174 papers found
Refreshing results…
Fast and Sensitive Total Protein and Peptide Assays for Proteomic Analysis
Absolute protein quantification allows differentiation of cell-specific metabolic routes and functions
Absolute Quantitative Profiling of the Key Metabolic Pathways in Slow and Fast Skeletal Muscle
Quantifying the impact of transporters on cellular drug permeability.
Pattern of melanotransferrin expression in human colorectal tissues: an immunohistochemical study on potential clinical application
The Impact of High-Fat Diet on Metabolism and Immune Defense in Small Intestine Mucosa
Astrocyte‐neuron crosstalk regulates the expression and subcellular localization of carbohydrate metabolism enzymes
A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards*
Multi-enzyme digestion FASP and the 'Total Protein Approach'-based absolute quantification of the Escherichia coli proteome
Ultradeep Human Phosphoproteome Reveals a Distinct Regulatory Nature of Tyr and Ser/Thr-Based Signaling
Quantitative analysis of the Escherichia coli proteome
Hepatic Uptake of Atorvastatin: Influence of Variability in Transporter Expression on Uptake Clearance and Drug-Drug Interactions
Proteomics approaches to identifying proteins involved in adenoma-to-colorectal carcinoma progression
Proteomic Sample Preparation from Formalin Fixed and Paraffin Embedded Tissue
Proteomic workflow for analysis of archival formalin-fixed and paraffin-embedded clinical samples to a depth of 10 000 proteins
Quantification of the N-glycosylated Secretome by Super-SILAC During Breast Cancer Progression and in Human Blood Samples*
The use of laser microdissection and mass spectrometry in colorectal cancer tissue to identify protein profiles
Three aspects of clinical proteomics - routine diagnostics, biomarker search, basic search
Spektroskopia mas w proteomice klinicznej na przykładzie badań nad analizą proteomu gruczolakoraka jelita grubego
The NUCKS: a novel tumor biomarker
Missing publications? Read more about our data sources.