HD phenocopies--possible role of Saitohin gene.

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Euglycemic agent-mediated hypothalamic transcriptomic manipulation in the N171-82Q model of Huntington disease is related to their physiological efficacy.

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Q36234711-914E9C6A-0412-44FC-8104-67E8FB325C30

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HD phenocopies--possible role of Saitohin gene.

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2008 nî lūn-bûn

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2008年の論文

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2008年学术文章

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HD phenocopies--possible role of Saitohin gene.

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HD phenocopies--possible role of Saitohin gene.

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HD phenocopies--possible role of Saitohin gene.

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HD phenocopies--possible role of Saitohin gene.

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HD phenocopies--possible role of Saitohin gene.

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HD phenocopies--possible role of Saitohin gene.

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HD phenocopies--possible role of Saitohin gene.

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D Keckarević

http://www.w3.org/2001/XMLSchema#string

D Savić Pavicević

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M Keckarević Marković

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M Kecmanović

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N Janković

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R Dimitrijević

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S Romac

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V Dobricić

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A polymorphic gene nested within an intron of the tau gene: implications for Alzheimer's disease.

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

Strong association of the Saitohin gene Q7 variant with progressive supranuclear palsy

Is the saitohin gene involved in neurodegenerative diseases?

Saitohin, which is nested in the tau locus and confers allele-specific susceptibility to several neurodegenerative diseases, interacts with peroxiredoxin 6

Mice with targeted mutation of peroxiredoxin 6 develop normally but are susceptible to oxidative stress

Augmented expression of peroxiredoxin VI in rat lung and kidney after birth implies an antioxidative role.

Huntington disease phenocopy is a familial prion disease.

Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease.

A repeat expansion in the gene encoding junctophilin-3 is associated with Huntington disease-like 2.

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391-397

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scholarly article

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10.1080/00207450701593103

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118

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2008-03-01T00:00:00Z

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18300012

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HD phenocopies--possible role of Saitohin gene.

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HD phenocopies--possible role of Saitohin gene.

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