Linked Life Data

17517099

Source:http://linkedlifedata.com/resource/pubmed/id/17517099

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2007-5-22
pubmed:abstractText
Elevated proliferative response to allergen in cord blood mononuclear cells (CBMCs) is related to subsequent allergy development of the neonate and has been suggested as a screening marker for high allergy risk.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Allergens, http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD, http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD3, http://linkedlifedata.com/resource/pubmed/chemical/CCR4 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/CXCR5 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Endotoxins, http://linkedlifedata.com/resource/pubmed/chemical/IL4 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Integrin alpha Chains, http://linkedlifedata.com/resource/pubmed/chemical/Interferon-gamma, http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-4, http://linkedlifedata.com/resource/pubmed/chemical/Ki-67 Antigen, http://linkedlifedata.com/resource/pubmed/chemical/Lactoglobulins, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, CCR4, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, CXCR5, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Chemokine, http://linkedlifedata.com/resource/pubmed/chemical/alpha E integrins
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0954-7894
pubmed:author
pubmed:issnType
Print
pubmed:volume
37
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
856-64
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:17517099-Adult, pubmed-meshheading:17517099-Allergens, pubmed-meshheading:17517099-Animals, pubmed-meshheading:17517099-Antigens, CD, pubmed-meshheading:17517099-Antigens, CD3, pubmed-meshheading:17517099-Cattle, pubmed-meshheading:17517099-Cell Communication, pubmed-meshheading:17517099-Cell Movement, pubmed-meshheading:17517099-Cell Proliferation, pubmed-meshheading:17517099-Endotoxins, pubmed-meshheading:17517099-Female, pubmed-meshheading:17517099-Fetal Blood, pubmed-meshheading:17517099-Flow Cytometry, pubmed-meshheading:17517099-Gene Expression Regulation, pubmed-meshheading:17517099-Humans, pubmed-meshheading:17517099-Hypersensitivity, pubmed-meshheading:17517099-Infant, Newborn, pubmed-meshheading:17517099-Integrin alpha Chains, pubmed-meshheading:17517099-Interferon-gamma, pubmed-meshheading:17517099-Interleukin-4, pubmed-meshheading:17517099-Ki-67 Antigen, pubmed-meshheading:17517099-Lactoglobulins, pubmed-meshheading:17517099-Male, pubmed-meshheading:17517099-Maternal-Fetal Exchange, pubmed-meshheading:17517099-Pregnancy, pubmed-meshheading:17517099-Receptors, CCR4, pubmed-meshheading:17517099-Receptors, CXCR5, pubmed-meshheading:17517099-Receptors, Chemokine, pubmed-meshheading:17517099-T-Lymphocytes
pubmed:year
2007
pubmed:articleTitle
Maternal allergy influences the proliferation of neonatal T cells expressing CCR4, CXCR5 or CD103.
pubmed:affiliation
Laboratory for Immunohistochemistry and Immunopathology (LIIPAT), Department and Institute of Pathology, University of Oslo, Rikshospitalet-Radiumhospitalet Medical Centre, Oslo, Norway.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't