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1,514 results for “Widespread”
Widespread alternative polyadenylation regulation reprograms the prostate cancer cell transcriptome upon androgen receptor inhibition.
GEO Series GSE190153. Homo sapiens. 6 samples. Type: Expression profiling by high throughput sequencing.
Widespread Expression of piRNA-like Molecules in Somatic Tissues
GEO Series GSE27369. Mus musculus; Macaca mulatta. 8 samples. Type: Non-coding RNA profiling by high throughput sequencing.
ANP32E Restricts Widespread Chromatin Accessibility Through Regulation of H2A.Z
GEO Series GSE145705. Mus musculus. 30 samples. Type: Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing.
Widespread Misinterpretable ChIP-seq Bias in Yeast
GEO Series GSE51251. Saccharomyces cerevisiae. 26 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
FIGURES 55–56 in Taxonomy of widespread Neotropical species of Podisus Herrich-Schäffer (Hemiptera: Pentatomidae: Asopinae): redescription of P. distinctus (Stål, 1860) and revalidation of P. fuscescens (Dallas, 1851)
FIGURES 55–56. Geographic distribution of Podisus fuscescens (55, yellow spots) and of Podisus distinctus (56, orange spots).
FIGURES 47–54 in Taxonomy of widespread Neotropical species of Podisus Herrich-Schäffer (Hemiptera: Pentatomidae: Asopinae): redescription of P. distinctus (Stål, 1860) and revalidation of P. fuscescens (Dallas, 1851)
FIGURES 47–54. Female genitalia of Podisus distinctus (47–50) and of Podisus fuscescens (51–54). Genital plates in posterior view (47–48, 51–52). Internal genitalia (49–50, 53–54). Abbreviations: aaf = anterior annular flange; cs = capsula seminalis; dpdr = distal part of ductus receptaculi; gcVIII = gonocoxites 8; gcIX = gonocoxites 9; laVIII = laterotergites 8; laIX = laterotergites 9; paf = posterior annular flange; pi = pars intermedialis; ppdr = proximal part of ductus receptaculi; rs = ring sclerites; st = secondary thickening of gonapophyses IX; tvi = thickening of vaginal intima; va = vesicular area; X = 10th abdominal segment. Scale bars: 47–48, 51–52 = 1 mm; 49–50, 53–54 = 0,1mm.
FIGURES 31–40 in Taxonomy of widespread Neotropical species of Podisus Herrich-Schäffer (Hemiptera: Pentatomidae: Asopinae): redescription of P. distinctus (Stål, 1860) and revalidation of P. fuscescens (Dallas, 1851)
FIGURES 31–40. Pygophore, paramere and superior process of dorsal rim of Podisus distinctus (31–33, 37–38) and of Podisus fuscescens (34–36, 39–40). Pygophore in dorsal (31, 34), posterior (32, 35) and ventral (33, 36) views. Paramere (37, 39). Superior process of dorsal rim (38, 40). Abbreviations: ao = anterior opening; dr = dorsal rim; ib = inner branch; par = paramere; slvr = superior layer of ventral rim; ilvr = inferior layer of ventral rim; spdr = superior process of dorsal rim. Scale bars: 31–36= 0,2 mm; 37–40 = 0,1 mm.
Subspecies and Distribution. . t. theobaldi Dobson, 1872 - Tenasserim, Myanmar. . t. secatus Thomas, 1915 - Madhya Pradesh, India. Boundaries and complete distribution for subspecies are unknown, but T theobaldi is patchily distributed from C & SW India (Madhya Pradesh, Maharashtra, Karnataka, and Kerala), S China (Yunnan, imprecise locality and therefore not mapped), and SE Asia to Greater Sundas (Borneo, Java) and Sulawesi. Distribution is poorly known in India, and. theobaldi likely is more widespread than presently understood. It presumably will be found on other islands of the Indonesian Archipelago. in Emballonuridae
Subspecies and Distribution. . t. theobaldi Dobson, 1872 - Tenasserim, Myanmar. . t. secatus Thomas, 1915 - Madhya Pradesh, India. Boundaries and complete distribution for subspecies are unknown, but T theobaldi is patchily distributed from C & SW India (Madhya Pradesh, Maharashtra, Karnataka, and Kerala), S China (Yunnan, imprecise locality and therefore not mapped), and SE Asia to Greater Sundas (Borneo, Java) and Sulawesi. Distribution is poorly known in India, and. theobaldi likely is more widespread than presently understood. It presumably will be found on other islands of the Indonesian Archipelago.
