Fig. 1. Photomicrograph of an epizoic acoelomorph flatworm (Waminoa sp

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Scanning electron microscopy analysis of EGK-I to -V chick embryos.
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Fig. 2. Effect of endurance training on gene expression, and protein content and activity in heart muscle. Effect of endurance training on gene expression,
Fig. 6. Ultrastructural changes in the glycocalyx of N
Fig. 5. Prip silencing enhances the co-localization of GABARAP with insulin vesicles and β-tubulin.Co-localization of GABARAP (green) with insulin (red)
Fig. 2. Outline of the two types of stimulus sequences employed in the analysis.(A) Environment information stimuli; (B) adaptation stimuli. Outline of.
Fig. 8. CCA and ChQ treatment induce accumulation of F-actin rings.
Fig. 1. Representative images of the four cell lines using fluorescence microscopy. Representative images of the four cell lines using fluorescence microscopy.
Fig. 2. Morphological changes of cultured adherent fibroblastic cells after OA treatment related to actin microfilament reorganization.(A) Cells observed.
Fig. 7. Motion adaptation increases time-dependent response modulations (TDRM) relatively to the average cell response.TDRM normalized to the value obtained.
Fig. 5. Ovary of the white shark Carcharodon carcharies.
Fig. 4. A primary screen based on scrape closure
Fig. 6. Cross-section of the stomach wall and spiral intestine of the embryo, stained with PAS. (A) Surface of the stomach wall (SW) and ingested material.
Fig. 8. The cohort of 3KO/CCS-LacZ embryos that survived to later timepoints showed marked hyperplasia of the ventricular conduction system (A–F).(B) Severe.
Fig. 2. Long-term CCH increases SDH activity after 6 weeks and does not prevent an increase of the fibre cross-sectional area.Fish were kept for 3 or 6.
Fig. 1. Mitochondrial internalization in cardiomyocytes.
Fig. 4. Expression of p75NTR and time-course of TrkA autophosphorylation at the Y751 and Y490 sites in PC12-27 cells transfected with the vector, empty.
Fig. 1. Morphological and growth characterization of hBMCs and hPDCs
Fig. 2. Transfection and clonal selection of rat pluripotent stem cells to generate stable transgenic lines. Transfection and clonal selection of rat pluripotent.
Fig. 4. The model of malate metabolism in fruit cells under different K level conditions. The model of malate metabolism in fruit cells under different.
Fig. 1. Pigmentation and melanophore counts of rainbow trout parr and smolt caudal fins.Pigmentation of (A) parr and (B) smolt. Pigmentation and melanophore.
Fig. 7. E2F1 acetylation in A1/A2-KO MEFs
Fig. 4. Brood size of four successive births by male seahorses Hippocampus erectus in the two groups (TR-1, TR-2).In TR-1 groups: male and female seahorses.
Fig. 4. Detection of dFMR1 mRNA in dFMRP granules by FISH
Fig. 5. Morphological changes of the N
Fig. 5. The bulk of Cep135 localizes distantly from Sas-6 and STIL
Fig. 6. Comparison of Plk4 with Sas-6 localization
Fig. 2. The localisation of integrins β1 and α6 in the hES cells grown in a colony and as a single-cell culture. hES cells were harvested manually as small.
Fig. 2. Morphological analysis of acentriolar mitotic spindles
Fig. 7. Lhx1-RNAi reduces the eye size
Fig. 3. Rnd proteins induce stronger responses in subconfluent endothelial cells.HUVECs were transfected with Rnd1, Rnd2, Rnd3 or GFP-encoding plasmids.
Fig. 5. UV reflections from the eye cup.
Fig. 2. Soluble sugar and organic acid levels with different K fertilization during fruit development. Soluble sugar and organic acid levels with different.
Fig. 1. Aboveground biomass of Caragana and herbaceous plants, and proportional abundance of Caragana, under different grazing management treatments. Aboveground.
Fig. 4. BKA values for different species.
Fig. 7. Representative images of control (Cas9+GFP) and Cas9+gRNA+GFP co-injected embryos on day 4 of culture, showing nuclear-imported GFP (green) and.
Fig. 1. Mitotic arrest results in differential RNA association with coilin.Untreated or nocodazole treated HeLa cell lysate was used for RNA immunoprecipitations.
Fig. 7. Force–displacement curves from porcine skin.
Fig. 6. STK35 KO mice show ovary defects.
