-
1
-
-
84880960483
-
Muscle histone deacetylase 4 upregulation in amyotrophic lateral sclerosis: potential role in reinnervation ability and disease progression
-
Bruneteau, G., Simonet, T., Bauche, S., Mandjee, N., Malfatti, E., Girard, E., et al. (2013). Muscle histone deacetylase 4 upregulation in amyotrophic lateral sclerosis: potential role in reinnervation ability and disease progression. Brain 136, 2359-2368. doi: 10.1093/brain/awt164
-
(2013)
Brain
, vol.136
, pp. 2359-2368
-
-
Bruneteau, G.1
Simonet, T.2
Bauche, S.3
Mandjee, N.4
Malfatti, E.5
Girard, E.6
-
2
-
-
56349130281
-
Use of hand-held dynamometry in the evaluation of lower limb muscle strength in people with Huntington's disease
-
Busse, M. E., Hughes, G., Wiles, C. M., and Rosser, A. E. (2008). Use of hand-held dynamometry in the evaluation of lower limb muscle strength in people with Huntington's disease. J. Neurol. 255, 1534-1540. doi: 10.1007/s00415-008-0964-x
-
(2008)
J. Neurol
, vol.255
, pp. 1534-1540
-
-
Busse, M.E.1
Hughes, G.2
Wiles, C.M.3
Rosser, A.E.4
-
3
-
-
0033560924
-
Characterization of progressive motor deficits in mice transgenic for the human Huntington's disease mutation
-
Carter, R. J., Lione, L. A., Humby, T., Mangiarini, L., Mahal, A., Bates, G. P., et al. (1999). Characterization of progressive motor deficits in mice transgenic for the human Huntington's disease mutation. J. Neurosci. 19, 3248-3257.
-
(1999)
J. Neurosci.
, vol.19
, pp. 3248-3257
-
-
Carter, R.J.1
Lione, L.A.2
Humby, T.3
Mangiarini, L.4
Mahal, A.5
Bates, G.P.6
-
4
-
-
67650061723
-
Impaired PGC-1alpha function in muscle in Huntington's disease
-
Chaturvedi, R. K., Adhihetty, P., Shukla, S., Hennessy, T., Calingasan, N., Yang, L., et al. (2009). Impaired PGC-1alpha function in muscle in Huntington's disease. Hum. Mol. Genet. 18, 3048-3065. doi: 10.1093/hmg/ddp243
-
(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
-
5
-
-
33750975898
-
Increased apoptosis Huntingtin inclusions and altered differentiation in muscle cell cultures from Huntington's disease subjects
-
Ciammola, A., Sassone, J., Alberti, L., Meola, G., Mancinelli, E., Russo, M. A., et al. (2006). Increased apoptosis, Huntingtin inclusions and altered differentiation in muscle cell cultures from Huntington's disease subjects. Cell Death Differ. 13, 2068-2078. doi: 10.1038/sj.cdd.4401967
-
(2006)
Cell Death Differ
, vol.13
, pp. 2068-2078
-
-
Ciammola, A.1
Sassone, J.2
Alberti, L.3
Meola, G.4
Mancinelli, E.5
Russo, M.A.6
-
6
-
-
79951492653
-
Low anaerobic threshold and increased skeletal muscle lactate production in subjects with Huntington's disease
-
Ciammola, A., Sassone, J., Sciacco, M., Mencacci, N. E., Ripolone, M., Bizzi, C., et al. (2011). Low anaerobic threshold and increased skeletal muscle lactate production in subjects with Huntington's disease. Mov. Disord. 26, 130-137. doi: 10.1002/mds.23258
-
(2011)
Mov. Disord.
, vol.26
, pp. 130-137
-
-
Ciammola, A.1
Sassone, J.2
Sciacco, M.3
Mencacci, N.E.4
Ripolone, M.5
Bizzi, C.6
-
7
-
-
79551655290
-
Huntington's disease: can mice lead the way to treatment?
