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1,183 results for “Insertion”
EVE: Software to identify novel viral insertions in wild-caught arthropod hosts from next-generation short read data
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Data from: A 4-lineage statistical suite to evaluate the support of large-scale retrotransposon insertion data to reconstruct evolutionary trees
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Data from: Critical role of insertion preference for invasion trajectory of transposons
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Data for: Epistatic effects between amino acid insertions and substitutions mediate toxin-resistance of vertebrate Na+, K+-ATPases
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ARPIP: Ancestral sequence Reconstruction with insertions and deletions under the Poisson Indel Process
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Reunion of Australasian possums by shared SINE insertions
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Data from: An intronic transposon insertion associates with a trans-species color polymorphism in Midas cichlid fishes
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Chemical modification of proteins by insertion of synthetic peptides using tandem protein trans-splicing
<p>Source data underlying Figs 2c-e, 3c,e-f, 6c,d,f, and Supplementary Figs S1c, S3a, S4c-e,h-j, S5c, S8b, S9d-e, S10d-e, S11d</p>
Insertion sites sizes (FR) and phalangeal size (PTA)
<p>Data to replicate the results of the paper "Insertion sites in manual proximal phalanges of African apes and modern humans. Looking for behavioral traces in phalanges"</p> <p> </p> <p>The database includes the insertion sites sizes (mm<sup>2</sup>) for the A2 pulley in a sample of gorilla, chimpanzee and human hands. These areas in anthropology are called "flexor ridges" (FR). They were measured in 3D models of manual proximal phalanges 2-5 (PP2-PP5) It also includes the area (mm<sup>2</sup>) of the corresponding phalanges (PTA), the length of the first metacarpal of the corresponding hand (MC1_length) and the sex of the individuals, when known. </p> <p> </p> <p>Please cite: Bucchi, A., Luengo, J., Del Bove, A & Lorenzo, C. (2020) Lorenzo. Insertion sites in manual proximal phalanges of African apes and modern humans. American Journal of Physical Anthropology 173(3), 556-567. doi: 10.1002/ajpa.24127.</p>
The insertion of a mitochondrial selfish element into the nuclear genome and its consequences: supporting data sets and scripts
<p>Supplementary data sets and script for the article "The insertion of a mitochondrial selfish element into the nuclear genome and its consequences".</p> <p>The original source code with versioning is available at https://gitlab.gwdg.de/molsysevol/umag_11064 .</p>
Clinical Usefulness of Capnographic Monitoring for Feeding Tube Insertion in Critically Ill Patients: Retrospective Cohort Study
<p><strong>Background</strong>: It is not rare for a small-bore feeding tube to be inserted incorrectly into the respiratory system in critically ill patients. Thus, monitoring is necessary to prevent respiratory malplacement of the tube. We investigated the utility of capnographic monitoring for the prevention of respiratory complications due to feeding tube mispositioning in critically ill patients.</p> <p><strong>Methods:</strong> This study is a pre- and post-intervention study, including a total of 445 feeding tube placements events that were retrospectively studied in the medical and surgical intensive care units of the Samsung Medical Center. We compared the outcomes between the time periods before and after the capnographic monitoring and respiratory complications.</p> <p><strong>Results:</strong> Feeding tubes were inserted in 275 cases without capnographic monitoring. Capnographic monitoring was performed in 170 cases. Sixteen patients (4%) had respiratory complications in total tube placements. Tracheal insertion was in 11 (2%) patients and pneumothorax in 5 (1%) patients. Fourteen cases of respiratory complications were detected in control group (14/275, 5%, ten tracheal insertions and four pneumothoraxes). Two cases of respiratory complications were detected in the capnographic monitoring group (2/170, 1%, one tracheal insertions and one pneumothorax). Respiratory complications were less detected in capnographic monitoring group than control group.</p> <p><strong>Conclusions:</strong> Capnographic monitoring is simple, easy to learn, and may be useful to prevent respiratory complication during feeding tube insertion in critically ill patients.</p>
Confined diffusion of nanoparticles inserted into a diblock polymer membrane captured by fluorescence microscopy
<p>The membrane average pore size was 1µm with a standard deviation of 0.25µm. The video was record by 50 FPS. For more information please see </p> <p>Haramagatti CR, Schacher FH, Müller AHE, Köhler J. Diblock copolymer<br> membranes investigated by single-particle tracking. Phys Chem Chem Phys.<br> 2011;13(6):2278–2284. doi:10.1039/c0cp01658f</p>
FIGURE 4 in A revision of the genera Galeolaria and Pyrgopolon (Polychaeta: Serpulidae), with discussions on opercular insertion as a character in their taxonomy and relationships, and their zoogeography
FIGURE 4. Result of test to determine the relationships/grouping of Galeolaria and Pyrgopolon with 10 other serpulid genera. The names of the 12 genera tested (Table 2, Appendix 2) appear numbered 0–11 in the cladogram.
