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592 results for “tendon”
Figure 2 in Air sac attachments or tendon scars: the distinction between soft tissue traces in archosaur bone
Figure 2. Sharpey's fibres in a dorsal vertebra of Arrudatitan (MPMA 12-0001-97-1024; A-F) and in a spinosaurine theropod tibia (LPP-PV-0042; G-I). Note that these fibres are visible at low magnifications (5×; arrowheads). G, H show a cross pattern of Sharpey's fibres. Silhouettes in A and G indicate sampled elements (not to scale; art by Felipe A. Elias). All polarized light. Crossed nicols in A-F. Parallel nicols in. Compensator in G, H. The relative angle to the bone surface is approximately 150° in A-C; 90° in D; 70° in E; 120° in F; 90° in G-I. Scale bar in A = 300 µm; in D, I = 250 µm; in B, C, E, F = 100 µm; in G, H = 500 µm.
Optimization of an ex vivo gene transfer to the hamstrings tendons muscle remnants: potential for genetic enhancement of bone healing
<p>Human muscle tissue samples obtained from 31 patients was used in this in vitro analytical and experimental study. To optimize transduction protocol, samples from 28 patients were transduced with the adenoviral vector carrying firefly luciferase cDNA (Ad.luc) using different doses, times of transduction and addition of positive ions for transduction enhancement. The optimized protocol was further tested on muscle samples from 3 new patients, which were transduced with Ad.BMP-2. Released bone morphogenetic protein 2 (BMP-2) levels in osteogenic medium were measured every 3 days during the period of 21 days. Expression of osteogenic markers was at day 14 and 21. After 21 days of cultivation, muscle tissue was prepared for immunohistochemical staining for collagen type I (COL-I). </p>
scRNA-seq of murine tendon from sham and injured group
<p>ScRNA-seq was performed on murine single cell suspension collected from sham and injured group. <span>Tendon</span><span> tissues were collected and dissected into pieces. Then they were digested in </span><span>a mix of collagenase II (Roche, 3 mg/ml) and dispase II (Sigma-Aldrich, 4 mg/ml), prepared in DMEM for 1 hour at 37 °C. Digestions were subsequently quenched with 10% FBS DMEM and filtered through 40μm sterile strainers. Cells were then washed in PBS with 0.04% BSA, counted and resuspended at a concentration of ~1000 cells/μl. Cell viability was assessed with Trypan blue exclusion on a Countess II (Thermo Fisher Scientific) automated counter and only samples with >85% viability were processed for further sequencing.</span><span> </span></p>
v7172-40 possible tendon or gastralia
Open the record for dataset details and reuse information.
The effects of cholesterol accumulation on Achilles tendon biomechanics: A cross-sectional study DATASET
<p>Data set for "The effects of cholesterol accumulation on Achilles tendon biomechanics: A cross-sectional study"</p>
Figure 6 in The first record of fossilized soft parts in ossified tendons and implications for the understanding of tendon mineralization
Figure 6. Fossilized soft parts released from the demineralized tendons of Homalocephale calathocercos (A, C–E) and Edmontosaurus regalis (B, F–P). The sample of H. calathocercos (A) and E. regalis (B) during demineralization. Note the presence of tubular structures released from the mineral phosphate matrix of the fossilized tendons. Dense network of blood vessels forming a mesh-like structure with thicker and thinner vessel-like tubes adjacent to the surface sheath of the partially demineralized tendon of H. calathocercos, visible in: C, transmitted light; D, SEM image (yellow asterisk indicate spot for EDS survey); E, EDS spectrum collected from the blood vessel-like structures reveals the presence of alumino-silicates (Al, Si, O) as the main components; F, tubular structure resembling blood vessels released during the demineralization process; G, the surface of the tubular structure released after demineralization, note the presence of
Figure 5 in The first record of fossilized soft parts in ossified tendons and implications for the understanding of tendon mineralization
Figure 5. Structure of Homalocephale calathocercos tendons: A, a colour-scaled topographic image of surface of an individual vascular canal in the tendon (depth profiling); B, reflected light microscopic image of one of the examined vascular canals with lines expressing depth profiles (not to scale); C–H, detailed AFM images of one of the fibre bundles (fascicles) demonstrated in lock-in-amplitude (C, E, G) and lock-in-phase (D, F, H) images; I, AFM topographical image presenting fibre bundles and four measuring profiles; J, surface topology of one of the measure profiles (no. 2 in I) suggesting periodicity of about 24 nm expressed in tip displacement (Supporting Information, Data S2).
