-
1
-
-
0028050667
-
Creatine in humans with special reference to creatine supplementation
-
Balsom PD, Soderlund K, Ekhlom B (1994) Creatine in humans with special reference to creatine supplementation. Sports Med 18:268-280.
-
(1994)
Sports Med
, vol.18
, pp. 268-280
-
-
Balsom, P.D.1
Soderlund, K.2
Ekhlom, B.3
-
3
-
-
0032314696
-
Perspectives of the mitochondrial permeability transition
-
Bernardi P, Basso E, Colonna R, Costantini P, Di Lisa F, Eriksson O, Fontaine E, Forte M, Ichas F, Massari S, Nicolli A, Petronilli V, Scorrano L (1998) Perspectives of the mitochondrial permeability transition. Biochim Biophys Acta 1365:200-206.
-
(1998)
Biochim Biophys Acta
, vol.1365
, pp. 200-206
-
-
Bernardi, P.1
Basso, E.2
Colonna, R.3
Costantini, P.4
Di Lisa, F.5
Eriksson, O.6
Fontaine, E.7
Forte, M.8
Ichas, F.9
Massari, S.10
Nicolli, A.11
Petronilli, V.12
Scorrano, L.13
-
4
-
-
0031797267
-
Increased vulnerability to 3-nitropropionic acid in an animal model of huntington's disease
-
Bogdanov MB, Ferrante RJ, Kuemmerle S, Klivenyi P, Beal MF (1998) Increased vulnerability to 3-nitropropionic acid in an animal model of Huntington's disease. J Neurochcm 71:2652-2644.
-
(1998)
J Neurochcm
, vol.71
, pp. 2652-12644
-
-
Bogdanov, M.B.1
Ferrante, R.J.2
Kuemmerle, S.3
Klivenyi, P.4
Beal, M.F.5
-
5
-
-
0023636904
-
Spatial localization in NMR spectroscopy in vivo
-
Bottomley PA (1987) Spatial localization in NMR spectroscopy in vivo. Ann NY Acad Sci 508:333-348.
-
(1987)
Ann NY Acad Sci
, vol.508
, pp. 333-348
-
-
Bottomley, P.A.1
-
6
-
-
0032422634
-
The molecular structure of mitochondrial contact sites. Their role in regulation of energy metabolism and permeability transition
-
Brdiczka D, Beutner G, Ruck A, Dolder M, Wallimann T (1998) The molecular structure of mitochondrial contact sites. Their role in regulation of energy metabolism and permeability transition. Biofactors 8:235-242.
-
(1998)
Biofactors
, vol.8
, pp. 235-242
-
-
Brdiczka, D.1
Beutner, G.2
Ruck, A.3
Dolder, M.4
Wallimann, T.5
-
7
-
-
0029118136
-
Chronic mitochondrial energy impairment produces selective striatal degeneration and abnormal choreiform movements in primates
-
Brouillet E, Hantraye P, Ferrante RJ, Dolan R, Leroy-Willig A, Kowall NW, Beal MF (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
-
8
-
-
0030919567
-
Oxidative damage and metabolic dysfunction in Huntington's disease: Selective vulnerability of the basal ganglia
-
Browne SE, Bowling AC, MacGarvey U, Baik MJ, Berger SC, Muqit MMK, Bird ED, Beal MF (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.K.6
Bird, E.D.7
Beal, M.F.8
-
9
-
-
0029007479
-
Preincubation with creatine enhances levels of creatine phosphate and prevents anoxic damage in rat hippocampal slices
-
Carter AJ, Muller RE, Pschorn U, Stransky W (1995) Preincubation with creatine enhances levels of creatine phosphate and prevents anoxic damage in rat hippocampal slices. J Neurochem 64:2691-2699.
