Author:
Jevtić Predrag,Haakonsen Diane L.,Rapé Michael
Funder
Howard Hughes Medical Institute
Subject
Clinical Biochemistry,Drug Discovery,Pharmacology,Molecular Biology,Molecular Medicine,Biochemistry
Reference187 articles.
1. Mutations in C2orf37, encoding a nucleolar protein, cause hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndrome;Alazami;Am. J. Hum. Genet.,2008
2. Molecular architecture and assembly of the DDB1-CUL4A ubiquitin ligase machinery;Angers;Nature,2006
3. NEDD8 nucleates a multivalent cullin-RING-UBE2D ubiquitin ligation assembly;Baek;Nature,2020
4. NEDD8 and ubiquitin ligation by cullin-RING E3 ligases;Baek;Curr. Opin. Struct. Biol.,2020
5. Structure and function of the 26S proteasome;Bard;Annu. Rev. Biochem.,2018
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