Distribution. Widespread in the savanna regions of Africa, patchily N of the equator from Sierra Leone, Ivory Coast, Nigeria, Central African Republic, Ethiopia, Somalia, and Kenya; S of the equator recorded from SE DR Congo, Tanzania, Angola, Zambia, Malawi, Namibia, Botswana, Zimbabwe, Mozambique, and extreme NE South Africa; also in Zanzibar Archipelago (Pemba, Unguja, and Mafia Is). in Hipposideridae
Distribution. Widespread in the savanna regions of Africa, patchily N of the equator from Sierra Leone, Ivory Coast, Nigeria, Central African Republic, Ethiopia, Somalia, and Kenya; S of the equator recorded from SE DR Congo, Tanzania, Angola, Zambia, Malawi, Namibia, Botswana, Zimbabwe, Mozambique, and extreme NE South Africa; also in Zanzibar Archipelago (Pemba, Unguja, and Mafia Is).
Distribution. Widespread in tropical Africa from Senegal E to extreme S South Sudan, NE DR Congo, W Uganda, Rwanda, and Burundi, with isolated populations in W & SE Kenya and NE Tanzania; also on Bioko I. in Hipposideridae
Distribution. Widespread in tropical Africa from Senegal E to extreme S South Sudan, NE DR Congo, W Uganda, Rwanda, and Burundi, with isolated populations in W & SE Kenya and NE Tanzania; also on Bioko I.
Subspecies and Distribution. A. t. tridens E. Geoffroy Saint-Hilaire, 1813 widespread in N Africa, from Morocco, Mauritania, and Senegal E to Egypt, Sudan, Eritrea, Ethiopia, Djibouti, and Somalia. A. t. murraianaj. Anderson, 1881 widely in the Middle East, including Syria, Iraq, Israel, Palestine, Jordan, Arabian Peninsula, and Iran, and E to W Afghanistan and S Pakistan. in Hipposideridae
Subspecies and Distribution. A. t. tridens E. Geoffroy Saint-Hilaire, 1813 widespread in N Africa, from Morocco, Mauritania, and Senegal E to Egypt, Sudan, Eritrea, Ethiopia, Djibouti, and Somalia. A. t. murraianaj. Anderson, 1881 widely in the Middle East, including Syria, Iraq, Israel, Palestine, Jordan, Arabian Peninsula, and Iran, and E to W Afghanistan and S Pakistan.
Subspecies and Distribution. . l. lepidus Blyth, 1844 - most of India and Bangladesh; possibly in Bhutan. R..l. feae K. Andersen, 1907 — Myanmar, S China (Yunnan), N Thailand, SW Cambodia, and S Vietnam (possibly more widespread across Vietnam) including Con Son and Phu Quoc Is. . l. monticola K Andersen, 1905 - SE Uzbekistan, SW Kyrgyzstan, Afghanistan (Faryab, Kabul, Nangarhar, Parwan, and Zabul provinces), N Pakistan (Khyber Pakhtunkhwa and Punjab provinces), NW India (Himachal Pradesh and Uttarakhand), and Nepal. in Rhinolophidae
Subspecies and Distribution. . l. lepidus Blyth, 1844 - most of India and Bangladesh; possibly in Bhutan. R..l. feae K. Andersen, 1907 — Myanmar, S China (Yunnan), N Thailand, SW Cambodia, and S Vietnam (possibly more widespread across Vietnam) including Con Son and Phu Quoc Is. . l. monticola K Andersen, 1905 - SE Uzbekistan, SW Kyrgyzstan, Afghanistan (Faryab, Kabul, Nangarhar, Parwan, and Zabul provinces), N Pakistan (Khyber Pakhtunkhwa and Punjab provinces), NW India (Himachal Pradesh and Uttarakhand), and Nepal.
FIGURE 3 in The putative endemic Mexican reef coral Porites baueri Squires 1959 (Scleractinia Poritidae) is a synonym of the widespread coral Porites lobata Dana 1846
FIGURE 3. Porites lobata colonies in Marías Islands. Left upper: small colony growing over stony bottom (scale bar = 10 cm). Left lower: detail of a colony showing coral polyps and colony bumps (scale bar = 1 cm). Right: massive colony 2 m high, with some Pocillopora colonies attached (scale bar = 10 cm).
FIGURE 1 in The putative endemic Mexican reef coral Porites baueri Squires 1959 (Scleractinia Poritidae) is a synonym of the widespread coral Porites lobata Dana 1846
FIGURE 1. Images of the type specimens of Porites. Left side shows the corallum (scale bar= 1 cm) and right side shows the calical surface (scale bar= 0.1 cm). First row: Porites baueri Squires, 1959. Holotype, AMNH 3348. Maria Madre Island, Tres Marías Islands, México. Second row: Porites lobata Dana 1846. Syntype, USNM 652. Hawaii, United States. Third row: Porites excavata Verrill 1870. Syntype, YPM1677A. Pearl Islands, Panama. Fourth row: Porites paschalensis Vaughan 1906. Syntype, USNM 68279. Easter Island, Chile.