-
(1995)
J Neurochem
, vol.64
, pp. 2691-2699
-
-
Carter, A.J.1
Muller, R.E.2
Pschorn, U.3
Stransky, W.4
-
10
-
-
0032568517
-
Altered brain neurotransmitter receptors in transgenic mice expressing a portion of an abnormal human Huntington disease gene
-
Cha J-HJ, Kosinski CM, Kerner JA, Alsdorf SA, Mangiarini L, Davies SW, Penney JB, Bates GP, Young AB (1998) Altered brain neurotransmitter receptors in transgenic mice expressing a portion of an abnormal human Huntington disease gene. Proc Natl Acad Sci USA 95:6480-6485.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 6480-6485
-
-
Cha, J.-H.1
Kosinski, C.M.2
Kerner, J.A.3
Alsdorf, S.A.4
Mangiarini, L.5
Davies, S.W.6
Penney, J.B.7
Bates, G.P.8
Young, A.B.9
-
12
-
-
18544410106
-
Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation
-
Davies SW, Turmaine M, Cozens BA, DiFiglia M, Sharp AH, Ross CA, Scherzinger E, Wanker EE, Mangiari L, Bates GP (1997) Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation. Cell 90:537-548.
-
(1997)
Cell
, vol.90
, pp. 537-548
-
-
Davies, S.W.1
Turmaine, M.2
Cozens, B.A.3
DiFiglia, M.4
Sharp, A.H.5
Ross, C.A.6
Scherzinger, E.7
Wanker, E.E.8
Mangiari, L.9
Bates, G.P.10
-
13
-
-
0028928579
-
Neuroprotective effects of gangliosides may involve inhibition of nitric oxide synthase
-
Dawson TM, Hung K, Dawson VL, Steiner JP, Snyder SH (1995) Neuroprotective effects of gangliosides may involve inhibition of nitric oxide synthase. Ann Neurol 37:115-118.
-
(1995)
Ann Neurol
, vol.37
, pp. 115-118
-
-
Dawson, T.M.1
Hung, K.2
Dawson, V.L.3
Steiner, J.P.4
Snyder, S.H.5
-
15
-
-
0030752709
-
Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain
-
DiFiglia M, Sapp E, Chase KO, Davies SW, Bates GP, Vonsattel JP, Aronin N (1997) Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain. Science 277:1990-1993.
-
(1997)
Science
, vol.277
, pp. 1990-1993
-
-
DiFiglia, M.1
Sapp, E.2
Chase, K.O.3
Davies, S.W.4
Bates, G.P.5
Vonsattel, J.P.6
Aronin, N.7
-
16
-
-
0023959399
-
Energy metabolism and quantal acetylcholine release: Effects of botulinum toxin, 1-fluoro-2,4-dinitrobenzene, and diamide in the Torpedo electric organ
-
Dunant Y, Loctin F, Marsal J, Muller D, Parducz A, Rabasseda X (1988) Energy metabolism and quantal acetylcholine release: effects of botulinum toxin, 1-fluoro-2,4-dinitrobenzene, and diamide in the Torpedo electric organ. J Neurochem 50:431-439.
-
(1988)
J Neurochem
, vol.50
, pp. 431-439
-
-
Dunant, Y.1
Loctin, F.2
Marsal, J.3
Muller, D.4
Parducz, A.5
Rabasseda, X.6
-
17
-
-
0030950980
-
Heterogeneous topographic and cellular distribution of huntingtin expression in the normal human neostriatum
-
Ferrante RJ, Gutekunst CA, Persichetti F, McNeil SM, Kowall NW, Gusella JF, MacDonald ME, Beal MF, Hersch SM (1997) Heterogeneous topographic and cellular distribution of huntingtin expression in the normal human neostriatum. J Neurosci 17:3052-3063.
-
(1997)
J Neurosci
, vol.17
, pp. 3052-3063
-
-
Ferrante, R.J.1
Gutekunst, C.A.2
Persichetti, F.3
McNeil, S.M.4
Kowall, N.W.5
Gusella, J.F.6
MacDonald, M.E.7
Beal, M.F.8
Hersch, S.M.9
-
19
-
-
0030730498
-
The nutritional biochemistry of creatine
-
Greenhaff PL (1997) The nutritional biochemistry of creatine. J Nutr Biochem 8:610-618.
