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2,532 results for “at present”
Microenvironment Shapes Small Cell Lung Cancer Neuroendocrine States and Presents Therapeutic Opportunities
GEO Series GSE267310. Homo sapiens. 12 samples. Type: Expression profiling by high throughput sequencing.
A transcriptional and metabolic signature of primary aneuploidy is present in chromosomally-unstable cancer cells and informs clinical prognosis
GEO Series GSE49894. Mus musculus. 6 samples. Type: Expression profiling by array.
Trunk events present minimal intra- and inter-tumoral heterogeneity in hepatocellular carcinoma
GEO Series GSE98620. Homo sapiens. 315 samples. Type: Expression profiling by array; Genome variation profiling by SNP array.
Endocrine treatment potentiates antigen presentation and in combination with SMAC mimetics enhances an anti-tumor immune response in hormone receptor positive breast cancer
GEO Series GSE214054. Homo sapiens. 134 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
Gene expression profiling of novel antigen presenting cells (APC) inducing pathogenic T helper cells of lupus
GEO Series GSE36284. Mus musculus. 12 samples. Type: Expression profiling by array.
Mapping naturally presented T-cell antigens in medulloblastoma based on integrative multi-omics
GEO Series GSE250587. Homo sapiens. 56 samples. Type: Expression profiling by high throughput sequencing; Methylation profiling by genome tiling array.
Endocrine treatment potentiates antigen presentation and in combination with SMAC mimetics enhances an anti-tumor immune response in hormone receptor positive breast cancer (ATAC-seq WH/E2)
GEO Series GSE213484. Homo sapiens. 8 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Autophagy promotes MHC class II presentation of peptides from intracellular source proteins
GEO Series GSE2435. Homo sapiens. 6 samples. Type: Expression profiling by array.
Genome wide analysis of RNA species present in SMN-containing RNPs
GEO Series GSE40197. Mus musculus. 5 samples. Type: Expression profiling by array.
Mrp1 is involved in lipid presentation and iNKT cell activation by Streptococcus pneumoniae
GEO Series GSE109717. Mus musculus. 2 samples. Type: Expression profiling by array.
Spatially separated intraepithelial and lamina propria neutrophils present distinct functional identities in the inflamed colon mucosa
GEO Series GSE289035. Homo sapiens. 60 samples. Type: Other.
The Effect of Synonymous Single-Nucleotide Polymorphisms on an Atypical Cystic Fibrosis Clinical Presentation
GEO Series GSE154023. Homo sapiens. 2 samples. Type: Expression profiling by high throughput sequencing.
Fibrinogen promotes autoimmunity and demyelination via chemokine release and antigen presentation [Rn]
GEO Series GSE71083. Rattus norvegicus. 4 samples. Type: Expression profiling by array.
Microenvironment Shapes Small Cell Lung Cancer Neuroendocrine States and Presents Therapeutic Opportunities [DMS273 SCLC cell lines]
GEO Series GSE267560. Homo sapiens. 8 samples. Type: Expression profiling by high throughput sequencing.
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.
Subspecies and Distribution. M. n. nigrescensJ. E. Gray, 1843 - G Moluccas, including Bum, Seram, Ambon, and possibly other islands in that island group. M. n. papuana Thomas, 1914 - Sulawesi, N Moluccas (Morotai, Halmahera, Ternate, Bacan), Sula Is (Senana), Raja Ampat Is (Waigeo, Batanta, Salawati), New Guinea (including Supiori and Biak on Schouten Is and Umboi I) and Woodlark Is (Woodlark, Alcester), and Kai Is. Recent molecular work seems to indicate that papuana might include populations from Admiralty Is (Manus and Los Negros). M. n. solomonisThomas, 1904-Bismarck Archipelago (New Ireland, Duke ofYork, and New Britain Is), and in N Solomons (Buka, Nissan, Bougainville, Fauro, Shortland, Vella Lavella, New Georgia, Russell, Savo, Florida, Guadalcanal, Malaita, Makira, and Uki Ni Masi Is). Also present on Emirau I (Bismarck Archipelago), but subspecies not known. in Emballonuridae
Subspecies and Distribution. M. n. nigrescensJ. E. Gray, 1843 - G Moluccas, including Bum, Seram, Ambon, and possibly other islands in that island group. M. n. papuana Thomas, 1914 - Sulawesi, N Moluccas (Morotai, Halmahera, Ternate, Bacan), Sula Is (Senana), Raja Ampat Is (Waigeo, Batanta, Salawati), New Guinea (including Supiori and Biak on Schouten Is and Umboi I) and Woodlark Is (Woodlark, Alcester), and Kai Is. Recent molecular work seems to indicate that papuana might include populations from Admiralty Is (Manus and Los Negros). M. n. solomonisThomas, 1904-Bismarck Archipelago (New Ireland, Duke ofYork, and New Britain Is), and in N Solomons (Buka, Nissan, Bougainville, Fauro, Shortland, Vella Lavella, New Georgia, Russell, Savo, Florida, Guadalcanal, Malaita, Makira, and Uki Ni Masi Is). Also present on Emirau I (Bismarck Archipelago), but subspecies not known.
