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1  jaw articulation, which provides a powerful bite force.
2 skulls that allowed them to generate extreme bite forces.
3 lls that are optimized for exerting powerful bite forces.
4 ited both to cutting and to generating large bite forces.
5 cuspal inner incline surface with an applied biting force.
6 ble through a combination of: (1) prodigious bite forces (8,526-34,522 newtons [N]) and tooth pressur
7      The combination of a weak muscle-driven bite force, a very 'light' and 'open' skull architecture
8 iba, was not optimized to produce high molar bite force and appears to have been limited in its abili
9 ed significant positive correlations between bite force and flow rates for unstimulated whole saliva
10 ans), Didelphodon vorax has a high estimated bite force and other craniomandibular and dental feature
11 e results confirm an age-related decrease in bite force and salivary flow rates and show that, regard
12 and gender, the partial correlations between bite force and salivary flow rates remained significant
13 ing behaviour from trace evidence, estimated bite forces and tooth pressures, and studied tooth-bone
14  to balancing side muscle force ratios, peak bite forces, and joint reaction forces during unilateral
15 l that can be used to predict muscle forces, bite forces, and joint reaction forces would have many u
16 zed to study the biomechanics of feeding and bite force as well the effects of cranial kinesis on the
17            Root mean square electromyography/bite-force calibrations determined subject-specific mass
18 eth, reduced chewing muscles, weaker maximum bite force capabilities, and a relatively smaller gut.
19 ose observed in vivo and that peak predicted bite forces compare well to published experimental data.
20                  Mean salivary secretion and bite force decrease with advancing age.
21 s significantly greater than that of the low-bite-force group as well as that of the medium-high-bite
22  each saliva type, the flow rate of the high-bite-force group was significantly greater than that of
23 rce group as well as that of the medium-high-bite-force group.
24 ld not run rapidly, were capable of crushing bite forces, had accelerated growth rates and keen sense
25 ship between salivary flow rates and maximal bite force in a community-based sample of men and women
26  and show that, regardless of age or gender, bite force is correlated with salivary flow.
27 ticatory variables (masticatory performance, bite force, number of posterior functional tooth units,
28 g the cuspal incline surface with an applied biting force (off-axis loading).
29 gn, we quantified the ontogenetic profile of bite-force performance in post-metamorphic Ceratophrys c
30 ures of their tooth structure, the estimated bite force produced, and their diet.
31 ata were derived from clinical examinations, bite force recordings, masticatory performance measureme
32 ided into four groups based on their maximal bite force score (low, medium low, medium high, and high
33 er and temporalis muscle activities per 20-N bite-force (T20 N, microV), which defined thresholds.
34  that squirrels are more efficient at muscle-bite force transmission during incisor gnawing than guin
35                                              Bite force was assessed with a bilateral force transduce
36                         Electromyography and bite-forces were measured during right and left incisor
37 opes indicate positive allometric scaling of bite force with reference to head and body size, results
38  optimized to provide the tooth with maximum biting force, withstanding millions of cycles of loads w
39 ical advantage, jaw velocity, bite duration, bite force, work and power.

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