Davidson, M.M. and Manfredi, G. (2010) Mitochondrial DNA background modifies the bioenergetics of NARP/MILS ATP6 mutant cells. Hum. Mol. Genet., 19, 374-386.
-
(2010)
Hum. Mol. Genet.
, vol.19
, pp. 374-386
-
-
D'Aurelio, M.1
Vives-Bauza, C.2
Davidson, M.M.3
Manfredi, G.4
-
58
-
-
0038036024
-
Bioenergetic analysis of peroxisome proliferator-activated receptor gamma coactivators 1alpha and 1beta (PGC-1alpha and PGC-1beta) in muscle cells
-
St-Pierre, J., Lin, J., Krauss, S., Tarr, P.T., Yang, R., Newgard, C.B. and Spiegelman, B.M. (2003) Bioenergetic analysis of peroxisome proliferator-activated receptor gamma coactivators 1alpha and 1beta (PGC-1alpha and PGC-1beta) in muscle cells. J. Biol. Chem., 278, 26597-26603.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 26597-26603
-
-
St-Pierre, J.1
Lin, J.2
Krauss, S.3
Tarr, P.T.4
Yang, R.5
Newgard, C.B.6
Spiegelman, B.M.7
-
59
-
-
33947675275
-
Oxidative damage in Huntington's disease pathogenesis
-
Browne, S.E. and Beal, M.F. (2006) Oxidative damage in Huntington's disease pathogenesis. Antioxid. Redox Signal., 8, 2061-2073.
-
(2006)
Antioxid. Redox Signal.
, vol.8
, pp. 2061-2073
-
-
Browne, S.E.1
Beal, M.F.2
-
60
-
-
33644927838
-
Creatine in Huntington disease is safe, tolerable, bioavailable in brain and reduces serum 8OH2'dG
-
Hersch, S.M., Gevorkian, S., Marder, K., Moskowitz, C., Feigin, A., Cox, M., Como, P., Zimmerman, C., Lin, M., Zhang, L. et al. (2006) Creatine in Huntington disease is safe, tolerable, bioavailable in brain and reduces serum 8OH2'dG. Neurology, 66, 250-252.
-
(2006)
Neurology
, vol.66
, pp. 250-252
-
-
Hersch, S.M.1
Gevorkian, S.2
Marder, K.3
Moskowitz, C.4
Feigin, A.5
Cox, M.6
Como, P.7
Zimmerman, C.8
Lin, M.9
Zhang, L.10
-
61
-
-
34748821960
-
Myopathy as a first symptom of Huntington's disease in a Marathon runner
-
Kosinski, C.M., Schlangen, C., Gellerich, F.N., Gizatullina, Z., Deschauer, M., Schiefer, J., Young, A.B., Landwehrmeyer, G.B., Toyka, K.V., Sellhaus, B. et al. (2007) Myopathy as a first symptom of Huntington's disease in a Marathon runner. Mov. Disord., 22, 1637-1640.
-
(2007)
Mov. Disord.
, vol.22
, pp. 1637-1640
-
-
Kosinski, C.M.1
Schlangen, C.2
Gellerich, F.N.3
Gizatullina, Z.4
Deschauer, M.5
Schiefer, J.6
Young, A.B.7
Landwehrmeyer, G.B.8
Toyka, K.V.9
Sellhaus, B.10
-
62
-
-
35348941757
-
Clinical correlates of mitochondrial function in Huntington's disease muscle
-
Turner, C., Cooper, J.M. and Schapira, A.H. (2007) Clinical correlates of mitochondrial function in Huntington's disease muscle. Mov. Disord., 22, 1715-1721.
-
(2007)
Mov. Disord.
, vol.22
, pp. 1715-1721
-
-
Turner, C.1
Cooper, J.M.2
Schapira, A.H.3
-
63
-
-
32044473546
-
Low stability of Huntington muscle mitochondria against Ca2+ in R6/2 mice
-
Gizatullina, Z.Z., Lindenberg, K.S., Harjes, P., Chen, Y., Kosinski, C.M., Landwehrmeyer, B.G., Ludolph, A.C., Striggow, F., Zierz, S. and Gellerich, F.N. (2006) Low stability of Huntington muscle mitochondria against Ca2+ in R6/2 mice. Ann. Neurol., 59, 407-411.
