<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kunstman KJ</submitter><funding>NICHD NIH HHS</funding><funding>NIAID NIH HHS</funding><pagination>12310-8</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC254294</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>77(22)</volume><pubmed_abstract>A chemokine receptor from the seven-transmembrane-domain G-protein-coupled receptor superfamily is an essential coreceptor for the cellular entry of human immunodeficiency virus type 1 (HIV-1) and simian immunodeficiency virus (SIV) strains. To investigate nonhuman primate CC-chemokine receptor 5 (CCR5) homologue structure and function, we amplified CCR5 DNA sequences from peripheral blood cells obtained from 24 representative species and subspecies of the primate suborders Prosimii (family Lemuridae) and Anthropoidea (families Cebidae, Callitrichidae, Cercopithecidae, Hylobatidae, and Pongidae) by PCR with primers flanking the coding region of the gene. Full-length CCR5 was inserted into pCDNA3.1, and multiple clones were sequenced to permit discrimination of both alleles. Compared to the</pubmed_abstract><journal>Journal of virology</journal><pubmed_title>Structure and function of CC-chemokine receptor 5 homologues derived from representative primate species and subspecies of the taxonomic suborders Prosimii and Anthropoidea.</pubmed_title><pmcid>PMC254294</pmcid><funding_grant_id>AI40880</funding_grant_id><funding_grant_id>HD37356</funding_grant_id><funding_grant_id>AI41420</funding_grant_id><funding_grant_id>R01 HD037356</funding_grant_id><funding_grant_id>R01 AI040880</funding_grant_id><funding_grant_id>R01 AI041420</funding_grant_id><pubmed_authors>Korber BT</pubmed_authors><pubmed_authors>Pillai S</pubmed_authors><pubmed_authors>Wolinsky SM</pubmed_authors><pubmed_authors>Agy M</pubmed_authors><pubmed_authors>Puffer B</pubmed_authors><pubmed_authors>Kunstman J</pubmed_authors><pubmed_authors>Kuiken C</pubmed_authors><pubmed_authors>Yoder AD</pubmed_authors><pubmed_authors>Stanton J</pubmed_authors><pubmed_authors>Smith UR</pubmed_authors><pubmed_authors>Shibata R</pubmed_authors><pubmed_authors>Doms RW</pubmed_authors><pubmed_authors>Kunstman KJ</pubmed_authors><pubmed_authors>Marx P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Structure and function of CC-chemokine receptor 5 homologues derived from representative primate species and subspecies of the taxonomic suborders Prosimii and Anthropoidea.</name><description>A chemokine receptor from the seven-transmembrane-domain G-protein-coupled receptor superfamily is an essential coreceptor for the cellular entry of human immunodeficiency virus type 1 (HIV-1) and simian immunodeficiency virus (SIV) strains. To investigate nonhuman primate CC-chemokine receptor 5 (CCR5) homologue structure and function, we amplified CCR5 DNA sequences from peripheral blood cells obtained from 24 representative species and subspecies of the primate suborders Prosimii (family Lemuridae) and Anthropoidea (families Cebidae, Callitrichidae, Cercopithecidae, Hylobatidae, and Pongidae) by PCR with primers flanking the coding region of the gene. Full-length CCR5 was inserted into pCDNA3.1, and multiple clones were sequenced to permit discrimination of both alleles. Compared to the</description><dates><release>2003-01-01T00:00:00Z</release><publication>2003 Nov</publication><modification>2025-04-04T09:50:45.773Z</modification><creation>2019-03-27T00:35:56Z</creation></dates><accession>S-EPMC254294</accession><cross_references><pubmed>14581567</pubmed><doi>10.1128/jvi.77.22.12310-12318.2003</doi></cross_references></HashMap>