Improved blue, green, and red fluorescent protein tagging vectors for S. cerevisiae.
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The Development of Genetic Modification Techniques in Intracellular Parasites and Potential Applications to MicrosporidiaPositive feedback of NDT80 expression ensures irreversible meiotic commitment in budding yeastTargeting and plasticity of mitochondrial proteins revealed by proximity-specific ribosome profiling.Timely Closure of the Prospore Membrane Requires SPS1 and SPO77 in Saccharomyces cerevisiaeMetabolic Engineering of Probiotic Saccharomyces boulardiiIdentification of a Novel Regulatory Mechanism of Nutrient Transport Controlled by TORC1-Npr1-Amu1/Par32Rainbow Vectors for Broad-Range Bacterial Fluorescence Labeling.Improved Plasmids for Fluorescent Protein Tagging of Microtubules in Saccharomyces cerevisiaeOverexpression of the essential Sis1 chaperone reduces TDP-43 effects on toxicity and proteolysis.Plasmids for C-terminal tagging in Saccharomyces cerevisiae that contain improved GFP proteins, Envy and Ivy.PCR Duplication: A One-Step Cloning-Free Method to Generate Duplicated Chromosomal Loci and Interference-Free Expression Reporters in YeastRapid isolation and single-molecule analysis of ribonucleoproteins from cell lysate by SNAP-SiMPullSuperresolution live imaging of plant cells using structured illumination microscopy.Characterization of Fluorescent Proteins for Three- and Four-Color Live-Cell Imaging in S. cerevisiaeSingle-Molecule mRNA Detection in Live Yeast.Sensitive and Quantitative Three-Color Protein Imaging in Fission Yeast Using Spectrally Diverse, Recoded Fluorescent Proteins with Experimentally-Characterized In Vivo Maturation Kinetics.Parallel reorganization of protein function in the spindle checkpoint pathway through evolutionary paths in the fitness landscape that appear neutral in laboratory experimentsEngineering of synthetic, stress-responsive yeast promoters.Expression of varied GFPs in Saccharomyces cerevisiae: codon optimization yields stronger than expected expression and fluorescence intensity.Can terminators be used as insulators into yeast synthetic gene circuits?Comparative assessment of fluorescent proteins for in vivo imaging in an animal model systemDifferentiated cytoplasmic granule formation in quiescent and non-quiescent cells upon chronological agingMetabolic engineering of yeast to produce fatty acid-derived biofuels: bottlenecks and solutions.Phototoxicity in live fluorescence microscopy, and how to avoid it.The Nucleoporin Nup2 Contains a Meiotic-Autonomous Region that Promotes the Dynamic Chromosome Events of Meiosis.Multi-color imaging of the bacterial nucleoid and division proteins with blue, orange, and near-infrared fluorescent proteins.Analysis of the Localization of MEN Components by Live Cell Imaging Microscopy.Bacterial tail anchors can target to the mitochondrial outer membrane.Switch-like Arp2/3 activation upon WASP and WIP recruitment to an apparent threshold level by multivalent linker proteins in vivo.Fast two-photon imaging of subcellular voltage dynamics in neuronal tissue with genetically encoded indicators.Quantitative high-content imaging identifies novel regulators of Neo1 trafficking at endosomes.Modelling of diffraction grating based optical filters for fluorescence detection of biomolecules.CRISPR-UnLOCK: Multipurpose Cas9-Based Strategies for Conversion of Yeast Libraries and Strains.Genetically encoded fluorescent tags.Dynamic regulation of Cdr1 localization and phosphorylation during osmotic stress.Polyglutamine toxicity in yeast uncovers phenotypic variations between different fluorescent protein fusions.Dual display of proteins on the yeast cell surface simplifies quantification of binding interactions and enzymatic bioconjugation reactions.Hof1 and Chs4 Interact via F-BAR Domain and Sel1-like Repeats to Control Extracellular Matrix Deposition during Cytokinesis.The Mitotic Exit Network Regulates Spindle Pole Body Selection During Sporulation of Saccharomyces cerevisiae.New integrative modules for multicolor-protein labeling and live-cell imaging in Saccharomyces cerevisiae.
P2860
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P2860
Improved blue, green, and red fluorescent protein tagging vectors for S. cerevisiae.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
@yue
2013年學術文章
@zh
2013年學術文章
@zh-hant
name
Improved blue, green, and red fluorescent protein tagging vectors for S. cerevisiae.
@en
type
label
Improved blue, green, and red fluorescent protein tagging vectors for S. cerevisiae.
@en
prefLabel
Improved blue, green, and red fluorescent protein tagging vectors for S. cerevisiae.
@en
P2093
P2860
P1433
P1476
Improved blue, green, and red fluorescent protein tagging vectors for S. cerevisiae.
@en
P2093
Kurt S Thorn
Wendell A Lim
P2860
P304
P356
10.1371/JOURNAL.PONE.0067902
P407
P577
2013-07-02T00:00:00Z