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401 results for “Nuclear Genes”
Figure 4 in The tail tells the tale: taxonomy and biogeography of some Atlantic Chelidonura (Gastropoda: Cephalaspidea: Aglajidae) inferred from nuclear and mitochondrial gene data
Figure 4. Scanning electron micrographs of the protoconch morphology or apical shell morphology of some specimens examined. Arrows indicate transitions in growth line pattern. A–D, Chelidonura africana: A, specimen from Portugal (MNCN 15.05/46493); B, specimen from Portugal (MNCN 15.05/46488); C, specimen from Portugal (MNCN 15.05/44368); D, juvenile specimen from Azores, Portugal (MNCN 15.05/44367). E–G, Chelidonura berolina: E, specimen from Bahamas (LACM 172272); F, specimen from Bahamas (LACM 176427); G, specimen from Bahamas (LACM 176426). H–J, Chelidonura normani sp. nov.: H, specimen from Bahamas (LACM 3126); I-J, specimen from Bahamas (LACM 3127).
Figure 3 in The tail tells the tale: taxonomy and biogeography of some Atlantic Chelidonura (Gastropoda: Cephalaspidea: Aglajidae) inferred from nuclear and mitochondrial gene data
Figure 3. Drawings of the penis and prostate of several specimens examined. A–K, Chelidonura berolina: A, specimen from Bahamas (LACM 176428); B, specimen from Bahamas (LACM 176428); C, specimen from Bahamas (LACM 176431); D, specimen from Bahamas (LACM 176428); E, specimen from Bahamas (LACM 176432); F, specimen from Bahamas (LACM 176428); G, specimen from Bahamas (LACM 176435); H, specimen from Bahamas (LACM 176428); I, specimen from Bahamas (LACM 176428); J, specimen from Martinique (LACM 176437); K, specimen from Roatán, Honduras (LACM 176433). L–M, Chelidonura africana: L, specimen from Portugal (MNCN 15.05/46493); M, specimen from Portugal (MNCN 15.05/44368). N–O, Chelidonura normani sp. nov.: N, specimen from Bahamas (LACM 3126); O, specimen from Bahamas (LACM 3125). Abbreviations: pe, penis; pr, prostate.
Figure 2 in The tail tells the tale: taxonomy and biogeography of some Atlantic Chelidonura (Gastropoda: Cephalaspidea: Aglajidae) inferred from nuclear and mitochondrial gene data
Figure 2. Maximum likelihood bootstrap consensus tree for the analysis of the combined histone 3 (H3), 16S, and cytochrome oxidase I (COI) sequence alignments. Bootstrap values are indicated above each branch. Respective posterior probabilities resulting from the Bayesian analysis are also indicated below each branch.
Figure 1 in The tail tells the tale: taxonomy and biogeography of some Atlantic Chelidonura (Gastropoda: Cephalaspidea: Aglajidae) inferred from nuclear and mitochondrial gene data
Figure 1. External morphology of some specimens of Chelidonura showing the range of colour variation. Specimens are grouped according to the authors' interpretation of species boundary hypotheses proposed in the literature. A–G, specimens similar to the original description of Chelidonura berolina Er. Marcus & Ev. Marcus, 1970: A, original drawing of C. berolina (from Marcus & Marcus, 1970); B, specimen from Bahamas (LACM 176429); C, specimen from Bahamas (LACM 3127); D, specimens from Bahamas (LACM 176427); E, specimen from Bahamas (LACM 3127); F, specimen from Yucatan, Mexico; G. specimen from Bahamas (LACM 176425). H–M, specimens similar to the original description of Aglaja hummelincki Er. Marcus & Ev. Marcus, 1970: H, specimen from Bahamas (LACM 3127); I, specimen from Bahamas (LACM 176427); J, specimen from Bahamas (LACM 176425); K, specimen from Bahamas (LACM 176426); L, specimen from Bahamas (LACM 176425); M, original drawing of A. hummelincki (from Marcus & Marcus, 1970). N–P, specimens similar to the original description of Chelidonura juancarlosi Ortea & Espinosa 1998: N, original drawing of C. juancarlosi (from Ortea & Espinosa, 1998); O, specimen from Bermuda (LACM 176434); P, specimen from Bahamas (LACM 173215). Q–S, specimens similar to the original description of Chelidonura mariagordae Ortea et al. 2004: Q, specimen from Bahamas (LACM 176435); R, original photograph of C. mariagordae (from Ortea et al., 2004); S, specimen from Bahamas (LACM 3128).