Figure 3 in The first record of fossilized soft parts in ossified tendons and implications for the understanding of tendon mineralization
Figure 3. Light microscopy and SEM of petrographic thin sections and etched surfaces of fossilized ornithischian tendons of Pinacosaurus grangeri: A, cross-section of a larger tendon from the specimen with three associated tendons; B, C, centre of the large, single tendon showing extensive secondary remodelling under normal (B) and polarized (C) light; D, secondary remodelling close to the periphery of the same tendon under transmitted polarized light alpha-compensation mode; E, interfascicular spaces between secondary osteons surrounded by cement lines; F, higher magnification of interfascicular spaces. Note that the fascicles and interfascicular spaces appear to be present in primary tissue only. Green arrows (A–E) mark secondary osteons, orange arrows (E, F) point to cement lines, red arrows (B, C, E, F) indicate interfascicular spaces, and yellow (A, B) point at bone cell lacunae.
Figure 1 in The first record of fossilized soft parts in ossified tendons and implications for the understanding of tendon mineralization
Figure 1. Light microscopy and SEM of petrographic thin sections and etched surfaces of fossilized ornithischian tendons of Edmontosaurus regalis: A, B, ground section (transverse) of the smaller tendon under transmitted normal light (A) and polarized light alpha-compensation mode (B) exhibiting primary organization of tissue; C, D, ground section (transverse) of the periphery (C) (under transmitted normal light) and centre (D) (under polarized light) of the larger tendon; E, circular backscatter detector (CBS-SEM) image of the etched surface of the tendon shows structures interpreted as vascular canals with vessel-like morphology and attached cell-like structures, well visible branched protrusions (red arrow) are also visible; F, CBS-SEM image longitudinal section of the vessel-like canals with cell-like structures attached to the wall (blue arrow). White arrows indicate young Haversian canals, green mark secondary osteons, and yellow point at bone cell lacunae.
Figure 2 in The first record of fossilized soft parts in ossified tendons and implications for the understanding of tendon mineralization
Figure 2. Light microscopy and SEM of petrographic thin sections and etched surfaces of fossilized ornithischian tendons of Homalocephale calathocercos: A, B, general view of the cross-sectioned tendon under transmitted normal (A) and polarized (B) light; C, close-up of the middle of the tendon showing a lattice-like pattern of the coarse collagenous fibre bundles under polarized light; D, close-up of secondary osteons with poorly marked cement lines; E, close-up of the periphery of the tendon under normal light; F, longitudinal section of the tendon under polarized light showing the herringbone-like pattern; G, cross-sectioned tendon in the SEM. Green arrows mark primary osteons, yellow arrow points bone cell lacunae, red asterisk indicate secondary osteons.
A Comparison of ACL Repair With BEAR Device vs. Autograft Patellar Tendon ACL Reconstruction
ClinicalTrials.gov study NCT03776162. IPD Sharing: YES. Countries: 1. Publications: 2.
The Efficacy of Different Immobilization Times After Achilles Tendon Rupture Surgery
ClinicalTrials.gov study NCT04663542. IPD Sharing: NO. Countries: 1. Publications: 2.
Biomechanical and Viscoelastic Properties of Achilles Tendon in Pregnant Women-Pilot Study
ClinicalTrials.gov study NCT05308121. IPD Sharing: UNDECIDED. Countries: 1. Publications: 5.
Muscle-tendon Pathology and Metabolic Dysregulation in CP
ClinicalTrials.gov study NCT06330922. IPD Sharing: YES. Countries: 1. Publications: 6.
Use of Blood Flow Restriction (BFR) Therapy in Post-operative Rehabilitation Following Distal Biceps Tendon Repair
ClinicalTrials.gov study NCT04503421. IPD Sharing: UNDECIDED. Countries: 1. Publications: 5.
Treatment Results After Acute Rupture of the Achilles Tendon.
ClinicalTrials.gov study NCT01785264. IPD Sharing: NO. Countries: 1. Publications: 1.
Ultrasound Supraspinatus Tendon Assessment After 448kilohertz Radiofrequency Stimulation in a Sporty Population.
ClinicalTrials.gov study NCT04273633. IPD Sharing: UNDECIDED. Countries: 1. Publications: 1.
Use of Tendon Vibration and Mirror for the Improvement of Upper Limb Function and Pain Reduction
ClinicalTrials.gov study NCT01010607. IPD Sharing: Not stated. Countries: 1. Publications: 2.
Kinesophobia's Impact on Hand Tendon Rehabilitation
ClinicalTrials.gov study NCT06741215. IPD Sharing: NO. Countries: 1. Publications: 19.
Use of Ultrasonography for Measuring Achilles Tendon Thickness: a Novel Measurement Method
ClinicalTrials.gov study NCT06867211. IPD Sharing: NO. Countries: 1. Publications: 7.
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Allen Brain Atlas
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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.