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<OAI-PMH schemaLocation=http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd> <responseDate>2018-01-15T18:28:28Z</responseDate> <request identifier=oai:HAL:hal-01174899v1 verb=GetRecord metadataPrefix=oai_dc>http://api.archives-ouvertes.fr/oai/hal/</request> <GetRecord> <record> <header> <identifier>oai:HAL:hal-01174899v1</identifier> <datestamp>2018-01-11</datestamp> <setSpec>type:ART</setSpec> <setSpec>subject:chim</setSpec> <setSpec>collection:UNIV-RENNES1</setSpec> <setSpec>collection:ISCR</setSpec> <setSpec>collection:CNRS</setSpec> <setSpec>collection:UNIV-AG</setSpec> <setSpec>collection:ENSC-RENNES</setSpec> <setSpec>collection:IRSET</setSpec> <setSpec>collection:HL</setSpec> <setSpec>collection:UNIV-NANTES</setSpec> <setSpec>collection:SCR-COS</setSpec> <setSpec>collection:IRSET-HIAEC</setSpec> <setSpec>collection:IFR140</setSpec> <setSpec>collection:BIOSIT</setSpec> <setSpec>collection:UR1-SPM</setSpec> <setSpec>collection:INC-CNRS</setSpec> <setSpec>collection:UR1-UFR-SVE</setSpec> <setSpec>collection:UR1-UFR-SPM</setSpec> <setSpec>collection:STATS-UR1</setSpec> <setSpec>collection:ISCR-CORINT</setSpec> <setSpec>collection:UR1-HAL</setSpec> <setSpec>collection:EHESP</setSpec> <setSpec>collection:USPC</setSpec> <setSpec>collection:UR1-SDLM</setSpec> <setSpec>collection:UR1-SDLMJONCH</setSpec> <setSpec>collection:UR1-SDV</setSpec> <setSpec>collection:IRSET-2</setSpec> <setSpec>collection:UNIV-ANGERS</setSpec> </header> <metadata><dc> <publisher>HAL CCSD</publisher> <title lang=en>Leishmania cell wall as a potent target for antiparasitic drugs. A focus on the glycoconjugates</title> <creator>Cabezas, Yari</creator> <creator>Legentil, Laurent</creator> <creator>Robert-Gangneux, Florence</creator> <creator>Daligault, Franck</creator> <creator>Belaz, Sorya</creator> <creator>Nugier-Chauvin, Caroline</creator> <creator>Tranchimand, Sylvain</creator> <creator>Tellier, Charles</creator> <creator>Gangneux, Jean-Pierre</creator> <creator>Ferrières, Vincent</creator> <contributor>Institut des Sciences Chimiques de Rennes (ISCR) ; Université de Rennes 1 (UR1) - Ecole Nationale Supérieure de Chimie de Rennes - Institut National des Sciences Appliquées (INSA) - Centre National de la Recherche Scientifique (CNRS)</contributor> <contributor>Service de Parasitologie-Mycologie [Rennes] ; Université de Rennes 1 (UR1) - Hôpital Pontchaillou - CHU Pontchaillou [Rennes]</contributor> <contributor>Institut de recherche, santé, environnement et travail [Rennes] (Irset) ; Université d'Angers (UA) - Université des Antilles et de la Guyane (UAG) - Université de Rennes 1 (UR1) - École des Hautes Études en Santé Publique [EHESP] (EHESP) - Institut National de la Santé et de la Recherche Médicale (INSERM) - Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique )</contributor> <contributor>Fonctionnalité et Ingénierie des Protéines (UFIP) ; Université de Nantes (UN) - Centre National de la Recherche Scientifique (CNRS)</contributor> <contributor>Université européenne de Bretagne (UEB)</contributor> <description>International audience</description> <source>ISSN: 1477-0520</source> <source>EISSN: 1477-0539</source> <source>Organic and Biomolecular Chemistry</source> <publisher>Royal Society of Chemistry</publisher> <identifier>hal-01174899</identifier> <identifier>https://hal-univ-rennes1.archives-ouvertes.fr/hal-01174899</identifier> <source>https://hal-univ-rennes1.archives-ouvertes.fr/hal-01174899</source> <source>Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2015, 13 (31), pp.8393-8404 〈10.1039/c5ob00563a〉</source> <identifier>DOI : 10.1039/c5ob00563a</identifier> <relation>info:eu-repo/semantics/altIdentifier/doi/10.1039/c5ob00563a</relation> <identifier>PUBMED : 26130402</identifier> <relation>info:eu-repo/semantics/altIdentifier/pmid/26130402</relation> <language>en</language> <subject>[CHIM] Chemical Sciences</subject> <type>info:eu-repo/semantics/article</type> <type>Journal articles</type> <description lang=en>Although leishmaniasis has been studied for over a century, the fight against cutaneous, mucocutaneous and visceral forms of the disease remains a hot topic. This review refers to the parasitic cell wall and more particularly to the constitutive glycoconjugates. The structures of the main glycolipids and glycoproteins, which are species-dependent, are described. The focus is on the disturbance of the lipid membrane by existing drugs and possible new ones, in order to develop future therapeutic agents</description> <date>2015</date> </dc> </metadata> </record> </GetRecord> </OAI-PMH>