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Results: 1 to 20 of 111

Related Articles by Review for PubMed (Select 19642201)

1.

Mutant huntingtin and glycogen synthase kinase 3-beta accumulate in neuronal lipid rafts of a presymptomatic knock-in mouse model of Huntington's disease.

Valencia A, Reeves PB, Sapp E, Li X, Alexander J, Kegel KB, Chase K, Aronin N, DiFiglia M.

J Neurosci Res. 2010 Jan;88(1):179-90. doi: 10.1002/jnr.22184.

PMID:
19642201
2.

Selective neuronal degeneration in Huntington's disease.

Cowan CM, Raymond LA.

Curr Top Dev Biol. 2006;75:25-71. Review.

PMID:
16984809
3.

The early cellular pathology of Huntington's disease.

Li XJ.

Mol Neurobiol. 1999 Oct-Dec;20(2-3):111-24. Review.

PMID:
10966117
4.

Huntingtin and its role in neuronal degeneration.

Li SH, Li XJ.

Neuroscientist. 2004 Oct;10(5):467-75. Review.

PMID:
15359012
5.

Genetic manipulations of mutant huntingtin in mice: new insights into Huntington's disease pathogenesis.

Lee CY, Cantle JP, Yang XW.

FEBS J. 2013 Sep;280(18):4382-94. doi: 10.1111/febs.12418. Epub 2013 Jul 31. Review.

6.

Are there multiple pathways in the pathogenesis of Huntington's disease?

Aronin N, Kim M, Laforet G, DiFiglia M.

Philos Trans R Soc Lond B Biol Sci. 1999 Jun 29;354(1386):995-1003. Review.

7.

The selective vulnerability of nerve cells in Huntington's disease.

Sieradzan KA, Mann DM.

Neuropathol Appl Neurobiol. 2001 Feb;27(1):1-21. Review.

PMID:
11298997
8.

Molecular aspects of Huntington's disease.

Walling HW, Baldassare JJ, Westfall TC.

J Neurosci Res. 1998 Nov 1;54(3):301-8. Review.

PMID:
9819135
9.

Huntington's disease: From molecular basis to therapeutic advances.

Krobitsch S, Kazantsev AG.

Int J Biochem Cell Biol. 2011 Jan;43(1):20-4. doi: 10.1016/j.biocel.2010.10.014. Epub 2010 Nov 4. Review.

PMID:
21056115
10.

Mechanisms of neuronal cell death in Huntington's disease.

Sawa A, Tomoda T, Bae BI.

Cytogenet Genome Res. 2003;100(1-4):287-95. Review.

PMID:
14526190
11.

Nature and cause of mitochondrial dysfunction in Huntington's disease: focusing on huntingtin and the striatum.

Oliveira JM.

J Neurochem. 2010 Jul;114(1):1-12. doi: 10.1111/j.1471-4159.2010.06741.x. Epub 2010 Apr 9. Review.

PMID:
20403078
12.

The therapeutic potential of G-protein coupled receptors in Huntington's disease.

Dowie MJ, Scotter EL, Molinari E, Glass M.

Pharmacol Ther. 2010 Nov;128(2):305-23. doi: 10.1016/j.pharmthera.2010.07.008. Epub 2010 Aug 11. Review.

PMID:
20708032
13.

Mutant huntingtin can paradoxically protect neurons from death.

Zuchner T, Brundin P.

Cell Death Differ. 2008 Mar;15(3):435-42. Epub 2007 Nov 2. Review.

14.

Presynaptic dysfunction in Huntington's disease.

Rozas JL, Gómez-Sánchez L, Tomás-Zapico C, Lucas JJ, Fernández-Chacón R.

Biochem Soc Trans. 2010 Apr;38(2):488-92. doi: 10.1042/BST0380488. Review.

PMID:
20298208
15.

Huntingtin-protein interactions and the pathogenesis of Huntington's disease.

Li SH, Li XJ.

Trends Genet. 2004 Mar;20(3):146-54. Review.

PMID:
15036808
16.

Huntington's disease: from huntingtin function and dysfunction to therapeutic strategies.

Borrell-Pagès M, Zala D, Humbert S, Saudou F.

Cell Mol Life Sci. 2006 Nov;63(22):2642-60. Review.

PMID:
17041811
17.

Huntington's disease: seeing the pathogenic process through a genetic lens.

Gusella JF, MacDonald ME.

Trends Biochem Sci. 2006 Sep;31(9):533-40. Epub 2006 Jul 10. Review.

PMID:
16829072
18.

[Huntington's disease: intracellular signaling pathways and neuronal death].

Humbert S, Saudou F.

J Soc Biol. 2005;199(3):247-51. Review. French.

PMID:
16471265
19.

Huntington's disease: how does huntingtin, an anti-apoptotic protein, become toxic?

Rangone H, Humbert S, Saudou F.

Pathol Biol (Paris). 2004 Jul;52(6):338-42. Review.

PMID:
15261377
20.

Synaptic dysfunction in Huntington's disease: a new perspective.

Smith R, Brundin P, Li JY.

Cell Mol Life Sci. 2005 Sep;62(17):1901-12. Review.

PMID:
15968465
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