(Q40708696)

English

A newly established neuronal rho-0 cell line highly susceptible to oxidative stress accumulates iron and other metals. Relevance to the origin of metal ion deposits in brains with neurodegenerative disorders

scientific article published on 22 August 2002

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scholarly article

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Europe PubMed Central

PubMed publication ID

23 September 2017

A newly established neuronal rho-0 cell line highly susceptible to oxidative stress accumulates iron and other metals. Relevance to the origin of metal ion deposits in brains with neurodegenerative disorders (English)

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

neurodegeneration

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based on heuristic

inferred from title

author name string

Ryuichi Fukuyama

1

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

Akihiko Nakayama

2

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Europe PubMed Central

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23 September 2017

Taizen Nakase

3

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Europe PubMed Central

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23 September 2017

Hiroe Toba

4

1 reference

Europe PubMed Central

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23 September 2017

Teruo Mukainaka

5

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Europe PubMed Central

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23 September 2017

Hirofumi Sakaguchi

6

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

Takuya Saiwaki

7

1 reference

Europe PubMed Central

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23 September 2017

Hiromu Sakurai

8

1 reference

Europe PubMed Central

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23 September 2017

Mikio Wada

9

1 reference

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23 September 2017

Shinji Fushiki

10

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Europe PubMed Central

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23 September 2017

language of work or name

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publication date

22 August 2002

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23 September 2017

Journal of Biological Chemistry

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23 September 2017

277

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23 September 2017

44

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Europe PubMed Central

PubMed publication ID

23 September 2017

41455-41462

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

A novel pantothenate kinase gene (PANK2) is defective in Hallervorden-Spatz syndrome

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Iron and neurodegenerative disorders

1 reference

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Brain iron pathways and their relevance to Parkinson's disease.

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The genetics and pathology of oxidative phosphorylation

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Mitochondrial involvement in Alzheimer's disease

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Gene expression of ND4, a subunit of complex I of oxidative phosphorylation in mitochondria, is decreased in temporal cortex of brains of Alzheimer's disease patients.

1 reference

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The expression of several mitochondrial and nuclear genes encoding the subunits of electron transport chain enzyme complexes, cytochrome c oxidase, and NADH dehydrogenase, in different brain regions in Alzheimer's disease.

1 reference

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Frataxin activates mitochondrial energy conversion and oxidative phosphorylation

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Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron deposits

1 reference

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1 reference

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Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

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Abnormal mitochondrial morphology in sporadic Parkinson's and Alzheimer's disease cybrid cell lines

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Bcl-2 completely blocks Fas-mediated apoptosis in mtDNA-depleted HeLa cells

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Sequence and organization of the human mitochondrial genome

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Molecular structure of the human cytoplasmic beta-actin gene: interspecies homology of sequences in the introns

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Effects of ethidium bromide on the cytochrome content and ultrastructure of L cell mitochondria

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21 January 2018

On the effect of inhibitors of mitochondrial macromolecular-synthesizing systems and respiration on the growth of cultured chick embryo cells.

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Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome

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A unique junctional palindromic sequence in mitochondrial DNA from a patient with progressive external ophthalmoplegia

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21 January 2018

Methylmercury poisoning of the developing nervous system: morphological changes in neuronal mitochondria.

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Chloromethyl-X-Rosamine is an aldehyde-fixable potential-sensitive fluorochrome for the detection of early apoptosis.

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21 January 2018

Functional F1-ATPase essential in maintaining growth and membrane potential of human mitochondrial DNA-depleted rho degrees cells

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21 January 2018

Structure, functioning, and assembly of the ATP synthase in cells from patients with the T8993G mitochondrial DNA mutation. Comparison with the enzyme in Rho(0) cells completely lacking mtdna

1 reference

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21 January 2018

Targeted gene disruption reveals an essential role for ceruloplasmin in cellular iron efflux

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21 January 2018

Oxidative stress and mitochondria alterations in Alzheimer's disease

1 reference

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21 January 2018

Transferrin and iron in normal, Alzheimer's disease, and Parkinson's disease brain regions

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204176200

21 January 2018

Metal chelation as a potential therapy for Alzheimer's disease.

1 reference

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21 January 2018

An evaluation of the role of mitochondria in neurodegenerative diseases: mitochondrial mutations and oxidative pathology, protective nuclear responses, and cell death in neurodegeneration

1 reference

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21 January 2018

Cytochrome c-mediated apoptosis in cells lacking mitochondrial DNA. Signaling pathway involving release and caspase 3 activation is conserved

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204176200

21 January 2018

Selective induction of mitochondrial chaperones in response to loss of the mitochondrial genome

1 reference

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21 January 2018

Creation and characterization of mitochondrial DNA-depleted cell lines with "neuronal-like" properties.

1 reference

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21 January 2018

A new diagnostic method for chronic hepatitis, liver cirrhosis, and hepatocellular carcinoma based on serum metallothionein, copper, and zinc levels

1 reference

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Substrate changes in peripheral nerve during ischaemia and Wallerian degeneration

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Ultrastructural findings in endomyocardial biopsy of patients with Kearns-Sayre syndrome

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Mitochondrial cytopathy presenting as hereditary sensory neuropathy with progressive external ophthalmoplegia, ataxia and fatal myoclonic epileptic status

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21 January 2018

Ultrastructural abnormalities of mitochondria and deficiency of myocardial cytochrome c oxidase in a patient with ventricular tachycardia

1 reference

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21 January 2018

Identifiers

10.1074/JBC.M204176200

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

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