-
Crook, Z. R., and Housman, D. (2011). Huntington's disease: can mice lead the way to treatment? Neuron 69, 423-435. doi: 10.1016/j.neuron.2010.12.035
-
(2011)
Neuron
, vol.69
, pp. 423-435
-
-
Crook, Z.R.1
Housman, D.2
-
8
-
-
84892450038
-
p53 increases caspase-6 expression and activation in muscle tissue expressing mutant huntingtin
-
Ehrnhoefer, D. E., Skotte, N. H., Ladha, S., Nguyen, Y. T., Qiu, X., Deng, Y., et al. (2014). p53 increases caspase-6 expression and activation in muscle tissue expressing mutant huntingtin. Hum. Mol. Genet. 23, 717-729. doi: 10.1093/hmg/ddt458
-
(2014)
Hum. Mol. Genet
, vol.23
, pp. 717-729
-
-
Ehrnhoefer, D.E.1
Skotte, N.H.2
Ladha, S.3
Nguyen, Y.T.4
Qiu, X.5
Deng, Y.6
-
9
-
-
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., et al. (2005). Active HSF1 significantly suppresses polyglutamine aggregate formation in cellular and mouse models. J. Biol. Chem. 280, 34908-34916. doi: 10.1074/jbc.M506288200
-
(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
-
10
-
-
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., et al. (2006). Low stability of Huntington muscle mitochondria against Ca2+ in R6/2 mice. Ann. Neurol. 59, 407-411. doi: 10.1002/ana.20754
-
(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
-
11
-
-
0027490598
-
Molecular genetics of Huntington's disease
-
Gusella, J. F., MacDonald, M. E., Ambrose, C. M., and Duyao, M. P. (1993). Molecular genetics of Huntington's disease. Arch. Neurol. 50, 1157-1163. doi: 10.1001/archneur.1993.00540110037003
-
(1993)
Arch. Neurol.
, vol.50
, pp. 1157-1163
-
-
Gusella, J.F.1
MacDonald, M.E.2
Ambrose, C.M.3
Duyao, M.P.4
-
12
-
-
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
-
HDRG. (1993). A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. The Huntington's Disease Collaborative Research Group. Cell 72, 971-83. doi: 10.1016/0092-8674(93)90585-E
-
(1993)
Cell
, vol.72
, pp. 971-983
-
-
-
13
-
-
0027759564
-
Characterization and localization of the Huntington disease gene product
-
Hoogeveen, A. T., Willemsen, R., Meyer, N., de Rooij, K. E., Roos, R. A., van Ommen, G. J., et al. (1993). Characterization and localization of the Huntington disease gene product. Hum. Mol. Genet. 2, 2069-2073. doi: 10.1093/hmg/2.12.2069
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 2069-2073
-
-
Hoogeveen, A.T.1
Willemsen, R.2
Meyer, N.3
de Rooij, K.E.4
Roos, R.A.5
van Ommen, G.J.6
-
14
-
-
84863011541
-
Pharmacologic activation of mitochondrial biogenesis exerts widespread beneficial effects in a transgenic mouse model of Huntington's disease
-
Johri, A., Calingasan, N. Y., Hennessey, T. M., Sharma, A., Yang, L., Wille, E., et al. (2012). Pharmacologic activation of mitochondrial biogenesis exerts widespread beneficial effects in a transgenic mouse model of Huntington's disease. Hum. Mol. Genet. 21, 1124-1137. doi: 10.1093/hmg/ddr541
-
(2012)
Hum. Mol. Genet.
, vol.21
, pp. 1124-1137
-
-
Johri, A.1
Calingasan, N.Y.2
Hennessey, T.M.3
Sharma, A.4
Yang, L.5
Wille, E.6
-
15
-
-
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., et al. (2007). Myopathy as a first symptom of Huntington's disease in a Marathon runner. Mov. Disord. 22, 1637-1640. doi: 10.1002/mds.21550
-
(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
-
16
-
-
84880730823
-
Huntington's disease: underlying molecular mechanisms and emerging concepts
-
Labbadia, J., and Morimoto, R. I. (2013). Huntington's disease: underlying molecular mechanisms and emerging concepts. Trends Biochem. Sci. 38, 378-385. doi: 10.1016/j.tibs.2013.05.003
-
(2013)
Trends Biochem. Sci.
