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2,453 results for “Architecture”
Figure 4. Neochlamisus bebbianae I in Faecal case architecture in the gibbosus species group of Neochlamisus Karren, 1972 (Coleoptera: Chrysomelidae: Cryptocephalinae: Chlamisini)
Figure 4. Neochlamisus bebbianae I: Salix bebbianae (willow) host form. A, instar-I case, lateral aspect. B, instar-I case, ventral aspect. C, instar-II case, dorsal aspect. D, instar-II case, lateral aspect, scanning electron micrograph. E, instar-IV case, lateral aspect. F, instar-IV case, trichomes on external surface. G, instar-IV case, internal surface. H, instar-IV case, wall section showing trichome–faecal matrix.
Figure 3. Neochlamisus bebbianae I in Faecal case architecture in the gibbosus species group of Neochlamisus Karren, 1972 (Coleoptera: Chrysomelidae: Cryptocephalinae: Chlamisini)
Figure 3. Neochlamisus bebbianae I: Salix bebbianae (willow) host form. A, case series from egg case (left) to pupal case (right). B, egg case, lateral aspect, scanning electron micrograph. C, egg case, scanning electron micrograph.
Figure 12. Neochlamisus chamaedaphnes. A, adult habitus. B in Faecal case architecture in the gibbosus species group of Neochlamisus Karren, 1972 (Coleoptera: Chrysomelidae: Cryptocephalinae: Chlamisini)
Figure 12. Neochlamisus chamaedaphnes. A, adult habitus. B, case series from egg case (left) to pupal case (right). C–G, scanning electron micrographs. C, egg case, lateral aspect. D, egg case surface with trichomes. E, instar-I case, lateral aspect. F, instar-I case, egg section showing faecal plates. G, instar-I case, larval section with faecal rows.
Figure 10. Neochlamisus bebbianae IV in Faecal case architecture in the gibbosus species group of Neochlamisus Karren, 1972 (Coleoptera: Chrysomelidae: Cryptocephalinae: Chlamisini)
Figure 10. Neochlamisus bebbianae IV: Acer (maple) host form. A, instar-II case, ventral aspect. B, instar-II case, lateral aspect, orientation of faecal rows, scanning electron micrograph. C, Instar-III case, lateral aspect. D, instar-III case, base opening. E, instar-III case, ventral faecal wedge at base, scanning electron micrograph. F, instar-III case, internal surface, scanning electron micrograph. G, larval instar-IV, lateral aspect. H, Pupal case, lateral aspect.
Figure 7 in Faecal case architecture in the gibbosus species group of Neochlamisus Karren, 1972 (Coleoptera: Chrysomelidae: Cryptocephalinae: Chlamisini)
Figure 7. Neochlamisus bebbianae III: Betula (river birch) host form. A, adult habitus. B, case series from egg case (left) to pupal case (right). C–F, egg case, scanning electron micrographs. C, lateral aspect. E–F, external surface.
Figure 9. Neochlamisus bebbianae IV in Faecal case architecture in the gibbosus species group of Neochlamisus Karren, 1972 (Coleoptera: Chrysomelidae: Cryptocephalinae: Chlamisini)
Figure 9. Neochlamisus bebbianae IV: Acer (maple) host form. A, adult habitus. B, case series from egg case (left) to pupal case (right). Instar-II case: broken. C, egg case, with twisted egg stalk. D, egg-case roof sealed. E, egg-case roof unsealed by instar-I larva. F, instar-I case, egg stalk intact. G–I, scanning electron micrographs. G, instar-I case, internal aspect. H, instar-I case, cross-section of apex showing faecal matrix. I, instar-I case, cross-section of wall showing dense faecal matrix.
Figure 6. Neochlamisus bebbianae II in Faecal case architecture in the gibbosus species group of Neochlamisus Karren, 1972 (Coleoptera: Chrysomelidae: Cryptocephalinae: Chlamisini)
Figure 6. Neochlamisus bebbianae II: Alnus (alder) host form. A, adult habitus with prothorax unnaturally distended while preserved. B, case series from egg case (left) to pupal case (right). C, egg case apex showing egg stalk. D, egg case, sealed roof. E, instar-I case, lateral aspect. F, instar-II case, ventral aspect. G, instar-IV case, lateral aspect. H, pupal case, dorsolateral aspect. I–J, pupal case, surface textures, scanning electron micrographs.
Why choose Art and architecture tours in St Petersburg?
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Arabidopsis HapMap screen for salt-induced changes in root architecture and root:shoot ratio - images BA4 experiment
<p>Images of scanned agar plates collected for Arabidopsis accessions exposed to salt stress / control treatment. The data were collected during PhD of Magdalena Julkowska at University of Amsterdam, under supervision of Dr. Christa Testerink. </p>
Arabidopsis HapMap screen for salt-induced changes in root architecture and root:shoot ratio - images BA5 experiment
<p>Images of scanned agar plates collected for Arabidopsis accessions exposed to salt stress / control treatment. The data were collected during PhD of Magdalena Julkowska at University of Amsterdam, under supervision of Dr. Christa Testerink. </p>
Network of reference tree-ring chronologies for forensic botanical (dendrochronological) examinations and dating of architectural structures in the Tyva Republic.
