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TranscriptomicsTranscription profiling of mouse xenograft L2987 lung tumor tissue samples
Transcriptional profiling was conducted on RNA from 8 xenograft L2987lung tumor tissue samples to identify genes affected by treatment with a VEGFR-2 small molecule inhibitor Experiment Overall Design: Baseline and 14 days post treatement gene expression profiling was performed using 8 xenograft L29...
ORGANISM(S): Mus musculus 
2008-06-15 | E-GEOD-7209 | biostudies-arrayexpress
TranscriptomicsTranscription profiling of human colon tumor tissue samples to identify genes whose expression level correlates with VEGFR-2 expression
Transcriptional profiling was conducted on RNA from 59 human colon tumor tissue samples to identify genes whose expression level correlates VEGFR-2 Experiment Overall Design: Baseline gene expression profiling was performed using 59 human colon tumor tissue samples to identify genomic signatures hig...
ORGANISM(S): Homo sapiens 
2008-06-15 | E-GEOD-7208 | biostudies-arrayexpress
MetabolomicsCollected mass spectrometry data on monoterpene indole alkaloids from natural product chemistry research
MIADB: a cumulative collection of 172 tandem mass spectrometry (MS/MS) of a vast array of monoterpene indole alkaloids. Samples were analyzed using an Agilent LC-MS system composed of an Agilent 1260 Infinity HPLC coupled to an Agilent 6530 ESI-Q-TOF-MS operating in positive mode. A Sunfire analytic...
2018-12-03 | MTBLS142 | MetaboLights
UnknownCross-Sectional Evaluation of Humoral Responses against SARS-CoV-2 Spike.
Not available
S-EPMC7524645 | biostudies-literature
UnknownTocilizumab in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial.
Not available
S-EPMC8084355 | biostudies-literature
UnknownExome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes.
Not available
S-EPMC9980234 | biostudies-literature
UnknownExome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes.
Not available
S-EPMC11646479 | biostudies-literature
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