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173 results for “molecular recognition”
Figure 3 from: Sakuragui CM, Calazans LSB, de Oliveira LL, de Morais EB, Benko-Iseppon AM, Vasconcelos S, Schrago CEG, Joseph Mayo SJ (2018) Recognition of the genus Thaumatophyllum Schott − formerly Philodendron subg. Meconostigma (Araceae) − based on molecular and morphological evidence. PhytoKeys 98: 51-71. https://doi.org/10.3897/phytokeys.98.25044
Figure 3 Phylogenetic relationships amongst Philodendron, Thaumatophyllum, Homalomena and Adelonema recovered by previous authors. A Barabé et al. (2002) B Tam et al. (2004) C Loss-Oliveira et al. (2014) D Vasconcelos (2015).
Figure 4 from: Sakuragui CM, Calazans LSB, de Oliveira LL, de Morais EB, Benko-Iseppon AM, Vasconcelos S, Schrago CEG, Joseph Mayo SJ (2018) Recognition of the genus Thaumatophyllum Schott − formerly Philodendron subg. Meconostigma (Araceae) − based on molecular and morphological evidence. PhytoKeys 98: 51-71. https://doi.org/10.3897/phytokeys.98.25044
Figure 4 Thaumathophyllum petreum. A Habit B Longitudinal cut of the inflorescence C Staminode D Stamen E Longitudinal cut of a female flower F Transversal cut of a female flower showing the 6-locular ovary G Side view of a female flower H Infructescence. All from Calazans & Morais 28 (RB).
Figure 1 from: Sakuragui CM, Calazans LSB, de Oliveira LL, de Morais EB, Benko-Iseppon AM, Vasconcelos S, Schrago CEG, Joseph Mayo SJ (2018) Recognition of the genus Thaumatophyllum Schott − formerly Philodendron subg. Meconostigma (Araceae) − based on molecular and morphological evidence. PhytoKeys 98: 51-71. https://doi.org/10.3897/phytokeys.98.25044
Figure 1 Philodendron, Homalomena and Adelonema phylogenetic relationships markers by previous publications. A Gauthier et al. (2008), maximum parsimony. B Gauthier et al. (2008), Bayesian analysis; Wong et al. (2013), Wong et al. (2016).
Molecular basis for the increased affinity of an RNA recognition motif with re-engineered specificity: A molecular dynamics and enhanced sampling simulations study- PART 6
<p>Trajectories and input files of the simulations of the S151T Rbfox*·pre-miR20b* system.</p>
Molecular basis for the increased affinity of an RNA recognition motif protein engineered to re-direct its specificity -PART 4
<p>Trajectory and input files for the simulation of the Rbfox* variant. </p>
Molecular basis for the increased affinity of an RNA recognition motif with re-engineered specificity: A molecular dynamics and enhanced sampling simulations study- PART 1
<p>Simulations of the Rbfox protein.</p> <p> </p>
Figure 1 from: Vargas-Luna MD, Hernández-Ledesma P, Majure LC, Puente-Martínez R, Macías HMH, Luna RTB (2018) Splitting Echinocactus: morphological and molecular evidence support the recognition of Homalocephala as a distinct genus in the Cacteae. PhytoKeys 111: 31-59. https://doi.org/10.3897/phytokeys.111.26856
Figure 1 Echinocactus species. AE.platyacanthus from Querétaro BE.horizonthalonius from Chihuahua CH.texensis from Chihuahua DH.parryi from Chihuahua EH.polycephalasubsp.polycephala from Sonora FK.grusonii from Querétaro. Line bar in fruit photographs is 1 mm.
Figure 3 from: Vargas-Luna MD, Hernández-Ledesma P, Majure LC, Puente-Martínez R, Macías HMH, Luna RTB (2018) Splitting Echinocactus: morphological and molecular evidence support the recognition of Homalocephala as a distinct genus in the Cacteae. PhytoKeys 111: 31-59. https://doi.org/10.3897/phytokeys.111.26856
Figure 3 Phylogenetic relationships of Echinocactus inferred with the total evidence matrix. Maximum parsimony strict consensus tree of 2 most parsimonious trees of 863 steps with a consistency index of 0.790 and a retention index of 0.770. Values above/below nodes indicate maximum parsimony bootstrap (mpb) and posterior probabilities (pp), respectively. Black circles indicate synapomorphic characters identified by the character optimisation analyses. Numbers above/below circles indicate characters and character states, respectively (see Appendix 2). The HEA clade is labelled showing the three genera: Astrophytum, Echinocactus and Homalocephala. Line drawings illustrate the morphological synapomorphies for respective clades.
