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59 results for “myth”

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zenodo32/100

FIGURE 1 in The myth of monophagy in Paralobesia (Lepidoptera: Tortricidae)? A new species feeding on Cypripedium reginae (Orchidaceae)

FIGURE 1. Neighbor-joining tree of COI DNA barcodes for Paralobesia marilynae, P. monotropana and P. cypripediana.

opennotspecifiedJul 2018View details →
zenodo32/100

FIGURE 2 in The myth of monophagy in Paralobesia (Lepidoptera: Tortricidae)? A new species feeding on Cypripedium reginae (Orchidaceae)

FIGURE 2. Male genitalia of Paralobesia showing spine clusters (Spc) on projections from sacculus of valva.

opennotspecifiedJul 2018View details →
zenodo32/100

Fig. 4 A–D in Thecochaos is not a myth: study of the genus Thecochaos (Amoebozoa, Discosea) - a rediscovered group of lobose amoeba, with short SSU gene

Fig. 4 A–D Ultrastructure of the nucleus of Thecochaos fibrillosum. A Cross-section through the nucleus of amoeba and the contractile vacuole surrounded with tubulovesicular spongiom. B A portion of the nuclear membrane with the underlying microfilamentous layer (black arrow) and nuclear pores (black arrowheads). C The fragment of the patchy nucleolus showing several small lacunae filled with the karyoplasm (one is marked with a white asterisk). Small patches of electron-dense material, appearing darker than the nucleolus' main material, are labeled with white arrows. A granule of electron-dense material resembling chromatin is labeled with the white arrowhead. D The fragment of amoebae cell showing the nucleus and the spongiom of the contractile vacuole localized near the nucleus. This is another section of the same nucleus as illustrated in A. Abbreviations: nu, nucleolus; l, lacuna; b, bacteria; m, mitochondria; cv, contractile vacuole; pm, plasma membrane; nm, nuclear membrane; n, nucleus; s, spongiom. Scale bars: A, D, 1 μm; B, 200 nm; C, 500 nm

opennotspecifiedAug 2022View details →
zenodo32/100

Fig. 3 A–E in Thecochaos is not a myth: study of the genus Thecochaos (Amoebozoa, Discosea) - a rediscovered group of lobose amoeba, with short SSU gene

Fig. 3 A–E Ultrastructure of Thecochaos fibrillosum. A A fragment of the amoeba cell demonstrating the stratification of the cytoplasm into the peripheral hyaloplasm and the inner granuloplasm. Numerous vacuoles and vesicles are noticeable at the periphery of the granuloplasm. B Cell coat consisting of the loose filamentous layer (distinct filaments are pointed by black arrows), covering a thick basal layer of electron-dense amorphous glycocalyx (black double arrowheads). C The peripheral area of the hyaloplasm, containing microfilamentous bundles, perpendicular to the plasma membrane (black arrowheads). Black arrows indicate cross-sections of filaments belonging to the upper layer of the glycocalyx. D An area of the granuloplasm containing dictyosomes of the Golgi complex, mitochondria with tubular cristae and dense matrix, and a single-membraned microbody. E Vacuoles containing bacteria. Abbreviations: pm, plasma membrane; hl, hyaloplasm; gr, granuloplasm; m, mitochondria; d, dictyosome of the Golgi complex; b, bacteria. Scale bars: A, 1 μm; B and C, 200 nm; D and E, 500 nm

opennotspecifiedAug 2022View details →
zenodo32/100

Fig. 7 A–I in Thecochaos is not a myth: study of the genus Thecochaos (Amoebozoa, Discosea) - a rediscovered group of lobose amoeba, with short SSU gene

Fig. 7 A–I Materials on Thecochaos species hold in the collection of E. Penard's slides deposited with the British Museum of Natural History (London). DIC optics is used to enhance the contrast of these rather bleach ancient preparations. A Page from the collection catalog, listing seven slides of T. album and the only slide of T. fibrillosum. B, C Actual view of these slides, showing the high quality of mount and good conditions of the preparation. D, E Thecochaos album, the overall appearance of the cell. F Thecochaos album nuclei showing the peripheral position of the nucleolar material

opennotspecifiedAug 2022View details →
zenodo32/100

Fig. 2 A–M in Thecochaos is not a myth: study of the genus Thecochaos (Amoebozoa, Discosea) - a rediscovered group of lobose amoeba, with short SSU gene

