<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15(1)</volume><submitter>Wasinger VC</submitter><pubmed_abstract>Breakdown of the protective gut barrier releases effector molecules and degradation products into the blood stream making serum and plasma ideal as a diagnostic medium. The enriched low mass proteome is unexplored as a source of differentiators for diagnosing and monitoring inflammatory bowel disease (IBD) activity, that is less invasive than colonoscopy. Differences in the enriched low mass plasma proteome (&lt;25 kDa) were assessed by label-free quantitative mass-spectrometry. A panel of marker candidates were progressed to validation phase and "Tier-2" FDA-level validated quantitative assay. Proteins important in maintaining gut barrier function and homeostasis at the epithelial interface have been quantitated by multiple reaction monitoring in plasma and serum including both inflammatory;</pubmed_abstract><journal>Molecular &amp; cellular proteomics : MCP</journal><pagination>256-65</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4762526</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Low Mass Blood Peptides Discriminative of Inflammatory Bowel Disease (IBD) Severity: A Quantitative Proteomic Perspective.</pubmed_title><pmcid>PMC4762526</pmcid><pubmed_authors>Shin S</pubmed_authors><pubmed_authors>Leong RW</pubmed_authors><pubmed_authors>Duo X</pubmed_authors><pubmed_authors>Yau Y</pubmed_authors><pubmed_authors>Zeng M</pubmed_authors><pubmed_authors>Campbell B</pubmed_authors><pubmed_authors>Redmond D</pubmed_authors><pubmed_authors>Wasinger VC</pubmed_authors><pubmed_authors>Luber R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Low Mass Blood Peptides Discriminative of Inflammatory Bowel Disease (IBD) Severity: A Quantitative Proteomic Perspective.</name><description>Breakdown of the protective gut barrier releases effector molecules and degradation products into the blood stream making serum and plasma ideal as a diagnostic medium. The enriched low mass proteome is unexplored as a source of differentiators for diagnosing and monitoring inflammatory bowel disease (IBD) activity, that is less invasive than colonoscopy. Differences in the enriched low mass plasma proteome (&lt;25 kDa) were assessed by label-free quantitative mass-spectrometry. A panel of marker candidates were progressed to validation phase and "Tier-2" FDA-level validated quantitative assay. Proteins important in maintaining gut barrier function and homeostasis at the epithelial interface have been quantitated by multiple reaction monitoring in plasma and serum including both inflammatory;</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Jan</publication><modification>2026-05-04T00:58:50.57Z</modification><creation>2019-03-27T02:09:35Z</creation></dates><accession>S-EPMC4762526</accession><cross_references><pubmed>26530476</pubmed><doi>10.1074/mcp.m115.055095</doi><doi>10.1074/mcp.M115.055095</doi></cross_references></HashMap>