(Q33617779)

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Integrated transcriptome analysis across mitochondrial disease etiologies and tissues improves understanding of common cellular adaptations to respiratory chain dysfunction

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scholarly article

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Europe PubMed Central

28 July 2017

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Europe PubMed Central

Integrated transcriptome analysis across mitochondrial disease etiologies and tissues improves understanding of common cellular adaptations to respiratory chain dysfunction (English)

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Europe PubMed Central

28 July 2017

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mitochondrial disease

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based on heuristic

inferred from title

2

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Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24569120%20AND%20SRC:MED&resulttype=core&format=json

7 June 2020

author name string

Zhe Zhang

1

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7 June 2020

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publication date

22 February 2014

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Europe PubMed Central

28 July 2017

International Journal of Biochemistry & Cell Biology

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7 June 2020

50

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7 June 2020

106-111

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Europe PubMed Central

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7 June 2020

Stimulus-triggered fate conversion of somatic cells into pluripotency

1 reference

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1 reference

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An experimental approach to the generation of human embryonic stem cells equivalents.

1 reference

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14 July 2018

Primary respiratory chain disease causes tissue-specific dysregulation of the global transcriptome and nutrient-sensing signaling network

1 reference

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14 July 2018

Human embryonic stem cells derived by somatic cell nuclear transfer.

1 reference

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Survival transcriptome in the coenzyme Q10 deficiency syndrome is acquired by epigenetic modifications: a modelling study for human coenzyme Q10 deficiencies

1 reference

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Transcriptome analysis of a rotenone model of parkinsonism reveals complex I-tied and -untied toxicity mechanisms common to neurodegenerative diseases

1 reference

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Expression profiling of attenuated mitochondrial function identifies retrograde signals in Drosophila

1 reference

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Skeletal muscle transcriptional coactivator PGC-1α mediates mitochondrial, but not metabolic, changes during calorie restriction

1 reference

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PGC-1α induces mitochondrial and myokine transcriptional programs and lipid droplet and glycogen accumulation in cultured human skeletal muscle cells

1 reference

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Induced pluripotent stem cells--opportunities for disease modelling and drug discovery

1 reference

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14 July 2018

Transcriptional changes in OXPHOS complex I deficiency are related to anti-oxidant pathways and could explain the disturbed calcium homeostasis

1 reference

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Whole blood genome-wide expression profiling and network analysis suggest MELAS master regulators

1 reference

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14 July 2018

Probucol ameliorates renal and metabolic sequelae of primary CoQ deficiency in Pdss2 mutant mice

1 reference

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14 July 2018

Cross-platform expression microarray performance in a mouse model of mitochondrial disease therapy.

1 reference

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14 July 2018

TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy

1 reference

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14 July 2018

Primary coenzyme Q deficiency in Pdss2 mutant mice causes isolated renal disease

1 reference

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Metabolic pathway profiling of mitochondrial respiratory chain mutants in C. elegans.

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mTOR controls mitochondrial oxidative function through a YY1-PGC-1alpha transcriptional complex

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Hypomorphic mutation of PGC-1beta causes mitochondrial dysfunction and liver insulin resistance

1 reference

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14 July 2018

Systematic identification of human mitochondrial disease genes through integrative genomics

1 reference

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14 July 2018

Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles

1 reference

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Production of transmitochondrial mouse cell lines by cybrid rescue of rhodamine-6G pre-treated L-cells

1 reference

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14 July 2018

A systems approach for decoding mitochondrial retrograde signaling pathways.

1 reference

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30 October 2018

Mitochondrial dysfunction triggered by loss of HtrA2 results in the activation of a brain-specific transcriptional stress response

1 reference

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Transcriptional repression of PGC-1alpha by mutant huntingtin leads to mitochondrial dysfunction and neurodegeneration.

1 reference

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Skeletal muscle gene expression profiling in mitochondrial disorders.

1 reference

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30 October 2018

Identifiers

10.1016/J.BIOCEL.2014.02.012

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24569120%20AND%20SRC:MED&resulttype=core&format=json

7 June 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24569120%20AND%20SRC:MED&resulttype=core&format=json

7 June 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24569120%20AND%20SRC:MED&resulttype=core&format=json

7 June 2020

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