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1,061 results for “115”
Figure 1 from: Tanaka H (2016) A new genus and species of Rhizoecidae (Hemiptera, Sternorryncha, Coccomorpha) associated with Acropyga yaeyamensis (Hymenoptera, Formicidae, Formicinae). ZooKeys 616: 115-124. https://doi.org/10.3897/zookeys.616.9442
Figure 1 - A mature adult female of Ishigakicoccus shimadai sp. n.
Figure 28 from: Chen K, Zhang D, Li H (2018) Systematics of the new genus Spinosuncus Chen, Zhang & Li with descriptions of four new species (Lepidoptera, Crambidae, Pyraustinae). ZooKeys 799: 115-151. https://doi.org/10.3897/zookeys.799.23925
Figure 28 Distribution of Spinosuncus species in China. A Distance between Bubang and Nabang.
Figure 2 from: Chen K, Zhang D, Li H (2018) Systematics of the new genus Spinosuncus Chen, Zhang & Li with descriptions of four new species (Lepidoptera, Crambidae, Pyraustinae). ZooKeys 799: 115-151. https://doi.org/10.3897/zookeys.799.23925
Figure 2 Wing venation of Spinosuncuspraepandalis.
COADS_115-7
This is a diagnostic biface collected in Green Township, Ross County, Ohio. Material Type: Delaware Uploaded by: Sidney Travis Suggested Data Citation: Nolan, Kevin C., Eric Olson, Kelli Wathen, Abby Clark, and Michael Shott, 2017. COADS_#-#, 3D Model .ply file. Central Ohio Archaeological Digitization Survey, Department of Anthropology, University of Akron and Applied Anthropology Laboratories, Department of Anthropology, Ball State University. Source: Objaverse 1.0 / Sketchfab
A Phase II Study of DMP 115 to Assess Focal Liver Lesions
ClinicalTrials.gov study NCT00162058. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Lipid Management in Clinical Practice (MK-0524A-115)
ClinicalTrials.gov study NCT01071278. IPD Sharing: Not stated. Countries: 0. Publications: 0.
S E- GEOD-50881 Study Samples --- Candida albicans response to spaceflight (NASA STS-115)
https://c3.nasa.gov/genelab/accession/GLDS-20/ This study presents the first global transcriptional profiling and phenotypic characterization of the major human opportunistic fungal pathogen, Candida albicans, grown in spaceflight conditions. Microarray analysis revealed that C. albicans subjected to short-term spaceflight culture differentially regulated 454 genes compared to synchronous ground controls, which represented 8.4% of the analyzed ORFs. Spaceflight-cultured C. albicans induced genes involved in cell aggregation (similar to flocculation), which was validated by microscopic and flow cytometry analysis. We also observed enhanced random budding of spaceflight-cultured cells as opposed to more normal bipolar budding patterns for ground samples, in accordance with the gene expression data. Furthermore, genes involved in antifungal agent and stress resistance were differentially regulated in spaceflight, including induction of ABC transporters and members of the major facilitator family, downregulation of ergosterol-encoding genes, and upregulation of genes involved in oxidative stress resistance. Finally, downregulation of genes involved in the actin cytoskeleton was observed. Interestingly, the transcriptional regulator Cap1 and over 30% of the Cap1 regulon was differentially expressed in spaceflight-cultured C. albicans. A potential role for Cap1 in the spaceflight response of C. albicans is suggested, as this regulator is involved in random budding, cell aggregation, actin cytoskeleton, and oxidative stress resistance; all related to observed spaceflight-associated changes of C. albicans. While culture of C. albicans in microgravity potentiates a global change in gene expression that could induce a virulence-related phenotype, no increased virulence in a murine intraperitoneal (i.p.) infection model was observed. This study represents an important basis for the assessment of the risk that commensal flora could play during spaceflight missions. Furthermore, since the low fluid-shear environment of microgravity is relevant to physical forces encountered by pathogens during the infection process, insights gained from this study could identify novel infectious disease mechanisms, with downstream benefits for the general public. Cells were grown for 24 hours on the space shuttle or as ground-based controls, preserved in RNALater, and stored at -80C. Four samples of each flight- and ground-based controls were harvested for microarray analysis. GAP is Group Activation Pack and each GAP contains 8 FPAs. The numbers represent the # assigned to the particular GAP and the number assigned to the specific FPA (1-8) within the indicated GAP. The same hardware is used for the flight samples and the ground samples.