, vol.38
, pp. 378-385
-
-
Labbadia, J.1
Morimoto, R.I.2
-
17
-
-
84883464853
-
Genetic manipulations of mutant huntingtin in mice: new insights into Huntington's disease pathogenesis
-
Lee, C. Y., Cantle, J. P., and Yang, X. W. (2013). Genetic manipulations of mutant huntingtin in mice: new insights into Huntington's disease pathogenesis. FEBS J. 18, 4382-4394. doi: 10.1111/febs.12418
-
(2013)
FEBS J
, vol.18
, pp. 4382-4394
-
-
Lee, C.Y.1
Cantle, J.P.2
Yang, X.W.3
-
18
-
-
1242338856
-
Huntingtin-protein interactions and the pathogenesis of Huntington's disease
-
Li, S. H., and Li, X. J. (2004). Huntingtin-protein interactions and the pathogenesis of Huntington's disease. Trends Genet. 20, 146-154. doi: 10.1016/j.tig.2004.01.008
-
(2004)
Trends Genet
, vol.20
, pp. 146-154
-
-
Li, S.H.1
Li, X.J.2
-
19
-
-
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. doi: 10.1016/j.cmet.2005.05.004
-
(2005)
Cell Metab
, vol.1
, pp. 361-370
-
-
Lin, J.1
Handschin, C.2
Spiegelman, B.M.3
-
20
-
-
0033500593
-
Selective discrimination learning impairments in mice expressing the human Huntington's disease mutation
-
Lione, L. A., Carter, R. J., Hunt, M. J., Bates, G. P., Morton, A. J., and Dunnett, S. B. (1999). Selective discrimination learning impairments in mice expressing the human Huntington's disease mutation. J. Neurosci. 19, 10428-10437.
-
(1999)
J. Neurosci.
, vol.19
, pp. 10428-10437
-
-
Lione, L.A.1
Carter, R.J.2
Hunt, M.J.3
Bates, G.P.4
Morton, A.J.5
Dunnett, S.B.6
-
21
-
-
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., et al. (2000). Abnormal in vivo skeletal muscle energy metabolism in Huntington's disease and dentatorubropallidoluysian atrophy. Ann. Neurol. 48, 72-76. doi: 10.1002/1531-8249(200007)48:1<72::AID-ANA11>3.0.CO;2-I
-
(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
-
22
-
-
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., 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. doi: 10.1093/hmg/11.17.1911
-
(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
-
23
-
-
84944718721
-
Dysfunction of the CNS-Heart Axis in Mouse Models of Huntington's Disease
-
Mielcarek, M., Inuabasi, L., Bondulich, M. K., Muller, T., Osborne, G. F., Franklin, S. A., et al. (2014). Dysfunction of the CNS-Heart Axis in Mouse Models of Huntington's Disease. PLoS Genet. 10:e1004550. doi: 10.1371/journal.pgen.1004550
-
(2014)
PLoS Genet
, vol.10
, pp. e1004550
-
-
Mielcarek, M.1
Inuabasi, L.2
Bondulich, M.K.3
Muller, T.4
Osborne, G.F.5
Franklin, S.A.6
-
24
-
-
84889031644
-
HDAC4 reduction: a novel therapeutic strategy to target cytoplasmic huntingtin and ameliorate neurodegeneration
-
Mielcarek, M., Landles, C., Weiss, A., Bradaia, A., Seredenina, T., Inuabasi, L., et al. (2013b). HDAC4 reduction: a novel therapeutic strategy to target cytoplasmic huntingtin and ameliorate neurodegeneration. PLoS Biol. 11:e1001717. doi: 10.1371/journal.pbio.1001717
-
(2013)
PLoS Biol
, vol.11
, pp. e1001717
-
-
Mielcarek, M.1
Landles, C.2
Weiss, A.3
Bradaia, A.4
Seredenina, T.5
Inuabasi, L.6
-
25
-
-
84889000595
-
HDAC4 does not act as a protein deacetylase in the postnatal murine brain in vivo
-
Mielcarek, M., Seredenina, T., Stokes, M. P., Osborne, G. F., Landles, C., Inuabasi, L., et al. (2013a). HDAC4 does not act as a protein deacetylase in the postnatal murine brain in vivo. PLoS ONE 8:e80849. doi: 10.1371/journal.pone.0080849
-
(2013)
PLoS ONE
, vol.8
, pp. e80849
-
-
Mielcarek, M.1
Seredenina, T.2
Stokes, M.P.3
Osborne, G.F.4
Landles, C.5
Inuabasi, L.6
-
26
-
-
77950547661
-
Formation of polyglutamine inclusions in a wide range of non-CNS tissues in the HdhQ150 knock-in mouse model of Huntington's disease
-
Moffitt, H., McPhail, G. D., Woodman, B., Hobbs, C., and Bates, G. P. (2009). Formation of polyglutamine inclusions in a wide range of non-CNS tissues in the HdhQ150 knock-in mouse model of Huntington's disease. PLoS ONE 4:e8025. doi: 10.1371/journal.pone.0008025
-
(2009)
PLoS ONE
, vol.4
, pp. e8025
-
-
Moffitt, H.1
McPhail, G.D.2
Woodman, B.3
Hobbs, C.4
Bates, G.P.5
-
27
-
-
0034234519
-
Abnormal synaptic plasticity and impaired spatial cognition in mice transgenic for exon 1 of the human Huntington's disease mutation
-
Murphy, K. P., Carter, R. J., Lione, L. A., Mangiarini, L., Mahal, A., Bates, G. P., et al. (2000). Abnormal synaptic plasticity and impaired spatial cognition in mice transgenic for exon 1 of the human Huntington's disease mutation. J. Neurosci. 20, 5115-5123.