FIGURE 3 in A revision of the genera Galeolaria and Pyrgopolon (Polychaeta: Serpulidae), with discussions on opercular insertion as a character in their taxonomy and relationships, and their zoogeography
FIGURE 3. Dorsal view of anterior end of Pyrgopolon ctenactis (Mørch, 1863) from Station 212, Santa Barbara, Bonaire, collected, determined and presented by ten Hove, BM (NH) 1971:230. Note operculum inserted independently of branchial radioles of both sides, i.e., from the middle of the anterior end of the thorax.
FIGURE 2. A–I in A revision of the genera Galeolaria and Pyrgopolon (Polychaeta: Serpulidae), with discussions on opercular insertion as a character in their taxonomy and relationships, and their zoogeography
FIGURE 2. A–I: Galeolaria hystrix Mørch 1863, BM (NH) 1986.1.18.48 from New Zealand. A, juvenile specimen figured within its tube. B, The latter worm removed from its tube. C & D: A specimen from BM (NH) 10.19.20 from Cronulla, Australia, determined and presented by B. Dew. D, A specimen from BM (NH) 10.19.20 showing the operculum originating independently of the branchial radioles of both sides. E, Operculum of the juvenile specimen figured in B above. F: Opercular plate of a very large specimen from BM (NH) 1986.11.18.48, from New Zealand. G: Special collar chaeta from the latter specimen. H & I: Geniculate abdominal neurochaetae from the latter.
FIGURE 1. A–F in A revision of the genera Galeolaria and Pyrgopolon (Polychaeta: Serpulidae), with discussions on opercular insertion as a character in their taxonomy and relationships, and their zoogeography
FIGURE 1. A–F: Galeolaria caespitosa Lamarck 1818, from Port Hacking, NSW, BM (NH) 1959.10.19.9–19 determined and presented by B. Dew. A: Whole worm. B, Anterior end of worm; the operculum clearly inserted independently of the branchial radioles of both sides. C, Anterior end of a worm viewed from the left, showing the following. Unfringed interradiolar membranes, an opercular plate bearing a marginal palisade of short rods, a group of medial spines, and a winged opercular peduncle. Note the mid-dorsal longitudinal groove along the peduncle which is a continuation of the faecal groove. D, Opercular peduncle viewed dorsally, showing the longitudinal mid-dorsal groove for passage of faecal matter. It also shows that the mid-dorsal rod of the marginal palisade of rods is specially adapted for deflecting faecal material wafted along the faecal groove of the opercular peduncle outwards, and away from the branchial crown. E & F, show opercular spines and basal plates; see text for description.
FIGURE 7. A in The taxonomic value of the structures for the insertion of the stylet muscles in the Eutardigrada, and description of a new genus
FIGURE 7. A Buccal tube of Ramajendas (Isohypsibiidae); arrows indicate the long, uninterrupted, ridge-shaped AISM; B, Dastychius gen. nov. (Isohypsibiidae); arrows indicate the long, uninterrupted, ridge-shaped AISM with an incision and a septum. C, Isohypsibius and, D, Thulinius (Isohypsibiidae); arrows indicate the ridge-shaped AISM. Scale bar = 10 µm.
FIGURE 4. Buccal tubes with ventral lamina and without dorsal AISM. A, B in The taxonomic value of the structures for the insertion of the stylet muscles in the Eutardigrada, and description of a new genus
FIGURE 4. Buccal tubes with ventral lamina and without dorsal AISM. A, B, Doryphoribius (Isohypsibiidae). C, Hexapodibius (Calohysibiidae). D, Apodibius (Necopinatidae). Scale bar = 10 µm.
FIGURE 3. A in The taxonomic value of the structures for the insertion of the stylet muscles in the Eutardigrada, and description of a new genus
FIGURE 3. A, Buccal tube of Ramajendas (Isohypsibiidae); arrows indicate the dorsal and ventral long, uninterrupted, ridgeshaped AISM. B, C, Buccal tube of Halobiotus (Isohypsibiidae); arrows indicates hook-shaped AISM followed by a longitudinal thickening of the buccal tube wall. D-F, Buccal tube of Mixibius (Isohypsibiidae); arrows indicates hook-shaped AISM followed by a longitudinal thickening of the buccal tube wall. Scale bar = 10 µm.
FIGURE 6 in The taxonomic value of the structures for the insertion of the stylet muscles in the Eutardigrada, and description of a new genus
FIGURE 6. Buccal tubes of A, Hypsibius, B, Diphascon, C, Hebesuncus, D, Bindius (Hypsibiidae); arrows indicate the hookshaped dorsal and ventral AISM. Scale bar = 10 µm.
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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)
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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.