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FIGURE 11 in Collection management and study of microscope slides: Storage, profiling, deterioration, restoration procedures, and general recommendations
FIGURE 11. Chemical structure of the more volatile ingredients of Venetian turpentine from Larix decidua. Ac, acetyl.
FIGURE 7 in Collection management and study of microscope slides: Storage, profiling, deterioration, restoration procedures, and general recommendations
FIGURE 7. Chemical structure of the ingredients of sandarac resin from Tetraclinis articulata in Euparal. Me, methyl.
FIGURE 9 in Collection management and study of microscope slides: Storage, profiling, deterioration, restoration procedures, and general recommendations
FIGURE 9. Chemical structure of the potential ingredients of styrax or storax resin from Liquidambar orientalis. Me, methyl.
FIGURE 3 in Collection management and study of microscope slides: Storage, profiling, deterioration, restoration procedures, and general recommendations
FIGURE 3. Small-sized (A-E) or otherwise unusual slides (F-K). Notice bottom (A, arrowheads) or top glass bars (C, F, H), thick cardboard labels (D, G, I, K), label extending beyond glass slide (F, arrowheads mark end of slide), yellowed mounting medium in periphery of coverslips (G), and slide with top glass slide instead of coverslip (J). Coverslip mounted on pieces of glass as spacer (H, arrowheads). K. Trematode mounted between two glass bars (black arrowheads) under coverslip (white arrowheads mark coverslip margins); broken glass slide repaired with the help of a 2nd lower glass slide, cracks of upper slide indicated by black arrows. Specimens mounted in glycerol (now dry) 1868 by von Nathusius (A), in unknown media1888 by Stuhlmann (B), in the 19th century by Krabbe (C), before 1917 by Weltner (D), before 1918 by an unknown person (F), before 1914 by von Linstow (G), before 1918 by Gaffron (H), between 1904 and 1927 by Zelinka (I), between 1906 and 1937 by Wilhelmi (J), and before 1897 by Thoss (K). A-K: macro lens. Scalebars: A-K, 2 cm.
FIGURE 12 in Collection management and study of microscope slides: Storage, profiling, deterioration, restoration procedures, and general recommendations
FIGURE 12. Chemical structure of various synthetic polymers. Bu, butyl; Cl, chlorine; CMC, carboxy methyl cellulose; CN, cellulose nitrate; Et, ethyl; EtOH, hydroxyethyl; HPMC, hydroxypropyl cellulose; MC, methyl cellulose; Me, methyl; OAc, hydroxyacetyl; PBMA, poly(butyl methacrylate); PDMS, poly(dimethyl siloxane); PEMA, poly(ethyl methacrylate); Phe, phenyl; PHEMA, poly(2-hydroxyethyl methacrylate); PMMA, poly(methyl methacrylate); PMMA-PBMA, copolymer of PMMA and PBMA; PS, polystyrene; PVAc, poly(vinyl acetate); PVC, poly(vinyl chloride); PVC-co-PVOAc, copolymer of PVC and PVAc; PVOH, poly(vinyl alcohol); PVP, poly(vinyl pyrrolidone).
FIGURE 5. A in Collection management and study of microscope slides: Storage, profiling, deterioration, restoration procedures, and general recommendations
FIGURE 5. A. Glycerol-paraffin mount with spacers (arrowheads), probably some kind of modelling clay; made between 2000 and 2007 by Rückert. B, C. Glycerol mounts with metal spacers (B, arrowheads) and cavities because of evaporation of glycerol (C, arrowheads), sealed with a white varnish; early 1920s by Micoletzky. D, E. Pieces of epidermis and cuticle of nematomorphs; early 1930s by Heinze. Notice lack of coverslip (D) and coverslip fastened to slide with adhesive tape (E, arrowheads) and a small amount of a mounting medium. F. Unfinished histological sections still in paraffin, unstained, and without coverslip; early 1920s by Arndt. G. Specimen information inked on glass slide and covered with mounting medium and coverslips; before 1932 by Eckmann. H. Specimen information written with a "permanent" marker on glass side, partly wiped off during cleaning of slide with lab tissue; after 1974 by Kanev. I, J. Slides with self-adhesive labels; glued on back side of slide, and coverslips adhered with mounting medium to aluminum frame (I); mounted in Malinol between 1995 and 2004 by Schmelz (I) and in an unknown medium in 1996 by Erséus (J). K, L. Surface of dry borosilicate coverslip (K) and of wet sodalime glass slide (L) of same slide at same spot (note white crystal in mounting medium marked by asterisk). A-J: macro lens; K, L: DIC. Scalebars: A-J, 2 cm; K, L, 500 µm.
