<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-05-17T05:43:32Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/15784" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/15784</identifier><datestamp>2024-09-27T09:48:07Z</datestamp><setSpec>com_20.500.12105_19604</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>col_20.500.12105_19605</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Dalmasso, Giovanni</subfield>
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      <subfield code="a">Musy, Marco</subfield>
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      <subfield code="a">Niksic, Martina</subfield>
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      <subfield code="a">Robert-Moreno, Alexandre</subfield>
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      <subfield code="a">Badia-Careaga, Claudio</subfield>
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      <subfield code="a">Sanz-Ezquerro, Juan Jose</subfield>
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      <subfield code="a">Sharpe, James</subfield>
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      <subfield code="c">2022-09-12</subfield>
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      <subfield code="a">Normal organogenesis cannot be recapitulated in vitro for mammalian organs, unlike in species including Drosophila and zebrafish. Available 3D data in the form of ex vivo images only provide discrete snapshots of the development of an organ morphology. Here, we propose a computer-based approach to recreate its continuous evolution in time and space from a set of 3D volumetric images. Our method is based on the remapping of shape data into the space of the coefficients of a spherical harmonics expansion where a smooth interpolation over time is simpler. We tested our approach on mouse limb buds and embryonic hearts. A key advantage of this method is that the resulting 4D trajectory can take advantage of all the available data while also being able to interpolate well through time intervals for which there are little or no data. This allows for a quantitative, data-driven 4D description of mouse limb morphogenesis.</subfield>
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      <subfield code="a">Dev Cell. 2022 Sep 12;57(17):2140-2150.e5</subfield>
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      <subfield code="a">10.1016/j.devcel.2022.08.005</subfield>
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      <subfield code="a">1878-1551</subfield>
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      <subfield code="a">Developmental cell</subfield>
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      <subfield code="a">36055247</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12105/15784</subfield>
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   <datafield ind2="0" ind1="0" tag="245">
      <subfield code="a">4D reconstruction of murine developmental trajectories using spherical harmonics.</subfield>
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