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9,798 results for “muscles”
Figures 4-7 in The adductor pectoral fin muscle of Micropogonias furnieri (Perciformes: Sciaenidae): a morphological and histochemical study
Figures 4-7. Histochemical staining of red, pink and white fibers from the adductor fin muscle of Micropogonias furnieri. (4). Red fibers showing strong staining (SDH technique); pink fibers showing weak reaction to SDH (lp: large pink, lr: large red, mp: medium pink, mr: medium red, sp: small pink, sr: small red), (bar = 100 µm). (5). Periodic acid-Schiff (PAS) showing small red fibers (sr) with very strong stain intensity, and small pink (sp) fibers with moderate activity; medium and large fibers react weakly to PAS (lp: large pink, lr: large red, mp: medium pink, mr: medium red), (bar = 50 µm). (6). The small (swp) and medium (mwp) white fibers of the proximal zone show a weak reaction to SDH; large fibers (lwp) have no reaction, (bar = 100 µm). (7). White fibers of the proximal zone react weakly to PAS; white fibers of the distal zone have no reaction (lwd: large white distal, lwp: large white proximal, mwd: medium white distal, mwp: medium white proximal, swd: small white distal, swp: small white proximal), (bar = 150 µm).
Figure 7 in Biochemical composition of the hemolymph, hepatopancreas, ovary, and muscle during ovarian maturation in the penaeid shrimps Fenneropenaeus merguiensis and F. penicillatus (Crustacea: Decapoda)
Figure 7. Comparison of protein, carbohydrate, and lipid in hepatopancreas, hemolymph, and ovary of immature, maturing, and fully mature females of two species.
Figure 6 in Biochemical composition of the hemolymph, hepatopancreas, ovary, and muscle during ovarian maturation in the penaeid shrimps Fenneropenaeus merguiensis and F. penicillatus (Crustacea: Decapoda)
Figure 6. Mean ± standard deviation of proteins, lipids, and carbohydrates in the hepatopancreas of F. penicillatus in different stages of maturation. Logarithmic hepatopancreas protein, lipid, and carbohydrate regressed against logarithmic GSI. Means with different letters are significantly different at P <0.05.
Figure 3 in Biochemical composition of the hemolymph, hepatopancreas, ovary, and muscle during ovarian maturation in the penaeid shrimps Fenneropenaeus merguiensis and F. penicillatus (Crustacea: Decapoda)
Figure 3. Mean ± standard deviation of proteins, lipids, and carbohydrates in the ovaries of F. merguiensis in different stages of maturation. Logarithmic ovary protein, lipid, and carbohydrate regressed against logarithmic GSI. Means with different letters are significantly different at P <0.05.
Text-fig. 3. Patelliconus primulus (BARRANDE in PERNER, 1903). Specimen NM L 39616, internal mould. A – apical view, B – oblique left posterolateral view, both ×......; C – right posterolateral view showing the second and third successive positions of muscle band (arrowed), located on top of each elevation (= in the deepest place of the wide depression of shell interior at the periphery of a flat ramp), ×....... Šárka F., Volduchy – Díly near Rokycany. in Patelliconus Horný, 1961 And Mytoconula Gen. N. (Mollusca, Tergomya) From The Ordovician Of Perunica
Text-fig. 3. Patelliconus primulus (BARRANDE in PERNER, 1903). Specimen NM L 39616, internal mould. A – apical view, B – oblique left posterolateral view, both ×......; C – right posterolateral view showing the second and third successive positions of muscle band (arrowed), located on top of each elevation (= in the deepest place of the wide depression of shell interior at the periphery of a flat ramp), ×....... Šárka F., Volduchy – Díly near Rokycany.
Text-fig. 5. Mytoconula vonkai sp. n. The holotype NM L 31983, internal mould. A – apical, B – right apical and right antero-lateral views, both with visible series of muscle scars in two raised zones, ×......;. Note the two long divergent scar zones in A. Dobrotivá F., Mýto near Holoubkov. in Patelliconus Horný, 1961 And Mytoconula Gen. N. (Mollusca, Tergomya) From The Ordovician Of Perunica
Text-fig. 5. Mytoconula vonkai sp. n. The holotype NM L 31983, internal mould. A – apical, B – right apical and right antero-lateral views, both with visible series of muscle scars in two raised zones, ×......;. Note the two long divergent scar zones in A. Dobrotivá F., Mýto near Holoubkov.
Figure 6 in Investigations of the nervous system biomarkers in the brain and muscle of freshwater fish (Oreochromis niloticus) following accumulation of nanoparticles in the tissues
Figure 6. TEM images of brain tissue sample of fish (O. niloticus) exposed to 1 (A and B), 5 (C and D), and 25 (E and F) mg/L of CuO NPs for 14 days of uptake and 14 days of depuration periods, respectively.
Figure 10 in Investigations of the nervous system biomarkers in the brain and muscle of freshwater fish (Oreochromis niloticus) following accumulation of nanoparticles in the tissues
Figure 10. The mean ATPase activity and associated standard errors in the brain of O. niloticus exposed to Al2 O 3 (a), CuO (b), and TiO2 NPs for 14 days (n = 6). See Figure 8 for detail.