Candida albicans response to spaceflight (NASA STS-115) --- GSM1231690_Slide_43
https://c3.nasa.gov/genelab/accession/GLDS-20/ This study presents the first global transcriptional profiling and phenotypic characterization of the major human opportunistic fungal pathogen, Candida albicans, grown in spaceflight conditions. Microarray analysis revealed that C. albicans subjected to short-term spaceflight culture differentially regulated 454 genes compared to synchronous ground controls, which represented 8.4% of the analyzed ORFs. Spaceflight-cultured C. albicans induced genes involved in cell aggregation (similar to flocculation), which was validated by microscopic and flow cytometry analysis. We also observed enhanced random budding of spaceflight-cultured cells as opposed to more normal bipolar budding patterns for ground samples, in accordance with the gene expression data. Furthermore, genes involved in antifungal agent and stress resistance were differentially regulated in spaceflight, including induction of ABC transporters and members of the major facilitator family, downregulation of ergosterol-encoding genes, and upregulation of genes involved in oxidative stress resistance. Finally, downregulation of genes involved in the actin cytoskeleton was observed. Interestingly, the transcriptional regulator Cap1 and over 30% of the Cap1 regulon was differentially expressed in spaceflight-cultured C. albicans. A potential role for Cap1 in the spaceflight response of C. albicans is suggested, as this regulator is involved in random budding, cell aggregation, actin cytoskeleton, and oxidative stress resistance; all related to observed spaceflight-associated changes of C. albicans. While culture of C. albicans in microgravity potentiates a global change in gene expression that could induce a virulence-related phenotype, no increased virulence in a murine intraperitoneal (i.p.) infection model was observed. This study represents an important basis for the assessment of the risk that commensal flora could play during spaceflight missions. Furthermore, since the low fluid-shear environment of microgravity is relevant to physical forces encountered by pathogens during the infection process, insights gained from this study could identify novel infectious disease mechanisms, with downstream benefits for the general public. Cells were grown for 24 hours on the space shuttle or as ground-based controls, preserved in RNALater, and stored at -80C. Four samples of each flight- and ground-based controls were harvested for microarray analysis. GAP is Group Activation Pack and each GAP contains 8 FPAs. The numbers represent the # assigned to the particular GAP and the number assigned to the specific FPA (1-8) within the indicated GAP. The same hardware is used for the flight samples and the ground samples.
A E- GEOD-50881 Gene Chip Assay --- Candida albicans response to spaceflight (NASA STS-115)
https://c3.nasa.gov/genelab/accession/GLDS-20/ This study presents the first global transcriptional profiling and phenotypic characterization of the major human opportunistic fungal pathogen, Candida albicans, grown in spaceflight conditions. Microarray analysis revealed that C. albicans subjected to short-term spaceflight culture differentially regulated 454 genes compared to synchronous ground controls, which represented 8.4% of the analyzed ORFs. Spaceflight-cultured C. albicans induced genes involved in cell aggregation (similar to flocculation), which was validated by microscopic and flow cytometry analysis. We also observed enhanced random budding of spaceflight-cultured cells as opposed to more normal bipolar budding patterns for ground samples, in accordance with the gene expression data. Furthermore, genes involved in antifungal agent and stress resistance were differentially regulated in spaceflight, including induction of ABC transporters and members of the major facilitator family, downregulation of ergosterol-encoding genes, and upregulation of genes involved in oxidative stress resistance. Finally, downregulation of genes involved in the actin cytoskeleton was observed. Interestingly, the transcriptional regulator Cap1 and over 30% of the Cap1 regulon was differentially expressed in spaceflight-cultured C. albicans. A potential role for Cap1 in the spaceflight response of C. albicans is suggested, as this regulator is involved in random budding, cell aggregation, actin cytoskeleton, and oxidative stress resistance; all related to observed spaceflight-associated changes of C. albicans. While culture of C. albicans in microgravity potentiates a global change in gene expression that could induce a virulence-related phenotype, no increased virulence in a murine intraperitoneal (i.p.) infection model was observed. This study represents an important basis for the assessment of the risk that commensal flora could play during spaceflight missions. Furthermore, since the low fluid-shear environment of microgravity is relevant to physical forces encountered by pathogens during the infection process, insights gained from this study could identify novel infectious disease mechanisms, with downstream benefits for the general public. Cells were grown for 24 hours on the space shuttle or as ground-based controls, preserved in RNALater, and stored at -80C. Four samples of each flight- and ground-based controls were harvested for microarray analysis. GAP is Group Activation Pack and each GAP contains 8 FPAs. The numbers represent the # assigned to the particular GAP and the number assigned to the specific FPA (1-8) within the indicated GAP. The same hardware is used for the flight samples and the ground samples.
FIGURES 107–115 in Diagnostics and updated catalogue of Acalyptris Meyrick, the second largest genus of Nepticulidae (Lepidoptera) in the Americas
FIGURES 107–115. Bionomics and adults of Acalyptris yucatani Remeikis & Stonis, 2013 from Colombia, tropical western slopes of the Andes, Valle del Cauca (new distribution, host plant, and newly attributed male). 107, 108, host plant Gliricidia sepium (Jacq.) Kunth ex Walp., Fabaceae, Faboideae; 109, cocoon; 110, 111, leaf mines; 112, adult, female; 113–115, same, male.
