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Dataset results
21 results for “N requirement”
Subspecies and Distribution. R.f. frantisi Soisook et al, 2015 - known only from a few localities in N, SW & S Borneo. R.f. thailandicus Soisook & Bates, 2015 — known only from type locality in SW Thailand. Genetic data suggest that the species may also occur in Vietnam, but this requires more research. in Rhinolophidae
Subspecies and Distribution. R.f. frantisi Soisook et al, 2015 - known only from a few localities in N, SW & S Borneo. R.f. thailandicus Soisook & Bates, 2015 — known only from type locality in SW Thailand. Genetic data suggest that the species may also occur in Vietnam, but this requires more research.
Distribution. Tanzania (not extreme NW), extreme S DR Congo, Malawi, Mozambique, Zambia (not extreme N), S Angola, Namibia, Botswana, Zimbabwe, Swaziland, and N South Africa. Demarcation of the distribution between the Zambezi Kudu and the Northern Kudu (S. chora) in S Kenya and N Tanzania requires additional research. in Bovidae
Distribution. Tanzania (not extreme NW), extreme S DR Congo, Malawi, Mozambique, Zambia (not extreme N), S Angola, Namibia, Botswana, Zimbabwe, Swaziland, and N South Africa. Demarcation of the distribution between the Zambezi Kudu and the Northern Kudu (S. chora) in S Kenya and N Tanzania requires additional research.
Distribution. Recorded from two localities in Papua New Guinea, Mt Missim in Morobe Province and Trans-Fly region of Western Province; it likely has a wider distribution, and there is a third possible record (as N. timoriensis) from Daru I that requires validation. in Vespertilionidae
Distribution. Recorded from two localities in Papua New Guinea, Mt Missim in Morobe Province and Trans-Fly region of Western Province; it likely has a wider distribution, and there is a third possible record (as N. timoriensis) from Daru I that requires validation.
Distribution. SW Russian Far East (Ussuri region), North and South Korea, Japan including many offshore Is (Tsushima, Yakushima, Tanegashima, Kuchinoshima, Takarajima, Amami-Oshima, Kakeroma-Jima, Tokunoshima, Okinawajima, Miyakojima, Irabu, Ishigakijima, Iriomotejima, and Yonagunijima), C, E & S China, Taiwan and Hainan Is, N Myanmar, N Laos, N & C Vietnam (including Cat Ba and Kaitien Is), and scattered records in NC, SC & NE India (Uttar Pradesh, Arunachal Pradesh, and Andhra Pradesh); there is a record from Sakhalin I, but this requires confirmation. in Vespertilionidae
Distribution. SW Russian Far East (Ussuri region), North and South Korea, Japan including many offshore Is (Tsushima, Yakushima, Tanegashima, Kuchinoshima, Takarajima, Amami-Oshima, Kakeroma-Jima, Tokunoshima, Okinawajima, Miyakojima, Irabu, Ishigakijima, Iriomotejima, and Yonagunijima), C, E & S China, Taiwan and Hainan Is, N Myanmar, N Laos, N & C Vietnam (including Cat Ba and Kaitien Is), and scattered records in NC, SC & NE India (Uttar Pradesh, Arunachal Pradesh, and Andhra Pradesh); there is a record from Sakhalin I, but this requires confirmation.
Distribution. WC Afghanistan (Nangarhar and Paktika provinces) and along the S Himalayas of N India (Himachal Pradesh and Uttarakhand) and W Nepal; it apparently occurs in N Pakistan, but this requires confirmation. in Vespertilionidae
Distribution. WC Afghanistan (Nangarhar and Paktika provinces) and along the S Himalayas of N India (Himachal Pradesh and Uttarakhand) and W Nepal; it apparently occurs in N Pakistan, but this requires confirmation.
