<?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>2026-06-14T05:06:57Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/9651" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/9651</identifier><datestamp>2024-10-31T11:41:13Z</datestamp><setSpec>com_20.500.12105_19604</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>col_20.500.12105_19605</setSpec><setSpec>col_20.500.12105_19607</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">Bonzon-Kulichenko, Elena</subfield>
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      <subfield code="a">Camafeita, Emilio</subfield>
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      <subfield code="a">Lopez, Juan Antonio</subfield>
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      <subfield code="a">Jorge, Inmaculada</subfield>
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      <subfield code="a">Calvo, Enrique</subfield>
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      <subfield code="a">Nunez, Estefania</subfield>
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      <subfield code="a">Trevisan-Herraz, Marco</subfield>
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      <subfield code="a">Bagwan, Navratan</subfield>
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      <subfield code="a">Bárcena, José Antonio</subfield>
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      <subfield code="a">Vazquez, Jesus</subfield>
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      <subfield code="a">Changes in the oxidation state of protein Cys residues are involved in cell signalling and play a key role in a variety of pathophysiological states. We had previously developed GELSILOX, an in-gel method that enables the large-scale, parallel analysis of dynamic alterations to the redox state of Cys sites and protein abundance changes. Here we present FASILOX, a further development of the GELSILOX approach featuring: i) significantly increased peptide recovery, ii) enhanced sensitivity for the detection of Cys oxidative alterations, and iii) streamlined workflow that results in shortened assay duration. In mitochondria isolated from the adipose tissue of obese, diabetic patients, FASILOX revealed a sexually dimorphic trait of Cys oxidation involving mainly mitochondrial oxidative phosphorylation complexes. These results provide the first evidence for a decreased efficiency in the antioxidant response of men as compared to women.</subfield>
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      <subfield code="a">J Proteomics. 2020; 214:103624</subfield>
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      <subfield code="a">10.1016/j.jprot.2019.103624</subfield>
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      <subfield code="a">31874222</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12105/9651</subfield>
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      <subfield code="a">Thiol redox proteome</subfield>
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      <subfield code="a">Improved integrative analysis of the thiol redox proteome using filter-aided sample preparation</subfield>
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