Mutation in FBXO32 causes dilated cardiomyopathy through up-regulation of ER-stress mediated apoptosis

Al-Yacoub et al. investigate the consequences of FBXO32 mutation on dilated cardiomyopathy. ER stress, abnormal CHOP activation and CHOP-induced apoptosis with no UPR effector activation are found to underlie the FBXO32 mutation induced cardiomyopathy, suggesting an alternative pathway that can be c...

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Autores principales: Nadya Al-Yacoub, Dilek Colak, Salma Awad Mahmoud, Maya Hammonds, Kunhi Muhammed, Olfat Al-Harazi, Abdullah M. Assiri, Jehad Al-Buraiki, Waleed Al-Habeeb, Coralie Poizat
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/9414570eeefe4652ac8f265170617ea4
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spelling oai:doaj.org-article:9414570eeefe4652ac8f265170617ea42021-12-02T18:30:44ZMutation in FBXO32 causes dilated cardiomyopathy through up-regulation of ER-stress mediated apoptosis10.1038/s42003-021-02391-92399-3642https://doaj.org/article/9414570eeefe4652ac8f265170617ea42021-07-01T00:00:00Zhttps://doi.org/10.1038/s42003-021-02391-9https://doaj.org/toc/2399-3642Al-Yacoub et al. investigate the consequences of FBXO32 mutation on dilated cardiomyopathy. ER stress, abnormal CHOP activation and CHOP-induced apoptosis with no UPR effector activation are found to underlie the FBXO32 mutation induced cardiomyopathy, suggesting an alternative pathway that can be considered to develop new therapeutic targets for its treatment.Nadya Al-YacoubDilek ColakSalma Awad MahmoudMaya HammondsKunhi MuhammedOlfat Al-HaraziAbdullah M. AssiriJehad Al-BuraikiWaleed Al-HabeebCoralie PoizatNature PortfolioarticleBiology (General)QH301-705.5ENCommunications Biology, Vol 4, Iss 1, Pp 1-12 (2021)
institution DOAJ
collection DOAJ
language EN
topic Biology (General)
QH301-705.5
spellingShingle Biology (General)
QH301-705.5
Nadya Al-Yacoub
Dilek Colak
Salma Awad Mahmoud
Maya Hammonds
Kunhi Muhammed
Olfat Al-Harazi
Abdullah M. Assiri
Jehad Al-Buraiki
Waleed Al-Habeeb
Coralie Poizat
Mutation in FBXO32 causes dilated cardiomyopathy through up-regulation of ER-stress mediated apoptosis
description Al-Yacoub et al. investigate the consequences of FBXO32 mutation on dilated cardiomyopathy. ER stress, abnormal CHOP activation and CHOP-induced apoptosis with no UPR effector activation are found to underlie the FBXO32 mutation induced cardiomyopathy, suggesting an alternative pathway that can be considered to develop new therapeutic targets for its treatment.
format article
author Nadya Al-Yacoub
Dilek Colak
Salma Awad Mahmoud
Maya Hammonds
Kunhi Muhammed
Olfat Al-Harazi
Abdullah M. Assiri
Jehad Al-Buraiki
Waleed Al-Habeeb
Coralie Poizat
author_facet Nadya Al-Yacoub
Dilek Colak
Salma Awad Mahmoud
Maya Hammonds
Kunhi Muhammed
Olfat Al-Harazi
Abdullah M. Assiri
Jehad Al-Buraiki
Waleed Al-Habeeb
Coralie Poizat
author_sort Nadya Al-Yacoub
title Mutation in FBXO32 causes dilated cardiomyopathy through up-regulation of ER-stress mediated apoptosis
title_short Mutation in FBXO32 causes dilated cardiomyopathy through up-regulation of ER-stress mediated apoptosis
title_full Mutation in FBXO32 causes dilated cardiomyopathy through up-regulation of ER-stress mediated apoptosis
title_fullStr Mutation in FBXO32 causes dilated cardiomyopathy through up-regulation of ER-stress mediated apoptosis
title_full_unstemmed Mutation in FBXO32 causes dilated cardiomyopathy through up-regulation of ER-stress mediated apoptosis
title_sort mutation in fbxo32 causes dilated cardiomyopathy through up-regulation of er-stress mediated apoptosis
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/9414570eeefe4652ac8f265170617ea4
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AT salmaawadmahmoud mutationinfbxo32causesdilatedcardiomyopathythroughupregulationoferstressmediatedapoptosis
AT mayahammonds mutationinfbxo32causesdilatedcardiomyopathythroughupregulationoferstressmediatedapoptosis
AT kunhimuhammed mutationinfbxo32causesdilatedcardiomyopathythroughupregulationoferstressmediatedapoptosis
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AT waleedalhabeeb mutationinfbxo32causesdilatedcardiomyopathythroughupregulationoferstressmediatedapoptosis
AT coraliepoizat mutationinfbxo32causesdilatedcardiomyopathythroughupregulationoferstressmediatedapoptosis
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