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6,383 results for “isolates”
Expression data from mesenchymal stromal cells isolated from the umbilical cord tissue (UCX®) and cultivated in ATMP-compatible media
GEO Series GSE51869. Homo sapiens. 11 samples. Type: Expression profiling by array.
Transcriptomic profiling of MDA-MD-231 and MDA-MB-231-LM1 cells isolated from mouse lungs at micrometastatic stage
GEO Series GSE121944. Homo sapiens. 6 samples. Type: Expression profiling by array.
CUT&RUN of alveolar macophages sorted bronchoalveolar lavage fluid (BALF) isolated from naive mice or mice recovered from SARS-CoV-2 (mouse-adapted strain MA10)
GEO Series GSE266968. Mus musculus. 20 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Whole genome expression profiling of artemsinin-resistant Plasmodium falciparum field isolates [in vivo]
GEO Series GSE59097. Plasmodium falciparum. 1043 samples. Type: Expression profiling by array.
RNA-seq of human and mouse brain microvessels isolated by laser capture microdissection and matched whole brain samples
GEO Series GSE142209. Homo sapiens; Mus musculus. 12 samples. Type: Expression profiling by high throughput sequencing.
Comparison of C3 or C3156-181-peptide treated Isolated primary rat neonatal Sschwann Cells after 72 h
GEO Series GSE70748. Rattus norvegicus. 3 samples. Type: Expression profiling by array.
Expression data from freshly isolated murine muscle satellite cells
GEO Series GSE154082. Mus musculus. 4 samples. Type: Expression profiling by array.
Expanded MLST genotyping and comparative genomic hybridization of Campylobacter coli isolates from multiple hosts
GEO Series GSE16787. Campylobacter coli. 132 samples. Type: Genome variation profiling by array.
Regulation of gene expression in splenic cDC1 isolated from WT vs XCR1-/- miceNK cells orchestrate cDC1 migration to potentiate antiviral protective CD8+ T cell responses
GEO Series GSE142402. Mus musculus. 8 samples. Type: Expression profiling by array.
Distribution. Equatorial forest belt of W & C Africa, from S Guinea and Liberia to DR Congo and W Uganda, with isolated records from W Kenya and E Angola. in Emballonuridae
Distribution. Equatorial forest belt of W & C Africa, from S Guinea and Liberia to DR Congo and W Uganda, with isolated records from W Kenya and E Angola.
Distribution. Widely in tropical Africa, but boundaries of each lineage (presumably separate species) are not known; this species complex occurs almost continuously from Senegal, Gambia, and Guinea E to S Sudan and Ethiopia, and S to Gabon, Republic of the Congo, DR Congo, and Tanzania, with isolated populations in NW Angola, Zambia, Malawi, and N Mozambique; also on Principe and Sâo Tomé Is. in Hipposideridae
Distribution. Widely in tropical Africa, but boundaries of each lineage (presumably separate species) are not known; this species complex occurs almost continuously from Senegal, Gambia, and Guinea E to S Sudan and Ethiopia, and S to Gabon, Republic of the Congo, DR Congo, and Tanzania, with isolated populations in NW Angola, Zambia, Malawi, and N Mozambique; also on Principe and Sâo Tomé 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. R. h. hipposideros Borkhausen, 1797 — continental Europe E to S Ukraine and Romania. R. h. escaleraeK. Andersen, 1918 — N Morocco, N Algeria, and N Tunisia. R. h. majori K. Andersen, 1918 — Corsica. R. h. midas K Andersen, 1905 — SW Russia, Georgia, Azerbaijan, Armenia, N Iraq, N, W & S Iran (including Qeshm I), SW Turkmenistan, S Kazakhstan, E Uzbekistan, WKyrgyzstan, Tajikistan, N & E Afghanistan, NE Pakistan, and NW India (Kashmir). R. h. minimus Heuglin, 1862 - Mediterranean Europe from Iberian Peninsula E to Greece, Turkey, N & W Syria, Lebanon, Israel, Palestine, WJordan, NE Egypt (Sinai), and W Saudi Arabia, with isolated records in E Africa, from SW Sudan, C Eritrea, Djibouti, and C Ethiopia; also on a number of Mediterranean Is, including Balearic Is, Sardinia, Sicily, Pantelleria, Malta, Ionian Is (Corfu and Kefalonia), Aegean Is (Thasos, Euboea, Skyros, Lesbos, Chios, Kos, and Rhodes), Crete, and Cyprus. R h. minutus Montagu, 1808 — W Ireland and SW Britain. in Rhinolophidae
Subspecies and Distribution. R. h. hipposideros Borkhausen, 1797 — continental Europe E to S Ukraine and Romania. R. h. escaleraeK. Andersen, 1918 — N Morocco, N Algeria, and N Tunisia. R. h. majori K. Andersen, 1918 — Corsica. R. h. midas K Andersen, 1905 — SW Russia, Georgia, Azerbaijan, Armenia, N Iraq, N, W & S Iran (including Qeshm I), SW Turkmenistan, S Kazakhstan, E Uzbekistan, WKyrgyzstan, Tajikistan, N & E Afghanistan, NE Pakistan, and NW India (Kashmir). R. h. minimus Heuglin, 1862 - Mediterranean Europe from Iberian Peninsula E to Greece, Turkey, N & W Syria, Lebanon, Israel, Palestine, WJordan, NE Egypt (Sinai), and W Saudi Arabia, with isolated records in E Africa, from SW Sudan, C Eritrea, Djibouti, and C Ethiopia; also on a number of Mediterranean Is, including Balearic Is, Sardinia, Sicily, Pantelleria, Malta, Ionian Is (Corfu and Kefalonia), Aegean Is (Thasos, Euboea, Skyros, Lesbos, Chios, Kos, and Rhodes), Crete, and Cyprus. R h. minutus Montagu, 1808 — W Ireland and SW Britain.