-
(2006)
Ann. Neurol.
, vol.59
, pp. 407-411
-
-
Gizatullina, Z.Z.1
Lindenberg, K.S.2
Harjes, P.3
Chen, Y.4
Kosinski, C.M.5
Landwehrmeyer, B.G.6
Ludolph, A.C.7
Striggow, F.8
Zierz, S.9
Gellerich, F.N.10
-
64
-
-
33846369453
-
Cardiac dysfunction in the R6/2 mouse model of Huntington's disease
-
Mihm, M.J., Amann, D.M., Schanbacher, B.L., Altschuld, R.A., Bauer, J.A. and Hoyt, K.R. (2007) Cardiac dysfunction in the R6/2 mouse model of Huntington's disease. Neurobiol. Dis., 25, 297-308.
-
(2007)
Neurobiol. Dis.
, vol.25
, pp. 297-308
-
-
Mihm, M.J.1
Amann, D.M.2
Schanbacher, B.L.3
Altschuld, R.A.4
Bauer, J.A.5
Hoyt, K.R.6
-
65
-
-
0037102256
-
Transcriptional co-activator PGC-1 alpha drives the formation of slow-twitch muscle fibres
-
Lin, J., Wu, H., Tarr, P.T., Zhang, C.Y., Wu, Z., Boss, O., Michael, L.F., Puigserver, P., Isotani, E., Olson, E.N. et al. (2002) Transcriptional co-activator PGC-1 alpha drives the formation of slow-twitch muscle fibres. Nature, 418, 797-801.
-
(2002)
Nature
, vol.418
, pp. 797-801
-
-
Lin, J.1
Wu, H.2
Tarr, P.T.3
Zhang, C.Y.4
Wu, Z.5
Boss, O.6
Michael, L.F.7
Puigserver, P.8
Isotani, E.9
Olson, E.N.10
-
66
-
-
54849422301
-
Huntingtin modulates transcription, occupies gene promoters in vivo, and binds directly to DNA in a polyglutamine-dependent manner
-
Benn, C.L., Sun, T., Sadri-Vakili, G., McFarland, K.N., DiRocco, D.P., Yohrling, G.J., Clark, T.W., Bouzou, B. and Cha, J.H. (2008) Huntingtin modulates transcription, occupies gene promoters in vivo, and binds directly to DNA in a polyglutamine-dependent manner. J. Neurosci., 28, 10720-10733.
-
(2008)
J. Neurosci.
, vol.28
, pp. 10720-10733
-
-
Benn, C.L.1
Sun, T.2
Sadri-Vakili, G.3
McFarland, K.N.4
DiRocco, D.P.5
Yohrling, G.J.6
Clark, T.W.7
Bouzou, B.8
Cha, J.H.9
-
67
-
-
61449226493
-
Phosphodiesterase type IV inhibition prevents sequestration of CREB binding protein, protects striatal parvalbumin interneurons and rescues motor deficits in the R6/2 mouse model of Huntington's disease
-
Giampa, C., Middei, S., Patassini, S., Borreca, A., Marullo, F., Laurenti, D., Bernardi, G., Ammassari-Teule, M. and Fusco, F.R. (2009) Phosphodiesterase type IV inhibition prevents sequestration of CREB binding protein, protects striatal parvalbumin interneurons and rescues motor deficits in the R6/2 mouse model of Huntington's disease. Eur. J. Neurosci., 29, 902-910.
-
(2009)
Eur. J. Neurosci.
, vol.29
, pp. 902-910
-
-
Giampa, C.1
Middei, S.2
Patassini, S.3
Borreca, A.4
Marullo, F.5
Laurenti, D.6
Bernardi, G.7
Ammassari-Teule, M.8
Fusco, F.R.9
-
68
-
-
43649092175
-
Beneficial effects of rolipram in the R6/2 mouse model of Huntington's disease
-
DeMarch, Z., Giampa, C., Patassini, S., Bernardi, G. and Fusco, F.R. (2008) Beneficial effects of rolipram in the R6/2 mouse model of Huntington's disease. Neurobiol. Dis., 30, 375-387.
-
(2008)
Neurobiol. Dis.
