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FIGURE 72. Conglin personatus Zhao and Li, 2014, female. A, C Epigyne, ventral view B Epigyne, lateral view D in Survey of Linyphiidae (Arachnida: Araneae) spiders from Yunnan, China
FIGURE 72. Conglin personatus Zhao and Li, 2014, female. A, C Epigyne, ventral view B Epigyne, lateral view D Vulva, dorsal view.
Plate 3 a. Costus kupensis Maas & H.Maas. Basal inflorescence. – b. Costus lateriflorus Baker. Habit showing lateral inflorescences. – c. Costus tappenbeckianus J.Braun & K.Schum. Inflorescence with flower. – d. Costus lilaceus Maas & H.Maas. Lateral inflorescence. – e. Costus phyllocephalus K.Schum. Inflorescence. – f in Monograph of African Costaceae
Plate 3 a. Costus kupensis Maas & H.Maas. Basal inflorescence. – b. Costus lateriflorus Baker. Habit showing lateral inflorescences. – c. Costus tappenbeckianus J.Braun & K.Schum. Inflorescence with flower. – d. Costus lilaceus Maas & H.Maas. Lateral inflorescence. – e. Costus phyllocephalus K.Schum. Inflorescence. – f. Costus maboumiensis Pellegr. Inflorescence (a: Maas et al. 10575; b: photographed in Lyon Arboretum Hawaï, no specimen collected; c: Burgers' Bush number 20140016; d: photographed in Burgers' Bush, Arnhem, The Netherlands, no specimen collected; e: Maas et al. 10407; f: Maas et al. 10227). — Photos: a, c–f: P.J.M.Maas; b: J.Mood.
Figs 199–202. Tsacasiella species. Epandrium, lateral. 199–200. T in Afrotropical Asilinae (Asilidae): A provisional key to genera, with a review of the status of Neomochtherus Osten Sacken, 1878, and descriptions of new genera and species
Figs 199–202. Tsacasiella species. Epandrium, lateral. 199–200. T. blanda (Tsacas, 1969). 199. Kalina ơ holotype. 200. Kagera ơ holotype (callipygus). 201. T. debilis (Tsacas, 1969) (Komi ơ holotype). 202. T. exilis (Tsacas, 1969) (Lubumbashi ơ holotype). Scale lines = 1 mm.
Figs 21–25. Heligmonevra laevis Engel, 1927 male genitalia. 21. Lateral. 22. Dorsal. 23. Ventral. 24. Aedeagus, lateral. 25 in Afrotropical Asilinae (Asilidae): A provisional key to genera, with a review of the status of Neomochtherus Osten Sacken, 1878, and descriptions of new genera and species
Figs 21–25. Heligmonevra laevis Engel, 1927 male genitalia. 21. Lateral. 22. Dorsal. 23. Ventral. 24. Aedeagus, lateral. 25. Gonocoxite and gonostylus (outside view of left side). Scale lines = 1 mm.
Figs 8–10. Edenophorus male terminalia, lateral view. 8. E in Revision of the South African endemic genus Edenophorus Smith (Diptera: Empididae)
Figs 8–10. Edenophorus male terminalia, lateral view. 8. E. hiemalis sp. n. 9. E. simplex sp. n. 10. E. stuckenbergi sp. n. Sclerites of segment 8 marked by dashed outline (not shown in Fig. 9). Scale bar = 0.1 mm. [Abbreviations: cerc = cercus; ej apod = ejaculatory apodeme; epand = epandrium; epand lb = epandrial lobe; goncx apod = gonocoxal apodeme; pgt = postgonite; ph = phallus; sp ch = sperm chamber.]
Datset related to article "DUPLICATION OF EXONS 15 AND 16 IN MATRIN-3: A PHENOTYPE BRIDGING AMYOTROPHIC LATERAL SCLEROSIS AND IMMUNE-MEDIATED DISORDERS"
<p><strong>NGS analysis performed at Fondazione Besta carried out as part of the study reported at title </strong></p>
Datset related to article "G507D MUTATION IN FUS GENE CAUSES FAMILIAL AMYOTROPHIC LATERAL SCLEROSIS WITH A SPECIFIC GENOTYPE-PHENOTYPE CORRELATION"
<p><strong>NGS_analysis performed at Fondazione Besta carried out as part of the study reported at title</strong></p>
Dataset related to article"G507D MUTATION IN FUS GENE CAUSES FAMILIAL AMYOTROPHIC LATERAL SCLEROSIS WITH A SPECIFIC GENOTYPE-PHENOTYPE CORRELATION"
<p>NGS Analyses of patients included in the study reported at title followed at Fondazione Besta</p>
Figure |. Hystrignathus splendidus sp. n. female. A Esophageal region, lateral view. B Cephalic end, internal view C Cephalic end, external view D Spines at level of the end of procorpus E Tail, lateral view F Vulva, lateral view G Egg. H Genital tract I Habitus, lateral view. in Two new species of nematode (Oxyurida, Hystrignathidae) parasites of Passalus interstitialis Escholtz, 1829 (Coleoptera, Passalidae) from Cuba and a new locality for Longior similis Morffe, Garcia & Ventosa, 2009
Figure |. Hystrignathus splendidus sp. n. female. A Esophageal region, lateral view. B Cephalic end, internal view C Cephalic end, external view D Spines at level of the end of procorpus E Tail, lateral view F Vulva, lateral view G Egg. H Genital tract I Habitus, lateral view.
