<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>23(1)</volume><submitter>Bertone AL</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>The use of micro-particulate allografts is rising, but knowledge about the protein characterization and biocompatibility of umbilical cord-derived allografts (UC) in vivo is limited.&lt;h4>Methods&lt;/h4>Proteomic analyses using mass spectrometry (MS) determined equine UC protein relative quantification and functions using total spectral counts (TSC). UC cytokines were quantified by enzyme-linked immunosorbent assay (ELISA). Three in vivo studies assessed recipient clinical and tissue biocompatibility in joints and ligaments.&lt;h4>Results&lt;/h4>Proteomics revealed 2645 annotated TSCs. Proteins of > 89 TSC were considered abundant and were present in all donors. Proteins within the same donor had a 4.7% mean variation. Inflammatory cytokines were low in UC. In vivo, the prospective</pubmed_abstract><journal>BMC medicine</journal><pagination>439</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12288288</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Cryopreserved equine umbilical cord tissue allograft characterization and biocompatibility in vivo in musculoskeletal tissues: a controlled study.</pubmed_title><pmcid>PMC12288288</pmcid><pubmed_authors>Ragland D</pubmed_authors><pubmed_authors>Bertone AL</pubmed_authors><pubmed_authors>Leise B</pubmed_authors><pubmed_authors>Reinemeyer C</pubmed_authors><pubmed_authors>Tsaprailis G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cryopreserved equine umbilical cord tissue allograft characterization and biocompatibility in vivo in musculoskeletal tissues: a controlled study.</name><description>&lt;h4>Background&lt;/h4>The use of micro-particulate allografts is rising, but knowledge about the protein characterization and biocompatibility of umbilical cord-derived allografts (UC) in vivo is limited.&lt;h4>Methods&lt;/h4>Proteomic analyses using mass spectrometry (MS) determined equine UC protein relative quantification and functions using total spectral counts (TSC). UC cytokines were quantified by enzyme-linked immunosorbent assay (ELISA). Three in vivo studies assessed recipient clinical and tissue biocompatibility in joints and ligaments.&lt;h4>Results&lt;/h4>Proteomics revealed 2645 annotated TSCs. Proteins of > 89 TSC were considered abundant and were present in all donors. Proteins within the same donor had a 4.7% mean variation. Inflammatory cytokines were low in UC. In vivo, the prospective</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jul</publication><modification>2026-07-15T12:34:23.012Z</modification><creation>2025-08-28T03:05:57.642Z</creation></dates><accession>S-EPMC12288288</accession><cross_references><pubmed>40702469</pubmed><doi>10.1186/s12916-025-04231-7</doi></cross_references></HashMap>