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UnknownIdentification of oscillatory genes in somitogenesis from functional genomic analysis of a human mesenchymal stem cell model.
Not available
S-EPMC1899184 | biostudies-literature
TranscriptomicsEffect of EglN1 knockdown on smooth muscle expression
Ischemic preconditioning is the phenomenon whereby brief periods of sublethal ischemia protect against a subsequent, more prolonged, ischemic insult. In remote ischemic preconditioning (RIPC), ischemia to one organ protects other organs at a distance. We developed mouse models to ask if inhibition o...
ORGANISM(S): Mus musculus 
2016-02-11 | E-GEOD-77789 | biostudies-arrayexpress
GenomicsExome sequencing in classic Hairy cell leukaemia reveals widespread variation in acquired somatic mutations between individual tumours apart from the signature BRAF V(600)E lesion
Whole exome sequencing of 5 HCLc tumor-germline pairs. Genomic DNA from HCLc tumor cells and T-cells for germline was used. Whole exome enrichment was performed with either Agilent SureSelect (50Mb, samples S3G/T, S5G/T, S9G/T) or Roche Nimblegen (44.1Mb, samples S4G/T and S6G/T). The resulting exom...
ORGANISM(S): Homo sapiens 
2016-02-01 | E-MTAB-4313 | biostudies-arrayexpress
TranscriptomicsTranscription profiling of mouse C2C12 myoblast cell line to identify oscillatory genes in somitogenesis
During somitogenesis, oscillatory expression of genes in the notch and wnt signaling pathways plays a key role in regulating segmentation. These oscillations in expression levels are elements of a species-specific developmental mechanism. To date, the periodicity and components of the human clock re...
ORGANISM(S): Mus musculus 
2008-06-15 | E-GEOD-7012 | biostudies-arrayexpress
TranscriptomicsTranscription profiling of human mesenchymal stem cell model to identification of oscillatory genes in somitogenesis
This SuperSeries is composed of the following subset Series:; GSE7012: Identif. of oscillatory genes in somitogenesis from functional genomic analysis of C2C12 myoblast line; GSE7015: Identif. of oscillatory genes in somitogenesis from functional genomic analysis of a human mesenchymal stem cell mod...
ORGANISM(S): Homo sapiens 
2008-06-15 | E-GEOD-7054 | biostudies-arrayexpress
TranscriptomicsTranscription profiling of human mesenchymal stem cell model to identify of oscillatory genes in somitogenesis
During somitogenesis, oscillatory expression of genes in the notch and wnt signaling pathways plays a key role in regulating segmentation. These oscillations in expression levels are elements of a species-specific developmental mechanism. To date, the periodicity and components of the human clock re...
ORGANISM(S): Homo sapiens 
2008-06-15 | E-GEOD-7015 | biostudies-arrayexpress
GenomicsDetermining Genetic Role in Treatment Response to Anti-Platelet Interventions (The PAPI Study)

CHD is the leading cause of death in the United States. One of the most common ways to prevent CHD is to take an anti-platelet agent, which lessens platelet aggregation. Two of the most common anti-platelet agents are aspirin and clopidogrel. However, up to 25% to 30% of people do not r...

phs000391.v1.p1 | EGA
UnknownOutcomes in High-Risk Pulmonary Embolism Patients Undergoing FlowTriever Mechanical Thrombectomy or Other Contemporary Therapies: Results From the FLAME Study.
Not available
S-EPMC10573120 | biostudies-literature
UnknownNSD1 mutations generate a genome-wide DNA methylation signature.
Not available
S-EPMC4703864 | biostudies-literature
TranscriptomicsTranscription profiling of mouse Dll3 and Notch1 homozygous mutant embryos to investigate craniofacial malformations of human birth defects
Mutations in the Notch1 receptor and delta-like 3 (Dll3) ligand cause global disruptions in axial segmental patterning. Genetic interactions between members of the notch pathway have previously been shown to cause patterning defects not observed in single gene disruptions. We examined Dll3-Notch1 ...
ORGANISM(S): Mus musculus 
2008-06-15 | E-GEOD-8027 | biostudies-arrayexpress
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