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2,098 results for “acting”
SubComm Infographics - Subtitles: A Balancing Act
<p>An infographic describing the various challenges and considerations associated with subtitling.</p>
Dataset belonging to SNF project: Use of physiologically based pharmacokinetic modelling to simulate dosing requirements of long-acting intramuscular antiretroviral drugs in special populations and to manage drug-drug interactions
Open the record for dataset details and reuse information.
ACT group interventions of parents of children with special needs
Open the record for dataset details and reuse information.
Reporter CRISPR screens decipher cis- and trans-regulatory principles at the Xist locus [Microscope images - Xist act KDs]
<p>Microscope images related to Figure 5 in Schwämmle et al. 2025. </p> <p>The cells are day 2 differentiated TX1072 XX SP427 mESCs with the indicated knockdowns. (-2iLIF)</p> <p>Exonic Xist is stained using Cy5 Stellaris probes. The nuclei are stained using DAPI.</p> <p>These files were used to perform automated image analysis to detect and quantify Xist clouds (https://github.com/EddaSchulz/TFiScreen_Paper).</p>
FIGURE 1. RAxML tree resulting from analyzed partial ACT dataset. The scale bar indicates 0.05 in Sexual morph of Phaeoacremonium aureum from Rhizophora mucronata collected in southern Thailand
FIGURE 1. RAxML tree resulting from analyzed partial ACT dataset. The scale bar indicates 0.05 changes. ML, MP bootstrap support values> 65 % from 1,000 replicates and PP> 0.95 from 1 million generations in Markov chains are shown at the nodes. Newly generated sequences are in bold text. The tree was rooted to Pleurostoma richardsiae (CBS 270.33) (Pleurostomataceae).
Ion sensors based on organic semiconductors acting as quasi-reference electrodes
<p>We report electric double-layer transistors with organic semiconductors in single-crystal forms for ion sensing. High operational stability of our transistors enabled them to serve as quasi-reference electrodes, which show one-to-one relationship between the source electrode potential and device resistance. Differential measurements between our sensing and reference transistors demonstrated ion concentration sensing without a conventional reference electrode.</p>
Restored legume acts as a 'nurse' to facilitate plant compensatory growth and biomass production in mown grasslands
<p>Legume restoration was conducted in a temperate grassland in Hulunbuir, northeastern Inner Mongolia, China, by reseeding native legumes. This process was followed by annual mowing and phosphorus (P) application over a seven-year period (2014–2020). Throughout this period, we measured aboveground biomass, plant diversity, and the relative biomass of five functional plant groups each year. In 2020, we assessed six functional traits of 15 common plant species in both legume-restored and naturally-restored grasslands, respectively. Using these trait values and relative biomass data, we calculated community-weighted means and functional diversity indices for each plot.</p> <p> </p>
FIGURES 5–11 in New taxonomic and nomenclatural acts in Cephenniini (Coleoptera: Staphylinidae Scydmaeninae)
FIGURES 5–11. Syntype of Pseudocephennium integricolle Reitter. Dorsal habitus (5); head, pronotum and elytral base in dorsal view (6); head, prothorax and anterior portion of mesothorax in ventral view (7); pterothorax in ventral view (8); aedeagus in ventral (9), dorsal (10) and lateral (11) views.
FIGURES 1–4 in New taxonomic and nomenclatural acts in Cephenniini (Coleoptera: Staphylinidae Scydmaeninae)
FIGURES 1–4. Syntype female of Cephennium breviusculum Motschulsky (1); aedeagus of Cephennodes zwaluwenburgi Zim- merman in ventral (2) and lateral (3) views; holotype female of Cephennium felicitas Scott (4).
FIGURE 5 in <p><strong>Nomenclatural and taxonomic problems related to</strong> <strong>the electronic publication of new nomina and nomenclatural acts in zoology, with brief comments on optical discs and on the situation in botany</strong></p>
FIGURE 5. Accompanying letters of four documents received by the Paris Museum library: facsimiles of PDFs of (a–c) three works published by Parasites & Vectors (Andrade Filho et al. 2009, Freeman & Sommerville 2010, Poinar 2009) and (d) a work published by BMC evolutionary Biology (Tan et al. 2012), letter received on 14 January 2013.
FIGURE 2 in <p><strong>Nomenclatural and taxonomic problems related to</strong> <strong>the electronic publication of new nomina and nomenclatural acts in zoology, with brief comments on optical discs and on the situation in botany</strong></p>
FIGURE 2. First page of Yamaguchi et al. (2012) under two different versions: (a) PDF dated 8 March 2012, downloaded from the BMC website on 6 November 2012; (b) paper facsimile dated 8 March 2012, received by the Paris Museum library before 5 November 2012 (two pages on one, successive pages printed upside down).