-
(1997)
J Nutr Biochem
, vol.8
, pp. 610-618
-
-
Greenhaff, P.L.1
-
20
-
-
0029875381
-
Mitochondrial defect in Huntington's disease caudate nucleus
-
Gu M, Gash MT, Mann VM, Javoy-Agid F, Cooper JM, Schapira AHV (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.V.6
-
21
-
-
0000531709
-
Mitochondrial calcium homeostasis in Huntington's disease fibroblasts
-
Gutekunst C-A, Peng T-I, Whaley WL, Rock B, Hersch SM, Greenamyre JT (1996) Mitochondrial calcium homeostasis in Huntington's disease fibroblasts. Soc Neurosci Abstr 22:227.
-
(1996)
Soc Neurosci Abstr
, vol.22
, pp. 227
-
-
Gutekunst, C.-A.1
Peng, T.-I.2
Whaley, W.L.3
Rock, B.4
Hersch, S.M.5
Greenamyre, J.T.6
-
22
-
-
0033119123
-
Nuclear and neuropil aggregates in Huntington's disease: Relationship to neuropathology
-
Gutekunst CA, Li SH, Yi H, Mulroy JS, Kuemmerle S, Jones R, Rye D, Ferrante RJ, Hersch SM, Li XJ (1999) Nuclear and neuropil aggregates in Huntington's disease: relationship to neuropathology. J Neurosci 19:2522-2534.
-
(1999)
J Neurosci
, vol.19
, pp. 2522-2534
-
-
Gutekunst, C.A.1
Li, S.H.2
Yi, H.3
Mulroy, J.S.4
Kuemmerle, S.5
Jones, R.6
Rye, D.7
Ferrante, R.J.8
Hersch, S.M.9
Li, X.J.10
-
23
-
-
0027724925
-
Functional aspects of creatine kinase in brain
-
Hemmer W, Wallimann T (1993) Functional aspects of creatine kinase in brain. Dev Neurosci 15:249-260.
-
(1993)
Dev Neurosci
, vol.15
, pp. 249-260
-
-
Hemmer, W.1
Wallimann, T.2
-
24
-
-
0033136692
-
A YAC mouse model for huntington's disease with full-length mutant huntingtin, cytoplasmic toxicity, and selective striatal neurodegeneration
-
Hodgson JG, Agopyan N, Gutekunst CA, Leavitt BR, LePiane F, Singaraja R, Smith DJ, Bissada N, McCutcheon K, Nasir J, Jamot L, Li XJ, Stevens ME, Rosemond E, Roder JC, Phillips AG, Rubin EM, Hersch SM, Hayden MR (1999) A YAC mouse model for Huntington's disease with full-length mutant huntingtin, cytoplasmic toxicity, and selective striatal neurodegeneration. Neuron 23:181-192.
-
(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
Jamot, L.11
Li, X.J.12
Stevens, M.E.13
Rosemond, E.14
Roder, J.C.15
Phillips, A.G.16
Rubin, E.M.17
Hersch, S.M.18
Hayden, M.R.19
-
25
-
-
0033009587
-
Mice transgenic for an expanded CAG repeat in the Huntington's disease gene develop diabetes
-
Hurlbert MS, Zhou W, Wasmeier C, Kaddis FG, Hutton JC, Freed CR (1999) Mice transgenic for an expanded CAG repeat in the Huntington's disease gene develop diabetes. Diabetes 48:649-651.
-
(1999)
Diabetes
, vol.48
, pp. 649-651
-
-
Hurlbert, M.S.1
Zhou, W.2
Wasmeier, C.3
Kaddis, F.G.4
Hutton, J.C.5
Freed, C.R.6
-
26
-
-
0027741301
-
Evidence for an energy metabolism defect in huntington's disease using localized proton spectroscopy
-
Jenkins B, Koroshetz W, Beal MF, Rosen B (1993) Evidence for an energy metabolism defect in Huntington's disease using localized proton spectroscopy. Neurology 43:2689-2695.
-
(1993)
Neurology
, vol.43
, pp. 2689-2695
-
-
Jenkins, B.1
Koroshetz, W.2
Beal, M.F.3
Rosen, B.4
-
27
-
-
0031596998
-
1H NMR spectroscopy studies of Huntington's disease: Correlations with CAG repeat numbers
-
Jenkins BG, Rosas HD, Chen YC, Makabe T, Myers R, MacDonald M, Rosen BR, Beal MF, Koroshetz WJ (1998) 1H NMR spectroscopy studies of Huntington's disease: correlations with CAG repeat numbers. Neurology 50:1357-1365.