Fig. 38. Parageron orientalis Paramonov, 1929 stat. rev. a. Epiphallic complex ventral. b. Epiphallic complex lateral. c. Gonocoxite ventral. d. Gonocoxite lateral. e. Epandrium dorsal. f. Epandrium lateral. g. Female genitalia ventral. h. Female sternite 8 in A world review of the bee fly tribe Usiini (Diptera, Bombyliidae) - Part 3: Parageron Paramonov s. lat.
Fig. 38. Parageron orientalis Paramonov, 1929 stat. rev. a. Epiphallic complex ventral. b. Epiphallic complex lateral. c. Gonocoxite ventral. d. Gonocoxite lateral. e. Epandrium dorsal. f. Epandrium lateral. g. Female genitalia ventral. h. Female sternite 8 ventral.
Bicycle Tyre Data - Lateral Characteristics
<p>Measurement of lateral characteristics of bicycle tyres performed through indoor test-rig VeTyT (Department of Mechanical Engineering, Politecnico di Milano, Milan IT). The test-rig for bicycle tyres complies with the standard ISO 9001-2015.</p> <p>Specifically, we measured lateral force and self-aligning torque varying vertical load, inflation pressure, camber angles, for a batch of bicycle tyres. </p> <p> </p> <p><strong>Authors’ disclaimer</strong></p> <p><br> The data produced in this paper are not -and cannot be- related in any way on the quality of the products that have been tested. Actually, only one single tyre per type has been tested and the data have been acquired in a laboratory, which is not the real environment. Relevant factors defining the quality of tyres are not -and cannot be- addressed in this paper.</p> <p> </p>
Fig. 9. Antenna lateral. A in Revision of the genus Euscelidia Westwood, 1850 (Diptera: Asilidae: Leptogastrinae)
Fig. 9. Antenna lateral. A. Euscelidia abbreviata sp. n. B. E. venusta sp. n. Claw and empodium. C, D. E. abbreviata sp. n. C. Dorsal. D. Lateral. E. E. venusta sp. n. Dorsal. F. E. lata sp. n. Lateral. Arrows point at empodium. Scale line = 1 mm.
Fig. 7. Surstyli lateral. A. Euscelidia pallasii. B. E in Revision of the genus Euscelidia Westwood, 1850 (Diptera: Asilidae: Leptogastrinae)
Fig. 7. Surstyli lateral. A. Euscelidia pallasii. B. E. natalensis sp. n. C. E. bequaerti. D. E. acuminata sp. n. E. E. splendida sp. n. F. E. longibifida sp. n. Scale lines = 100 m.
Fig. 4. Aedeagi. A, B, D. Euscelidia pallasii. A. Lateral. B. Dorsal. D. Anterior. C, F. E in Revision of the genus Euscelidia Westwood, 1850 (Diptera: Asilidae: Leptogastrinae)
Fig. 4. Aedeagi. A, B, D. Euscelidia pallasii. A. Lateral. B. Dorsal. D. Anterior. C, F. E. pulchra sp. n. C. Lateral. F. Dorsal. E, G. E. splendida sp. n. E. Lateral. G. Dorsal. Scale lines = 100 m.
