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Conference Paper: Glycodelin-A modulates the functions of human macrophages: possible involvement in the maternal-fetal tolerogenic environment

TitleGlycodelin-A modulates the functions of human macrophages: possible involvement in the maternal-fetal tolerogenic environment
Authors
KeywordsMedical sciences
Allergology and immunology medical sciences
Obstetrics and gynecology
Issue Date2013
PublisherBlackwell Munksgaard. The Journal's web site is located at http://www.munksgaard.dk/ajri
Citation
The 12th Congress of the International Society for Immunology Reproduction (ISIR 2013), Boston Park Plaza Hotel, Boston, MA., 28 May-1 June 2013. In American Journal of Reproductive Immunology, 2013, v. 69 suppl. s2, p. 169, abstract P-198 How to Cite?
AbstractBACKGROUND: Glycodelin-A (GdA) is a glycoprotein abundant in the human secretory endometrium, decidua and amniotic fluid. Its concentration in the deciduas rises in early pregnancy, and peaks between 6 and 12th week of gestation. The most well studied role of GdA is its function as a regulator of immune cell function at the fetaomaternal interface. The glycosylation of GdA mediates its binding and therefore the biological functions. Macrophages represent the second major type of decidual leukocytes at the fetomaternal interface. Changes in macrophage number and activity are associated with fetal loss and …
DescriptionCongress Theme: Building Bridges in Reproductive Immunology
This journal suppl. entitled: Special Issue: Abstracts of the 14th International Symposium for Immunology of Reproduction, Boston Park Plaza Hotel, Boston, MA., 28 May-1 June 2013.
Persistent Identifierhttp://hdl.handle.net/10722/183948
ISSN

 

DC FieldValueLanguage
dc.contributor.authorChiu, PCNen_US
dc.contributor.authorLam, EYFen_US
dc.contributor.authorLam, KKen_US
dc.contributor.authorKoistinen, Hen_US
dc.contributor.authorSeppala, Men_US
dc.contributor.authorNg, EHYen_US
dc.contributor.authorYeung, WSBen_US
dc.contributor.authorLee, CL-
dc.date.accessioned2013-06-18T04:31:25Z-
dc.date.available2013-06-18T04:31:25Z-
dc.date.issued2013en_US
dc.identifier.citationThe 12th Congress of the International Society for Immunology Reproduction (ISIR 2013), Boston Park Plaza Hotel, Boston, MA., 28 May-1 June 2013. In American Journal of Reproductive Immunology, 2013, v. 69 suppl. s2, p. 169, abstract P-198en_US
dc.identifier.issn1600-0897 (Online)-
dc.identifier.urihttp://hdl.handle.net/10722/183948-
dc.descriptionCongress Theme: Building Bridges in Reproductive Immunology-
dc.descriptionThis journal suppl. entitled: Special Issue: Abstracts of the 14th International Symposium for Immunology of Reproduction, Boston Park Plaza Hotel, Boston, MA., 28 May-1 June 2013.-
dc.description.abstractBACKGROUND: Glycodelin-A (GdA) is a glycoprotein abundant in the human secretory endometrium, decidua and amniotic fluid. Its concentration in the deciduas rises in early pregnancy, and peaks between 6 and 12th week of gestation. The most well studied role of GdA is its function as a regulator of immune cell function at the fetaomaternal interface. The glycosylation of GdA mediates its binding and therefore the biological functions. Macrophages represent the second major type of decidual leukocytes at the fetomaternal interface. Changes in macrophage number and activity are associated with fetal loss and …-
dc.languageengen_US
dc.publisherBlackwell Munksgaard. The Journal's web site is located at http://www.munksgaard.dk/ajrien_US
dc.relation.ispartofAmerican Journal of Reproductive Immunologyen_US
dc.rightsThe definitive version is available at www.blackwell-synergy.com-
dc.subjectMedical sciences-
dc.subjectAllergology and immunology medical sciences-
dc.subjectObstetrics and gynecology-
dc.titleGlycodelin-A modulates the functions of human macrophages: possible involvement in the maternal-fetal tolerogenic environmenten_US
dc.typeConference_Paperen_US
dc.identifier.emailChiu, PCN: pchiucn@hku.hken_US
dc.identifier.emailNg, EHY: nghye@hku.hken_US
dc.identifier.emailYeung, WSB: wsbyeung@hkucc.hku.hken_US
dc.identifier.emailLee, CL: kcllee@hku.hken_US
dc.identifier.authorityChiu, PCN=rp00424en_US
dc.identifier.authorityNg, EHY=rp00426en_US
dc.identifier.authorityYeung, WSB=rp00331en_US
dc.identifier.doi10.1111/aji.12124-
dc.identifier.hkuros214970en_US
dc.identifier.volume69en_US
dc.identifier.issuesuppl. s2-
dc.identifier.spage169en_US
dc.identifier.epage169en_US
dc.publisher.placeDenmark-

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