Fig. 2 A–M Light microscopy of Thecochaos fibrillosum, DIC. A–C Moving cells on the glass surface. D–M Light microscopy of the cytoplasm and nuclei of Thecochaos fibrillosum, showing variants of

opennotspecifiedAug 2022View details →
zenodo32/100

Fig. 6 A, B in Thecochaos is not a myth: study of the genus Thecochaos (Amoebozoa, Discosea) - a rediscovered group of lobose amoeba, with short SSU gene

Fig. 6 A, B Multigene phylogeny of Thecochaos fibrillosum. A Tree based on the alignment of 58 genes, each individual gene alignment contained both Thecochaos (11 021 AA positions in total) and Stratorugosa gene sequences (18 761 AA positions in total). RAxML (LGX+ G4m model + I)/ Phylobayes (LG model with CAT approximation)/IqTree/ (LG+ F + R4 model). Black circles indicate full support by all methods used. "–" indicates that the pattern of branching was not recovered by one of the reconstruction methods used. Gray arrow indicates the alterative position of Stratorugosa clade under PhyloBayes analysis. B Tree based on the alignment of 151 protein-coding genes including either Thecochaos (13 898 AA positions) or Stratorugosa sequences (42 744 AA positions) or both, so the 58 gene set is also in. IQTree; Sh-aLRT supports values are indicated

opennotspecifiedAug 2022View details →
zenodo32/100

Fig. 8 A–E in Thecochaos is not a myth: study of the genus Thecochaos (Amoebozoa, Discosea) - a rediscovered group of lobose amoeba, with short SSU gene

Fig. 8 A–E Schemes or phylogenetic trees of Discosea obtained in SSU and multigene phylogenetic analyses and comparison of two alternative configurations obtained in the present SSU phylogenetic analysis

opennotspecifiedAug 2022View details →
zenodo32/100

Fig. 5 in Thecochaos is not a myth: study of the genus Thecochaos (Amoebozoa, Discosea) - a rediscovered group of lobose amoeba, with short SSU gene

Fig. 5 SSU phylogenetic tree showing the position of Thecochaos fibrillosum. PhyML analysis (GTRGAMMA model and a proportion of invariant sites; 1620 sites used) and Bayesian analysis (GTR- GAMMA model (8 rate categories) and the covarion model, same mask). Black circles indicate full support (100/1.0 of BS/PP). Open

opennotspecifiedAug 2022View details →
zenodo32/100

Figure 7 in Revised systematics of Palaeozoic 'horseshoe crabs' and the myth of monophyletic Xiphosura

Figure 7. Summary cladogram of higher-level relationships retrieved from the phylogenetic analysis. Chelicerata consists of Pycnogonida and Euchelicerata, with megacheirans forming a polytomy on the node below. Trilobites and xenopods form a basal clade which is here considered to represent Antennata. For the full consensus tree see the Supporting information.

opennotspecifiedDec 2012View details →
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Figure 2 in Revised systematics of Palaeozoic 'horseshoe crabs' and the myth of monophyletic Xiphosura

Figure 2. Schematic of a generalized synziphosurine arthropod, showing the distinction between the preabdominal and postabdominal non-functional pseudotagmata and the true tagmata of the prosoma, mesosoma, and metasoma.

opennotspecifiedDec 2012View details →
zenodo32/100

Figure 10 in Revised systematics of Palaeozoic 'horseshoe crabs' and the myth of monophyletic Xiphosura

Figure 10. Weinbergina opitzi Richter & Richter, 1929 from the Lower Devonian (Emsian) of Bundenbach, Germany. Holotype specimen SMF VIII 7a, showing a flat articulating facet at the anterior of each tergite. Scale bar = 10 mm.

opennotspecifiedDec 2012View details →
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Figure 5. Limulus polyphemus Linnaeus, 1758 in Revised systematics of Palaeozoic 'horseshoe crabs' and the myth of monophyletic Xiphosura

