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Links from GEO DataSets

Items: 20

1.

Circadian skeletal muscle_wt and Clock mutants

(Submitter supplied) One hundred ninety wildtype male C57BL/6J mice age 7-10 weeks were purchased from Jackson Laboratory and entrained to a 12:12 light:dark cycle for 2 weeks. Mice were placed in light-tight boxes on a 12:12 LD cycle for 4 weeks, then released into constant darkness. Starting 30 hours after entry into DD (CT18), the left leg muscle from 5 wildtype mice, and the right leg muscle from the same wildtype mice were collected every 4 hours for 48 hours, for a total of 12 timepoints. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1073
38 Samples
Download data: CEL
Series
Accession:
GSE3746
ID:
200003746
2.

Circadian rhythm in clock mutants

(Submitter supplied) One hundred ninety wildtype male C57BL/6J mice age 7-10 weeks were purchased from Jackson Laboratory and entrained to a 12:12 light:dark cycle for 2 weeks. Mice were placed in light-tight boxes on a 12:12 LD cycle for 4 weeks, then released into constant darkness. Starting 30 hours after entry into DD (CT18), tissues from 5 (skeletal muscle) or 10 (liver or SCN) wildtype mice were collected every 4 hours for 48 hours, for a total of 12 timepoints. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1073
76 Samples
Download data: CEL
Series
Accession:
GSE3751
ID:
200003751
3.

Circadian liver_wt and Clock mutants

(Submitter supplied) One hundred ninety wildtype male C57BL/6J mice age 7-10 weeks were purchased from Jackson Laboratory and entrained to a 12:12 light:dark cycle for 2 weeks. Mice were placed in light-tight boxes on a 12:12 LD cycle for 4 weeks, then released into constant darkness. Starting 30 hours after entry into DD (CT18), tissues from 5 (skeletal muscle) or 10 (liver or SCN) wildtype mice were collected every 4 hours for 48 hours, for a total of 12 timepoints. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1073
38 Samples
Download data: CEL
Series
Accession:
GSE3748
ID:
200003748
4.

Circadian rhythm in Clock mutant and Cry deficient mice

(Submitter supplied) Molecular analysis of circadian rhythm in mice. Liver tissue of wildtype, Clock mutant and Cry deficient C57BL/6 8- to 10-week-old male mice examined. Keywords = circadian rhythm Keywords: other
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS413
Platform:
GPL81
6 Samples
Download data
Series
Accession:
GSE454
ID:
200000454
5.
Full record GDS413

Circadian rhythm in Clock and Cry mutants

Identification of CLOCK and CRY-regulated genes expressed in circadian manner in liver. Wild-type, Clock mutant and Cry-deficient C57BL/6 8-10 week old male mice examined at circadian times (CT) 14 and 2.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 3 strain, 2 time sets
Platform:
GPL81
Series:
GSE454
6 Samples
Download data
DataSet
Accession:
GDS413
ID:
413
6.

Cry2 and Fbxl3 promote circadian destruction of c-Myc

(Submitter supplied) Examination of gene expression changes caused by genetic deletion of Cry2 in MEFs with samples collected over a 24 hour time course after circadian synchronization
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
48 Samples
Download data: XLSX
Series
Accession:
GSE89018
ID:
200089018
7.

Binge Alcohol Disrupts Skeletal Muscle Core Molecular Clock Independent of Glucocorticoids

(Submitter supplied) Circadian rhythms are central to optimal physiological functioning and their interruption contributes to the development of several chronic diseases. Alcohol (EtOH) intoxication disrupts circadian rhythms within liver, brain, and intestines, but it is unknown whether alcohol also disrupts components of the core clock in skeletal muscle. Female C57BL/6Hsd mice were randomized to receive either saline (control) or alcohol (EtOH) (5g/kg) via intraperitoneal injection at the start of the dark cycle (ZT12), and gastrocnemius was collected every 4hr from Control and EtOH treated mice for the next 48hr following isoflurane anesthetization. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
10 Samples
Download data: XLSX
Series
Accession:
GSE183665
ID:
200183665
8.

MYOD1 functions as a clock amplifier as well as a critical co-factor for downstream circadian gene expression in muscle

(Submitter supplied) In the present study we show that the master myogenic regulatory factor, MYOD1, is a positive modulator of molecular clock amplitude and functions with the core clock factors for expression of clock-controlled genes in skeletal muscle. We demonstrate that MYOD1 directly regulates the expression and circadian amplitude of the positive core clock factor Bmal1. We identify a non-canonical E-box element in Bmal1 and demonstrate that is required for full MYOD1-responsiveness. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13112
1 Sample
Download data: BED, TXT
Series
Accession:
GSE122082
ID:
200122082
9.

Wildtype and Per2Cry1 double mutant mice: temporal gene expression profiling of adrenal gland

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
30 Samples
Download data
Series
Accession:
GSE4253
ID:
200004253
10.

Transcriptome regulation in the adrenal gland of circadian clock deficient Per2Cry1 double mutant mice

(Submitter supplied) This array set was used to determine clock regulated genes in the adrenal gland that are not necessarily rhythmic but still controlled by the circadian TTL. Keywords: comparative genomic hybridization / time series
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS2233
Platform:
GPL1261
6 Samples
Download data
Series
Accession:
GSE4239
ID:
200004239
11.
Full record GDS2233

Circadian clock deficient Per2/Cry1 double mutant adrenal gland in constant darkness: time course

Analysis of adrenal glands of Per2/Cry1 double mutant animals at 46 and 54 hours after transferring the animals from a light-day cycle to constant darkness. Per2/Cry1 double mutants lack a circadian clock. Results identify clock-regulated genes in the adrenal that are not necessarily rhythmic.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 time sets
Platform:
GPL1261
Series:
GSE4239
6 Samples
Download data
DataSet
Accession:
GDS2233
ID:
2233
12.