, vol.30
, pp. 375-387
-
-
DeMarch, Z.1
Giampa, C.2
Patassini, S.3
Bernardi, G.4
Fusco, F.R.5
-
69
-
-
12244298155
-
Cell death triggered by polyglutamine-expanded huntingtin in a neuronal cell line is associated with degradation of CREB-binding protein
-
Jiang, H., Nucifora, F.C. Jr, Ross, C.A. and DeFranco, D.B. (2003) Cell death triggered by polyglutamine-expanded huntingtin in a neuronal cell line is associated with degradation of CREB-binding protein. Hum. Mol. Genet., 12, 1-12.
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 1-12
-
-
Jiang, H.1
Nucifora F.C., Jr.2
Ross, C.A.3
DeFranco, D.B.4
-
70
-
-
33747170869
-
Depletion of CBP is directly linked with cellular toxicity caused by mutant huntingtin
-
Jiang, H., Poirier, M.A., Liang, Y., Pei, Z., Weiskittel, C.E., Smith, W.W., DeFranco, D.B. and Ross, C.A. (2006) Depletion of CBP is directly linked with cellular toxicity caused by mutant huntingtin. Neurobiol. Dis., 23, 543-551.
-
(2006)
Neurobiol. Dis.
, vol.23
, pp. 543-551
-
-
Jiang, H.1
Poirier, M.A.2
Liang, Y.3
Pei, Z.4
Weiskittel, C.E.5
Smith, W.W.6
DeFranco, D.B.7
Ross, C.A.8
-
71
-
-
33749999530
-
Suppression of reactive oxygen species and neurodegeneration by the PGC-1 transcriptional coactivators
-
St-Pierre, J., Drori, S., Uldry, M., Silvaggi, J.M., Rhee, J., Jager, S., Handschin, C., Zheng, K., Lin, J., Yang, W. et al. (2006) Suppression of reactive oxygen species and neurodegeneration by the PGC-1 transcriptional coactivators. Cell, 127, 397-408.
-
(2006)
Cell
, vol.127
, pp. 397-408
-
-
St-Pierre, J.1
Drori, S.2
Uldry, M.3
Silvaggi, J.M.4
Rhee, J.5
Jager, S.6
Handschin, C.7
Zheng, K.8
Lin, J.9
Yang, W.10
-
72
-
-
0035855905
-
CREB regulates hepatic gluconeogenesis through the coactivator PGC-1
-
Herzig, S., Long, F., Jhala, U.S., Hedrick, S., Quinn, R., Bauer, A., Rudolph, D., Schutz, G., Yoon, C., Puigserver, P. et al. (2001) CREB regulates hepatic gluconeogenesis through the coactivator PGC-1. Nature, 413, 179-183.
-
(2001)
Nature
, vol.413
, pp. 179-183
-
-
Herzig, S.1
Long, F.2
Jhala, U.S.3
Hedrick, S.4
Quinn, R.5
Bauer, A.6
Rudolph, D.7
Schutz, G.8
Yoon, C.9
Puigserver, P.10
-
73
-
-
0942298545
-
Endogenous mitochondrial oxidative stress: neurodegeneration, proteomic analysis, specific respiratory chain defects, and efficacious antioxidant therapy in superoxide dismutase 2 null mice
-
Hinerfeld, D., Traini, M.D., Weinberger, R.P., Cochran, B., Doctrow, S.R., Harry, J. and Melov, S. (2004) Endogenous mitochondrial oxidative stress: neurodegeneration, proteomic analysis, specific respiratory chain defects, and efficacious antioxidant therapy in superoxide dismutase 2 null mice. J. Neurochem., 88, 657-667.
-
(2004)
J. Neurochem.
, vol.88
, pp. 657-667
-
-
Hinerfeld, D.1
Traini, M.D.2
Weinberger, R.P.3
Cochran, B.4
Doctrow, S.R.5
Harry, J.6
Melov, S.7
-
74
-
-
67650242167
-
Sensitivity of lipid metabolism and insulin signaling to genetic alterations in hepatic peroxisome proliferator-activated receptor-gamma coactivator-1alpha expression
-
Estall, J.L., Kahn, M., Cooper, M.P., Fisher, F.M., Wu, M.K., Laznik, D., Qu, L., Cohen, D.E., Shulman, G.I. and Spiegelman, B.M. (2009) Sensitivity of lipid metabolism and insulin signaling to genetic alterations in hepatic peroxisome proliferator-activated receptor-gamma coactivator-1alpha expression. Diabetes, 58, 1499-1508.
