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Links from GEO DataSets

Items: 20

1.

Transcriptomic Profiling of Trophoblast Subpopulations in Severe Preeclampsia Reveals Novel Aspects of RNA Dysregulation

(Submitter supplied) The maternal signs of preeclampsia, principally the new onset of high blood pressure, are thought to occur secondary to faulty placentation. Previous studies profiled the gene expression patterns of chorionic villi, the maternal-fetal interface or isolated cytotrophoblasts in this pregnancy complication. We theorized that transcriptomic analyses of trophoblast subpopulations in situ would give us new insights into the role of these cells in preeclampsia pathogenesis.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL16686
23 Samples
Download data: CEL, TXT
Series
Accession:
GSE93839
ID:
200093839
2.

Placenta-specific genes and their regulation during villous trophoblast differentiation.

(Submitter supplied) Analysis of genome-wide gene expression during the differentiation of villous trophoblasts isolated from healthy term placentas.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
24 Samples
Download data: TXT
Series
Accession:
GSE130339
ID:
200130339
3.

Placental gene expression profiling for the identification of subtypes of human fetal growth restriction

(Submitter supplied) Fetal growth restriction (FGR) is a heterogeneous disorder of pregnancy associated with pathologically low fetal and neonatal weights. We hypothesized that FGR consists of multiple placental subtypes, similar to what we have observed in preeclampsia. To address this hypothesis, we assembled a fetal growth-focused human placental microarray data set (N=97) consisting of 20 new normotensive suspected FGR samples (below), in addition to term controls (N=26) and hypertensive suspected FGR samples (N=51) from GSE75010.
Organism:
Homo sapiens
Type:
Expression profiling by array; Third-party reanalysis
Platform:
GPL6244
20 Samples
Download data: CEL, TXT
Series
Accession:
GSE100415
ID:
200100415
4.

Placental gene expression profiling for the identification of clinically relevant subclasses of human preeclampsia

(Submitter supplied) Preeclampsia (PE) is a complex, heterogeneous disorder of pregnancy, demonstrating considerable variability in observed maternal symptoms and fetal outcomes. We hypothesized that this heterogeneity is due to the existence of multiple molecular forms of PE. To address our hypothesis, we created a large (N=330) human placental microarray data set consisting of seven previously published studies (GSE30186, GSE10588, GSE24129, GSE25906, GSE43942, GSE4707, and GSE44711) and 157 highly annotated samples from a BioBank (below). more...
Organism:
Homo sapiens
Type:
Expression profiling by array; Third-party reanalysis
Platform:
GPL6244
157 Samples
Download data: CEL, CSV
Series
Accession:
GSE75010
ID:
200075010
5.

Histopathologic and transcriptome profiling identify novel trophoblast lineage-specific defects in preeclampsia

(Submitter supplied) Preeclampsia (PE) is a heterogeneous disease which lacks pathophysiology-based subclassification. Current clinical classification is based on gestational age at diagnosis and severity of disease. However, PE placentas have heterogeneous findings on pathologic exam. We combined clinical, pathological, immunohistochemical (IHC), and transcriptomic profiling to better subclassify this disease. 303 PE and 1388 non-hypertensive controls were included, with subgroups of samples used for each analysis. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
44 Samples
Download data: TXT
6.

Regulatory small RNA profiling of first-trimester maternal plasma-derived exosome content in preeclampsia aggravated with intrauterine growth restriction

(Submitter supplied) Preeclampsia (PE) is a pregnancy related multisystemic syndrome, which shows symptomes after the 20th week of the pregnancy. It affects 5-8% of all pregnancies, caused by placental disfunction and commonly combined with fetal intrauterine growth restriction (IUGR). Exosomes mediate cell-to-cell communication with their cargo, such as different types of RNA molecules. The exosomal RNA cargo is unique, gives information about the molecular condition of the donor cells and promotes altered gene expression in the acceptor cells. more...
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL30173
10 Samples
Download data: CSV
Series
Accession:
GSE241815
ID:
200241815
7.

RNA profiling of laser microdissected human trophoblast subtypes at mid-gestation

(Submitter supplied) Human placental architecture is complex. Its surface epithelium, specialized for transport, forms by fusion of cytotrophoblast progenitors into multinucleated syncytiotrophoblasts. Near the uterine surface, these progenitors assume a different fate, becoming cancer-like cells that invade its lining and blood vessels. The latter process physically connects the placenta to the mother and shunts uterine blood to the syncytiotrophoblasts. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL16686
12 Samples
Download data: CEL, TXT
Series
Accession:
GSE156766
ID:
200156766
8.

