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ProteomicsThe complexome contextualizes proteomics data to fingerprint biological states and highlight perturbed functional modules in disease
Proteins organize into functional assemblies that drive diverse biological activities. Leveraging a comprehensive dataset of manually curated annotations for the human protein complexome, we investigated biological perturbations at the protein complex level. Using proteomics and transcriptomics data...
ORGANISM(S): Homo sapiens (Human) 
2026-09-14 | PXD048352 | Pride
ProteomicsHigh-throughput nano-flow proteomics using a dual-column electrospray source
With current trends in proteomics, especially regarding clinical and low input (to single cell) samples, it is increasingly important to both maximize the throughput of the analysis and maintain as much sensitivity as possible. The new generation of mass spectrometers (MS) are taking a huge leap in ...
ORGANISM(S): Homo sapiens (Human) 
2024-04-22 | PXD050034 | Pride
Dia Nanolc Tandem setup High-throughput 
UnknownEye morphogenesis in the blind Mexican cavefish.
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S-EPMC8565469 | biostudies-literature
UnknownTwelve Years of Drug Prioritization to Help Accelerate Disease Modification Trials in Parkinson's Disease: The International Linked Clinical Trials Initiative.
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S-EPMC11191436 | biostudies-literature
UnknownIntegrating Pulmonary and Systemic Transcriptomic Profiles to Characterize Lung Injury after Pediatric Hematopoietic Stem Cell Transplant.
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S-EPMC11998824 | biostudies-literature
UnknownREGEN-COV Antibody Combination and Outcomes in Outpatients with Covid-19.
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S-EPMC8522800 | biostudies-literature
UnknownPulmonary microbiome and transcriptome signatures reveal distinct pathobiologic states associated with mortality in two cohorts of pediatric stem cell transplant patients.
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S-EPMC10705623 | biostudies-literature
UnknownDiscontinuation versus continuation of hypertonic saline or dornase alfa in modulator treated people with cystic fibrosis (SIMPLIFY): results from two parallel, multicentre, open-label, randomised, controlled, non-inferiority trials.
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S-EPMC10065895 | biostudies-literature
UnknownDisruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior.
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S-EPMC9472083 | biostudies-literature
UnknownFive-year outcome in the copaxone observatory: a nationwide cohort of patients with multiple sclerosis starting treatment with glatiramer acetate in France.
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S-EPMC6420902 | biostudies-literature
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