................................................................................................................................................. Fig. 4. DNA fingerprint analysis of the four new isolates and other Bartonella species by ERICPCR. Lanes: M, molecular mass markers; 1, negative control; 2, R1T; 3, R3; 4, R4; 5, R6; 6, Bartonella henselae; 7, Bartonella quintana; 8, Bartonella bacilliformis; 9, Bartonella elizabethae; 10, Bartonella clarridgeiae; 11, Bartonella alsatica; 12, Bartonella tribocorum; 13, Bartonella grahamii; 14, Bartonella doshiae; 15, Bartonella vinsonii spp. arupensis; 16, Bartonella vinsonii spp. berkhoffii; 17, Bartonella vinsonii spp. vinsonii; 18, Bartonella koehlerae. in Bartonella schoenbuchii sp. nov., isolated from the blood of wild roe deer.
................................................................................................................................................. Fig. 4. DNA fingerprint analysis of the four new isolates and other Bartonella species by ERICPCR. Lanes: M, molecular mass markers; 1, negative control; 2, R1T; 3, R3; 4, R4; 5, R6; 6, Bartonella henselae; 7, Bartonella quintana; 8, Bartonella bacilliformis; 9, Bartonella elizabethae; 10, Bartonella clarridgeiae; 11, Bartonella alsatica; 12, Bartonella tribocorum; 13, Bartonella grahamii; 14, Bartonella doshiae; 15, Bartonella vinsonii spp. arupensis; 16, Bartonella vinsonii spp. berkhoffii; 17, Bartonella vinsonii spp. vinsonii; 18, Bartonella koehlerae.
................................................................................................................................................. Fig. 2. Negative staining of strain R1T. Bar, 1 lm. in Bartonella schoenbuchii sp. nov., isolated from the blood of wild roe deer.
................................................................................................................................................. Fig. 2. Negative staining of strain R1T. Bar, 1 lm.
................................................................................................................................................. Fig. 1. Colony dimorphism of strain R1T at secondpassage on blood agar after 8 d of growth. Bar, 2 mm. in Bartonella schoenbuchii sp. nov., isolated from the blood of wild roe deer.
................................................................................................................................................. Fig. 1. Colony dimorphism of strain R1T at secondpassage on blood agar after 8 d of growth. Bar, 2 mm.
Rapid phagosome isolation enables unbiased multiomic analysis of human microglia phagosomes 1
<p><span>Proteomic data of patient microglia phagosomes and controls</span></p>
FIGURE 5 in New cyanobacterium Aliterella vladivostokensis sp. nov. (Aliterellaceae, Chroococcidiopsidales), isolated from temperate monsoon climate zone (Vladivostok, Russia)
FIGURE 5. Map showing distribution of sampling locations of Aliterella genus members according of Rigonato et al. (2016), Zhang et al. (2018), Jung et al. (2020), present study and GenBank data (created with https://www.simplemappr.net, CC 1.0; Shorthouse 2010). For the uncultured bacterial clones and Synechocystis sp. PCC 7509 GenBank accessions are given (see the legend).
FIGURE 1 in New cyanobacterium Aliterella vladivostokensis sp. nov. (Aliterellaceae, Chroococcidiopsidales), isolated from temperate monsoon climate zone (Vladivostok, Russia)
FIGURE 1. Light micrographs of Aliterella vladivostokensis. A–C. Compact and irregular thallus composed of numerous irregular or rounded colonies or solitary cells with colorless and firm mucilaginous envelopes. D. Cylindrical or irregular cells. Scale bars: 10 μm.
FIGURE 4. Secondary structures for the Box-B in New cyanobacterium Aliterella vladivostokensis sp. nov. (Aliterellaceae, Chroococcidiopsidales), isolated from temperate monsoon climate zone (Vladivostok, Russia)
FIGURE 4. Secondary structures for the Box-B helices in the ITS regions for five Aliterella species and putative genus member Synechocystis sp. PCC 7509. Conservative nucleotides are grey colored. Arrowheads show compensatory (CBCs) and hemi-compensatory base changes (hCBCs). Homological base pairs among different species are indicated by dotted lines.
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.