<p>The database consists of tables. First sheet - general description of tree-ring chronologies (general information: name of chronology, authors, data type, tree-ring parameter, notes, key words; description of sample collection site: site name, location, region, latitude, longitude, height; description of sample collection: collection code designation, number of series, year of first ring, year of last ring, maximum length of sample, average width of year ring; species affiliation - species; support - grant number). Second sheet, first column - years, second column - standardized growth value. The third sheet is a PDF document containing the results of independent testing in the program COFECA (the file is opened by the command: right-click/Acrobat Document object/open). The database is implemented in the OpenOffice.org Calc spreadsheet processor. The table file format is an internal OpenOffice.org Calc format, with the extension .ods. The data is accessed and structured using the standard tools "Sort", "Autofilter", etc. In the database, the integrity restriction control is not implemented, the user is invited to monitor the integrity of the database himself. Computer type: IBM PC. PC; OS: Windows 10.</p> <p>Type and version of the database management system: OpenOffice.org Calc.</p> <p>Database size: 5.6 MB</p>
Molecular architecture of nucleosome remodeling and deacetylase sub-complexes by integrative structure determination
<p>Drawing on information from SEC-MALLS, DIA-MS, XLMS, negative-stain EM, X-ray crystallography, NMR spectroscopy, secondary structure predictions, and homology models, we applied Bayesian integrative structure determination to investigate the molecular architecture of three NuRD sub-complexes: MTA1-HDAC1-RBBP4 (MHR), MTA1<sup>N</sup>-HDAC1-MBD3<sup>GATAD2CC</sup> (MHM), and MTA1-HDAC1-RBBP4-MBD3-GATAD2A (NuDe). The present dataset pertains to the results of this study.</p>
Dataset related to: Empagliflozin protects glomerular endothelial cell architecture in experimental diabetes through the VEGF-A/caveolin-1/PV-1 signaling pathway
<p>The files contain all the dataset included in the manuscript divided by figures.</p> <p>Abstract<br> In addition to having blood glucose-lowering effects, inhibitors of sodium glucose cotransporter 2 (SGLT2) afford renoprotection in diabetes. We sought to investigate which components of the glomerular filtration barrier could be involved in the antiproteinuric and renoprotective effects of SGLT2 inhibition in diabetes. BTBR (black and tan, brachyuric) <em>ob/ob</em> mice that develop a type 2 diabetic nephropathy received a standard diet with or without empagliflozin for 10 weeks, starting at 8 weeks of age, when animals had developed albuminuria. Empagliflozin caused marked decreases in blood glucose levels and albuminuria but did not correct glomerular hyperfiltration. The protective effect of empagliflozin against albuminuria was not due to a reduction in podocyte damage as empagliflozin did not affect the larger podocyte filtration slit pore size nor the defective expression of nephrin and nestin. Empagliflozin<br> did not reduce the thickening of the glomerular basement membrane. In BTBR <em>ob/ob</em> mice, the most profound abnormality seen using electron microscopy was in the endothelial aspect of the glomerular capillary, with significant loss of endothelial fenestrations. Remarkably, empagliflozin ameliorated the subverted microvascular endothelial ultrastructure. Caveolae and bridging diaphragms between adjacent endothelial fenestrae were seen in diabetic mice and associated with increased expression of caveolin-1 and the appearance of PV-1. These endothelial abnormalities were limited by the SGLT2 inhibitor. Although no expression of SGLT2 was found in glomerular endothelial cells, SGLT2 was expressed in the podocytes of diabetic mice. VEGF-A, which is a known stimulus for endothelial caveolin-1 and PV-1, was increased in podocytes of BTBR <em>ob/ob</em> mice and normalized by SGLT2 inhibitor treatment.<br> Thus, empagliflozin’s protective effect on the glomerular endothelium of diabetic mice could be due to a limitation of the paracrine signaling of podocyte-derived VEGF-A that resulted in a reduction of the abnormal endothelial caveolin-1 and PV-1, with the consequent preservation of glomerular endothelial function and permeability.</p>
A Novel Architecture for room temperature microwave optomechanical experiments
<p>The dataset contains cavity optomechanical measurements of the Si<sub>3</sub>N<sub>4</sub> membrane at room temperature. These datasets correspond to different techniques to extract single photon coupling rate g<sub>0</sub>. The files with the name starting with fig_2 are about the characterization of the microwave cavity (S<sub>21</sub>) and Si<sub>3</sub>N<sub>4</sub> membrane (noise spectrum). The file names with initials as fig_3 is contains data of noise spectrum when Si<sub>3</sub>N<sub>4</sub> membrane is driven by white noise using piezoelectric transducer. It is the file names with initials as fig_4 that are about the optically induced transparency/absorption, while the file names with initials as fig_5 are about the driven nonlinear Si<sub>3</sub>N<sub>4</sub> membrane.</p>