-
(2000)
J. Neurosci.
, vol.20
, pp. 5115-5123
-
-
Murphy, K.P.1
Carter, R.J.2
Lione, L.A.3
Mangiarini, L.4
Mahal, A.5
Bates, G.P.6
-
28
-
-
77956069555
-
Huntington's disease
-
Novak, M. J., and Tabrizi, S. J. (2010). Huntington's disease. BMJ 340:c3109. doi: 10.1136/bmj.c3109
-
(2010)
BMJ
, vol.340
, pp. c3109
-
-
Novak, M.J.1
Tabrizi, S.J.2
-
29
-
-
0141866674
-
Inclusion formation in Huntington's disease R6/2 mouse muscle cultures
-
Orth, M., Cooper, J. M., Bates, G. P., and Schapira, A. H. (2003). Inclusion formation in Huntington's disease R6/2 mouse muscle cultures. J. Neurochem. 87, 1-6. doi: 10.1046/j.1471-4159.2003.02009.x
-
(2003)
J. Neurochem.
, vol.87
, pp. 1-6
-
-
Orth, M.1
Cooper, J.M.2
Bates, G.P.3
Schapira, A.H.4
-
30
-
-
70349422148
-
Role of mitochondrial dysfunction in the pathogenesis of Huntington's disease
-
Quintanilla, R. A., and Johnson, G. V. W. (2009). Role of mitochondrial dysfunction in the pathogenesis of Huntington's disease. Brain Res. Bull. 80, 242-247. doi: 10.1016/j.brainresbull.2009.07.010
-
(2009)
Brain Res. Bull.
, vol.80
, pp. 242-247
-
-
Quintanilla, R.A.1
Johnson, G.V.W.2
-
31
-
-
84893193971
-
Correlations of behavioral deficits with brain pathology assessed through longitudinal MRI and histopathology in the R6/2 mouse model of HD
-
Rattray, I., Smith, E., Gale, R., Matsumoto, K., Bates, G. P., and Modo, M. (2013). Correlations of behavioral deficits with brain pathology assessed through longitudinal MRI and histopathology in the R6/2 mouse model of HD. PLoS ONE 8:e60012. doi: 10.1371/journal.pone.0060012
-
(2013)
PLoS ONE
, vol.8
, pp. e60012
-
-
Rattray, I.1
Smith, E.2
Gale, R.3
Matsumoto, K.4
Bates, G.P.5
Modo, M.6
-
32
-
-
84903779388
-
Increased mitochondrial fission and neuronal dysfunction in Huntington's disease: implications for molecular inhibitors of excessive mitochondrial fission
-
Reddy, P. H. (2014). Increased mitochondrial fission and neuronal dysfunction in Huntington's disease: implications for molecular inhibitors of excessive mitochondrial fission. Drug Discov. Today 19, 951-955. doi: 10.1016/j.drudis.2014.03.020
-
(2014)
Drug Discov. Today.
