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821 results for “Molecular Systematics”
Fig. 2 in New insights into the systematics and molecular phylogeny of the Malagasy snake genus Liopholidophis suggest at least one rapid reversal of extreme sexual dimorphism in tail length
Fig. 2 Head drawings of Liopholidophis baderi sp. nov. (holotype, ZFMK 62235) in (a) dorsal and (b) lateral view
Fig. 5 in Systematics and phylogenetic species delimitation within Polinices s.l. (Caenogastropoda: Naticidae) based on molecular data and shell morphology
Fig. 5 Pictures of type specimens and protoconchs of a Nerita mammilla Linnaeus, 1758 [ZMUU#386] b Mamma albula Chemnitz, 1758 [nonbinomial, ZMUC] and c Natica pyriformis Recluz, 1844 [BMNH#1991089.1]. For further information see Table 1. Bars 0.5 cm
Fig. 3 in Systematics and phylogenetic species delimitation within Polinices s.l. (Caenogastropoda: Naticidae) based on molecular data and shell morphology
Fig. 3 Phylogram obtained through Bayesian inference based on the COI gene fragment. Posterior probabilities are indicated at the nodes. Branches supported by values>0.95 are indicated in bold. Polytomies are due to the cut-off value specified for the consensus tree (50 % used as the default value in MrBayes)
Fig. 2 in Systematics and phylogenetic species delimitation within Polinices s.l. (Caenogastropoda: Naticidae) based on molecular data and shell morphology
Fig. 2 Phylogram obtained through Bayesian inference based on the concatenated data set (COI, 16S, 18S, 28S, H3) for a reduced number of taxa. Posterior probabilities are indicated at the nodes. Branches supported by values>0.95 are indicated in bold. Polytomies are due to the cut-off value specified for the consensus tree (50 % used as the default value in MrBayes)
Fig. 6 in Systematics and phylogenetic species delimitation within Polinices s.l. (Caenogastropoda: Naticidae) based on molecular data and shell morphology
Fig. 6 Analysed type specimens or figured type specimens of taxa that could potentially represent Polinices sp. 2, Polinices sp. 3 or Polinices sp. 4. a Natica controversa Pritchard & Gatliff, 1913 [MV#F7695]. b Natica dubia Récluz, 1844 [BMNH#1991085] (0 P. constanti Huelsken and Hollmann, herein; replacement name). c Natica deiodosa Reeve, 1855 [BMNH#1991069]. d Uber mellosum Hedley, 1924 [AMS#C20058]. e Natica phytelephas Reeve 1855 [BMNH#1991096]. f Polinices putealis Garrard, 1961 [AMS#C63344]. g Natica jukesii Reeve, 1855 [BMNH#1991067]. (h) Polinices tawhitirahia Powell, 1965 [Auckland Museum #71242]. i Natica vavaosi Reeve, 1855 [figured type]. j Natica galactites Philippi, 1851 [figured type]. k Natica cygnea Philippi, 1850 [figured type]. l Natica virginea Philippi, 1850 [figured type]. For further information see Table 1. Bars 0.5 cm
Fig. 4 in Molecular and phytochemical systematics of the subtribe Hypochaeridinae (Asteraceae, Cichorieae)
Fig. 4 Overview of the distribution of isoetin derivatives within the phylogenetic context of the Hypochaeridinae
Fig. 1 in Molecular and phytochemical systematics of the subtribe Hypochaeridinae (Asteraceae, Cichorieae)
Fig. 1 Maximum likelihood (ML) phylogram. Bootstrap support values of ML and posterior probabilities of the Bayesian Likelihood (BL) analysis are given above branches (ML/BL). H I and H II denote clades
Fig. 2 in Molecular and phytochemical systematics of the subtribe Hypochaeridinae (Asteraceae, Cichorieae)
Fig. 2 Maximum parsimony (MP) 50% majority rule consensus tree. Bootstrap support values given above branches. Clades contain species according to Fig. 1
FIGURE 2 in Systematics and molecular phylogenetics of Asian snail-eating snakes (Pareatidae)
FIGURE 2. Variation in the frontal scale (top row) and the anterior pair of the chin shields (lower row) in Pareas. Both characters are shaded black. A & H: P. hamptoni (A–C, H–J all modified from Pope 1935); B & I: P. stanleyi; C & J: P. boulengeri; D & K: P. iwasakii (modified from Ota et al. 1997); E & L: P. nigriceps (modified from Guo and Deng 2009); F & M: P. carinatus (modified from Rao and Yang 1992); G & N: P. nuchalis (modified from Boulenger 1900).
