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TranscriptomicsGene expression profile of Dicer-deficient oocytes
Small RNAs, such as miRNAs and siRNAs, are involved in gene regulation in a variety of systems, including mouse oocytes. Dicer is a ribonuclease III enzyme essential for miRNA and siRNA biosynthesis. In an effort to uncover the function of small RNAs during oocyte growth, we specifically deleted Dic...
ORGANISM(S): Mus musculus 
2010-04-06 | E-GEOD-17985 | biostudies-arrayexpress
ProteomicsInducible synthetic protein degradation system for phenotype control
Synthetic control of cell factory phenotypes is needed for redirecting resources from cell growth to production. To achieve that ClpXP proteasome was introduced to yeast Saccharomyces cerevisiae under control of TetON induction. Growth essential (in synthetic defined medium) metabolic enzymes Acc1, ...
ORGANISM(S): Saccharomyces cerevisiae (Baker's yeast) 
2023-05-10 | PXD034451 | Pride
Saccharomyces cerevisiae Clpxp proteasome 
UnknownETV4-Dependent Transcriptional Plasticity Maintains MYC Expression and Results in IMiD Resistance in Multiple Myeloma.
Not available
S-EPMC10772538 | biostudies-literature
UnknownSevere lower respiratory tract infection in infants and toddlers from a non-affluent population: viral etiology and co-detection as risk factors.
Not available
S-EPMC3598993 | biostudies-literature
UnknownRare loss of function variants in candidate genes and risk of colorectal cancer.
Not available
S-EPMC6283057 | biostudies-literature
UnknownExome sequencing of extreme phenotypes identifies DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis.
Not available
S-EPMC3702264 | biostudies-literature
UnknownEffects of body size on estimation of mammalian area requirements.
Not available
S-EPMC7496598 | biostudies-literature
UnknownCommon and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project.
Not available
S-EPMC3724194 | biostudies-literature
UnknownJoint linkage and association analysis with exome sequence data implicates SLC25A40 in hypertriglyceridemia.
Not available
S-EPMC3852929 | biostudies-literature
UnknownRare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence Project.
Not available
S-EPMC4673986 | biostudies-literature
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