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

Slides:

Advertisements

Similar presentations

Candidates with a PVM localization.

Advertisements

Localization of PBANKA_ and PBANKA_ during blood and liver stage development. Localization of PBANKA_ and PBANKA_ during blood.

Differential secretion profiles of C. elegans TTR models.

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. Overview of the nervous system of the adult S. roscoffensis.

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. In vitro effect of CMPs on adult DSS-treated stomach explants.

Fig. 3. Hts and Dlg are in a complex at the postsynaptic membrane of larval NMJs.(A–B″) PLA with HtsM and Dlg antibodies (green) performed on third instar.

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. 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. 4. Seeding density modulates cell shape in both cell types

Fig. 6. Hts regulates par-1 and camkII mRNA distribution and levels in the muscle.(A–J) Views of muscles 6/7 in abdominal segment 4, probed for either.

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.

Tbx1 regulates the Mef2c AHF enhancer in vivo.

Fig. 1. Exogenous folic acid and Folr1 rescues the function of a Rho-kinase binding mutation in Shroom3. Exogenous folic acid and Folr1 rescues thefunction.

Fig. 1. Mitochondrial internalization in cardiomyocytes.

Fig. 1. Loss of PC following INT depletion

Indirect fluorescence assay of N. gruberi cells.

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. 2. Salivary glands from RasV12-expressing larvae produce MMP1, release tissue fragments into the hemolymph and express apoptotic markers.Salivary.

Fig. 1. E-cadherin localizes in nano-scale clusters.

PfSec13 does not co-localize with P. falciparum heterochromatin.

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. 2. DDR1 over-expression enhances collagen fibril reorganization

Fig. 1. Ovarian cancer spheroids can bud from a monolayer

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.

Kinetics of induced and non-induced AR, and its relationship to cell death and motility. Kinetics of induced and non-induced AR, and its relationship to.

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

Fig. 4. Detection of dFMR1 mRNA in dFMRP granules by FISH

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

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

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. 6. Comparison of Plk4 with Sas-6 localization

Fig. 3. The checkpoint proteins Mad2 and BubR1 remain associated with the kinetochores of unaligned chromosomes in cenp-metaΔ mutant cells entering anaphase.(A–C)

Fig. 5. GFP fluorescence colocalization of Gcn5.

Fig. 2. Morphological analysis of acentriolar mitotic spindles

Fig. 7. Lhx1-RNAi reduces the eye size

The TER94-p47 complex isinvolved in Notch signaling regulation

Fig. 3. Rnd proteins induce stronger responses in subconfluent endothelial cells.HUVECs were transfected with Rnd1, Rnd2, Rnd3 or GFP-encoding plasmids.

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. 6. STK35 KO mice show ovary defects.

Fig. 2. Sorting in chimeric embryoid bodies of wildtype with E- or N-cadherin null ES cells.Wildtype, E-cadherin null (9J), and N-cadherin null (Ncad95)

Fig. 2. Fluorescent images indicating the cytoskeleton of human bone marrow-derived mesenchymal stem cells (hBMSCs) subjected to cyclic stretching. Fluorescent.

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

Axial organisation of gastruloids.

Fig. 3. Analysis of mitotic and post-mitotic specificity of recombination in the cerebral cortices of Emx1cre and Nestin-cre mice using the MADM-11 genetic.

Effect of the plastid translation inhibitor Spec on LR development

EpiDEG efficiently degrades GFP-tagged proteins that localize to different subcellular localizations. epiDEG efficiently degrades GFP-tagged proteins that.

Two domains of KHC act to position the nucleus.

Tau–RFP–RBPs colocalize with mRNA on microtubules and lead to the wetting of stress granules on microtubules. Tau–RFP–RBPs colocalize with mRNA on microtubules.

Exo70 is recruited to the plasma membrane at sites of mechanical wounding. Exo70 is recruited to the plasma membrane at sites of mechanical wounding. NRK.

Fig. 2. Non-homogeneous subcellular distribution of Vangl2 along the anteroposterior axis. Non-homogeneous subcellular distribution of Vangl2 along the.

Fig. 2. iPSCs produce functional osteoblasts.

Fig. 2. Tbx1 lineage is largely complementary to the NSD

dcn1-deletion results in attenuated cohesin cleavage at anaphase

Fig. 6. IIS affected the soma area of most neurons in pharate adults, but not in larvae.(A,B) Pan-peptidergic expression pattern of 386-Gal4,UAS-CD8::GFP.

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. 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. 4. CR4.2 may be active in amacrine cells but not in ganglion cells.Chick retinas were electroporated with either the control CAG-GFP construct or.

Fig. 2. Acetylation stiffens primary cilia.

Fig. 7. Eye defects in STK35 KO mouse.

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.

Fig. 1. Expression of a Ror-eGFP fusion protein under control of the endogenous Ror promoter in Drosophila embryos. Expression of a Ror-eGFP fusion protein.

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.

WT MARCH8, but not the CS mutant, specifically ubiquitinates and downregulates TfR. WT MARCH8, but not the CS mutant, specifically ubiquitinates and downregulates.

Failure of chromosome disassembly in mip120 null ovarian nurse cells

Fig. 7. Analysis of dFMRP kinetics in dFMRP granules by FRAP

Presentation transcript:

Fig. 2. abu/pqn genes are expressed in the pharyngeal cuticle Fig. 2. abu/pqn genes are expressed in the pharyngeal cuticle.(A) Expression of abu-5 (red) and abu-11 (green) in pharyngeal cells. abu/pqn genes are expressed in the pharyngeal cuticle.(A) Expression of abu-5 (red) and abu-11 (green) in pharyngeal cells. Scale bar is 10 µm. (B) Differential interference contrast (DIC) and fluorescence image of the anterior pharynx of an adult transgenic animal containing the transgene abu-14>abu-14::sfGFP. The fluorescence localizes to the pharyngeal corpus and buccal cavity cuticle (arrows). A non-transgenic sister (marked with “non-Tg”) shows no fluorescence. Anterior is to the left. Scale bar is 10 µm. (C) DIC and fluorescence image of the pharynx of a fourth larval stage molting animal containing the transgene abu-14>abu-14::sfGFP. Green fluorescence is seen in both the L4 and adult pharyngeal grinders, in the pharyngeal cuticle, and in the buccal cap. Anterior is to the left. Scale bar is 10 µm. (D) DIC (left) and fluorescence (right) images of a larval animal containing the transgene abu-7>abu-7::GFP. The pharyngeal grinder is brightly fluorescent. Scale bar is 10 µm. Julia B. George-Raizen et al. Biology Open 2014;bio.20147500 © 2014. Published by The Company of Biologists Ltd