Figure 2. Maximum-likelihood tree for 95 in Molecular phylogeny of the Forcipulatacea (Asteroidea: Echinodermata): systematics and biogeography
Figure 2. Maximum-likelihood tree for 95 forcipulate taxa and nine velatidan taxa, rooted on 111 taxa belonging to the Valvatida, Paxillosida, and Notomyotida (these taxa have been omitted for clarity), and based on 261 bp of sequence data for the 12S rDNA gene and 437 bp for the 16S rDNA gene. Bootstrap support values are based on 250 pseudoreplicates and are shown as percentages when ± 50%. Named clades correspond either to traditional taxonomic groups or to geographically restricted lineages.
Figure 3 in Morphological and molecular taxonomy of a new Daptonema (Nematoda, Xyalidae) with comments on the systematics of some related taxa
Figure 3. Scanning electron micrographs of Daptonema matrona sp. nov. male: A, anterior region; B, amphid; C, tail; D, external structure of the gubernuculum.
Figure 2 in Morphological and molecular taxonomy of a new Daptonema (Nematoda, Xyalidae) with comments on the systematics of some related taxa
Figure 2. Photographs of Daptonema matrona sp. nov. holotype: A, habitus; B, anterior region; C, amphid; D, buccal cavity; E, spicule; F, tail.
Figure 6 in Morphological and molecular taxonomy of a new Daptonema (Nematoda, Xyalidae) with comments on the systematics of some related taxa
Figure 6. Maximum parsimony (stricto consensus) topology based on 18S sequences from 25 specimens of Xyalidae and three outgroups (Monhystera riemanni, Sphaerolaimus hirsute, and Spirinia parasitifera). Numbers are bootstrap and jack-knife values (10 000 replicates), respectively, both with branch support over 50%.
FIGURE 3. The genus Antroxestoblatta gen.n. A–H in Molecular systematics and genital morphology of the Neotropical cockroaches from the genus Xestoblatta (Blattellidae)
FIGURE 3. The genus Antroxestoblatta gen.n. A–H, Antroxestoblatta immaculata (Hebard) comb.nov. (male) (BLA 222). A, Habitus (dorsal); B, Abdominal segment I; C, Left paraproct (ventral); D, Supra-anal plate (dorsal); E, Subgenital plate (ventral), Left style = L, Right style = R. F–H, Genital sclerites, (F) L2 (dorsal), (G) L3 (ventral) and (H) R (dorsal). Scale bar 1mm.
Fig. 2 in Molecular systematics of the Reithrodontomys tenuirostris group (Rodentia: Cricetidae) highlighting the Reithrodontomys microdon species complex
Fig. 2.—Phylogenetic relationships among species of the Reithrodontomys tenuirostris group using sequences data of the mitochondrial gene Cytochrome b. Values below branches represent nodal support for BI/ML analysis. Terminal labels are named according to mammal collection voucher numbers (see Supplementary Appendix I).
Systematic analysis of purified astrocytes after spinal cord injury unveils lncRNA Zeb2os as a novel molecular target for astrogliosis
GEO Series GSE153721. Mus musculus. 29 samples. Type: Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing.
FIGURE 3 in Molecular systematics and biogeography of the genus Zizina (Lepidoptera: Lycaenidae)
FIGURE 3. Plots of uncorrected p-distance against the number of transitions and transversions.
Fig. 5 in New insights into the systematics and molecular phylogeny of the Malagasy snake genus Liopholidophis suggest at least one rapid reversal of extreme sexual dimorphism in tail length
Fig. 5 Liopholidophis rhadinaea in life, from Talatakely, Ranomafana National Park (ZSM 1602/2008)
Fig. 4 in New insights into the systematics and molecular phylogeny of the Malagasy snake genus Liopholidophis suggest at least one rapid reversal of extreme sexual dimorphism in tail length
Fig. 4 Holotype of Liopholidophis oligolepis sp. nov. in (a) dorsal and (b) ventral view
Systematic identification of molecular pathways driving GBM invasion
GEO Series GSE87535. Homo sapiens. 4 samples. Type: Expression profiling by high throughput sequencing.
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Allen Brain Atlas
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