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9,798 results for “muscles”
Fig. 32 in Dorsolateral head muscles of the catfish families Nematogenyidae and Trichomycteridae (Siluriformes: Loricarioidei): comparative anatomy and phylogenetic analysis
Fig. 32. Most parsimonious phylogram of relationships of Trichomycteridae derived from character matrix in Table 2 with diagnostic characters plotted according to the most parsimonious reconstruction. Characters numbered as in text and Table 2; synapomorphic state indicated after a period (.) for multistate characters.
Fig. 21 in Dorsolateral head muscles of the catfish families Nematogenyidae and Trichomycteridae (Siluriformes: Loricarioidei): comparative anatomy and phylogenetic analysis
Fig. 21. Medial view of right adductor mandibulae and attached lower jaw of Tridentopsis pearsoni (Tridentinae), MZUSP 38671 (18.3 mm SL). Image flipped horizontally to facilitate comparisons.
Fig. 25 in Dorsolateral head muscles of the catfish families Nematogenyidae and Trichomycteridae (Siluriformes: Loricarioidei): comparative anatomy and phylogenetic analysis
Fig. 25. Dorsolateral view of left adductor mandibulae and attached lower jaw of Parastegophilus paulensis (Stegophilinae), LISDEBE 1312 (46.5 mm SL).
Fig. 26 in Dorsolateral head muscles of the catfish families Nematogenyidae and Trichomycteridae (Siluriformes: Loricarioidei): comparative anatomy and phylogenetic analysis
Fig. 26. Dorsal view of right anterior region of head of Ochmacanthus flabelliferus (Stegophilinae), LIRP 7439 (33.0 mm SL). Arrow indicates attachment ofA2' section of adductor mandibulae to buccopalatal membrane.
Fig. 17 in Dorsolateral head muscles of the catfish families Nematogenyidae and Trichomycteridae (Siluriformes: Loricarioidei): comparative anatomy and phylogenetic analysis
Fig. 17. Medial view of left adductor mandibulae and attached lower jaw of Microcambeva ribeirae (Sarcoglanidinae), MZUSP 65764 (41.8 mm SL).
Fig. 20 in Dorsolateral head muscles of the catfish families Nematogenyidae and Trichomycteridae (Siluriformes: Loricarioidei): comparative anatomy and phylogenetic analysis
Fig. 20. Left lateral view of head of Tridentopsis pearsoni (Tridentinae), MZUSP 38671 (18.3 mm SL).
Fig. 24 in Dorsolateral head muscles of the catfish families Nematogenyidae and Trichomycteridae (Siluriformes: Loricarioidei): comparative anatomy and phylogenetic analysis
Fig. 24. Posterior view of left adductor mandibulae and attached lower jaw of Haemomaster venezuelae (Stegophilinae), LIRP 7438 (36.9 mm SL).
Figure 8 in Ontogeny of the jaw and maxillary barbel musculature in the armoured catfish families Loricariidae and Callichthyidae (Loricarioidea, Siluriformes), with a discussion on muscle homologies
Figure 8. Cross-sections of adult Corydoras aeneus. Only the right half of each section is shown. A, halfway along lower jaw; B, at posterior end of lower jaw (39.0-mm SL) (black indicates bone, dark grey indicates cartilage, light grey indicates muscle, stippled areas indicate nerves). Scale bar = 1 mm.
Figure 6 in Ontogeny of the jaw and maxillary barbel musculature in the armoured catfish families Loricariidae and Callichthyidae (Loricarioidea, Siluriformes), with a discussion on muscle homologies
Figure 6. Cross-sections of subadult Ancistrus cf. triradiatus. Only the right half of each section is shown. A, at lower jaw; B, at hyoid bar (33.5-mm SL) (black indicates bone, dark grey indicates cartilage, light grey indicates muscle, stippled areas indicate nerves). Scale bar = 1 mm.
Figure 4 in Ontogeny of the jaw and maxillary barbel musculature in the armoured catfish families Loricariidae and Callichthyidae (Loricarioidea, Siluriformes), with a discussion on muscle homologies
Figure 4. Three-dimensional reconstruction of the head of an 8.0-mm SL Ancistrus cf. triradiatus free-living embryo. Only the skeleton and the jaw and maxillary barbel musculature are shown, as well as the principal nerve branches in the jaw region (the buccal branches have been omitted). A, dorsal view (left half of neurocranium removed); B, ventral view (left suspensorium, hyoid and mandibular arch removed); C, lateral view. Scale bar = 0.5 mm.