FIGURE 4. A-I in Collection management and study of microscope slides: Storage, profiling, deterioration, restoration procedures, and general recommendations
FIGURE 4. A-I. Double-coverslip slides with frames of different materials: aluminum (A, Cobb slides), plastic (B, C: Higgins-Shirayama slide with rectangular opening in B and circular opening in C; D, E: aged plastic, coverslip held in place by label paper and detached in D, see arrowheads), thin (F) or thick (G, H) cardboard, and wood (I, coverslip held in place by paper strips). Notice that certain types of plastic and cardboard slides bend upwards centrally (C, E, H) or get easily distorted (D). J. Stains faded and unknown mounting medium yellowed in the periphery of the coverslip. K. Slide with cardboard labels and spacer consisting possibly of coloured paper tissue. Mounted as glycerol-paraffin mounts between 1999 and 2010 by Neuhaus (A), in Hoyer's medium between 2000 and 2001 by Song and Chang (B) and between 1998 and 2004 by Higgins (C), in Canada balsam after 1925 by Schultze or Heider (D, probably E), in gum dammar dissolved in xylene after 1925 by Heider (F-H), and between 1874 and 1890 by Marenzeller (K). A-K: macro lens. Scalebars: A-K, 2 cm.
FIGURE 1 in Collection management and study of microscope slides: Storage, profiling, deterioration, restoration procedures, and general recommendations
FIGURE 1. Storage of slide collections at the Museum für Naturkunde Berlin (A–E) and National Museum of Natural History, Washington, D.C. (F–I). A–D. Wooden cabinets with drawers and cardboard trays for horizontal storage. Note replacement label for slide on loan (D) and slide mounts of Aphidina between two coverslips previously stored with insect on needle (E, arrows mark holes from needle in cardboard envelopes). F–I. Metal cabinets composed of several units by Technicon (F–H) and Fisherbrand™ (I). G. Metal tray with holes (arrows) for easy access to standard slides from below. Arrowheads mark bentup slide holders. H. Frontal view of opened single unit. I. Dense vertical storage of slides of similar size. Photographs F–I courtesy of Cheryl Bright. D–F: macro lens.
FIGURE 2. A, D in Collection management and study of microscope slides: Storage, profiling, deterioration, restoration procedures, and general recommendations
FIGURE 2. A, D. Cestode (A) and nematodes (D) on oversized blue and white-opaque glass plates, respectively; before 1901 by Borchmann (A) and 19th century by an unknown person (D). Specimen in A without coverslip. B, C, E, G. Histological sections of flatworms (B, E, G) and oligochaete (C) on oversized glass plates; before 1927 by Schulze (B), before 1897 by Michaelsen (C), before 1914 by Böhmig (E), and in the 1980s in DPX in the lab of Sluys (G). Label in C glued and covered with mounting medium. Self-adhesive label in G with glue having migrated through the label indicated by dark spots on the surface of the label. F. Hirudinea on large glass plate with top glass bars; before 1917 by Weltner. Notice yellowed mounting medium in periphery of coverslips in B–F. H. Cestodes on painted pieces of glass; middle of the 19th century by Küchenmeister. A–H: macro lens. Scalebars: A–H, 5 cm.
Supplementary material 1 from: Vaníčková L, Břízová R, Pompeiano A, Ferreira LL, de Aquino NC, Tavares RF, Rodriguez LD, Mendonça AL, Canal NA, do Nascimento RR (2015) Characterisation of the chemical profiles of Brazilian and Andean morphotypes belonging to the Anastrepha fraterculus complex (Diptera, Tephritidae). In: De Meyer M, Clarke AR, Vera MT, Hendrichs J (Eds) Resolution of Cryptic Species Complexes of Tephritid Pests to Enhance SIT Application and Facilitate International Trade. ZooKeys 540: 193-209. https://doi.org/10.3897/zookeys.540.9649
Table S1. Anastrepha fraterculus male and female characteristic.: Explanation note: Anastrepha fraterculus male (m) and female (f) characteristic cuticular hydrocarbons identified by principal component analyses.
