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ProteomicsInteractions between basic helix-loop-helix transcription factors and nucleosomes
In solution crosslinking mass spectrometry of transcription factors in complex with nucleosomes
ORGANISM(S): Homo sapiens (Human) 
2023-05-23 | PXD033181 | Pride
Dsso crosslinking xlinkx pd transcription factor nucleosome human 
UnknownRapid, scalable assembly of stereochemically rich, mono- and bicyclic acyl sultams.
Not available
S-EPMC4179432 | biostudies-literature
TranscriptomicsIRF-8 extinguishes neutrophil production and promotes dendritic cell lineage commitment in both myeloid and lymphoid progenitors (Illumina).
While most blood lineages are assumed to mature through a single cellular and developmental route downstream of hematopoietic stem cells (HSCs), dendritic cells (DCs) can be derived from both myeloid and lymphoid progenitors in vivo. To determine how distinct progenitors can generate similar downst...
ORGANISM(S): Mus musculus 
2012-01-07 | E-GEOD-34915 | biostudies-arrayexpress
ProteomicsModular Vinyl-Phosphonamidates for Cysteine Directed Protein Targeting
Covalent inhibitors and chemical probes targeting ligandable cysteine residues have emerged as powerful tools in drug discovery and proteomics. In this study, we introduce vinyl-phosphonamidates (VPAs) as a novel class of latent cysteine electrophiles and assess their reactivity, selectivity, and po...
ORGANISM(S): Homo sapiens (Human) 
2026-03-09 | PXD064073 | Pride
Chemoproteomics Covalent inhibitors 
TranscriptomicsAdaptation of Bacillus subtilis carbon core metabolism to simultaneous nutrient limitation and osmotic challenge
Here, we investigated for the first time the systems-wide response of B. subtilis to different simultaneous stresses, i.e. nutrient limitation and high osmolarity. To address the anticipated complexity of the cellular response networks, we combined chemostat experiments under conditions of carbon li...
ORGANISM(S): Bacillus subtilis 
2014-03-31 | E-GEOD-53333 | biostudies-arrayexpress
TranscriptomicsCNV_Kasumi-1_U-2 OS_Patient
Arrays were used to determine the copy numbers of genomic regions harboring gene mutations and to identify heterozygous single nucleotide polymorphisms (SNPs) that were located close to these gene mutations. The gene mutations were identified through the COSMIC database and sequencing. The SNPs were...
ORGANISM(S): Homo sapiens 
2016-10-10 | E-MTAB-4950 | biostudies-arrayexpress
UnknownClinical role of microRNAs in cytogenetically normal acute myeloid leukemia: miR-155 upregulation independently identifies high-risk patients.
Not available
S-EPMC3731981 | biostudies-literature
UnknownAge-related prognostic impact of different types of DNMT3A mutations in adults with primary cytogenetically normal acute myeloid leukemia.
Not available
S-EPMC3295550 | biostudies-literature
UnknownCrossing cultural barriers: an initial cross-cultural validation of the Arabic compared to the German version of the Posttraumatic Stress Disorder Checklist for DSM-5 using multi-group confirmatory factor analysis.
Not available
S-EPMC12512762 | biostudies-literature
UnknownSystematic review on effects of experimental orthodontic tooth displacement on brain activation assessed by fMRI.
Not available
S-EPMC10982672 | biostudies-literature
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