<?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>2026-05-27T05:23:32Z</responseDate><request verb="GetRecord" identifier="oai:riuma.uma.es:10630/20636" metadataPrefix="marc">https://riuma.uma.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:riuma.uma.es:10630/20636</identifier><datestamp>2026-02-03T11:59:31Z</datestamp><setSpec>com_10630_2254</setSpec><setSpec>col_10630_37959</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">García-León, Juan Antonio</subfield>
      <subfield code="e">author</subfield>
   </datafield>
   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Cáceres Palomo, Laura</subfield>
      <subfield code="e">author</subfield>
   </datafield>
   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Dávila-Cansino, José Carlos</subfield>
      <subfield code="e">author</subfield>
   </datafield>
   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Vitorica Ferrández, Javier</subfield>
      <subfield code="e">author</subfield>
   </datafield>
   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Gutiérrez-Pérez, Antonia</subfield>
      <subfield code="e">author</subfield>
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   <datafield ind2=" " ind1=" " tag="260">
      <subfield code="c">2020-12-18</subfield>
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      <subfield code="a">Background:&#xd;
Alzheimer's disease (AD) is characterized by presenting a complex pathology,&#xd;
not fully resolved yet. This fact, together with the lack of reliable models, has&#xd;
impeded the development of effective therapies. Recently, several studies have&#xd;
shown that functional glial cell defects have a key role in the pathology of AD.&#xd;
However, this glial dysfunction, currently, cannot be correctly modeled using&#xd;
the available animal models, so we hypothesized that cells derived from&#xd;
Alzheimer's patients can serve as a better platform for studying the disease. In&#xd;
this sense, human pluripotent stem cells (hPSC) allow the generation of&#xd;
different types of neural cells, which can be used for disease modeling,&#xd;
identification of new targets and drugs development.&#xd;
Methods:&#xd;
We have a collection of hiPSCs derived from patients with sporadic forms of&#xd;
AD. We have differentiated these cells towards neural lineage to obtain neurons&#xd;
and astrocytes. For the generation of oligodendrocytes (OLs), we have&#xd;
developed a fast and robust protocol to generate mature OLs in just 22 days.&#xd;
Results:&#xd;
We have generated neural precursors from all the lines tested. In the case of&#xd;
OLs, the cells generated resemble primary OLs and can myelinate neurons in&#xd;
vivo and in vitro using a screening compatible platform. This platform is being&#xd;
transferred for the generation of the other glial cells.&#xd;
Conclusions:&#xd;
This methodology can be used to elucidate the pathogenic pathways associated&#xd;
with neurodegeneration and to identify new therapeutic targets susceptible to&#xd;
modulation, contributing to the development of new effective drugs against AD.</subfield>
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      <subfield code="a">https://hdl.handle.net/10630/20636</subfield>
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      <subfield code="a">Alzheimer, Enfermedad de</subfield>
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   <datafield ind2="0" ind1="0" tag="245">
      <subfield code="a">Human pluripotent stem cells as a research tool for elucidating the role of glial cells in Alzheimer´s disease</subfield>
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