CRY2 missense mutations suppress P53 and enhance cell growth

(Submitter supplied) Disruption of circadian rhythms increases the risk of several types of cancer. Mammalian cryptochromes (CRY1 and CRY2) are circadian transcriptional repressors that are related to DNA repair enzymes. While CRYs lack DNA repair activity, they modulate the transcriptional response to DNA damage, and CRY2 can promote SCFFBXL3-mediated ubiquitination of c-MYC and other targets. Here, we characterize five mutations in CRY2 observed in human cancers in The Cancer Genome Atlas. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL23479
30 Samples
Download data: XLSX
Series
Accession:
GSE165647
ID:
200165647
13.

Genome-Wide And Phase-Specific DNA-Binding Rhythms Of BMAL1 Control Circadian Output Functions In Mouse Liver

(Submitter supplied) Using chromatin immuno-precipitation (ChIP) combined with deep sequencing (ChIP-seq) we obtained a time resolved and genome-wide map of BMAL1 binding in mouse liver, which allowed to identify over two thousand binding sites with peak binding narrowly centered around Zeitgeber time (ZT) 6. Annotation of BMAL1 targets confirms carbohydrate and lipid metabolism as the major output of the circadian clock in mouse liver. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL9185
13 Samples
Download data: BEDGRAPH
Series
Accession:
GSE26602
ID:
200026602
14.

Ribosome profiling reveals the rhythmic liver translatome and circadian clock regulation by upstream open reading frames

(Submitter supplied) Mammalian gene expression displays widespread circadian oscillations. Rhythmic transcription underlies the core clock mechanism, but it cannot explain numerous observations made at the level of protein rhythmicity. We have used ribosome profiling in mouse liver to measure the translation of mRNAs into protein around-the-clock and at high temporal and nucleotide resolution. Transcriptome-wide, we discovered extensive rhythms in ribosome occupancy, and identified a core set of ≈150 mRNAs subject to particularly robust daily changes in translation efficiency. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
48 Samples
Download data: TXT
Series
Accession:
GSE67305
ID:
200067305
15.

The Skeletal Muscle Molecular Clock Regulates Sarcomere Length Through Titin Splicing

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL24247 GPL17021
12 Samples
Download data
Series
Accession:
GSE189865
ID:
200189865
16.

The Skeletal Muscle Molecular Clock Regulates Sarcomere Length Through Titin Splicing [2]

(Submitter supplied) Circadian rhythms have been implicated in regulating skeletal muscle structure and function, but no mechanisms have connected the molecular clock to sarcomeric proteins. We identified an isoform shift in the sarcomeric ruler, titin, and showed that the skeletal muscle molecular clock regulates titin isoform and subsequently sarcomere length through RBM20, an RNA binding protein that controls titin splicing. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
6 Samples
Download data: CSV
Series
Accession:
GSE189863
ID:
200189863
17.

The Skeletal Muscle Molecular Clock Regulates Sarcomere Length Through Titin Splicing [1]

(Submitter supplied) Circadian rhythms have been implicated in regulating skeletal muscle structure and function, but no mechanisms have connected the molecular clock to sarcomeric proteins. We identified an isoform shift in the sarcomeric ruler, titin, and showed that the skeletal muscle molecular clock regulates titin isoform and subsequently sarcomere length through RBM20, an RNA binding protein that controls titin splicing.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
6 Samples
Download data: CSV
Series
Accession:
GSE172067
ID:
200172067
18.

Achilles-mediated and sex-specific regulation of circadian mRNA rhythms in Drosophila

(Submitter supplied) The circadian clock is an evolutionarily conserved mechanism that drives rhythmic expression of downstream genes. The core circadian clock drives the expression of clock-controlled genes either directly or indirectly, which in turn play critical roles in carrying out many rhythmic physiological processes. Nevertheless, the molecular mechanisms by which clock output genes orchestrate rhythmic signals from the brain to peripheral tissues are largely unknown. more...
Organism:
Drosophila melanogaster
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21306
96 Samples
Download data: TXT
Series
Accession:
GSE120100
ID:
200120100
19.

Circadian gene profiling in the distal nephron and collecting ducts

(Submitter supplied) Renal excretion of water and major electrolytes exhibits a significant circadian rhythm. This functional periodicity is believed to result, at least in part, from circadian changes in secretion/reabsorption capacities of the distal nephron and collecting ducts. Here, we studied the molecular mechanisms underlying circadian rhythms in the distal nephron segments, i.e. distal convoluted tubule (DCT) and connecting tubule (CNT) and, the cortical collecting duct (CCD). more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS4023
Platform:
GPL1261
24 Samples
Download data: CEL
Series
Accession:
GSE17739
ID:
200017739
20.
Full record GDS4023

Molecular clock effect on distal nephron segments: time course

Temporal analysis of microdissected distal nephron convoluted/connecting tubules (DCT/CNT) or cortical collecting ducts (CCD). Renal excretion of water and major electrolytes exhibits a significant circadian rhythm. Results provide insight into the role of molecular clock in renal function.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 6 time, 2 tissue sets
Platform:
GPL1261
Series:
GSE17739
24 Samples
Download data: CEL
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