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49 results for “CBF”
Raw diffraction data (CBF) for a structure of SARS-CoV-2 Main Protease bound to 2-Methyl-1-tetralone
<p>Data collected at beamline P11/PETRAIII Deutsches Elektronen Synchrotron DESY</p> <p>Info:</p> <p>run type: regular<br> run name: l6p17_09_001<br> start angle: 0.000000deg<br> frames: 1000<br> degrees/frame: 0.200000deg<br> exposure time: 40.000000ms<br> energy: 11.999832keV<br> wavelength: 1.033214A<br> detector distance: 200.000000mm<br> resolution: 1.304257A<br> aperture: 100um<br> filter transmission: 71.798748%<br> filter thickness: 75um<br> ring current: 119.222664mA</p> <p>Crystal-info:</p> <p>Co-crystallization of Sars-CoV-2 MPro with the compound was achieved by equlibrating a 6.25 mg/ml protein solution in 20 mM HEPES buffer (pH 7.8) containing 1 mM DTT, 1mM EDTA, and 150 mM NaCl against a reservoir solution of 100 mM MIB buffer (2:3:3 molar ratio of malonic acid, imidazole, and boric acid), pH 7.5, containing 25% v/v PEG 1500 and 5% v/v DMSO. Prior to crystallization compound solutions in DMSO were dried onto the wells of SwissCI 96-well plates. To achieve reproducible crystal growth seeding was used. Crystals appeared within a few hours and reached their final size after 2 -3 days. Crystals were manually harvested and flash cooled in liquid nitrogen for subsequent X-ray diffraction data collection.</p>
Fig. 4. Brachyhypopomus alberti. a. CBF 10284 in A taxonomic revision of the Neotropical electric fish genus Brachyhypopomus (Ostariophysi: Gymnotiformes: Hypopomidae), with descriptions of 15 new species
Fig. 4. Brachyhypopomus alberti. a. CBF 10284 (WC24.280607), holotype, male, 97 mm TL (head in lateral view, and body in lateral and dorsal views); b. ANSP 197573 (WC03.250607), paratype, female, 91 mm TL (body in lateral view); Bolivia, río Beni, Amazonas dr. Note the sexual dimorphism in body pigmentation, in which females are darker. Specimens fixed in formalin and preserved in EtOH. Scale bars = 5mm.
Effect of Raised CBF During CEA on Cognition in DM Patients
ClinicalTrials.gov study NCT00597545. IPD Sharing: Not stated. Countries: 1. Publications: 1.
CBF-Based Motion Planning for Socially Responsible Robot Navigation Guaranteeing STL Specification
<p>Video of submitted paper entitled "CBF-Based Motion Planning for Socially Responsible Robot Navigation Guaranteeing STL Specification"</p>
Robust CBF-based STL motion planning for socially responsible robot navigation in the presence of measurement noise
<p>Video of submitted paper entitled "Robust CBF-based STL motion planning for socially responsible robot navigation in the presence of measurement noise"</p>
Quantitative CBF values across different off-resonance correction methods used in 7T PCASL
<p>The data correspond to the underlying plots depicted in Figure 7 of the paper titled 'Dynamic B0 field shimming for improving pseudo-continuous arterial spin labeling at 7 Tesla'."</p>
Transcranial Electrical Stimulation (TCES) / Cerebral Blood Flow (CBF) / Xenon Under Computerized Tomography (Xe/CT)
ClinicalTrials.gov study NCT00273663. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Combination of Sorafenib With Standard Therapy in Newly Diagnosed Adult CBF AML
ClinicalTrials.gov study NCT05404516. IPD Sharing: Not stated. Countries: 1. Publications: 3.
Timed-Sequential Induction in CBF-AML
ClinicalTrials.gov study NCT00428558. IPD Sharing: Not stated. Countries: 1. Publications: 4.
Cerebral Blood Flow (CBF) Disturbances Following Traumatic Brain Injury (TBI) and Subarachnoid Hemorrhage (SAH)
ClinicalTrials.gov study NCT00807833. IPD Sharing: Not stated. Countries: 1. Publications: 18.
Dasatinib (Sprycel™) in Patients With Newly Diagnosed Core Binding Factor (CBF) Acute Myeloid Leukemia (AML)
ClinicalTrials.gov study NCT00850382. IPD Sharing: Not stated. Countries: 2. Publications: 1.
