Association between the candidate susceptibility gene ACVR2A on chromosome 2q22 and pre-eclampsia in a large Norwegian population-based study (the HUNT study).
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Nodal signals through activin receptor-like kinase 7 to inhibit trophoblast migration and invasion: implication in the pathogenesis of preeclampsiaSTOX2 but not STOX1 is differentially expressed in decidua from pre-eclamptic women: data from the Second Nord-Trondelag Health StudyNetwork of microRNAs-mRNAs interactions in pancreatic cancer.Genetic and molecular functional characterization of variants within TNFSF13B, a positional candidate preeclampsia susceptibility gene on 13qGenetic aspects of preeclampsia and the HELLP syndrome.Polymorphisms of the endothelial nitric oxide synthase (NOS3) gene in preeclampsia: a candidate-gene association studyAssociation of the rs1424954 polymorphism of the ACVR2A gene with the risk of pre-eclampsia is not replicated in a Finnish study population.Genome-wide association scan identifies a risk locus for preeclampsia on 2q14, near the inhibin, beta B gene.Uncoupled embryonic and extra-embryonic tissues compromise blastocyst development after somatic cell nuclear transfer.STOX1: Key player in trophoblast dysfunction underlying early onset preeclampsia with growth retardation.Two variants of the C-reactive protein gene are associated with risk of pre-eclampsia in an American Indian population.The ERAP2 gene is associated with preeclampsia in Australian and Norwegian populations.The genetics of pre-eclampsia and other hypertensive disorders of pregnancyGene expression profiling of placentae from women with early- and late-onset pre-eclampsia: down-regulation of the angiogenesis-related genes ACVRL1 and EGFL7 in early-onset diseaseInterPregGen: genetic studies of pre-eclampsia in three continents.The role of genetics in pre-eclampsia and potential pharmacogenomic interventions.Genetic dissection of the pre-eclampsia susceptibility locus on chromosome 2q22 reveals shared novel risk factors for cardiovascular disease.Genetic association of the activin A receptor gene (ACVR2A) and pre-eclampsiaIntegrative transcriptome analysis reveals dysregulation of canonical cancer molecular pathways in placenta leading to preeclampsia(Epi)genetics of pregnancy-associated diseasesActivins in reproductive biology and beyond.The TGF-β Family in the Reproductive Tract.Protective Low-Frequency Variants for Preeclampsia in the Fms Related Tyrosine Kinase 1 Gene in the Finnish Population.Genetic Approaches in Preeclampsia.Genetic predisposition to preeclampsia is conferred by fetal DNA variants near FLT1, a gene involved in the regulation of angiogenesis.The STOX1 genotype associated with pre-eclampsia leads to a reduction of trophoblast invasion by alpha-T-catenin upregulation.
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Association between the candidate susceptibility gene ACVR2A on chromosome 2q22 and pre-eclampsia in a large Norwegian population-based study (the HUNT study).
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 10 September 2008
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Association between the candid ...... -based study (the HUNT study).
@en
Association between the candid ...... rwegian population-based study
@nl
type
label
Association between the candid ...... -based study (the HUNT study).
@en
Association between the candid ...... rwegian population-based study
@nl
prefLabel
Association between the candid ...... -based study (the HUNT study).
@en
Association between the candid ...... rwegian population-based study
@nl
P2093
P2860
P50
P356
P1476
Association between the candid ...... -based study (the HUNT study).
@en
P2093
Elizabeth Fitzpatrick
Linda T Roten
Matthew P Johnson
Thomas D Dyer
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P2888
P304
P356
10.1038/EJHG.2008.158
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2008-09-10T00:00:00Z