-
1
-
-
25444474703
-
Mitochondria take center stage in aging and neurodegeneration
-
Beal M.F. Mitochondria take center stage in aging and neurodegeneration. Ann. Neurol. 58 (2005) 495-505
-
(2005)
Ann. Neurol.
, vol.58
, pp. 495-505
-
-
Beal, M.F.1
-
2
-
-
0027433553
-
Neurochemical and histologic characterization of striatal excitotoxic lesions produced by the mitochondrial toxin 3-nitropropionic acid
-
Beal M.F., Brouillet E., Jenkins B.G., Ferrante R.J., Kowall N.W., Miller J.M., Storey E., Srivastava R., Rosen B.R., and Hyman B.T. Neurochemical and histologic characterization of striatal excitotoxic lesions produced by the mitochondrial toxin 3-nitropropionic acid. J. Neurosci. 13 (1993) 4181-4192
-
(1993)
J. Neurosci.
, vol.13
, pp. 4181-4192
-
-
Beal, M.F.1
Brouillet, E.2
Jenkins, B.G.3
Ferrante, R.J.4
Kowall, N.W.5
Miller, J.M.6
Storey, E.7
Srivastava, R.8
Rosen, B.R.9
Hyman, B.T.10
-
3
-
-
2342598416
-
Experimental therapeutics in transgenic mouse models of Huntington's disease
-
Beal M.F., and Ferrante R.J. Experimental therapeutics in transgenic mouse models of Huntington's disease. Nat. Rev. Neurosci. 5 (2004) 373-384
-
(2004)
Nat. Rev. Neurosci.
, vol.5
, pp. 373-384
-
-
Beal, M.F.1
Ferrante, R.J.2
-
4
-
-
0037316303
-
A comparison of normalization methods for high density oligonucleotide array data based on variance and bias
-
Bolstad B.M., Irizarry R.A., Astrand M., and Speed T.P. A comparison of normalization methods for high density oligonucleotide array data based on variance and bias. Bioinformatics 19 (2003) 185-193
-
(2003)
Bioinformatics
, vol.19
, pp. 185-193
-
-
Bolstad, B.M.1
Irizarry, R.A.2
Astrand, M.3
Speed, T.P.4
-
5
-
-
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. Chronic mitochondrial energy impairment produces selective striatal degeneration and abnormal choreiform movements in primates. Proc. Natl. Acad. Sci. USA 92 (1995) 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
-
6
-
-
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. Oxidative damage and metabolic dysfunction in Huntington's disease: selective vulnerability of the basal ganglia. Ann. Neurol. 41 (1997) 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
-
7
-
-
3042763187
-
Frataxin acts as an iron chaperone protein to modulate mitochondrial aconitase activity
-
Bulteau A.L., O'Neill H.A., Kennedy M.C., Ikeda-Saito M., Isaya G., and Szweda L.I. Frataxin acts as an iron chaperone protein to modulate mitochondrial aconitase activity. Science 305 (2004) 242-245
-
(2004)
Science
, vol.305
, pp. 242-245
-
-
Bulteau, A.L.1
O'Neill, H.A.2
Kennedy, M.C.3
Ikeda-Saito, M.4
Isaya, G.5
Szweda, L.I.6
-
8
-
-
0347989317
-
Brown adipose tissue: function and physiological significance
-
Cannon B., and Nedergaard J. Brown adipose tissue: function and physiological significance. Physiol. Rev. 84 (2004) 277-359
-
(2004)
Physiol. Rev.
, vol.84
, pp. 277-359
-
-
Cannon, B.1
Nedergaard, J.2
-
9
-
-
17744386955
-
Alpha1- and beta1-adrenoceptor signaling fully compensates for beta3-adrenoceptor deficiency in brown adipocyte norepinephrine-stimulated glucose uptake
-
Chernogubova E., Hutchinson D.S., Nedergaard J., and Bengtsson T. Alpha1- and beta1-adrenoceptor signaling fully compensates for beta3-adrenoceptor deficiency in brown adipocyte norepinephrine-stimulated glucose uptake. Endocrinology 146 (2005) 2271-2284
-
(2005)
Endocrinology
, vol.146
, pp. 2271-2284
-
-
Chernogubova, E.1
Hutchinson, D.S.2
Nedergaard, J.3
Bengtsson, T.4
-
10
-
-
33749042331
-
Repression of PGC-1a gene by mutant huntingtin leads to mitochondrial dysfunction in Huntington's disease
-
Cui L., Jeong H., Borovecki F., Parkhurst C.N., Tanese N., and Krainc D. Repression of PGC-1a gene by mutant huntingtin leads to mitochondrial dysfunction in Huntington's disease. Cell 127 (2006) 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
-
11
-
-
0037972522
-
Mitochondrial respiratory-chain diseases
-
DiMauro S., and Schon E.A. Mitochondrial respiratory-chain diseases. N. Engl. J. Med. 348 (2003) 2656-2668
-
(2003)
