<?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>2026-07-21T09:09:09Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/26135" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/26135</identifier><datestamp>2025-12-18T13:00:12Z</datestamp><setSpec>com_20.500.12105_19586</setSpec><setSpec>com_20.500.12105_2202</setSpec><setSpec>col_20.500.12105_19587</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">Silva-Rojas, Roberto</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Pérez-Guàrdia, Laura</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Lafabrie, Emma</subfield>
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   </datafield>
   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Moulaert, David</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Laporte, Jocelyn</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Böhm, Johann</subfield>
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      <subfield code="c">2022-06-23</subfield>
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      <subfield code="a">Tubular aggregate myopathy (TAM) and Stormorken syndrome (STRMK) form a clinical continuum associating progressive muscle weakness with additional multi-systemic anomalies of the bones, skin, spleen, and platelets. TAM/STRMK arises from excessive extracellular Ca entry due to gain-of-function mutations in the Ca sensor STIM1 or the Ca channel ORAI1. Currently, no treatment is available. Here we assessed the therapeutic potential of ORAI1 downregulation to anticipate and reverse disease development in a faithful mouse model carrying the most common TAM/STRMK mutation and recapitulating the main signs of the human disorder. To this aim, we crossed  mice with  mice expressing 50% of ORAI1. Systematic phenotyping of the offspring revealed that the  mice were born with a normalized ratio and showed improved postnatal growth, bone architecture, and partly ameliorated muscle function and structure compared with their  littermates. We also produced AAV particles containing -specific shRNAs, and intramuscular injections of  mice improved the skeletal muscle contraction and relaxation properties, while muscle histology remained unchanged. Altogether, we provide the proof-of-concept that  silencing partially prevents the development of the multi-systemic TAM/STRMK phenotype in mice, and we also established an approach to target  expression in postnatal tissues.</subfield>
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      <subfield code="a">Int J Mol Sci. 2022 Jun 23;23(13):6968.</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">International Journal of Molecular Sciences</subfield>
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      <subfield code="a">35805973</subfield>
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      <subfield code="a">https://hdl.handle.net/20.500.12105/26135</subfield>
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   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">ORAI1</subfield>
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   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">STIM1</subfield>
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   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">Stormorken syndrome</subfield>
   </datafield>
   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">calcium</subfield>
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   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">ion channel</subfield>
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      <subfield code="a">mouse model</subfield>
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      <subfield code="a">muscle disorder</subfield>
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      <subfield code="a">shRNA</subfield>
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   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">tubular aggregate myopathy</subfield>
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   <datafield ind2="0" ind1="0" tag="245">
      <subfield code="a">Silencing of the Ca Channel ORAI1 Improves the Multi-Systemic Phenotype of Tubular Aggregate Myopathy (TAM) and Stormorken Syndrome (STRMK) in Mice.</subfield>
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