Distribution. Tanzania (not extreme NW), extreme S DR Congo, Malawi, Mozambique, Zambia (not extreme N), S Angola, Namibia, Botswana, Zimbabwe, Swaziland, and N South Africa. Demarcation of the distribution between the Zambezi Kudu and the Northern Kudu (S. chora) in S Kenya and N Tanzania requires additional research. in Bovidae
Distribution. Tanzania (not extreme NW), extreme S DR Congo, Malawi, Mozambique, Zambia (not extreme N), S Angola, Namibia, Botswana, Zimbabwe, Swaziland, and N South Africa. Demarcation of the distribution between the Zambezi Kudu and the Northern Kudu (S. chora) in S Kenya and N Tanzania requires additional research.
Distribution. Widely distributed in S Africa (S DR Congo, Angola, Zambia, Malawi, S Tanzania, Mozambique, NE Namibia, N & SE Botswana, Zimbabwe, N South Africa, and Swaziland; isolated records from Ethiopia and Kenya require verification. in Nesomyidae
Distribution. Widely distributed in S Africa (S DR Congo, Angola, Zambia, Malawi, S Tanzania, Mozambique, NE Namibia, N & SE Botswana, Zimbabwe, N South Africa, and Swaziland; isolated records from Ethiopia and Kenya require verification.
Distribution. NE Madagascar, known only from the Mananara-Nord region, with the only confirmed reports coming from the Ivontaka-Sud and Verezanantsoro (Ambinanibeorana) parcels of the Mananara-Nord Biosphere Reserve. The N and S limits of the range have not been defined, but they are tentatively assumed to be S of the Fahambahy or Mananara rivers and N of the Simianona, Sandratsio, or Maningory rivers, respectively. Additional surveys are required to determine the full extent of the distribution. in Lepilemuridae
Distribution. NE Madagascar, known only from the Mananara-Nord region, with the only confirmed reports coming from the Ivontaka-Sud and Verezanantsoro (Ambinanibeorana) parcels of the Mananara-Nord Biosphere Reserve. The N and S limits of the range have not been defined, but they are tentatively assumed to be S of the Fahambahy or Mananara rivers and N of the Simianona, Sandratsio, or Maningory rivers, respectively. Additional surveys are required to determine the full extent of the distribution.
Distribution. NW DR Congo and NE Republic of the Congo, in lowland forests of the Congo Basin on both sides of the lower and middle Congo (c.16" E to 26°-27° E); S of the Congo Riverits distribution extends E to the Lomami River system (c.3° N to 6° 30° S); it has also been recorded on twoislands in the Sangha River. Its presence in NE Angola requires confirmation. in Cercopithecidae
Distribution. NW DR Congo and NE Republic of the Congo, in lowland forests of the Congo Basin on both sides of the lower and middle Congo (c.16" E to 26°-27° E); S of the Congo Riverits distribution extends E to the Lomami River system (c.3° N to 6° 30° S); it has also been recorded on twoislands in the Sangha River. Its presence in NE Angola requires confirmation.
