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

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inhibits BMP signalling.

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Scanning electron microscopy analysis of EGK-I to -V chick embryos.

Pigment patterns: fish in stripes and spots

CK2 is required for early cell divisions in C. elegans embryos

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. 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. 2. Proportion of motile objects and track length

A highly conserved six-amino-acid region in the C-terminal CT domain of MARCH8 is responsible for its ability to downregulate TfR. A highly conserved six-amino-acid.

Fig. 2. abu/pqn genes are expressed in the pharyngeal cuticle

No significant functional difference could be observed between N1ICD and N2ICD in maintaining skin barrier function and promoting tumorigenesis. No significant.

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. 1. Mitochondrial internalization in cardiomyocytes.

Fig. 1. Morphological and growth characterization of hBMCs and hPDCs

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.

Scanning EM shows cilia abnormalities in the neural tube.

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.

Setdb1 has cell-intrinsic functions in B cell development.

eb1a-2 eb1b-3 double-mutant plants display skewed and shorter roots

Fig. 2. DDR1 over-expression enhances collagen fibril reorganization

Fig. 3. Genetic interactions between unc-53 and unc-6 and between unc-53 and unc-5 affect intracellular UNC-40::GFP localization.(A–H) Photomicrographs.

Fig. 6. LR phenotype of plastid translation-defective mutants with/without Spec. LR phenotype of plastid translation-defective mutants with/without Spec.

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. 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.

Connective tissue cells, but not myogenic cells, obey the rule of distal transformation in axolotl limb regeneration. Connective tissue cells, but not.

Fig. 5. Morphological changes of the N

Fig. 2. The kar phenotype arises during metamorphosis

Fig. 5. Differentiated cells sort to the outer layer, regardless of E- or N-cadherin status.Wildtype and mutant ES cells were distinguished by GFP expression.

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. 7. Lhx1-RNAi reduces the eye size

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.

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Fig. 6. Apical polarity of primitive endoderm cells on surface of embryoid bodies.Embryoid bodies were analyzed by immunofluorescence microscopy for GATA4.

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The idefix phenotype first becomes visible during metamorphosis

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Reb does not play a significant role in regulating TGF-β signaling

Fig. 1. Phenotypes of RasV12 transformed Drosophila lines

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

Depleting CK2 restores centrosomal ZYG-1 levels in zyg-1(it25) embryos

Fig. 3. Enhanced EGFR signaling in Rhbdf2P159L/P159L mice.

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Ibm1 and edm2 mutants generate more stomatal divisions in the leaf epidermis. ibm1 and edm2 mutants generate more stomatal divisions in the leaf epidermis.

Prophase nuclear movements in wild-type, rec8 and rec7 mutant cells.

dcn1-deletion results in attenuated cohesin cleavage at anaphase

Amplicon sequencing analysis of on-target sites in trβ crispants

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)

Expression of smc3 in whole-mount and cryosectioned regenerating fins

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Fig. 3. Mean force and velocity during jumping

Fig. 5. EGL-20 inhibits anterior and posterior orientation of UNC-40 asymmetric localization and the formation of axons from these sites.(A–D) HSN neurons.

mip120 null egg chambers have a condensed nurse cell DNA phenotype

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.

Fig. 3. Inclusion of E-cadherin into stationary clusters requires cis-, trans-, and cytoplasmic interactions. Inclusion of E-cadherin into stationary clusters.

Fig. 7. Rho family GTPase signaling is required for cyst formation in Ptp4E Ptp10D mutants.(A–C) Expression of DN Rho1 and Rac1 mutants in wild-type (w1118)

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

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Spatial cues direct neuronal diversification with respect to OR gene selection. Spatial cues direct neuronal diversification with respect to OR gene selection.

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Fig. 3. idefix mutant chromatophores contribute to a wild-type pattern in chimeric animals. idefix mutant chromatophores contribute to a wild-type pattern in chimeric animals. Chimeric animals derived from blastomere transplantations of ide mutant cells into (A) pfeffer (n=8), (B) rose (n=6) and (C) nacre (n=4) hosts. In all three cases the normally striped wild-type pattern is restored in the regions of donor-derived xanthophores (A), iridophores (B) or melanophores (C), indicated by the brackets. Scale bar: 1 mm. Hans Georg Frohnhöfer et al. Biology Open 2016;5:736-744 © 2016. Published by The Company of Biologists Ltd