(Q42959191)

11 November 2017

Mitochondrial myopathy induces a starvation-like response (English)

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11 November 2017

mitochondrial myopathy

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1

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11 November 2017

11

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11 November 2017

14

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11 November 2017

Sofia Ahola-Erkkilä

4

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Christopher J Carroll

object named as

Christopher J Carroll

2

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Kirsi H Pietiläinen

object named as

Kirsi Pietiläinen

13

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Akseli Hemminki

8

object named as

Akseli Hemminki

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11 November 2017

Nuno Raimundo

3

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11 November 2017

Tina Wenz

5

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11 November 2017

Heini Ruhanen

6

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11 November 2017

Kilian Guse

7

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11 November 2017

Katja E Peltola-Mjøsund

9

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11 November 2017

Valtteri Tulkki

10

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11 November 2017

Carlos T Moraes

12

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11 November 2017

Anu Suomalainen

15

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11 November 2017

23 July 2010

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11 November 2017

Human Molecular Genetics

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11 November 2017

19

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11 November 2017

20

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11 November 2017

3948-3958

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Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia

11 November 2017

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ310

Role of adenine nucleotide translocator 1 in mtDNA maintenance

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ310

Mutant POLG2 disrupts DNA polymerase gamma subunits and causes progressive external ophthalmoplegia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ310

Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ310

A heterozygous truncating mutation in RRM2B causes autosomal-dominant progressive external ophthalmoplegia with multiple mtDNA deletions

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ310

Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ310

Autosomal dominant progressive external ophthalmoplegia with multiple deletions of mtDNA: clinical, biochemical, and molecular genetic features of the 10q-linked disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ310

Mutant mitochondrial helicase Twinkle causes multiple mtDNA deletions and a late-onset mitochondrial disease in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ310

Transcriptional profile of a myotube starvation model of atrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ310

Hepatic fibroblast growth factor 21 is regulated by PPARalpha and is a key mediator of hepatic lipid metabolism in ketotic states

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ310

Endocrine regulation of the fasting response by PPARalpha-mediated induction of fibroblast growth factor 21

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ310

Nutritional control of gene expression: how mammalian cells respond to amino acid limitation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ310

Ketogenic diet slows down mitochondrial myopathy progression in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ310

Involvement of the Akt/PKB signaling pathway with disease processes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ310

FGF21 is an Akt-regulated myokine

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ310

PGC-1alpha negatively regulates hepatic FGF21 expression by modulating the heme/Rev-Erb(alpha) axis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ310

RETRACTED: Activation of the PPAR/PGC-1alpha pathway prevents a bioenergetic deficit and effectively improves a mitochondrial myopathy phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ310

Twinkle helicase is essential for mtDNA maintenance and regulates mtDNA copy number

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ310

Large GLUT4 vesicles are stationary while locally and reversibly depleted during transient insulin stimulation of skeletal muscle of living mice: imaging analysis of GLUT4-enhanced green fluorescent protein vesicle dynamics

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ310

Adipose fibroblast growth factor 21 is up-regulated by peroxisome proliferator-activated receptor gamma and altered metabolic states.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ310

FGF-21 as a novel metabolic regulator

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ310

Mice lacking COX10 in skeletal muscle recapitulate the phenotype of progressive mitochondrial myopathies associated with cytochrome c oxidase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ310

Fibroblast growth factor-21 as a therapeutic agent for metabolic diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ310

Fast/Glycolytic muscle fiber growth reduces fat mass and improves metabolic parameters in obese mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ310

CHOP (C/EBP homologous protein) and ASNS (asparagine synthetase) induction in cybrid cells harboring MELAS and NARP mitochondrial DNA mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ310

A mitochondrial specific stress response in mammalian cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ310

Molecular insights into the klotho-dependent, endocrine mode of action of fibroblast growth factor 19 subfamily members

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ310

The metabolic state of diabetic monkeys is regulated by fibroblast growth factor-21.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ310

FGF21 induces PGC-1alpha and regulates carbohydrate and fatty acid metabolism during the adaptive starvation response

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ310

FGF21: a missing link in the biology of fasting.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ310

Fibroblast growth factor-21 is induced in human skeletal muscles by hyperinsulinemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ310

Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): biochemical features and therapeutic approaches

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ310

The expression of mitochondrial methylenetetrahydrofolate dehydrogenase-cyclohydrolase supports a role in rapid cell growth

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ310

Summaries of Affymetrix GeneChip probe level data

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ310

Adult mouse brain gene expression patterns bear an embryologic imprint

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ310

An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ310

21 January 2018

Identifiers

DOI

10.1093/HMG/DDQ310

1 reference

11 November 2017

1 reference