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189 results for “scale development;”
PROSEECO developement, 0.8 scaling, POPC + Na, Ca ions
<p>POPC membrane, 200 lipids, 9000 waters</p> <p>310 K, gromacs 2018</p> <p> </p> <p>Test of 0.8 scaling</p>
Tradeoffs with utility-scale solar development and ungulates on western rangelands
<p>Utility scale solar energy (USSE) has become an efficient and cost-effective form of renewable energy, with an expanding footprint into rangelands that provide important habitat for many ungulate populations. Using GPS data collected before and after construction, we documented the potential impacts of USSE on pronghorn, including direct habitat loss, indirect habitat loss, and barrier effects to both resident and migratory population segments. Our case study highlights the challenges that USSE poses to ungulate conservation, including 1) impermeable security fencing that removes habitat and reduces connectivity, and 2) the lack of guidelines for minimizing solar impacts to ungulates. We encourage agencies and industry to work towards a unified siting process and develop ungulate-specific best management practices to minimize habitat loss and retain landscape connectivity. Ungulate biodiversity and ecosystem services (e.g., long-distance migrations) in arid rangelands are important considerations when balancing the global benefits of renewable energy with local wildlife impacts.</p>
Text-fig. 12. Silutanispermum kvacekiorum gen. et sp. nov. seeds from the Early Cretaceous Famalicão locality (sample 025), Portugal; Synchrotron radiation X-ray tomographic microscopy (SRXTM, orthoslices). a) Longitudinal orthoslice (yz1170) through the median plane of the seed (S170238) in the micropylar region showing exotestal cells lining the micropylar slit (mi) and hilum (hi); note the well-preserved mesotestal cells (me). b) Longitudinal orthoslice (xz0805) of seed perpendicular to the median plane through the micropylar region showing the transverse micropylar slit (mi) lined by radiating exotestal cells; note abundant mesotestal cells (me). c) Transverse orthoslice (xy0768) through seed below hilum and micropyle showing exotesta (ex) and mesotesta (me) that is strongly developed along the raphe (ra) (S174352). d) Transverse orthoslice (xy2113) through middle of the seed showing well-preserved cellular nutritive tissue with empty cells; note that the raphe (ra) is enclosed in mesotestal tissue (S174352). e) Longitudinal orthoslice (yz0970) through seed coat showing exotesta (ex) of tall palisade-shaped cells and thick mesotesta (me) of low cells (S174352). Scale bars = 500 µm (a, c, d); 250 µm (b); 125 µm (e). in Extinct Taxa Of Exotestal Seeds Close To Austrobaileyales And Nymphaeales From The Early Cretaceous Of Portugal
Text-fig. 12. Silutanispermum kvacekiorum gen. et sp. nov. seeds from the Early Cretaceous Famalicão locality (sample 025), Portugal; Synchrotron radiation X-ray tomographic microscopy (SRXTM, orthoslices). a) Longitudinal orthoslice (yz1170) through the median plane of the seed (S170238) in the micropylar region showing exotestal cells lining the micropylar slit (mi) and hilum (hi); note the well-preserved mesotestal cells (me). b) Longitudinal orthoslice (xz0805) of seed perpendicular to the median plane through the micropylar region showing the transverse micropylar slit (mi) lined by radiating exotestal cells; note abundant mesotestal cells (me). c) Transverse orthoslice (xy0768) through seed below hilum and micropyle showing exotesta (ex) and mesotesta (me) that is strongly developed along the raphe (ra) (S174352). d) Transverse orthoslice (xy2113) through middle of the seed showing well-preserved cellular nutritive tissue with empty cells; note that the raphe (ra) is enclosed in mesotestal tissue (S174352). e) Longitudinal orthoslice (yz0970) through seed coat showing exotesta (ex) of tall palisade-shaped cells and thick mesotesta (me) of low cells (S174352). Scale bars = 500 µm (a, c, d); 250 µm (b); 125 µm (e).
