rdf:type |
|
lifeskim:mentions |
umls-concept:C0015272,
umls-concept:C0017262,
umls-concept:C0019704,
umls-concept:C0039194,
umls-concept:C0524914,
umls-concept:C0542341,
umls-concept:C1171362,
umls-concept:C1332653,
umls-concept:C1332824,
umls-concept:C1515670,
umls-concept:C1705154,
umls-concept:C1879547
|
pubmed:issue |
9
|
pubmed:dateCreated |
1998-2-3
|
pubmed:abstractText |
Chemokines bind to specific receptors and mediate leukocyte migration to sites of inflammation. Recently, some chemokine receptors, notably CXCR4 and CCR5, have been shown to be essential fusion factors on target cells for infection by human immunodeficiency virus (HIV); the chemokines bound by these receptors have also been shown to act as potent inhibitors of HIV infection. Here, we describe the isolation of a novel, putative chemokine receptor.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/CCR1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/DNA, Complementary,
http://linkedlifedata.com/resource/pubmed/chemical/Ligands,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, CCR1,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Chemokine,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, HIV,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Interleukin,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Interleukin-8B
|
pubmed:status |
MEDLINE
|
pubmed:month |
Sep
|
pubmed:issn |
0960-9822
|
pubmed:author |
pubmed-author:AmareMM,
pubmed-author:Arenzana-SeisdedosFF,
pubmed-author:BaggioliniMM,
pubmed-author:BrassNN,
pubmed-author:D'ApuzzoMM,
pubmed-author:LeglerDD,
pubmed-author:LoetscherMM,
pubmed-author:LoetscherPP,
pubmed-author:MeeseEE,
pubmed-author:MosesCC,
pubmed-author:OberlinEE,
pubmed-author:RoussetDD,
pubmed-author:VirelizierJ LJL
|
pubmed:issnType |
Print
|
pubmed:day |
1
|
pubmed:volume |
7
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
652-60
|
pubmed:dateRevised |
2007-11-15
|
pubmed:meshHeading |
pubmed-meshheading:9285716-Amino Acid Sequence,
pubmed-meshheading:9285716-Chromosome Mapping,
pubmed-meshheading:9285716-Cloning, Molecular,
pubmed-meshheading:9285716-DNA, Complementary,
pubmed-meshheading:9285716-HIV-1,
pubmed-meshheading:9285716-Humans,
pubmed-meshheading:9285716-Ligands,
pubmed-meshheading:9285716-Lymphocyte Activation,
pubmed-meshheading:9285716-Molecular Sequence Data,
pubmed-meshheading:9285716-Open Reading Frames,
pubmed-meshheading:9285716-Polymerase Chain Reaction,
pubmed-meshheading:9285716-Receptors, CCR1,
pubmed-meshheading:9285716-Receptors, Chemokine,
pubmed-meshheading:9285716-Receptors, HIV,
pubmed-meshheading:9285716-Receptors, Interleukin,
pubmed-meshheading:9285716-Receptors, Interleukin-8B,
pubmed-meshheading:9285716-Sequence Alignment,
pubmed-meshheading:9285716-T-Lymphocytes
|
pubmed:year |
1997
|
pubmed:articleTitle |
TYMSTR, a putative chemokine receptor selectively expressed in activated T cells, exhibits HIV-1 coreceptor function.
|
pubmed:affiliation |
Theodor-Kocher Institute University of Bern P.O. Box 99, CH-3000 Bern 9, Switzerland.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|