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Links from GEO DataSets

Items: 20

1.

The RNA-binding proteins TIA1 and TIAL1 are required for the expression of the DNA damage repair machinery during B cell lymphopoiesis

(Submitter supplied) B-cell lymphopoiesis requires dynamic modulation of the B-cell transcriptome at the post-transcriptional level, although the implication of RNA-binding proteins (RBPs) remain largely unknown. Here we show that the RBPs TIA1 and TIAL1 are essential in B cells and, if deleted, there is a developmental block at the pro-B cell stage. TIA1 and TIAL1 have redundant functions. They act together as global splicing regulators for the expression of mRNAs including those involved in DNA damage repair in pro-B cells. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28457
8 Samples
Download data: CSV
Series
Accession:
GSE188556
ID:
200188556
2.

The RNA-binding proteins TIA1 and TIAL1 are required for the expression of the DNA damage repair machinery during B cell lymphopoiesis.

(Submitter supplied) B-cell lymphopoiesis requires dynamic modulation of the B-cell transcriptome at the post-transcriptional level, although the implication of RNA binding proteins (RBPs) remain largely unknown. Here we show that the RBPs TIA1 and TIAL1 are essential in B cells and, if deleted, there is a developmental block at the pro-B cell stage. TIA1 and TIAL1 have redundant functions. They act together as global splicing regulators for the expression of mRNAs including those involved in DNA damage repair in pro-B cells. more...
Organism:
Mus musculus
Type:
Other
Platform:
GPL28330
1 Sample
Download data: BEDGRAPH
Series
Accession:
GSE186701
ID:
200186701
3.

The RNA binding proteins TIA1 and TIAL1 protect germinal centre responses from apoptosis [iCLIP]

(Submitter supplied) Germinal centres (GC) are essential for the establishment of long-lasting antibody responses. In there, GC B cells rely on post-transcriptional RNA mechanisms for translating activation-associated transcriptional programs into functional changes in the cell proteome. However, we still lack knowledge about which are the critical proteins driving these key mechanisms. Here we show that the RNA binding proteins TIA1 and TIAL1 are required for the generation of long-lasting GC responses. more...
Organism:
Mus musculus
Type:
Other
Platform:
GPL21626
2 Samples
Download data: TSV
Series
Accession:
GSE235655
ID:
200235655
4.

The RNA binding proteins TIA1 and TIAL1 protect germinal centre responses from apoptosis

(Submitter supplied) Germinal centres (GC) are essential for the establishment of long-lasting antibody responses. In there, GC B cells rely on post-transcriptional RNA mechanisms for translating activation-associated transcriptional programs into functional changes in the cell proteome. However, we still lack knowledge about which are the critical proteins driving these key mechanisms. Here we show that the RNA binding proteins TIA1 and TIAL1 are required for the generation of long-lasting GC responses. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
13 Samples
Download data: CSV
Series
Accession:
GSE235358
ID:
200235358
5.

Transcriptome-wide analysis links the short-term expression of the b isoforms of T-cell intracellular antigens to protective proteostasis-mediated survival and quiescence

(Submitter supplied) Control of gene expression depends on genetics and environmental factors. The T-cell intracellular antigens T-cell intracellular antigen 1 (TIA1), TIA1-like/related protein (TIAL1/TIAR) and human antigen R (HuR/ELAVL1) are RNA-binding proteins that play crucial roles in regulating gene expression in both situations. This study used massive sequencing analysis to uncover molecular and functional mechanisms resulting from the short-time expression of the b isoforms of TIA1 and TIAR and HuR in HEK293 cells.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
12 Samples
Download data: TXT
6.

Regulation of mRNA translation and subcellular location controls protein synthesis of key modulators of the DNA damage response during B cell activation

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Other
Platforms:
GPL11002 GPL15103
171 Samples
Download data: BED
Series
Accession:
GSE93576
ID:
200093576
7.

Regulation of mRNA translation and subcellular location controls protein synthesis of key modulators of the DNA damage response during B cell activation [CLIP-seq]

(Submitter supplied) Post-transcriptional regulation of cellular mRNA is essential for protein synthesis. Here we describe the importance of mRNA translational repression and mRNA subcellular location for protein expression during B lymphocyte activation and the DNA damage response. Cytoplasmic RNA granules are formed upon cell activation with mitogens, including stress granules that contain the RNA binding protein Tia1. more...
Organism:
Mus musculus
Type:
Other
Platform:
GPL11002
2 Samples
Download data: BED
Series
Accession:
GSE93575
ID:
200093575
8.

Regulation of mRNA translation and subcellular location controls protein synthesis of key modulators of the DNA damage response during B cell activation [RNA-seq]

(Submitter supplied) Post-transcriptional regulation of cellular mRNA is essential for protein synthesis. Here we describe the importance of mRNA translational repression and mRNA subcellular location for protein expression during B lymphocyte activation and the DNA damage response. Cytoplasmic RNA granules are formed upon cell activation with mitogens, including stress granules that contain the RNA binding protein Tia1. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL15103
12 Samples
Download data: CSV
Series
Accession:
GSE93574
ID:
200093574
9.

Regulation of mRNA translation and subcellular location controls protein synthesis of key modulators of the DNA damage response during B cell activation [PolyRiboSeq]

(Submitter supplied) Post-transcriptional regulation of cellular mRNA is essential for protein synthesis. Here we describe the importance of mRNA translational repression and mRNA subcellular location for protein expression during B lymphocyte activation and the DNA damage response. Cytoplasmic RNA granules are formed upon cell activation with mitogens, including stress granules that contain the RNA binding protein Tia1. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL15103
157 Samples
Download data: TXT
Series
Accession:
GSE93573
ID:
200093573
10.

