| P2093 | author name string | Joan M Kelly | |
| | Md Ashiqul Alam | |
| P2860 | cites work | Characterization of a protein complex containing spliceosomal proteins SAPs 49, 130, 145, and 155 | Q22010545 |
| | Mammalian mediator subunit mMED8 is an Elongin BC-interacting protein that can assemble with Cul2 and Rbx1 to reconstitute a ubiquitin ligase | Q24302474 |
| | Ubiquitin-dependent regulation of COPII coat size and function | Q24305964 |
| | Mass spectrometry reveals modularity and a complete subunit interaction map of the eukaryotic translation factor eIF3 | Q24309617 |
| | Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources | Q27860739 |
| | Sequential interactions with Sec23 control the direction of vesicle traffic | Q27929972 |
| | Nuclear FKBPs, Fpr3 and Fpr4 affect genome-wide genes transcription | Q27931855 |
| | Apg2 is a novel protein required for the cytoplasm to vacuole targeting, autophagy, and pexophagy pathways | Q27933193 |
| | Bro1 coordinates deubiquitination in the multivesicular body pathway by recruiting Doa4 to endosomes. | Q27933270 |
| | Med9/Cse2 and Gal11 modules are required for transcriptional repression of distinct group of genes | Q27933388 |
| | Srb7p is a physical and physiological target of Tup1p | Q27933607 |
| | Proline isomerization of histone H3 regulates lysine methylation and gene expression | Q27933713 |
| | Two-color cell array screen reveals interdependent roles for histone chaperones and a chromatin boundary regulator in histone gene repression | Q27933893 |
| | Pam17 is required for architecture and translocation activity of the mitochondrial protein import motor | Q27935671 |
| | Yeast Npi3/Bro1 is involved in ubiquitin-dependent control of permease trafficking | Q27940285 |
| | Histone variant H2A.Z is required for early mammalian development | Q28214088 |
| | The GeneMANIA prediction server: biological network integration for gene prioritization and predicting gene function | Q29614950 |
| | Tryptic peptide reference data sets for MALDI imaging mass spectrometry on formalin-fixed ovarian cancer tissues. | Q30580264 |
| | Analysis of the creA gene, a regulator of carbon catabolite repression in Aspergillus nidulans | Q33409712 |
| | Quantifying the biological significance of gene ontology biological processes--implications for the analysis of systems-wide data. | Q33517420 |
| | Histone variants: dynamic punctuation in transcription | Q33588109 |
| | H2A.Z is required for global chromatin integrity and for recruitment of RNA polymerase II under specific conditions | Q33969518 |
| | Autophosphorylation within the Atg1 activation loop is required for both kinase activity and the induction of autophagy in Saccharomyces cerevisiae | Q34007927 |
| | A versatile and efficient gene-targeting system for Aspergillus nidulans. | Q34587921 |
| | Analysis of protein complexes using mass spectrometry | Q34642068 |
| | Phylogenetic analysis of the core histones H2A, H2B, H3, and H4 | Q34662571 |
| | An Atg13 protein-mediated self-association of the Atg1 protein kinase is important for the induction of autophagy | Q35309677 |
| | Histone modifications influence mediator interactions with chromatin | Q35447589 |
| | Prolyl isomerases in yeast | Q35880640 |
| | p21 transcription is regulated by differential localization of histone H2A.Z. | Q35917048 |
| | Monoubiquitylation of H2A.Z distinguishes its association with euchromatin or facultative heterochromatin | Q36177449 |
| | KEGG as a reference resource for gene and protein annotation | Q36434599 |
| | Essential and nonessential histone H2A variants in Tetrahymena thermophila | Q36561455 |
| | A two-step database search method improves sensitivity in peptide sequence matches for metaproteomics and proteogenomics studies. | Q36787600 |
| | Direct and indirect gene replacements in Aspergillus nidulans | Q36903665 |
| | Functional characterisation of the non-essential protein kinases and phosphatases regulating Aspergillus nidulans hydrolytic enzyme production | Q36972815 |