Deccan region, Madras, India. Genus Vandeleuria is masculine, so widely used specific name oleracea has been changed for gender agreement. Vandeleuria oleraceusis possibly a composite of species. Polytypic, but subspecific taxonomy requires reassessment. Distribution. Widespread in S Asia (India, Nepal, Bhutan, Bangladesh, and Sri Lan-ka), S China (W & S Yunnan), and mainland SE Asia N of the Isthmus of Kra. Descriptive notes. Head-body 68 mm, tail 105 mm, ear 13 mm, hindfoot 17 mm; weight 10 g. The Indomalayan Long-tailed Climbing Mouse is small, with flat nail on outer finger and outertoe; tail is slender, brown, twice as long as head-body length, and lacks distal tuft. Dorsal pelageis silky and salmon in color; venter is white, with fulvous hues. Habitat. Tall cane and tangled vines in primary and secondary forest such as bamboo forest, moist deciduous forest, temperate forests, montane wet zone, and disturbed secondary forests, and perhaps agricultural areas at elevations of 150-1500 m. Food and Feeding. Indomalayan [Long-tailed Climbing Mice eat fruits, buds, and flowers. Breeding. Litters of the Indomalayan Long-tailed Climbing Mouse have 3-6 young. Activity patterns. Indomalayan Long-tailed Climbing Mice are arboreal and nocturnal, although one individual was caught duringthe day. Movements, Home range and Social organization. Indomalayan Long-tailed Climbing Mice build nests in tall bushes or cane to rear their young. Status and Conservation. Classified as Least Concern on The IUCN Red Last (as V. olacea). The Indomalayan Long-tailed Climbing Mouse occurs in several habitats and a wide distribution that includes national parks. Further taxonomical studies are required to assess conservation status ofthis potentially diverse species complex. Bibliography. Corbet & Hill (1992), Dang Huy Huynh et al. (1994), Ellerman (1941), Marshall (1977b), Musser & Carleton (2005), Osgood (1932), Phillips (1980), Wang Yingxiang (2003). in Muridae
Deccan region, Madras, India. Genus Vandeleuria is masculine, so widely used specific name oleracea has been changed for gender agreement. Vandeleuria oleraceusis possibly a composite of species. Polytypic, but subspecific taxonomy requires reassessment. Distribution. Widespread in S Asia (India, Nepal, Bhutan, Bangladesh, and Sri Lan-ka), S China (W & S Yunnan), and mainland SE Asia N of the Isthmus of Kra. Descriptive notes. Head-body 68 mm, tail 105 mm, ear 13 mm, hindfoot 17 mm; weight 10 g. The Indomalayan Long-tailed Climbing Mouse is small, with flat nail on outer finger and outertoe; tail is slender, brown, twice as long as head-body length, and lacks distal tuft. Dorsal pelageis silky and salmon in color; venter is white, with fulvous hues. Habitat. Tall cane and tangled vines in primary and secondary forest such as bamboo forest, moist deciduous forest, temperate forests, montane wet zone, and disturbed secondary forests, and perhaps agricultural areas at elevations of 150-1500 m. Food and Feeding. Indomalayan [Long-tailed Climbing Mice eat fruits, buds, and flowers. Breeding. Litters of the Indomalayan Long-tailed Climbing Mouse have 3-6 young. Activity patterns. Indomalayan Long-tailed Climbing Mice are arboreal and nocturnal, although one individual was caught duringthe day. Movements, Home range and Social organization. Indomalayan Long-tailed Climbing Mice build nests in tall bushes or cane to rear their young. Status and Conservation. Classified as Least Concern on The IUCN Red Last (as V. olacea). The Indomalayan Long-tailed Climbing Mouse occurs in several habitats and a wide distribution that includes national parks. Further taxonomical studies are required to assess conservation status ofthis potentially diverse species complex. Bibliography. Corbet & Hill (1992), Dang Huy Huynh et al. (1994), Ellerman (1941), Marshall (1977b), Musser & Carleton (2005), Osgood (1932), Phillips (1980), Wang Yingxiang (2003).
N-3 Fatty Acid Requirements for Human Development
ClinicalTrials.gov study NCT00620672. IPD Sharing: Not stated. Countries: 1. Publications: 4.
Supplementary material 1 from: Vissers J, Bosch FV, Bogaerts A, Cocquyt C, Degreef J, Diagre D, de Haan M, De Smedt S, Engledow H, Ertz D, Fabri R, Godefroid S, Hanquart N, Mergen P, Ronse A, Sosef M, Stévart T, Stoffelen P, Vanderhoeven S, Groom Q (2017) Scientific user requirements for a herbarium data portal. PhytoKeys 78: 37-57. https://doi.org/10.3897/phytokeys.78.10936
Gathered needs per type of researcher :
Figure 1 from: Vissers J, Bosch FV, Bogaerts A, Cocquyt C, Degreef J, Diagre D, de Haan M, De Smedt S, Engledow H, Ertz D, Fabri R, Godefroid S, Hanquart N, Mergen P, Ronse A, Sosef M, Stévart T, Stoffelen P, Vanderhoeven S, Groom Q (2017) Scientific user requirements for a herbarium data portal. PhytoKeys 78: 37-57. https://doi.org/10.3897/phytokeys.78.10936
Figure 1 - Stakeholders interacting with the Botanic Garden Meise and potentially using its data portal. The stakeholders prefixed by the words 'internal' refer to those that work at the Botanic Garden, whereas those referred to as 'external' refer to researchers in other institutions.
