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259
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ShareScore release 0.9.0
Dataset results
259 results for “camelina”
Camelina alyssum (Mill.) Thell. (BR0000010448236)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Camelina alyssum (Mill.) Thell. (BR0000010446935)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Camelina alyssum (Mill.) Thell. (BR0000010446829)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Camelina alyssum (Mill.) Thell. (BR0000010448182)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Camelina alyssum (Mill.) Thell. (BR0000010448069)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Camelina alyssum (Mill.) Thell. (BR0000010448519)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Camelina alyssum (Mill.) Thell. (BR0000010448076)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Camelina alyssum (Mill.) Thell. (BR0000010448212)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Camelina alyssum (Mill.) Thell. (BR0000010448038)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Data from: Early spring-flowering winter cover crop (<em>Camelina sativa</em>) increases insect flower visits in Wisconsin (USA)
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Targeted sequencing of T-DNA borders in OCP1xOGC transgenic lines of Camelina
<p>Background: Genetic engineering of crop plants has been successful in transferring traits into elite lines beyond what can be achieved with breeding techniques. Introduction of transgenes originating from other species has conferred resistance to biotic and abiotic stresses, increased efficiency, and modified developmental programs. The next challenge is now to combine multiple transgenes into elite varieties via gene stacking to combine traits. Generating stable homozygous lines with multiple transgenes requires selection of segregating generations which is time consuming and labor intensive, especially if the crop is polyploid. Insertion site effects and transgene copy number are important metrics for commercialization and trait efficiency.</p> <p>Results: We have developed a simple method to identify the sites of transgene insertions using T-DNA-specific primers and high-throughput sequencing that enables identification of multiple insertion sites in the T1 generation of any crop transformed via <em>Agrobacterium</em>. We present an example using the allohexaploid oil-seed plant <em>Camelina sativa</em> to determine insertion site location of two transgenes.</p> <p>Conclusion: This new methodology enables the early selection of desirable transgene location and copy number to generate homozygous lines within two generations.</p>
Text-fig. 4. Lectotype specimen of Camelina sylvestris WALLROTH. in Wallroth´S Collection Of Vascular Plants In The Herbarium Of The National Museum, Prague
Text-fig. 4. Lectotype specimen of Camelina sylvestris WALLROTH.
Targeted sequencing of T-DNA borders in OCP1xOGC transgenic lines of Camelina
Open the record for dataset details and reuse information.
FIGURES 17–21. Illustrations for Notocera camelina Sakakibara, 1977 in Two remakable new species of Notocera Amyot and Serville, 1843 (Hemiptera, Membracidae, Hypsoprorini) from the Brazilian Caatinga
FIGURES 17–21. Illustrations for Notocera camelina Sakakibara, 1977. (17–20) Male holotype (DZUP) in frontal (17), lateral (18), and dorsal (19) view. (20) Photograph of the original labels from holotype. (21) Sakakibara's original illustrations of N. camelina (published in Sakakibara, 1997), depicting a female specimen (above) and a male specimen (below), in frontal and lateral view. Sakakibara's handwriting can be seen above the drawings.
FIGURES 3A–3G. Amapeza camelina new species. A in Amapeza and Nigripeza, new genera of Neotropical micropezid flies (Diptera, Micropezidae, Taeniapterinae)
FIGURES 3A–3G. Amapeza camelina new species. A, female, Ecuador; B, female abdomen to show humped oviscape; C, male sternite 5 (genital fork); D, male terminalia, left lateral; E, male abdominal segments 4, 5 and terminalia, ventral; F, spermathecae; G, spermathecae and associated ducts.
Fig. 3 in Extracellular lipids of Camelina sativa: Characterization of cutin and suberin reveals typical polyester monomers and unusual dicarboxylic fatty acids
Fig. 3. Annotated chromatograms of TMSi derivatives of C. sativa leaf cutin (A) and root suberin (B) monomers. Peak numbers correspond to monomers listed in Table 2 (cutin monomers) and Table 3 (suberin monomers). Internal standard (IS): 17:0 fatty acid methyl ester (IS1) and 15-hydroxy 15:0 fatty acid methyl ester (IS2). Asterisks indicate peaks of residual unsaturated fatty acids from membranes, not considered part of the polyester.
Fig. 2 in Extracellular lipids of Camelina sativa: Characterization of cutin and suberin reveals typical polyester monomers and unusual dicarboxylic fatty acids
Fig. 2. Suberin deposition in roots and seed coats of Camelina sativa. Root cross sections showing suberized root periderm stained with Sudan Red (A) or viewed via blue-yellow suberin autofluorescence (B). Transmission electron microscopy (TEM) image of root endodermis (C) and TEM image of root periderm (D). TEM image of seed coat showing suberized palisade cell walls (E, F). Scale bars: 100 μm (A, B), 100 nm (C, D), 5 μm (E), and 500 nm (F). CW, cell wall; P, palisade layer; S, suberin.
Fig. 1 in Extracellular lipids of Camelina sativa: Characterization of cutin and suberin reveals typical polyester monomers and unusual dicarboxylic fatty acids
Fig. 1. Ultrastructure of Camelina sativa cuticles. Transmission electron microscopy images of cross-sections of adaxial (A) and abaxial (B) leaves, and top (C) and bottom (D) stems. Scanning electron microscopy images of adaxial (E) and abaxial (F) petal surfaces. Scale bars: 500 nm (A), 200 nm (B, C, D), and 10 μm (E, F). C, cuticle; CW, cell wall.
Fig. 4 in Extracellular lipids of Camelina sativa: Characterization of cutin and suberin reveals typical polyester monomers and unusual dicarboxylic fatty acids
Fig. 4. Lipid polyester monomer distribution in seed tissues. Comparison of transmethylation products from whole seeds, embryo-enriched and seed coatenriched delipidated residues. (A) Relative content of cutin monomer classes. (B–G) Detailed seed coat, embryo and whole seed monomer composition in each component class, namely hydroxy fatty acids (HFA; B), 1,ω-Diols (C), primary alcohols (PA; D), dicarboxylic acids (DCA; E) and hydroxycinnamic acids (HCA; F). Error bars represent SE; n =3. Fatty acids did not present any particular distribution between seed tissues and are not included in this figure.
Fig. 6 in Evolutionary changes in the glucosinolate biosynthetic capacity in species representing Capsella, Camelina and Neslia genera
Fig. 6. Diversification of CYP81F enzymes in the Camelineae species.A neighbor-joining tree of CYP81F proteins from the investigated species. AtCYP83B1 was used as an outgroup. The bar represents 10% sequence divergence.
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International Brain Laboratory public data
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OpenNeuro
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