Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

ABSTRACT: Optimizing Embryoid Bodies and Organoids by Chemical Cytoprotection

PROVIDER: PRJNA815659 | ENA |

REPOSITORIES: ENA

ACCESS DATA

Json Xml

Dataset's files

Source:

			Action	DRS
	SRR18312900_1.fastq.gz	Fastqsanger.gz
	SRR18312900_2.fastq.gz	Fastqsanger.gz
	SRR18312901_1.fastq.gz	Fastqsanger.gz
	SRR18312901_2.fastq.gz	Fastqsanger.gz
	SRR18312902_1.fastq.gz	Fastqsanger.gz

Items per page:

1 - 5 of 116

Similar Datasets

Project description:Optimizing Embryoid Bodies and Organoids by Chemical Cytoprotection

| PRJNA816454 | ENA

Optimizing Embryoid Bodies and Organoids by Chemical Cytoprotection [RASL-Seq]

Project description:Optimizing Embryoid Bodies and Organoids by Chemical Cytoprotection [RASL-Seq]

| PRJNA816058 | ENA

Control or KZFP KD hESC-derived organoids RNA-seqs

Project description:Control or KD hESC were differentiated into organoids as decribed in Methods. RNA was extracted from individual organoids at day 20 after commencing the STEMdiff™ Cerebral Organoid Kit protocol. Day 0 was designated as the day of transfer of hESC to a 96-well plate for differentiation into embryoid bodies .

2020-02-18 | GSE145406 | GEO

CGR8 mouse embryonic stem cells time-course experiment 0 days old vs 3 days old , 0days old vs 10 days old

Project description:time-course experiment with embryoid bodies of CGR8 mouse embryonic stem cells ; in the whole time-series RNA from 0 days old embryoid bodies were hybridized against RNA from 3 days and 10 days old embryoid bodies Keywords = embryoid bodies Keywords = mouse Keywords = time-course Keywords = oligonucleotide array Keywords: time-course

2006-04-01 | GSE2469 | GEO

Characterization of miRNomes in two mouse Embryonic Stem Cell lines subjected to differentiation

Project description:We used high throughput miRNA sequencing to investigate differences between two mESC lines (D3 and B8 ESCs). Undifferentiated ESCs, cells differentiating in embryoid bodies (day 7), and also cells from embryoid bodies outgrowth (day 21) were analyzed.

2018-01-18 | GSE102719 | GEO

Mus musculus

Project description:Expression data from Mst knockout embryoid bodies and wild type embryoid bodies

| PRJNA217311 | ENA

Polycomb-dependent H3K27me1 and H3K27me2 regulate active transcription and enhancer fidelity

Project description:These data include the genome wide location of different histone modifications by ChIP sequencing in mouse ES cells, and RNA Seq data generated from wild type and EED KO mouse ES cells and knocked down for unrelated protein and Setd2 protein. ChIP-Seq: Immuno-precipitation of formaldehyde cross-linked chromatin prepared from wild type mouse E14 ES cells, wild type E36 ES cells, EED KO E36 ES cells, wild type Embryoid bodies (Ebs), EED KO Embryoid bodies (Ebs EED KO) using specific antibody against different histone modifications. RNA-Seq: Total RNA extracted from wild type E36 ES cells, EED KO E36 ES cells, wild type E36 Embryoid bodies (Ebs), EED KO Embryoid bodies (Ebs EED KO), E14 Ctrl KD, E14 Setd2 KD.

2013-12-05 | E-GEOD-51006 | biostudies-arrayexpress

Ultrasound-directed emergence of pluripotent-like spheroids from human fibroblasts

Project description:We have developed a gene- and chemical-free method of generating pluripotency from HDF cell, we called pluripotent-like spheroids yielded by ultrasonic stimulus (Physics). Physics were very similar to embryoid bodies (EB) in terms of cluster formation, pluripotency with three germ layer markers, and multi-lineage differentiation potential.

2019-05-30 | GSE82038 | GEO

Human pluripotent stem cell derived hematopoietic cells using expanded potential stem cell media

Project description:We recently developed a novel chemical media formulation, Expanded Potential Stem Cell Medium (EPSCM), that maintains mouse pluripotent stem cells (PSCs) in a unique cellular state that affords extraembryonic differentiation capacity. Here, we have used EPSCM to stably maintain human PSCs and used EPSCM-maintained iPSCs (EC-EPSCM) to study in vitro hematopoietic differentiation by embryoid body (EB) formation. We found that human PSCs maintained in EPSCM can spontaneously form embryoid bodies and efficiently undergo in vitro hematopoiesis using a simple differentiation protocol. EC-EPSCM PSCs generated primitive-wave and definitive-wave hematopoietic cells, which were chracterized by RNA-sequencing analysis.

2022-04-26 | GSE130662 | GEO

Mus musculus

Project description:HOXB4 expression in iRUNX embryoid bodies

| PRJNA403805 | ENA