N. Engl. J. Med.
, vol.348
, pp. 2656-2668
-
-
DiMauro, S.1
Schon, E.A.2
-
12
-
-
27144524290
-
Active HSF1 significantly suppresses polyglutamine aggregate formation in cellular and mouse models
-
Fujimoto M., Takaki E., Hayashi T., Kitaura Y., Tanaka Y., Inouye S., and Nakai A. Active HSF1 significantly suppresses polyglutamine aggregate formation in cellular and mouse models. J. Biol. Chem. 280 (2005) 34908-34916
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 34908-34916
-
-
Fujimoto, M.1
Takaki, E.2
Hayashi, T.3
Kitaura, Y.4
Tanaka, Y.5
Inouye, S.6
Nakai, A.7
-
13
-
-
0037096365
-
Polyglutamine-expanded ataxin-7 promotes non-cell-autonomous purkinje cell degeneration and displays proteolytic cleavage in ataxic transgenic mice
-
Garden G.A., Libby R.T., Fu Y.H., Kinoshita Y., Huang J., Possin D.E., Smith A.C., Martinez R.A., Fine G.C., Grote S.K., et al. Polyglutamine-expanded ataxin-7 promotes non-cell-autonomous purkinje cell degeneration and displays proteolytic cleavage in ataxic transgenic mice. J. Neurosci. 22 (2002) 4897-4905
-
(2002)
J. Neurosci.
, vol.22
, pp. 4897-4905
-
-
Garden, G.A.1
Libby, R.T.2
Fu, Y.H.3
Kinoshita, Y.4
Huang, J.5
Possin, D.E.6
Smith, A.C.7
Martinez, R.A.8
Fine, G.C.9
Grote, S.K.10
-
14
-
-
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. Bioconductor: open software development for computational biology and bioinformatics. Genome Biol. 5 (2004) 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
-
15
-
-
0033373421
-
Bioenergetics in Huntington's disease
-
Grunewald T., and Beal M.F. Bioenergetics in Huntington's disease. Ann. N Y Acad. Sci. 893 (1999) 203-213
-
(1999)
Ann. N Y Acad. Sci.
, vol.893
, pp. 203-213
-
-
Grunewald, T.1
Beal, M.F.2
-
16
-
-
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. Mitochondrial defect in Huntington's disease caudate nucleus. Ann. Neurol. 39 (1996) 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
-
17
-
-
0028284779
-
Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation
-
Gurney M.E., Pu H., Chiu A.Y., Dal Canto M.C., Polchow C.Y., Alexander D.D., Caliendo J., Hentati A., Kwon Y.W., Deng H.X., et al. Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation. Science 264 (1994) 1772-1775
-
(1994)
Science
, vol.264
, pp. 1772-1775
-
-
Gurney, M.E.1
Pu, H.2
Chiu, A.Y.3
Dal Canto, M.C.4
Polchow, C.Y.5
Alexander, D.D.6
Caliendo, J.7
Hentati, A.8
Kwon, Y.W.9
Deng, H.X.10
-
18
-
-
0031035154
-
Decreased N-acetyl-aspartate/choline ratio and increased lactate in the frontal lobe of patients with Huntington's disease: a proton magnetic resonance spectroscopy study
-
Harms L., Meierkord H., Timm G., Pfeiffer L., and Ludolph A.C. Decreased N-acetyl-aspartate/choline ratio and increased lactate in the frontal lobe of patients with Huntington's disease: a proton magnetic resonance spectroscopy study. J. Neurol. Neurosurg. Psychiatry 62 (1997) 27-30
-
(1997)
J. Neurol. Neurosurg. Psychiatry
, vol.62
, pp. 27-30
-
-
Harms, L.1
Meierkord, H.2
Timm, G.3
Pfeiffer, L.4
Ludolph, A.C.5
-
19
-
-
33644783812
-
Regional and cellular gene expression changes in human Huntington's disease brain
-
Hodges A., Strand A.D., Aragaki A.K., Kuhn A., Sengstag T., Hughes G., Elliston L.A., Hartog C., Goldstein D.R., Thu D., et al. Regional and cellular gene expression changes in human Huntington's disease brain. Hum. Mol. Genet. 15 (2006) 965-977
-
(2006)
Hum. Mol. Genet.
