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
Full title
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 , Dalle, Stéphane , Gual, Philippe , Muller, Dany , Rutter, Guy , Servais, Stéphane , Iovanna, Juan and Carrier, Alice
Publisher
Wiley Open Access
Journal title
Language
English
Formats
Publication information
Publisher
Wiley Open Access
Subjects
More information
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 not iden...
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
Dalle, Stéphane
Gual, Philippe
Muller, Dany
Rutter, Guy
Servais, Stéphane
Iovanna, Juan
Carrier, Alice
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_hal_primary_oai_HAL_hal_04496734v1
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_hal_primary_oai_HAL_hal_04496734v1
Other Identifiers
ISSN
1757-4676
E-ISSN
1757-4684
DOI
10.15252/emmm.201404318