Figure 1 in Patients profiling for Botox® (onabotulinum toxin A) treatment for migraine: a look at white matter lesions in the MRI as a potential marker
Figure 1 Coronar brain MRI slices (FLAIR), in (a), on the left side, with one WML in a responder and in (b), on the right side, with three WML in a non-responder.
Few juveniles or males were collected. Only four males from groups 7, 8, 9, and 11, all in clade D, were included in the dataset. The male in Fig. 13E–H conforms to the general morphological description of males in Lobocriconema with an undifferentiated labial region, the absence of a stylet, a degenerate pharyngeal region, a FIGURE 7. SEM images of specimens representing clades D (A–H) and B (I). NID numbers are associated with unique specimens, all are females except image C. A) Lobocriconema sp., face view with conspicuous labial disc surrounded by irregular labial structure, Nine-Mile Prairie, Nebraska, NID 4533. B) Lobocriconema sp., face view lacking submedian lobes and displaying subcuticular labial structure, Big Thicket National Preserve, Texas, NID 4560. C) Lobocriconema sp., juvenile, head with visible submedian lobes, body scales with fine terminal projections, Spring Creek Prairie, Nebraska, NID 4514. D) Lobocriconema sp., face view lacking submedian lobes and displaying subcuticular labial structure, Nine-Mile Prairie, Nebraska, NID 4527 E) Lobocriconema sp., cephalic profile with protruding stylet, Nine-Mile Prairie, Nebraska, NID 4529. F) Lobocriconema sp., head profile lacking submedian lobes, Tunica Hills, Louisiana, NID 4574. G) Lobocriconema sp., tail with closed vulva, Nine-Mile Prairie, Nebraska, NID 4533. H) Lobocriconema sp., tail with closed vulva, Nine-Mile Prairie, Nebraska, NID 4526. I) Lobocriconema sp., face view lacking submedian lobes, Great Smoky Mountains National Park, Purchase Knob, NID 4570. in Species discovery and diversity in Lobocriconema (Criconematidae: Nematoda) and related plant-parasitic nematodes from North American ecoregions
Few juveniles or males were collected. Only four males from groups 7, 8, 9, and 11, all in clade D, were included in the dataset. The male in Fig. 13E–H conforms to the general morphological description of males in Lobocriconema with an undifferentiated labial region, the absence of a stylet, a degenerate pharyngeal region, a FIGURE 7. SEM images of specimens representing clades D (A–H) and B (I). NID numbers are associated with unique specimens, all are females except image C. A) Lobocriconema sp., face view with conspicuous labial disc surrounded by irregular labial structure, Nine-Mile Prairie, Nebraska, NID 4533. B) Lobocriconema sp., face view lacking submedian lobes and displaying subcuticular labial structure, Big Thicket National Preserve, Texas, NID 4560. C) Lobocriconema sp., juvenile, head with visible submedian lobes, body scales with fine terminal projections, Spring Creek Prairie, Nebraska, NID 4514. D) Lobocriconema sp., face view lacking submedian lobes and displaying subcuticular labial structure, Nine-Mile Prairie, Nebraska, NID 4527 E) Lobocriconema sp., cephalic profile with protruding stylet, Nine-Mile Prairie, Nebraska, NID 4529. F) Lobocriconema sp., head profile lacking submedian lobes, Tunica Hills, Louisiana, NID 4574. G) Lobocriconema sp., tail with closed vulva, Nine-Mile Prairie, Nebraska, NID 4533. H) Lobocriconema sp., tail with closed vulva, Nine-Mile Prairie, Nebraska, NID 4526. I) Lobocriconema sp., face view lacking submedian lobes, Great Smoky Mountains National Park, Purchase Knob, NID 4570.