-
(2009)
Diabetes
, vol.58
, pp. 1499-1508
-
-
Estall, J.L.1
Kahn, M.2
Cooper, M.P.3
Fisher, F.M.4
Wu, M.K.5
Laznik, D.6
Qu, L.7
Cohen, D.E.8
Shulman, G.I.9
Spiegelman, B.M.10
-
75
-
-
58649094617
-
The gene coding for PGC-1alpha modifies age at onset in Huntington's Disease
-
Weydt, P., Soyal, S.M., Gellera, C., Didonato, S., Weidinger, C., Oberkofler, H., Landwehrmeyer, G.B. and Patsch, W. (2009) The gene coding for PGC-1alpha modifies age at onset in Huntington's Disease. Mol. Neurodegener., 4,3.
-
(2009)
Mol. Neurodegener.
, vol.4
, pp. 3
-
-
Weydt, P.1
Soyal, S.M.2
Gellera, C.3
Didonato, S.4
Weidinger, C.5
Oberkofler, H.6
Landwehrmeyer, G.B.7
Patsch, W.8
-
76
-
-
60849109499
-
PGC-1alpha as modifier of onset age in Huntington disease
-
Taherzadeh-Fard, E., Saft, C., Andrich, J., Wieczorek, S. and Arning, L. (2009) PGC-1alpha as modifier of onset age in Huntington disease. Mol. Neurodegener., 4, 10.
-
(2009)
Mol. Neurodegener.
, vol.4
, pp. 10
-
-
Taherzadeh-Fard, E.1
Saft, C.2
Andrich, J.3
Wieczorek, S.4
Arning, L.5
-
77
-
-
67749124479
-
GCN5-mediated transcriptional control of the metabolic coactivator PGC-1beta through lysine acetylation
-
Kelly, T.J., Lerin, C., Haas, W., Gygi, S.P. and Puigserver, P. (2009) GCN5-mediated transcriptional control of the metabolic coactivator PGC-1beta through lysine acetylation. J. Biol. Chem., 284, 19945-19952.
-
(2009)
J. Biol. Chem.
, vol.284
, pp. 19945-19952
-
-
Kelly, T.J.1
Lerin, C.2
Haas, W.3
Gygi, S.P.4
Puigserver, P.5
-
78
-
-
64549127790
-
PGC-1alpha, SIRT1 and AMPK, an energy sensing network that controls energy expenditure
-
Canto, C. and Auwerx, J. (2009) PGC-1alpha, SIRT1 and AMPK, an energy sensing network that controls energy expenditure. Curr. Opin. Lipidol., 20, 98-105.
-
(2009)
Curr. Opin. Lipidol.
, vol.20
, pp. 98-105
-
-
Canto, C.1
Auwerx, J.2
-
79
-
-
77955018413
-
Nutrient-dependent regulation of PGC-1alpha's acetylation state and metabolic function through the enzymatic activities of Sirt1/GCN5
-
In press
-
Dominy, J.E. Jr, Lee, Y., Gerhart-Hines, Z. and Puigserver, P. (2009) Nutrient-dependent regulation of PGC-1alpha's acetylation state and metabolic function through the enzymatic activities of Sirt1/GCN5. Biochim. Biophys. Acta. In press.
-
(2009)
Biochim. Biophys. Acta.
-
-
Dominy J.E. Jr1
Lee, Y.2
Gerhart-Hines, Z.3
Puigserver, P.4
-
80
-
-
54449092109
-
Rosiglitazone treatment prevents mitochondrial dysfunction in mutant huntingtin-expressing cells: possible role of peroxisome proliferator-activated receptor-gamma (PPARgamma) in the pathogenesis of Huntington disease
-
Quintanilla, R.A., Jin, Y.N., Fuenzalida, K., Bronfman, M. and Johnson, G.V. (2008) Rosiglitazone treatment prevents mitochondrial dysfunction in mutant huntingtin-expressing cells: possible role of peroxisome proliferator-activated receptor-gamma (PPARgamma) in the pathogenesis of Huntington disease. J. Biol. Chem., 283, 25628-25637.
