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Overlap Between Pediatric Nodal Marginal Zone Lymphoma (PNMZL) and Pediatric-Type Follicular Lymphoma (PTFL) : Morphological and Molecular Analysis (OncoScan)
GEO Series GSE154831. Ignicoccus hospitalis; Homo sapiens; Cavia porcellus; Mus musculus; Capra hircus. 53 samples. Type: Genome variation profiling by genome tiling array.
Figure 18 in Tanaidacea (Crustacea: Peracarida) of the northeast Atlantic: Chauliopleona Dojiri and Sieg, 1997 and Saurotipleona n. gen. from the 'Atlantic Margin'
Figure 18. Distribution of Chauliopleona species in the Atlantic Margin area. Filled triangles C. amdrupii, filled squares C. armata, and filled circles C. hastata; crosses indicate Ingolf records of C. hastata.
Figure 4 in Tanaidacea (Crustacea: Peracarida) of the northeast Atlantic: Chauliopleona Dojiri and Sieg, 1997 and Saurotipleona n. gen. from the 'Atlantic Margin'
Figure 4. Chauliopleona amdrupii. Non-ovigerous female, BIOICE Stn 3282: (A–F) pereopods 1–6 respectively. Scale bar 0.25 mm.
Figure 5 in Tanaidacea (Crustacea: Peracarida) of the northeast Atlantic: Chauliopleona Dojiri and Sieg, 1997 and Saurotipleona n. gen. from the 'Atlantic Margin'
Figure 5. Chauliopleona armata. Non-ovigerous female, BIOICE Stn 2856: (A) habitus; (B) pleonal sternites, lateral; (C) antennule; (D) antenna; (E) uropod. Scale bars: (i) 1 mm for A; (ii) 0.5 mm for B; (iii) 0.25 mm for C–E.
Mantle heterogeneity generated by melt depletion and melt-rock interaction: the West Iberian margin peridotites (ODP Legs 149 and 173)
<p>This database contains mineral major and trace element data from the homonymous manuscript of Secchiari et al (submitted to Journal of Petrology). The study is based on IODP material (rock samples) and deals with a petrological and geochemical investigation of mantle samples drilled in the Iberia Abyssal Plain. More specifically the material comes from ODP Leg 149 (Hole 899 B) and Leg 173 (Holes 1068A and 1070A).</p> <p>The folder contains Table 1 and Supplementary Table material (mineral major and trace element data) of the homonymous manuscript of Secchiari et al. submitted to JPET.<br>Mineral major element data were obtained with EMPA, while trace element data were analyzed using LA-ICP-MS. Further details are provided in the related manuscript.<br>The investigated samples are from ODP Holes 899B, 1068A, and 1070A. The geographic coordinates of the Hole locations are provided below:<br>Hole 899B: Lat: 40.766667, Lon: -12.200000<br>Hole 1068A: Lat: 40.683333, Lon: -11.616667<br>Hole 1070A:Lat: 40.800000, Lon: -12.716667<br>Sample location is provided in Table 1.</p> <p> </p> <p><strong>This research was funded by the Italian Ministry of University and Research (MUR) through the grant “ECORD-IODP Italia 2021” attributed to A. Secchiari.</strong></p>
Subspecies and Distribution. H.a.aquaticusOgilby,1841—WAfricafromGuineaandSierraLeonetoGhana. H.a.bates:Lydekker,1906—Nigeria,Cameroon,andpresumablyneighboringcountries. H. a. cottoni Lydekker, 1906 — Republic of the Congo, DR Congo, and presumably Uganda. The Water Chevrotain reportedly has a disjunct distribution, occurring in coastal forests from West Africa and in the rainforests of Central Africa from Nigeria to DR Congo, marginally entering Uganda. It has been listed for the following countries in Central Africa: Angola (Cabinda), Cameroon, Central African Republic, DR Congo, Equatorial Guinea, Gabon, Nigeria, Republic of the Congo, and Uganda (Semliki Valley). A record from Angola's Lunda Norte Province, near the Cassai River,is the southernmost record of the species. The species' status in some countries remains unclear. It is apparently absent from the Republic of Benin and Togo (but the speciesis listed as probable in the Ot Basin in Togo); its supposed occurrence in Guinea Bissau and Senegal remains unsupported by evidence. The species was listed for Sierra Leone, although its presence had been called into question. Photographic evidence seems to clarify that the species occurs in Sierra Leone. In 1850, a specimen was recorded from Gambia, but the present status of the species is unclear. Local people report the species from the Boké Préfecture in NW Guinea, which might be the northernmost area from which the species has been recently reported. Extensive field and market surveys there and in the southern Guinea savanna belt did notfind evidence for the species' presence. in Tragulidae