-
(1998)
Neurology
, vol.50
, pp. 1357-1365
-
-
Jenkins, B.G.1
Rosas, H.D.2
Chen, Y.C.3
Makabe, T.4
Myers, R.5
MacDonald, M.6
Rosen, B.R.7
Beal, M.F.8
Koroshetz, W.J.9
-
28
-
-
0034006477
-
Non-linear decrease over time in N-acetylaspartate levels in the absence of neuronal loss and increases in glutamine and glucose in transgenic Huntington's disease mice
-
Jenkins BG, Klivenyi P, Kustermann E, Andreassen OA, Ferrante RJ, Rosen BR, Beal MF (2000) Non-linear decrease over time in N-acetylaspartate levels in the absence of neuronal loss and increases in glutamine and glucose in transgenic Huntington's disease mice. J Neurochem 74:2108-2119.
-
(2000)
J Neurochem
, vol.74
, pp. 2108-2119
-
-
Jenkins, B.G.1
Klivenyi, P.2
Kustermann, E.3
Andreassen, O.A.4
Ferrante, R.J.5
Rosen, B.R.6
Beal, M.F.7
-
29
-
-
0033051815
-
Neuroprotective effects of creatine in a transgenic animal model of ALS
-
Klivenyi P, Ferrante RJ, Matthews RT, Bogdanov MB, Klein AM, Andreassen OA, Mueller G, Wcrmer M, Kaddurah-Daouk R, Beal MF (1999) Neuroprotective effects of creatine in a transgenic animal model of ALS. Nat Med 5:347-350.
-
(1999)
Nat Med
, vol.5
, pp. 347-350
-
-
Klivenyi, P.1
Ferrante, R.J.2
Matthews, R.T.3
Bogdanov, M.B.4
Klein, A.M.5
Andreassen, O.A.6
Mueller, G.7
Wcrmer, M.8
Kaddurah-Daouk, R.9
Beal, M.F.10
-
31
-
-
0032590053
-
Huntingtin aggregates may not predict neuronal death in Huntington's disease
-
Kuemmerle S, Gutekunst CA, Klein AM, Li XJ, Li SH, Beal MF, Hersch SM, Ferrante RJ (1999) Huntingtin aggregates may not predict neuronal death in Huntington's disease. Ann Neurol 46:842-849.
-
(1999)
Ann Neurol
, vol.46
, pp. 842-849
-
-
Kuemmerle, S.1
Gutekunst, C.A.2
Klein, A.M.3
Li, X.J.4
Li, S.H.5
Beal, M.F.6
Hersch, S.M.7
Ferrante, R.J.8
-
32
-
-
0028891145
-
Huntington's disease gene: Regional and cellular expression in brain of normal and affected individuals
-
Landwehrmeyer GB, McNeil SM, Dure I, LS, Ge P, Aizawa H, Huang Q, Ambrose CM, Duyao MP, Bird ED, Bonilla E, de Young M, Avila-Gonzales AJ, Wexler NS, DiFiglia M, Gusella JF, MacDonald ME, Penney JB, Young AB, Vonsattel J-P (1995) Huntington's disease gene: regional and cellular expression in brain of normal and affected individuals. Ann Neurol 37:218-230.
-
(1995)
Ann Neurol
, vol.37
, pp. 218-230
-
-
Landwehrmeyer, G.B.1
McNeil, S.M.2
Dure, I.3
Ge, P.4
Aizawa, H.5
Huang, Q.6
Ambrose, C.M.7
Duyao, M.P.8
Bird, E.D.9
Bonilla, E.10
De Young, M.11
Avila-Gonzales, A.J.12
Wexler, N.S.13
DiFiglia, M.14
Gusella, J.F.15
Macdonald, M.E.16
Penney, J.B.17
Young, A.B.18
Vonsattel, J.-P.19
-
33
-
-
0031816414
-
Apoptosis, excitotoxicity, and neuropathology
-
Leist M, Nicotera P (1998) Apoptosis, excitotoxicity, and neuropathology. Exp Cell Res 239:183-201.
