Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
12
pubmed:dateCreated
2009-11-26
pubmed:databankReference
pubmed:abstractText
In patients with long-standing type 1 diabetes, we investigated whether improved beta-cell function can be achieved by combining intensive insulin therapy with agents that may 1) promote beta-cell growth and/or limit beta-cell apoptosis and 2) weaken the anti-beta-cell autoimmunity.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Monoclonal, http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Monoclonal, Humanized, http://linkedlifedata.com/resource/pubmed/chemical/HLA-DR Antigens, http://linkedlifedata.com/resource/pubmed/chemical/HLA-DRB1 Chains, http://linkedlifedata.com/resource/pubmed/chemical/Hemoglobin A, Glycosylated, http://linkedlifedata.com/resource/pubmed/chemical/Hypoglycemic Agents, http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin G, http://linkedlifedata.com/resource/pubmed/chemical/Immunosuppressive Agents, http://linkedlifedata.com/resource/pubmed/chemical/Insulin, http://linkedlifedata.com/resource/pubmed/chemical/Peptides, http://linkedlifedata.com/resource/pubmed/chemical/Venoms, http://linkedlifedata.com/resource/pubmed/chemical/daclizumab, http://linkedlifedata.com/resource/pubmed/chemical/exenatide
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
1935-5548
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
32
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2251-7
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:19808924-Adult, pubmed-meshheading:19808924-Age of Onset, pubmed-meshheading:19808924-Antibodies, Monoclonal, pubmed-meshheading:19808924-Antibodies, Monoclonal, Humanized, pubmed-meshheading:19808924-Autoimmunity, pubmed-meshheading:19808924-Cross-Over Studies, pubmed-meshheading:19808924-Diabetes Mellitus, Type 1, pubmed-meshheading:19808924-Drug Therapy, Combination, pubmed-meshheading:19808924-Female, pubmed-meshheading:19808924-HLA-DR Antigens, pubmed-meshheading:19808924-HLA-DRB1 Chains, pubmed-meshheading:19808924-Hemoglobin A, Glycosylated, pubmed-meshheading:19808924-Humans, pubmed-meshheading:19808924-Hypoglycemic Agents, pubmed-meshheading:19808924-Immunoglobulin G, pubmed-meshheading:19808924-Immunosuppressive Agents, pubmed-meshheading:19808924-Insulin, pubmed-meshheading:19808924-Insulin-Secreting Cells, pubmed-meshheading:19808924-Male, pubmed-meshheading:19808924-Peptides, pubmed-meshheading:19808924-Questionnaires, pubmed-meshheading:19808924-Research Design, pubmed-meshheading:19808924-United States, pubmed-meshheading:19808924-Venoms, pubmed-meshheading:19808924-Young Adult
pubmed:year
2009
pubmed:articleTitle
Effects of exenatide alone and in combination with daclizumab on beta-cell function in long-standing type 1 diabetes.
pubmed:affiliation
National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland, USA. kristina.rother@nih.gov
pubmed:publicationType
Journal Article, Randomized Controlled Trial, Research Support, N.I.H., Intramural