, vol.15
, pp. 965-977
-
-
Hodges, A.1
Strand, A.D.2
Aragaki, A.K.3
Kuhn, A.4
Sengstag, T.5
Hughes, G.6
Elliston, L.A.7
Hartog, C.8
Goldstein, D.R.9
Thu, D.10
-
20
-
-
0033136692
-
A YAC mouse model for Huntington's disease with full-length mutant huntingtin, cytoplasmic toxicity, and selective striatal neurodegeneration
-
Hodgson J.G., Agopyan N., Gutekunst C.A., Leavitt B.R., LePiane F., Singaraja R., Smith D.J., Bissada N., McCutcheon K., Nasir J., et al. A YAC mouse model for Huntington's disease with full-length mutant huntingtin, cytoplasmic toxicity, and selective striatal neurodegeneration. Neuron 23 (1999) 181-192
-
(1999)
Neuron
, vol.23
, pp. 181-192
-
-
Hodgson, J.G.1
Agopyan, N.2
Gutekunst, C.A.3
Leavitt, B.R.4
LePiane, F.5
Singaraja, R.6
Smith, D.J.7
Bissada, N.8
McCutcheon, K.9
Nasir, J.10
-
21
-
-
0027480960
-
A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
-
Huntington's Disease Collaborative Research Group
-
Huntington's Disease Collaborative Research Group. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. Cell 72 (1993) 971-983
-
(1993)
Cell
, vol.72
, pp. 971-983
-
-
-
22
-
-
17944370599
-
Polyglutamine-expanded ataxin-7 antagonizes CRX function and induces cone-rod dystrophy in a mouse model of SCA7
-
La Spada A.R., Fu Y., Sopher B.L., Libby R.T., Wang X., Li L.Y., Einum D.D., Huang J., Possin D.E., Smith A.C., et al. Polyglutamine-expanded ataxin-7 antagonizes CRX function and induces cone-rod dystrophy in a mouse model of SCA7. Neuron 31 (2001) 913-927
-
(2001)
Neuron
, vol.31
, pp. 913-927
-
-
La Spada, A.R.1
Fu, Y.2
Sopher, B.L.3
Libby, R.T.4
Wang, X.5
Li, L.Y.6
Einum, D.D.7
Huang, J.8
Possin, D.E.9
Smith, A.C.10
-
23
-
-
4344619319
-
Nucleotide release provides a mechanism for airway surface liquid homeostasis
-
Lazarowski E.R., Tarran R., Grubb B.R., van Heusden C.A., Okada S., and Boucher R.C. Nucleotide release provides a mechanism for airway surface liquid homeostasis. J. Biol. Chem. 279 (2004) 36855-36864
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 36855-36864
-
-
Lazarowski, E.R.1
Tarran, R.2
Grubb, B.R.3
van Heusden, C.A.4
Okada, S.5
Boucher, R.C.6
-
24
-
-
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. PGC-1alpha deficiency causes multi-system energy metabolic derangements: muscle dysfunction, abnormal weight control and hepatic steatosis. PLoS Biol. 3 (2005) 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
-
25
-
-
0041632303
-
Lack of huntingtin-associated protein-1 causes neuronal death resembling hypothalamic degeneration in Huntington's disease
-
Li S.H., Yu Z.X., Li C.L., Nguyen H.P., Zhou Y.X., Deng C., and Li X.J. Lack of huntingtin-associated protein-1 causes neuronal death resembling hypothalamic degeneration in Huntington's disease. J. Neurosci. 23 (2003) 6956-6964
-
(2003)
