<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Belsley G</submitter><funding>NIHR Oxford Biomedical Research Centre</funding><funding>Engineering and Physical Sciences Research Council (EPSRC), Medical Research Council (MRC)</funding><pagination>2331-2345</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11971508</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>93(6)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>To develop an accurate and precise liver 3D T1$$ {T}_1 $$ mapping method using only scanner-agnostic sequences.&lt;h4>Methods&lt;/h4>While the spoiled gradient-recalled echo sequence is widely available on clinical scanners, variable flip angle T1$$ {T}_1 $$ mapping methods based on this sequence provide biased T1$$ {T}_1 $$ estimates, with the largest systematic error arising from B1+$$ {B}_1^{+} $$ inhomogeneities. To correct for this, the flip angle was mapped using a 2D gradient-echo double-angle method approach. To correct for the confounding effect of fat on liver T1$$ {T}_1 $$ and B1+$$ {B}_1^{+} $$ , Dixon and fat saturation techniques were used in combination with the variable flip angle and the B1+$$ {B}_1^{+} $$ map acquisitions, respectively. The T1$$ {T}_1 $$ and B1+</pubmed_abstract><journal>Magnetic resonance in medicine</journal><pubmed_title>Accurate and precise in vivo liver 3D T&amp;lt;sub&amp;gt;1&amp;lt;/sub&amp;gt; mapping at 3T.</pubmed_title><pmcid>PMC11971508</pmcid><funding_grant_id>EP/L016052/1</funding_grant_id><pubmed_authors>Tyler DJ</pubmed_authors><pubmed_authors>Tunnicliffe EM</pubmed_authors><pubmed_authors>Belsley G</pubmed_authors><pubmed_authors>Robson MD</pubmed_authors><pubmed_authors>Mozes FE</pubmed_authors></additional><is_claimable>false</is_claimable><name>Accurate and precise in vivo liver 3D T&amp;lt;sub&amp;gt;1&amp;lt;/sub&amp;gt; mapping at 3T.</name><description>&lt;h4>Purpose&lt;/h4>To develop an accurate and precise liver 3D T1$$ {T}_1 $$ mapping method using only scanner-agnostic sequences.&lt;h4>Methods&lt;/h4>While the spoiled gradient-recalled echo sequence is widely available on clinical scanners, variable flip angle T1$$ {T}_1 $$ mapping methods based on this sequence provide biased T1$$ {T}_1 $$ estimates, with the largest systematic error arising from B1+$$ {B}_1^{+} $$ inhomogeneities. To correct for this, the flip angle was mapped using a 2D gradient-echo double-angle method approach. To correct for the confounding effect of fat on liver T1$$ {T}_1 $$ and B1+$$ {B}_1^{+} $$ , Dixon and fat saturation techniques were used in combination with the variable flip angle and the B1+$$ {B}_1^{+} $$ map acquisitions, respectively. The T1$$ {T}_1 $$ and B1+</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jun</publication><modification>2025-07-08T03:13:38.555Z</modification><creation>2025-07-08T03:13:38.555Z</creation></dates><accession>S-EPMC11971508</accession><cross_references><pubmed>39902594</pubmed><doi>10.1002/mrm.30448</doi></cross_references></HashMap>