(Q41059087)

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Nuclear-recessive mutations of factors involved in mitochondrial translation are responsible for age-related respiration deficiency of human skin fibroblasts

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Europe PubMed Central

PubMed publication ID

26 September 2017

Nuclear-recessive mutations of factors involved in mitochondrial translation are responsible for age-related respiration deficiency of human skin fibroblasts (English)

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Europe PubMed Central

PubMed publication ID

26 September 2017

author name string

Isobe K

1

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Europe PubMed Central

PubMed publication ID

26 September 2017

Ito S

2

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Europe PubMed Central

PubMed publication ID

26 September 2017

Hosaka H

3

1 reference

Europe PubMed Central

PubMed publication ID

26 September 2017

Iwamura Y

4

1 reference

Europe PubMed Central

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26 September 2017

Kondo H

5

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Europe PubMed Central

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26 September 2017

Kagawa Y

6

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Europe PubMed Central

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26 September 2017

Hayashi JI

7

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26 September 2017

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publication date

1 February 1998

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Europe PubMed Central

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26 September 2017

Journal of Biological Chemistry

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Europe PubMed Central

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26 September 2017

273

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Europe PubMed Central

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26 September 2017

8

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Europe PubMed Central

PubMed publication ID

26 September 2017

4601-4606

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Europe PubMed Central

PubMed publication ID

26 September 2017

An integrated theory of aging as the result of mitochondrial-DNA mutation in differentiated cells

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.8.4601

21 January 2018

Mitochondrial genetics: a paradigm for aging and degenerative diseases?

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.8.4601

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.273.8.4601

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.273.8.4601

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.273.8.4601

21 January 2018

Mosaicism for a specific somatic mitochondrial DNA mutation in adult human brain

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.8.4601

21 January 2018

Mitochondrial DNA deletions in human brain: regional variability and increase with advanced age

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.8.4601

21 January 2018

Aging-dependent functional alterations of mitochondrial DNA (mtDNA) from human fibroblasts transferred into mtDNA-less cells

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.8.4601

21 January 2018

Increase of deleted mitochondrial DNA in the striatum in Parkinson's disease and senescence

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.8.4601

21 January 2018

Ageing-associated 5 kb deletion in human liver mitochondrial DNA.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.8.4601

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.273.8.4601

21 January 2018

Transcription of the mammalian mitochondrial genome

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.8.4601

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.8.4601

21 January 2018

THE LIMITED IN VITRO LIFETIME OF HUMAN DIPLOID CELL STRAINS

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.8.4601

21 January 2018

Replicative senescence: the human fibroblast comes of age.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.8.4601

21 January 2018

Energy metabolism in cultured human fibroblasts during aging in vitro

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.8.4601

21 January 2018

Pearson's marrow-pancreas syndrome. A multisystem mitochondrial disorder in infancy

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.8.4601

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.273.8.4601

21 January 2018

Molecular genetic aspects of human mitochondrial disorders

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.8.4601

21 January 2018

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.8.4601

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.8.4601

21 January 2018

Identifiers

10.1074/JBC.273.8.4601

1 reference

Europe PubMed Central

PubMed publication ID

26 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 September 2017

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