Text-fig. 36. Synchrotron radiation X-ray tomographic microscopy (SRXTM, a–e) images of "Paisia-like follicle"; Catefica locality, Portugal. a, b) Volume rendering of follicle in lateral (a) and ventral (b) views showing the decurrent stigmatic region that extends from the follicle base to the apex but lacks a distinct papillate zone; c) Longitudinal section (volume rendering cut at orthoslice yz0341) of follicle showing under-developed ovules towards the base and numerous well-developed ovules/seeds in the upper part suggesting that the follicle is probably mature; d) Dorsal view of follicle apex showing the cleft in the presumed stigmatic apical region; e) Transverse section (orthoslice xy1294) of follicle with one dorsal and two ventral bundles and two placentae bulging into the locule, one on either side of the ventral suture; note the strongly compressed outer epidermis and the homogenized cells of the mesocarp. Specimen, Catefica 49-S174915 (a–e). Scale bars = 300 Μm (a–d), 100 Μm (e). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms
Text-fig. 36. Synchrotron radiation X-ray tomographic microscopy (SRXTM, a–e) images of "Paisia-like follicle"; Catefica locality, Portugal. a, b) Volume rendering of follicle in lateral (a) and ventral (b) views showing the decurrent stigmatic region that extends from the follicle base to the apex but lacks a distinct papillate zone; c) Longitudinal section (volume rendering cut at orthoslice yz0341) of follicle showing under-developed ovules towards the base and numerous well-developed ovules/seeds in the upper part suggesting that the follicle is probably mature; d) Dorsal view of follicle apex showing the cleft in the presumed stigmatic apical region; e) Transverse section (orthoslice xy1294) of follicle with one dorsal and two ventral bundles and two placentae bulging into the locule, one on either side of the ventral suture; note the strongly compressed outer epidermis and the homogenized cells of the mesocarp. Specimen, Catefica 49-S174915 (a–e). Scale bars = 300 Μm (a–d), 100 Μm (e).
Figure 2 in Large-scale snake genome analyses provide insights into vertebrate development
Figure 2. Evolutionary features of snake genomes (A) Chromosome evolution in snakes. A total of 23 proto-chromosomes of Serpentes were reconstructed using four lizards as outgroups (only eight species are shown here for clarity, with more species listed in Figure S2A). (B) Genome size, TE size, and TE type content in chicken, non-snake reptiles (four lizards, one turtle, and one crocodile), and snakes. (C) GC content and CpG island density of snake genomes.
Figure S4 in Large-scale snake genome analyses provide insights into vertebrate development
Figure S4. Genetic bases of snake limb loss, body elongation, lung asymmetry, and eye structure simplification, related to Figures 3 and 4 (A) Multiple alignments of PTCH1. Fish, mammals, frogs, birds, crocodiles, turtles, lizards, and snakes are indicated in different colors. (B) CPLANE1 multiple alignments. The gene structure is outlined by the black line with yellow blocks representing CDSs. The position span is obtained based on the European glass lizard reference genome. The ''378–381'' and ''473'' show the positions of snake-specific missing amino acids. The ''His472Try'' and ''Gln474Glu'' indicate the two snake-specific amino acid mutations. (C) Relative body mass and relative body length of WT mice and PTCH1-mutated mice with snake deletion. Mean ± SD is shown by error bar. (D) Microstructural characteristics of the proximal shinbone (colored in red) in 1-week-old WT mice and PTCH1-mutated mice with snake deletion. The trabecular bone volume (BV) and bone volume per tissue volume (BV/TV) of WT type and PTCH1-mutated mice. Significantly smaller *p <0.05 (independent Student's t test). Mean ± SD is shown by error bar. (E) Statistics of phalanx relative length (absolute length divided by body length) in WT mice and PTCH1-mutated mice with snake deletion. Mutated mice had significantly shorter fourth forelimb phalanx (n = 8, *p <0.05, independent Student's t test) and third hindlimb phalanx (n = 8, *p <0.05, independent Student's t test). Mean ± SD is shown by error bar. (F) Expressions of genes related to limb development in stage E11.5 forelimb bud (left) and hindlimb (right) of WT mice and PTCH1-mutated mice with snake deletion. (G) The 17-bp deletion of snake ZRS enhancer in our newly sequenced snakes. (H) Expression levels of somite development-related