<?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>2026-04-19T12:48:40Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/11670" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/11670</identifier><datestamp>2025-06-13T08:30:31Z</datestamp><setSpec>com_20.500.12105_15322</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>com_20.500.12105_2052</setSpec><setSpec>col_20.500.12105_16938</setSpec><setSpec>col_20.500.12105_19617</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">Segura-Collar, Berta</subfield>
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      <subfield code="a">Mata-Martínez, Pablo</subfield>
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      <subfield code="a">Hernández-Laín, Aurelio</subfield>
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      <subfield code="a">Sánchez-Gómez, Pilar</subfield>
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      <subfield code="a">Gargini, Ricardo</subfield>
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      <subfield code="c">2021-01-15</subfield>
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      <subfield code="a">The brain is endowed with a unique cellular composition and organization, embedded within a vascular network and isolated from the circulating blood by a specialized frontier, the so-called blood-brain barrier (BBB), which is necessary for its proper function. Recent reports have shown that increments in the permeability of the blood vessels facilitates the entry of toxic components and immune cells to the brain parenchyma and alters the phenotype of the supporting astrocytes. All of these might contribute to the progression of different pathologies such as brain cancers or neurodegenerative diseases. Although it is well known that BBB breakdown occurs due to pericyte malfunctioning or to the lack of stability of the blood vessels, its participation in the diverse neural diseases needs further elucidation. This review summarizes what it is known about BBB structure and function and how its instability might trigger or promote neuronal degeneration and glioma progression, with a special focus on the role of pericytes as key modulators of the vasculature. Moreover, we will discuss some recent reports that highlights the participation of the BBB alterations in glioma growth. This pan-disease analysis might shed some light into these otherwise untreatable diseases and help to design better therapeutic approaches.</subfield>
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      <subfield code="a">Neuroscientist. 2022 Jun;28(3):222-237.</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12105/11670</subfield>
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      <subfield code="a">The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry</subfield>
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      <subfield code="a">Blood-brain barrier (BBB)</subfield>
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      <subfield code="a">Neurovascular unit (NVU)</subfield>
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      <subfield code="a">Blood-Brain Barrier Disruption: A Common Driver of Central Nervous System Diseases</subfield>
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