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1,140 results for “TOPS”
Data used for publication on 'Analysis of blue corona discharges at the top of tropical thunderstorm clouds in different phases of convection'
<p>This data was used from implementing Figures 1-4 in the main manuscript and all the Figures in the Supportive Information of the submitted publication 'Analysis of blue corona discharges at the top of tropical thunderstorm clouds in different phases of convection'.</p>
FIGURE 5. Pestalotiopsis hydei. a. Colony top view. b. Colony reverse view. c in Additions to pestalotioid fungi in Thailand: Neopestalotiopsis hydeana sp. nov. and Pestalotiopsis hydei sp. nov.
FIGURE 5. Pestalotiopsis hydei. a. Colony top view. b. Colony reverse view. c. Conidiomata on PDA. d–e. Conidiogenous cells. f–k. Conidia. Scale bars d, e = 10 µm, f–k = 20 µm.
FIGURE 3. Neopestalotiopsis hydeana. a. Colony top view. b. Colony reverse view. c in Additions to pestalotioid fungi in Thailand: Neopestalotiopsis hydeana sp. nov. and Pestalotiopsis hydei sp. nov.
FIGURE 3. Neopestalotiopsis hydeana. a. Colony top view. b. Colony reverse view. c. Conidiomata on PDA. d–f. Conidiogenous cells. g–k. Conidia. Scale bars d = 20 µm, e–g = 10 µm, h–k = 10 µm.
FIGURE. Typical habitats of Ramalina species on northern South America. A. High paramo, Laguna Anteojos, Sierra Nevada de Merida, where grows on rocks R. anteojina at 4100 m. B. Sub-paramo (timberline), La Aguada, Sierra Nevada de Merida, 3100 m, where are found R. dictyota and R. reducta on shrubs. C. Andean cloud forest, La Victoria, Sierra Nevada de Merida where R. cochlearis, R. cumanensis and R. victoriana are found growing as epiphytes. D. Populations of R. usnea, R. morrocoyensis and R. paradisensis growing as epiphytes on mangroves and Suriana maritima at sea level, National Park Morrocoy, state Falcón; the latter two species are known only from this locality. E. Ramalina usnea is the only species of this genus reported from the Alto Orinoco, Amazonas, near La Esmeralda, 150 m, growing as corticolous in submontane forests, at the top of the picture the Cerro Duida. F. Xerophytic forests from the National Park Cerro Santa Ana, state Falcón, where Ramalina santanensis and R. microphylla are known only growing on soil and rocks at 200–400 m. Photos V. Marcano. in The genus Ramalina Acharius (Ascomycota, Lecanoromycetes, Ramalinaceae) in northern South America
FIGURE. Typical habitats of Ramalina species on northern South America. A. High paramo, Laguna Anteojos, Sierra Nevada de Merida, where grows on rocks R. anteojina at 4100 m. B. Sub-paramo (timberline), La Aguada, Sierra Nevada de Merida, 3100 m, where are found R. dictyota and R. reducta on shrubs. C. Andean cloud forest, La Victoria, Sierra Nevada de Merida where R. cochlearis, R. cumanensis and R. victoriana are found growing as epiphytes. D. Populations of R. usnea, R. morrocoyensis and R. paradisensis growing as epiphytes on mangroves and Suriana maritima at sea level, National Park Morrocoy, state Falcón; the latter two species are known only from this locality. E. Ramalina usnea is the only species of this genus reported from the Alto Orinoco, Amazonas, near La Esmeralda, 150 m, growing as corticolous in submontane forests, at the top of the picture the Cerro Duida. F. Xerophytic forests from the National Park Cerro Santa Ana, state Falcón, where Ramalina santanensis and R. microphylla are known only growing on soil and rocks at 200–400 m. Photos V. Marcano.
FIGURE 1. Myrcia excelsa. A. fruiting branch. B. flowering branch. C. flower bud, top view. D. open flower. E. fruit, side view. F. fruit, top view. G. embryo. H in Myrcia excelsa (Myrtaceae), a new species from Espírito Santo, Brazil
FIGURE 1. Myrcia excelsa. A. fruiting branch. B. flowering branch. C. flower bud, top view. D. open flower. E. fruit, side view. F. fruit, top view. G. embryo. H. flower bud, side view (A,G: D.A. Folli 5360; B,H: D.A. Folli 81; C: G.L. Farias 274; D: M. Gibran 138; E,F: D.A.Folli 6650). All photographs taken from material deposited at the SORO herbarium.
