Association of maternal KIR and fetal HLA-C genes with the risk of preeclampsia in the Chinese Han population.

doi:10.1016/j.placenta.2014.05.008

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Back to search

Article

Association of maternal KIR and fetal HLA-C genes with the risk of preeclampsia in the Chinese Han population.

Placenta - 1 Apr 2015

Long W, Shi Z, Fan S, Liu L, Lu Y, Guo X, Rong C, Cui X, Ding H

Abstract excerpt

INTRODUCTION: This study is to investigate the distribution of inhibitory and activating killer-cell immunoglobulin-like receptors (KIRs) and the combination of KIR/human leukocyte antigen (HLA)-C in women with preeclampsia in the Chinese Han population. METHODS: A total of 271 patients and 295 controls were enrolled in our study. The inhibitory/activating KIR and HLA-C genes were detected using the PCR-SSP...

Topics

Adult
Alleles
Asian People
China
Cohort Studies
Female
Fetal Blood
Gene Frequency
Genetic Association Studies
Genetic Predisposition to Disease
HLA-C Antigens

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Histocompatibility, Maternal-Fetal

Homozygote

Humans

Pre-Eclampsia

Pregnancy

Receptors, KIR

Receptors, KIR2DL1

Source

Open in PubMed

Identifiers

PMID: 24951171
DOI: 10.1016/j.placenta.2014.05.008

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

discussions

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Association of maternal KIR and fetal HLA-C genes with the risk of preeclampsia in the Chinese Han population.PMID 24951171Read ↗

Interaction of parental KIR and fetal HLA-C genotypes with the risk of preeclampsia.Semantic proximity Read ↗

Significance of inhibitory maternal killer-cell immunoglobulin-like receptor (KIR) and fetal KIR ligand genotype combinations in placenta related obstetric complications.Semantic proximity Read ↗

Combined maternal KIR2DL4 and fetal HLA-G polymorphisms were associated with preeclampsia in a Han Chinese populationSemantic proximity Read ↗

Polymorphism in killer cell immunoglobulin-like receptors and human leukocyte antigen-c and predisposition to preeclampsia in Ethiopian pregnant women population.Semantic proximity Read ↗

The Roles of Uterine Natural Killer (NK) Cells and KIR/HLA-C Combination in the Development of Preeclampsia: A Systematic Review.Semantic proximity Read ↗

Combinations of maternal KIR and fetal HLA-C genes influence the risk of preeclampsia and reproductive success.Semantic proximity Read ↗

KIR2DL4 expression rather than its single nucleotide polymorphisms correlates with pre-eclampsia.Semantic proximity Read ↗

[Correlation between killer cell immunoglobulin-like receptors genes and pre-eclampsia].Semantic proximity Read ↗

Maternal activating KIRs protect against human reproductive failure mediated by fetal HLA-C2.Semantic proximity Read ↗

Association between HLA-A gene polymorphism and early-onset preeclampsia in Chinese pregnant women early-onset.Semantic proximity Read ↗

Recurrent Pregnancy Loss in Women with Killer Cell Immunoglobulin-Like Receptor KIR2DS1 is Associated with an Increased HLA-C2 Allelic Frequency.Semantic proximity Read ↗

Possible gene-gene interaction of KIR2DL4 with its cognate ligand HLA-G in modulating risk for preeclampsia.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.