(Q43757469)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11588181%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

title

Late-onset corticohippocampal neurodepletion attributable to catastrophic failure of oxidative phosphorylation in MILON mice (English)

1 reference

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11 November 2019

0 references

8

N G Larsson

1 reference

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11 November 2019

author name string

L Sörensen

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11588181%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

M Ekstrand

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11588181%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

J P Silva

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11588181%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

E Lindqvist

4

1 reference

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11 November 2019

B Xu

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11588181%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

P Rustin

6

1 reference

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11 November 2019

L Olson

7

1 reference

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11 November 2019

language of work or name

English

0 references

publication date

1 October 2001

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11588181%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

published in

Journal of Neuroscience

1 reference

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11 November 2019

volume

21

1 reference

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11 November 2019

issue

20

1 reference

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11 November 2019

page(s)

8082-8090

1 reference

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Subacute necrotizing encephalomyelopathy in an infant

11 November 2019

cites work

1 reference

12 December 2020

Neuropathology in Kearns-Sayre syndrome

1 reference

12 December 2020

Revolution in mitochondrial medicine

1 reference

12 December 2020

Cytochrome c oxidase deficient cells accumulate in the hippocampus and choroid plexus with age.

1 reference

12 December 2020

The incidence of mitochondrial encephalomyopathies in childhood: clinical features and morphological, biochemical, and DNA abnormalities

1 reference

12 December 2020

Localization of cellular retinoid-binding proteins suggests specific roles for retinoids in the adult central nervous system

1 reference

12 December 2020

Role of mitochondrial DNA mutations in human aging: implications for the central nervous system and muscle

1 reference

12 December 2020

Mitochondrial diseases in man and mouse

1 reference

12 December 2020

Cortical degeneration in the absence of neurotrophin signaling: dendritic retraction and neuronal loss after removal of the receptor TrkB.

1 reference

12 December 2020

Superoxide-induced massive apoptosis in cultured skin fibroblasts harboring the neurogenic ataxia retinitis pigmentosa (NARP) mutation in the ATPase-6 gene of the mitochondrial DNA.

1 reference

12 December 2020

Intracellular adenosine triphosphate (ATP) concentration: a switch in the decision between apoptosis and necrosis

1 reference

12 December 2020

Molecular genetic aspects of human mitochondrial disorders

1 reference

12 December 2020

Mitochondrial DNA deletions in inclusion body myositis.

1 reference

12 December 2020

Immunohistochemical localization of three catecholamine synthesizing enzymes: aspects on methodology

1 reference

12 December 2020

Biochemical and molecular investigations in respiratory chain deficiencies

1 reference

12 December 2020

Neuropathological and histochemical changes in a multiple mitochondrial DNA deletion disorder

1 reference

12 December 2020

Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndrome

1 reference

12 December 2020

Genetic modification of survival in tissue-specific knockout mice with mitochondrial cardiomyopathy

1 reference

12 December 2020

Kainic acid-induced seizures: dose-relationship of behavioural, neurochemical and histopathological changes.

1 reference

12 December 2020

A single mouse gene encodes the mitochondrial transcription factor A and a testis-specific nuclear HMG-box protein

1 reference

12 December 2020

Dilated cardiomyopathy and atrioventricular conduction blocks induced by heart-specific inactivation of mitochondrial DNA gene expression.

1 reference

12 December 2020

Increased in vivo apoptosis in cells lacking mitochondrial DNA gene expression

1 reference

12 December 2020

Tissue distribution and disease manifestations of the tRNA(Lys) A-->G(8344) mitochondrial DNA mutation in a case of myoclonus epilepsy and ragged red fibres

1 reference

12 December 2020

Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia

1 reference

12 December 2020

Mitochondrial transcription factor A is necessary for mtDNA maintenance and embryogenesis in mice

1 reference

12 December 2020

Mitochondrial genetics: a paradigm for aging and degenerative diseases?

1 reference

12 December 2020

The epidemiology of pathogenic mitochondrial DNA mutations

1 reference

12 December 2020

Sensitive mRNA detection using unfixed tissue: combined radioactive and non-radioactive in situ hybridization histochemistry

1 reference

12 December 2020

Impaired insulin secretion and beta-cell loss in tissue-specific knockout mice with mitochondrial diabetes.

1 reference

12 December 2020

10.1523/JNEUROSCI.21-20-08082.2001

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11588181%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11588181%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

PubMed publication ID

11588181

1 reference