FIGURE. Inflorescence of Hylaeaicum. A. H. myrmecophilum (Leme 2555). B. H. levianum (Leme 5639-A). C–D. H. wurdackii (Leme 2567). C. Top view. D. Outer primary fascicle, with secondary fascicles indicated by an arrow. E–G. H. eleutheropetalum var. eleutheropetalum (Leme 4491). E. Top view. F. Secondary fascicles indicated by an arrow. G. Outer primary fascicles, with secondary fascicles indicated by an arrow. H. H. margaretae (Leme 2331). I. H. tarapotoense (Leme 1977). J. H. aff. myrmecophilum (Leme 3487). K. H. pendulum (Leme 1979). in Re-evaluation of the Amazonian Hylaeaicum (Bromeliaceae: Bromelioideae) based on neglected morphological traits and molecular evidence
FIGURE. Inflorescence of Hylaeaicum. A. H. myrmecophilum (Leme 2555). B. H. levianum (Leme 5639-A). C–D. H. wurdackii (Leme 2567). C. Top view. D. Outer primary fascicle, with secondary fascicles indicated by an arrow. E–G. H. eleutheropetalum var. eleutheropetalum (Leme 4491). E. Top view. F. Secondary fascicles indicated by an arrow. G. Outer primary fascicles, with secondary fascicles indicated by an arrow. H. H. margaretae (Leme 2331). I. H. tarapotoense (Leme 1977). J. H. aff. myrmecophilum (Leme 3487). K. H. pendulum (Leme 1979).
Text-fig. 11. Cheek teeth of Sayimys giganteus from Keseköy. Anterior sides are indicated by arrows. Top row: labial sides of M3, M2, M1 and DP4, images horizontally-mirrored. Second row: occlusal surfaces of M3, M2, M1 and DP4 of the same specimens. Third row: lingual sides of m3, m2, m1 and dp4, images horizontally-mirrored. Lower row: occlusal surfaces of m3, m2, m1 and dp4 of the same specimens. in An Exceptional Large Sample Of The Early Miocene Ctenodactyline Rodent Sayimys Giganteus, Specific Variation And Taxonomic Implications
Text-fig. 11. Cheek teeth of Sayimys giganteus from Keseköy. Anterior sides are indicated by arrows. Top row: labial sides of M3, M2, M1 and DP4, images horizontally-mirrored. Second row: occlusal surfaces of M3, M2, M1 and DP4 of the same specimens. Third row: lingual sides of m3, m2, m1 and dp4, images horizontally-mirrored. Lower row: occlusal surfaces of m3, m2, m1 and dp4 of the same specimens.
Code & Data for "Adoption of Transparency and Openness Promotion (TOP) guidelines across journals"
<p>This entry contains code and data that was used in the publication: "Adoption of Transparency and Openness Promotion (TOP) guidelines across journals" submitted in Publications journal.</p> <p>*It was version 2 when we added Fig_3_Tab2_Defining_science_disciplines_plus_plot.R script to version 1.</p> <p>*It was version 3 because we added script that calculates median and mean values of the stringency levels to version 2 data.</p> <p>*Latest version is version 4: we added supplementary data.</p> <p>#IDEA:</p> <p>This project was about analyzing policies of two thousand journals within the framework of eight TOP standards: <br> data citation, transparency of data, material, code and design and analysis, replication, plan and study pre-registration, <br> and two effective interventions: “Registered reports” and “Open science badges”. </p> <p># MATERIALS & METHODS<br> We downloaded the TOP Factor (v33, 2022-08-29 3:12 PM) metric from the https://osf.io/kgnva/files/osfstorage/5e13502257341901c3805317 <br> website and analyzed its content with an in-house R script (in this repo):<br> 1) SCRIPT: fig1_Analyzing_journals_policies_and_TOP_guidelines.R<br> 2) SCRIPT: Figure2a_b_TOP_impl_journal_statistist_0_1_piechart_barplot.R<br> In order to get statistics about implementation of the TOP guidelines across discipline-specific journals, <br> we extracted information about journal’s disciplines from the Scopus content database. <br> We downloaded SCOPUS content coverage from the https://www.elsevier.com/solutions/scopus/how-scopus-works/content?dgcid=RN_AGCM_Sourced_300005030 (existJuly2022.xlsx)<br> and used the first Sheet.<br> We identified match between those 2 tables: <br> 3) SCRIPT: Rscript_overlapping_TOP_dataframe_and_SCOPUS_db.R<br> And resulted in Overlap_SCOPUS_TOP.rds file<br> And performed visualization and statistics:<br> 4) SCRIPT: Fig_3_Tab2_Defining_science_disciplines_plus_plot.R</p> <p> </p> <p>#RESULTS Submitted to Publications 30.9.2022.</p> <p>Reviewed 2.11.2022.</p> <p>Latest version: 25.11.2022.</p>
