(Q42792348)

English

Peroxisome-proliferator-activated receptor gamma coactivator 1 α contributes to dysmyelination in experimental models of Huntington's disease

scientific article published on June 2011

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scholarly article

1 reference

Europe PubMed Central

7 November 2017

Peroxisome-proliferator-activated receptor gamma coactivator 1 α contributes to dysmyelination in experimental models of Huntington's disease (English)

1 reference

Europe PubMed Central

7 November 2017

Huntington's disease

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11

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7 November 2017

object named as

Marta Valenza

2

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Jiangyang Zhang

7

object named as

Jiangyang Zhang

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Europe PubMed Central

7 November 2017

author name string

Zhongmin Xiang

1

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Europe PubMed Central

7 November 2017

Libin Cui

3

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Europe PubMed Central

7 November 2017

Valerio Leoni

4

1 reference

Europe PubMed Central

7 November 2017

Hyun-Kyung Jeong

5

1 reference

Europe PubMed Central

7 November 2017

Elisa Brilli

6

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Europe PubMed Central

7 November 2017

Qi Peng

8

1 reference

Europe PubMed Central

7 November 2017

Wenzhen Duan

9

1 reference

Europe PubMed Central

7 November 2017

Steven A Reeves

10

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Europe PubMed Central

7 November 2017

Dimitri Krainc

12

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7 November 2017

language of work or name

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publication date

1 June 2011

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Europe PubMed Central

7 November 2017

Journal of Neuroscience

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7 November 2017

31

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7 November 2017

9544-9553

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Europe PubMed Central

7 November 2017

26

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7 November 2017

describes a project that uses

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Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3132810/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

Structural MRI detects progressive regional brain atrophy and neuroprotective effects in N171-82Q Huntington's disease mouse model

1 reference

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Smaller intracranial volume in prodromal Huntington's disease: evidence for abnormal neurodevelopment

1 reference

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The role of PGC-1α in the pathogenesis of neurodegenerative disorders

1 reference

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Nicotinamide improves motor deficits and upregulates PGC-1α and BDNF gene expression in a mouse model of Huntington's disease

1 reference

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Cholesterol defect is marked across multiple rodent models of Huntington's disease and is manifest in astrocytes

1 reference

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Inhibition of transglutaminase 2 mitigates transcriptional dysregulation in models of Huntington disease.

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Molecular mechanisms and potential therapeutical targets in Huntington's disease

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Impairment of PGC-1alpha expression, neuropathology and hepatic steatosis in a transgenic mouse model of Huntington's disease following chronic energy deprivation

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Contrasting gray and white matter changes in preclinical Huntington disease: an MRI study

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Altered white matter microstructure in the corpus callosum in Huntington's disease: implications for cortical "disconnection".

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Impaired PGC-1alpha function in muscle in Huntington's disease.

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The gene coding for PGC-1alpha modifies age at onset in Huntington's Disease

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Full-length human mutant huntingtin with a stable polyglutamine repeat can elicit progressive and selective neuropathogenesis in BACHD mice

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Detection of Huntington's disease decades before diagnosis: the Predict-HD study

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Localization of the transcriptional coactivator PGC-1alpha to GABAergic neurons during maturation of the rat brain

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Cholesterol dysfunction in neurodegenerative diseases: is Huntington's disease in the list?

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An oligodendrocyte-specific zinc-finger transcription regulator cooperates with Olig2 to promote oligodendrocyte differentiation

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Diffusion tensor imaging in presymptomatic and early Huntington's disease: Selective white matter pathology and its relationship to clinical measures.

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PGC-1 coactivators: inducible regulators of energy metabolism in health and disease

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Regional white matter change in pre-symptomatic Huntington's disease: a diffusion tensor imaging study

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PGC-1alpha deficiency causes multi-system energy metabolic derangements: muscle dysfunction, abnormal weight control and hepatic steatosis

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Defects in adaptive energy metabolism with CNS-linked hyperactivity in PGC-1alpha null mice

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In vivo evidence of cerebellar atrophy and cerebral white matter loss in Huntington disease

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Identifiers

10.1523/JNEUROSCI.1291-11.2011

1 reference

Europe PubMed Central

7 November 2017

1 reference

Europe PubMed Central

7 November 2017

1 reference

Europe PubMed Central

7 November 2017

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