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TranscriptomicsSf1+ mouse adrenocortical cells vs. Wnt-responsive mouse adrenocortical cells
We sought to determine which gene transcripts are enriched in Wnt-responsive adrenocortical mouse cells compared to the entire adrenocortical mouse cell population in vivo. To this end, we employed transgenic reporter mice that label Wnt-responsive cells with GFP expression (TCF/Lef:H2B-GFP mice) or...
ORGANISM(S): Mus musculus 
2014-07-11 | E-GEOD-53981 | biostudies-arrayexpress
UnknownDrug-induced aneuploidy and polyploidy is a mechanism of disease relapse in MYC/BCL2-addicted diffuse large B-cell lymphoma.
Not available
S-EPMC6267596 | biostudies-literature
UnknownHigh-Dimensional Analysis of Type 2 Lymphocyte Dynamics During Mepolizumab or Dupilumab Treatment in Severe Asthma.
Not available
S-EPMC12444942 | biostudies-literature
MetabolomicsDivergent relationships between faecal microbiota and metabolome following distinct antibiotic-induced disruptions
The intestinal microbiome plays an essential role in regulating many aspects of host physiology, and its disruption through antibiotic exposure has been implicated in the development of a range of serious pathologies. The complex metabolic relationships that exist between members of the intestinal m...
2017-03-03 | MTBLS422 | MetaboLights
TranscriptomicsMisregulation of alternative splicing of BIN1 leads to T-tubule alterations and muscle weakness in myotonic dystrophy
Myotonic dystrophes (DM), the most common adult muscular dystrophy, are the first recognized examples of RNA-mediated diseases in which expression of mutant RNAs containing expanded CUG or CCUG repeats interfere with the splicing of other mRNAs. Using whole-genome microarrays, we found that alternat...
ORGANISM(S): Homo sapiens 
2011-05-26 | E-GEOD-21795 | biostudies-arrayexpress
UnknownThe development of a HAMstring InjuRy (HAMIR) index to mitigate injury risk through innovative imaging, biomechanics, and data analytics: protocol for an observational cohort study.
Not available
S-EPMC9288010 | biostudies-literature
UnknownA framework for the investigation of rare genetic disorders in neuropsychiatry.
Not available
S-EPMC8656349 | biostudies-literature
UnknownPopulation-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia.
Not available
S-EPMC8863274 | biostudies-literature
UnknownModeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores.
Not available
S-EPMC4596916 | biostudies-literature
TranscriptomicsTranscription profiling of multiple human tumour specimens of different anatomical origin arrayed against a common reference
Multiple tumour specimens of different anatomical origin arrayed against a common reference.
ORGANISM(S): Homo sapiens 
2005-09-20 | E-MEXP-113 | biostudies-arrayexpress
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