J. Neurosci.
, vol.23
, pp. 6956-6964
-
-
Li, S.H.1
Yu, Z.X.2
Li, C.L.3
Nguyen, H.P.4
Zhou, Y.X.5
Deng, C.6
Li, X.J.7
-
26
-
-
0028803757
-
A huntingtin-associated protein enriched in brain with implications for pathology
-
Li X.J., Li S.H., Sharp A.H., Nucifora Jr. F.C., Schilling G., Lanahan A., Worley P., Snyder S.H., and Ross C.A. A huntingtin-associated protein enriched in brain with implications for pathology. Nature 378 (1995) 398-402
-
(1995)
Nature
, vol.378
, pp. 398-402
-
-
Li, X.J.1
Li, S.H.2
Sharp, A.H.3
Nucifora Jr., F.C.4
Schilling, G.5
Lanahan, A.6
Worley, P.7
Snyder, S.H.8
Ross, C.A.9
-
27
-
-
24144463983
-
Metabolic control through the PGC-1 family of transcription coactivators
-
Lin J., Handschin C., and Spiegelman B.M. Metabolic control through the PGC-1 family of transcription coactivators. Cell Metab. 1 (2005) 361-370
-
(2005)
Cell Metab.
, vol.1
, pp. 361-370
-
-
Lin, J.1
Handschin, C.2
Spiegelman, B.M.3
-
28
-
-
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. Defects in adaptive energy metabolism with CNS-linked hyperactivity in PGC-1alpha null mice. Cell 119 (2004) 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
-
29
-
-
0028834086
-
Oligonucleotides with fluorescent dyes at opposite ends provide a quenched probe system useful for detecting PCR product and nucleic acid hybridization
-
Livak K.J., Flood S.J., Marmaro J., Giusti W., and Deetz K. Oligonucleotides with fluorescent dyes at opposite ends provide a quenched probe system useful for detecting PCR product and nucleic acid hybridization. PCR Methods Appl. 4 (1995) 357-362
-
(1995)
PCR Methods Appl.
, vol.4
, pp. 357-362
-
-
Livak, K.J.1
Flood, S.J.2
Marmaro, J.3
Giusti, W.4
Deetz, K.5
-
30
-
-
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. Abnormal in vivo skeletal muscle energy metabolism in Huntington's disease and dentatorubropallidoluysian atrophy. Ann. Neurol. 48 (2000) 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
-
31
-
-
0034611678
-
Towards a molecular understanding of adaptive thermogenesis
-
Lowell B.B., and Spiegelman B.M. Towards a molecular understanding of adaptive thermogenesis. Nature 404 (2000) 652-660
-
(2000)
Nature
, vol.404
, pp. 652-660
-
-
Lowell, B.B.1
Spiegelman, B.M.2
-
32
-
-
0642303113
-
Peroxisome proliferator-activated receptor delta controls muscle development and oxidative capability
-
Luquet S., Lopez-Soriano J., Holst D., Fredenrich A., Melki J., Rassoulzadegan M., and Grimaldi P.A. Peroxisome proliferator-activated receptor delta controls muscle development and oxidative capability. FASEB J. 17 (2003) 2299-2301
-
(2003)
FASEB J.
, vol.17
, pp. 2299-2301
-
-
Luquet, S.1
Lopez-Soriano, J.2
Holst, D.3
Fredenrich, A.4
Melki, J.5
Rassoulzadegan, M.6
Grimaldi, P.A.7
-
33
-
-
0034702030
-
Decreased expression of striatal signaling genes in a mouse model of Huntington's disease
-
Luthi-Carter R., Strand A., Peters N.L., Solano S.M., Hollingsworth Z.R., Menon A.S., Frey A.S., Spektor B.S., Penney E.B., Schilling G., et al. Decreased expression of striatal signaling genes in a mouse model of Huntington's disease. Hum. Mol. Genet. 9 (2000) 1259-1271
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 1259-1271
-
-
Luthi-Carter, R.1
Strand, A.2
Peters, N.L.3
Solano, S.M.4
Hollingsworth, Z.R.5
Menon, A.S.6
Frey, A.S.7
Spektor, B.S.8
Penney, E.B.9
Schilling, G.10
-
34
-
-
16044373842
-
Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice
-
Mangiarini L., Sathasivam K., Seller M., Cozens B., Harper A., Hetherington C., Lawton M., Trottier Y., Lehrach H., Davies S.W., and Bates G.P. Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice. Cell 87 (1996) 493-506
-
(1996)
Cell
, vol.87
, pp. 493-506
-
-
Mangiarini, L.1
Sathasivam, K.2
Seller, M.3
Cozens, B.4
Harper, A.5
Hetherington, C.6
Lawton, M.7
Trottier, Y.8
Lehrach, H.9
Davies, S.W.10
Bates, G.P.11
-
35
-
-
0041691176
-
Time course of early motor and neuropathological anomalies in a knock-in mouse model of Huntington's disease with 140 CAG repeats
-
Menalled L.B., Sison J.D., Dragatsis I., Zeitlin S., and Chesselet M.F. Time course of early motor and neuropathological anomalies in a knock-in mouse model of Huntington's disease with 140 CAG repeats. J. Comp. Neurol. 465 (2003) 11-26
-
(2003)
