Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
1999-3-11
pubmed:abstractText
A double-blind, placebo-controlled phase III study was performed to assess whether basiliximab, a chimeric anti-interleukin-2 receptor monoclonal antibody, reduced the incidence of acute rejection episodes in renal allograft recipients.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0041-1337
pubmed:author
pubmed:issnType
Print
pubmed:day
27
pubmed:volume
67
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
276-84
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:10075594-Acute Disease, pubmed-meshheading:10075594-Adult, pubmed-meshheading:10075594-Antibodies, Monoclonal, pubmed-meshheading:10075594-Cause of Death, pubmed-meshheading:10075594-Creatinine, pubmed-meshheading:10075594-Double-Blind Method, pubmed-meshheading:10075594-Female, pubmed-meshheading:10075594-Follow-Up Studies, pubmed-meshheading:10075594-Graft Rejection, pubmed-meshheading:10075594-Humans, pubmed-meshheading:10075594-Immunosuppressive Agents, pubmed-meshheading:10075594-Incidence, pubmed-meshheading:10075594-Kidney Transplantation, pubmed-meshheading:10075594-Male, pubmed-meshheading:10075594-Middle Aged, pubmed-meshheading:10075594-Postoperative Complications, pubmed-meshheading:10075594-Receptors, Interleukin-2, pubmed-meshheading:10075594-Recombinant Fusion Proteins, pubmed-meshheading:10075594-Time Factors
pubmed:year
1999
pubmed:articleTitle
Reduction of the occurrence of acute cellular rejection among renal allograft recipients treated with basiliximab, a chimeric anti-interleukin-2-receptor monoclonal antibody. United States Simulect Renal Study Group.
pubmed:affiliation
Division of Immunology and Organ Transplantation, University of Texas Medical School, Houston 77030, USA.
pubmed:publicationType
Journal Article, Clinical Trial, Randomized Controlled Trial, Research Support, Non-U.S. Gov't, Multicenter Study, Clinical Trial, Phase III