Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4-5
pubmed:dateCreated
2007-8-2
pubmed:abstractText
The predominant mode of HIV-1 transmission is by heterosexual contact. The cervical/vaginal mucosa is the main port of HIV entry in women. A safe and effective topical microbicide against HIV is urgently needed to prevent sexual transmission. Hence, we evaluated griffithsin (GRFT), a 12.7 kDa carbohydrate-binding protein, both native and recombinant GRFT, potently inhibited both CXCR4-and CCR5-tropic HIV infection and transmission in vitro.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
0047-2565
pubmed:author
pubmed:issnType
Print
pubmed:volume
36
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
244-53
pubmed:dateRevised
2007-12-3
pubmed:meshHeading
pubmed-meshheading:17669213-Algal Proteins, pubmed-meshheading:17669213-Animals, pubmed-meshheading:17669213-Anti-HIV Agents, pubmed-meshheading:17669213-Cell Line, pubmed-meshheading:17669213-Cell Survival, pubmed-meshheading:17669213-Disease Models, Animal, pubmed-meshheading:17669213-Female, pubmed-meshheading:17669213-HIV Infections, pubmed-meshheading:17669213-Humans, pubmed-meshheading:17669213-Hydrogen-Ion Concentration, pubmed-meshheading:17669213-Kinetics, pubmed-meshheading:17669213-Lectins, pubmed-meshheading:17669213-Macaca nemestrina, pubmed-meshheading:17669213-Receptors, CCR5, pubmed-meshheading:17669213-Receptors, CXCR4, pubmed-meshheading:17669213-Simian Acquired Immunodeficiency Syndrome, pubmed-meshheading:17669213-Simian immunodeficiency virus, pubmed-meshheading:17669213-Vaginal Douching
pubmed:year
2007
pubmed:articleTitle
Griffithsin, a potent HIV entry inhibitor, is an excellent candidate for anti-HIV microbicide.
pubmed:affiliation
Washington National Primate Research Center, University of Washington, Seattle, WA 98195, USA.
pubmed:publicationType
Journal Article, Research Support, N.I.H., Extramural, Research Support, N.I.H., Intramural