Culturing Cytotrophoblasts Reverses Gene Dysregulation in Preeclampsia Revealing Possible Causes

(Submitter supplied) During human pregnancy, a subset of placental cytotrophoblasts (CTBs) differentiates into cells that aggressively invade the uterus and its vasculature, anchoring the progeny and rerouting maternal blood to the placenta. In preeclampsia (PE), CTB invasion is limited, reducing placental perfusion and/or creating intermittent flow. This syndrome, affecting 4-8% of pregnancies, entails maternal vascular alterations (e.g., high blood pressure, proteinuria, and edema) ± fetal growth restriction. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
39 Samples
Download data: CEL, TXT
Series
Accession:
GSE40182
ID:
200040182
9.

LncRNAs Expression in Preeclampsia Placenta Reveals the Potential Role of LncRNAs Contributing to Preeclampsia Pathogenesis

(Submitter supplied) Background: Long non-coding RNAs (lncRNAs) are an important class of pervasive genes involved in a variety of biological functions. They are aberrantly expressed in many types of diseases. We want to study the lncRNAs profiles in preeclampsia. Preeclampsia has been observed in patients with molar pregnancy where a fetus is absent demonstrating that the placenta is sufficient to cause the condition. So we analyze the lncRNAs profiles in preeclampsia placentas. In this study, we described the lncRNAs profiles in 6 preeclampsia placentas (T) and 5 matched normal pregnancy placentas (N) tissues by microarray. Methodology/Principal Findings: With abundant and varied probes accounting 33,045 LncRNAs in our microarray, the number of lncRNAs that expressed at a certain level could be detected is 28,443. From the data we found there were 738 lncRNAs that differentially expressed (≥1.5 fold-change) among preeclampsia placentas compared with matched controls. Up to 18,063 coding transcripts could be detected in placenta samples through 30,215 coding transcripts probes. Coding-non-coding gene co-expression networks (CNC network) were constructed based on the correlation analysis between the differential expressed lncRNAs and mRNAs. According to the GO-Pathway analysis of differential expressed lncRNAs/mRNAs, we choose three lncRNAs to analyze the relationship between lncRNAs and preeclampsia. LOC391533, LOC284100, CEACAMP8 were evaluated by qPCR in 40 of preeclampsia placentas and 40 of controls. The results showed three lncRNAs were aberrantly expressed in preeclampsia placentas compared with controls. Conclusions/Significance: Our study is the first one to determine genome-wide lncRNAs expression patterns in preeclampsia placenta by microarray. The results displayed that clusters of lncRNAs were aberrantly expressed in preeclampsia placenta compared with controls, which revealed that lncRNAs differentially expressed in preeclampsia placenta may exert a partial or key role in preeclampsia development. Misregulation of LOC391533, LOC284100, CEACAMP8 might be associated with preeclampsia. Taken together, this study may provide potential targets for future treatment of preeclampsia and novel insights into preeclampsia biology.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL15314
11 Samples
Download data: TXT
Series
Accession:
GSE50783
ID:
200050783
10.

Genome-wide analysis of placental gene expression in severe preterm preeclampsia

(Submitter supplied) Analysis of genome-wide gene expression in placentas from women with preterm severe preeclampsia, with or without HELLP syndrome, compared to gestational age-matched controls. The hypothesis tested in the present study was that placental transcriptomic changes in preeclampsia are considerably different from controls. The results provide important information on placental transcriptomic changes in preeclampsia.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL4133
17 Samples
Download data: TXT
Series
Accession:
GSE66273
ID:
200066273
11.

Genome-wide analysis of gene expression in HTR8/SVneo cells treated with ZNF554 siRNA

(Submitter supplied) Analysis of the effect of ZNF554 knock-down on genome-wide gene expression in trophoblastic cells. The hypothesis tested in the present study was that ZNF554 regulates the expression of genes involved in trophoblastic cell migration and invasion. The results provide important information on the functions of ZNF554 in trophoblastic cells.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL10558
6 Samples
Download data: TXT
Series
Accession:
GSE65940
ID:
200065940
12.

Genome-wide analysis of gene expression in BeWo cells treated with ZNF554 siRNA

(Submitter supplied) Analysis of the effect of ZNF554 knock-down on genome-wide gene expression in BeWo trophoblast-like cells. The hypothesis tested in the present study was that ZNF554 regulates the expression of genes involved in key functions of trophoblastic cells. The results provide important information on the functions of ZNF554 in BeWo trophoblast-like cells.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
6 Samples
Download data: TXT
Series
Accession:
GSE65866
ID:
200065866
13.

