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TranscriptomicsAth_Agilent_v2_Riechmann array expression profile AP1-GR ap1cal inflorescences - chx experiment
This experiment describes gene expression after the activation of APETALA1-GR, to study and identify AP1 target genes. We used a 35S:AP1-GR ap1 cal line to induce a synchronized response activating the AP1-GR fusion protein in ap1 cal inflorescence-like meristems through dexamethasone or dexamethaso...
ORGANISM(S): Arabidopsis thaliana 
2011-01-01 | E-GEOD-20175 | biostudies-arrayexpress
UnknownMechanism of drug resistance in clonally related clinical isolates of Vibrio fluvialis isolated in Kolkata, India.
Not available
S-EPMC1489780 | biostudies-literature
UnknownRectifying calibration error of Goldmann applanation tonometer is easy!
Not available
S-EPMC4290199 | biostudies-literature
UnknownSuperfast Synthesis of Stabilized Silver Nanoparticles Using Aqueous Allium sativum (Garlic) Extract and Isoniazid Hydrazide Conjugates: Molecular Docking and In-Vitro Characterizations.
Not available
S-EPMC8746848 | biostudies-literature
UnknownMaternal MUAC and fetal outcome in an Indian tertiary care hospital: A prospective observational study.
Not available
S-EPMC7083480 | biostudies-literature
UnknownPhase IV postmarketing surveillance study shows continued efficacy and safety of Stempeucel in patients with critical limb ischemia due to Buerger's disease.
Not available
S-EPMC8641082 | biostudies-literature
UnknownNovel C-3 and C-20 derived analogs of betulinic acid as potent cytotoxic agents: design, synthesis, <i>in vitro</i> and <i>in silico</i> studies.
Not available
S-EPMC12061048 | biostudies-literature
UnknownHuman T cell responses to Japanese encephalitis virus in health and disease.
Not available
S-EPMC4925015 | biostudies-literature
UnknownImpact of a package of diagnostic tools, clinical algorithm, and training and communication on outpatient acute fever case management in low- and middle-income countries: protocol for a randomized controlled trial.
Not available
S-EPMC7687811 | biostudies-literature
GenomicsEGAS00001000167-sc-20150720 - samples
This project is to explore the contribution of de novo mutations to severe structural malformations diagnosed prenatally using ultrasound. These malformations include heart, CNS, renal and GI abnormalities. In this pilot project we aim to exome sequence 30 parent-foetus trios to ~50X mean coverage a...
EGAD00001001442 | EGA
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