<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Liu J</submitter><funding>NIBIB NIH HHS</funding><funding>NCRR NIH HHS</funding><funding>NINDS NIH HHS</funding><pubmed_abstract>&lt;h4>Purpose&lt;/h4>To demonstrate the feasibility and performance of mesoscopic whole brain T&lt;sub>2&lt;/sub>*-weighted (T&lt;sub>2&lt;/sub>*w) MRI at 10.5 T by combining a motion-robust multi-echo gradient-echo (GRE) method with high-density RF receive arrays.&lt;h4>Methods&lt;/h4>Multi-echo GRE data were collected in healthy adults at isotropic 0.5 mm resolution using a custom-built 16-channel transmit/80-channel receive (16Tx/80Rx) RF coil. Whole brain images were reconstructed with navigator-guided joint motion and field correction and were used for quantitative &lt;i>R&lt;/i> &lt;sub>2&lt;/sub>* and susceptibility (&lt;i>χ&lt;/i>) mapping. Intrinsic signal-to-noise ratio (iSNR) and quantification precision for &lt;i>R&lt;/i> &lt;sub>2&lt;/sub>* and &lt;i>χ&lt;/i> were also estimated. The results were compared with those obtained in the sa</pubmed_abstract><journal>bioRxiv : the preprint server for biology</journal><pagination>2025.04.21.649819</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12190817</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Mesoscopic whole-brain T&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;*-weighted and associated quantitative MRI in healthy humans at 10.5 T.</pubmed_title><pmcid>PMC12190817</pmcid><funding_grant_id>R01 NS136490</funding_grant_id><funding_grant_id>P41 EB027061</funding_grant_id><funding_grant_id>S10 RR029672</funding_grant_id><funding_grant_id>U01 EB025144</funding_grant_id><pubmed_authors>Waks M</pubmed_authors><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Auerbach E</pubmed_authors><pubmed_authors>Eryaman Y</pubmed_authors><pubmed_authors>Lagore R</pubmed_authors><pubmed_authors>Ugurbil K</pubmed_authors><pubmed_authors>Adriany G</pubmed_authors><pubmed_authors>Grant A</pubmed_authors><pubmed_authors>Duyn JH</pubmed_authors><pubmed_authors>Delabarre L</pubmed_authors><pubmed_authors>Huang Y</pubmed_authors><pubmed_authors>Sadeghi-Tarakameh A</pubmed_authors><pubmed_authors>van Gelderen P</pubmed_authors><pubmed_authors>de Zwart JA</pubmed_authors><pubmed_authors>Wu X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Mesoscopic whole-brain T&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;*-weighted and associated quantitative MRI in healthy humans at 10.5 T.</name><description>&lt;h4>Purpose&lt;/h4>To demonstrate the feasibility and performance of mesoscopic whole brain T&lt;sub>2&lt;/sub>*-weighted (T&lt;sub>2&lt;/sub>*w) MRI at 10.5 T by combining a motion-robust multi-echo gradient-echo (GRE) method with high-density RF receive arrays.&lt;h4>Methods&lt;/h4>Multi-echo GRE data were collected in healthy adults at isotropic 0.5 mm resolution using a custom-built 16-channel transmit/80-channel receive (16Tx/80Rx) RF coil. Whole brain images were reconstructed with navigator-guided joint motion and field correction and were used for quantitative &lt;i>R&lt;/i> &lt;sub>2&lt;/sub>* and susceptibility (&lt;i>χ&lt;/i>) mapping. Intrinsic signal-to-noise ratio (iSNR) and quantification precision for &lt;i>R&lt;/i> &lt;sub>2&lt;/sub>* and &lt;i>χ&lt;/i> were also estimated. The results were compared with those obtained in the sa</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Apr</publication><modification>2026-04-08T16:12:25.21Z</modification><creation>2026-04-08T06:11:04.806Z</creation></dates><accession>S-EPMC12190817</accession><cross_references><pubmed>40568064</pubmed><doi>10.1101/2025.04.21.649819</doi></cross_references></HashMap>