J. Comp. Neurol.
, vol.465
, pp. 11-26
-
-
Menalled, L.B.1
Sison, J.D.2
Dragatsis, I.3
Zeitlin, S.4
Chesselet, M.F.5
-
36
-
-
0038054341
-
PGC-1alpha-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes
-
Mootha V.K., Lindgren C.M., Eriksson K.F., Subramanian A., Sihag S., Lehar J., Puigserver P., Carlsson E., Ridderstrale M., Laurila E., et al. PGC-1alpha-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes. Nat. Genet. 34 (2003) 267-273
-
(2003)
Nat. Genet.
, vol.34
, pp. 267-273
-
-
Mootha, V.K.1
Lindgren, C.M.2
Eriksson, K.F.3
Subramanian, A.4
Sihag, S.5
Lehar, J.6
Puigserver, P.7
Carlsson, E.8
Ridderstrale, M.9
Laurila, E.10
-
37
-
-
0030848204
-
Clinical aspects of CAG repeat diseases
-
Nance M.A. Clinical aspects of CAG repeat diseases. Brain Pathol. 7 (1997) 881-900
-
(1997)
Brain Pathol.
, vol.7
, pp. 881-900
-
-
Nance, M.A.1
-
38
-
-
0033965329
-
Higher sedentary energy expenditure in patients with Huntington's disease
-
Pratley R.E., Salbe A.D., Ravussin E., and Caviness J.N. Higher sedentary energy expenditure in patients with Huntington's disease. Ann. Neurol. 47 (2000) 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
-
39
-
-
0037326196
-
Peroxisome proliferator-activated receptor-gamma coactivator 1 alpha (PGC-1 alpha): transcriptional coactivator and metabolic regulator
-
Puigserver P., and Spiegelman B.M. Peroxisome proliferator-activated receptor-gamma coactivator 1 alpha (PGC-1 alpha): transcriptional coactivator and metabolic regulator. Endocr. Rev. 24 (2003) 78-90
-
(2003)
Endocr. Rev.
, vol.24
, pp. 78-90
-
-
Puigserver, P.1
Spiegelman, B.M.2
-
40
-
-
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. A cold-inducible coactivator of nuclear receptors linked to adaptive thermogenesis. Cell 92 (1998) 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
-
41
-
-
0037072886
-
Regulatory motifs for CREB-binding protein and Nfe2l2 transcription factors in the upstream enhancer of the mitochondrial uncoupling protein 1 gene
-
Rim J.S., and Kozak L.P. Regulatory motifs for CREB-binding protein and Nfe2l2 transcription factors in the upstream enhancer of the mitochondrial uncoupling protein 1 gene. J. Biol. Chem. 277 (2002) 34589-34600
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 34589-34600
-
-
Rim, J.S.1
Kozak, L.P.2
-
43
-
-
0037461730
-
Pivotal role of oligomerization in expanded polyglutamine neurodegenerative disorders
-
Sanchez I., Mahlke C., and Yuan J. Pivotal role of oligomerization in expanded polyglutamine neurodegenerative disorders. Nature 421 (2003) 373-379
-
(2003)
Nature
, vol.421
, pp. 373-379
-
-
Sanchez, I.1
Mahlke, C.2
Yuan, J.3
-
44
-
-
0031743066
-
UCP2, UCP3 and leptin gene expression: modulation by food restriction and leptin
-
Scarpace P.J., Nicolson M., and Matheny M. UCP2, UCP3 and leptin gene expression: modulation by food restriction and leptin. J. Endocrinol. 159 (1998) 349-357
-
(1998)