Fig. 1 in The architecture of the physid musculature of Physa acuta Draparnaud, 1805 (Gastropoda: Physidae)
Fig. 1. (A) Dorsal view of P. acuta with all visceral structures removed to show the broad insertion of the physid muscle s.s. (Pm) in the columellar muscle (Cm) in the snail foot. The Cm has two pedal horns that run anteriorly towards the head while the thicker posterior part runs a short distance towards the tail. The anterior horns start as thick bundles but taper as they near the head. (B) Dorsal view of P. acuta with its visceral hump removed to show the Pm and its five branches numbered Pm1–5. Pm1 runs anteriorly from the origin to the neck and head, Pm2 across the neck to the left hand side of the head, Pm3 and Pm4 descend to the left side of the body and Pm5 wraps around the Cm before passing anteriorly, also to the left hand side of the body. The columellar muscle was not drawn but is located inside the loop made by Pm5. (C) Dorsolateral view of P. acuta with the skin and visceral hump removed. The branches of the Pm are seen coming from right to left over the anterior part of body, intertwining as they do so with Cm fibres that run from the middle to the anterior part of the body. Pm fibres are overlain by Cm fibres. (D) Lateral view of P. acuta showing the location of Pm branches 2–5 within the snail body where they overlie each other. Pm1 is obscured. The fan muscle (Pf) radiates posteriorly from its origin on the physid muscle s.s. (Pm) to a diffuse insertion beneath the mantle.
Fig. 4 in The architecture of the physid musculature of Physa acuta Draparnaud, 1805 (Gastropoda: Physidae)
Fig. 4. (A) Lateral view of P. acuta showing the columellar muscle (Cm) and its relationship with the female and male pores. Also shown are Cm branches running towards the head and side, the insertion of Cm into the foot and the posterior part of the Cm that attaches to the shell. (B) Lateral view of P. acuta showing the relationship between the Pm (dotted line), the Cm, fan muscle (Pf) and the pneumostome–mantle band" of fibres (Pp) on the roof of the mantle. (C) Dorsal view of P. acuta (visceral hump removed) showing the relationship between the branches Pm2–Pm5 of the physid muscle s.s. associated with the 'cervical septum' (dotted lines) and the columellar muscle (Cm).
Fig. 2 in The architecture of the physid musculature of Physa acuta Draparnaud, 1805 (Gastropoda: Physidae)
Fig. 2. (A) Dorsal view of P. acuta showing the muscles overlying the lung floor, viz. thin bands of fibres (Plu) from the main trunk of the physid muscle s.s. (Pm) and from the columellar muscle (Cm). The anterior corner of the pneumostome is indicated in the lower mid-portion of the visceral hump but is not drawn. (B) Lateral view of P. acuta showing the pneumostome–mantle band of muscle fibres (Pp). This band runs from the left anterior part of the mantle roof (i.e. the anterior corner of the pneumostome) towards the right hand side of the roof, anchoring on the fan muscle (see also Fig. 2C). (C) Floor of the mantle cavity after removal of the lung tissue, showing in its mid-portion the pneumostome–mantle band of muscle fibres (Pp) that seems to give support to the opening of the pneumostome. The uppermost of these fibres converge at the edge of the mantle collar and immediately below are those (removed) that support the kidney.
Fig. 3 in The architecture of the physid musculature of Physa acuta Draparnaud, 1805 (Gastropoda: Physidae)
Fig. 3. (A) Transverse view of the body at the level of the lung floor as seen from below showing the physid muscle s.s. (Pm) and columellar muscle (Cm). Fibres from the Pm (Plu) and columellar muscle (Cm) cross the lung floor (fine detail indicated in upper right hand corner of the lung floor). The lung floor is surrounded by mantle collar tissue. (B) Dorsal view of P. acuta with the visceral hump removed to show the dorsal components of the columellar muscle (Cm). These have been flattened slightly. No detail is shown on the lung floor. (C) Above – dissection of the columellar muscle (Cm) and its four elements (slightly flattened). Below – detail of Cm overlying Pm4 and Pm5 fibres as they pass into the foot.
Petrucco et al, Neural dynamics and architecture of the heading direction circuit in a vertebrate brain [Dataset]
<p>Data supporting the paper <a href="https://www.biorxiv.org/content/10.1101/2022.04.27.489672v1.full">Neural dynamics and architecture of the heading direction circuit in a vertebrate brain</a>. </p>
Architecture-based Uncertainty Impact Analysis to ensure Confidentiality - Data Set
<p>Data set of the Paper "Architecture-based Uncertainty Impact Analysis to ensure Confidentiality". For more information, please see the README.md. For more information please visit https://abunai.dev</p>
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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.