Figure 1 in Ontogeny of the jaw and maxillary barbel musculature in the armoured catfish families Loricariidae and Callichthyidae (Loricarioidea, Siluriformes), with a discussion on muscle homologies
Figure 1. Schematic lateral view of jaw and maxillary barbel musculature in (A) Ancistrus cf. triradiatus and (B) Corydoras aeneus. Redrawn from Schaefer & Lauder (1986) and adjusted according to Geerinckx et al. (2007b). Names as featured in the current paper.
Figure 2 in Ontogeny of the jaw and maxillary barbel musculature in the armoured catfish families Loricariidae and Callichthyidae (Loricarioidea, Siluriformes), with a discussion on muscle homologies
Figure 2. Three-dimensional reconstruction of the head of a 6.1-mm SL Ancistrus cf. triradiatus embryo. Only the skeleton and the jaw and maxillary barbel musculature are shown. A, dorsal view (left half of neurocranium removed); B, ventral view (left suspensorium, hyoid and mandibular arch removed); C, lateral view. Scale bar = 0.5 mm.
Figure 7 in Ontogeny of the jaw and maxillary barbel musculature in the armoured catfish families Loricariidae and Callichthyidae (Loricarioidea, Siluriformes), with a discussion on muscle homologies
Figure 7. Cross-sections of larval Corydoras aeneus. Only the right half of each section is shown. A, anterior to lower jaw; B, at lower jaw (A, B: 4.9-mm SL); C, at lower jaw; D, posterior to lower jaw (C, D: 9.3-mm SL) (black indicates bone, dark grey indicates cartilage, light grey indicates muscle, stippled areas indicate nerves). Scale bar = 0.2 mm.
Figure 5 in Ontogeny of the jaw and maxillary barbel musculature in the armoured catfish families Loricariidae and Callichthyidae (Loricarioidea, Siluriformes), with a discussion on muscle homologies
Figure 5. Cross-sections of embryonic Ancistrus cf. triradiatus. Only the right half of each section is shown (only adductor mandibulae complex in E). A, at lower jaw; B, at posterior side of hyoid bar (A, B: 8.0-mm SL); C, at lower jaw; D, at anterior side of hyoid bar (C, D: 12.4-mm SL); E, at anterior side of hyoid bar (10.2-mm SL) (black indicates bone, dark grey indicates cartilage, light grey indicates muscle, stippled areas indicate nerves). Scale bar = 0.5 mm.
Figure 3. P in Mammals with a long diastema typically also have dominant masseter and pterygoid muscles
Figure 3. P/A = 3/7. Lengthening the jaw (from i to i′′′) increases A (to A″″). Rotation of the vector (from Post to Ant) increases the length of P (to P′′′) and changes the length of A″″ (to A′′′′′′′′′). P′′′/A′′′′′′′′′ = 3/7.
Figure 1 in Mammals with a long diastema typically also have dominant masseter and pterygoid muscles
Figure 1. The distances from the jaw joint to the third molar (Jm) and the length of the tooth row (mi) are both projected onto lines that are perpendicular to the arrow that represents the resultant vector of jaw muscle force. The ratio of P to A is 3: 7.
Oblique profile of a Tyrannosaurus torosus head. Note the good degree of binocular vision, and the bulgingjaw-closing muscles on what is in effect a little frill at the back-top of the head. in Predatory Dinosaurs of the World
Oblique profile of a Tyrannosaurus torosus head. Note the good degree of binocular vision, and the bulgingjaw-closing muscles on what is in effect a little frill at the back-top of the head.
BeMAGIC_Deep neural (and muscle) wireless stimulation using magnetoelectric particles
<p>BeMAGIC ITN (GA861145)_Deep neural (and muscle) wireless stimulation using magnetoelectric particles. Results from ICN2 and G.TEC.</p>
Prenatal skeletogenesis partially recovers from absent skeletal muscle as development progresses
<p>Raw data (measurements made) for paper entitled "Prenatal skeletogenesis partially recovers from absent skeletal muscle as development progresses"</p>
Arthrogenic Muscle Inhibition - decomposed EMG
<p>ACL-injured and healthy controls performed isometric contractions (10-50% maximal voluntary contractions) while EMG was being measured of the quadriceps and hamstrings. The EMG was decomposed to individual motor unit characteristics. </p>
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Allen Brain Atlas
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OpenNeuro
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