Identification of TIA1 mRNA targets during human neuronal development

(Submitter supplied) Background: Neuronal development is a tightly controlled process involving multi-layered regulatory mechanisms. While transcriptional pathways regulating neurodevelopment are well characterized, post-transcriptional programs are still poorly understood. TIA1 is an RNA-binding protein that can regulate splicing, stability, or translation of target mRNAs, and has been shown to play critical roles in neurodevelopment. more...
Organism:
Homo sapiens
Type:
Other
Platform:
GPL16791
27 Samples
Download data: CSV
Series
Accession:
GSE166306
ID:
200166306
11.

Dynamics of alternative splicing during somatic cell reprogramming reveals functions for RNA-binding proteins CPSF3, hnRNP UL1 and TIA1

(Submitter supplied) Background. Somatic cell reprogramming is the process that allows differentiated cells to revert to a pluripotent state. In contrast to the extensively studied rewiring of epigenetic and transcriptional programs required for reprogramming, the dynamics of post-transcriptional changes and their associated regulatory mechanisms remain poorly understood. Here we study the dynamics of alternative splicing changes occurring during efficient reprogramming of mouse B cells into induced pluripotent stem (iPS) cells and compare them to those occurring during reprogramming of mouse embryonic fibroblasts. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
18 Samples
Download data: TAB, TXT
Series
Accession:
GSE158633
ID:
200158633
12.

Interplay between genome topology and gene regulation during somatic cell reprogramming

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Other
Platforms:
GPL19057 GPL13112
57 Samples
Download data: BEDGRAPH, BW, TSV
Series
Accession:
GSE96611
ID:
200096611
13.

Interplay between genome topology and gene regulation during somatic cell reprogramming [RNA-seq]

(Submitter supplied) Studies of genome topology, chromatin state and transcriptome dynamics during highly-efficient somatic cell reprogramming
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
16 Samples
Download data: BW
Series
Accession:
GSE96608
ID:
200096608
14.

Interplay between genome topology and gene regulation during somatic cell reprogramming [ATAC-seq]

(Submitter supplied) Studies of genome topology, chromatin state and transcriptome dynamics during highly-efficient somatic cell reprogramming
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13112
8 Samples
Download data: BW
Series
Accession:
GSE96554
ID:
200096554
15.

Interplay between genome topology and gene regulation during somatic cell reprogramming [HiC-seq]

(Submitter supplied) Studies of genome topology, chromatin state and transcriptome dynamics during highly-efficient somatic cell reprogramming
Organism:
Mus musculus
Type:
Other
Platform:
GPL13112
14 Samples
Download data: TSV
Series
Accession:
GSE96553
ID:
200096553
16.

Interplay between genome topology and gene regulation during somatic cell reprogramming [ChIP-seq]

(Submitter supplied) Studies of genome topology, chromatin state and transcriptome dynamics during highly-efficient somatic cell reprogramming
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL19057 GPL13112
11 Samples
Download data: BW
Series
Accession:
GSE96548
ID:
200096548
17.

Interplay between genome topology and gene regulation during somatic cell reprogramming [4C-seq]

(Submitter supplied) Studies of genome topology, chromatin state and transcriptome dynamics during highly-efficient somatic cell reprogramming
Organism:
Mus musculus
Type:
Other
Platform:
GPL13112
8 Samples
Download data: BEDGRAPH
Series
Accession:
GSE96546
ID:
200096546
18.

T-cell intracellular antigen (TIA) proteins deficiency in murine embryonic fibroblasts alters cell cycle progression and induces autophagy

(Submitter supplied) Background: Mice lacking either T-cell intracellular antigen 1 (TIA1) or TIA1-related/like protein (TIAR/TIAL1) show high rates of embryonic lethality, suggesting a relevant role for these proteins during embryonic development. However, intrinsic molecular and cellular consequences of either TIA1 or TIAR deficiency remain poorly defined. Results: By using genome-wide expression profiling approach, we demonstrate that either TIA1 or TIAR inactivation broadly alter normal development-associated signaling pathways in murine embryonic fibroblasts (MEF). more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL13912
6 Samples
Download data: TXT
Series
Accession:
GSE43077
ID:
200043077
19.

Dysregulation of RNA splicing in tauopathies

(Submitter supplied) Pathological aggregation of RNA binding proteins (RBPs) has emerged as an important driver of multiple neurodegenerative diseases. Since RBP aggregation may result in a loss of normal RBP function, we examined whether dysregulation of RNA metabolism contributes to tauopathies. We find that the PS19 P301S tau mouse model exhibits a dysregulation of RNA splicing that is also apparent upon analysis of human Alzheimer’s disease brain tissues. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
12 Samples
Download data: TXT
Series
Accession:
GSE109226
ID:
200109226
20.

RNA binding protein TIA1 cytoplasmic expression as an Independent Prognostic Factor in Human Esophageal Squamous Cell Carcinoma (ESCC).

(Submitter supplied) T-cell intracellular antigen-1 (TIA1) is an RNA-binding protein modulating many regulatory aspects of target mRNA metabolism. Despite several reports referring to the role of TIA1 in carcinogenesis, little is known about the significance of its expression and function in human cancers including esophageal squamous cell carcinoma (ESCC). In the present study, we found that ectopic localization of overexpressed TIA1 in the cytoplasm was observed in a cohort of 143 ESCC patients using immunohistochemistry, and the cytoplasmic TIA1 was an independent prognosticator for worse overall survival. more...
Organism:
Homo sapiens
Type:
Other
Platform:
GPL17077
4 Samples
Download data: TXT
Series
Accession:
GSE71342
ID:
200071342
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