Figure 3 from: Vissers J, Bosch FV, Bogaerts A, Cocquyt C, Degreef J, Diagre D, de Haan M, De Smedt S, Engledow H, Ertz D, Fabri R, Godefroid S, Hanquart N, Mergen P, Ronse A, Sosef M, Stévart T, Stoffelen P, Vanderhoeven S, Groom Q (2017) Scientific user requirements for a herbarium data portal. PhytoKeys 78: 37-57. https://doi.org/10.3897/phytokeys.78.10936
Figure 3 - A summary of the data elements mentioned by the different researcher types, showing which data elements researchers had in common and which were unique. This does not mean that any particular data element is not of interest to another group, only that it did not arise in the series of interviews. Details of these data elements can be found in the supplementary information. The full list of common data elements is listed in Table 2.
Figure 2 from: Vissers J, Bosch FV, Bogaerts A, Cocquyt C, Degreef J, Diagre D, de Haan M, De Smedt S, Engledow H, Ertz D, Fabri R, Godefroid S, Hanquart N, Mergen P, Ronse A, Sosef M, Stévart T, Stoffelen P, Vanderhoeven S, Groom Q (2017) Scientific user requirements for a herbarium data portal. PhytoKeys 78: 37-57. https://doi.org/10.3897/phytokeys.78.10936
Figure 2 - A user experience researcher using affinity diagramming to cluster user requirements from the results of the interviews.
Disordered N-Terminal DNMT3A Domain Is Required for Mouse Postnatal Development
GEO Series GSE164265. Mus musculus. 75 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Methylation profiling by high throughput sequencing.
An intact heterotrimeric G-Protein complex is required for the N-acylethanolamine-induced, transcriptionally-mediated chloroplast response in developing Arabidopsis seedlings
GEO Series GSE140294. Arabidopsis thaliana. 24 samples. Type: Expression profiling by high throughput sequencing.
Multi-center Study to Investigate the Effects of Citrasate® on Heparin N Requirements During Hemodialysis Treatment
ClinicalTrials.gov study NCT01092455. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Efficient Mammary Gland Involution Requires c-Jun N-terminal kinase
GEO Series GSE89495. Mus musculus. 12 samples. Type: Expression profiling by high throughput sequencing.
Subspecies and Distribution. D.d.dorsalisFraser,1855—BiokoI. D.d.eminiThomas,1887—N&EDRCongo. D.d.latratorThomas,1910—CDRCongo. D.d.marmotaThomas,1901—forestislandsofUganda. D.d.nigricansPeters,1879—NigeriatorightbankofCongoRiver. D. d. sylvestris Temminck, 1853 — W Africa. The distribution information for this species is still incomplete; the Western Tree Hyrax is also present in SW Sudan and S Central African Republic, but the subspecific identity of these populationsstill requires confirmation. in Procaviidae
Subspecies and Distribution. D.d.dorsalisFraser,1855—BiokoI. D.d.eminiThomas,1887—N&EDRCongo. D.d.latratorThomas,1910—CDRCongo. D.d.marmotaThomas,1901—forestislandsofUganda. D.d.nigricansPeters,1879—NigeriatorightbankofCongoRiver. D. d. sylvestris Temminck, 1853 — W Africa. The distribution information for this species is still incomplete; the Western Tree Hyrax is also present in SW Sudan and S Central African Republic, but the subspecific identity of these populationsstill requires confirmation.
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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.