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Fig. 3 in Molecular characterization of the re-emerging West Nile virus in avian species and equids in Israel, 2018, and pathological description of the disease
Fig. 3 Brain histopathology of WNV-infected horses. Perivascular cuffs composed of lymphocytes and plasma cells in the brain of two horses, characteristic of viral encephalitis (marked by arrows). a Horse no. Eq111 (324085). b Horse no. Eq117 (325903). 100× magnification
Fig. 6 in Molecular and physiological characterization of the chitin synthase B gene isolated from CUlex pipieNS palleNS (Diptera: Culicidae)
Fig. 6 Effect of CpCHSB silencing in third instar larvae on chitin content. a Relative chitin content in fourth-instar larvae at 72 h after siCHSB injection (n = 10). b Rhodamine B staining of the midgut of fourth-instar larvae isolated after 72 h after siCHSB injection. c Chitin staining in the midgut at 48 and 72 h after siCHSB injection (n = 10). Results are shown as the mean ± SE (Student's t-tests; *P <0.05, **P <0.01). Scale-bar: 50 μm
Fig. 5 in Molecular and physiological characterization of the chitin synthase B gene isolated from CUlex pipieNS palleNS (Diptera: Culicidae)
Fig. 5 CpCHSB gene suppression by RNAi at 1 day after injection (n = 200) in adult mosquitoes. a Expression levels of CpCHSB at 72 h after injecting siCHSB assessed by RT-qPCR. The group injected with siCHSB show a reduction in CpCHSB expression of 53% compared with the control group. b Relative chitin content at 72 h after siCHSB injection. c Midgut length at 72 h after siCHSB injection. d Number of follicles per ovary and number of eggs per female mosquito (e) after injecting siCHSB. Results are shown as the mean ± SE (Student's t-tests; **P <0.01, ***P <0.001, ns, not significant)
Fig. 2 in Molecular and physiological characterization of the chitin synthase B gene isolated from CUlex pipieNS palleNS (Diptera: Culicidae)
Fig. 2 Expression profiles of CpCHSB in different tissues of fourth-instar C. pipiens pallens larvae. Tissues include head (HE), foregut (FG), midgut (MG), hindgut (HG), Malpighian tubules (MT) and carcass (CA). Relative expression levels were calculated based on the lowest expression value, which was ascribed an arbitrary value of 1. Results are shown as the mean ± SE
Fig. 1 in Molecular and physiological characterization of the chitin synthase B gene isolated from CUlex pipieNS palleNS (Diptera: Culicidae)
Fig. 1 Alignment of the conserved catalytic domain of chitin synthases from three mosquito species Seven characteristic motifs (M1–M7) in insect chitin synthases are highlighted. Dashes are used to denote gaps introduced to maximise alignment. Abbreviations: Ae, Aedes aegypti; Ag, Anopheles gambiae; Cp, Culex pipiens pallens
Fig. 2 in Molecular characterization of the re-emerging West Nile virus in avian species and equids in Israel, 2018, and pathological description of the disease
Fig. 2 Brain histopathology of WNV-infected long-eared owl (Asio otus) AV156. a A glial nodule in the brain stem (marked by an arrow). 100× magnification. b A glial nodule in the brain stem with few adjacent necrotic neurons, 400× magnification
Figure 6 in Molecular and morphological characterization of Tylenchus zeae n. sp. (Nematoda: Tylenchida) from Corn (Zea mays) in South Carolina
Figure 6: Phylogenetic relationships of Tylenchus zeae n. sp. with other select Tylenchidae, as inferred from a 418 bp alignment of mitochondrial COI sequences, according to the GTR + I + G model of nucleotide substitution and incorporated into MrBayes (MB) as described. A 50% majority rule consensus tree was generated with posterior probabilities (PP) shown on appropriate branches, with Bursaphelenchus cOnicaudatus as the outgroup. New sequences are indicated in bold.
Figure 4 in Molecular and morphological characterization of Tylenchus zeae n. sp. (Nematoda: Tylenchida) from Corn (Zea mays) in South Carolina
Figure 4: Phylogenetic relationships of Tylenchus zeae n. sp. with other select Tylenchidae, as inferred from a 1585 bp alignment of 18S rRNA sequences, according to the GTR + I + G model of nucleotide substitution and incorporated into MrBayes (MB) as described. A 50% majority rule consensus tree was generated with posterior probabilities (PP) shown on appropriate branches, with AphelenchOides besseyi as the outgroup. New sequences are indicated in bold.
Figure 3 in Molecular and morphological characterization of Tylenchus zeae n. sp. (Nematoda: Tylenchida) from Corn (Zea mays) in South Carolina
Figure 3: Line drawings of Tylenchus zeae n. sp. A: Female pharyngeal region; B: Female lip region showing stylet; C: Areolated lateral field; D: Male spicule, gubernaculum, and bursa. E: Vulval region showing vulva, uterus, and spermatheca; F–G: female tails.
Figure 2 in Molecular and morphological characterization of Tylenchus zeae n. sp. (Nematoda: Tylenchida) from Corn (Zea mays) in South Carolina
Figure 2: Photomicrographs of Tylenchus zeae n. sp. males and females. A–B: Anterior end with arrows pointing toward the excretory pore; C: Excretory pore; D: Areolated lateral field; E: Entire female body; F: Female basal bulb; G: Female gonad; H–I: female posterior end with arrow pointing the anal area (H); J: Female vulva region with arrow pointing toward the spermatheca; K: Male spicule.
