Fig. 3. transparent is required cell-autonomously in iridophores

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Pigment patterns: fish in stripes and spots

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Fig. 3. Effect of NH4Cl (0 or 30 mM) on percentage of motile spermatozoa and VAP after 1 and 5 min after activation. Effect of NH4Cl (0 or 30 mM) on percentage.

Fig. 2. Outline of the two types of stimulus sequences employed in the analysis.(A) Environment information stimuli; (B) adaptation stimuli. Outline of.

Fig. 2. Spectral sensitivity of smolt melanophores and candidate photopigments involved in melanophore photosensitive processes.(A,B) Incident light triggered.

Fig. 5. Effect of MPO on surface elasticity of human platelets

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. 2. Proportion of motile objects and track length

Fig. 4. transparent encodes Mpv17.(A) tra maps to chromosome 20.

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.

TC-1 silencing sensitized A549 and SPC-A-1 cells to radiation therapy

Fig. 6. Comparison between the response against transformed tissues and capsule formation.At the cellular level the two responses share many similarities.

Fig. 1. Mitochondrial internalization in cardiomyocytes.

Fig. 3. Read-outs of mTORC1 (P-S6(S235/236)) and mTORC2 (P-Akt(S473)) in wtPC12 and PC12-27 cells.(A,B) wtPC12 and PC12-27 cells were treated for 48 hr.

Fig. 3. Inactivation of the Wnt/β-catenin signaling pathway inhibited cell proliferation and induced apoptosis in A549 and SPC-A-1 cells. Inactivation.

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. 4. Mutations induced by TALENs are heritable through the germline

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. 2. Dispersal pattern and walking distances of the two wingless strains of Acyrthosiphon pisum in 24 h. Dispersal pattern and walking distances of.

Fig. 2. Two signal-producing behaviours of wild-type Canton-S males and per mutant males relative to whether the wild-type female is moving or immobile.

Fig. 3. Low power hemi retinal image of the RPE surface showing the albino central and equatorial retina and pigment distribution in the periphery. Low.

Doxorubicin viability in the presence and absence of Herceptin

Fig. 4. Non-autonomous rescue of puc expression in DME cells

Table 3. Penetrance of cuticle defects seen in ush2 mutants embryos and in the progeny from rescue experiments (genotypes indicated in the table) with.

Fig. 2. The kar phenotype arises during metamorphosis

Fig. 3. Cell-autonomous loss of GABAergic interneurons in the OB of newborn and adult conditional GFRα1 mutants. Cell-autonomous loss of GABAergic interneurons.

Fig. 6. Effect of SAHA and ML on histone acetylation, BAX, and p21CDKN1A expression.PANC-1 and BxPC-3 cells were incubated for 48 hours with 5 µM.

Fig. 7. Lhx1-RNAi reduces the eye size

The TER94-p47 complex isinvolved in Notch signaling regulation

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. 4. Co-immunostaining of nocodazole or ASNase treated RPE-1 cells with anti-hASNS and anti-alpha tubulin showed defect in both mitotic spindle formation.

Fig. 7. Force–displacement curves from porcine skin.

Delayed formation of sensory hair cells in dlx3b/4b-deficient embryos

Effects of overexpressing pk on polarity of cells in which either the Stan/Fz system (stan–) or the Ds/Ft system is broken (ft– d–), or both are broken.

Fig. 6. Increased oxidative stress in Nrf2-deficient cells

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

Fig. 2. Kinetics of OptoEphB2 activation.

Fig. 1. Polarized F-actin cables in the Xenopus neural plate.

Fig. 3. idefix mutant chromatophores contribute to a wild-type pattern in chimeric animals. idefix mutant chromatophores contribute to a wild-type pattern.

Fig. 5. Flatworm density and activity on coral polyps

Fig. 2. Analysis of morphology, pluripotency marker expression and transgene silencing in the colonies emerging during reprogramming. Analysis of morphology,

Fig. 2. RGD and KGD motifs in N. vectensis thrombospondins

Fig. 3. Effects of Tec on IL-1β-induced apoptosis in chondrocytes.

Amplicon sequencing analysis of on-target sites in trβ crispants

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. 2. Coupling of actin to cell–cell junctions requires α-catenin and is necessary for the establishment of the barrier.(A) Effect of Cytochalasin D.

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. 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.

Fig. 7. Quantal size of NMJs is decreased in lola RNAi mutants

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

Fig. 5. Behaviours of the wild-types Oregon-R at two temperatures.

Phenotypic analysis of the CNS in mutants for Ror, otk and otk2

Failure of chromosome disassembly in mip120 null ovarian nurse cells

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. 3. transparent is required cell-autonomously in iridophores Fig. 3. transparent is required cell-autonomously in iridophores.(A–C) Mutants used in transplantation experiments: (A) nac;pfe, (B) tra, (C) rse. transparent is required cell-autonomously in iridophores.(A–C) Mutants used in transplantation experiments: (A) nac;pfe, (B) tra, (C) rse. (D) nac;pfe mutant which received tra mutant xanthophores and melanophores, showing that both cell types contribute normally to stripes. (E) tra mutant which received nac;pfe mutant iridophores, showing that the supply with iridophores is sufficient to normalize the pigment pattern. Jana Krauss et al. Biology Open 2013;2:703-710 © 2013. Published by The Company of Biologists Ltd