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.

Slides:



Advertisements
Similar presentations
Immuno-gold localisation of COPI in N. gruberi cells.
Advertisements

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.
Fig. 1. Representative images of the four cell lines using fluorescence microscopy. Representative images of the four cell lines using fluorescence microscopy.
Fig. 2. Chd1l is a candidate developmental regulator
Fig. 1. Chlamydia infection causes elevated levels of sortilin.
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. 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. 4. A primary screen based on scrape closure
Fig. 1. Blood lactate, blood glucose and blood corticosterone concentration from crawl until 4 hours of frenzy swimming in loggerhead (C. caretta) and.
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. 2. Mapping of the interaction domain on coilin for association with the dyskerin complex. Mapping of the interaction domain on coilin for association.
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. 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.
Fig. 1. Lack of Hmga1 and Hmga2 expression in A1/A2-KO mice
Fig. 1. Morphological and growth characterization of hBMCs and hPDCs
Fig. 3. Changes of sugar- and malate-metabolic enzyme activities during fruit development under different K treatment conditions. Changes of sugar- and.
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. 2. Dispersal pattern and walking distances of the two wingless strains of Acyrthosiphon pisum in 24 h. Dispersal pattern and walking distances of.
Obesity affected the metabolic response to stroke.
Fig. 8. C. elegans susceptibility to α-terthienyl was affected by the activities of skn-1 and wdr-23. C. elegans susceptibility to α-terthienyl was affected.
Fig. 5. GFP fluorescence colocalization of Gcn5.
Fig. 2. Morphological analysis of acentriolar mitotic spindles
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.
The TER94-p47 complex isinvolved in Notch signaling regulation
Fig. 4. One-dimensional gel electrophoresis of DIMs
Fig. 3. Rnd proteins induce stronger responses in subconfluent endothelial cells.HUVECs were transfected with Rnd1, Rnd2, Rnd3 or GFP-encoding plasmids.
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. 7. Ror-GFP binds to Myc-tagged Wnts and Wnt receptors.
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. 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. 3. Effect of substrate orientation on growth rate for bottom-dwelling tadpoles with similar oral configuration. Effect of substrate orientation on.
Fig. 2. Fluorescent images indicating the cytoskeleton of human bone marrow-derived mesenchymal stem cells (hBMSCs) subjected to cyclic stretching. Fluorescent.
Fig. 4. SMXL6 is degraded in response to SL treatment.
Fig. 1. Nrf2 affects the mitochondrial membrane potential
Fig. 4. Schematic representing clock contribution to Fgf21 regulation in the liver. Schematic representing clock contribution to Fgf21 regulation in the.
Statistical chart of significantly differentially expressed genes
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. 4. Spectra of monochromatic light from the OLS
Fig. 2. RGD and KGD motifs in N. vectensis thrombospondins
The AUX and PIN auxin carrier proteins are transported by both ESCRT-dependent and ESCRT-independent pathways. The AUX and PIN auxin carrier proteins are.
Fig. 8. Tracking details and coordinate systems.
Localization and cellular function of spectraplakins.
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.
Morphological changes induced by T3 treatment 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)
Fig. 2. Acetylation stiffens primary cilia.
Fig. 8. Compared mobilities of passenger proteins in G2/M-prophase, metaphase and anaphase.FRAP experiments were performed on HeLa cells stably expressing.
Fig. 1. p85β localizes at adhesion plaques and associates with FAK
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.
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.
Presentation transcript:

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 K level conditions. Different colored shapes located on the tonoplast and plasma membrane represent different transport proteins. The brown ovals in the cytosol indicate enzymes involved in malate metabolism. (A) Malate metabolism in fruit under low K level condition; (B) malate metabolism in fruit under high K level condition. Wen Zhang et al. Biology Open 2018;7:bio024745 © 2018. Published by The Company of Biologists Ltd