-
(1998)
Exp Cell Res
, vol.239
, pp. 183-201
-
-
Leist, M.1
Nicotera, P.2
-
34
-
-
0033571743
-
Enhanced sensitivity to N-methyl-D-aspartate receptor activation in transgenic and knockin mouse models of Huntington's disease
-
Levine MS, Klapstein GJ, Koppel A, Gruen E, Cepeda C, Vargas ME, Jokel ES, Carpenter EM, Zanjani H, Hurst RS, Efstratiadis A, Zeitlin S, Chesselet MF (1999) Enhanced sensitivity to N-methyl-D-aspartate receptor activation in transgenic and knockin mouse models of Huntington's disease. J Neurosci Res 58:515-532.
-
(1999)
J Neurosci Res
, vol.58
, pp. 515-532
-
-
Levine, M.S.1
Klapstein, G.J.2
Koppel, A.3
Gruen, E.4
Cepeda, C.5
Vargas, M.E.6
Jokel, E.S.7
Carpenter, E.M.8
Zanjani, H.9
Hurst, R.S.10
Efstratiadis, A.11
Zeitlin, S.12
Chesselet, M.F.13
-
35
-
-
0031713541
-
Excitotoxicity, free radicals, necrosis, and apoptosis
-
Lipton SA, Nicotera P (1998) Excitotoxicity, free radicals, necrosis, and apoptosis. Neuroscientist 4:345-352.
-
(1998)
Neuroscientist
, vol.4
, pp. 345-352
-
-
Lipton, S.A.1
Nicotera, P.2
-
36
-
-
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 SW, Bates GP (1996) Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice. Cell 87:493-506.
-
(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
-
37
-
-
0031964359
-
Neuroprotective effects of creatine and cyclocreatine in animal models of Huntington's disease
-
Matthews RT, Yang L, Jenkins BG, Ferrante RJ, Rosen BR, Kaddurah-Daouk R, Beal MF (1998) Neuroprotective effects of creatine and cyclocreatine in animal models of Huntington's disease. J Neurosci 18:156-163.
-
(1998)
J Neurosci
, vol.18
, pp. 156-163
-
-
Matthews, R.T.1
Yang, L.2
Jenkins, B.G.3
Ferrante, R.J.4
Rosen, B.R.5
Kaddurah-Daouk, R.6
Beal, M.F.7
-
38
-
-
0032914740
-
Creatine and cyclocreatine attenuate MPTP neurotoxicity
-
Matthews RT, Ferrante RJ, Klivenyi P, Yang L, Klein AM, Mueller G, Kaddurah-Daouk R, Beal MF (1999) Creatine and cyclocreatine attenuate MPTP neurotoxicity. Exp Neurol 157:142-149.
-
(1999)
Exp Neurol
, vol.157
, pp. 142-149
-
-
Matthews, R.T.1
Ferrante, R.J.2
Klivenyi, P.3
Yang, L.4
Klein, A.M.5
Mueller, G.6
Kaddurah-Daouk, R.7
Beal, M.F.8
-
39
-
-
0001477910
-
Differential effects of creatine depletion on the regulation of enzyme activities and on creatine-stimulated mitochondrial respiration in skeletal muscle, heart, and brain
-
O'Gorman E, Beutner G, Wallimann T, Brdiczka D (1996) Differential effects of creatine depletion on the regulation of enzyme activities and on creatine-stimulated mitochondrial respiration in skeletal muscle, heart, and brain. Biochim Biophys Acta 1276:161-170.
-
(1996)
Biochim Biophys Acta
, vol.1276
, pp. 161-170
-
-
O'Gorman, E.1
Beutner, G.2
Wallimann, T.3
Brdiczka, D.4
-
40
-
-
0031559949
-
The role of creatine kinase inhibition of mitochondrial permeability transition
-
O'Gorman E, Beutner G, Dolder M, Koretsky AP, Brdiczka D, Wallimann T (1997) The role of creatine kinase inhibition of mitochondrial permeability transition. FEBS Lett 414:253-257.