Subspecies and Distribution. H.a.aquaticusOgilby,1841—WAfricafromGuineaandSierraLeonetoGhana. H.a.bates:Lydekker,1906—Nigeria,Cameroon,andpresumablyneighboringcountries. H. a. cottoni Lydekker, 1906 — Republic of the Congo, DR Congo, and presumably Uganda. The Water Chevrotain reportedly has a disjunct distribution, occurring in coastal forests from West Africa and in the rainforests of Central Africa from Nigeria to DR Congo, marginally entering Uganda. It has been listed for the following countries in Central Africa: Angola (Cabinda), Cameroon, Central African Republic, DR Congo, Equatorial Guinea, Gabon, Nigeria, Republic of the Congo, and Uganda (Semliki Valley). A record from Angola's Lunda Norte Province, near the Cassai River,is the southernmost record of the species. The species' status in some countries remains unclear. It is apparently absent from the Republic of Benin and Togo (but the speciesis listed as probable in the Ot Basin in Togo); its supposed occurrence in Guinea Bissau and Senegal remains unsupported by evidence. The species was listed for Sierra Leone, although its presence had been called into question. Photographic evidence seems to clarify that the species occurs in Sierra Leone. In 1850, a specimen was recorded from Gambia, but the present status of the species is unclear. Local people report the species from the Boké Préfecture in NW Guinea, which might be the northernmost area from which the species has been recently reported. Extensive field and market surveys there and in the southern Guinea savanna belt did notfind evidence for the species' presence.
Distribution. Brazilian Amazon, S from the Rio Iriri at least as far as the S (left) margin of the Rio Peixoto de Azevedo (E tributary of the Rio Teles Pires), the S limits are not beyond the headwaters and upper Rio Paraguay (c.14° 30' S), the upper Rio Teles Pires evidently marks the W limit. in Callitrichiade
Distribution. Brazilian Amazon, S from the Rio Iriri at least as far as the S (left) margin of the Rio Peixoto de Azevedo (E tributary of the Rio Teles Pires), the S limits are not beyond the headwaters and upper Rio Paraguay (c.14° 30' S), the upper Rio Teles Pires evidently marks the W limit.
Distribution. Nepal, N India (Kumaon, Garwhal), NE India (including Sikkim), Bhutan, and marginally extreme S Xizang, China. in Bovidae
Distribution. Nepal, N India (Kumaon, Garwhal), NE India (including Sikkim), Bhutan, and marginally extreme S Xizang, China.
Continental Influence on the Fertilization of Marine Waters during the Late Quaternary in the South of the Brazilian Continental Margin
<p>Concentration and percentages of palynomorphs, diatoms and marine indicators.</p>
Distribution. SE Peru, N Bolivia (LLa Paz, Pando), and Brazil S of the Amazon River (Acre, Rondonia, S Amazonas, N Mato Grosso, and Para, up to the E margin of the Rio Xingu, and on the Marajo I). in Didelphidae
Distribution. SE Peru, N Bolivia (LLa Paz, Pando), and Brazil S of the Amazon River (Acre, Rondonia, S Amazonas, N Mato Grosso, and Para, up to the E margin of the Rio Xingu, and on the Marajo I).
FIGURES –. Relatively rare Achnanthales (SEM, New Caledonia, Melanesia). Cocconeis margaritata Riaux-Gobin & Al-Handal, oblong SV areolae bordered by siliceous small beads (37–38), Cocconeis paucistriata Riaux-Gobin, Romero, Compère & Al-Handal (39, 40), SV striae composed of a unique areola on each side of the SV sternum (40, arrow), two (to three) marginal areolae (39, 40), simple process apertures on SV mantle (40, twin arrowheads). Cocconeis sigillata Riaux-Gobin & Al-Handal (41), low marginal crista marginalis and biseriate striae (41, arrowhead) split in two parts by an axial raised area. Achnanthidium glyphos Riaux-Gobin, Compère & Witkowski (42), naviculoïd SV shape, one row of marginal oblong SV areolae (42, arrowhead). See the RV of these taxa on their original description (refs cited above). Scale bars = 3 µm (37), 2 µm (42), 500 nm (40), 400 nm (38). in Marine Achnanthales (Bacillariophyceae) from New Caledonia (Melanesia): assemblage specificities, ultramafic environment
FIGURES –. Relatively rare Achnanthales (SEM, New Caledonia, Melanesia). Cocconeis margaritata Riaux-Gobin & Al-Handal, oblong SV areolae bordered by siliceous small beads (37–38), Cocconeis paucistriata Riaux-Gobin, Romero, Compère & Al-Handal (39, 40), SV striae composed of a unique areola on each side of the SV sternum (40, arrow), two (to three) marginal areolae (39, 40), simple process apertures on SV mantle (40, twin arrowheads). Cocconeis sigillata Riaux-Gobin & Al-Handal (41), low marginal crista marginalis and biseriate striae (41, arrowhead) split in two parts by an axial raised area. Achnanthidium glyphos Riaux-Gobin, Compère & Witkowski (42), naviculoïd SV shape, one row of marginal oblong SV areolae (42, arrowhead). See the RV of these taxa on their original description (refs cited above). Scale bars = 3 µm (37), 2 µm (42), 500 nm (40), 400 nm (38).
