<?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>2026-06-14T03:46:46Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/8374" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/8374</identifier><datestamp>2024-09-27T09:49:21Z</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">dc</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">del Fresno, Carlos</subfield>
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      <subfield code="a">Cueto, Francisco J.</subfield>
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      <subfield code="a">Sancho, David</subfield>
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      <subfield code="c">2019-09</subfield>
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      <subfield code="a">Myeloid C-type lectin receptors (CLRs) comprise a family of receptors expressed by immune myeloid cells that share homologous C-type lectin domains. The implication of these CLRs in the regulation of homeostasis and activation of myeloid cells has generated a buoyant growth in the number of studies involving these receptors. Since their first description, diverse nomenclature has been used to refer to each of them, ranging from systematic classifications, such as gene name or cluster of differentiation, to non-systematic ones that include terminology based on gene expression patterns or function. In this review, we aim to summarize the different names used for the main myeloidCLRs and analyzewhich of themhave beenmore frequently used in the literature. In addition, we have examined the evolution of the terminology applied to these myeloid CLRs over time. Based on this analysis, we propose a consensus alias for each of those myeloid CLRs. However, we acknowledge that systematicity is required beyond this terminology based on use frequency. Therefore, we have included gene names as the standardization tool to gather the maximum agreement. We suggest that a standard nomenclature consisting of both gene names and consensus alias should be included at least in scientific abstracts, which would help to identify relevant literature, saving time and effort and fostering the research in this field in a more systematic manner.</subfield>
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      <subfield code="a">Front Immunol. 2019; 10:2098</subfield>
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      <subfield code="a">10.3389/fimmu.2019.02098</subfield>
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      <subfield code="a">1664-3224</subfield>
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      <subfield code="a">Frontiers in Immunology</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12105/8374</subfield>
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   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">Lectin receptors</subfield>
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      <subfield code="a">Signaling</subfield>
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      <subfield code="a">Monocytes</subfield>
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      <subfield code="a">Macrophage</subfield>
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      <subfield code="a">Dentritic cells</subfield>
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      <subfield code="a">Innate immunity</subfield>
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      <subfield code="a">Nomenclature</subfield>
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   <datafield ind2="0" ind1="0" tag="245">
      <subfield code="a">A Proposal for Nomenclature in Myeloid C-Type Lectin Receptors</subfield>
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