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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
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
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
UnknownClinical complexity and impact of the ABC (Atrial fibrillation Better Care) pathway in patients with atrial fibrillation: a report from the ESC-EHRA EURObservational Research Programme in AF General Long-Term Registry.
Not available
S-EPMC9440492 | biostudies-literature
UnknownImpact of clinical phenotypes on management and outcomes in European atrial fibrillation patients: a report from the ESC-EHRA EURObservational Research Programme in AF (EORP-AF) General Long-Term Registry.
Not available
S-EPMC8527730 | biostudies-literature
UnknownImpact of renal impairment on atrial fibrillation: ESC-EHRA EORP-AF Long-Term General Registry.
Not available
S-EPMC9287022 | biostudies-literature
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