-
(1997)
FEBS Lett
, vol.414
, pp. 253-257
-
-
O'Gorman, E.1
Beutner, G.2
Dolder, M.3
Koretsky, A.P.4
Brdiczka, D.5
Wallimann, T.6
-
41
-
-
0033587128
-
Inhibition of caspase-1 slows disease progression in a mouse model of Huntington's disease
-
Ona VO, Li M, Vonsattel JPG, Andrews LJ, Khan SQ, Chung WM, Frey AS, Menon AS, Li X-J, Stieg PE, Yuan J, Penney JB, Young AB, Cha J-HJ, Friedlander RM (1999) Inhibition of caspase-1 slows disease progression in a mouse model of Huntington's disease. Nature 399:263-267.
-
(1999)
Nature
, vol.399
, pp. 263-267
-
-
Ona, V.O.1
Li, M.2
Vonsattel, J.P.G.3
Andrews, L.J.4
Khan, S.Q.5
Chung, W.M.6
Frey, A.S.7
Menon, A.S.8
Li, X.-J.9
Stieg, P.E.10
Yuan, J.11
Penney, J.B.12
Young, A.B.13
Cha, J.-H.14
Friedlander, R.M.15
-
42
-
-
17344367977
-
Behavioural abnormalities and selective neuronal loss in HD transgenic mice expressing mutated full-length HD cDNA
-
Reddy PH, Williams M, Charles V, Garrett L, Pike-Buchanan L, Whetsell Jr WO, Miller G, Tagle DA (1998) Behavioural abnormalities and selective neuronal loss in HD transgenic mice expressing mutated full-length HD cDNA. Nat Genet 20:198-202.
-
(1998)
Nat Genet
, vol.20
, pp. 198-202
-
-
Reddy, P.H.1
Williams, M.2
Charles, V.3
Garrett, L.4
Pike-Buchanan, L.5
Whetsell W.O., Jr.6
Miller, G.7
Tagle, D.A.8
-
43
-
-
0027504939
-
Determination of creatine kinase parameters in rat brain by NMR magnetization transfer: Correlation with brain function
-
Sauter A, Rudin M (1993) Determination of creatine kinase parameters in rat brain by NMR magnetization transfer: correlation with brain function. J Biol Chem 268:13166-13171.
-
(1993)
J Biol Chem
, vol.268
, pp. 13166-13171
-
-
Sauter, A.1
Rudin, M.2
-
44
-
-
0032851595
-
Increased apoptosis of Huntington disease lymphoblasts associated with repeat length-dependent mitochondrial depolarization
-
Sawa A, Wiegand GW, Cooper J, Margolis RL, Sharp AH, Lawler Jr JF, Greenamyre JT, Snyder SH, Ross CA (1999) Increased apoptosis of Huntington disease lymphoblasts associated with repeat length-dependent mitochondrial depolarization. Nat Med 5:1194-1198.
-
(1999)
Nat Med
, vol.5
, pp. 1194-1198
-
-
Sawa, A.1
Wiegand, G.W.2
Cooper, J.3
Margolis, R.L.4
Sharp, A.H.5
Lawler J.F., Jr.6
Greenamyre, J.T.7
Snyder, S.H.8
Ross, C.A.9
-
45
-
-
0029034511
-
Widespread expression of the Huntington's disease gene (IT-15) protein product
-
Sharp NH, Loev SJ, Schilling G, Li S-H, Li X-J, Bao J, Wagster MV, Kotzuk JA, Steiner JP, Lo A, Hedreen J, Sisodia S, Snyder SH, Dawson TM, Ryugo DK, Ross CA (1995) Widespread expression of the Huntington's disease gene (IT-15) protein product. Neuron 14:1065-1074.
-
(1995)
Neuron
, vol.14
, pp. 1065-1074
-
-
Sharp, N.H.1
Loev, S.J.2
Schilling, G.3
Li, S.-H.4
Li, X.-J.5
Bao, J.6
Wagster, M.V.7
Kotzuk, J.A.8
Steiner, J.P.9
Lo, A.10
Hedreen, J.11
Sisodia, S.12
Snyder, S.H.13
Dawson, T.M.14
Ryugo, D.K.15
Ross, C.A.16
-
46
-
-
0019511040
-
Supplementary creatine as a treatment for gyrate atrophy of the choroid and retina
-
Sipila I, Rapola J, Simell O, Vannas A (1981) Supplementary creatine as a treatment for gyrate atrophy of the choroid and retina. N Engl J Med 304:867-870.
