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TranscriptomicsIdentification of Genes and Networks Driving Cardiovascular and Metabolic Phenotypes in a Mouse F2 Intercross
To identify the genes and pathways that underlie cardiovascular and metabolic phenotypes we performed an integrated analysis of a mouse C57BL/6J x A/J F2 (B6AF2) cross by relating genome-wide gene expression data from adipose, kidney, and liver tissues to physiological endpoints measured in the popu...
ORGANISM(S): Mus musculus 
2011-01-13 | E-GEOD-25506 | biostudies-arrayexpress
UnknownGenetic and Environmental Factors of Non-Ability-Based Confidence.
Not available
S-EPMC11244733 | biostudies-literature
UnknownThe role of fatty acid desaturase (FADS) genes in oleic acid metabolism: FADS1 Δ7 desaturates 11-20:1 to 7,11-20:2.
Not available
S-EPMC5806126 | biostudies-literature
UnknownImaging trace element distributions in single organelles and subcellular features.
Not available
S-EPMC4766485 | biostudies-literature
TranscriptomicsA combinatorial Interplay Among the ACC Synthase Isoforms Regulates Ethylene Biosynthesis in Arabidopsis thaliana
ACC Synthase (ACS) is the key regulatory enzyme in the ethylene biosynthesis in plants. It catalyzes the conversion of s-adenosylmethionine (SAM) to 1-aminocyclopropane-1-carboxylic acid (ACC), the precursor of ethylene. Arabidopsis has nine ACS genes. The goal of the project is to inactivate each g...
ORGANISM(S): Arabidopsis thaliana 
2009-12-15 | E-GEOD-14496 | biostudies-arrayexpress
UnknownHuman monoclonal antibodies against West Nile virus induced by natural infection neutralize at a postattachment step.
Not available
S-EPMC2698525 | biostudies-literature
UnknownPhosphatidylinositol 3-kinase: the oncoprotein.
Not available
S-EPMC2955792 | biostudies-literature
UnknownEffects of simvastatin on white matter integrity in healthy middle-aged adults.
Not available
S-EPMC8351379 | biostudies-literature
UnknownThe gain of function SCN1A disorder spectrum: novel epilepsy phenotypes and therapeutic implications.
Not available
S-EPMC9679167 | biostudies-literature
UnknownNot all SCN1A epileptic encephalopathies are Dravet syndrome: Early profound Thr226Met phenotype.
Not available
S-EPMC5589790 | biostudies-literature
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