Dataset for the paper "Ensemble optimization retrieval algorithm of hydrometeor profiles for the Ice Cloud Imager submillimeter-wave radiometer'
<p>1. "Retrieval_Database" file contains the pre-calculated retrieval database.</p> <p>2. "Algorithm_Input" file contains the input of the ensemble optimization retrieval algorithm.</p> <p>3. "TrueProfiles" file contains the true profiles corresponding to the input brightness temperatures. </p> <p>4. "Algorithm_Output" file contains the output of the ensemble optimization retrieval algorithm.</p>
Prokaryotic gene catalog, prokaryotic Metagenome-Assembled Genomes (MAGs) and taxonomic profiling of metagenomic data of NEREA Augmented Observatory
<p>The NEREA_metaG directory is dedicated to the in-depth analysis of NEREA microbial communities using metagenomic sequencing data. </p> <p><strong>Gene catalog:</strong> This directory contains the gene catalog compiled from metagenomic data, which includes: Protein and nucleotide sequence files for genes; Cluster files grouping similar genes; Annotation files mapping genes to KEGG pathways; Normalized gene abundance profiles.</p> <div><strong>MAGs:</strong> Directory for Metagenome-Assembled Genomes (MAGs). It contains comprehensive annotation files for the MAGs, providing insights into gene functions, metabolic pathways, and other genomic features. It also contains the individual MAGs categorized by sample origin. Each MAG is stored in a compressed FASTA format.</div> <p><strong>mOTUs</strong>: Contains files related to microbial taxonomic units identified and quantified using the mOTUs profiler. </p>
Single cell suppression profiling of human regulatory T cells
<p>FCS files were generated on a CyTOF Helios (Standard BioTools).</p> <p>Password to unzip the fcs-file folder “scSPOT2024”</p>
Dataset - Instagram Posts from Academic Libraries Profiles
<p>The current dataset comprises a total of 1681 instances (rows) of Instagram posts that originate from 120 academic library profiles across the globe. Each post instance comes with a range of features, including the publication date, text caption, profile name, post interaction rate, post link, post type (image, carousel, reel), and the thematic category to which it belongs out of 14 proposed categories. This dataset provides a valuable resource for researchers and practitioners interested in investigating the social media practices and content structure strategies of academic libraries worldwide. </p> <p><strong>Note: </strong>This dataset was developed by the authors and has been utilized in the publication of the paper titled "Unveiling the Feed: Academic Libraries' Instagram Unpacked" in <em>The Journal of Academic Librarianship. </em>Find more for this publication at: <a href="https://doi.org/10.1016/j.acalib.2024.102924" target="_blank" rel="noopener">https://doi.org/10.1016/j.acalib.2024.102924.</a></p>
Figure S2 Extra- and intra-oral photographs of the patient at 5 years after treatment. Frontal view and smile(A,B), right profile(C), 45 profile and smile(D,E), right lateral occlusion(F), frontal occlusion(G), left lateral occlusion(H), upper arch(I), and lower arch(J).))
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Inorganic biomaterials shape the transcriptome profile to induce endochondral differentiation
<div> <p>Minerals play a vital role, working synergistically with enzymes and other cofactors to regulate physiological functions including tissue healing and regeneration. The bioactive characteristics of mineral-based nanomaterials can be harnessed to facilitate in situ tissue regeneration by attracting endogenous progenitor and stem cells and subsequently directing tissue-specific differentiation. Here, we investigate cellular responses of human mesenchymal stem/stromal cells (hMSCs) to traditional bioactive mineral-based nanomaterials, such as hydroxyapatite (nHA), whitlockite (nWH), silicon-dioxide (nSiO<sub>2</sub>), and the emerging synthetic 2D nanosilicates (nSi). We utilized transcriptome sequencing (RNA-seq) to probe the cellular response and determine the significantly affected signaling pathways due to exposure to these inorganic nanomaterials. Transcriptome profiles of stem cells treated with nanosilicates revealed a stabilized skeletal progenitor state suggestive of endochondral differentiation. This observation is bolstered by enhanced deposition of matrix mineralization in nanosilicate treated stem cells compared to control or other treatments. Specifically, use of 2D nanosilicates directs osteogenic differentiation of stem cells via activation of bone morphogenetic proteins (BMP) and hypoxia-inducible factor 1-alpha (HIF-1<span><span>a</span></span>) signaling pathway. This study provides a holistic transcriptomic insight into nanomaterial-cell interactions and predicts downstream effects of nanomaterial induction of endochondral differentiation.</p> </div>
Proteomic and Metabolomic Profiling of Plasma Predict Immune-related Adverse Events in Older Patients with Advanced Non-small Cell Lung Cancer
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Temporal Dynamics and Demographic Profiles: Evaluating the Cultural Impact of Public Engagements with Civil War Shelters in Alicante (Spain)
<p>In the context of sustainable tourism, understanding visitors' needs and preferences is crucial for planning effective strategies that promote the conservation of historical and cultural heritage. In this regard, the quantitative analysis of survey results from visitors to Civil War air-raid shelters in Alicante, Spain, emerges as a valuable tool for gaining detailed insights that enable the planning of specific visits and events. This paper aims to explore the significance of using quantitative data in developing strategies for sustainable tourism within this particular context.</p>
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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.