Source data for "Inhibitory top-down projections from zona incerta mediate neocortical memory"
<p>These files contain the data that are presented in the figures in the article: "Inhibitory top-down projections from zona incerta mediate neocortical memory".</p>
Data for "Nonagenarian men and women in Switzerland at the end of the 19th century: Inspecting verified outliers at the top end of the historical age distribution"
<p>Datasets underlying the analysis of the paper: "Nonagenarian men and women in Switzerland at the end of the 19th century: Inspecting verified outliers at the top end of the historical age distribution"</p> <ul> <li><strong>Data_1888_1900.xlsx</strong> : Individual data of persons aged 90 and older from the 1888 and 1900 censuses</li> <li><strong>Cofactors.xlsx</strong> : Ecological co-factors for each Swiss district</li> </ul>
Highly variable (no clear pattern). All portions of the dorsal views were equally used. In head images the area around the eye, the top of the head, the snout and the throat were all used in similar proportions. P. carbonelli Variable for both views. Snout and middle of the dorsum used in dorsal view. Top of the head most frequently (but not strictly) used in lateral view. P. guadarramae Whole body used for dorsal view (but variable); either throat (most common) or ear region used in head lateral views. P. hispanicus Variable. Anterior portion of snout used more frequently than in other species for both dorsal and head lateral views. P. liolepis Highly variable. Whole body used in most dorsal images, area around the eye and throat used in head lateral views, but other patterns common. P. lusitanicus Highly variable. All parts of the dorsum used (but frequently the most posterior part); area around the ear frequently used in head lateral images. P. tunesiacus Highly variable. Dorsal area near the insertion of the posterior limbs used more frequently than in other species; different regions of the head used, often simultaneously. P. Ʋaucheri Highly variable. Different regions of dorsum (from head to the posterior region) used in dorsal images, all portions of the head, but most frequently the throat, used in lateral images. P. Ʋirescens Highly variable. All parts of both images used. Head and anterior part of the dorsum more used than in other species. in Identification of morphologically cryptic species with computer vision models: wall lizards (Squamata: Lacertidae: Podarcis) as a case study
Highly variable (no clear pattern). All portions of the dorsal views were equally used. In head images the area around the eye, the top of the head, the snout and the throat were all used in similar proportions. P. carbonelli Variable for both views. Snout and middle of the dorsum used in dorsal view. Top of the head most frequently (but not strictly) used in lateral view. P. guadarramae Whole body used for dorsal view (but variable); either throat (most common) or ear region used in head lateral views. P. hispanicus Variable. Anterior portion of snout used more frequently than in other species for both dorsal and head lateral views. P. liolepis Highly variable. Whole body used in most dorsal images, area around the eye and throat used in head lateral views, but other patterns common. P. lusitanicus Highly variable. All parts of the dorsum used (but frequently the most posterior part); area around the ear frequently used in head lateral images. P. tunesiacus Highly variable. Dorsal area near the insertion of the posterior limbs used more frequently than in other species; different regions of the head used, often simultaneously. P. Ʋaucheri Highly variable. Different regions of dorsum (from head to the posterior region) used in dorsal images, all portions of the head, but most frequently the throat, used in lateral images. P. Ʋirescens Highly variable. All parts of both images used. Head and anterior part of the dorsum more used than in other species.