J. Endocrinol.
, vol.159
, pp. 349-357
-
-
Scarpace, P.J.1
Nicolson, M.2
Matheny, M.3
-
45
-
-
0033054555
-
Intranuclear inclusions and neuritic aggregates in transgenic mice expressing a mutant N-terminal fragment of huntingtin
-
Schilling G., Becher M.W., Sharp A.H., Jinnah H.A., Duan K., Kotzuk J.A., Slunt H.H., Ratovitski T., Cooper J.K., Jenkins N.A., et al. Intranuclear inclusions and neuritic aggregates in transgenic mice expressing a mutant N-terminal fragment of huntingtin. Hum. Mol. Genet. 8 (1999) 397-407
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 397-407
-
-
Schilling, G.1
Becher, M.W.2
Sharp, A.H.3
Jinnah, H.A.4
Duan, K.5
Kotzuk, J.A.6
Slunt, H.H.7
Ratovitski, T.8
Cooper, J.K.9
Jenkins, N.A.10
-
46
-
-
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., and MacDonald M.E. HD CAG repeat implicates a dominant property of huntingtin in mitochondrial energy metabolism. Hum. Mol. Genet. 14 (2005) 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
MacDonald, M.E.11
-
47
-
-
33646556703
-
Hypothalamic huntingtin-associated protein 1 as a mediator of feeding behavior
-
Sheng G., Chang G.Q., Lin J.Y., Yu Z.X., Fang Z.H., Rong J., Lipton S.A., Li S.H., Tong G., Leibowitz S.F., and Li X.J. Hypothalamic huntingtin-associated protein 1 as a mediator of feeding behavior. Nat. Med. 12 (2006) 526-533
-
(2006)
Nat. Med.
, vol.12
, pp. 526-533
-
-
Sheng, G.1
Chang, G.Q.2
Lin, J.Y.3
Yu, Z.X.4
Fang, Z.H.5
Rong, J.6
Lipton, S.A.7
Li, S.H.8
Tong, G.9
Leibowitz, S.F.10
Li, X.J.11
-
48
-
-
0032980686
-
Fasting and leptin modulate adipose and muscle uncoupling protein: divergent effects between messenger ribonucleic acid and protein expression
-
Sivitz W.I., Fink B.D., and Donohoue P.A. Fasting and leptin modulate adipose and muscle uncoupling protein: divergent effects between messenger ribonucleic acid and protein expression. Endocrinology 140 (1999) 1511-1519
-
(1999)
Endocrinology
, vol.140
, pp. 1511-1519
-
-
Sivitz, W.I.1
Fink, B.D.2
Donohoue, P.A.3
-
49
-
-
18744369640
-
Use of within-array replicate spots for assessing differential expression in microarray experiments
-
Smyth G.K., Michaud J., and Scott H.S. Use of within-array replicate spots for assessing differential expression in microarray experiments. Bioinformatics 21 (2005) 2067-2075
-
(2005)
Bioinformatics
, vol.21
, pp. 2067-2075
-
-
Smyth, G.K.1
Michaud, J.2
Scott, H.S.3
-
50
-
-
0022446708
-
PET studies of cerebral glucose metabolism in idiopathic torticollis
-
Stoessl A.J., Martin W.R., Clark C., Adam M.J., Ammann W., Beckman J.H., Bergstrom M., Harrop R., Rogers J.G., Ruth T.J., et al. PET studies of cerebral glucose metabolism in idiopathic torticollis. Neurology 36 (1986) 653-657
-
(1986)
Neurology
, vol.36
, pp. 653-657
-
-
Stoessl, A.J.1
Martin, W.R.2
Clark, C.3
Adam, M.J.4
Ammann, W.5
Beckman, J.H.6
Bergstrom, M.7
Harrop, R.8
Rogers, J.G.9
Ruth, T.J.10
-
51
-
-
0042424602
-
Statistical significance for genomewide studies
-
Storey J.D., and Tibshirani R. Statistical significance for genomewide studies. Proc. Natl. Acad. Sci. USA 100 (2003) 9440-9445
-
(2003)
Proc. Natl. Acad. Sci. USA
, vol.100
, pp. 9440-9445
-
-
Storey, J.D.1
Tibshirani, R.2
-
52
-
-
0037408279
-
Transcriptional abnormalities in Huntington disease
-
Sugars K.L., and Rubinsztein D.C. Transcriptional abnormalities in Huntington disease. Trends Genet. 19 (2003) 233-238
-
(2003)
Trends Genet.