Figure 5 from: Vargas-Luna MD, Hernández-Ledesma P, Majure LC, Puente-Martínez R, Macías HMH, Luna RTB (2018) Splitting Echinocactus: morphological and molecular evidence support the recognition of Homalocephala as a distinct genus in the Cacteae. PhytoKeys 111: 31-59. https://doi.org/10.3897/phytokeys.111.26856
Figure 5 Bayesian 50% majority rule consensus tree showing phylogenetic relationship of Echinocactus inferred with 5GT. Values in tree nodes correspond (left to right) to bootstrap values from maximum parsimony (mpb), maximum likelihood (mlb) and posterior probabilities (pp). The clades highlighted in dark and light grey correspond to the Echinocactus, Homalocephala and K.grusonii-Ferocactus clades.
Figure 4 from: Vargas-Luna MD, Hernández-Ledesma P, Majure LC, Puente-Martínez R, Macías HMH, Luna RTB (2018) Splitting Echinocactus: morphological and molecular evidence support the recognition of Homalocephala as a distinct genus in the Cacteae. PhytoKeys 111: 31-59. https://doi.org/10.3897/phytokeys.111.26856
Figure 4 Phylogenetic relationship of Echinocactus inferred with cpDNA plus morphology. Bayesian 50% majority rule consensus tree. Values in nodes correspond (left to right) to bootstrap values from maximum parsimony (mpb) and posterior probabilities (pp). The black star indicates the HEA clade and its three subclades Astrophytum, Echinocactus and Homalocephala highlighted.
Figure 2 from: Vargas-Luna MD, Hernández-Ledesma P, Majure LC, Puente-Martínez R, Macías HMH, Luna RTB (2018) Splitting Echinocactus: morphological and molecular evidence support the recognition of Homalocephala as a distinct genus in the Cacteae. PhytoKeys 111: 31-59. https://doi.org/10.3897/phytokeys.111.26856
Figure 2 Phylogenetic relationship of Echinocactus inferred with the cpDNA matrix. Maximum parsimony 50% majority rule consensus tree of 4 most parsimonious trees of 347 steps with a consistency index of 0.681 and retention index of 0.848. Values in nodes correspond (from left to right) to maximum parsimony bootstrap (mpb), maximum likelihood bootstrap (mlb) and posterior probabilities (pp). The black star indicates the HEA clade with three subclades: Astrophytum, Echinocactus and Homalocephala highlighted.
Fig. 53 in Molecular and morphological recognition of species boundaries in the neglected ant genus Brachymyrmex (Hymenoptera: Formicidae): toward a taxonomic revision
Fig. 53 Brachymyrmex tristis: a–c head, dorsal, and lateral view of the lectotype worker
Fig. 42 in Molecular and morphological recognition of species boundaries in the neglected ant genus Brachymyrmex (Hymenoptera: Formicidae): toward a taxonomic revision
Fig. 42 Brachymyrmex myops: a–c head, dorsal, and lateral view of the lectotype worker
Fig. 28 in Molecular and morphological recognition of species boundaries in the neglected ant genus Brachymyrmex (Hymenoptera: Formicidae): toward a taxonomic revision
Fig. 28 Brachymyrmex donisthorpei: a–c head, dorsal, and lateral view of the lectotype worker
Fig. 26 in Molecular and morphological recognition of species boundaries in the neglected ant genus Brachymyrmex (Hymenoptera: Formicidae): toward a taxonomic revision
Fig. 26 Brachymyrmex delabiei: a–c head, dorsal, and lateral view of the holotype worker
Fig. 45 in Molecular and morphological recognition of species boundaries in the neglected ant genus Brachymyrmex (Hymenoptera: Formicidae): toward a taxonomic revision
Fig. 45 Brachymyrmex oculatus: a–c head, dorsal, and lateral view of the lectotype worker
Fig. 12 Brachymyrmex bahamensis n in Molecular and morphological recognition of species boundaries in the neglected ant genus Brachymyrmex (Hymenoptera: Formicidae): toward a taxonomic revision
Fig. 12 Brachymyrmex bahamensis n.sp.: a–c head, dorsal, and lateral view of the holotype worker
Fig. 15 in Molecular and morphological recognition of species boundaries in the neglected ant genus Brachymyrmex (Hymenoptera: Formicidae): toward a taxonomic revision
Fig. 15 Brachymyrmex brasiliensis: a–c head, dorsal, and lateral view of the holotype worker
Fig. 41 in Molecular and morphological recognition of species boundaries in the neglected ant genus Brachymyrmex (Hymenoptera: Formicidae): toward a taxonomic revision
Fig. 41 Brachymyrmex musculus: a–c head, dorsal, and lateral view of the lectotype worker
Fig. 37 Brachymyrmex iridescens n in Molecular and morphological recognition of species boundaries in the neglected ant genus Brachymyrmex (Hymenoptera: Formicidae): toward a taxonomic revision
Fig. 37 Brachymyrmex iridescens n. sp.: a–c head, dorsal, and lateral view of the holotype worker
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
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.