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179 results for “50(2)”
Figure 2 from: Penev L, Agosti D, Georgiev T, Catapano T, Miller J, Blagoderov V, Roberts D, Smith V, Brake I, Ryrcroft S, Scott B, Johnson N, Sautter G, Chavan V, Robertson T, Remsen D, Stoev P, Parr C, Knapp S, Kress W, Thompson F, Erwin T (2010) Semantic tagging of and semantic enhancements to systematics papers: ZooKeys working examples. ZooKeys 50: 1-16. https://doi.org/10.3897/zookeys.50.538
Figure 2 - Four stages of an XML-based editorial, publication and dissemination workflow applied in ZooKeys (stages 1, 2, 4) and/or Plazi (stages 3, 4). Forms in blue are either implemented or prototyped, forms in red are in a process of development.
Figure 50 from: Lehmann T, Heß M, Melzer R (2014) Common littoral pycnogonids of the Mediterranean Sea. Zoosystematics and Evolution 90(2): 163-224. https://doi.org/10.3897/zse.90.7520
Figure 50 - Anoplodactylus pygmaeus, male; A: Mouth opening; scale 20 µm; B: Left chelifore with developed chela; scale 20 µm; C: Ventral view of right palp, reduced to a small tubercle; scale 40 µm; D: Ocular tubercle with lateral sense organ; scale 40 µm; E: 6-articled oviger; scale 100 µm; F: Distal articles of left oviger; scale 20 µm.
Figure 2 from: Renner MAM, Engel JJ, Patzak SDF, Heinrichs J (2015) A new species of Brevianthus (Brevianthaceae, Marchantiophyta) from New Caledonia with unusual underleaf production. PhytoKeys 50: 43-60. https://doi.org/10.3897/phytokeys.50.4998
Figure 2 - Brevianthus hypocanthidium: A leaf apex B cells at base of sinus on abaxial leaf surface C abaxial leaf surface at mid-leaf D abaxial leaf surface scale E adaxial leaf surface scale F adaxial leaf surface detail scale. All from NSW791547. Scale: 40 µm (A); 20 µm (B, E, F); 10 µm (C, D).
Figure 2 from: Larraín J, Carter B, Shaw B, Hentschel J, Strozier LS, Furuki T, Heinrichs J, Crandall-Stotler B, Engel J, von Konrat M (2015) The resurrection of Neohattoria Kamim. (Jubulaceae, Marchantiophyta): a six decade systematic conflict resolved through a molecular perspective. PhytoKeys 50: 101-122. https://doi.org/10.3897/phytokeys.50.4940
Figure 2 - Maximum likelihood (ML) tree showing the systematic position of Neohattoria herzogii within the Jubulaceae. Only 1/2 of the length of the branch between the Frullaniaceae and the Lejeuneaceae/Jubulaceae clade is depicted. Wide black branches indicate ML bootstrap support > 90 % and PP > 0.95.
Figure 2 from: Valdespino IA, Heringer G, Salino A, Góes-Neto LAA, Ceballos J (2015) Seven new species of Selaginella subg. Stachygynandrum (Selaginellaceae) from Brazil and new synonyms for the genus. PhytoKeys 50: 61-99. https://doi.org/10.3897/phytokeys.50.4873
Figure 2 - Selaginella alstonii G. Heringer, Salino & Valdespino. A Megaspore proximal face B Close-up of megaspore proximal face surface C Megaspore distal face D Close-up of megaspore distal face surface E Microspore proximal face F Microspore distal face G Close-up of microspore distal face surface H Close-up of microspore equatorial view surface A–H taken from isotype, Almeida et al. 533 (PMA).
Figure 2 from: Tagane S, Dang VS, Yahara T, Toyama H, Tran H (2015) Goniothalamus flagellistylus Tagane & V. S. Dang (Annonaceae), a new species from Mt. Hon Ba, Vietnam. PhytoKeys 50: 1-8. https://doi.org/10.3897/phytokeys.50.4427
Figure 2 - Line drawing of Goniothalamus flagellistylus sp. nov. (a) leafy twig, (b) flower on main trunk, (c) outer petal (adaxial), (d) inner petals (ad- and abaxial), (e) Stamens, (f) Carpel. Materials from Tagane et al. V1497.
