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Reconstructing regulatory pathways by systematically mapping protein localization interdependency networks

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Heterologous modules for efficient and versatile PCR-based gene targeting inSchizosaccharomyces pombe
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Featured Organism: Schizosaccharomyces pombe, the fission yeast
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New drug‐resistant cassettes for gene disruption and epitope tagging in Schizosaccharomyces pombe
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Visualization of Fluorescence-Tagged Proteins in Fission Yeast: The Analysis of Mitotic Spindle Dynamics Using GFP-Tubulin Under the Native Promoter
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[56] Molecular genetic analysis of fission yeast Schizosaccharomyces pombe
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Interactome Networks and Human Disease
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A Systematic Mammalian Genetic Interaction Map Reveals Pathways Underlying Ricin Susceptibility
inferredcites →https://doi.org/10.1016/j.cell.2014.10.050openalex-snapshot
A Proteome-Scale Map of the Human Interactome Network
inferredcites →https://doi.org/10.1016/j.cellsig.2007.12.017openalex-snapshot
Activation of the cell integrity pathway is channelled through diverse signalling elements in fission yeast
inferredcites →https://doi.org/10.1016/j.cub.2008.02.005openalex-snapshot
Pom1 DYRK Regulates Localization of the Rga4 GAP to Ensure Bipolar Activation of Cdc42 in Fission Yeast
inferredcites →https://doi.org/10.1016/j.cub.2012.10.042openalex-snapshot
Cdc42 Explores the Cell Periphery for Mate Selection in Fission Yeast
inferredcites →https://doi.org/10.1016/j.devcel.2014.09.005openalex-snapshot
A Genomic Multiprocess Survey of Machineries that Control and Link Cell Shape, Microtubule Organization, and Cell-Cycle Progression
inferredcites →https://doi.org/10.1016/j.semcdb.2011.07.013openalex-snapshot
Cell polarity in fission yeast: A matter of confining, positioning, and switching growth zones
inferredcites →https://doi.org/10.1016/j.tcb.2009.06.003openalex-snapshot
Microtubule-dependent cell morphogenesis in the fission yeast
inferredcites →https://doi.org/10.1038/35089520openalex-snapshot
A journey into space
inferredcites →https://doi.org/10.1038/nature05773openalex-snapshot
Alp7/TACC is a crucial target in Ran-GTPase-dependent spindle formation in fission yeast
inferredcites →https://doi.org/10.1038/nature08779openalex-snapshot
Systems survey of endocytosis by multiparametric image analysis
inferredcites →https://doi.org/10.1038/nature08869openalex-snapshot
Phenotypic profiling of the human genome by time-lapse microscopy reveals cell division genes
inferredcites →https://doi.org/10.1038/nature12748openalex-snapshot
High-content genome-wide RNAi screens identify regulators of parkin upstream of mitophagy
inferredcites →https://doi.org/10.1038/nbt.1628openalex-snapshot
Analysis of a genome-wide set of gene deletions in the fission yeast Schizosaccharomyces pombe
inferredcites →https://doi.org/10.1038/nbt.3146openalex-snapshot
High-throughput fluorescence correlation spectroscopy enables analysis of proteome dynamics in living cells
inferredcites →https://doi.org/10.1038/nmeth.1220openalex-snapshot
Lifeact: a versatile marker to visualize F-actin
inferredcites →https://doi.org/10.1038/nmeth.1581openalex-snapshot
Mapping of signaling networks through synthetic genetic interaction analysis by RNAi
inferredcites →https://doi.org/10.1038/nmeth.2089openalex-snapshot
NIH Image to ImageJ: 25 years of image analysis
inferredcites →https://doi.org/10.1038/nmeth.2398openalex-snapshot
Quantitative genetic-interaction mapping in mammalian cells
inferredcites →https://doi.org/10.1038/nmeth.2436openalex-snapshot
Mapping genetic interactions in human cancer cells with RNAi and multiparametric phenotyping
inferredcites →https://doi.org/10.1038/nmeth1098openalex-snapshot
High-throughput genetic interaction mapping in the fission yeast Schizosaccharomyces pombe
inferredcites →https://doi.org/10.1038/nmeth876openalex-snapshot
High-throughput RNAi screening by time-lapse imaging of live human cells
inferredcites →https://doi.org/10.1038/nrg1272openalex-snapshot
Network biology: understanding the cell's functional organization
inferredcites →https://doi.org/10.1042/bc20060048openalex-snapshot
Fission yeast cytoskeletons and cell polarity factors: connecting at the cortex
inferredcites →https://doi.org/10.1042/bj20091823openalex-snapshot
Rho GTPases: regulation of cell polarity and growth in yeasts
inferredcites →https://doi.org/10.1046/j.1365-2443.2001.00414.xopenalex-snapshot
Identification and functional analysis of the gene for type I myosin in fission yeast
inferredcites →https://doi.org/10.1073/pnas.87.21.8272openalex-snapshot
A putative protein kinase gene (kin1+) is important for growth polarity in Schizosaccharomyces pombe.