genes (under positive selection) in P. dhumnades (40 days post oviposition). (I) AP3B1 multiple alignments of snakes and outgroup. The gene structure is outlined by the black line with orange sticks representing CDSs and the numbers indicating the position span according to the European glass lizard reference genome. The positions of snake lost amino acids residues are indicated by the interval number ''796–800.''and number "802". (J) Example of differentially expressed genes (DEGs) between embryonic left and right lungs (40 days post oviposition) of P. dhumnades. The significance is indicated as *p <0.05, **p <0.01, or ***p <0.001. Mean ± SD is shown by error bar. (K) The SD-CNE located at ~13 kb downstream of YAP1. The identities (compared with the 31 reptile species ancestor sequence) of the SD-CNE were decreasing along the evolution of snakes. (L) A SSSV inserted to the 5 kb upstream of the TITF1 transcriptional start site. The SSSV was predicted to have one binding site of HOXA5 transcription factor. Heatmap (left) displays the expressions (log10(quantiled FPKMs)) of HOXA5 and TITF1 in lung, liver, heart, and muscle of green anole (Acar), keeled slug snake (Pber), and many-banded krait (Bmul). TITF1 and HOXA5 were highly expressed in the lung of all species but the expressions of TITF1 were significantly higher in the two snakes than in green anole (Student's t test p values: 0.0048 [Pber] and 0.0077 [Bmul]). (M) Snake-specific amino acid residues loss of CC2D2A. The black line layouts the gene structure with blue sticks representing CDSs and the numbers indicating the position span based on the European glass lizard reference genome. The interval number ''41–74'' points out the sites of lost amino acid residues in CC2D2A based on European glass lizard sequence. The lost amino acid residues were indicated in red on 3D structure.
Development and Validation of a Scale to Measure Fear of ACTivity in Patients With Coronary Artery Disease
ClinicalTrials.gov study NCT03858829. IPD Sharing: UNDECIDED. Countries: 0. Publications: 1.
Community Development Teams to Scale-Up Multidimensional Treatment Foster Care (MTFC) in California
ClinicalTrials.gov study NCT00880126. IPD Sharing: Not stated. Countries: 0. Publications: 3.
Development of a Qualitative Scale to Asses the Acceptability of Percutaneous Techniques. A Delphi Study
ClinicalTrials.gov study NCT07380100. IPD Sharing: YES. Countries: 1. Publications: 0.
Development and Validation of the Air Quality Awareness Scale (AQAS) for Parents
ClinicalTrials.gov study NCT07283250. IPD Sharing: NO. Countries: 1. Publications: 0.
Development of a Constipation Risk Assessment Scale for Hospitalized Patients.
ClinicalTrials.gov study NCT04068415. IPD Sharing: NO. Countries: 0. Publications: 0.
Turkish Affordances in the Home Environment for Motor Development-Infant Scale (AHEMD-IS)
ClinicalTrials.gov study NCT04556487. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.
Data from: The Urban Heat Island and its spatial scale dependent impact on survival and development in butterflies of different thermal sensitivity
Open the record for dataset details and reuse information.
Tradeoffs with utility-scale solar development and ungulates on western rangelands
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Data from: Does the cost of development scale allometrically with offspring size?
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Developing and validating the psychosocial burden among people seeking abortion scale (PB-SAS)
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Postnatal Development is Associated with Genome-scale Changes in DNA Methylation in Mouse Liver
GEO Series GSE79775. Mus musculus. 104 samples. Type: Methylation profiling by high throughput sequencing.
Leveraging large-scale datasets and single cell omics data to develop a polygenic score for cisplatin-induced ototoxicity
GEO Series GSE281324. Mus musculus. 4 samples. Type: Expression profiling by high throughput sequencing.
Postnatal Development is Associated with Genome-scale Changes in DNA methylation in Mouse Liver
GEO Series GSE58129. Mus musculus. 55 samples. Type: Methylation profiling by high throughput sequencing.
Multi-scale 3D genome rewiring during mouse neural development
GEO Series GSE96107. Mus musculus. 92 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Other.
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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.