Cisd2 deficiency drives premature aging and causes mitochondria-mediated defects in mice (Q28594937)

1 February 2017

title

Cisd2 deficiency drives premature aging and causes mitochondria-mediated defects in mice (English)

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CDGSH iron sulfur domain 2

1 February 2017

main subject

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GOA release 2020-03-11

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Yi-Fan Chen

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1 February 2017

Cheng-Heng Kao

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1 February 2017

Ya-Ting Chen

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1 February 2017

Chih-Hao Wang

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1 February 2017

Chia-Yu Wu

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1 February 2017

Ching-Yen Tsai

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1 February 2017

Fu-Chin Liu

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1 February 2017

Chu-Wen Yang

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1 February 2017

Yau-Huei Wei

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1 February 2017

Ming-Ta Hsu

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1 February 2017

Shih-Feng Tsai

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1 February 2017

Ting-Fen Tsai

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1 February 2017

publication date

15 May 2009

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1 February 2017

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1 February 2017

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1 February 2017

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1 February 2017

page(s)

1183–1194

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Autophagy fights disease through cellular self-digestion

1 February 2017

cites work

1 reference

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17 March 2017

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17 March 2017

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MitoNEET is an iron-containing outer mitochondrial membrane protein that regulates oxidative capacity

17 March 2017

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17 March 2017

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17 March 2017

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WFS1-deficiency increases endoplasmic reticulum stress, impairs cell cycle progression and triggers the apoptotic pathway specifically in pancreatic beta-cells

17 March 2017

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17 March 2017

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17 March 2017

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17 March 2017

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17 March 2017

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17 March 2017

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17 March 2017

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17 March 2017

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17 March 2017

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A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome)

17 March 2017

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Mutation of the mouse klotho gene leads to a syndrome resembling ageing

17 March 2017

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17 March 2017

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7 April 2017

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7 April 2017

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29 September 2017

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29 September 2017

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Beneficial effects of subcutaneous fat transplantation on metabolism

29 September 2017

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A homozygous mutation in a novel zinc-finger protein, ERIS, is responsible for Wolfram syndrome 2

29 September 2017

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Noxp20 and Noxp70, two new markers of early neuronal differentiation, detected in teratocarcinoma-derived neuroectodermic precursor cells.

29 September 2017

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29 September 2017

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29 September 2017

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29 September 2017

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29 September 2017

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29 September 2017

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29 September 2017

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29 September 2017

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29 September 2017

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Wolfram (DIDMOAD) syndrome.

3 June 2018

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Fine structure of the autophagosome.

3 June 2018

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Coordinated changes of mitochondrial biogenesis and antioxidant enzymes during osteogenic differentiation of human mesenchymal stem cells

27 November 2018

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Genetic analysis of the diabetes-prone C57BLKS/J mouse strain reveals genetic contribution from multiple strains

27 November 2018

1 reference

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Mice conditionally lacking the Wolfram gene in pancreatic islet beta cells exhibit diabetes as a result of enhanced endoplasmic reticulum stress and apoptosis

27 November 2018

1 reference

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Insulin infusion induces endothelin-1-dependent hypertension in rats

27 November 2018

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Disruption of the WFS1 gene in mice causes progressive beta-cell loss and impaired stimulus-secretion coupling in insulin secretion

27 November 2018

1 reference

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A progeroid syndrome in mice is caused by defects in A-type lamins

27 November 2018

1 reference

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Impact of genetic background and ablation of insulin receptor substrate (IRS)-3 on IRS-2 knock-out mice

27 November 2018

1 reference

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Wolfram syndrome: a mitochondrial-mediated disorder?

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2685531

Visualization of the transport pathways of low density lipoproteins across the endothelial cells in the branched regions of rat arteries.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2685531

Protein kinase C beta and prolyl isomerase 1 regulate mitochondrial effects of the life-span determinant p66Shc

27 November 2018

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12 December 2020

DNA deletions and clonal mutations drive premature aging in mitochondrial mutator mice

1 reference

12 December 2020

Optic atrophy in Wolfram syndrome

1 reference

12 December 2020

Mitochondrial abnormalities in the DIDMOAD syndrome

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12 December 2020

The influence of genetic background on the expression of mutations at the diabetes (db) locus in the mouse. VI: Hepatic malic enzyme activity is associated with diabetes severity

1 reference

12 December 2020

Deletion of mitochondrial DNA in a case of early-onset diabetes mellitus, optic atrophy and deafness (DIDMOAD, Wolfram syndrome)

1 reference

12 December 2020

Wolfram (DIDMOAD) syndrome and Leber hereditary optic neuropathy (LHON) are associated with distinct mitochondrial DNA haplotypes

1 reference

12 December 2020

Optic atrophy in Wolfram (DIDMOAD) syndrome

1 reference

12 December 2020

Oxidative damage and mutation to mitochondrial DNA and age-dependent decline of mitochondrial respiratory function

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12 December 2020

Identifiers

DOI

10.1101/GAD.1779509

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release_onuxw4bnrjfbziq6ox2khunwf4

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/onuxw4bnrjfbziq6ox2khunwf4

24 November 2022

mapped directly with Wikidata item

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1 reference

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