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241 results for “long bones”
Figure 11 in Growth and textural ageing in long bones of the American alligator Alligator mississippiensis (Crocodylia: Alligatoridae)
Figure 11. Relationships between bone texture type and femur length body-size proxy for individuals with known habitat. A, femora. B, tibiae. C, humeri.
Figure 5 in Growth and textural ageing in long bones of the American alligator Alligator mississippiensis (Crocodylia: Alligatoridae)
Figure 5. Relationships between femur length body-size proxy and element percentage maturity based on cluster analyses of long bone landmarks. A, femora: three individuals 25% mature, 21 individuals 50% mature, 61 individuals 75% mature, 24 individuals 100% mature. B, tibiae: one individual 0% mature, 16 individuals 33% mature, 24 individuals 67% mature, four individuals 100% mature. C, humeri: three individuals 0% mature, seven individuals 33% mature, 32 individuals 67% mature, six individuals 100% mature.
Figure 4 in Long-bone geometry in columnar-limbed animals: allometry of the proboscidean appendicular skeleton
Figure 4. Branch-length standardizations for the total sample of proboscideans. A, humerus (log transformed branch lengths, r = 0.025); B, ulna (cube root transformed branch lengths, r = 0.010); C, femur (Pagel's arbitrary transformation method, r = 0.052); D, tibia (square root transformed branch lengths, r = 0.028).
Figure 2 in Bone surface texture as an ontogenetic indicator in long bones of the Canada goose Branta canadensis (Anseriformes: Anatidae)
Figure 2. Strict consensus trees resulting from parsimony analyses. Numbered ontogenetic stages are defined in Table 4. Femur: strict consensus of four trees, tree length = 28, consistency index = 0.7500. Tibiotarsus: strict consensus of 40 trees, tree length = 31, consistency index = 0.6452. Humerus: strict consensus of six trees, tree length = 19, consistency index = 0.8333.
Fig. 11 in The first dsungaripterid pterosaur from the Kimmeridgian of Germany and the biomechanics of pterosaur long bones
Fig. 11. Geometric parameters in a hollow circular cross−section. D, diameter; KR, inner radius; R, outer radius; t, wall thickness. After Currey and Alexander (1985).
Fig. 8 in The first dsungaripterid pterosaur from the Kimmeridgian of Germany and the biomechanics of pterosaur long bones
Fig. 8. Comparative reconstructions of pterosaurian pelves. A. Dsungaripteridae gen. et sp. indet., DFMMh/FV 500. B. Pterodactylus sp. C. Ornithocheirus sp. D. "Queensland pterosaur". E. Germanodactylus sp. F. Dsungaripterus weii. All drawn to the same size.
Fig. 7 in The first dsungaripterid pterosaur from the Kimmeridgian of Germany and the biomechanics of pterosaur long bones
Fig. 7. Dsungaripteridae gen. et sp. indet., DFMMh/FV 500. A. Fragment of?tibia. B. Cross−section of?tibia. Scale bars 10 mm. Note exceptionally thick cortex and consequent constricted lumen in the diaphysis.
Fig. 12 in The first dsungaripterid pterosaur from the Kimmeridgian of Germany and the biomechanics of pterosaur long bones
Fig. 12. Frequency of R/t−values in samples of different tetrapod groups, based on data from Currey and Alexander (1985), and my own data.
Fig. 18 in The first dsungaripterid pterosaur from the Kimmeridgian of Germany and the biomechanics of pterosaur long bones
Fig. 18. Three hypothetical step cycles in bipedal locomotion of DFMMh/FV 500. Lines of action of the major hip muscles shown in start of retraction phase (A), intermediate (B), and start of protraction phase (C). Note inclined position of the pelvis reconstructed after Bennett (1990) and relatively poor mechanical advantage of the muscle lever arms through all stages.
Fig. 1 in The first dsungaripterid pterosaur from the Kimmeridgian of Germany and the biomechanics of pterosaur long bones
Fig. 1. Map of north−central Germany, showing the locality of Oker near Goslar, Lower Saxony, Germany, enclosed by the motorways A2 and A7.
Fig. 6 in The first dsungaripterid pterosaur from the Kimmeridgian of Germany and the biomechanics of pterosaur long bones
Fig. 6. Dsungaripteridae gen. et sp. indet., DFMMh/FV 500, dorsal view of left femur. For anatomical explanations see text and Fig. 2. Scale bar 10 mm.
Fig. 4 in The first dsungaripterid pterosaur from the Kimmeridgian of Germany and the biomechanics of pterosaur long bones
Fig. 4. Dsungaripteridae gen. et sp. indet., DFMMh/FV 500, posterior view of pelvis. For anatomical explanations see text and Fig. 2. Scale bar 10 mm.
Fig. 5 in The first dsungaripterid pterosaur from the Kimmeridgian of Germany and the biomechanics of pterosaur long bones
Fig. 5. Dsungaripteridae gen. et sp. indet., DFMMh/FV 500, dorsal view of right femur. For anatomical explanations see text and Fig. 2. Scale bar 10 mm.
Fig. 17 in The first dsungaripterid pterosaur from the Kimmeridgian of Germany and the biomechanics of pterosaur long bones
Fig. 17. Three hypothetical step cycles in quadrupedal locomotion of DFMMh/FV 500. Lines of action of the major hip muscles shown in start of retraction phase (A), intermediate (B), and start of protraction phase (C). Note vertical position of the pelvis and relatively good mechanical advantage of the muscle lever arms through all stages.
Fig. 10 in The first dsungaripterid pterosaur from the Kimmeridgian of Germany and the biomechanics of pterosaur long bones
Fig. 10. Cross sections of typical pterosaur long bones from the Santana Formation (Lower Cretaceous, Brazil). A. Longitudinal section of wing bone SMF R 4919a. B. Transverse section of wing bone SMF R 4915a. Note different density of trabercula, relative bone wall thickness of the bones and triangular cross−section including a thickened angular cortex in B. Scale bars 10 mm.
Fig. 9 in The first dsungaripterid pterosaur from the Kimmeridgian of Germany and the biomechanics of pterosaur long bones
Fig. 9. Original drawings of Dsungaripterus weii by Young (1964). Note strong curvature of the diaphysis, reminiscent of the condition in the studied specimen. Scale bar 100 mm.
Fig.13 in The first dsungaripterid pterosaur from the Kimmeridgian of Germany and the biomechanics of pterosaur long bones
Fig.13. Frequency of K−values in samples of different tetrapod groups, based on data from Currey and Alexander (1985), and my own data.
Fig. 2 in The first dsungaripterid pterosaur from the Kimmeridgian of Germany and the biomechanics of pterosaur long bones
Fig. 2. Dsungaripteridae gen. et sp. indet., DFMMh/FV 500. A. Dorsal view of specimen. B. Interpretative drawing. Scale bar 100 mm.
Pre-market Study to Evaluate Safety and Performance of GreenBone Implant (Long Bone Study)
ClinicalTrials.gov study NCT03884790. IPD Sharing: UNDECIDED. Countries: 6. Publications: 0.
The Use Of Growing Rods In Pediatric Long Bones Deformity Correction
ClinicalTrials.gov study NCT05251961. IPD Sharing: Not stated. Countries: 0. Publications: 2.
ScienceDex guides
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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.