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Huntingtin
LE WE PMID CA
Huntingtin5589Huntingtin

AHSP

Ataxia (spinocerebellar)

Autophagy

Bax

BimEL

CA8

Chaperone

Collagen

ERS UFR (Induced Mediators)

HAP1 Huntingtin associated protein1

Huntingtin

HYPK

InsP3R

Ion channel (Calcium)

Mitochondria (Dysfunction)

opt mouse

Organelle migration

P47

Presenilin

Receptor (Inositol trisphosphate)

Spinocerebellar ataxia15

Spinocerebellar ataxia16

Spinocerebellar ataxia2

Spinocerebellar ataxia3

Tubulin

waddles wdl mouse

1999  
1
The localization and interactions of huntingtin.
[10434301] Philos Trans R Soc Lond B Biol Sci 354(1386): 1021-7 (1999)
2011  
2
2004  
3
Huntingtin and the molecular pathogenesis of Huntington's disease. Fourth in molecular medicine review series.
[15459747] EMBO Rep 5(10): 958-63 (2004)
2009  
4
Huntingtin as an essential integrator of intracellular vesicular trafficking.
[19269181] Trends Cell Biol 19(4): 147-55 (2009)
2010  
5
Inositol trisphosphate receptor Ca2+ release channels in neurological diseases.
[20383523] Pflugers Arch 460(2): 481-94 (2010)
2008  
6
A stress sensitive ER membrane-association domain in Huntingtin protein defines a potential role for Huntingtin in the regulation of autophagy.
[17986868] Autophagy 4(1): 91-3 (2008)
2010  
7
BimEL as a possible molecular link between proteasome dysfunction and cell death induced by mutant huntingtin.
[20497470] Eur J Neurosci 31(11): 1915-25 (2010)
2008  
8
Mutant huntingtin and mitochondrial dysfunction.
[18951640] Trends Neurosci 31(12): 609-16 (2008)

Downloaded from http://www.kidney.de - The Database of Free Medical Reviews - The Metatextbook of Medicine - Ossip Groth

All Medline data shown were primarily retrieved from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.


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