<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sahota A</submitter><funding>Cancer Research UK</funding><funding>European Research Council</funding><funding>Medical Research Council</funding><funding>Wellcome Trust</funding><funding>Academy of Medical Sciences</funding><funding>Engineering and Physical Sciences Research Council</funding><pagination>18522-18533</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12096465</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>19(19)</volume><pubmed_abstract>Emerging techniques for mapping mRNAs within the subcellular compartments of live cells hold great promise for advancing our understanding of the spatial distribution of transcripts and enabling the study of single-cell dynamics in health and disease. This is particularly critical for polarized cells, such as neurons, where mRNA compartmentalization is essential for regulating gene expression, and defects in these localization mechanisms are linked to numerous neurological disorders. However, many subcellular analysis techniques require a compromise between subcellular precision, live-cell measurements, and nondestructive access to single cells in their native microenvironment. To overcome these challenges, we employ a single-cell technology that we have recently developed, the nanotweezer</pubmed_abstract><journal>ACS nano</journal><pubmed_title>Spatial and Temporal Single-Cell Profiling of RNA Compartmentalization in Neurons with Nanotweezers.</pubmed_title><pmcid>PMC12096465</pmcid><funding_grant_id>EP/T022000/1</funding_grant_id><funding_grant_id>SBF008\1179</funding_grant_id><funding_grant_id>724300</funding_grant_id><funding_grant_id>EP/V049070/1</funding_grant_id><funding_grant_id>CC2206</funding_grant_id><funding_grant_id>875525</funding_grant_id><pubmed_authors>Kittler JT</pubmed_authors><pubmed_authors>Edel JB</pubmed_authors><pubmed_authors>Kwan Z</pubmed_authors><pubmed_authors>Claxton S</pubmed_authors><pubmed_authors>Paulose Nadappuram B</pubmed_authors><pubmed_authors>Lesept F</pubmed_authors><pubmed_authors>Sahota A</pubmed_authors><pubmed_authors>Howden JH</pubmed_authors><pubmed_authors>Ivanov AP</pubmed_authors><pubmed_authors>Devine MJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Spatial and Temporal Single-Cell Profiling of RNA Compartmentalization in Neurons with Nanotweezers.</name><description>Emerging techniques for mapping mRNAs within the subcellular compartments of live cells hold great promise for advancing our understanding of the spatial distribution of transcripts and enabling the study of single-cell dynamics in health and disease. This is particularly critical for polarized cells, such as neurons, where mRNA compartmentalization is essential for regulating gene expression, and defects in these localization mechanisms are linked to numerous neurological disorders. However, many subcellular analysis techniques require a compromise between subcellular precision, live-cell measurements, and nondestructive access to single cells in their native microenvironment. To overcome these challenges, we employ a single-cell technology that we have recently developed, the nanotweezer</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 May</publication><modification>2026-07-15T11:12:37.621Z</modification><creation>2026-07-05T03:08:36.612Z</creation></dates><accession>S-EPMC12096465</accession><cross_references><pubmed>40326740</pubmed><doi>10.1021/acsnano.5c02056</doi></cross_references></HashMap>