-
(1981)
N Engl J Med
, vol.304
, pp. 867-870
-
-
Sipila, I.1
Rapola, J.2
Simell, O.3
Vannas, A.4
-
47
-
-
0039530026
-
Octamer-dimer transitions of mitochondrial creatine kinase in heart disease
-
Soboll S, Brdiczka D, Jahnke D, Schmidt A, Schlattner U, Wendt S, Wyss M, Wallimann T (1999) Octamer-dimer transitions of mitochondrial creatine kinase in heart disease. J Mol Cell Cardiol 31:857-866.
-
(1999)
J Mol Cell Cardiol
, vol.31
, pp. 857-866
-
-
Soboll, S.1
Brdiczka, D.2
Jahnke, D.3
Schmidt, A.4
Schlattner, U.5
Wendt, S.6
Wyss, M.7
Wallimann, T.8
-
48
-
-
0032479147
-
Mitochondrial creatine kinase is a prime target of peroxynitrite-induced modification and inactivation
-
Stachowiak O, Dolder M, Wallimann T, Richter C (1998) Mitochondrial creatine kinase is a prime target of peroxynitrite-induced modification and inactivation. J Biol Chem 273:16694-16699.
-
(1998)
J Biol Chem
, vol.273
, pp. 16694-16699
-
-
Stachowiak, O.1
Dolder, M.2
Wallimann, T.3
Richter, C.4
-
49
-
-
0030611177
-
2+ responses in muscles with combined mitochondrial and cytosolic creatine kinase deficiencies
-
2+ responses in muscles with combined mitochondrial and cytosolic creatine kinase deficiencies. Cell 89:93-103.
-
(1997)
Cell
, vol.89
, pp. 93-103
-
-
Steeghs, K.1
Benders, A.2
Oerlemans, F.3
De Haan, A.4
Heerschap, A.5
Ruitenbeck, W.6
Jost, C.7
Van Deursen, J.8
Perryman, B.9
Pette, D.10
Bruckwilder, M.11
Koudijs, J.12
Jap, P.13
Veerkamp, J.14
Wieringa, B.15
-
50
-
-
0027994133
-
Creatine deficiency in the brain: A new, treatable inborn error of metabolism
-
Stockler S, Holzbach U, Hanefeld F, Marquardt I, Helms G, Requart M, Hanicke W, Frahm J (1994) Creatine deficiency in the brain: a new, treatable inborn error of metabolism. Pediatr Res 36:409-413.
-
(1994)
Pediatr Res
, vol.36
, pp. 409-413
-
-
Stockler, S.1
Holzbach, U.2
Hanefeld, F.3
Marquardt, I.4
Helms, G.5
Requart, M.6
Hanicke, W.7
Frahm, J.8
-
51
-
-
0030596907
-
Creatine replacement therapy in quanidinoacetate methyltransferase deficiency, a novel inborn error of metabolism
-
Stockler S, Hanefeld F, Frahn J (1996) Creatine replacement therapy in quanidinoacetate methyltransferase deficiency, a novel inborn error of metabolism. Lancet 348:789-790.
-
(1996)
Lancet
, vol.348
, pp. 789-790
-
-
Stockler, S.1
Hanefeld, F.2
Frahn, J.3
-
52
-
-
0027432418
-
Widespread expression of the human and rat Huntington's disease gene in brain and nonneural tissues
-
Strong TV, Tagle DA, Valdes JM, Elmer LW, Boehm K, Swaroop M, Kaatz KW, Collins FS, Albin RL (1993) Widespread expression of the human and rat Huntington's disease gene in brain and nonneural tissues. Nat Genet 5:259-265.
