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ShareScore release 0.9.0
Dataset results
37 results for “sil”
KSR inhibitor APS-2-79 sensitivity test in JURKAT and ALL-SIL T-cell acute lymphoblastic leukemia cell lines measured by Cell Counting Kit 8
<p>APS-2-79 compound was purchased from MedChemExpress (Monmoutyh Junction, NJ, USA). The 20 mg/ml stock solution was prepared in DMSO. To calculate the IC50, JURKAT and ALL-SIL cells were cultured for 72h with a range of APS-2-79 concentrations (5-15 µM) added as equal volumes. Cells treated with 0.5% DMSO (vehicle) were used as negative control. Cells treated with 10% DMSO were used as positive control. The viability of cells was measured using Cell Counting Kit 8 (Sigma Aldrich) and GloMax Microplate Reader system (Promega) with 450 nm wavelength and 600 nm as reference wavelength. The relevant reads are made from following wells: 2A-2D (15 µM APS-2-79), 3A-3D (12.5 µM APS-2-79), 4A-4D (10 µM APS-2-79), 5A-5D (7.5 µM APS-2-79), 6A-6D (5 µM APS-2-79), 7A-7D (vehicle), 8A-8D (positive control).</p>
Deliverable 2.1 Aero-hydro-elastic model definition - SOFTWIND 10 MW FOWT (wave-tank SIL version)
<p>For the detailed validation and verification of the capabilities of QBladeOcean in work package 2 of FLOATECH, a detailed definition of the models is needed. This database presents the QBladeOcean model of the DTU 10MW Reference Wind Turbine mounted on the SOFTWIND floater.</p> <p>Update V2.0.0: <br>Structure files are modified according to the requirements of the QBladeCE version</p> <p>Update V3.0.0:<br>- Added controller from SOFTWIND experiments (Modified from DTU 10MW to have oO star controller parameters)<br>- Modified mooring line length<br>- Shifted platform COG slightly towards centerline<br>- Modified blade definition to AD14 blade def.<br>- Included STATICBUOYANCY flag</p> <p>Update V3.1.0:<br>- Included ADVANCEDBUOYANCY flag<br>- Corrected excitation file (.3), previously: incorrect assignment of wave headings and excitation force coefficients<br>- Addition of mean drift file (.8)<br>- Corrected error in added mass matrix entry [4,2] (sway-roll coupling)</p> <p>Update V3.2.0:<br>- DELTA_DIR_DIFF 1-->20<br>- STATICBUOYANCY --> true</p> <p>Update V3.3.0:<br>- updated Substructure .txt file to format compatible with new QBlade version 2.0.6.4+<br>- extrapolation stretching activated<br>- depth dependent drag coefficient of 0.6 until z = -4m<br>- adjusted "DAMP_[-]" paremeter in the "MOORELEMENTS" table of ths Substructure .dat file to be zero due to numerical instabilities</p>
Functional anaysis of miR-143-3p/KSR2 interaction and oncogenic function in JURKAT and ALL-SIL T-cell acute lymphoblastic leukemia cell lines
<p>1. FCS files from GFP competition assay performed in ALL-SIL and JURKAT cell lines upon transduction with hsa-mir-143 expression vector (pCDH miR-143-3p) or empty vector (pCDH EV) as control.</p><p>2. Uncropped chemiluminescent immunoblot in JURKAT and ALL-SIL cell lines transduced with hsa-mir-143 expression vector (pCDH miR-143-3p) or empty vector (pCDH EV) as control. Upper band is KSR2 protein (~100 kDa) and lower band is loading control GAPDH protein (~37 kDa). Order of samples on the membrane: JURKAT pCDH miR-143-3p replicate 1, pCDH EV replicate 1, pCDH EV replicate 2, pCDH miR-143-3p replicate 2, pCDH EV replicate 3, pCDH miR-143-3p replicate 3, ALL-SIL pCDH miR-143-3p replicate 1, pCDH miR-143-3p replicate 2, pCDH EV replicate 1, pCDH miR-143-3p replicate 3, pCDH EV replicate 2, pCDH EV replicate 3.