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Items: 14

1.

The IGF-1/Akt pathway is neuroprotective in Huntington's disease and involves Huntingtin phosphorylation by Akt.

Humbert S, Bryson EA, Cordelières FP, Connors NC, Datta SR, Finkbeiner S, Greenberg ME, Saudou F.

Dev Cell. 2002 Jun;2(6):831-7.

2.

[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
3.

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.

4.

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
5.

Huntington's disease: from pathology and genetics to potential therapies.

Imarisio S, Carmichael J, Korolchuk V, Chen CW, Saiki S, Rose C, Krishna G, Davies JE, Ttofi E, Underwood BR, Rubinsztein DC.

Biochem J. 2008 Jun 1;412(2):191-209. doi: 10.1042/BJ20071619. Review.

PMID:
18466116
6.

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
7.

Protein aggregation in Huntington's disease.

Hoffner G, Djian P.

Biochimie. 2002 Apr;84(4):273-8. Review.

PMID:
12106904
8.

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.

9.

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
10.

Huntingtin processing in pathogenesis of Huntington disease.

Qin ZH, Gu ZL.

Acta Pharmacol Sin. 2004 Oct;25(10):1243-9. Review.

11.

Loss of normal huntingtin function: new developments in Huntington's disease research.

Cattaneo E, Rigamonti D, Goffredo D, Zuccato C, Squitieri F, Sipione S.

Trends Neurosci. 2001 Mar;24(3):182-8. Review.

PMID:
11182459
12.

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
13.

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
14.

Huntington's disease: degradation of mutant huntingtin by autophagy.

Sarkar S, Rubinsztein DC.

FEBS J. 2008 Sep;275(17):4263-70. doi: 10.1111/j.1742-4658.2008.06562.x. Epub 2008 Jul 15. Review.

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