Figure 5 in Molecular and morphological characterization of Tylenchus zeae n. sp. (Nematoda: Tylenchida) from Corn (Zea mays) in South Carolina
Figure 5: Phylogenetic relationships of Tylenchus zeae n. sp. with other select Tylenchidae, as inferred from an 822 bp alignment of 28S rRNA sequences, according to the GTR + I + G model of nucleotide substitution and incorporated into MrBayes (MB) as described. A 50% majority rule consensus tree was generated with posterior probabilities (PP) shown on appropriate branches, with Bursaphelenchus mucrOnatus as the outgroup. New sequences are indicated in bold.
Figure 1 in Molecular and morphological characterization of Tylenchus zeae n. sp. (Nematoda: Tylenchida) from Corn (Zea mays) in South Carolina
Figure 1: Scanning electron micrograph (SEM) images of Tylenchus zeae n. sp. A: Female specimen, anterior end, arrow pointing toward the excretory pore; B: Female specimen, head; C: Female specimen, face view; D: Lateral field (midbody); E: Female specimen, anal opening; F: Female specimen, vulval opening; G: Male specimen, spicule; H: Female specimen, arrow showing the anal opening; I: Female specimen, tail; J: Male specimen, posterior end.
Figure 3 in Characterization of root-knot nematodes infecting mulberry in Southern China
Figure 3: Phylogenetic relationships within root-knot nematodes on mulberry as inferred from Bayesian analysis of the D2-D3 region of the 28S gene sequences. Posterior probability values more than 70% are given on appropriate clades.
Figure 1 in Characterization of root-knot nematodes infecting mulberry in Southern China
Figure 1: Representative morphological characteristics of M. enterolobii. (A, whole female; B, C, female head; D, E, female perineal pattern; F, male entire; G, male head and tail; H, male posture; I, head of G second instar larva; J, middle of second instar larva; K, tail of second instar larva).
Figure 2 in Characterization of root-knot nematodes infecting mulberry in Southern China
Figure 2: Phylogenetic relationships within root-knot nematodes on mulberry as inferred from Bayesian analysis of the rDNA-ITS gene sequences. Posterior probability values more than 70% are given on appropriate clades.
Fig. 1 in Characterization of Crude and Biodiesel Oils of Jatropha curcas and Calophyllum inophyllum in Guam
Fig. 1. Potential biofuel crops in Guam. Flow chart is indicating processing to produce biofuels. (from Marutani and Martinez, presented at the 5th Regional Conference of Island Sustainability on April 15, 2014)
Fig. 3 in Characterization of Crude and Biodiesel Oils of Jatropha curcas and Calophyllum inophyllum in Guam
Fig. 3. Jatropha curcas showing: field planting in Guam (3A); a close-up tree (3B); inflorescences (3C), different stages of fruits (3D); open fruit with three seeds in each fruit (3E); dried seeds and ground seeds before extracted oil (3F); oil extracts (3G); and final product of crude oils of jatropha (left) and da'ok (right) after removing sediments (3H).
Figure 5 in Characterizing the complete mitochondrial genome of Psephenothrips eriobotryae Dang & Qiao (Thysanoptera: Phlaeothripidae) with massive gene arrangement in Phlaeothripidae
Figure 5. Comparison of the nucleotide sequences of the two putative control regions in the mitogenome of P. eriobotryae. The structural elements were recognized: repeat unit, TATA motif, TA(A)n motif, stem and loop, Poly T-stretch sequence, A + T-rich sequence and G(A)nT motif.
Figure 6 in Characterizing the complete mitochondrial genome of Psephenothrips eriobotryae Dang & Qiao (Thysanoptera: Phlaeothripidae) with massive gene arrangement in Phlaeothripidae
Figure 6. Gene rearrangement, transposition, inversion and inverse transposition. A. Comparison with the ancestor gene sequence of arthropods, Drosophila yakuba and P. eriobotryae gene sequence. B. Comparison with P. eriobotryae and other five known mitogenomes of Phlaeothripidae species. Yellow blocks show PCGs, blue ones show tRNA, red ones show rRNA and Colourless ones show CRs. Red dashes boxes represent conserve gene blocks. Red dotted ovals represent that the reverse transposition happened in the gene blocks. '+' indicates H-strand, and '-' indicates L-strand. Black arrows indicate the direction of gene translation.
Figure 1 in Characterizing the complete mitochondrial genome of Psephenothrips eriobotryae Dang & Qiao (Thysanoptera: Phlaeothripidae) with massive gene arrangement in Phlaeothripidae
Figure 1. The circular representation of the complete mitogenome of P. eriobotryae. The direction of gene transcription is indicated by the arrows. PCGs are showed as blue purple arrows, rRNA genes as green arrows, tRNA genes as pink purple arrow and CRs as orange arrows. The inner black circles show GC content and GC-skew plotted as the deviation from the average value of the entire sequence. The image was taken from slide-mounted specimen with an Olympus BX53 and edited manually in Adobe Photoshop 2022 v23.0.2.101.
ScienceDex guides
Understand access before you commit
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.