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Links from GEO DataSets

Items: 20

1.
Full record GDS5434

Articular and growth plate cartilage zones: 10-day old normal proximal tibia

Analysis of superficial (SZ) and intermediate/deep (IDZ) zones microdissected from articular cartilage and resting (RZ) zone from growth plate cartilage of proximal tibial epiphyses of 10-day old rats. Results provide insight into molecular basis of articular and growth plate cartilage divergence.
Organism:
Rattus norvegicus
Type:
Expression profiling by array, transformed count, 3 tissue sets
Platform:
GPL6247
Series:
GSE54216
12 Samples
Download data: CEL
2.

Expression data of articular and growth plate cartilage zones in 10-day-old rat proximal tibial epiphysis

(Submitter supplied) Articular and growth plate cartilage have comparable structures consisting of three distinct layers of chondrocytes, suggesting similar differentiation programs and therefore similar gene expression profiles. To address this hypothesis and to explore transcriptional changes that occur during the onset of articular and growth plate cartilage divergence, we used microdissection of 10-day-old rat proximal tibial epiphyses, microarray analysis, and bioinformatics to compare gene expression profiles in individual layers of articular and growth plate cartilage. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Dataset:
GDS5434
Platform:
GPL6247
12 Samples
Download data: CEL
Series
Accession:
GSE54216
ID:
200054216
3.

Spatial Regulation of Gene Expression in Articular Cartilage Assessed by Laser Captured Microdissection and Microarray

(Submitter supplied) We used laser capture microdissection to isolate different zones of the articular cartilage from proximal tibiae of 1-week old mice, and used microarray to analyze global gene expression. Bioinformatic analysis corroborated previously known signaling pathways, such as Wnt and Bmp signaling, and implicated novel pathways, such as ephrin and integrin signaling, for spatially associated articular chondrocyte differentiation and proliferation. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS5433
Platform:
GPL1261
14 Samples
Download data: CEL, CHP
Series
Accession:
GSE51994
ID:
200051994
4.
Full record GDS5433

Articular cartilage zones: 1-week old normal proximal tibia

Analysis of superficial (SZ), intermediate/deep (IDZ), and resting (RZ) zones microdissected from articular cartilage of the proximal tibiae of 1-week old mice. Results provide insight into the spatial regulation of gene expression in articular cartilage.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 3 tissue sets
Platform:
GPL1261
Series:
GSE51994
14 Samples
Download data: CEL, CHP
5.

Gene expression analysis of ER-stressed growth plate chondrocytes in two mouse models of Schmid chondrodysplasia

(Submitter supplied) We set out to generate transcriptional maps of chondrocyte UPR gene networks in vivo using two mouse models (Schmid and Cog) of Schmid chondrodysplasia, in order to define the consequences of UPR activation for the adaptation, differentiation, and survival of chondrocytes experiencing ER stress during hypertrophy, thus providing insights into ER stress signaling and its impact on cartilage pathophysiology. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7202
12 Samples
Download data: TXT
Series
Accession:
GSE30628
ID:
200030628
6.

Single-cell RNA-seq of long bone epiphyses from control and Sox9 mutant mice

(Submitter supplied) Using a conditional inactivation approach in the mouse, we examined the importance of SOX9 in adult growth plate and articular cartilage. We specifically investigated the roles of SOX9 in the expression of the pancartilaginous, growth-plate and articular programs and in maintaining the chondrocyte lineage fate.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
4 Samples
Download data: MTX, TSV, XLSX
Series
Accession:
GSE162033
ID:
200162033
7.

Bulk RNA-seq of articular and growth plate chondrocytes from control and Sox9 mutant mice

(Submitter supplied) Using a conditional inactivation approach in the mouse, we examined the importance of SOX9 in adult growth plate and articular cartilage. We specifically investigated the roles of SOX9 in the expression of the pancartilaginous, growth-plate and articular programs and in maintaining the chondrocyte lineage fate.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
12 Samples
Download data: XLSX
Series
Accession:
GSE154381
ID:
200154381
8.

Expression data from hyaline cartilages

(Submitter supplied) Comparison of human prepuberal articular and growth plate cartilage
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL9828
13 Samples
Download data: CEL
Series
Accession:
GSE32398
ID:
200032398
9.

Spatial and Temporal Regulation of Gene Expression in the Mammalian Growth Plate

(Submitter supplied) To explore the mechanisms responsible for spatial and temporal regulation of the growth plate, we microdissected postnatal rat growth plates into their constituent zones and then used microarray analysis to characterize the changes in gene expression that occur as chondrocytes undergo spatially-associated differentiation and temporally-associated senescence.
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL1355
35 Samples
Download data: CEL
Series
Accession:
GSE16981
ID:
200016981
10.

Microarray analysis of perichondral and reserve growth plate zones

(Submitter supplied) In the growth plate, the reserve and perichondral zones have been hypothesized to have similar functions, but their exact functions are poorly understood. Our hypothesis was that significant differential gene expression exists between perichondral and reserve chondrocytes that may differentiate the respective functions of these two zones. Normal Sprague-Dawley rat growth plate chondrocytes from the perichondral zone (PC), reserve zone (RZ), proliferative zone (PZ), and hypertrophic zone (HZ) were isolated by laser microdissection and then subjected to microarray analysis. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL1355
8 Samples
Download data: CEL, CHP
Series
Accession:
GSE9537
ID:
200009537
11.

