A scalable strategy for high-throughput GFP tagging of endogenous human proteins.
about
Inducible LAP-tagged Stable Cell Lines for Investigating Protein Function, Spatiotemporal Localization and Protein Interaction Networks.The mechanisms and functions of interorganelle interactionsSystematic morphological profiling of human gene and allele function via Cell Painting.Systematic gene tagging using CRISPR/Cas9 in human stem cells to illuminate cell organization.Precision genome editing in the CRISPR era.Quantitative microscopy based on single-molecule fluorescence.High-Throughput Imaging for the Discovery of Cellular Mechanisms of Disease.Improved split fluorescent proteins for endogenous protein labelingGenetically encoded fluorescent tags.Split GFP technologies to structurally characterize and quantify functional biomolecular interactions of FTD-related proteinsCovalent Protein Labeling by SpyTag-SpyCatcher in Fixed Cells for Super-Resolution Microscopy.Spatiotemporal Monitoring of Pseudomonas syringae Effectors via Type III Secretion Using Split Fluorescent Protein Fragments.Emerging Chemistry Strategies for Engineering Native Chromatin.Determining direct binders of the Androgen Receptor using a high-throughput Cellular Thermal Shift Assay.Precision genome editing using synthesis-dependent repair of Cas9-induced DNA breaks.Clathrin Assembly Defines the Onset and Geometry of Cortical Patterning.Methods and Applications of CRISPR-Mediated Base Editing in Eukaryotic Genomes.A Single-Cell Biochemistry Approach Reveals PAR Complex Dynamics during Cell Polarization.Histone phosphorylation by TRPM6's cleaved kinase attenuates adjacent arginine methylation to regulate gene expression.SAC1 degrades its lipid substrate PtdIns4P in the endoplasmic reticulum to maintain a steep chemical gradient with donor membranes.Versatile approach for functional analysis of human proteins and efficient stable cell line generation using FLP-mediated recombination system.Integrating images from multiple microscopy screens reveals diverse patterns of change in the subcellular localization of proteins.Characterization of Split Fluorescent Protein Variants and Quantitative Analyses of Their Self-Assembly Process.
P2860
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P2860
A scalable strategy for high-throughput GFP tagging of endogenous human proteins.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
A scalable strategy for high-throughput GFP tagging of endogenous human proteins.
@ast
A scalable strategy for high-throughput GFP tagging of endogenous human proteins.
@en
type
label
A scalable strategy for high-throughput GFP tagging of endogenous human proteins.
@ast
A scalable strategy for high-throughput GFP tagging of endogenous human proteins.
@en
prefLabel
A scalable strategy for high-throughput GFP tagging of endogenous human proteins.
@ast
A scalable strategy for high-throughput GFP tagging of endogenous human proteins.
@en
P2093
P2860
P356
P1476
A scalable strategy for high-throughput GFP tagging of endogenous human proteins.
@en
P2093
Daichi Kamiyama
Manuel D Leonetti
Sayaka Sekine
P2860
P304
P356
10.1073/PNAS.1606731113
P407
P577
2016-06-06T00:00:00Z