FIGURE 4 in <p><strong>Nomenclatural and taxonomic problems related to</strong> <strong>the electronic publication of new nomina and nomenclatural acts in zoology, with brief comments on optical discs and on the situation in botany</strong></p>
FIGURE 4. Four pages of Bargues et al. (2011) under two different versions: (a) page 11 of PDF dated 12 July 2011, downloaded from the BMC website on 11 November 2012, showing its fig. 8 with its correct legend; (b–d) pages 6, 9 and 15 of paper facsimile dated 12 July 2011, received by the Paris Museum library before 5 November 2012, showing its fig. 2 (legend of fig. 2 in PDF, tree of fig. 8 in PDF), its fig. 4 (legend of fig. 4 in PDF, photograph of fig. 10 in PDF) and its fig. 10 (legend and photograph of fig. 10 in PDF).
FIGURE 3. Page 9 in <p><strong>Nomenclatural and taxonomic problems related to</strong> <strong>the electronic publication of new nomina and nomenclatural acts in zoology, with brief comments on optical discs and on the situation in botany</strong></p>
FIGURE 3. Page 9 of Malm & Johanson (2011) under two different versions: (a) PDF dated 12 January 2011, downloaded from the BMC website on 11 November 2012; (b) paper facsimile dated 12 January 2011, received by the Paris Museum library before 5 November 2012 (compared to the PDF, throughout the printed document blue was replaced by violet and red by orange).
FIGURE 6 in <p><strong>Nomenclatural and taxonomic problems related to</strong> <strong>the electronic publication of new nomina and nomenclatural acts in zoology, with brief comments on optical discs and on the situation in botany</strong></p>
FIGURE 6. First page of PDFs of Tan et al. (2012) under two different versions, both dated 9 July 2012, as downloaded from the BMC website on: (a) 6 November 2012 (prepublication); (b) 16 December 2012 (final publication). In (b), the small boxes surrounded with green are taken from pages 18 (dates) and 19 (DOI and reference).
FIGURE 7 in <p><strong>Nomenclatural and taxonomic problems related to</strong> <strong>the electronic publication of new nomina and nomenclatural acts in zoology, with brief comments on optical discs and on the situation in botany</strong></p>
FIGURE 7. Four figures of prepublication of Tan et al. (2012), as downloaded from the BMC website on 6 November 2012. Note than fig. 3 and 4 are identical but with different legends.
Figure 2 in The Zagros Mountains acting as a natural barrier to gene flow in the Middle East: more evidence from the evolutionary history of spiny-tailed lizards (Uromasticinae: Saara)
Figure 2. The phylogenetic tree of the Uromasticinae subfamily, including the genera Saara and Uromastyx, based two mtDNA (Cytb and 16S) and one nDNA (ACM4) genes. The trees showed the same topologies for both ML and BI trees, and therefore, only the BI tree is presented. The ML bootstrap values and BI posterior probabilities are next to the nodes, respectively.
Figure 5 in The Zagros Mountains acting as a natural barrier to gene flow in the Middle East: more evidence from the evolutionary history of spiny-tailed lizards (Uromasticinae: Saara)
Figure 5. The biogeographic analysis of Saara with S-DIVA (A) and BBM (B) based on Cytb. For these analyses, three regions were considered: (A: blue nodes) the Mesopotamian plain [or western part of Zagros Mountains (WZM); distribution of S. loricata], (B: green nodes) the central Iranian Plateau [or eastern part of Zagros Mountains (EZM); distribution of S. asmussi] and (C: pink nodes) India/Pakistan (IP); distribution of S. hardwickii. The dark blue and dark green circles around nodes show dispersal and vicariance events, respectively.
Figure 1 in The Zagros Mountains acting as a natural barrier to gene flow in the Middle East: more evidence from the evolutionary history of spiny-tailed lizards (Uromasticinae: Saara)
Figure 1. Geographical distribution range of the genus Saara. The grey circles represent distribution points (the points were obtained from valid references e.g. GBIF, reptile database, etc.) and black circles refer to locations of samples that were used in the genetic analyses. Distribution ranges of S. loricata, S. asmussi and S. hardwickii are illustrated with blue, green and pink cross-hatches, respectively.
Figure 3 in The Zagros Mountains acting as a natural barrier to gene flow in the Middle East: more evidence from the evolutionary history of spiny-tailed lizards (Uromasticinae: Saara)
Figure 3. Parsimony haplotype networks of Saara loricata and S. asmussi based on two mtDNA (Cytb and 16S) genes. The haplogroups (A) and (B) refer to S. loricata with Cytb and 16S, respectively. The haplogroups (C) and (D) refer to S. asmussi with Cytb and 16S, respectively.
Figs. 34 –42 in Colydiine Genera (Coleoptera: Zopheridae: Colydiinae) of the New World: A Key and Nomenclatural Acts 30 Years in the Making
Figs. 34 –42. Dorsal habitus of New World colydiine genera, tribe Synchitini. 34) Megataphrus tenuicornis; 35) Microprius rufulus; 36) Monoedus guttatus; 37) Namunaria guttulata; 38) Neotrichus verrucatus; 39) Notocoxelus sp., Chile; 40) Paha laticollis; 41) Paryphus serratus; 42) Paxillobitoma clinei.
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
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.