Defects in mitophagy promote redox‐driven metabolic syndrome in the absence of TP53INP1
Defects in mitophagy promote redox‐driven metabolic syndrome in the absence of TP53INP1
About this item
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Author / Creator
Seillier, Marion , Pouyet, Laurent , N'Guessan, Prudence , Nollet, Marie , Capo, Florence , Guillaumond, Fabienne , Peyta, Laure , Dumas, Jean‐François , Varrault, Annie , Bertrand, Gyslaine , Bonnafous, Stéphanie , Tran, Albert , Meur, Gargi , Marchetti, Piero , Ravier, Magalie A , Dalle, Stéphane , Gual, Philippe , Muller, Dany , Rutter, Guy A , Servais, Stéphane , Iovanna, Juan L and Carrier, Alice
Publisher
London: Nature Publishing Group UK
Journal title
Language
English
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Publication information
Publisher
London: Nature Publishing Group UK
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Scope and Contents
Contents
The metabolic syndrome covers metabolic abnormalities including obesity and type 2 diabetes (T2D). T2D is characterized by insulin resistance resulting from both environmental and genetic factors. A genome‐wide association study (GWAS) published in 2010 identified
TP53INP1
as a new T2D susceptibility locus, but a pathological mechanism was no...
Alternative Titles
Full title
Defects in mitophagy promote redox‐driven metabolic syndrome in the absence of TP53INP1
Authors, Artists and Contributors
Author / Creator
Pouyet, Laurent
N'Guessan, Prudence
Nollet, Marie
Capo, Florence
Guillaumond, Fabienne
Peyta, Laure
Dumas, Jean‐François
Varrault, Annie
Bertrand, Gyslaine
Bonnafous, Stéphanie
Tran, Albert
Meur, Gargi
Marchetti, Piero
Ravier, Magalie A
Dalle, Stéphane
Gual, Philippe
Muller, Dany
Rutter, Guy A
Servais, Stéphane
Iovanna, Juan L
Carrier, Alice
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Primary Identifiers
Record Identifier
TN_cdi_doaj_primary_oai_doaj_org_article_a391b04c6a3242c3a64fb5dbffab3422
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_a391b04c6a3242c3a64fb5dbffab3422
Other Identifiers
ISSN
1757-4676
E-ISSN
1757-4684
DOI
10.15252/emmm.201404318