Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Inhibitory input directs astrocyte morphogenesis through glial GABABR [scRNA-Seq]

ABSTRACT: Inhibitory input directs astrocyte morphogenesis through glial GABABR [scRNA-Seq]

PROVIDER: PRJNA814686 | ENA |

REPOSITORIES: ENA

ACCESS DATA

Json Xml

Dataset's files

Source:

			Action	DRS
	SRR18292607_1.fastq.gz	Fastqsanger.gz
	SRR18292607_2.fastq.gz	Fastqsanger.gz
	SRR18292608_1.fastq.gz	Fastqsanger.gz
	SRR18292608_2.fastq.gz	Fastqsanger.gz
	SRR18292609_1.fastq.gz	Fastqsanger.gz

Items per page:

1 - 5 of 16

Similar Datasets

Inhibitory input directs astrocyte morphogenesis through glial GABABR

Project description:Inhibitory input directs astrocyte morphogenesis through glial GABABR

| PRJNA816188 | ENA

Inhibitory input directs astrocyte morphogenesis through glial GABABR [bulk RNA-Seq]

Project description:Inhibitory input directs astrocyte morphogenesis through glial GABABR [bulk RNA-Seq]

| PRJNA816191 | ENA

Inhibitory input directs astrocyte morphogenesis through glial GABABR

Project description:This SuperSeries is composed of the SubSeries listed below.

2022-03-16 | GSE198633 | GEO

Inhibitory input directs astrocyte morphogenesis through glial GABABR [scRNA-Seq]

Project description:The goal of the study is to profile molecular signature of different cell populations between Gabbr1 control and Gabbr1 cKO animals.

2022-03-16 | GSE198357 | GEO

Inhibitory input directs astrocyte morphogenesis through glial GABABR [bulk RNA-Seq]

Project description:The goal of the study is to profile (1) molecular signature of astrocytes in different developmental stages across different brain regions, (2) differential gene expression between Gabbr1 control and Gabbr1 cKO animals.

2022-03-16 | GSE198632 | GEO

Spatiotemporal expression of regulatory kinases directs the transition from mitosis to cellular morphogenesis in Drosophila

Project description:Embryogenesis depends on a tightly regulated balance between mitosis, differentiation, and morphogenesis. Understanding how the embryo uses a relatively small number of proteins to transition between growth and morphogenesis is a central question of developmental biology, but the mechanisms controlling mitosis and differentiation are considered to be fundamentally distinct. Here we show the mitotic kinase Polo, which regulates all steps of mitosis in Drosophila, also directs cellular morphogenesis after cell cycle exit.

2022-01-14 | PXD030953 | Pride

Cis-Regulatory Accessibility Directs Muller Glial Development and Regenerative Capacity

Project description:Cis-Regulatory Accessibility Directs Muller Glial Development and Regenerative Capacity

| PRJNA565157 | ENA

A BMP-controlled metabolic-epigenetic signaling cascade directs midfacial morphogenesis

Project description:A BMP-controlled metabolic-epigenetic signaling cascade directs midfacial morphogenesis

| PRJNA1040221 | ENA

Genetic control of cellular morphogenesis in Müller glia

Project description:How the various cell-types of the body achieve their specific shapes is fundamentally unknown. Here, we explore this issue by identifying genes involved in the elaboration of the complex, yet conserved, cellular morphology of Müller glial (MG) cells in the retina. Using genomic based strategies in zebrafish, we found more than 40 candidate genes involved in specific aspects of MG morphogenesis. The successive steps of cell morphogenesis correlate with the timing of the expression of cohorts of inter-related genes that have roles in generating the particular anatomical features of these cells, suggesting that a sequence of genetic regulomes govern stepwise cellular morphogenesis in this system.

2019-06-20 | GSE120275 | GEO

Astrocyte morphogenesis is dependent on BDNF signaling via astrocytic TrkB.T1

Project description:Astrocytic morphogenesis and maturation are critical steps in CNS development. The time window of astrocyte morphological development is well defined, but the molecular underpinnings are still unclear. BDNF is a critical growth factor involved in the development of the CNS, including synapse refinement. Here we demonstrate the BDNF receptor at Ntrk2 is enriched in astrocytes relative to all CNS cell populations. RNA sequencing indicates Ntrk2 falls in the top 0.001% of all gene transcripts expressed in juvenile astrocytes, almost exclusively due to truncated TrkB.T1. Astrocyte complexity is increased in the presence of BNDF in vitro, which is dependent upon the presence of TrkB.T1. Furthermore, deletion of TrkB.T1 in vivo revealed astrocytes with significantly reduced volume and branching complexities. Indicating a role for functional astrocyte maturation via BDNF/TrkB.T1 signaling, TrkB.T1 KO astrocytes do not support normal excitatory synaptogenesis. Together, these data suggest a significant role for BDNF/TrkB.T1 signaling in astrocyte morphogenesis and indicate this signaling may contribute to astrocyte regulation of neuronal synapse development.

2019-08-26 | GSE122176 | GEO

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data