Figure 6 in The tail tells the tale: taxonomy and biogeography of some Atlantic Chelidonura (Gastropoda: Cephalaspidea: Aglajidae) inferred from nuclear and mitochondrial gene data
Figure 6. Type specimens of Chelidonura normani sp. nov. A, holotype (LACM 3125). B, paratype (LACM 3127). C, paratypes (LACM 3126). D, paratype (LACM 3128).
Systematic Gene Expression Mapping Clusters Nuclear Receptors According to Their Function in the Brain - Website save
<p>This is a copy of the website that was related to mousepat.ics-mci.fr</p>
Data for: Both Conifer II and Gnetales are characterized by a high frequency of ancient mitochondrial gene transfer to the nuclear genome
<p><strong>Background:</strong> Mitochondrial gene transfer/loss is common in land plants, and therefore the fate of missing mitochondrial genes has attracted more and more attention. The gene content of gymnosperm mitochondria varies greatly, supplying a system for studying the evolutionary fate of missing mitochondrial genes.</p> <p><strong>Results:</strong> Here we studied the tempo and pattern of mitochondrial gene loss/transfer in gymnosperms represented by all 13 families, using high-throughput sequencing of both DNA and cDNA. All 41 mitochondrial protein-coding genes were found in cycads, <em>Ginkgo</em> and Pinaceae, whereas multiple mitochondrial genes were absent in Conifer II and Gnetales. In Conifer II, gene transfer from mitochondria to the nucleus followed by loss of the mitochondrial copy was common, but complete loss of a gene in both mitochondrial and nuclear genomes was rare. In contrast, both gene transfer and loss were commonly found in Gnetales. Notably, in Conifer II and Gnetales, the same five mitochondrial genes were transferred to the nuclear genome, and these gene transfer events occurred, respectively, in ancestors of the two lineages. A two-step transfer mechanism (retroprocessing and subsequent DNA-mediated gene transfer) may be responsible for mitochondrial gene transfer in Conifer II and Gnetales. Moreover, the mitochondrial gene content variation is correlated with gene length, GC content, hydrophobicity, and nucleotide substitution rates in land plants.</p> <p><strong>Conclusions: </strong>This study reveals a complete evolutionary scenario for mitochondrial genes of gymnosperms and the factors responsible for mitochondrial gene content variation in land plants.</p>
Data from: Molecular systematics of armadillos (Xenarthra, Dasypodidae): contribution of maximum likelihood and Bayesian analyses of mitochondrial and nuclear genes
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Data from: Single nucleotide polymorphisms reveal genetic structuring of the Carpathian newt and provide evidence of interspecific gene flow in the nuclear genome
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Data from: Phylogenetic relationships in Orobanchaceae inferred from low-copy nuclear genes: consolidation of major clades and identification of a novel position of the non-photosynthetic Orobanche clade sister to all other parasitic Orobanchaceae
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Data from: Gene flow among wild and domesticated almond species: insights from chloroplast and nuclear markers
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Data from: Out of sight, out of mind: Widespread nuclear and plastid-nuclear discordance in the flowering plant genus Polemonium (Polemoniaceae) suggests widespread historical gene flow despite limited nuclear signal
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Data from: A reconsideration of the classification of the spider infraorder Mygalomorphae based on three nuclear genes and morphology (Arachnida: Araneae)
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Data from: Rodent phylogeny and a timescale for the evolution of Glires: evidence from an extensive taxon sampling using three nuclear genes.
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Data from: Local molecular clocks in three nuclear genes: divergence times for rodents and other mammals and incompatibility among fossil calibrations.
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Data for: Both Conifer II and Gnetales are characterized by a high frequency of ancient mitochondrial gene transfer to the nuclear genome
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Data from: Perched at the mito-nuclear crossroads: divergent mitochondrial lineages correlate with environment in the face of ongoing nuclear gene flow in an Australian bird
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Data from: Phylogenetic relationships and timing of diversification in gonorynchiform fishes inferred using nuclear gene DNA sequences (Teleostei: Ostariophysi)
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Data from: Molecular evolution of the nuclear factor (erythroid-derived 2)-like 2 gene Nrf2 in Old World fruit bats (Chiroptera: Pteropodidae)
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Data from: Ancient onset of geographic divergence, interpopulation genetic exchange, and natural selection on the Mc1r coat-color gene in the house mouse (Mus musculus) inferred from tandemly arranged nuclear gene markers
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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.