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173 results for “molecular recognition”
Fig. 10 in Molecular and morphological recognition of species boundaries in the neglected ant genus Brachymyrmex (Hymenoptera: Formicidae): toward a taxonomic revision
Fig. 10 Brachymyrmex attenuatus: a−c head, dorsal, and lateral view of the lectotype worker
Fig. 33 in Molecular and morphological recognition of species boundaries in the neglected ant genus Brachymyrmex (Hymenoptera: Formicidae): toward a taxonomic revision
Fig. 33 Brachymyrmex gaucho: a–c head, dorsal, and lateral view of a worker
Fig. 44 in Molecular and morphological recognition of species boundaries in the neglected ant genus Brachymyrmex (Hymenoptera: Formicidae): toward a taxonomic revision
Fig. 44 Brachymyrmex obscurior: a–c head, dorsal, and lateral view of the lectotype worker
Fig. 8 in Molecular and morphological recognition of species boundaries in the neglected ant genus Brachymyrmex (Hymenoptera: Formicidae): toward a taxonomic revision
Fig. 8 Brachymyrmex antennatus: a–c head, dorsal, and lateral view of the lectotype worker
Fig. 40 in Molecular and morphological recognition of species boundaries in the neglected ant genus Brachymyrmex (Hymenoptera: Formicidae): toward a taxonomic revision
Fig. 40 Brachymyrmex modestus: a–c head, dorsal, and lateral view of the lectotype worker
Fig. 32 in Molecular and morphological recognition of species boundaries in the neglected ant genus Brachymyrmex (Hymenoptera: Formicidae): toward a taxonomic revision
Fig. 32 Brachymyrmex gagates: a–c head, dorsal, and lateral view of the lectotype worker
Fig. 39 in Molecular and morphological recognition of species boundaries in the neglected ant genus Brachymyrmex (Hymenoptera: Formicidae): toward a taxonomic revision
Fig. 39 Brachymyrmex minutus: a–c head, dorsal, and lateral view of the lectotype worker
Fig. 51 Brachymyrmex sosai n in Molecular and morphological recognition of species boundaries in the neglected ant genus Brachymyrmex (Hymenoptera: Formicidae): toward a taxonomic revision
Fig. 51 Brachymyrmex sosai n. sp.: a–c head, dorsal, and lateral view of the holotype worker
Fig. 1 in Molecular and morphological recognition of species boundaries in the neglected ant genus Brachymyrmex (Hymenoptera: Formicidae): toward a taxonomic revision
Fig. 1 Morphological measurements for Brachymyrmex workers. See text for details
FIGURE 4 in Recognition of a new species of Hedysarum (Fabaceae, Hedysareae) from China based on morphological and molecular evidence
FIGURE 4. Living plant of Hedysarum cuonanum. A, in the habitat; B, upper part of the plant.
FIGURE 3 in Recognition of a new species of Hedysarum (Fabaceae, Hedysareae) from China based on morphological and molecular evidence
FIGURE 3. Holotype of Hedysarum cuonanum.
Fig. 1 in A morphological and molecular study supports the recognition of Rhipilia psammophila sp. nov. and Rhipilia baculifera comb. nov. (Halimedaceae, Chlorophyta) from southern Australia
Fig. 1. (Caption on next page)
Figures 3 from: Guilliams CM, Jang T, Baldwin BG (2016) Molecular and morphological evidence for recognition of two species within Harpagonella (Amsinckiinae, Boraginaceae). PhytoKeys 70: 17-30. https://doi.org/10.3897/phytokeys.70.9053
Figures 3 - Maximum clade credibility trees from phylogenetic analysis of the: A combined, partitioned nuclear DNA regions, and B combined, partitioned chloroplast DNA regions. Values on branches are Bayesian posterior probabilities followed by maximum likelihood bootstrap values.
Figure 4 from: Guilliams CM, Jang T, Baldwin BG (2016) Molecular and morphological evidence for recognition of two species within Harpagonella (Amsinckiinae, Boraginaceae). PhytoKeys 70: 17-30. https://doi.org/10.3897/phytokeys.70.9053
Figure 4 - Box and whisker plots by taxon of A average maximum fruit length (mm), B average maximum fruit width (mm), C average maximum subterete appendage length (mm). Asterisks denote the measured values of type specimens. Note significant differentiation in all features measured.
Figure 2 from: Guilliams CM, Jang T, Baldwin BG (2016) Molecular and morphological evidence for recognition of two species within Harpagonella (Amsinckiinae, Boraginaceae). PhytoKeys 70: 17-30. https://doi.org/10.3897/phytokeys.70.9053
Figure 2 - Fruits of Harpagonella in lateral view, from A) southern Arizona (Tedford 1043, ARIZ403065) and B) southern California (Bramlet 2301, ARIZ345225). Although morphologically similar, note overall difference in size. Scale bars are each approximately 1 mm. Labels: (AAS) sepals away from inflorescence axis in flower; (IA) inflorescence axis; (N) nutlet; (P) pedicel; (SA) sepal appendages; (TAS) sepals toward inflorescence axis in flower.
Figure 1 from: Guilliams CM, Jang T, Baldwin BG (2016) Molecular and morphological evidence for recognition of two species within Harpagonella (Amsinckiinae, Boraginaceae). PhytoKeys 70: 17-30. https://doi.org/10.3897/phytokeys.70.9053
Figure 1 - Map of western North America showing Harpagonella collections in major herbaria based on available specimen data from GBIF and Bajaflora. Type collection localities are indicated with black star for Harpagonella palmeri and a red star for Harpagonella arizonica.
Data from: Molecular adaptation in flowering and symbiotic recognition pathways: insights from patterns of polymorphism in the legume Medicago truncatula
Open the record for dataset details and reuse information.
Molecular mechanism of flocculation self-recognition in yeast and its role in mating and survival
Saccharomyces cerevisiae flocculation occurs when fermentable sugars are limiting and is therefore considered as a way to enhance the survival chance of Flo-expressing yeast cells. In this paper the role of Flo1p in mating was demonstrated by showing that the mating efficiency which contributes to the increased survival rate as well by generating genetic variability is increased when cells flocculate. This was revealed by liquid growth experiments in a low shear environment and differential transcriptome analysis of FLO1 expressing cells compared to the non-flocculent wild-type cells. The results show that a floc provides a uniquely organized multicellular ultrastructure that provides a suitable microenvironment to induce and perform cell conjugation. S. cerevisiae strains BY4742 WT BY4742::FLO8 and BY4742 [FLO1] were grown in microgravity and 1-g. A transcriptomic analysis was performed and the transcriptome data were integrated with the high quality protein-protein interaction networks. The identified high score sub-networks (qvalue < 0.001) were considered and further evaluated concerning their GO enrichment using a hypogeometric test. The data were from the Ying B-1 experiment.
A Protein-Protein Interaction Underlies the Molecular Basis for Substrate Recognition by an Adenosine to Inosine RNA Editing Enzyme
GEO Series GSE112367. Caenorhabditis elegans. 12 samples. Type: Expression profiling by high throughput sequencing; Other.
Identification of mRNAs bound and regulated by human LIN28 proteins and molecular requirements for RNA recognition
GEO Series GSE44616. Homo sapiens. 16 samples. Type: Expression profiling by array; Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing.
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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.