Highly variable. Mid-portion of the dorsum used frequently (although other areas as well). Tip of the snout used often, but area around the ear and throat are also relevant. P. carbonelli Variable. In the dorsal view, the tip of the snout is frequently used. In the head lateral view, the tip of the snout is also com- monly used, as well as the most posterior region of the head. P. guadarramae Variable. Mid portion of the dorsum and tip of the snout are the regions used more frequently in dorsal and head lateral views, respectively. P. hispanicus Variable. The head and most anterior part of the dorsum are frequently used in the dorsal view. Snout and/or top of posterior region of head used. P. liolepis Variable. Different parts of the dorsum are used, whereas the tip of the snout is used in most head lateral images. P. lusitanicus Anterior dorsum, in the dorsal view, and both snout and posterior side of the head (in head lateral views) frequently used. P. tunesiacus Variable. Tip of the snout and posterior part of the trunk more used than in other species; snout and top head region behind the eye used with some frequency. P. Ʋaucheri Highly variable. All parts of the dorsum used in dorsal images, various parts of the head (but frequently snout and throat combined) used in head lateral images. P. Ʋirescens Highly variable. All portions of the dorsum used in dorsal images, region around and behind the ear more used than in other species for head lateral images. in Identification of morphologically cryptic species with computer vision models: wall lizards (Squamata: Lacertidae: Podarcis) as a case study
Highly variable. Mid-portion of the dorsum used frequently (although other areas as well). Tip of the snout used often, but area around the ear and throat are also relevant. P. carbonelli Variable. In the dorsal view, the tip of the snout is frequently used. In the head lateral view, the tip of the snout is also com- monly used, as well as the most posterior region of the head. P. guadarramae Variable. Mid portion of the dorsum and tip of the snout are the regions used more frequently in dorsal and head lateral views, respectively. P. hispanicus Variable. The head and most anterior part of the dorsum are frequently used in the dorsal view. Snout and/or top of posterior region of head used. P. liolepis Variable. Different parts of the dorsum are used, whereas the tip of the snout is used in most head lateral images. P. lusitanicus Anterior dorsum, in the dorsal view, and both snout and posterior side of the head (in head lateral views) frequently used. P. tunesiacus Variable. Tip of the snout and posterior part of the trunk more used than in other species; snout and top head region behind the eye used with some frequency. P. Ʋaucheri Highly variable. All parts of the dorsum used in dorsal images, various parts of the head (but frequently snout and throat combined) used in head lateral images. P. Ʋirescens Highly variable. All portions of the dorsum used in dorsal images, region around and behind the ear more used than in other species for head lateral images.
Fig. 6. Overlapped top-scored poses for ligands 19 in Monoterpene indole alkaloids from Vinca minor L. (Apocynaceae): Identification of new structural scaffold for treatment of Alzheimer's disease
Fig. 6. Overlapped top-scored poses for ligands 19 (blue) and crystal structure of tacrine (green) in the active site of hBuChE (PDB ID: 4BDS). Amino acid residues involved in the interactions with ligands are depicted as either grey or yellow (catalytic triad) lines. The rest of the receptor is displayed in light-grey cartoon conformation. The Figure was created with The PyMOL Molecular Graphics System, Version 2.4.1, Schr¨odinger, LLC. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Fig. 4. Top 10 in In silico approach on sequential and structural variability in oryzacystatin and its interaction with cysteine protease enzymes of insect
Fig. 4. Top 10 protein-protein interaction of oryzacystatins and cysteine protease enzymes based on docking scores. A) OC XI – cathepsin B. B) OC II – cathepsin B. C) OC IV – cathepsin B. D) OC IV – cathepsin O2 like. E) OC III – cathepsin B. F) OC IV – caspase 1. G) OC I – cathepsin B. H) OC V – cathepsin F like. I) OC VI – cathepsin B. J) OC XI – cathepsin O2 like protease enzyme. The protease cathepsin B showed the interaction in the wedge region of OC I (G), OC II (B), OC III (E), OC IV (C), OC VI (I) and OC XI (A). OC IV showed higher docking score with caspase 1 (F) and cathepsin O2 like (D), similarly, OC V and OC XI interacted with cathepsin F like (H) and cathepsin O2 (J) like respectively. The hydrogen bond between the oryzacystatins and cysteine protease enzymes are shown in dotted line (—). Structural graphics were produced by using BIOVIA Discovery studio visualizer software, version 20.1.0.
B9219 Top
Source: Objaverse 1.0 / Sketchfab
ITC Focus 12 Set-top Box
Cable Box from Manhattan Cable. Source: Objaverse 1.0 / Sketchfab
Cognitive Remediation in Schizophrenia: Efficacy and Role of Neuroplasticity in "Top-down" and "Bottom-up" Mechanisms
ClinicalTrials.gov study NCT06482918. IPD Sharing: Not stated. Countries: 1. Publications: 18.
Phase Ib First in Human Dose Escalation of GT103 in Refractory, Advanced Stage Non-Small Cell Lung Cancer (TOP 1902)
ClinicalTrials.gov study NCT04314089. IPD Sharing: NO. Countries: 1. Publications: 1.
A Study Select Top-grade Embryo by Time-lapse Imaging
ClinicalTrials.gov study NCT02965222. IPD Sharing: Not stated. Countries: 1. Publications: 3.
Top-down Infliximab Study in Kids With Crohn's Disease
ClinicalTrials.gov study NCT02517684. IPD Sharing: Not stated. Countries: 3. Publications: 4.
ScienceDex guides
Understand access before you commit
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.