(Q58853777)

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Identification of Inheritance Modes of Mitochondrial Diseases by Introduction of Pure Nuclei from mtDNA-less HeLa Cells to Patient-derived Fibroblasts

scientific article published in Journal of Biological Chemistry

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9139714%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

Identification of inheritance modes of mitochondrial diseases by introduction of pure nuclei from mtDNA-less HeLa cells to patient-derived fibroblasts (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9139714%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

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S Kishino

2

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9139714%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

K Inoue

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9139714%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

D Takai

4

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9139714%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

H Hirawake

5

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9139714%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

S Miyabayashi

7

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9139714%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

J I Hayashi

8

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Europe PubMed Central

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3 November 2019

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publication date

1 May 1997

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9139714%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

Journal of Biological Chemistry

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9139714%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

272

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9139714%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

19

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9139714%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

12606-12610

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9139714%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

Diseases of the mitochondrial DNA.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.19.12606

21 January 2018

Molecular genetic aspects of human mitochondrial disorders

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.19.12606

21 January 2018

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.19.12606

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.19.12606

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.19.12606

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.19.12606

21 January 2018

In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondria

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.19.12606

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.19.12606

21 January 2018

MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.19.12606

21 January 2018

Mitochondrial DNA is required for regulation of glucose-stimulated insulin secretion in a mouse pancreatic beta cell line, MIN6.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.19.12606

21 January 2018

Biochemistry of dystrophic muscle. Mitochondrial succinate-tetrazolium reductase and adenosine triphosphatase

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.19.12606

21 January 2018

Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.19.12606

21 January 2018

Recovery of the missing tumorigenicity in mitochondrial DNA-less HeLa cells by introduction of mitochondrial DNA from normal human cells

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.19.12606

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.19.12606

21 January 2018

Cytochrome c oxidase deficiency in Leigh's syndrome: genetic evidence for a nuclear DNA-encoded mutation.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.19.12606

21 January 2018

Nuclear DNA origin of cytochrome c oxidase deficiency in Leigh's syndrome: genetic evidence based on patient's-derived rho degrees transformants

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.19.12606

21 January 2018

Mitochondrial myopathies

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.19.12606

21 January 2018

Accumulation of mtDNA with a mutation at position 3271 in tRNA(Leu)(UUR) gene introduced from a MELAS patient to HeLa cells lacking mtDNA results in progressive inhibition of mitochondrial respiratory function

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.19.12606

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.19.12606

21 January 2018

Mitochondrial genomes in intraspecies mammalian cell hybrids display codominant or dominant/recessive behavior

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.19.12606

21 January 2018

Identifiers

10.1074/JBC.272.19.12606

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9139714%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9139714%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

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