Widespread Ranavirus and Perkinsea infections in Cuban Treefrogs (Osteopilus septentrionalis) invading New Orleans, USA
<p>Invasive species can negatively impact ecosystems in numerous ways, including vectoring pathogenic organisms. In amphibians, a lineage globally threatened by multiple pathogens, this spread of disease via invasive species could contribute to declines in native populations. The Cuban Treefrog (<i>Osteopilus septentrionalis</i>) is invasive in the southeastern USA. To assess whether <i>O. septentrionalis</i> is a potential reservoir host for the pathogens <i>Batrachochytrium dendrobatidis</i> (Bd), Ranavirus (Rv), and Perkinsea (Pr), we sampled 82 individuals from a recently invaded site in New Orleans, Louisiana, USA. We used quantitative PCR to assess prevalence and intensity of Bd,<i> </i>Rv and Pr in mouthparts and tail clips from 22 larvae and in toe clips from 60 metamorphosed frogs. We compared infection prevalence and intensity across host characteristics, including Fulton's body condition (K), sex, and life stage. None of the individuals were infected with Bd, 72% were infected with Rv, and 44% were infected with Pr. Twenty-three individuals (28%) were co-infected with Rv and Pr, but co-infection did not significantly predict the prevalence or intensity of either Rv or Pr. Although we did not observe any disease signs, Pr infections were significantly associated with lower body condition, suggesting sub-lethal fitness costs. Our study establishes that invasive <i>O. septentrionalis</i> in New Orleans are infected with two pathogens of global concern for amphibians. Understanding host-pathogen dynamics in <i>O. septentrionalis</i> in Louisiana is a critical step towards understanding how this invasive species could threaten amphibian biodiversity in the region by transmitting infectious pathogens.</p>
Figure 5 in Modern hydrophilid clades present and widespread in the Late Jurassic and Early Cretaceous (Coleoptera: Hydrophiloidea: Hydrophilidae)
Figure 5. Well-preserved specimens of Hydroyixia gen. nov., Yixian Formation, China. Hydroyixia elongata sp. nov.: holotype CNU 2010005, piece and counterpiece (A, B); paratype CNU 2009075, whole specimen (C), detail of head and pronotum (D); detail of elytral apices (E). Hydroyixia latissima sp. nov.: holotype, CNU 2009074, whole specimen (F), detail of abdominal apex (G); posterior leg of paratype CNU 2010014 (H); paratype CNU 2009107 (I). Abbreviations: abem, apical emargination of abdominal ventrite 5; aes3, metanepisternum; apls, anapleural sutures; cl, clypeus; fcs, frontoclypeal suture; gs, gular suture; lb, labrum; men, mentum; msv, mesoventrite; mtv, metaventrite; mttr1, metatarsomere 1; pros, prosternum; sstr, sutural stria; trich, trichobothrium.
FIGURE 5 in A new species of Cis Latreille (Coleoptera: Ciidae) widespread in Brazil but with similarities to the African fauna
FIGURE 5. Geographic distribution of Cis caramelo sp. nov. in the North, Northeast and Southeast Regions of Brazil (red circles).
Figure 3 in First reports of protists in land crabs of the family Gecarcinidae (Crustacea: Decapoda: Brachyura) suggest a relatively widespread phenomenon
Figure 3. Percentage occurrence of the various items in stomachs of Gecarcinus lateralis (Guérin, 1832) without (n = 62) and with (n = 8) eccrinids; the relative frequency of stomachs containing a specified item is pooled for the three locations analysed.
Distribution. Very widespread throughout Africa from Morocco, Algeria, and N Egypt (Cairo) to SW South Africa (Cape Town), as well as SW Saudi Arabia, Yemen, and E Oman, S Iran, E Afghanistan, Pakistan, India, and Sr1 Lanka; while it 1s more continuously distributed in S Africa, its distribution N of the Zambezi Riveris very patchy. in Molossidae
Distribution. Very widespread throughout Africa from Morocco, Algeria, and N Egypt (Cairo) to SW South Africa (Cape Town), as well as SW Saudi Arabia, Yemen, and E Oman, S Iran, E Afghanistan, Pakistan, India, and Sr1 Lanka; while it 1s more continuously distributed in S Africa, its distribution N of the Zambezi Riveris very patchy.
Fig. 18 in A Comprehensive Phylogeny of Tettigoniidae (Orthoptera: Ensifera) Reveals Extensive Ecomorph Convergence and Widespread Taxonomic Incongruence
Fig. 18. Pseudophylline group: supertribe 'Pleminiiti'. Vertical bars indicate subtribes, tribes, and subfamilies. Paraphyletic groups are marked with an asterisk. Posterior probability values over 90 are marked with a circle at the node. Photo credits are as follows: (Pterophylla camellifolia (Fabricius, 1775)) Tom Murray, (Championica sp. (Saussure & Pictet, 1898) and Balboana sp.(Uvarov, 1939)) Arthur Anker.
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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.