Data from: Adaptation to warmer climates by parallel functional evolution of CBF genes in Arabidopsis thaliana
The evolutionary processes and genetics underlying local adaptation at a specieswide level are largely unknown. Recent work has indicated that a frameshift mutation in a member of a family of transcription factors, C-repeat binding factors or CBFs, underlies local adaptation and freezing tolerance divergence between two European populations of Arabidopsis thaliana. To ask whether the specieswide evolution of CBF genes in Arabidopsis is consistent with local adaptation, we surveyed CBF variation from 477 wild accessions collected across the species' range. We found that CBF sequence variation is strongly associated with winter temperature variables. Looking specifically at the minimum temperature experienced during the coldest month, we found that Arabidopsis from warmer climates exhibit a significant excess of nonsynonymous polymorphisms in CBF genes and revealed a CBF haplotype network whose structure points to multiple independent transitions to warmer climates. We also identified a number of newly described mutations of significant functional effect in CBF genes, similar to the frameshift mutation previously indicated to be locally adaptive in Italy, and find that they are significantly associated with warm winters. Lastly, we uncover relationships between climate and the position of significant functional effect mutations between and within CBF paralogs, suggesting variation in adaptive function of different mutations. Cumulatively, these findings support the hypothesis that disruption of CBF gene function is adaptive in warmer climates, and illustrate how parallel evolution in a transcription factor can underlie adaptation to climate.
Figure 2 from: Mezzonato-Pires AC, Milward-de-Azevedo MA, Mendonça CBF, Gonçalves-Esteves V (2018) Taxonomy, palynology and distribution notes of seven new records of Passiflora L. (Passifloraceae s.s.) for Brazil. PhytoKeys 95: 1-14. https://doi.org/10.3897/phytokeys.95.22342
Figure 2 Illustrations of leaves and flowers in longitudinal section. A, B Passiflora amoena (S.V. Costa Neto et al. 2818, HAMAB) C, D Passiflora fuchsiiflora (S. Sakagawa et al. 248, INPA) E, F Passiflora jussieui (D.C. Daly et al. 7423, UPCB) G, H Passiflora ovata (S. Sakagawa et al. 668, INPA) I, J Passiflora plumosa (C.A. Cid et al. 561, MG) K, L Passiflora quelchii (R.C. Forzza et al. 8321, RB) M, N Passiflora tessmannii (C.A. Sothers & E.C. Pereira 612, INPA).
Figure 4 from: Mezzonato-Pires AC, Milward-de-Azevedo MA, Mendonça CBF, Gonçalves-Esteves V (2018) Taxonomy, palynology and distribution notes of seven new records of Passiflora L. (Passifloraceae s.s.) for Brazil. PhytoKeys 95: 1-14. https://doi.org/10.3897/phytokeys.95.22342
Figure 4 Passiflora amoena L.K. Escobar. A habit B inflorescence C flower D fruits. Scale bars: 10 mm (A, C, D); 2 mm (B). Photographs by S.C. Neto (S.V. Costa Neto et al. 2818, HAMAB)
Figure 3 from: Mezzonato-Pires AC, Milward-de-Azevedo MA, Mendonça CBF, Gonçalves-Esteves V (2018) Taxonomy, palynology and distribution notes of seven new records of Passiflora L. (Passifloraceae s.s.) for Brazil. PhytoKeys 95: 1-14. https://doi.org/10.3897/phytokeys.95.22342
Figure 3 Photomicrographs and electron photomicrographs of pollen grains of the species of Passiflora. A, B Passiflora amoena C, D Passiflora fuchsiiflora E, F Passiflora jussieui G, H Passiflora ovata I, J Passiflora quelchii K, L Passiflora tessmannii A, C, E, G, K general aspect of polar view B, F, H, I, L general aspect of equatorial view, D and J ornamentation detail. Scale bars: 10 µm (C, E, F, G, H, I, K, L); 5 µm (A, B, J); 1 µm (D).
Data from: Adaptation to warmer climates by parallel functional evolution of CBF genes in Arabidopsis thaliana
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Nenana Ice Classic: Tanana River Ice Annual Breakup Dates, Version 2
The Tanana river in the Interior of Alaska usually freezes over during October and November. The ice continues to grow throughout the winter accumulating an average maximum thickness of about 110 cm, depending upon winter weather conditions.The Nenana Ice Classic competition began in 1917 when railroad engineers bet a total of 800 dollars, winner takes all, guessing the exact time (month, day, hour, minute) ice on the Tanana River would break up. Each year since then, Alaska residents have guessed at the timing of the river breakup. A tripod, connected to an on-shore clock with a string, is planted in two feet of river ice during river freeze-up in October or November. The following spring, the clock automatically stops when the tripod moves as the ice breaks up. The time on the clock is used as the river ice breakup time.Many factors influence the river ice breakup, such as air temperature, ice thickness, snow cover, wind, water temperature, and depth of water below the ice. Generally, the Tanana river ice breaks up in late April or early May (historically, April 20 to May 20). The time series of Tanana river ice breakup dates can be used to indicate climate change in the region.
Core binding factor (CBF) is required for Epstein-Barr virus EBNA3 proteins to regulate target gene expression
GEO Series GSE88729. Homo sapiens. 7 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Nanostring based analysis of CBF-AML patients
GEO Series GSE196177. Homo sapiens. 48 samples. Type: Other.
STCH4/REIL2 confers cold stress tolerance in Arabidopsis by promoting rRNA processing and CBF protein translation
GEO Series GSE141304. Arabidopsis thaliana. 18 samples. Type: Expression profiling by high throughput sequencing.
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.