Asymmetric mechanotransduction by hair cells of the zebrafish lateral line (Part 1/2)
<p>In the lateral line system, water motion is detected by neuromast organs, fundamental units that are arrayed on a fish's surface. Each neuromast contains hair cells, specialized mechanoreceptors that convert mechanical stimuli, in the form of water movement, into electrical signals. The orientation of hair cells' mechanosensitive structures ensures that the opening of mechanically-gated channels is maximal when deflected in a single direction. In each neuromast organ, hair cells have two opposing orientations, enabling bi-directional detection of water movement. Interestingly, Tmc2b and Tmc2a proteins, which constitute the mechanotransduction channels in neuromasts, distribute asymmetrically so that Tmc2a is expressed in hair cells of only one orientation. Here, using both<em> in vivo</em> recording of extracellular potentials and calcium imaging of neuromasts, we demonstrate that hair cells of one orientation have larger mechanosensitive responses. The associated afferent neuron processes that innervate neuromast hair cells faithfully preserve this functional difference. Moreover, Emx2, a transcription factor required for the formation of hair cells with opposing orientations, is necessary to establish this functional asymmetry within neuromasts. Remarkably, loss of Tmc2a does not impact hair cell orientation but abolishes the functional asymmetry as measured by recording extracellular potentials and calcium imaging. Overall, our work indicates that oppositely oriented hair cells within a neuromast employ different proteins to alter mechanotransduction to sense the direction of water motion.</p>
Asymmetric mechanotransduction by hair cells of the zebrafish lateral line (Part 2/2)
<p>In the lateral line system, water motion is detected by neuromast organs, fundamental units that are arrayed on a fish's surface. Each neuromast contains hair cells, specialized mechanoreceptors that convert mechanical stimuli, in the form of water movement, into electrical signals. The orientation of hair cells' mechanosensitive structures ensures that the opening of mechanically-gated channels is maximal when deflected in a single direction. In each neuromast organ, hair cells have two opposing orientations, enabling bi-directional detection of water movement. Interestingly, Tmc2b and Tmc2a proteins, which constitute the mechanotransduction channels in neuromasts, distribute asymmetrically so that Tmc2a is expressed in hair cells of only one orientation. Here, using both<em> in vivo</em> recording of extracellular potentials and calcium imaging of neuromasts, we demonstrate that hair cells of one orientation have larger mechanosensitive responses. The associated afferent neuron processes that innervate neuromast hair cells faithfully preserve this functional difference. Moreover, Emx2, a transcription factor required for the formation of hair cells with opposing orientations, is necessary to establish this functional asymmetry within neuromasts. Remarkably, loss of Tmc2a does not impact hair cell orientation but abolishes the functional asymmetry as measured by recording extracellular potentials and calcium imaging. Overall, our work indicates that oppositely oriented hair cells within a neuromast employ different proteins to alter mechanotransduction to sense the direction of water motion.</p>
Antigravitropic PIN polarization maintains non-vertical growth in lateral roots
<p>Datasets and gel images associated with the manuscript: <strong>Antigravitropic PIN polarization maintains non-vertical growth in lateral roots. </strong></p>
FIGS. 297–302. Orus dentiger. 297. Head, left lateral. 298. Trichobothrium, enlarged. 299. Mesoventrite. 300. Metaventrite. 301. Metaventrite, left lateral margin. 302 in Generic Revisions Of The Scopaeina And The Sphaeronina (Coleoptera: Staphylinidae: Paederinae: Lathrobiini)
FIGS. 297–302. Orus dentiger. 297. Head, left lateral. 298. Trichobothrium, enlarged. 299. Mesoventrite. 300. Metaventrite. 301. Metaventrite, left lateral margin. 302. Mesofemur, right base.
FIGS. 303–308. Orus. 303–304. O. dentiger. 303. Sternites II and III. 304. Sternite IV, midanterior margin. 305–308. O. punctatus. 305. Metaventrite. 306. Metaventrite, left lateral margin. 307. Mesofemur, left base. 308 in Generic Revisions Of The Scopaeina And The Sphaeronina (Coleoptera: Staphylinidae: Paederinae: Lathrobiini)
FIGS. 303–308. Orus. 303–304. O. dentiger. 303. Sternites II and III. 304. Sternite IV, midanterior margin. 305–308. O. punctatus. 305. Metaventrite. 306. Metaventrite, left lateral margin. 307. Mesofemur, left base. 308. Mesoventrite, posteroventral.
FIGS. 286–296. Orus. 286–295. Orus rubens. 286. Head. 287. Prothorax. 288. Labrum, male. 289. Tergites IX, X, female. 290. Lateral gonocoxal plates. 291. Sternite IX, male. 292. Tergites IX, X, male. 293. Labrum, female. 294–295. Mandibles, dorsal. 296 in Generic Revisions Of The Scopaeina And The Sphaeronina (Coleoptera: Staphylinidae: Paederinae: Lathrobiini)
FIGS. 286–296. Orus. 286–295. Orus rubens. 286. Head. 287. Prothorax. 288. Labrum, male. 289. Tergites IX, X, female. 290. Lateral gonocoxal plates. 291. Sternite IX, male. 292. Tergites IX, X, male. 293. Labrum, female. 294–295. Mandibles, dorsal. 296. Orus dentiger, labrum, female.
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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.