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Links from GEO DataSets

Items: 17

1.

The single cell transcriptional landscape of female primordial germ cell differentiation

(Submitter supplied) Female primordial germ cell differentiation undergoes sex determination and meiosis initiation asynchronously. Here we investigate the transcriptional profiles of 20519 single cells collected from E12.5, E14.5 and E16.5 mouse fetal ovaries. Clustering analysis identifies ten clusters and defines dozens of corresponding marker genes and provides a global view of cellular differentiation from undifferentiated primordial germ cells towards meiotic oocytes. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
3 Samples
Download data: TXT
Series
Accession:
GSE130212
ID:
200130212
2.

Single-cell RNA-seq of the developing C57BL/6 mouse ovary from E11.5 to E14.5

(Submitter supplied) We profiled a time-course single-cell RNA-seq on C57BL/6 mouse ovary from E11.5 to E14.5 to study the cell population heterogeneity and regulation of meiosis initiation. We collected single cell from XX gonads at E11.5, E12.5, E13.5 and E14.5, and were further captured with 10x Genomics based single-cell system. By using single-cell RNA seq, we recapitulated the progression of meiosis using pseudotime ordering of all germ cells and delineated key molecular network among all germ cell clusters. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
4 Samples
Download data: TXT
Series
Accession:
GSE128553
ID:
200128553
3.

Ex vivo reconstitution of fetal oocyte development in humans and cynomolgus monkeys [sc3seq_mouse]

(Submitter supplied) In vitro oogenesis is key to elucidating the mechanism of human female germ-cell development and its anomalies. Accordingly, pluripotent stem cells have been induced into primordial germ cell-like cells and into oogonia with epigenetic reprogramming, yet further reconstitutions remain a challenge. Here, we demonstrate ex vivo reconstitution of fetal oocyte development in both humans and cynomolgus monkeys (Macaca fascicularis). more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
37 Samples
Download data: TXT
Series
Accession:
GSE195990
ID:
200195990
4.

Ex vivo reconstitution of fetal oocyte development in humans and cynomolgus monkeys [sc3seq_macfas]

(Submitter supplied) In vitro oogenesis is key to elucidating the mechanism of human female germ-cell development and its anomalies. Accordingly, pluripotent stem cells have been induced into primordial germ cell-like cells and into oogonia with epigenetic reprogramming, yet further reconstitutions remain a challenge. Here, we demonstrate ex vivo reconstitution of fetal oocyte development in both humans and cynomolgus monkeys (Macaca fascicularis). more...
Organism:
Macaca fascicularis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL22523
153 Samples
Download data: TXT
Series
Accession:
GSE195989
ID:
200195989
5.

Ex vivo reconstitution of fetal oocyte development in humans and cynomolgus monkeys [sc3seq_human]

(Submitter supplied) In vitro oogenesis is key to elucidating the mechanism of human female germ-cell development and its anomalies. Accordingly, pluripotent stem cells have been induced into primordial germ cell-like cells and into oogonia with epigenetic reprogramming, yet further reconstitutions remain a challenge. Here, we demonstrate ex vivo reconstitution of fetal oocyte development in both humans and cynomolgus monkeys (Macaca fascicularis). more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
120 Samples
Download data: TXT
Series
Accession:
GSE195988
ID:
200195988
6.

Ex vivo reconstitution of fetal oocyte development in humans and cynomolgus monkeys

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; Mus musculus; Macaca fascicularis
Type:
Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing
5 related Platforms
320 Samples
Download data: MTX, TSV, TXT
Series
Accession:
GSE194266
ID:
200194266
7.

Ex vivo reconstitution of fetal oocyte development in humans and cynomolgus monkeys [10x_macfas]

(Submitter supplied) In vitro oogenesis is key to elucidating the mechanism of human female germ-cell development and its anomalies. Accordingly, pluripotent stem cells have been induced into primordial germ cell-like cells and into oogonia with epigenetic reprogramming, yet further reconstitutions remain a challenge. Here, we demonstrate ex vivo reconstitution of fetal oocyte development in both humans and cynomolgus monkeys (Macaca fascicularis). more...
Organism:
Macaca fascicularis
Type:
Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing
Platform:
GPL28212
9 Samples
Download data: MTX, TSV
Series
Accession:
GSE194264
ID:
200194264
8.

Ex vivo reconstitution of fetal oocyte development in humans and cynomolgus monkeys [10x_human]

(Submitter supplied) In vitro oogenesis is key to elucidating the mechanism of human female germ-cell development and its anomalies. Accordingly, pluripotent stem cells have been induced into primordial germ cell-like cells and into oogonia with epigenetic reprogramming, yet further reconstitutions remain a challenge. Here, we demonstrate ex vivo reconstitution of fetal oocyte development in both humans and cynomolgus monkeys (Macaca fascicularis). more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing
Platform:
GPL24676
1 Sample
Download data: MTX, TSV
Series
Accession:
GSE194091
ID:
200194091
9.

Generation of human oogonia from induced pluripotent stem cells in vitro

(Submitter supplied) Human in vitro gametogenesis may transform reproductive medicine. Human pluripotent stem cells (hPSCs) have been induced into primordial germ cell-like cells (hPGCLCs); however, further differentiation to a mature germ cell has not been achieved. Here, we show that hPGCLCs differentiate progressively into oogonia-like cells during a long-term in vitro culture (approximately 4 months) in xenogeneic reconstituted ovaries with mouse embryonic ovarian somatic cells. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
27 Samples
Download data: TXT
Series
Accession:
GSE117101
ID:
200117101
10.

