
Publikationen von Judith Müller
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Zeitschriftenartikel (2)
1.
Zeitschriftenartikel
598 (9), S. 978 - 994 (2024)
Skraban-Deardorff intellectual disability syndrome-associated mutations in WDR26 impair CTLH E3 complex assembly. FEBS Letters 2.
Zeitschriftenartikel
84 (2), S. 293 - 308 (2024)
Multisite phosphorylation dictates selective E2-E3 pairing as revealed by Ubc8/UBE2H-GID/CTLH assemblies. Molecular Cell