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TranscriptomicsTranscription profiling of homozygous Commd1 null mouse embryos to elucidate the underlying mechanism leading to embryonic lethality
A gene expression study using microarray analysis was performed to elucidate the underlying mechanism leading to embryonic lethality in homozygous Commd1 null (Commd1-/-) mouse embryos. A gene expression profile of 9.5 dpc Commd1-/- embryos were generated and were compared to a gene expression profi...
ORGANISM(S): Mus musculus 
2006-09-01 | E-MEXP-832 | biostudies-arrayexpress
TranscriptomicsTranscription profiling of MIII celiac disease patients vs controls (M0) individuals
Comparison of MIII celiac disease patients to controls (M0) individuals.
ORGANISM(S): Homo sapiens 
2005-01-01 | E-MEXP-42 | biostudies-arrayexpress
TranscriptomicsInduced genomic rearrangements and chromothripsis by micronucleus-mediated chromosome transfer [850K]
Chromosome segregation errors have been linked to DNA damage and genomic rearrangements. Accumulating evidence has shown that catastrophic genomic rearrangements, like chromothripsis, can result from lagging chromosomes undergoing aberrant DNA replication and DNA damage in micronuclei. Detailed char...
ORGANISM(S): Homo sapiens 
2015-08-13 | E-GEOD-71928 | biostudies-arrayexpress
TranscriptomicsInduced genomic rearrangements and chromothripsis by micronucleus-mediated chromosome transfer [CytoSNP12]
Chromosome segregation errors have been linked to DNA damage and genomic rearrangements. Accumulating evidence has shown that catastrophic genomic rearrangements, like chromothripsis, can result from lagging chromosomes undergoing aberrant DNA replication and DNA damage in micronuclei. Detailed char...
ORGANISM(S): Homo sapiens 
2015-08-13 | E-GEOD-71978 | biostudies-arrayexpress
TranscriptomicsChromothripsis in healthy individuals affects multiple protein-coding genes and can result in severe congenital abnormalities in offspring [case 2]
Chromothripsis represents an extreme class of complex chromosome rearrangements (CCRs) with major effects on chromosomal architecture. Although recent studies have associated chromothripsis with congenital abnormalities, the incidence and pathogenic effects of this phenomenon require further investi...
ORGANISM(S): Homo sapiens 
2015-01-31 | E-GEOD-65452 | biostudies-arrayexpress
TranscriptomicsAnalysis of copy number changes and complex rearrangements in patients with congenital abnormalities
Chromothripsis represents a novel phenomenon in the structural variation landscape of cancer genomes. Here, we analyzed the genomes of ten patients with congenital disease that were preselected to carry complex chromosomal rearrangements (CCRs) with more than two breakpoints. The rearrangements disp...
ORGANISM(S): Homo sapiens 
2012-05-10 | E-GEOD-37906 | biostudies-arrayexpress
UnknownDesign and Baseline Characteristics of the Finerenone in Reducing Kidney Failure and Disease Progression in Diabetic Kidney Disease Trial.
Not available
S-EPMC6888890 | biostudies-literature
UnknownElective surgery cancellations due to the COVID-19 pandemic: global predictive modelling to inform surgical recovery plans.
Not available
S-EPMC7272903 | biostudies-literature
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