Age-dependent changes in the calcium sensitivity of striatal mitochondria in mouse models of Huntington's Disease
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Mouse models of polyglutamine diseases: review and data table. Part IThe chicken or the egg: mitochondrial dysfunction as a cause or consequence of toxicity in Huntington's diseaseHomeostatic adaptations in brain energy metabolism in mouse models of Huntington diseaseThe operant serial implicit learning task reveals early onset motor learning deficits in the Hdh knock-in mouse model of Huntington's diseaseElucidating a normal function of huntingtin by functional and microarray analysis of huntingtin-null mouse embryonic fibroblasts.Mouse models of Huntington's disease and methodological considerations for therapeutic trials.N-terminal mutant huntingtin associates with mitochondria and impairs mitochondrial trafficking.Mitochondrial calcium uptake capacity as a therapeutic target in the R6/2 mouse model of Huntington's disease.Cardiac dysfunction in the R6/2 mouse model of Huntington's diseaseCa(2+) handling in isolated brain mitochondria and cultured neurons derived from the YAC128 mouse model of Huntington's diseaseCalcium Handling by Endoplasmic Reticulum and Mitochondria in a Cell Model of Huntington's Disease.Mitochondrial Ca(2+) and neurodegenerationImpaired regulation of brain mitochondria by extramitochondrial Ca2+ in transgenic Huntington disease ratsCalpain-mediated signaling mechanisms in neuronal injury and neurodegenerationMitochondrial calcium function and dysfunction in the central nervous system.Mitochondria and energetic depression in cell pathophysiologyThe dysregulation of intracellular calcium in Alzheimer disease.Mitochondrial Ca2+ sequestration and precipitation revisited.Molecular mechanisms and potential therapeutical targets in Huntington's disease.Huntington's disease: can mice lead the way to treatment?Huntington's disease, calcium, and mitochondria.Neuronal Ca(2+) dyshomeostasis in Huntington disease.Metabotropic glutamate receptor 5 as a potential therapeutic target in Huntington's disease.Mutant Huntingtin and Elusive Defects in Oxidative Metabolism and Mitochondrial Calcium Handling.Huntington's Disease: Calcium Dyshomeostasis and Pathology ModelsIsolation and functional assessment of mitochondria from small amounts of mouse brain tissueThe calpain-suppressing effects of olesoxime in Huntington's disease.The path from mitochondrial ROS to aging runs through the mitochondrial permeability transition pore.Catecholamine exocytosis is diminished in R6/2 Huntington's disease model mice.
P2860
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P2860
Age-dependent changes in the calcium sensitivity of striatal mitochondria in mouse models of Huntington's Disease
description
2005 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի հունիսին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2005
@ast
scientific journal article
@en
vedecký článok (publikovaný 2005/06/01)
@sk
vědecký článek publikovaný v roce 2005
@cs
wetenschappelijk artikel (gepubliceerd op 2005/06/01)
@nl
наукова стаття, опублікована в червні 2005
@uk
مقالة علمية (نشرت في يونيو 2005)
@ar
name
Age-dependent changes in the c ...... models of Huntington's Disease
@ast
Age-dependent changes in the c ...... models of Huntington's Disease
@en
Age-dependent changes in the c ...... models of Huntington's Disease
@nl
type
label
Age-dependent changes in the c ...... models of Huntington's Disease
@ast
Age-dependent changes in the c ...... models of Huntington's Disease
@en
Age-dependent changes in the c ...... models of Huntington's Disease
@nl
prefLabel
Age-dependent changes in the c ...... models of Huntington's Disease
@ast
Age-dependent changes in the c ...... models of Huntington's Disease
@en
Age-dependent changes in the c ...... models of Huntington's Disease
@nl
P2093
P921
P3181
P1476
Age-dependent changes in the c ...... models of Huntington's Disease
@en
P2093
C. D. Keene
J. M. Dubinsky
K. J. Purl
N. Brustovetsky
R. LaFrance
T. Brustovetsky
P304
P3181
P356
10.1111/J.1471-4159.2005.03036.X
P407
P577
2005-06-01T00:00:00Z