Figure 5. Limulus polyphemus Linnaeus, 1758 from the Recent of North America. A, ventral view of opisthosoma showing opercula. B, dorsal view of opisthosoma with prosoma and telson removed. C, schematic of opisthosoma in dorsal view with apodemes (shallow pits indicating sites of muscle attachment) marked in black and the insertion points of the opercula shown by grey ovals. D, ventral view of opisthosoma with prosoma, telson, and opercula removed. It can be clearly seen that the opercula are not attached to the lateral regions of the opisthosoma. Scale bars = 10 mm.

opennotspecifiedDec 2012View details →
zenodo32/100

Figure 4. A in Revised systematics of Palaeozoic 'horseshoe crabs' and the myth of monophyletic Xiphosura

Figure 4. A, Pasternakevia podolica Selden & Drygant, 1987 from the late Silurian (Ludlow) of Zalissia, Ukraine. Specimen ISEA I - F/MP/3/1499/08, isolated opsithosoma with articulated microtergite of somite VII (arrowed). Image courtesy of Ewa Krzemin´ ska. Scale bar = 10 mm. B, undescribed chasmataspidid from the Lower Devonian (Emsian) of Siberia, Russia. Specimen PIN 5116-6, disarticulated buckler with microtergite of somite VII (arrowed) still firmly attached to its anterior margin. Image courtesy of Dave Marshall. Scale bar = 2 mm.

opennotspecifiedDec 2012View details →
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Figure 8 in Revised systematics of Palaeozoic 'horseshoe crabs' and the myth of monophyletic Xiphosura

Figure 8. Summary cladogram of the internal relationships of Prosomapoda. Arachnids, eurypterids, and chasmataspidids form a clade, here termed Dekatriata. Xiphosurans are paraphyletic with respect to Dekatriata, with xiphosurids forming a monophyletic clade of their own. All taxa outside the two labels are synziphosurines, which would here be polyphyletic. For the full consensus tree see the Supporting information.

opennotspecifiedDec 2012View details →
zenodo32/100

Figure 3. A, Bunodes lunula d in Revised systematics of Palaeozoic 'horseshoe crabs' and the myth of monophyletic Xiphosura

Figure 3. A, Bunodes lunula d'Eichwald, 1854 from the late Silurian (Ludlow) of Oesel, Estonia. Specimen ELM G1:262:2, clearly showing the partially reduced pre-opercula tergite of somite VII (arrowed) between the downturned carapace and the hypertrophied tergite of somite VIII. Scale bar = 10 mm. B, 'Eurypterus' stoermeri Novojilov, 1959, a chasmataspidid from the early Devonian (Lochkovian) of Siberia, Russia. Specimen PIN 1138-1, exhibiting the microtergite of somite VII (arrowed) positioned between the carapace and the buckler. The microtergite curves anteriorly towards its lateral edges, and is particularly noticeable on the left-hand side. The occurrence of ridges associated with the lateral eye on the carapace is also labelled. Image courtesy of Dave Marshall. Scale bar = 2 mm.

opennotspecifiedDec 2012View details →
ClinicalTrials.gov32/100

MYTHS - MYocarditis THerapy With Steroids

ClinicalTrials.gov study NCT05150704. IPD Sharing: NO. Countries: 9. Publications: 9.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov32/100

Myths and Misconceptions About HSCT in a Limited Resource Region

ClinicalTrials.gov study NCT05151406. IPD Sharing: YES. Countries: 1. Publications: 1.

controlledIPD-YESFeb 2026View details →
ClinicalTrials.gov32/100

MYTHS-MR Trial (MYocarditis THerapy With Steroids in Patients With Mildly Reduced Ejection Fraction)

ClinicalTrials.gov study NCT05974462. IPD Sharing: NO. Countries: 4. Publications: 10.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov32/100

The Effect of Simulation Training on Nursing Students' Perception, Myths and Attitudes of Dating Violence

ClinicalTrials.gov study NCT07297992. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →

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Annotated Behaviour and Observability Dataset (ABODe)

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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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

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behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

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neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record

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