Figure 2 from: Nilsson RH, Wurzbacher C, Bahram M, Coimbra VRM, Larsson E, Tedersoo L, Eriksson J, Duarte Ritter C, Svantesson S, Sánchez-García M, Ryberg M, Kristiansson E, Abarenkov K (2016) Top 50 most wanted fungi. MycoKeys 12: 29-40. https://doi.org/10.3897/mycokeys.12.7553
Figure 2 - A compound cluster displayed in the web browser of the user. The INSDC accession numbers and their taxonomic annotation are shown in columns 1 and 2. The DNA source and the country of collection are shown in columns 3 and 4. Column 5 shows the inclusiveness of the species hypotheses at the 97% similarity level (rightmost filled column), the 97.5% similarity level (second-to-rightmost filled column), and so on up to 100% similarity. The aligned sequence data are shown in column 6.
Figures 50-55 from: Markee A, Dikow T (2018) Taxonomic revision of the assassin-fly genus Microphontes Londt, 1994 (Insecta, Diptera, Asilidae). African Invertebrates 59(2): 195-237. https://doi.org/10.3897/afrinvertebr.59.30684
Figures 50-55 Microphonteswhittingtoni: 50 ♂ Holotype (NMSA-DIP-4777), dorsal (Morphbank #861895) 51 same, lateral (#861897) 52 same, head anterior (#861899) 53 ♀ Paratype (NMSA-DIP-74619), head anterior (#861902) 54 same, dorsal (#861904) 55 same, lateral (#861906). Scale bars: 5 mm (50–51, 54–55), 1 mm (52–53).
Text-fig. 16. Scanning electron microscope (SEM) images of "Stamen fragments with in situ Clavatipollenites- or Asteropollis-type pollen" (sp. 1: a–c; sp. 2: d–f; sp. 3: g–i); Catefica locality, Portugal. a) Stamen fragment showing pollen sacs; b) Distal view of pollen grain from (a) showing semitectate-reticulate tectum; c) Detail of pollen wall showing the semitectate-reticulate tectum and long, scattered, columellae supporting muri with fine pits and rounded supratectal ornamentation; note orbiculae with a finely spiny surface (arrows); d) Stamen showing very short filament, lateral pollen sacs and short apical extension of the narrow connective; e) Folded pollen grain from (d) showing semitectate-reticulate tectum; f) Detail of pollen wall from (d) showing the semitectatereticulate tectum and muri with fine rounded ornamentation; g) Stamen fragment; h, i) Detail of pollen grains from (g) showing the semitectate-reticulate tectum with smooth muri, long scattered columellae and tiny scattered orbicules (arrow). Specimens, Catefica 50-S170395 (a–c), Catefica 49-S172561 (d–f), Catefica 50-S170390 (g–i). Scale bars = 600 Μm (a, d, g), 6 Μm (b, e, h), 1.5 Μm (c, f, i). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms
Text-fig. 16. Scanning electron microscope (SEM) images of "Stamen fragments with in situ Clavatipollenites- or Asteropollis-type pollen" (sp. 1: a–c; sp. 2: d–f; sp. 3: g–i); Catefica locality, Portugal. a) Stamen fragment showing pollen sacs; b) Distal view of pollen grain from (a) showing semitectate-reticulate tectum; c) Detail of pollen wall showing the semitectate-reticulate tectum and long, scattered, columellae supporting muri with fine pits and rounded supratectal ornamentation; note orbiculae with a finely spiny surface (arrows); d) Stamen showing very short filament, lateral pollen sacs and short apical extension of the narrow connective; e) Folded pollen grain from (d) showing semitectate-reticulate tectum; f) Detail of pollen wall from (d) showing the semitectatereticulate tectum and muri with fine rounded ornamentation; g) Stamen fragment; h, i) Detail of pollen grains from (g) showing the semitectate-reticulate tectum with smooth muri, long scattered columellae and tiny scattered orbicules (arrow). Specimens, Catefica 50-S170395 (a–c), Catefica 49-S172561 (d–f), Catefica 50-S170390 (g–i). Scale bars = 600 Μm (a, d, g), 6 Μm (b, e, h), 1.5 Μm (c, f, i).
Fig. 2. Bayesian 50 in Checklist and molecular phylogenetics reveal three taxonomic novelties in Habenaria (Orchidaceae, Orchidoideae) from Chapada dos Veadeiros, Goiás, Brazil
Fig. 2. Bayesian 50% majority-rule consensus tree of the combined ITS, ETS, matK-trnK and rps16– trnK datasets. Numbers next to the nodes represent the posterior probabilities (PP) from the Bayesian analyses and bootstrap percentages (BP) from the parsimony analyses. Only the values of the main clades are shown. Neotropical subclades are numbered according to Batista et al. (2013). The new species described here are highlighted in bold and indicated by an arrow. Species with the petal anterior segment inserted above the base of the posterior segment are highlighted by an asterisk. Subclades in which it was possible to associate with one of the sections of Kränzlin's sectional treatment are identified accordingly.