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 25628-25637
-
-
Quintanilla, R.A.1
Jin, Y.N.2
Fuenzalida, K.3
Bronfman, M.4
Johnson, G.V.5
-
81
-
-
50049118173
-
Activation of the PPAR/PGC-1alpha pathway prevents a bioenergetic deficit and effectively improves a mitochondrial myopathy phenotype
-
Wenz, T., Diaz, F., Spiegelman, B.M. and Moraes, C.T. (2008) Activation of the PPAR/PGC-1alpha pathway prevents a bioenergetic deficit and effectively improves a mitochondrial myopathy phenotype. Cell Metab., 8, 249-256.
-
(2008)
Cell Metab.
, vol.8
, pp. 249-256
-
-
Wenz, T.1
Diaz, F.2
Spiegelman, B.M.3
Moraes, C.T.4
-
82
-
-
34548095002
-
Metformin therapy in a transgenic mouse model of Huntington's disease
-
Ma, T.C., Buescher, J.L., Oatis, B., Funk, J.A., Nash, A.J., Carrier, R.L. and Hoyt, K.R. (2007) Metformin therapy in a transgenic mouse model of Huntington's disease. Neurosci. Lett., 411, 98-103.
-
(2007)
Neurosci. Lett.
, vol.411
, pp. 98-103
-
-
Ma, T.C.1
Buescher, J.L.2
Oatis, B.3
Funk, J.A.4
Nash, A.J.5
Carrier, R.L.6
Hoyt, K.R.7
-
83
-
-
34347272966
-
Overexpression of peroxisome proliferator-activated receptor gamma co-activator-1alpha leads to muscle atrophy with depletion of ATP
-
Miura, S., Tomitsuka, E., Kamei, Y., Yamazaki, T., Kai, Y., Tamura, M., Kita, K., Nishino, I. and Ezaki, O. (2006) Overexpression of peroxisome proliferator-activated receptor gamma co-activator-1alpha leads to muscle atrophy with depletion of ATP. Am. J. Pathol., 169, 1129-1139.
-
(2006)
Am. J. Pathol.
, vol.169
, pp. 1129-1139
-
-
Miura, S.1
Tomitsuka, E.2
Kamei, Y.3
Yamazaki, T.4
Kai, Y.5
Tamura, M.6
Kita, K.7
Nishino, I.8
Ezaki, O.9
-
84
-
-
0033803048
-
Peroxisome proliferator-activated receptor gamma coactivator-1 promotes cardiac mitochondrial biogenesis
-
Lehman, J.J., Barger, P.M., Kovacs, A., Saffitz, J.E., Medeiros, D.M. and Kelly, D.P. (2000) Peroxisome proliferator-activated receptor gamma coactivator-1 promotes cardiac mitochondrial biogenesis. J. Clin. Invest., 106, 847-856.
-
(2000)
J. Clin. Invest.
, vol.106
, pp. 847-856
-
-
Lehman, J.J.1
Barger, P.M.2
Kovacs, A.3
Saffitz, J.E.4
Medeiros, D.M.5
Kelly, D.P.6
-
85
-
-
65649148341
-
Whole body overexpression of PGC-1alpha has opposite effects on hepatic and muscle insulin sensitivity
-
Liang, H., Balas, B., Tantiwong, P., Dube, J., Goodpaster, B.H., O'Doherty, R.M., DeFronzo, R.A., Richardson, A., Musi, N. and Ward, W.F. (2009) Whole body overexpression of PGC-1alpha has opposite effects on hepatic and muscle insulin sensitivity. Am. J. Physiol. Endocrinol. Metab., 296, E945-E954.
-
(2009)
Am. J. Physiol. Endocrinol. Metab.
, vol.296
-
-
Liang, H.1
Balas, B.2
Tantiwong, P.3
Dube, J.4
Goodpaster, B.H.5
O'Doherty, R.M.6
DeFronzo, R.A.7
Richardson, A.8
Musi, N.9
Ward, W.F.10
|