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42
datasets available to search
ShareScore release 0.9.0
Dataset results
42 results for “esterase”
Study to Evaluate the Clinical Efficacy and Safety of Subcutaneously Administered C1 Esterase Inhibitor for the Prevention of Angioedema Attacks in Adolescents and Adults With Hereditary Angioedema
ClinicalTrials.gov study NCT02584959. IPD Sharing: YES. Countries: 7. Publications: 2.
A Study to Evaluate the Clinical Pharmacology and Safety of C1-esterase Inhibitor Administered by the Subcutaneous Route
ClinicalTrials.gov study NCT01576523. IPD Sharing: Not stated. Countries: 2. Publications: 1.
C1 Esterase Inhibitor (C1INH-nf) for the Prevention of Acute Hereditary Angioedema (HAE) Attacks
ClinicalTrials.gov study NCT01005888. IPD Sharing: Not stated. Countries: 1. Publications: 4.
C1 Esterase Inhibitor (C1INH-nf) for the Treatment of Acute Hereditary Angioedema (HAE) Attacks
ClinicalTrials.gov study NCT00289211. IPD Sharing: Not stated. Countries: 1. Publications: 3.
Efficacy and Safety of Human Plasma-derived C1-esterase Inhibitor as add-on to Standard of Care for the Treatment of Refractory Antibody Mediated Rejection (AMR) in Adult Renal Transplant Recipients
ClinicalTrials.gov study NCT03221842. IPD Sharing: NO. Countries: 7. Publications: 1.
C1-esterase Inhibitor (Cinryze) for Acute Treatment of Neuromyelitis Optica Exacerbation
ClinicalTrials.gov study NCT01759602. IPD Sharing: Not stated. Countries: 1. Publications: 1.
C1 Esterase Inhibitor in Hereditary Angioedema (HAE)(Extension Study)
ClinicalTrials.gov study NCT00292981. IPD Sharing: Not stated. Countries: 2. Publications: 7.
Human C1 Esterase Inhibitor (C1-INH) in Subjects With Acute Abdominal or Facial Hereditary Angioedema (HAE) Attacks
ClinicalTrials.gov study NCT00168103. IPD Sharing: Not stated. Countries: 15. Publications: 4.
A Study to Evaluate the Clinical Efficacy and Safety of Subcutaneously Administered C1-esterase Inhibitor in the Prevention of Hereditary Angioedema
ClinicalTrials.gov study NCT01912456. IPD Sharing: Not stated. Countries: 10. Publications: 3.
Open-Label C1 Esterase Inhibitor (C1INH-nf) for the Treatment of Acute Hereditary Angioedema (HAE) Attacks
ClinicalTrials.gov study NCT00438815. IPD Sharing: Not stated. Countries: 1. Publications: 5.
Open-Label C1 Esterase Inhibitor (C1INH-nf) for the Prevention of Acute Hereditary Angioedema (HAE) Attacks
ClinicalTrials.gov study NCT00462709. IPD Sharing: Not stated. Countries: 1. Publications: 4.
A Study to Evaluate the Long-term Clinical Safety and Efficacy of Subcutaneously Administered C1-esterase Inhibitor in the Prevention of Hereditary Angioedema
ClinicalTrials.gov study NCT02316353. IPD Sharing: Not stated. Countries: 11. Publications: 4.
A Pilot Study to Evaluate the Use of C1 Esterase Inhibitor (Human) in Patients With Acute Antibody-Mediated Rejection
ClinicalTrials.gov study NCT01147302. IPD Sharing: Not stated. Countries: 2. Publications: 1.
high-resolution data set of esterase vb_24B_21 from Shiga toxin-encoding bacteriophage phi24B; PDB id is 6YP6
<p>high-resolution data set of esterase vb_24B_21 from Shiga toxin-encoding bacteriophage phi24B; PDB id is 6YP6</p> <p>Data were collected at Diamond I04 on February 8, 2012 using an ADSC detector.</p>
medium resolution data set of esterase vb_24B_21 from Shiga toxin-encoding bacteriophage phi24B; PDB id 6YP6
<p>medium resolution data set of esterase vb_24B_21 from Shiga toxin-encoding bacteriophage phi24B; PDB id 6YP6</p> <p>Data were collected at Diamond I04-1 on February 6, 2012</p>
Data from: Selection at the Esterase-2 locus of Drosophila buzzatii? Perturbation-reperturbation experiments
Apparent selection affecting starch gel electrophoretic alleles at the Esterase-2 locus of Drosophila buzzatii has been detected in laboratory and natural populations. Perturbation-reperturbation of allele frequencies in replicated laboratory populations attempts to test direct selective effects at the locus versus effects of linked loci. Sequential gel electrophoresis has identified more alleles within starch classes, and three of these alleles (within the a, b and c starch alleles) were used in cage population experiments. Allele a/1.00/1.00/1.00 was set up in 10 replicate populations with allele c/1.00/1.00/1.00, and in an independent 10 replicate populations with allele b/0.99/1.01/1.00. For each set, three reperturbations were done. Replicate populations generally showed similar patterns of allele frequency change and clear directionality: effects of selection, not drift. However, four populations deviated from their replicates, indicating dissipation of linkage disequilibrium. Estimates of pre-adult viability in the F2 of pair-wise crosses among 12 sequential gel electrophoretic alleles showed very variable modes of inheritance and relative viability fitnesses. Together with the diversity of patterns of allele frequency change in the cage populations, these results suggest a gene complex, with selection acting on an interacting set of loci which may include Esterase-2.
Raw diffraction images of a crystal of Ferulic Acid Esterase (FAE) solved by SAD from data collected by Direct Data Collection (DDC) using the ESRF RoboDiff goniometer
<p>In order to demonstrate the data collection capabilities of the RoboDiff diffraction data were collected from a crystal of FAE to demonstrate the suitability of the beamline MASSIF-1 and RoboDiff for ab initio phasing experiments using diffraction data collected at wavelengths at or remote from the absorption edges of the anomalous scattering elements contained in crystals.</p>
Treatment With Acetyl-Choline Esterase Inhibitors in Children With Autism Spectrum Disorders
ClinicalTrials.gov study NCT01098383. IPD Sharing: Not stated. Countries: 1. Publications: 2.
Enhanced Vascular Function Following Intake of Feruloyl Esterase-processed High Fibre Bread.
ClinicalTrials.gov study NCT03946293. IPD Sharing: NO. Countries: 1. Publications: 1.
Recombinant Human C1 Esterase Inhibitor in the Prevention of Contrast-induced Nephropathy in High-risk Subjects
ClinicalTrials.gov study NCT02869347. IPD Sharing: UNDECIDED. Countries: 1. Publications: 1.
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