| | Post-translational modifications of the histone variant H2AZ. | Q38169520 |
| | A global requirement for the HIR complex in the assembly of chromatin | Q38181504 |
| | Chromosomal landscape of nucleosome-dependent gene expression and silencing in yeast. | Q38317749 |
| | Increased and decreased sensitivity to carbon catabolite repression of enzymes of acetate metabolism in mutants of Aspergillus nidulans | Q39180000 |
| | Genetic and biochemical studies of nitrate reduction in Aspergillus nidulans | Q39273629 |
| | Carbon Catabolite Repression in Aspergillus nidulans | Q39942602 |
| | Pleiotropic mutants ofAspergillus nidulans altered in carbon metabolism | Q40752243 |
| | Diverse Regulation of the CreA Carbon Catabolite Repressor in Aspergillus nidulans | Q41091197 |
| | Human Mediator enhances basal transcription by facilitating recruitment of transcription factor IIB during preinitiation complex assembly | Q42493019 |
| | Yeast Num1p associates with the mother cell cortex during S/G2 phase and affects microtubular functions | Q42952999 |
| | RcoA has pleiotropic effects on Aspergillus nidulans cellular development | Q43548958 |
| | Unique residues on the H2A.Z containing nucleosome surface are important for Xenopus laevis development | Q45010246 |
| | Patterns of nucleosomal organization in the alc regulon of Aspergillus nidulans: roles of the AlcR transcriptional activator and the CreA global repressor | Q46424896 |
| | SEC16 in COPII coat dynamics at ER exit sites | Q46782581 |
| | A role for creD, a carbon catabolite repression gene from Aspergillus nidulans, in ubiquitination | Q48182439 |
| | Identification of protein complexes from filamentous fungi with tandem affinity purification | Q48336324 |
| | Carbon catabolite repression in Aspergillus nidulans involves deubiquitination | Q48354827 |
| | CreA-mediated repression in Aspergillus nidulans does not require transcriptional auto-regulation, regulated intracellular localisation or degradation of CreA. | Q50654998 |
| | The CreB deubiquitinating enzyme does not directly target the CreA repressor protein in Aspergillus nidulans. | Q51308766 |
| | The CreB deubiquitinating enzyme does not directly target the CreA repressor protein in Aspergillus nidulans. | Q51536188 |
| | Nitrogen metabolite repression in Aspergillus nidulans | Q54154831 |
| | Conserved Histone Variant H2A.Z Protects Euchromatin from the Ectopic Spread of Silent Heterochromatin | Q58212661 |
| | The Aspergillus nidulans creC gene involved in carbon catabolite repression encodes a WD40 repeat protein | Q62648385 |
| | The WD40-repeat protein CreC interacts with and stabilizes the deubiquitinating enzyme CreB in vivo in Aspergillus nidulans | Q62652320 |
| | The function of CreA, the carbon catabolite repressor of Aspergillus nidulans, is regulated at the transcriptional and post-transcriptional level | Q62654960 |
| | Fusion PCR and gene targeting in Aspergillus nidulans | Q62658531 |
| | The induction and repression of nitrate reductase in the fungus Aspergillus nidulans | Q62667879 |
| | The role of CRE1 in nucleosome positioning within the cbh1 promoter and coding regions of Trichoderma reesei | Q62693165 |
| | Patterns of histone variant synthesis can distinguish G0 from G1 cells | Q70561137 |
| | The essential histone variant H2A.Z regulates the equilibrium between different chromatin conformational states | Q77649147 |
| | Med8, a subunit of the mediator CTD complex of RNA polymerase II, directly binds to regulatory elements of SUC2 and HXK2 genes | Q77905989 |
| | Qualitative ubiquitome unveils the potential significances of protein lysine ubiquitination in hyphal growth of Aspergillus nidulans | Q86049056 |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Aspergillus nidulans | Q683881 |
| P577 | publication date | 2016-12-03 | |
| P1433 | published in | Current Genetics | Q15765847 |
| P1476 | title | Proteins interacting with CreA and CreB in the carbon catabolite repression network in Aspergillus nidulans | |