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UnknownPrognostic potential of CUL3 ligase with differential roles in luminal A and basal type breast cancer tumors.
Not available
S-EPMC11213933 | biostudies-literature
TranscriptomicsTranscription profiling of Drosophila wild type and Ada2b knockout L3 larvae synchronized to spiracle eversion
Effect of the Ada2b mutation on L3 larvae synchronized to spiracle eversion (compared to w1118)
ORGANISM(S): Drosophila melanogaster 
2009-04-25 | E-MEXP-2125 | biostudies-arrayexpress
TranscriptomicsAda2b isoforms
Gene expression profiling of the two ADA2b protein (ADA2bS and ADA2bL) in Drosophila melanogaster
ORGANISM(S): Drosophila melanogaster 
2012-09-30 | E-MEXP-3747 | biostudies-arrayexpress
TranscriptomicsTranscription profiling of Drosophila wild type and Ada2b knock out pupa
The study of the role of Drosophila Ada2b SAGA histone acetyltransferase component at early pupal stage (P4)
ORGANISM(S): Drosophila melanogaster 
2009-04-25 | E-MEXP-2126 | biostudies-arrayexpress
TranscriptomicsTranscription profiling by array of Drosophila dAda2a amd dAda3 mutants at the puparium formation stage
Analyze the Drosophila ATAC complex function at the puparium formation stage. dAda2a and dAda3 were used.
ORGANISM(S): Drosophila melanogaster 
2010-06-24 | E-MEXP-2765 | biostudies-arrayexpress
ProteomicsK63-Linked Ubiquitylation of S2P-RNAPII Regulates Transcription in a DNA-PK Inter-Dependent Manner in Response to Double-Strand Breaks
DNA double-strand breaks (DSBs) pose a constant challenge to essential biological functions, including transcription, potentially leading to genomic instability. RNA polymerase II (RNAPII) plays a central role in detecting DNA lesions. Due to difficult-to-repair DSBs, RNAPII removal becomes challeng...
ORGANISM(S): Homo sapiens (Human) 
2026-05-25 | PXD058988 | Pride
Dsbs Ubiquitylation substrates Cul3 Nhej. Ir Ubiquitin ligase 
ProteomicsK63-Linked Ubiquitylation of S2P-RNAPII Regulates Transcription in a DNA-PK Inter-Dependent Manner in Response to Double-Strand Breaks
The goal of this experiment was to conduct immunoprecipitation (IP) on lysates from control and neocarzinostatin (NCS)-treated U2OS cells (at 30 minutes and 2 hours) to identify the proteins that interact with Polr2a and to investigate how NCS treatment influences the relative abundance of Polr2a an...
ORGANISM(S): Homo sapiens (Human) 
2026-05-25 | PXD059497 | Pride
U2os cells Mass spectrometry Immunoprecipitation Ip Lfq Label-free quantitation 
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