Subspecies and Distribution. . n. nudiventris Cretzschmar, 1830 - N, W, C & E Africa, also in Israel, Palestine, and the Arabian Peninsula. . n. magnus Wettstein, 1913 - Turkey, Iraq, and Bahrain. . n. kachhensis Dobson, 1872 - South Asia in Afghanistan, Pakistan, India, Nepal, Bhutan, and Bangladesh. . n. nudaster Thomas, 1915-NWMyanmar; however, complete distribution is unknown.. n. zayidi D. L. Harrison, 1955 - Oman; however, complete distribution is unknown. Present also in Georgia, Armenia, Azerbaijan, Turkmenistan, Lebanon, Syria, Jordan, and Iran, but distributions of subspecies in SW & C Asia are only partially understood and clarification awaits future systematic resolution in Emballonuridae
Subspecies and Distribution. . n. nudiventris Cretzschmar, 1830 - N, W, C & E Africa, also in Israel, Palestine, and the Arabian Peninsula. . n. magnus Wettstein, 1913 - Turkey, Iraq, and Bahrain. . n. kachhensis Dobson, 1872 - South Asia in Afghanistan, Pakistan, India, Nepal, Bhutan, and Bangladesh. . n. nudaster Thomas, 1915-NWMyanmar; however, complete distribution is unknown.. n. zayidi D. L. Harrison, 1955 - Oman; however, complete distribution is unknown. Present also in Georgia, Armenia, Azerbaijan, Turkmenistan, Lebanon, Syria, Jordan, and Iran, but distributions of subspecies in SW & C Asia are only partially understood and clarification awaits future systematic resolution
Distribution. Known from scattered records in S Senegal (Niokolo-Koba National Park and Diattacounda), SW & SE Guinea (near Kindia, Simandou Range, and Mt Nimba), C Sierra Leone, N Liberia (including Liberian Mt Nimba), and E Ivory Coast; it is potentially present in Gambia in patches of relict forest. in Rhinolophidae
Distribution. Known from scattered records in S Senegal (Niokolo-Koba National Park and Diattacounda), SW & SE Guinea (near Kindia, Simandou Range, and Mt Nimba), C Sierra Leone, N Liberia (including Liberian Mt Nimba), and E Ivory Coast; it is potentially present in Gambia in patches of relict forest.
APPENDIX Individuals included in the genetic and/or skull morphology analyses are presented with source and locality information (reference to sites in Fig. 1 are given in parentheses when available). Voucher numbers are provided for individuals that were collected: AMNH — American Museum of Natural History, New York, NY, USA, BMNH — Natural History Museum, London, UK, FMNH — Field Museum, Chicago, IL, USA, HZM — Harrison Zoological Museum, Kent, UK, MCZ — Museum of Comparative Zoology, Harvard, MA, USA, MZB — Muzeum Zoologicum Bogoriense, Bogor, Indonesia, RMNH — National Museum of Natural History Naturalis, Leiden, Netherlands, SEN — Senckenberg Museum, Frankfurt, Germany, TK — tissue collection and TTU — specimen numbers; Texas Tech. University, Lubbock, TX, USA, and USNM — Smithsonian Institute, Washington D.C., USA. All specimens from peninsular Malaysia with THK or MBCRU field numbers were collected by A. Zubaid, and the specimens or duplicate wing punches were deposited at UKM (Universiti Kebangsaan Malaysia, Bangi, Selangor, Malaysia). The original taxonomy of type specimens (type) are listed. Haplotypes (Hap) are given for individuals of H. bicolor (=H. bicolor-131) and H. kunzi (=H. bicolor-142). GenBank accession numbers are given for one representative of each unique haplotype in A new species in the Hipposideros bicolor group (Chiroptera: Hipposideridae) from Peninsular Malaysia
APPENDIX Individuals included in the genetic and/or skull morphology analyses are presented with source and locality information (reference to sites in Fig. 1 are given in parentheses when available). Voucher numbers are provided for individuals that were collected: AMNH — American Museum of Natural History, New York, NY, USA, BMNH — Natural History Museum, London, UK, FMNH — Field Museum, Chicago, IL, USA, HZM — Harrison Zoological Museum, Kent, UK, MCZ — Museum of Comparative Zoology, Harvard, MA, USA, MZB — Muzeum Zoologicum Bogoriense, Bogor, Indonesia, RMNH — National Museum of Natural History Naturalis, Leiden, Netherlands, SEN — Senckenberg Museum, Frankfurt, Germany, TK — tissue collection and TTU — specimen numbers; Texas Tech. University, Lubbock, TX, USA, and USNM — Smithsonian Institute, Washington D.C., USA. All specimens from peninsular Malaysia with THK or MBCRU field numbers were collected by A. Zubaid, and the specimens or duplicate wing punches were deposited at UKM (Universiti Kebangsaan Malaysia, Bangi, Selangor, Malaysia). The original taxonomy of type specimens (type) are listed. Haplotypes (Hap) are given for individuals of H. bicolor (=H. bicolor-131) and H. kunzi (=H. bicolor-142). GenBank accession numbers are given for one representative of each unique haplotype
Constraining present-day anthropogenic total iron emissions using model and observations
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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.