<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>22(11)</volume><submitter>Aref S</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Bone marrow myelofibrosis (BMF) that develop on top of Polycythaemia vera (PV) and essential thrombocythemia leads to shortening of the patient's overall survival. This study aimed to address the impact of miR-146a rs2431697 polymorphism on inflammatory biomarkers and genes expression and the hazards of myelofibrosis progression.&lt;h4>Patients and methods&lt;/h4>The study included 88 myeloproliferative neoplasm (40 PV; 27 ET; 21 MF) and 90 healthy controls. For all investigated subjects miR-146a rs2431697 genotypes were identified by sequencing and the expression of miR-146a; IL-1β; NF-κB; a NOD-like receptor family, pyrin domain containing 3 (NLRP3) (NLRP3) genes were estimated by real time PCR.&lt;h4>Results&lt;/h4>miR146a genotypes revealed that there was significant association</pubmed_abstract><journal>Asian Pacific journal of cancer prevention : APJCP</journal><pagination>3585-3589</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9068196</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Predictive Value of miR-146a rs2431697 Polymorphism to Myelofibrosis Progression in Patients with Myeloproliferative Neoplasm.</pubmed_title><pmcid>PMC9068196</pmcid><pubmed_authors>Atia D</pubmed_authors><pubmed_authors>Al Boghdady M</pubmed_authors><pubmed_authors>Aref S</pubmed_authors><pubmed_authors>Al Tantawy A</pubmed_authors><pubmed_authors>Gouda E</pubmed_authors></additional><is_claimable>false</is_claimable><name>Predictive Value of miR-146a rs2431697 Polymorphism to Myelofibrosis Progression in Patients with Myeloproliferative Neoplasm.</name><description>&lt;h4>Background&lt;/h4>Bone marrow myelofibrosis (BMF) that develop on top of Polycythaemia vera (PV) and essential thrombocythemia leads to shortening of the patient's overall survival. This study aimed to address the impact of miR-146a rs2431697 polymorphism on inflammatory biomarkers and genes expression and the hazards of myelofibrosis progression.&lt;h4>Patients and methods&lt;/h4>The study included 88 myeloproliferative neoplasm (40 PV; 27 ET; 21 MF) and 90 healthy controls. For all investigated subjects miR-146a rs2431697 genotypes were identified by sequencing and the expression of miR-146a; IL-1β; NF-κB; a NOD-like receptor family, pyrin domain containing 3 (NLRP3) (NLRP3) genes were estimated by real time PCR.&lt;h4>Results&lt;/h4>miR146a genotypes revealed that there was significant association</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Nov</publication><modification>2025-04-22T09:48:10.345Z</modification><creation>2025-04-05T23:17:07.013Z</creation></dates><accession>S-EPMC9068196</accession><cross_references><pubmed>34837916</pubmed><doi>10.31557/APJCP.2021.22.11.3585</doi></cross_references></HashMap>