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700 results for “molecular identification”
Fig. 5 in Molecular identification of a new myxozoan, Myxobolus dermiscalis n. sp. (Myxosporea) infecting scales of Labeo rohita Hamilton in Harike Wetland, Punjab (India)
Fig. 5. Estimates of evolutionary divergence between the sequences of M. dermiscalis and other Myxosporea available in GenBank.
Fig. 2 in Molecular identification of a new myxozoan, Myxobolus dermiscalis n. sp. (Myxosporea) infecting scales of Labeo rohita Hamilton in Harike Wetland, Punjab (India)
Fig. 2. Infected scales of L. rohita showing creamish white pseudocysts of M. dermiscalis n. sp scale bar = 1 cm.
Fig. 4 in Molecular identification and characterization of partial COX1 gene from caecal worm (Aulonocephalus pennula) in Northern bobwhite (Colinus virginianus) from the Rolling Plains Ecoregion of Texas
Fig. 4. Molecular Phylogenetic analysis by Maximum Likelihood method. The evolutionary history was inferred using the ML method based on the General Time Reversible model. The phylogenetic tree illustrates COX1 gene sequences of nematodes related to A. pennula. Bootstrap values above 50 are shown in the tree. The tree is drawn to scale, with branch lengths measured in the number of substitutions-per-site. All positions containing gaps and missing data were eliminated. Evolutionary analyses were conducted in MEGA7.
Fig. 1. A in Molecular identification and characterization of partial COX1 gene from caecal worm (Aulonocephalus pennula) in Northern bobwhite (Colinus virginianus) from the Rolling Plains Ecoregion of Texas
Fig. 1. A. Caecum of the wild quail B. Morphology of male and female caecal worm. All the parts of male and female caecal worm Aulonocephalus pennula are marked in Fig. 1B.
Fig. 3 in Molecular identification and characterization of partial COX1 gene from caecal worm (Aulonocephalus pennula) in Northern bobwhite (Colinus virginianus) from the Rolling Plains Ecoregion of Texas
Fig. 3. Pairwise alignment of the sequences of A. pennula and H. gallinarum. Sequence variations between A. pennula and H. gallinarum are highlighted in red. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
Fig. 2. A in Molecular identification and characterization of partial COX1 gene from caecal worm (Aulonocephalus pennula) in Northern bobwhite (Colinus virginianus) from the Rolling Plains Ecoregion of Texas
Fig. 2. A. PCR amplification of COX1 gene using nematode primers. Lane M: 100 bp DNA ladder (Fermentas); lane 1‾4 COX1 gene amplicon (750 bp). B. PCR amplification of partial COX1 gene using gene specific primers. Lane M: 100 bp DNA Marker (Fermentas); lane 1‾4 partial COX1 amplified products (405bp).
Fig. 3 in Molecular insights into the identification and phylogenetics of the cosmopolitan marine fish blood parasite, Haemogregarina bigemina (Adeleorina: Haemogregarinidae)
Fig. 3. Phylogenetic identification of Haemogregarina bigemina from the UK based on 18S rDNA sequences. (a) Maximum parsimony and (b) Maximum likelihood reconstructions revealing the unique position of UK H. bigemina samples outside of the adeleorine groups. For both phylogenies nodal support was calculated using 1000 bootstrap replicates with only values> 50% presented.
Fig. 1 in Molecular insights into the identification and phylogenetics of the cosmopolitan marine fish blood parasite, Haemogregarina bigemina (Adeleorina: Haemogregarinidae)
Fig. 1. Photograph of the fish host Lipophrys pholis, one of the type hosts of Haemogregarina bigemina, screened in this study.
Fig. 2 in Molecular insights into the identification and phylogenetics of the cosmopolitan marine fish blood parasite, Haemogregarina bigemina (Adeleorina: Haemogregarinidae)
Fig. 2. Stages of Haemogregarina bigemina from Giemsa-stained blood films of Lipophrys pholis from the UK. (a) trophozoite, (b) meront, (c–e) dividing meronts, and (f) paired gamonts. Scale bar = 10 μm.
Fig. 5 in First molecular identification of Vorticella sp. from freshwater shrimps in Tainan, Taiwan
Fig. 5. Bayesian phylogenetic tree of Vorticella sp. constructed from the nuclear ITS1-5.8S-ITS2 sequences. Sequences investigated in this study is in bold. Numbers numbers given at nodes of branches are the posterior probability (BI) and bootstrap (ML) values. The scale bar corresponds to 10 substitutions per 100 nucleotide positions. Classification follows that of Lynn (2008).
