Mitochondrial dysfunction in cybrid lines expressing mitochondrial genes from patients with progressive supranuclear palsy. (Q30306088)

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10 November 2019

title

Mitochondrial dysfunction in cybrid lines expressing mitochondrial genes from patients with progressive supranuclear palsy (English)

1 reference

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10 November 2019

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4

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10 November 2019

Irene Litvan

7

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10 November 2019

author name string

R H Swerdlow

1

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10 November 2019

L I Golbe

2

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10 November 2019

J K Parks

3

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10 November 2019

D R Binder

5

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10 November 2019

A E Grawey

6

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10 November 2019

J P Bennett

8

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10 November 2019

G F Wooten

9

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10 November 2019

W D Parker

10

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10 November 2019

language of work or name

English

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publication date

1 October 2000

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Journal of Neurochemistry

10 November 2019

published in

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10 November 2019

volume

75

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10 November 2019

page(s)

1681-1684

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10 November 2019

issue

4

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Evidence for oxidative stress in the subthalamic nucleus in progressive supranuclear palsy.

10 November 2019

cites work

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Association of an extended haplotype in the tau gene with progressive supranuclear palsy.

21 January 2018

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Comparative biochemistry of tau in progressive supranuclear palsy, corticobasal degeneration, FTDP-17 and Pick's disease

21 January 2018

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Elevated reactive oxygen species and antioxidant enzyme activities in animal and cellular models of Parkinson's disease

21 January 2018

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Genetic evidence for the involvement of tau in progressive supranuclear palsy

21 January 2018

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Identification of a novel polymorphism in the promoter region of the tau gene highly associated to progressive supranuclear palsy in humans.

21 January 2018

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Mitochondrial DNA transmission of the mitochondrial defect in Parkinson's disease

21 January 2018

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Preliminary NINDS neuropathologic criteria for Steele-Richardson-Olszewski syndrome (progressive supranuclear palsy).

21 January 2018

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Mutational analysis of the tau gene in progressive supranuclear palsy.

21 January 2018

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The tau gene A0 allele and progressive supranuclear palsy.

21 January 2018

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Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17

21 January 2018

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Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

21 January 2018

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Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome): report of the NINDS-SPSP international workshop

21 January 2018

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Leber's hereditary optic neuropathy. New genetic considerations

21 January 2018

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Clinical genetics of familial progressive supranuclear palsy.

21 January 2018

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PROGRESSIVE SUPRANUCLEAR PALSY. A HETEROGENEOUS DEGENERATION INVOLVING THE BRAIN STEM, BASAL GANGLIA AND CEREBELLUM WITH VERTICAL GAZE AND PSEUDOBULBAR PALSY, NUCHAL DYSTONIA AND DEMENTIA.

21 January 2018

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Origin and functional consequences of the complex I defect in Parkinson's disease

21 January 2018

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Matrilineal inheritance of complex I dysfunction in a multigenerational Parkinson's disease family

21 January 2018

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