Fig. 3. Electron micrographs showing presynaptic autophagosomes in hippocampal neurons treated with ShhN.(A–D,F) Examples of early autophagosomes (avi).
Fig. 2. mip120 null mutants have abnormal egg chamber development.
Table 1. Average ± S.E. of level of dissimilarity scores of each feature per stripe per pattern comparison of sides of the same fish (“Same Individual”),
The idefix phenotype first becomes visible during metamorphosis
Statistical chart of significantly differentially expressed genes
Table 1. Effects of flatworm presence and prey concentration on coral feeding rates and flatworm behaviour.Two-way mixed factorial ANOVA, showing main.
Fig. 4. Quantitative mRNA expression of two membrane-bound trehalase genes in Harmonia axyridis in response to starvation (0–72 h). Quantitative mRNA expression.
Fig. 1. Phenotypes of RasV12 transformed Drosophila lines
Fig. 2. Immunostaining for ClC-5 in isolated hog gastric mucosa
Fig. 3. idefix mutant chromatophores contribute to a wild-type pattern in chimeric animals. idefix mutant chromatophores contribute to a wild-type pattern.
Fig. 2. RFC3 function in chloroplasts.
Fig. 3. Enhanced EGFR signaling in Rhbdf2P159L/P159L mice.
Fig. 5. Flatworm density and activity on coral polyps
Fig. 2. RGD and KGD motifs in N. vectensis thrombospondins
Fig. 3. Overview of an epizoic flatworm capturing a single Artemia nauplius.(A) Flatworm (Waminoa sp.) on the oral disc of its coral host (G. fascicularis),
Fig. 2. Effects of pH on percentage of motile spermatozoa and VAP after 1 and 5 min after activation. Effects of pH on percentage of motile spermatozoa.
Fig. 12. Overview of the molecular program essential to build mdDA neurons.The genes identified in this study (in red) have been added to the programming.
Fig. 3. transparent is required cell-autonomously in iridophores
Fig. 2. Expression of Cx43 mutant T154A resulted in non-radial spreading and formation of protrusions in J558µm3 cells spreading in response to BCR signaling.(A)
Peroxisome speeds were slower in patient and control cells.
Fig. 5. Upregulation and subcellular relocalization of Hsp70 in striated muscles overexpressing either DVAP-V260I or DVAP-WT constructs.(A) NMJs of BG57-Gal4/+
Fig. 7. Eye defects in STK35 KO mouse.
Fig. 3. Mean force and velocity during jumping
mip120 null egg chambers have a condensed nurse cell DNA phenotype
Fig. 4. Representative still images of behaviour and characteristics typical of inshore foraging strategy of Australasian gannets. Representative still.
Fig. 1. Microarray analyses of genes whose expression is regulated by innervation during synaptogenesis.(A) Schematic drawings of the experimental design.
Fig. 5. Co-expression analyses of disease mutations in YFP-RPGRIP1α1 with wild-type RFP-RPGR1–19 or RFP-RPGRORF15 in COS7 cells.YFP-RPGRIP1α1 with disease-associated.
Table 1. Measurement of ring diameters of proteins localizing in ring-like patterns around centrioles.Consideration of the size of IgG (about 8 nm) raises.
Fig. 7. Nrf2-dependent enzyme activities in wild-type, Nrf2- and Keap1-deficient tissues.Hepatic (A,C,E) and cortical (B,D,F) enzyme activities of NQO1.
Fig. 5. Behaviours of the wild-types Oregon-R at two temperatures.
Fig. 3. Changes in the total EPS/Chl a ratio and bend interval of trichomes before and after the removal of polysaccharide from the BG11-cultured N. flagelliforme.
Fig. 1. lgl interacts genetically with Argonaute 1 (AGO1) in the eye.
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Fig. 1. Photomicrograph of an epizoic acoelomorph flatworm (Waminoa sp Fig. 1. Photomicrograph of an epizoic acoelomorph flatworm (Waminoa sp.) isolated from Galaxea fascicularis.Note the abundant symbiotic dinoflagellates in the worm's parenchyma. Photomicrograph of an epizoic acoelomorph flatworm (Waminoa sp.) isolated from Galaxea fascicularis.Note the abundant symbiotic dinoflagellates in the worm's parenchyma. Scale bar: 100 µm. Tim Wijgerde et al. Biology Open 2013;2:10-17 © 2012. Published by The Company of Biologists Ltd