<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhang A</submitter><funding>CAMS Innovation Fund for Medical Sciences</funding><funding>National Natural Science Foundation of China</funding><pagination>154</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11228008</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(1)</volume><pubmed_abstract>Essential thrombocythemia (ET) and prefibrotic primary myelofibrosis (pre-PMF) are Philadelphia chromosome-negative myeloproliferative neoplasms. These conditions share overlapping clinical presentations; however, their prognoses differ significantly. Current morphological diagnostic methods lack reliability in subtype differentiation, underlining the need for improved diagnostics. The aim of this study was to investigate the multi-omics alterations in bone marrow biopsies of patients with ET and pre-PMF to improve our understanding of the nuanced diagnostic characteristics of both diseases. We performed proteomic analysis with 4D direct data-independent acquisition and microbiome analysis with 2bRAD-M sequencing technology to identify differential protein and microbe levels between untrea</pubmed_abstract><journal>Clinical and experimental medicine</journal><pubmed_title>Multi-omics differences in the bone marrow between essential thrombocythemia and prefibrotic primary myelofibrosis.</pubmed_title><pmcid>PMC11228008</pmcid><funding_grant_id>82000136</funding_grant_id><funding_grant_id>82270152</funding_grant_id><funding_grant_id>2023-I2M-QJ-015</funding_grant_id><funding_grant_id>82100151</funding_grant_id><pubmed_authors>Fu R</pubmed_authors><pubmed_authors>Xue F</pubmed_authors><pubmed_authors>Li H</pubmed_authors><pubmed_authors>Chen J</pubmed_authors><pubmed_authors>Gu W</pubmed_authors><pubmed_authors>Sun T</pubmed_authors><pubmed_authors>Yu D</pubmed_authors><pubmed_authors>Zhang L</pubmed_authors><pubmed_authors>Liu W</pubmed_authors><pubmed_authors>Dai X</pubmed_authors><pubmed_authors>Liu X</pubmed_authors><pubmed_authors>Dong H</pubmed_authors><pubmed_authors>Wang W</pubmed_authors><pubmed_authors>Yang R</pubmed_authors><pubmed_authors>Chen Y</pubmed_authors><pubmed_authors>Ju M</pubmed_authors><pubmed_authors>Chi Y</pubmed_authors><pubmed_authors>Zhang A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Multi-omics differences in the bone marrow between essential thrombocythemia and prefibrotic primary myelofibrosis.</name><description>Essential thrombocythemia (ET) and prefibrotic primary myelofibrosis (pre-PMF) are Philadelphia chromosome-negative myeloproliferative neoplasms. These conditions share overlapping clinical presentations; however, their prognoses differ significantly. Current morphological diagnostic methods lack reliability in subtype differentiation, underlining the need for improved diagnostics. The aim of this study was to investigate the multi-omics alterations in bone marrow biopsies of patients with ET and pre-PMF to improve our understanding of the nuanced diagnostic characteristics of both diseases. We performed proteomic analysis with 4D direct data-independent acquisition and microbiome analysis with 2bRAD-M sequencing technology to identify differential protein and microbe levels between untrea</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jul</publication><modification>2025-04-26T05:42:14.143Z</modification><creation>2025-04-06T11:35:24.609Z</creation></dates><accession>S-EPMC11228008</accession><cross_references><pubmed>38972952</pubmed><doi>10.1007/s10238-024-01350-y</doi></cross_references></HashMap>