, vol.19
, pp. 951-955
-
-
Reddy, P.H.1
-
33
-
-
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., et al. (2004). Progressive abnormalities in skeletal muscle and neuromuscular junctions of transgenic mice expressing the Huntington's disease mutation. Eur. J. Neurosci. 20, 3092-3114. doi: 10.1111/j.1460-9568.2004.03783.x
-
(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
-
34
-
-
78751517878
-
Increased neurotransmitter release at the neuromuscular junction in a mouse model of polyglutamine disease
-
Rozas, J. L., Gomez-Sanchez, L., Tomas-Zapico, C., Lucas, J. J., and Fernandez-Chacon, R. (2011). Increased neurotransmitter release at the neuromuscular junction in a mouse model of polyglutamine disease. J. neurosci. 31, 1106-1113. doi: 10.1523/JNEUROSCI.2011-10.2011
-
(2011)
J. neurosci.
, vol.31
, pp. 1106-1113
-
-
Rozas, J.L.1
Gomez-Sanchez, L.2
Tomas-Zapico, C.3
Lucas, J.J.4
Fernandez-Chacon, R.5
-
35
-
-
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., et al. (2005). Mitochondrial impairment in patients and asymptomatic mutation carriers of Huntington's disease. Mov. Disord. 20, 674-679. doi: 10.1002/mds.20373
-
(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
-
36
-
-
69949102831
-
Huntington's disease: the current state of research with peripheral tissues
-
Sassone, J., Colciago, C., Cislaghi, G., Silani, V., and Ciammola, A. (2009). Huntington's disease: the current state of research with peripheral tissues. Exp. Neurol. 219, 385-397. doi: 10.1016/j.expneurol.2009.05.012
-
(2009)
Exp. Neurol.
, vol.219
, pp. 385-397
-
-
Sassone, J.1
Colciago, C.2
Cislaghi, G.3
Silani, V.4
Ciammola, A.5
-
37
-
-
0032919205
-
Formation of polyglutamine inclusions in non-CNS tissue
-
Sathasivam, K., Hobbs, C., Turmaine, M., Mangiarini, L., Mahal, A., Bertaux, F., et al. (1999). Formation of polyglutamine inclusions in non-CNS tissue. Hum. Mol. Genet. 8, 813-822. doi: 10.1093/hmg/8.5.813
-
(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
-
38
-
-
84873463075
-
Aberrant splicing of HTT generates the pathogenic exon 1 protein in Huntington disease
-
Sathasivam, K., Neueder, A., Gipson, T. A., Landles, C., Benjamin, A. C., Bondulich, M. K., et al. (2013). Aberrant splicing of HTT generates the pathogenic exon 1 protein in Huntington disease. Proc. Natl. Acad. Sci. U.S.A. 110, 2366-2370. doi: 10.1073/pnas.1221891110
-
(2013)
Proc. Natl. Acad. Sci. U. S. A.
, vol.110
, pp. 2366-2370
-
-
Sathasivam, K.1
Neueder, A.2
Gipson, T.A.3
Landles, C.4
Benjamin, A.C.5
Bondulich, M.K.6
-
39
-
-
79959589571
-
Molecular characterization of skeletal muscle atrophy in the R6/2 mouse model of Huntington's disease
-
She, P., Zhang, Z., Marchionini, D., Diaz, W. C., Jetton, T. J., Kimball, S. R., et al. (2011). Molecular characterization of skeletal muscle atrophy in the R6/2 mouse model of Huntington's disease. Am. J. Physiol. Endocrinol. Metab. 301, E49-E61. doi: 10.1152/ajpendo.00630.2010
-
(2011)
Am. J. Physiol. Endocrinol. Metab.
, vol.301
, pp. E49-E61
-
-
She, P.1
Zhang, Z.2
Marchionini, D.3
Diaz, W.C.4
Jetton, T.J.5
Kimball, S.R.6
-
40
-
-
25844526181
-
Gene expression in Huntington's disease skeletal muscle: a potential biomarker
-
Strand, A. D., Aragaki, A. K., Shaw, D., Bird, T., Holton, J., Turner, C., et al. (2005). Gene expression in Huntington's disease skeletal muscle: a potential biomarker. Hum. Mol. Genet. 14, 1863-1876. doi: 10.1093/hmg/ddi192
-
(2005)
Hum. Mol. Genet
, vol.14
, pp. 1863-1876
-
-
Strand, A.D.1
Aragaki, A.K.2
Shaw, D.3
Bird, T.4
Holton, J.5
Turner, C.6
-
41
-
-
0027432418
-
Widespread expression of the human and rat Huntington's disease gene in brain and nonneural tissues
-
Strong, T. V., Tagle, D. A., Valdes, J. M., Elmer, L. W., Boehm, K., Swaroop, M., et al. (1993). Widespread expression of the human and rat Huntington's disease gene in brain and nonneural tissues. Nat. Genet. 5, 259-265. doi: 10.1038/ng1193-259
-
(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
-
42
-
-
0029055601
-
Cellular localization of the Huntington's disease protein and discrimination of the normal and mutated form
-
Trottier, Y., Devys, D., Imbert, G., Saudou, F., An, I., Lutz, Y., et al. (1995). Cellular localization of the Huntington's disease protein and discrimination of the normal and mutated form. Nat. Genet. 10, 104-110. doi: 10.1038/ng0595-104
-
(1995)
Nat. Genet.