Distribution. NE India, marginally in the states of Arunachal Pradesh (Lohit and Lower Dibang Valley districts) and Assam (Tinsukia District), E Myanmar (E of the Chindwin River), and S China in W Yunnan Province. in Hylobatidae
Distribution. NE India, marginally in the states of Arunachal Pradesh (Lohit and Lower Dibang Valley districts) and Assam (Tinsukia District), E Myanmar (E of the Chindwin River), and S China in W Yunnan Province.
Distribution. Forest-savanna margin of the African forest block; there are records from Cameroon, Central African Republic, DR Congo, Uganda, Rwanda, Tanzania, and NE Angola, and possibly present in South Sudan. in Soricidae
Distribution. Forest-savanna margin of the African forest block; there are records from Cameroon, Central African Republic, DR Congo, Uganda, Rwanda, Tanzania, and NE Angola, and possibly present in South Sudan.
Figure 12 in Tanaidacea (Crustacea: Peracarida) of the North-east Atlantic: the genera Leptognathioides and Portaratrum of the 'Atlantic Margin'
Figure 12. Distribution of Leptognathioides and Portaratrum species in Atlantic Margin studies. Small black filled circles indicate all tanaidacean records, large black filled circles L. polita, red filled circles L. biarticulata, and blue filled circles P. holdichi; red arrow indicates joint record of L. biarticulata and P. holdichi.
FIGURE 3 in The sand shrimp genus Philocheras (Caridea: Crangonidae) from the continental margin of Western Australia including the description of a new species and a key to Australian species*
FIGURE 3. Carapace (dorsal view) of Philocheras species reported from Australian waters: P. angustirostris redrawn from De Man (1918: pl. 22 fig. 67); P. anthonyi reproduced from type illustration herein (fig. 1B); P. brucei redrawn from Komai (2004: fig. 1); P. flindersi redrawn from Poore (2004: fig. 36g); P. incisus redrawn from Kemp (1916: pl. 8 fig. 1); P. intermedius redrawn from Poore (2004: fig. 36h); P.japonicus redrawn from De Man (1918: pl. 23 fig. 69); P. lowisi redrawn from Kemp (1916: pl. 8 fig. 2).
Switzerland 2022 Field Campaign - 360 degree Alpine Tethys rifted margin outcrops
<p>360 degree photospheres acquired during the summer data acquisition campaign targeting the pristine remnant outcrops of the Alpine Tethys rifted margins that are exposed in the Swiss Alps</p>
FIGURE 14. Crossaster penicillatus USNM 1122950. A. Abactinal surface. B. Closeup showing abactinal paxillae. C. Actinal surface. D. Abactinal-lateral view showing marginal paxillae. E. Actinal intermediate and adambulacral spination. F in New Genera, Species, and observations on the biology of Antarctic Valvatida (Asteroidea)
FIGURE 14. Crossaster penicillatus USNM 1122950. A. Abactinal surface. B. Closeup showing abactinal paxillae. C. Actinal surface. D. Abactinal-lateral view showing marginal paxillae. E. Actinal intermediate and adambulacral spination. F. Closeup of adambulacral spination showing furrow and subambulacral spines.
Artificial Intelligence Enhanced Optical Coherence Tomography (AI-OCT) Imaging for Pre-surgical Margin Detection of Basal Cell Carcinoma
ClinicalTrials.gov study NCT07358637. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Effect of Different Drilling Techniques on Primary Stability and Marginal Bone Loss of Extra Short Implants
ClinicalTrials.gov study NCT06234566. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Zanubrutinib, Rituximab, and Lenalidomide in the First-Line Treatment of Marginal Zone Lymphoma
ClinicalTrials.gov study NCT07299331. IPD Sharing: Not stated. Countries: 0. Publications: 0.
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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.