Data for high-clay content submarine slope failure flume experiments. Experiment 50% clay, static 1, part 2.
<p>These video and photographic data support the following manuscripts:</p><p>Silver, M.M.W., Dugan, B., 2020, The influence of clay content on submarine slope failure: insights from laboratory experiments and numerical models, Geological Society of London, Special Publications, 500, 301-309, <a href="https://doi.org/10.1144/SP500-2019-186">https://doi.org/10.1144/SP500-2019-186</a>. </p><p>Silver, M.M.W., Dugan, B., 2023, Cohesion, permeability, and slope failure dynamics: implications for failure morphology and tsunamigenesis from benchtop flume experiments, Marine Geology, 462, <a href="https://doi.org/10.1016/j.margeo.2023.107079">https://doi.org/10.1016/j.margeo.2023.107079</a>.</p><p>Log sheets are included for each experiment file.</p>
Investigating Efficacy and Safety of Biphasic Insulin Aspart 50 Twice Daily Versus Biphasic Human Insulin 50 Twice Daily Both in Combination With Metformin in Chinese Subjects With Type 2 Diabetes Mel
ClinicalTrials.gov study NCT01892020. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Effect of Biphasic Insulin Aspart 50 on Blood Glucose Control in Subjects With Type 2 Diabetes
ClinicalTrials.gov study NCT00627445. IPD Sharing: Not stated. Countries: 1. Publications: 0.
24-week Study Comparing Lixisenatide to Sitagliptin as add-on to Metformin in Obese Type 2 Diabetic Patients Younger Than 50 Years
ClinicalTrials.gov study NCT00976937. IPD Sharing: Not stated. Countries: 13. Publications: 0.
MD simulation of POPC bilayer with OPLS3e force field, 50 mM CaCl2 part 2
<p>MD simulation of POPC bilayer with OPLS3e force field, 50 mM CaCl<sub>2</sub> part 2 (500-1000ns)</p> <p>Dataset contains trajectories (_trj) for the last 500ns of the 1000ns trajectory, topology (-out.cms), and other files.</p> <p>For the ease of the upload, trajectory files (_trj) are divided to 100ns pieces and tarred (named desmond_md_cacl50_x-xns.tar.gz)</p> <p>System: POPC bilayer in water</p> <p>Number of lipids: 200 (100/leaflet)</p> <p>Number of waters: 8880</p> <p>Salt: CaCl<sub>2</sub></p> <p>Concentration: 50 mM</p> <p>Number of cations: 8</p> <p>Simulation time: 1000 ns (in this dataset 500-1000ns)</p> <p>Simulation engine: Desmond 2019-4</p> <p>Temperature: 300 K</p> <p>Related dataset: MD simulation of POPC bilayer with OPLS3e force field, 50 mM CaCl<sub>2</sub> part 1</p>
Figure 2 from: Blagoderov V, Hippa H, Nel A (2010) Parisognoriste, a new genus of Lygistorrhinidae (Diptera: Sciaroidea) from the Oise amber with redescription of Palaeognoriste Meunier. ZooKeys 50: 79-90. https://doi.org/10.3897/zookeys.50.506
Figure 2 - Parisognoriste eocenica, sp. n., wing
Figure 2 from: Blagoderov V, Brake I, Georgiev T, Penev L, Roberts D, Ryrcroft S, Scott B, Agosti D, Catapano T, Smith V (2010) Streamlining taxonomic publication: a working example with Scratchpads and ZooKeys. ZooKeys 50: 17-28. https://doi.org/10.3897/zookeys.50.539
Figure 2 - Selecting images to be included in the manuscript.
Using Three Different Doses of Hyperbaric Prilocaine 2% Local Anaesthetic ( 40,50 and 60mg ),Through Spinal Anaesthesia in Knee Arthroscopy Patients to Compare Time to Void
ClinicalTrials.gov study NCT06703580. IPD Sharing: YES. Countries: 1. Publications: 0.
Vildagliptin 50 mg Twice Daily in Patients With Type 2 Diabetes Mellitus Inadequately Controlled With Metformin
ClinicalTrials.gov study NCT01426802. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Serplulimab for Patients With Non-small Cell Lung Cancer (NSCLC) With TPS ≥ 50%: a Prospective, Single-center, Single-arm Phase 2 Study.
ClinicalTrials.gov study NCT06195683. IPD Sharing: NO. Countries: 1. Publications: 0.
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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.