</p><p>3. RT-qPCR amplification data for relative quantification of <i>KSR2 </i>expression in reference to <i>ACTB </i>and <i>GAPDH </i>in JURKAT and ALL-SIL cell lines expressing deadCas9-KRAB system for transcriptional repression, upon transduction with sgRNA targeting <i>KSR2 </i>transcription start site vector (<i>KSR2 </i>sgRNA1 and <i>KSR2 </i>sgRNA2) or non-targeting sgRNA vector (NT) as control.</p><p>4. FCS files from GFP competition assay performed in ALL-SIL and JURKAT cell lines expressing deadCas9-KRAB system for transcriptional repression, upon transduction with sgRNA targeting <i>KSR2 </i>transcription start site vector (<i>KSR2 </i>sgRNA1 and <i>KSR2 </i>sgRNA2) or non-targeting sgRNA vector (NT) as control.</p>
Single-incision Laparoscopic (SILS) Versus Conventional Laparoscopic Appendectomy for the Treatment of Acute Appendicitis
ClinicalTrials.gov study NCT00997516. IPD Sharing: Not stated. Countries: 1. Publications: 3.
SILS™ Port Laparoscopic Cholecystectomy Post Market Study
ClinicalTrials.gov study NCT00832767. IPD Sharing: Not stated. Countries: 3. Publications: 1.
Hydrozoanthus sils decontaminated FSCR
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Hydrozoanthus sils decontaminated gx
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Single Incision Laparoscopic Surgery (SILS) Versus Conventional Laparoscopic Hysterectomy
ClinicalTrials.gov study NCT01483417. IPD Sharing: Not stated. Countries: 1. Publications: 4.
Prospective Randomized Study of SILS Versus CLS for Rectal Cancer
ClinicalTrials.gov study NCT01579721. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Single Incision Laparoscopic Surgery (SILS) Versus Laparoscopic Cholecystectomy
ClinicalTrials.gov study NCT00981604. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Short-term Outcomes of SILS+1 Versus CLS for Distal Gastric Cancer
ClinicalTrials.gov study NCT05035446. IPD Sharing: NO. Countries: 1. Publications: 9.
Single Incision Laparoscopic Surgery (SILS) Versus Laparoscopic Appendectomy
ClinicalTrials.gov study NCT00981136. IPD Sharing: Not stated. Countries: 1. Publications: 3.
Effect of LEGALON SIL on Hepatitis C Virus Recurrence in Stable Liver Transplanted Patients
ClinicalTrials.gov study NCT01518933. IPD Sharing: Not stated. Countries: 1. Publications: 1.
A Study to Investigate Interleukin-6 (IL-6) and IL-6/Soluble IL-6 Receptor (sIL-6R) Complex Levels in Subjects With Active Inflammatory Bowel Disease
ClinicalTrials.gov study NCT02790281. IPD Sharing: Not stated. Countries: 2. Publications: 0.
H3K27ac ChIP-Seq in ALL-SIL
GEO Series GSE70734. Homo sapiens. 2 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
H3K4me1 ChIP-seq in ALL-SIL
GEO Series GSE110631. Homo sapiens. 3 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Development of gene expression signatures for RUNX1 knockdown in the ALL-SIL cell line.
GEO Series GSE62140. Homo sapiens. 9 samples. Type: Expression profiling by array.
TLX1 ChIP-Seq in ALL-SIL
GEO Series GSE62264. Homo sapiens. 2 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Development of gene expression signatures for ETS1 knockdown in the ALL-SIL cell line.
GEO Series GSE62135. Homo sapiens. 9 samples. Type: Expression profiling by array.
Development of gene expression signatures for GSI treatment of the ALL-SIL cell line.
GEO Series GSE70629. Homo sapiens. 6 samples. Type: Expression profiling by array.
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OpenNeuro
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