Fig. 2 in First molecular identification of Vorticella sp. from freshwater shrimps in Tainan, Taiwan
Fig. 2. Vorticella aequilata-like pop TW infected freshwater shrimps (Neocaridina Denticulata). (st) stalk. (sc) scopula. (FV) food vacuole. Scale bar: A = 500 μm; B- D = 100 μm.
Fig. 6 in Molecular identification of two Eimeria species, E. uekii and E. raichoi as type B, in wild Japanese rock ptarmigans, Lagopus muta japonica
Fig. 6. Histopathologic sections of ceca which were obtained from dead chicks infected with Eimeria spp. Arrowhead indicates macrogametocytes with a prominent wall-forming body (A), and arrows indicate zygotes or early oocysts, which are surrounded by an oocyst wall (A and B). Pathological lesions could not be observed because of severe degradation after death. Scale bars indicate 20 μm.
Fig. 3 in Molecular identification of two Eimeria species, E. uekii and E. raichoi as type B, in wild Japanese rock ptarmigans, Lagopus muta japonica
Fig. 3. Phylogram of E. uekii, type B, other Eimeria spp., and related parasites (Cyclospora spp.) inferred by the neighbor-joining method using partial 18S rRNA gene sequences. Accession numbers and derived hosts are shown in parentheses. Scale bar represents substitutions per nucleotide, and bootstrap values are indicated (> 1000). Cystoisospora spp. are used as an outgroup taxon.
Fig. 4 in Molecular identification of two Eimeria species, E. uekii and E. raichoi as type B, in wild Japanese rock ptarmigans, Lagopus muta japonica
Fig. 4. Phylogram of E. uekii, type B, and other related Eimeria spp. inferred by the neighbor-joining method using partial mitochondrial cytochrome c oxidase subunit I gene sequences. Accession numbers and derived hosts are shown in parentheses. Scale bar represents substitutions per nucleotide, and bootstrap values are indicated (> 1000). Toxoplasma gondii is used as an outgroup taxon.
Fig. 2 in Molecular identification of two Eimeria species, E. uekii and E. raichoi as type B, in wild Japanese rock ptarmigans, Lagopus muta japonica
Fig. 2. Eimeria oocysts detected in the feces of Japanese rock ptarmigans. (A) E. uekii and (B) type B. Scale bars indicate 10 μm.
Fig. 1 in Molecular identification of two Eimeria species, E. uekii and E. raichoi as type B, in wild Japanese rock ptarmigans, Lagopus muta japonica
Fig. 1. Location of three sampled areas in Japan, Mt. Tateyama (36̊35′N, 137̊36′E), Norikuradake (36̊6′N, 137̊33′E), and Kitadake (35̊40′N, 138̊14′E) (triangle boxes 1–3).
Fig. 4 in First molecular identification of Vorticella sp. from freshwater shrimps in Tainan, Taiwan
Fig. 4. Bayesian phylogenetic tree of peritrich ciliates constructed from the nuclear ITS1-5.8S-ITS2 sequences. Sequence investigated in this study is in bold. Numbers given at nodes of branches are the posterior probability (BI) and bootstrap (ML) values. The scale bar corresponds to 10 substitutions per 100 nucleotide positions. Classification follows that of Lynn (2008).
Fig. 3 in First molecular identification of Vorticella sp. from freshwater shrimps in Tainan, Taiwan
Fig. 3. Scutariella sp. infected freshwater shrimps (Neocaridina Denticulata). (b) brain. (e) eye. (m) mouth. (p) pharynx. (t) testis. (te) tentacle. (vg) vitelline glands. Scale bar: A = 500 μm; B, D = 200 μm; C = 100 μm.
Fig. 5 in Molecular identification of two Eimeria species, E. uekii and E. raichoi as type B, in wild Japanese rock ptarmigans, Lagopus muta japonica
Fig. 5. Composite line drawing of oocyst of Eimeria raichoi n. sp (previously referred as type B). Scale bars indicate 10 μm.
Fig. 1 in Toxocariasis in Carnivora from Argentinean Patagonia: Species molecular identification, hosts, and geographical distribution
Fig. 1. Collection sites of specimens of Felidae, Mustelidae, and Canidae in Lanín and Nahuel Huapi National Parks from Argentinean Patagonia.
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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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.