<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wang S</submitter><funding>NIDDK NIH HHS</funding><funding>National Institutes of Health</funding><funding>NIAMS NIH HHS</funding><pagination>dev195388</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7648600</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>147(20)</volume><pubmed_abstract>Between embryonic days 10.5 and 14.5, active proliferation drives rapid elongation of the murine midgut epithelial tube. Within this pseudostratified epithelium, nuclei synthesize DNA near the basal surface and move apically to divide. After mitosis, the majority of daughter cells extend a long, basally oriented filopodial protrusion, building a &lt;i>de novo&lt;/i> path along which their nuclei can return to the basal side. WNT5A, which is secreted by surrounding mesenchymal cells, acts as a guidance cue to orchestrate this epithelial pathfinding behavior, but how this signal is received by epithelial cells is unknown. Here, we have investigated two known WNT5A receptors: ROR2 and RYK. We found that epithelial ROR2 is dispensable for midgut elongation. However, loss of &lt;i>Ryk&lt;/i> phenocopies th</pubmed_abstract><journal>Development (Cambridge, England)</journal><pubmed_title>RYK-mediated filopodial pathfinding facilitates midgut elongation.</pubmed_title><pmcid>PMC7648600</pmcid><funding_grant_id>R01 AR055926</funding_grant_id><funding_grant_id>R01 DK121166</funding_grant_id><funding_grant_id>R01 AR067203</funding_grant_id><funding_grant_id>R56 DK089933</funding_grant_id><funding_grant_id>P30 DK034933</funding_grant_id><funding_grant_id>R01 DK089933</funding_grant_id><funding_grant_id>R01 DK117981</funding_grant_id><pubmed_authors>Cameron L</pubmed_authors><pubmed_authors>Lechler T</pubmed_authors><pubmed_authors>Wang S</pubmed_authors><pubmed_authors>Tsai YH</pubmed_authors><pubmed_authors>Underwood J</pubmed_authors><pubmed_authors>Tomlinson AJ</pubmed_authors><pubmed_authors>Roy JP</pubmed_authors><pubmed_authors>Wang EB</pubmed_authors><pubmed_authors>Walton KD</pubmed_authors><pubmed_authors>Gumucio DL</pubmed_authors><pubmed_authors>Stacker SA</pubmed_authors><pubmed_authors>Spence JR</pubmed_authors></additional><is_claimable>false</is_claimable><name>RYK-mediated filopodial pathfinding facilitates midgut elongation.</name><description>Between embryonic days 10.5 and 14.5, active proliferation drives rapid elongation of the murine midgut epithelial tube. Within this pseudostratified epithelium, nuclei synthesize DNA near the basal surface and move apically to divide. After mitosis, the majority of daughter cells extend a long, basally oriented filopodial protrusion, building a &lt;i>de novo&lt;/i> path along which their nuclei can return to the basal side. WNT5A, which is secreted by surrounding mesenchymal cells, acts as a guidance cue to orchestrate this epithelial pathfinding behavior, but how this signal is received by epithelial cells is unknown. Here, we have investigated two known WNT5A receptors: ROR2 and RYK. We found that epithelial ROR2 is dispensable for midgut elongation. However, loss of &lt;i>Ryk&lt;/i> phenocopies th</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Oct</publication><modification>2026-05-03T10:11:13.115Z</modification><creation>2025-04-04T19:50:17.122Z</creation></dates><accession>S-EPMC7648600</accession><cross_references><pubmed>32994164</pubmed><doi>10.1242/dev.195388</doi></cross_references></HashMap>