Experiments

Searchable full-text extractions: founding hypothesis, core claims, experimental setups, key results and statistics — pulled out of each paper as structure. Search a cell line, an assay or an entity (e.g. HUH7) and find every paper that worked with it. This corpus stands on its own: most entries carry no reproduction assessment (yet).

• A quantitative proteomics analysis of subcellular proteome localization and changes induced by DNA damage.

  PMID 20026476 · PMC2849709 · Molecular & cellular proteomics : MCP · 2010 · 6 claims · 5 setups

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  A SILAC-based 'spatial proteomics' method can quantitatively measure the relative subcellular distribution of thousands of proteins across cytoplasm, nucleus, and nucleolus.

  hct116 silac silac-based immunofluorescence

• Quantitative membrane proteomics reveals new cellular targets of viral immune modulators.

  PMID 17238276 · PMC1626102 · PLoS pathogens · 2006 · 8 claims · 8 setups

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  SILAC-based quantitative membrane proteomics can identify novel targets of viral immunomodulators in an unbiased manner

  hela silac immunoblot flow

• Identification of novel proteins affected by rotenone in mitochondria of dopaminergic cells.

  PMID 17705834 · PMC2000881 · BMC neuroscience · 2007 · 6 claims · 5 setups

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  SILAC-based quantitative proteomics combined with SDS-PAGE and LC-MS/MS can identify and quantify mitochondrial protein abundance changes in dopaminergic MES cells exposed to rotenone vs. control

  mes silac western confocal

• The impact of microRNAs on protein output.

  PMID 18668037 · PMC2745094 · Nature · 2008 · 8 claims · 8 setups

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  MicroRNA targeting for protein repression occurs primarily through seed-matched sites (6mer, 7mer-A1, 7mer-m8, 8mer) located in favourable predicted contexts within 3′ UTRs

  hela neutrophils bone mir-223 quantitative blot microarray

• Evolution of organelle-associated protein profiling.

  PMID 19110081 · PMC2680700 · Journal of proteomics · 2009 · 8 claims · 8 setups

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  Traditional biochemical organelle isolation followed by MS cataloguing suffers high false-positive rates because organelles cannot be purified to homogeneity and are structurally heterogeneous

  golgi nuclear lipid clathrin-coated density qualitative silac