, vol.19
, pp. 233-238
-
-
Sugars, K.L.1
Rubinsztein, D.C.2
-
53
-
-
0842310006
-
Regulation of ATP/ADP in pancreatic islets
-
Sweet I.R., Cook D.L., DeJulio E., Wallen A.R., Khalil G., Callis J., and Reems J. Regulation of ATP/ADP in pancreatic islets. Diabetes 53 (2004) 401-409
-
(2004)
Diabetes
, vol.53
, pp. 401-409
-
-
Sweet, I.R.1
Cook, D.L.2
DeJulio, E.3
Wallen, A.R.4
Khalil, G.5
Callis, J.6
Reems, J.7
-
54
-
-
0036412160
-
Continuous measurement of oxygen consumption by pancreatic islets
-
Sweet I.R., Khalil G., Wallen A.R., Steedman M., Schenkman K.A., Reems J.A., Kahn S.E., and Callis J.B. Continuous measurement of oxygen consumption by pancreatic islets. Diabetes Technol. Ther. 4 (2002) 661-672
-
(2002)
Diabetes Technol. Ther.
, vol.4
, pp. 661-672
-
-
Sweet, I.R.1
Khalil, G.2
Wallen, A.R.3
Steedman, M.4
Schenkman, K.A.5
Reems, J.A.6
Kahn, S.E.7
Callis, J.B.8
-
55
-
-
0034703869
-
Dominant phenotypes produced by the HD mutation in STHdh(Q111) striatal cells
-
Trettel F., Rigamonti D., Hilditch-Maguire P., Wheeler V.C., Sharp A.H., Persichetti F., Cattaneo E., and MacDonald M.E. Dominant phenotypes produced by the HD mutation in STHdh(Q111) striatal cells. Hum. Mol. Genet. 9 (2000) 2799-2809
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 2799-2809
-
-
Trettel, F.1
Rigamonti, D.2
Hilditch-Maguire, P.3
Wheeler, V.C.4
Sharp, A.H.5
Persichetti, F.6
Cattaneo, E.7
MacDonald, M.E.8
-
56
-
-
0033977890
-
The coactivator PGC-1 cooperates with peroxisome proliferator-activated receptor alpha in transcriptional control of nuclear genes encoding mitochondrial fatty acid oxidation enzymes
-
Vega R.B., Huss J.M., and Kelly D.P. The coactivator PGC-1 cooperates with peroxisome proliferator-activated receptor alpha in transcriptional control of nuclear genes encoding mitochondrial fatty acid oxidation enzymes. Mol. Cell. Biol. 20 (2000) 1868-1876
-
(2000)
Mol. Cell. Biol.
, vol.20
, pp. 1868-1876
-
-
Vega, R.B.1
Huss, J.M.2
Kelly, D.P.3
-
57
-
-
27844551588
-
The orphan nuclear receptor SHP regulates PGC-1alpha expression and energy production in brown adipocytes
-
Wang L., Liu J., Saha P., Huang J., Chan L., Spiegelman B., and Moore D.D. The orphan nuclear receptor SHP regulates PGC-1alpha expression and energy production in brown adipocytes. Cell Metab. 2 (2005) 227-238
-
(2005)
Cell Metab.
, vol.2
, pp. 227-238
-
-
Wang, L.1
Liu, J.2
Saha, P.3
Huang, J.4
Chan, L.5
Spiegelman, B.6
Moore, D.D.7
-
58
-
-
0034094873
-
Glutamine repeats and neurodegeneration
-
Zoghbi H.Y., and Orr H.T. Glutamine repeats and neurodegeneration. Annu. Rev. Neurosci. 23 (2000) 217-247
-
(2000)
Annu. Rev. Neurosci.
, vol.23
, pp. 217-247
-
-
Zoghbi, H.Y.1
Orr, H.T.2
|