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Links from GEO DataSets

Items: 9

1.
Full record GDS4784

Post-pneumonectomy lung regeneration: time course

Analysis of right lung medial lobe, right lung cardiac lobe, and whole right lung following left pneumonectomy. Surgical resection of pulmonary tissue triggers a proregenerative stretch stimulus in the remaining lung. Results provide insight into molecular basis of stretch-induced lung regeneration.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 2 protocol, 6 time, 3 tissue sets
Platform:
GPL6246
Series:
GSE39817
21 Samples
Download data: CEL
2.

Identification of de-differentiation and re-development phases during post-pneumonectomy lung growth.

(Submitter supplied) The medial and cardiac lobes of the right lung and whole right lung of (initially) 10-12 week old C57BL/6 mice were transcriptome profiled at days 0, 3, 7, 14, 28 and 56 post left pneumonectomy, with day 0 being pre-pneumonectomy, and an additional day 56 post sham surgery to control for 8 week aging post left pneumonectomy.
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS4784
Platform:
GPL6246
21 Samples
Download data: CEL
Series
Accession:
GSE39817
ID:
200039817
3.

Age-dependent decline in lung regeneration with loss of clonogenicity and myofibroblastic differentiation of lung fibroblasts

(Submitter supplied) While aging leads to a reduction in the capacity for regeneration after pneumonectomy (PNX) in most mammals, this biological phenomenon has not been characterized over the lifetime of mice. We measured the age-specific (3, 9, 24 month) effects of PNX on physiology, morphometry, cell proliferation and apoptosis, global gene expression, and lung fibroblast phenotype and clonogenicity in female C57BL6 mice. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6887
36 Samples
Download data: TXT
Series
Accession:
GSE27964
ID:
200027964
4.

Mesenchymal signature of post-pneumonectomy lung regeneration in adult mice

(Submitter supplied) The adult human lung has a very limited capacity to regenerate functional alveoli. In contrast, adult mice have a remarkable capacity for neoalveolarization following either lung resection or injury. The molecular basis for this unique capability to regenerate lung tissue in mice is largely unknown. We examined the transcriptomic responses to single lung pneumonectomy in adult mice in order to elucidate prospective molecular signaling used in this species during lung regeneration. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
8 Samples
Download data: CEL
Series
Accession:
GSE15999
ID:
200015999
5.

The single cell RNA seq of pulmonary alveolar epithelial cells

(Submitter supplied) The pulmonary alveolar epithelium which play key role in lung biological function is mainly composed of two types of epithelial cells: alveolar type I (AT1) and type II (AT2) cells. We know very little about developmental heterogeneity of the AT1 cell population. By using 10X genomics “Chromium Single Cell” technology, we performed single-cell RNA-seq (scRNA-seq) analyses of AT1 cells at postnatal day 3 (P3), P15, and P60, along with AT2 cells (P60) in mice. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
4 Samples
Download data: CSV
Series
Accession:
GSE106960
ID:
200106960
6.

Hydrostatic pressure controls angiogenesis through endothelial YAP1 during lung regeneration

(Submitter supplied) Pulmonary artery (PA) pressure increases during lung growth after unilateral pneumonectomy (PNX). Mechanosensitive transcriptional co-activator, yes-associated protein (YAP1), in endothelial cells (ECs) is necessary for angiogenesis during post-PNX lung growth. We investigate whether increases in PA pressure following PNX controls angiogenesis through YAP1. When hydrostatic pressure is applied to human pulmonary arterial ECs (HPAECs), the expression of YAP1, transcription factor TEAD1, and angiogenic factor receptor Tie2 increases, while these effects are inhibited when HPAECs are treated with YAP1 siRNA or YAP1S94A mutant that fails to bind to TEAD1. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
4 Samples
Download data: TXT
Series
Accession:
GSE154110
ID:
200154110
7.

FOXF1 transcription factor promotes lung regeneration after partial pneumonectomy

(Submitter supplied) FOXF1, a member of the forkhead box family of transcription factors, has been previously shown to be critical for lung development, homeostasis, and injury responses. However, the role of FOXF1 in lung regeneration is unknown. Herein, we performed partial pneumonectomy, a model of lung regeneration, in mice lacking one Foxf1 allele in endothelial cells (PDGFb-iCre/Foxf1fl/+ mice). Endothelial cell proliferation was significantly reduced in regenerating lungs from mice deficient for endothelial Foxf1. more...
Organism:
Mus
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platform:
GPL23575
3 Samples
Download data: CSV, XLSX
Series
Accession:
GSE100149
ID:
200100149
8.

Regeneration in sponge Sycon ciliatum partly mimics postlarval development

(Submitter supplied) We performed high-throughput sequencing on regenerating samples and compared the data with regular embryonic and postlarval development of Sycon ciliatum. Our comparative transcriptomic analysis illuminates that sponge regeneration is equally dynamic as embryogenesis.
Organism:
Sycon ciliatum
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL28463 GPL28462
26 Samples
Download data: TXT
Series
Accession:
GSE149471
ID:
200149471
9.

Genome wide gene expression during lung development in three inbred mouse strains

(Submitter supplied) To better understand the temporal dynamics of gene expression during normal murine lung development we characterized global gene expression at 26 time points in three common inbred strains of mice (A/J, C57BL/6J, and C3H/HeJ). The data set provides a unique resource for identifying patterns of gene expression changes during normal lung development and for investigating the developmental origins of respiratory disease. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL20894
216 Samples
Download data: CEL, TSV, TXT
Series
Accession:
GSE74243
ID:
200074243
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