Competing endogenous RNA expression dataset from placenta tissues of normal human and patients with severe preeclampsia.

(Submitter supplied) We used microarray to detail Competing endogenous RNA expreession in placenta tissues from normal human and patients with severe preeclampsia
Organism:
Homo sapiens
Type:
Expression profiling by array; Non-coding RNA profiling by array
Platform:
GPL22120
6 Samples
Download data: TXT
Series
Accession:
GSE102897
ID:
200102897
14.

Chorionic villus sampling (CVS) microarray in preeclampsia

(Submitter supplied) 4 chorionic villus sampling specimens in pregnancies destined for preeclampsia and 8 matched controls were analyzed 36 genes were differentially expressed using J5 score and prediction modeling in caGEDA computer program Keywords: snap frozen, banked CVS specimens with known pregnancy outcomes revealed genes differentially expressed in preeclampsia pregnancies
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS3467
Platform:
GPL570
12 Samples
Download data: CEL
Series
Accession:
GSE12767
ID:
200012767
15.
Full record GDS3467

Preeclampsia: first trimester placentas of pre-symptomatic women

Analysis of first trimester placenta tissues obtained by chorionic villus sampling from women destined to develop preeclampsia. Preeclampsia is a cause of maternal, fetal, and neonatal morbidity and mortality. Results provide insight into the molecular pathogenesis of preeclampsia.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 disease state sets
Platform:
GPL570
Series:
GSE12767
12 Samples
Download data: CEL
16.

Epigenome analysis of normal and preeclamptic placenta samples

(Submitter supplied) Preeclampsia (PE), a hypertensive disorder of pregnancy, is hypothesized to be associated with, if not mechanistically related to abnormal placental function. However, the exact mechanisms regulating the pathogenesis of PE remain unclear. While many studies have investigated changes in gene expression in the PE placenta, the role of epigenetics in PE associated placental dysfunction remains unclear. more...
Organism:
Homo sapiens
Type:
Methylation profiling by array
Platform:
GPL13534
45 Samples
Download data: TXT
Series
Accession:
GSE57767
ID:
200057767
17.

Isolation and Characterisation of a Novel Trophoblast Hoescht Side-Population with Stem Cell Properties from First Trimester Placentae

(Submitter supplied) In this work, we have isolated a Hoescht side-population of trophoblasts from first trimester human placentae that cluster separately from more differentiated trophoblast populations, and have a transcriptomic profile indicative of a stem cell population.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL15207
15 Samples
Download data: CEL
Series
Accession:
GSE57834
ID:
200057834
18.

Severe Preeclampsia-Related Changes in Gene Expression at the Maternal-Fetal Interface Include Siglec-6 and Pappalysin-2

(Submitter supplied) Preeclampsia (PE), which affects 4-8% of human pregnancies, causes significant maternal and neonatal morbidity and mortality. Within the basal plate, placental cytotrophoblasts (CTBs) of fetal origin invade the uterus and extensively remodel the maternal vasculature. In PE, CTB invasion is often shallow, and vascular remodeling is rudimentary. To better understand possible causes, we conducted a global analysis of gene expression at the maternal-fetal interface in placental samples from women with PE (n = 12; 24-36 wk) vs. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL97 GPL96
46 Samples
Download data: CEL
Series
Accession:
GSE14722
ID:
200014722
19.

Small non-coding RNA contents in preeclamptic and normotensive trophobalst debris

(Submitter supplied) Small RNA sequencing on trophoblast debris samples was employed to profile the small RNA contents in either normotensive or preeclamptic trophoblast debris. We have identified 1278 miRNAs and 2646 non-miRNA small RNA fragments across all trophoblast debris samples. Differential expression analysis was executed by iSRAP small RNA sequencing analysis pipeline and we identified 16 miRNAs, 5 tRNA fragments from 3 different tRNAs, 13 snRNA fragments and 85 rRNA fragments differentially contained between preeclamptic and normotensive trophoblast debris
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL11154
8 Samples
Download data: CSV
Series
Accession:
GSE85926
ID:
200085926
20.

Transcriptional analysis of bone morphogenetic protein 2 signaling in human placental trophoblast development and function

(Submitter supplied) Previous studies have demonstrated the pro-invasive action of BMP2 signaling in human trophoblast cells in vitro. In this study, we investigated downstream transcriptional targets of BMP2 signaling using mRNA-sequencing on control and BMP2-treated primary human trophoblast cells (n=5). Gene ontology annotations revealed that differentially expressed genes were involved in multiple organ development and cellular functions. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
10 Samples
Download data: FPKM_TRACKING
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