, vol.10
, pp. 104-110
-
-
Trottier, Y.1
Devys, D.2
Imbert, G.3
Saudou, F.4
An, I.5
Lutz, Y.6
-
43
-
-
67650095269
-
Beyond the brain: widespread pathology in Huntington's disease
-
van der Burg, J. M., Bjorkqvist, M., and Brundin, P. (2009). Beyond the brain: widespread pathology in Huntington's disease. Lancet Neurol. 8, 765-774. doi: 10.1016/S1474-4422(09)70178-4
-
(2009)
Lancet Neurol
, vol.8
, pp. 765-774
-
-
van der Burg, J.M.1
Bjorkqvist, M.2
Brundin, P.3
-
45
-
-
37349066159
-
Atrophy and degeneration in sciatic nerve of presymptomatic mice carrying the Huntington's disease mutation
-
Wade, A., Jacobs, P., and Morton, A. J. (2008). Atrophy and degeneration in sciatic nerve of presymptomatic mice carrying the Huntington's disease mutation. Brain Res. 1188, 61-68. doi: 10.1016/j.brainres.2007.06.059
-
(2008)
Brain Res
, vol.1188
, pp. 61-68
-
-
Wade, A.1
Jacobs, P.2
Morton, A.J.3
-
46
-
-
33846225133
-
Huntington's disease
-
Walker, F. O. (2007). Huntington's disease. Lancet 369, 218-228. doi: 10.1016/S0140-6736(07)60111-1
-
(2007)
Lancet
, vol.369
, pp. 218-228
-
-
Walker, F.O.1
-
47
-
-
84878459469
-
Huntington disease skeletal muscle is hyperexcitable owing to chloride and potassium channel dysfunction
-
Waters, C. W., Varuzhanyan, G., Talmadge, R. J., and Voss, A. A. (2013). Huntington disease skeletal muscle is hyperexcitable owing to chloride and potassium channel dysfunction. Proc. Natl. Acad. Sci. U.S.A. 110, 9160-9165. doi: 10.1073/pnas.1220068110
-
(2013)
Proc. Natl. Acad. Sci. U. S. A.
, vol.110
, pp. 9160-9165
-
-
Waters, C.W.1
Varuzhanyan, G.2
Talmadge, R.J.3
Voss, A.A.4
-
48
-
-
84993912315
-
Increased apoptosis and early embryonic lethality in mice nullizygous for the Huntington's disease gene homologue
-
Zeitlin, S., Liu, J. P., Chapman, D. L., Papaioannou, V. E., and Efstratiadis, A. (1995). Increased apoptosis and early embryonic lethality in mice nullizygous for the Huntington's disease gene homologue. Nat. Genet. 11, 155-163. doi: 10.1038/ng1095-155
-
(1995)
Nat. Genet.
, vol.11
, pp. 155-163
-
-
Zeitlin, S.1
Liu, J.P.2
Chapman, D.L.3
Papaioannou, V.E.4
Efstratiadis, A.5
-
49
-
-
84905862069
-
Cardiac Dysfunction in Huntington's Disease
-
Available online at
-
Zielonka, D., Piotrowska, I., and Mielcarek, M. (2014). Cardiac Dysfunction in Huntington's Disease. Exp. Clin. Cardiol. 20, 2547-2554. Available online at: http://cardiologyacademicpress.com/soap/pdf/delme_1788_53e3f6e3313354.90986595.pdf
-
(2014)
Exp. Clin. Cardiol.
, vol.20
, pp. 2547-2554
-
-
Zielonka, D.1
Piotrowska, I.2
Mielcarek, M.3
|