Figure 5 in Investigations of the nervous system biomarkers in the brain and muscle of freshwater fish (Oreochromis niloticus) following accumulation of nanoparticles in the tissues
Figure 5. TEM images of brain tissue sample of fish (O. niloticus) exposed to 1 (A and B), 5 (C and D), and 25 (E and F) mg/L of Al2 O 3 NPs for 14 days of uptake and 14 days of depuration periods, respectively.
Figure 9 in Investigations of the nervous system biomarkers in the brain and muscle of freshwater fish (Oreochromis niloticus) following accumulation of nanoparticles in the tissues
Figure 9. The mean Ca-ATPase activity and associated standard errors in the muscle of O. niloticus. See Figure 8 for details.
Figure 3 in Investigations of the nervous system biomarkers in the brain and muscle of freshwater fish (Oreochromis niloticus) following accumulation of nanoparticles in the tissues
Figure 3. TEM images of muscle tissue sample of fish (O. niloticus) exposed to 1 (A and B), 5 (C and D), and 25 (E and F) mg/L of CuO NPs for 14 days of uptake and 14 days of depuration periods, respectively.
Figure 6 in Effects of in vivo exposures to nanoparticles (Al O , CuO, TiO ) on the activities of ATPases in the gill and muscle of freshwater mussel (Unio tigridis)
Figure 6. Effects of NPs on Ca-ATPase activity in the muscle of mussels after 14 days. * indicates significant (p <0.05) differences compared to control.
Figure 4 in Effects of in vivo exposures to nanoparticles (Al O , CuO, TiO ) on the activities of ATPases in the gill and muscle of freshwater mussel (Unio tigridis)
Figure 4. Effects of NPs on Ca-ATPase activity in the gill of mussels after 14 days. * indicates significant (p <0.05) differences compared to control.
Figure 3 in Effects of in vivo exposures to nanoparticles (Al O , CuO, TiO ) on the activities of ATPases in the gill and muscle of freshwater mussel (Unio tigridis)
Figure 3. Effects of NPs on Mg-ATPase activity in the gill of mussels after 14 days. * indicates significant (p <0.05) differences compared to control.
Figure 5 in Effects of in vivo exposures to nanoparticles (Al O , CuO, TiO ) on the activities of ATPases in the gill and muscle of freshwater mussel (Unio tigridis)
Figure 5. Effects of NPs on Mg-ATPase activity in the muscle of mussels after 14 days. * indicates significant (p <0.05) differences compared to control.
Figure 1 in Effects of in vivo exposures to nanoparticles (Al O , CuO, TiO ) on the activities of ATPases in the gill and muscle of freshwater mussel (Unio tigridis)
Figure 1. TEM images of Al O (a), CuO (b), and TiO (c) nanoparticles in stock solutions (Canli and Canli, 2020).
Fig. 1 in Craniolateral forearm muscles of the crab-eating raccoon (Procyon cancrivorus) and a comparative review with other carnivorans
Fig. 1. Cranial view of a left forearm (a), and lateral view of a left forearm (b). 1, m. brachioradialis; 2, m. extensor carpi radialis; 2', cranial belly; 2", caudal belly; 3, m. eXtensor digitorum communis; 3', tendon of the m. eXtensor digitorum communis; 4, m. eXtensor digitorum lateralis; 4', tendon of insertion of the m. extensor digitorum lateralis; 5, m. extensor carpi ulnaris; 5', tendon; 6, m. abductor digiti I longus; 7; extensor retinaculum.
Fig. 5 in Craniolateral forearm muscles of the crab-eating raccoon (Procyon cancrivorus) and a comparative review with other carnivorans
Fig. 5. Lateral view of a left forearm where the m. brachioradialis had been retracted toward medial (a), and lateral view of a left forearm (b). 1, m. brachioradialis; 2, m. eXtensor carpi radialis; 3, m. eXtensor digitorum communis; 4, m. eXtensor digitorum lateralis; 5, m. eXtensor carpi ulnaris; 6, cranial interosseous artery; 7, m. supinator; 8, transverse cubital artery; 1', 2', 7', branches of the deep branch of radial nerve to the respective muscle.
Fig. 3 in Craniolateral forearm muscles of the crab-eating raccoon (Procyon cancrivorus) and a comparative review with other carnivorans
Fig. 3. Dorsal view of a left hand, dorsal view of a right hand (b), deep dorsal view of a left hand (c). 1, Extensor digitorum communis tendon; 1', tendon to the digit I; 2, extensor digiti I et II tendons; 2', medial tendon, 2", lateral tendon; 3, extensor digitorum lateralis tendons; 3', medial; 3", intermediate; 3"', lateral; 4, eXtensor carpi radialis tendon; 4', tendon of the cranial belly; 4", tendon of the caudal belly; 5, EXtensor retinaculum.
Fig. 4 in Craniolateral forearm muscles of the crab-eating raccoon (Procyon cancrivorus) and a comparative review with other carnivorans
Fig. 4. Deep lateral views of a two left forearms (a-b), and deep cranial view of a left forearm (c). 1, m. brachioradialis; 2, m. eXtensor carpi radialis; 3, m. supinator; 4, m. abductor digiti I longus; 4', tendon; 5, m. eXtensor digiti I et II; 5', medial tendon; 5", lateral tendon; 6, m. eXtensor carpi ulnaris.
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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.