Research Article

Open Access
p62 and NBR1 functions are dispensable for aggrephagy in mouse ESCs and ESC-derived neurons
View ORCID ProfileRiccardo Trapannone Correspondence email, Julia Romanov, View ORCID ProfileSascha Martens Correspondence email
Riccardo Trapannone
1Max Perutz Labs, Vienna Biocenter Campus, Vienna, Austria
2Department of Biochemistry and Cell Biology, Center for Molecular Biology, University of Vienna, Vienna, Austria
Roles: Conceptualization, Data curation, Formal analysis, Validation, Investigation, Visualization, Methodology, Writing—original draft, Writing—review and editing
Julia Romanov
1Max Perutz Labs, Vienna Biocenter Campus, Vienna, Austria
2Department of Biochemistry and Cell Biology, Center for Molecular Biology, University of Vienna, Vienna, Austria
Roles: Investigation, Methodology, Writing—review and editing
Sascha Martens
1Max Perutz Labs, Vienna Biocenter Campus, Vienna, Austria
2Department of Biochemistry and Cell Biology, Center for Molecular Biology, University of Vienna, Vienna, Austria
Roles: Conceptualization, Resources, Supervision, Funding acquisition, Writing—original draft, Project administration, Writing—review and editing
Published 24 August 2023. DOI: 10.26508/lsa.202301936

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p62 and NBR1-independent aggrephagy
Riccardo Trapannone, Julia Romanov, Sascha Martens
Life Science Alliance Aug 2023, 6 (11) e202301936; DOI: 10.26508/lsa.202301936
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Volume 6, No. 11
November 2023
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