inferredcites →https://doi.org/10.1074/jbc.m109.071027openalex-snapshot
Rga4 Modulates the Activity of the Fission Yeast Cell Integrity MAPK Pathway by Acting as a Rho2 GTPase-activating Protein
inferredcites →https://doi.org/10.1074/jbc.m506467200openalex-snapshot
Stress-induced Response, Localization, and Regulation of the Pmk1 Cell Integrity Pathway in Schizosaccharomyces pombe
inferredcites →https://doi.org/10.1074/jbc.m806391200openalex-snapshot
Cell Wall Integrity MAPK Pathway Is Essential for Lipid Homeostasis
inferredcites →https://doi.org/10.1091/mbc.12.4.1061openalex-snapshot
Roles of a Fimbrin and an α-Actinin-like Protein in Fission Yeast Cell Polarization and Cytokinesis
inferredcites →https://doi.org/10.1093/bioinformatics/bth448openalex-snapshot
Advances to Bayesian network inference for generating causal networks from observational biological data
inferredcites →https://doi.org/10.1093/bioinformatics/btq342openalex-snapshot
TRANSWESD: inferring cellular networks with transitive reduction
inferredcites →https://doi.org/10.1093/nar/gkr853openalex-snapshot
PomBase: a comprehensive online resource for fission yeast
inferredcites →https://doi.org/10.1093/nar/gku1204openalex-snapshot
The BioGRID interaction database: 2015 update
inferredcites →https://doi.org/10.1101/gad.12.9.1356openalex-snapshot
Pom1p, a fission yeast protein kinase that provides positional information for both polarized growth and cytokinesis
inferredcites →https://doi.org/10.1109/icdm.2010.133openalex-snapshot
Network Simplification with Minimal Loss of Connectivity
inferredcites →https://doi.org/10.1111/j.1365-2958.2010.07281.xopenalex-snapshot
Kin1 is a plasma membrane-associated kinase that regulates the cell surface in fission yeast
inferredcites →https://doi.org/10.1111/j.2517-6161.1995.tb02031.xopenalex-snapshot
Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing
inferredcites →https://doi.org/10.1126/science.1091317openalex-snapshot
Global Mapping of the Yeast Genetic Interaction Network
inferredcites →https://doi.org/10.1126/science.1105809openalex-snapshot
Causal Protein-Signaling Networks Derived from Multiparameter Single-Cell Data
inferredcites →https://doi.org/10.1126/science.1180823openalex-snapshot
The Genetic Landscape of a Cell
inferredcites →https://doi.org/10.1242/jcs.00206openalex-snapshot
Mob2p interacts with the protein kinase Orb6p to promote coordination of cell polarity with cell cycle progression
inferredcites →https://doi.org/10.1242/jcs.01585openalex-snapshot
The novel fission yeast (1,3)β-D-glucan synthase catalytic subunit Bgs4p is essential during both cytokinesis and polarized growth
inferredcites →https://doi.org/10.1242/jcs.01690openalex-snapshot
Ste20/GCK kinase Nak1/Orb3 polarizes the actin cytoskeleton in fission yeast during the cell cycle
inferredcites →https://doi.org/10.1242/jcs.112.20.3569openalex-snapshot
Schizosaccharomyces pombe protein kinase C homologues, pck1p and pck2p, are targets of rho1p and rho2p and differentially regulate cell integrity
inferredcites →https://doi.org/10.1242/jcs.75.1.357openalex-snapshot
Growth in cell length in the fission yeast Schizosaccharomyces pombe
inferredcites →https://doi.org/10.1371/journal.pcbi.1002732openalex-snapshot
Linkers of Cell Polarity and Cell Cycle Regulation in the Fission Yeast Protein Interaction Network

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1042/ebc20180044openalex-snapshot
From observing to predicting single-cell structure and function with high-throughput/high-content microscopy
inferred← citeshttps://doi.org/10.1101/2023.08.25.554841openalex-snapshot
Generative adversarial networks in cell microscopy for image augmentation. A systematic review
inferred← citeshttps://doi.org/10.1109/iccv.2017.245openalex-snapshot
GANs for Biological Image Synthesis
inferred← citeshttps://doi.org/10.1371/journal.pbio.3002491openalex-snapshot
Rho1 and Rgf1 establish a new actin-dependent signal to determine growth poles in yeast independently of microtubules and the Tea1–Tea4 complex
inferred← citeshttps://doi.org/10.1371/journal.pone.0291217openalex-snapshot
Systematic review of generative adversarial networks (GANs) in cell microscopy: Trends, practices, and impact on image augmentation
inferred← citeshttps://doi.org/10.3390/cells10061422openalex-snapshot
The Multiple Functions of Rho GTPases in Fission Yeasts
inferred← citeshttps://doi.org/10.3390/jof8010032openalex-snapshot
The Fission Yeast Cell Integrity Pathway: A Functional Hub for Cell Survival upon Stress and Beyond
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