FIGURE 115 Uroptychus lacunatus n in Chirostylidae of the Western and Central Pacific: Uroptychus and a new genus (Crustacea: Decapoda: Anomura)
FIGURE 115 Uroptychus lacunatus n.sp.,A-C, E-H, holotype,male 6.1 mm (MNHN-IU-2014-16609);D, paratype,ovigerous female (MNHN-IU-2014-16610). A, carapace and anterior part of abdomen,proximal part of right P1 included,dorsal.B, same, lateral.C, sternal plastron,with excavated sternum and basal parts of Mxp1. D, telson. E, left antenna, ventral.F, right Mxp3, setae omitted, ventral.G, left P3, setae omitted from distal articles, lateral. H, right P1, dorsal. Scale bars: 1 mm.
FIGURES 115–118 in Damselflies of the genus Argia (Odonata: Coenagrionidae) from Ecuador with descriptions of five new species
FIGURES 115–118. Male caudal appendages. (a) lateral view; (b) dorsal view; (c) mediodorsal view; (d) posterior view.
FIGURES 113–115. Lanceopora formosa Harmer, 1957, RGM.1350571 in Early Pleistocene and Holocene bryozoans from Indonesia
FIGURES 113–115. Lanceopora formosa Harmer, 1957, RGM.1350571, Holocene, UPGG041, off South Sulawesi. 113. View of the lanceolate, bilaminar colony. 114. Group of zooids. 115. Close-up of an orifice. Scale bars: Fig. 113 = 500 µm; Fig. 114 = 100 µm; Fig. 115 = 20 µm.
FIGURES 106–115 in The Chinese Hecalina (Hemiptera: Cicadellidae: Deltocephalinae: Hecalini) with descriptions of a new genus and seven new species
FIGURES 106–115. Thomsonia breviaea, sp. n. 106, male adult, dorsal view; 107, female adult, dorsal view; 108, female left forewing; 109, female 7th abdominal sternum; 110–111, aedeagus, lateral and ventral view respectively; 112, style, dorsal view; 113, connective, dorsal view; 114, male pygofer, lateral view; 115, subgenital plate.
FIGURES 115–118 in Review of the Oriental genus Indocloeon Müller-Liebenau 1982 (Ephemeroptera: Baetidae) with descriptions of two new species
FIGURES 115–118. Indocloeon (Hindocloeon) sp. «Java». 115–116, female subimago; 117–118, male subimago.
FIGURES 115–121 in Three new synonyms within the flower chafer genus Goliathopsis Janson, 1881 (Coleoptera: Scarabaeidae: Cetoniinae) from China
FIGURES 115–121. Type specimens of Goliathopsis capreolus Gestro, 1888 in MSNG. 115–118, male lectotype and labels; 119–121, female paralectotype and labels.
FIGURES 110–115. Ptiloneura tunkywasi n in An appraisal of the genus Ptiloneura Enderlein (Insecta: Psocodea: Psocomorpha Ptiloneuridae), new species from Colombia and Peru, and a key to the males
FIGURES 110–115. Ptiloneura tunkywasi n. sp. Female. 110. Forewing. 111. Hindwing. 112. Front view of head. 113. Left paraproct and epiproct. 114. Subgenital plate. 115. Ninth sternum and left gonapophyses. Scales in mm.
FIGURE 115. Pterygosoma pseudorbicularis Jack, 1962, female. A in A systematic revision of the scale mite genus Pterygosoma Peters, 1849 (Acariformes: Pterygosomatidae)
FIGURE 115. Pterygosoma pseudorbicularis Jack, 1962, female. A, gnathosoma in dorsal view; B, tarsus I in ventro-lateral view; C, tarsus II in dorsal view.
FIGURES 115-118 in Taxonomic revision of the genus Nychiodes Lederer, 1853 (Geometridae: Ennominae: Boarmiini) with description of three new species-an integrative approach
FIGURES 115-118. Male genitalia of Nychiodes species. 115: Syntype of N. divergaria achtyca syn. nov. of N. divergaria (Dagestan, Ackty, g.prep. 7272); 116: Uncus, lateral view, N. divergaria (Turkey, Hakkari, g.prep. 0395/2019 D. Wanke); 117: Lectotype (herewith designated) of N. divergaria (Turkey, Mardin, g.prep. 2106/2017 H. Rajaei); 118: Paralectotype (herewith designated) of N. divergaria (Turkey, Egin, g.prep. 2107/2017 H. Rajaei); a = genitalia capsule; b = aedeagus. Scale-bar 1 mm.
FIGURES 106–115. Andraegoidus variegatus male. 106 in Revision of the genus Andraegoidus Aurivillius (Insecta: Coleoptera: Cerambycidae)
FIGURES 106–115. Andraegoidus variegatus male. 106, sternite VIII; 107, tergite VIII; 108, ventral arc; 109, dorsal arc; 110– 112, tegmen: 110, dorsal view, 111, lateral view, 112, ventral view; 113–115, median lobe: 113, dorsal view, 114, lateral view, 115, ventral view.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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OpenNeuro
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