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MetabolomicsExtreme genome diversity and cryptic speciation in a harmful algal bloom forming eukaryote

Harmful algal blooms (HABs) of the toxic haptophyte Prymnesium parvum are a recurrent problem in many inland and estuarine waters around the world. Strains of P. parvum vary in the toxins they produce and in other physiological traits associated with HABs, but the genetic basis ...

2023-04-26 | MTBLS5893 | MetaboLights
UnknownComplex And Simple Appendicitis: REstrictive or Liberal postoperative Antibiotic eXposure (CASA RELAX) using Desirability of Outcome Ranking (DOOR) and Response Adjusted for Duration of Antibiotic Risk (RADAR): study protocol for a randomized controlled trial.
Not available
S-EPMC9486380 | biostudies-literature
UnknownContributions of PTSD polygenic risk and environmental stress to suicidality in preadolescents.
Not available
S-EPMC8569631 | biostudies-literature
TranscriptomicsAsthma III
Bronchial Epithelial Cells were isolated processed as described (Chu et al., 2002 and Zhao et al., 2011). The objective of the study was to identify differentially expressed genes between normal control (NC), mild-moderate asmathic (notSA) and severe asthmatic (SA) patients. For demographics data,...
ORGANISM(S): Homo sapiens 
2015-10-27 | E-GEOD-67940 | biostudies-arrayexpress
ProteomicsNRS1, a nitrogen source-regulated microprotein, confers an alternative mechanism of G1/S transcriptional activation in budding yeast
Commitment to cell division at the end of G1 phase, termed Start in the budding yeast Saccharomyces cerevisiae, is strongly influenced by nutrient availability. To identify newdominant activators of Start that might operate under different nutrient conditions, we screened a genome-wide ORF overexpr...
ORGANISM(S): Saccharomyces cerevisiae (Baker's yeast) 
2021-08-25 | PXD018681 | Pride
G1/s transcription Start Quantitative microscopy Nutrient limitation Evolution Microprotein Genetic screen Transcription factor Saccharomyces cerevisiae 
UnknownEmerging phenotypes linked to variants in SAMD9 and MIRAGE syndrome.
Not available
S-EPMC9433874 | biostudies-literature
UnknownSNX14 mutations affect endoplasmic reticulum-associated neutral lipid metabolism in autosomal recessive spinocerebellar ataxia 20.
Not available
S-EPMC5961352 | biostudies-literature
UnknownMutations in SNX14 cause a distinctive autosomal-recessive cerebellar ataxia and intellectual disability syndrome.
Not available
S-EPMC4225633 | biostudies-literature
UnknownMultiple congenital melanocytic nevi and neurocutaneous melanosis are caused by postzygotic mutations in codon 61 of NRAS.
Not available
S-EPMC3678977 | biostudies-literature
UnknownAerosol precautions and airway complications: a national prospective multicentre cohort study.
Not available
S-EPMC10087829 | biostudies-literature
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