Persistent Requirement and Alteration of the Key Targets of PRDM1 during Primordial Germ Cell Development in Mice

(Submitter supplied) Primordial germ cells (PGCs) are the foundation of totipotency and vital for reproduction and heredity. PGCs in mice arise from the epiblast around Embryonic Day (E) 7.0, migrate through the hindgut endoderm, and colonize and proliferate in the embryonic gonads until around E13.5 prior to their differentiation either into pro-spermatogonia or oogonia. PRDM1, a transcriptional repressor, plays an essential role in PGC specification that includes robustly repressing a somatic mesodermal program. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL15907
16 Samples
Download data: TXT
Series
Accession:
GSE74094
ID:
200074094
11.

Defining the developmental program leading to meiosis in maize

(Submitter supplied) We isolated pre-meiotic and early meiotic cells from 24 maize anthers, covering a week of development from the day after archesporial (AR) cell specification to the early zygotene stage of meiotic prophase I. Starting material was staged by anther length, and anther stages were densely sampled from throughout this period. High quality reads were obtained from 144 cells.
Organism:
Zea mays
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17628
56 Samples
Download data: CSV, TXT
Series
Accession:
GSE121039
ID:
200121039
12.

Rapid protein turnover and dynamic mRNA regulation drive the mitosis-meiosis transition in maize germinal cells

(Submitter supplied) Transcriptional profiling of mitotic archesporial cells, early pollen mother cells and pollen mother cells comparing control tapetal cells, pollen, parenchyma cells and seedling. Goal was explain the mitosis/meiosis transition at the molecular level.
Organism:
Zea mays
Type:
Expression profiling by array
Platform:
GPL20611
20 Samples
Download data: TXT
Series
Accession:
GSE70215
ID:
200070215
13.

Regulatory complexity revealed by integrated cytological and RNA-seq analyses of meiotic substages in mouse spermatocytes

(Submitter supplied) The juvenile onset of spermatogenesis in mice is analyzed by combining cytological and transcriptomic data in a novel computational analysis, resulting in meiotic substage-specific transcriptomes and the discovery of a transcription factor network that regulates the substages of meiosis.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL17021 GPL13112
32 Samples
Download data: TXT, XLSX
Series
Accession:
GSE72833
ID:
200072833
14.

Intercellular bridges coordinate the transition from pluripotency to meiosis in mouse fetal oocytes 

(Submitter supplied) Purpose: Investigate the transcriptomes of Tex14 heterogygous sample (with intercellular bridges intact) compared to Tex14 homozygous mutant (lacking intracellular bridges) to ascertain what effects the loss of cytoplasmic sharing has on mitotic to meiotic mouse ovary Methods: Single cell RNA sequencing libaries were created from embryonic day 13.5 mouse ovaries from Tex14 +/- and Tex14 -/- samples. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL24247 GPL21103
4 Samples
Download data: TXT
Series
Accession:
GSE166121
ID:
200166121
15.

Whole genome bisulfite sequencing of E13.0 and E13.5 Tex14 mutant, heterozygote and wild-type murine female germ cells

(Submitter supplied) Meiosis is critical to generating oocytes however, the mechanisms regulating the switch from mitotic primordial germ cells (PGCs) to meiotic germ cells are poorly understood in females. We showed that the onset of meiosis in the fetal murine ovary propagates via intercellular bridges between developing germ cells by using Tex14 mutant (Tex14-/-) mice. Tex14-/- germ cells, which lack intercellular bridges, initiates meiosis prematurely and they more rapidly extinguish pluripotency-associated transcripts (such as Dppa3) upon entering meiosis. more...
Organism:
Mus musculus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL24247
7 Samples
Download data: BIGWIG
Series
Accession:
GSE165010
ID:
200165010
16.

Single cell RNA sequencing reveals fetal ovary development in Macaca fascicularis

(Submitter supplied) The germ cells are vital for reproduction and heredity. However, the mechanisms for female germ cell development in primates, especially in late embryonic stage, has remained elusive. Here, we performed single-cell RNA sequencing of 12471 cells from fetal ovaries. We identified five cell types (germ cell, granulosa cell, theca cell, endothelial cell, macrophage cell), and explored the interactions between germ cells and niche cells. more...
Organism:
Macaca fascicularis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28212
2 Samples
Download data: TXT
Series
Accession:
GSE149629
ID:
200149629
17.

Single-cell Definition of the full-term Developmental Program of Male Mouse Germline

(Submitter supplied) Germ cells are essential for the genetic information transition to subsequent generations of the species relying on sexual reproduction. Full-term developmental trajectory of germ cells provides a paradigm for understanding mammalian germline and germline niches with pivotal knowledge from tremendous in vivo and in vitro studies on the critical role of master regulators in regulating the initiation and maintenance of germline.To characterise the dynamic process of transcriptional programme underlying male mouse germline development, we generated single-cell RNA sequencing profiles for 28 developmental time-points from dissected early embryos or male gonads that were collected between embryonic day (E) 6.5 and postnatal day (P) 8 at one-day intervals, P10-P14 at two-day intervals and at juvenile stage of P30 and P35 as well as adult (8-10 weeks).
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21273
147 Samples
Download data: CSV
Series
Accession:
GSE148032
ID:
200148032
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