Fig. 4. Induction of a systemic immune response in RasV12-expressing larvae.(A) List of genes that are significantly induced (at q<0.05 and induction level.

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Bar plot representation of the transcriptomic changes in Δsaci_ptp and Δsaci_pp2a. Bar plot representation of the transcriptomic changes in Δsaci_ptp and.
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. 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.
Retinoic acid sentinels in live embryos and responding to exogenous RA in half-embryo cultures. Retinoic acid sentinels in live embryos and responding.
Fig. 4. E-cadherin expression level affects monomer dynamics.
Fig. 4. smc3 regulates the expression of cx43 in regenerating fins.
Fig. 7. Motion adaptation increases time-dependent response modulations (TDRM) relatively to the average cell response.TDRM normalized to the value obtained.
Fig. 4. Phosphorylation of the MARCKS-homology domain partially inhibits Hts' ability to disrupt Dlg postsynaptic targeting to the larval NMJ.(A–D″) High.
Fig. 1. Muscle-specific PITX1 over-expression in the Pitx1 transgenic mice.(A) Detection of Pitx1 mRNA expression in muscles of the Pitx1 transgenic mice.
Fig. 6. The cholinergic receptor subunits a6 (Chrna6) and b3 (Chrnb3) are (subset) specifically expressed in mdDA neurons during development.(A) The Chrna6.
Fig. 6. Comparison between the response against transformed tissues and capsule formation.At the cellular level the two responses share many similarities.
Fig. 4. Effect of royal jelly on silkmoth fat body cells and eggs.
Table 1. Menthol preference index (MPI) and average number of eggs laid per female (EPF) in F0 and F1 lines.The statistical significance of MPI was assessed.
Fig. 10. Ratiometric live imaging of di-4-ANEPPDHQ in growing pollen tubes.(A) Higher and lower membrane order distribution in control and BCD treated.
Fig. 4. Expression of miR-2 family mediates tissue growth of Hippo pathway.(A) Photomicrographs of adult wings of the indicated genotype. Expression of.
Identification of aging-related genes and affected biological processes. Identification of aging-related genes and affected biological processes. (A) Experimental.
Fig. 5. Onecut transcription factors are important for the correct generation of the mdDA neuronal population.(A) Schematic representation of the region.
Fig. 3. Inactivation of the Wnt/β-catenin signaling pathway inhibited cell proliferation and induced apoptosis in A549 and SPC-A-1 cells. Inactivation.
Ingenuity pathway analysis of the genes enriched in both 96-h-induced MMs and human ccRCC. Ingenuity pathway analysis of the genes enriched in both 96-h-induced.
Fig. 1. Lack of Hmga1 and Hmga2 expression in A1/A2-KO mice
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. 2. Salivary glands from RasV12-expressing larvae produce MMP1, release tissue fragments into the hemolymph and express apoptotic markers.Salivary.
Fig. 1. Body weight gain in Cbx7-KO mice
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. 5. Morphological changes of the N
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. Interaction between BAF60c and cardiac transcription factors.
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. 1. TSA at 165 nM induces maximal acetylation of histone H3 and near-maximal acetylation of histone H4.Immunoblot analysis of acetylated histones H3.
Fig. 6. STK35 KO mice show ovary defects.
Distribution and extent of expression.
Comparison ofMyc-induced zebrafish liver tumors with different stages of human HCC and seven mouse HCC models. Comparison ofMyc-induced zebrafish liver.
Functional classification and visualization of differentially expressed genes. Functional classification and visualization of differentially expressed.
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”),
Fig. 8. The morphology of the ventral nerve cord in Ror-Myc overexpressing embryos is normal. The morphology of the ventral nerve cord in Ror-Myc overexpressing.
Statistical chart of significantly differentially expressed genes
The genomic distribution of essential and non-essential mouse genes, separated into known and predicted essentiality. The genomic distribution of essential.
Fig. 4. Quantitative mRNA expression of two membrane-bound trehalase genes in Harmonia axyridis in response to starvation (0–72 h). Quantitative mRNA expression.
Nodal signalling is absolutely required for T/Bra induction and correct patterning. Nodal signalling is absolutely required for T/Bra induction and correct.
Fig. 1. Phenotypes of RasV12 transformed Drosophila lines
Fig. 6. The cholinergic receptor subunits a6 (Chrna6) and b3 (Chrnb3) are (subset) specifically expressed in mdDA neurons during development.(A) The Chrna6.
BAF60c transcriptionally affects cardiac morphogenesis and function
Systemic infection in Drosophila larvae by septic injury with a fine tungsten needle. Systemic infection in Drosophila larvae by septic injury with a fine.
Drs expression profiles for OreR flies infected with the various C
Participation of the ankle extensor muscle, LG, during RLMs in control posture and extension restraint. Participation of the ankle extensor muscle, LG,
Fig. 8. Tracking details and coordinate systems.
Fig. 2. iPSCs produce functional osteoblasts.
MMP16 upregulation during myofibroblast differentiation
Stage-specific expression modules of preimplantation development.
Model for TGF-β-induced myofibroblast differentiation involving MKL1 isoform-specific activities. Model for TGF-β-induced myofibroblast differentiation.
Delay of tail resorption in trβ crispants during natural metamorphosis
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.
Effects of dietary sucrose and fat on the expression of metabolic and stress-response genes in knee cartilage. Effects of dietary sucrose and fat on the.
Morphological changes induced by T3 treatment in trβ crispants
Overexpression of cyp7a1 in the liver ameliorates tumor-induced liver inflammation. Overexpression of cyp7a1 in the liver ameliorates tumor-induced liver.
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)
Fig. 3. Mean force and velocity during jumping
Fig. 2. Temporal map of genes clustering with the expression profile of Lmx1a.(A) Heat-map visualization obtained by HCL of genes clustering with Lmx1a.
Fig. 1. Microarray analyses of genes whose expression is regulated by innervation during synaptogenesis.(A) Schematic drawings of the experimental design.
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. 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. 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.
Fig. 1. Effects of royal jelly on silkmoth body size.
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Fig. 4. Induction of a systemic immune response in RasV12-expressing larvae.(A) List of genes that are significantly induced (at q<0.05 and induction level >10) in the RasV12-expressing glands (40 larvae were used for each replicate). Induction of a systemic immune response in RasV12-expressing larvae.(A) List of genes that are significantly induced (at q<0.05 and induction level >10) in the RasV12-expressing glands (40 larvae were used for each replicate). (B) The fat body transcription profile of RasV12-expressing larvae shows the hallmarks of an immune response GO classification of genes that are differentially expressed after Ras expression was performed using DAVID (see Materials and Methods for details). The most significant classifications are indicated (see supplementary material Table S2 for a more extensive list of annotations. (C) Induction kinetics of selected immune genes in RasV12-expressing larvae. Individual analysis of a Toll-regulated (Drosomycin) and two preferentially imd-dependent genes (Cecropin A1 and PGRP-SB1) confirms their differential regulation and reveals a complex pattern during the course of the 3rd instar. The ratio of expression between RasV12-expressing and control larvae was determined at the indicated time points after hatching. (Significance levels are: for CecA1: 0.0831; 0.0013; 0.0403 for Drs: 0.0015; 0.0035; 2.15 E−6; 0.0374; 0.0001; 0.0097; 0.0015 and for PRGP-SB1: 0.0151; 0.0167; 0.0321; 0.0436, Student T-test; unpaired, equal variance.)‏ Thomas Hauling et al. Biology Open 2014;bio.20146494 © 2014. Published by The Company of Biologists Ltd