Cilia defects upon loss of WDR4 are linked to proteasomal hyperactivity and ubiquitin shortage
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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1 Online-Ressource.
- Language
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Englisch
- Bibliographic citation
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Cilia defects upon loss of WDR4 are linked to proteasomal hyperactivity and ubiquitin shortage ; volume:15 ; number:9 ; day:9 ; month:9 ; year:2024 ; pages:1-14 ; date:9.2024
Cell death & disease ; 15, Heft 9 (9.9.2024), 1-14, 9.2024
- Creator
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Burkhalter, Martin D.
Stiff, Tom
Maerz, Lars D.
Casar Tena, Teresa
Wiese, Heike
Gerhards, Julian
Sailer, Steffen A.
Vu, Linh Anna Trúc
Duong Phu, Max
Donow, Cornelia
Alupei, Marius
Iben, Sebastian
Groth, Marco
Wiese, Sebastian Edgar
Church, Joseph A.
Jeggo, Penelope A.
Philipp, Melanie
- Contributor
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SpringerLink (Online service)
- DOI
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10.1038/s41419-024-07042-5
- URN
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urn:nbn:de:101:1-2411232100343.635521334126
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:33 AM CEST
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Burkhalter, Martin D.
- Stiff, Tom
- Maerz, Lars D.
- Casar Tena, Teresa
- Wiese, Heike
- Gerhards, Julian
- Sailer, Steffen A.
- Vu, Linh Anna Trúc
- Duong Phu, Max
- Donow, Cornelia
- Alupei, Marius
- Iben, Sebastian
- Groth, Marco
- Wiese, Sebastian Edgar
- Church, Joseph A.
- Jeggo, Penelope A.
- Philipp, Melanie
- SpringerLink (Online service)
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The structure of the ubiquitin-like modifier FAT10 reveals an alternative targeting mechanism for proteasomal degradation
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Molecular basis of SAP05-mediated ubiquitin-independent proteasomal degradation of transcription factors
Conjugation of the Ubiquitin Activating Enzyme UBE1 with the Ubiquitin-Like Modifier FAT10 Targets It for Proteasomal Degradation
Role of the ubiquitin-proteasomal system and HDAC6 in the maintenance of protein homeostasis
Erratum to: hCLP46 increases Smad3 protein stability via inhibiting its ubiquitin-proteasomal degradation
Role of the ubiquitin-proteasomal system and HDAC6 in the maintenance of protein homeostasis
E3 Ubiquitin Ligase RNF13 Suppresses TLR Lysosomal Degradation by Promoting LAMP‐1 Proteasomal Degradation
The Chaperone-associated Ubiquitin Ligase CHIP Is Able to Target p53 for Proteasomal Degradation
The ubiquitin-like modifier FAT10 inhibits retinal PDE6 activity and mediates its proteasomal degradation
Prokaryotic ubiquitin-like protein remains intrinsically disordered when covalently attached to proteasomal target proteins
Cilia
The structure of the ubiquitin-like modifier FAT10 reveals an alternative targeting mechanism for proteasomal degradation
FAT10, a ubiquitin-independent signal for proteasomal degradation
Molecular basis of SAP05-mediated ubiquitin-independent proteasomal degradation of transcription factors
Conjugation of the Ubiquitin Activating Enzyme UBE1 with the Ubiquitin-Like Modifier FAT10 Targets It for Proteasomal Degradation
Role of the ubiquitin-proteasomal system and HDAC6 in the maintenance of protein homeostasis
Erratum to: hCLP46 increases Smad3 protein stability via inhibiting its ubiquitin-proteasomal degradation
Role of the ubiquitin-proteasomal system and HDAC6 in the maintenance of protein homeostasis
E3 Ubiquitin Ligase RNF13 Suppresses TLR Lysosomal Degradation by Promoting LAMP‐1 Proteasomal Degradation
The Chaperone-associated Ubiquitin Ligase CHIP Is Able to Target p53 for Proteasomal Degradation
The ubiquitin-like modifier FAT10 inhibits retinal PDE6 activity and mediates its proteasomal degradation
Prokaryotic ubiquitin-like protein remains intrinsically disordered when covalently attached to proteasomal target proteins
Cilia