Inhibitor trials in chondrocytes - MAS 5.0 normalization

(Submitter supplied) Objectives: To identify similarities and differences in gene expression data in the MEK/ERK and PI3K pathways and to determine how histone modification affects these same pathways. Goal: To identify and functionally characterize novel targets of these signaling pathways in the context of chondrocyte differentiation. Keywords: Treatment, signaling, one-colour array, signaling pathway comparison
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
15 Samples
Download data: CEL, CHP
Series
Accession:
GSE15069
ID:
200015069
12.

Inhibitor Trials

(Submitter supplied) Objectives: To identify similarities and differences in gene expression data in the MEK/ERK and PI3K pathways and to determine how histone modification affects these same pathways. Goal: To identify and functionally characterize novel targets of these signaling pathways in the context of chondrocyte differentiation. Keywords: Teatment, signaling, one-colour array, signaling pathway comparison
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
15 Samples
Download data: CEL
Series
Accession:
GSE8488
ID:
200008488
13.

Expression data from articular and growth plate cartilage

(Submitter supplied) The aim of the current study was to identify molecular markers for articular cartilage that can be used for the quality control of tissue engineered cartilage. Therefore a genom-wide expression analysis was performed using RNA isolated from articular and growth plate cartilage, both extracted from the knee joints of minipigs. Keywords: Native material or primary cells isolated from articular cartilage and growth plate cartilage
Organism:
Sus scrofa
Type:
Expression profiling by array
Platform:
GPL3533
6 Samples
Download data: CEL, CHP
Series
Accession:
GSE23492
ID:
200023492
14.

mRNA-seq analysis of superficial zone (SFZ) and deeper layers (deep AC) of articular cartilage of adult rats

(Submitter supplied) We compared gene expression profiles of SFZ and deep AC of articular cartilage through laser microdissection (LMD) using adhesive tape, linear amplification of mRNA, and mRNA-seq analysis.
Organism:
Rattus norvegicus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL14844
4 Samples
Download data: XLSX
Series
Accession:
GSE57377
ID:
200057377
15.

Expression data from mandibular condylar cartilage of rats

(Submitter supplied) Mandibular condylar cartilage (MCC) has many distinctive features reviewed in the literature, hence it would be expected that the genetic regulation of the biological process in the MCC to be different from those of other articular hyaline cartilages and epiphyseal growth cartilages. In addition, The MCC is a multi-zonal fibrocartilage containing different types of cells, which are well characterized histomorphologically, but the factors governing their morphological transition across the zones are not fully understood. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL1355
5 Samples
Download data: CEL
Series
Accession:
GSE162823
ID:
200162823
16.

Fetal mesenchymal stromal cells differentiating towards chondrocytes acquire a gene expression profile resembling human growth plate cartilage.

(Submitter supplied) We used human fetal bone marrow-derived mesenchymal stromal cells (hfMSCs) differentiating towards chondrocytes as an alternative model for the human growth plate (GP). Our aims were to study gene expression patterns associated with chondrogenic differentiation to assess whether chondrocytes derived from hfMSCs are a suitable model for studying the development and maturation of the GP. hfMSCs efficiently formed hyaline cartilage in a pellet culture in the presence of TGFB3 and BMP6. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL16066
10 Samples
Download data: CEL
Series
Accession:
GSE40942
ID:
200040942
17.

Comparative bulk RNAseq analysis of label-retaining chondrocytes (LRCs) of the growth plate versus their progeny

(Submitter supplied) We revealed the unique molecular signature of slow-cycling chondrocytes of the postnatal growth plate.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21103
6 Samples
Download data: CSV
Series
Accession:
GSE160364
ID:
200160364
18.

Effect of different hydrostatic pressures on mouse metatarsal and hip cartilage tissues

(Submitter supplied) Chondrocytes are subject to continuous loads placed upon them throughout development and physical activity. Normal physiological loads enable the maintenance of the articular cartilage health, however abnormal loads contribute to pathological joint ageing. Similarly, the growth plate cartilage is exposed to a number of loads during growth and development. Due to the high-water content of cartilage, hydrostatic pressure is considered one of the main biomechanical influences on chondrocytes and it plays an important role in the mechanoregulation of cartilage. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
24 Samples
Download data: TXT
Series
Accession:
GSE234112
ID:
200234112
19.

Lineage-Specific Differences and Inference of Regulatory Networks Governing Human Chondrocyte Development

(Submitter supplied) In-vitro differentiation of chondrocyte populations recapitulate in-vivo behaviours, and reveal gene regulatory networks involved in chondrocyte development
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL20301 GPL18573 GPL19057
46 Samples
Download data: BED, NARROWPEAK, TXT, XLSX
Series
Accession:
GSE195688
ID:
200195688
20.

Human PSC-derived articular cartilage chondrocytes scRNA-seq

(Submitter supplied) Objectives Traditional approaches to study Progressive Pseudorheumatoid Arthropathy of Childhood (PPAC) failed to uncover how loss-of-function mutations in Wnt inducible secreted protein 3 (WISP3) cause premature cartilage failure in children. We developed a human induced pluripotent stem cell (hiPSC)-based model of cartilage development to elucidate pathological changes in WISP3-deficient articular cartilage tissues compared to WISP3-sufficient isogenic cartilage tissues. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL20301 GPL24676
6 Samples
Download data: CSV, TAR
Series
Accession:
GSE230195
ID:
200230195
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