-
(1993)
Nat Genet
, vol.5
, pp. 259-265
-
-
Strong, T.V.1
Tagle, D.A.2
Valdes, J.M.3
Elmer, L.W.4
Boehm, K.5
Swaroop, M.6
Kaatz, K.W.7
Collins, F.S.8
Albin, R.L.9
-
53
-
-
0033541016
-
Creatine monohydrate increases strength in patients with neuromuscular disease
-
Tarnopolsky M, Martin J (1999) Creatine monohydrate increases strength in patients with neuromuscular disease. Neurology 52:854-857.
-
(1999)
Neurology
, vol.52
, pp. 854-857
-
-
Tarnopolsky, M.1
Martin, J.2
-
54
-
-
0030731246
-
A randomized, controlled trial of creatine monohydrate in patients with mitochondrial cytopathies
-
Tarnopolsky MA, Roy BD, MacDonald JR (1997) A randomized, controlled trial of creatine monohydrate in patients with mitochondrial cytopathies. Muscle Nerve 20:1502-1509.
-
(1997)
Muscle Nerve
, vol.20
, pp. 1502-1509
-
-
Tarnopolsky, M.A.1
Roy, B.D.2
MacDonald, J.R.3
-
55
-
-
0027480960
-
A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
-
The Huntington's Disease Collaborative Research Group (1993) A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. Cell 72:971-983.
-
(1993)
Cell
, vol.72
, pp. 971-983
-
-
-
56
-
-
0022395922
-
Neuropathological classification of Huntington's disease
-
Vonsattel JP, Myers RH, Stevens TJ, Ferrante RJ, Bird ED, Richardson EP Jr (1985) Neuropathological classification of Huntington's disease. J Neuropathol Exp Neurol 44:559-577.
-
(1985)
J Neuropathol Exp Neurol
, vol.44
, pp. 559-577
-
-
Vonsattel, J.P.1
Myers, R.H.2
Stevens, T.J.3
Ferrante, R.J.4
Bird, E.D.5
Richardson E.P., Jr.6
-
57
-
-
0026585611
-
Intracellular compartmentation, structure and function of creatine kinase isoenzymes in tissues with high and fluctuating energy demands: The 'phosphocreatine circuit' for cellular energy homeostasis
-
Wallimann T, Wyss M, Brdiczka D, Nicolay K, Eppenberger HM (1992) Intracellular compartmentation, structure and function of creatine kinase isoenzymes in tissues with high and fluctuating energy demands: the 'phosphocreatine circuit' for cellular energy homeostasis. Biochem J 281:21-40.
-
(1992)
Biochem J
, vol.281
, pp. 21-40
-
-
Wallimann, T.1
Wyss, M.2
Brdiczka, D.3
Nicolay, K.4
Eppenberger, H.M.5
-
58
-
-
0032938295
-
Length-dependent gametic CAG repeat instability in the Huntington's disease knock-in mouse
-
Wheeler VC, Auerhach W, White JK, Srinidhi J, Auerbach A, Ryan A, Duyao MP, Vrbanac V, Weaver M, Gusella JF, Joyner AL, MacDonald ME (1999) Length-dependent gametic CAG repeat instability in the Huntington's disease knock-in mouse. Hum Mol Genet 8:115-122.
-
(1999)
Hum Mol Genet
, vol.8
, pp. 115-122
-
-
Wheeler, V.C.1
Auerhach, W.2
White, J.K.3
Srinidhi, J.4
Auerbach, A.5
Ryan, A.6
Duyao, M.P.7
Vrbanac, V.8
Weaver, M.9
Gusella, J.F.10
Joyner, A.L.11
Macdonald, M.E.12
-
59
-
-
0029993078
-
Phosphocreatine-dependent glutamate uptake by synaptic vesicles
-
Xu CJ, Klunk WE, Kanfer JN, Xiong Q, Miller G, Pettegrew JW (1996) Phosphocreatine-dependent glutamate uptake by synaptic vesicles. J Biol Chem 271:13435-13440.
-
(1996)
J Biol Chem
, vol.271
, pp. 13435-13440
-
-
Xu, C.J.1
Klunk, W.E.2
Kanfer, J.N.3
Xiong, Q.4
Miller, G.5
Pettegrew, J.W.6
|