Generation of mice with mitochondrial dysfunction by introducing mouse mtDNA carrying a deletion into zygotes (Q73035349)

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scientific article published on 01 October 2000

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English	Generation of mice with mitochondrial dysfunction by introducing mouse mtDNA carrying a deletion into zygotes	scientific article published on 01 October 2000

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scholarly article

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Europe PubMed Central

PubMed publication ID

11017072

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11017072%20AND%20SRC:MED&resulttype=core&format=json

retrieved

31 October 2019

title

Generation of mice with mitochondrial dysfunction by introducing mouse mtDNA carrying a deletion into zygotes (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11017072

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11017072%20AND%20SRC:MED&resulttype=core&format=json

retrieved

31 October 2019

author name string

Inoue K

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11017072

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11017072%20AND%20SRC:MED&resulttype=core&format=json

retrieved

31 October 2019

Nakada K

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11017072

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11017072%20AND%20SRC:MED&resulttype=core&format=json

retrieved

31 October 2019

Ogura A

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11017072

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11017072%20AND%20SRC:MED&resulttype=core&format=json

retrieved

31 October 2019

Isobe K

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11017072

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11017072%20AND%20SRC:MED&resulttype=core&format=json

retrieved

31 October 2019

Goto Y

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11017072

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11017072%20AND%20SRC:MED&resulttype=core&format=json

retrieved

31 October 2019

Nonaka I

series ordinal

6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11017072

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11017072%20AND%20SRC:MED&resulttype=core&format=json

retrieved

31 October 2019

Hayashi JI

series ordinal

7

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11017072

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11017072%20AND%20SRC:MED&resulttype=core&format=json

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31 October 2019

publication date

1 October 2000

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Europe PubMed Central

PubMed publication ID

11017072

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11017072%20AND%20SRC:MED&resulttype=core&format=json

retrieved

31 October 2019

published in

Nature Genetics

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stated in

Europe PubMed Central

PubMed publication ID

11017072

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11017072%20AND%20SRC:MED&resulttype=core&format=json

retrieved

31 October 2019

volume

26

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Europe PubMed Central

PubMed publication ID

11017072

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11017072%20AND%20SRC:MED&resulttype=core&format=json

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31 October 2019

issue

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11017072

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11017072%20AND%20SRC:MED&resulttype=core&format=json

retrieved

31 October 2019

page(s)

176-181

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Europe PubMed Central

PubMed publication ID

11017072

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11017072%20AND%20SRC:MED&resulttype=core&format=json

retrieved

31 October 2019

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Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction

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Defects in mitochondrial protein synthesis and respiratory chain activity segregate with the tRNA(Leu(UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes

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Complementation of mutant and wild-type human mitochondrial DNAs coexisting since the mutation event and lack of complementation of DNAs introduced separately into a cell within distinct organelles

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Functional integrity of mitochondrial genomes in human platelets and autopsied brain tissues from elderly patients with Alzheimer's disease

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Isolation of mitochondrial DNA-less mouse cell lines and their application for trapping mouse synaptosomal mitochondrial DNA with deletion mutations

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Isolation and characterization of mitochondrial DNA-less lines from various mammalian cell lines by application of an anticancer drug, ditercalinium

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Sequence analysis of a deleted mitochondrial DNA molecule in heteroplasmic mice

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7 January 2021

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Multiple deletions are detectable in mitochondrial DNA of aging mice

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7 January 2021

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Circular Dimer and Catenate Forms of Mitochondrial DNA in Human Leukaemic Leucocytes

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7 January 2021

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Elimination of paternal mitochondrial DNA in intraspecific crosses during early mouse embryogenesis

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7 January 2021

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Duplications of mitochondrial DNA in mitochondrial myopathy

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7 January 2021

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Maternally transmitted partial direct tandem duplication of mitochondrial DNA associated with diabetes mellitus

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7 January 2021

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Human mitochondria and mitochondrial genome function as a single dynamic cellular unit

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7 January 2021

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The interorganellar interaction between distinct human mitochondria with deletion mutant mtDNA from a patient with mitochondrial disease and with HeLa mtDNA

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Mitochondrial DNA deletion: a cause of chronic tubulointerstitial nephropathy

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7 January 2021

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Mitochondria transfer into mouse ova by microinjection

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Isolation and microinjection of somatic cell-derived mitochondria and germline heteroplasmy in transmitochondrial mice

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7 January 2021

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Stable heteroplasmy for a large-scale deletion in the coding region of Drosophila subobscura mitochondrial DNA

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A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies

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7 January 2021

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Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

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Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

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7 January 2021

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

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7 January 2021

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Transmitochondrial mice carrying resistance to chloramphenicol on mitochondrial DNA: developing the first mouse model of mitochondrial DNA disease.

1 reference

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7 January 2021

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inferred from DOI database lookup

Transfer of chloramphenicol-resistant mitochondrial DNA into the chimeric mouse

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Cytochrome C oxidase deficiency in two siblings with leigh encephalomyelopathy

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7 January 2021

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Identifiers

DOI

10.1038/82826

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11017072

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11017072%20AND%20SRC:MED&resulttype=core&format=json

retrieved

31 October 2019

PubMed publication ID

11017072

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11017072

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11017072%20AND%20SRC:MED&resulttype=core&format=json

retrieved

31 October 2019

 

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