scholarly article | Q13442814 |
P2093 | author name string | Paul J Cullen | |
Hema Adhikari | |||
P2860 | cites work | NIH Image to ImageJ: 25 years of image analysis | Q23319322 |
Stimulation of glucose transport by AMP-activated protein kinase via activation of p38 mitogen-activated protein kinase | Q24291657 | ||
Activation of the yeast SSK2 MAP kinase kinase kinase by the SSK1 two-component response regulator | Q24533167 | ||
Suppression of mitochondrial respiration through recruitment of p160 myb binding protein to PGC-1alpha: modulation by p38 MAPK | Q24598689 | ||
The transcriptional landscape of the yeast genome defined by RNA sequencing | Q24633693 | ||
TopHat: discovering splice junctions with RNA-Seq | Q24655505 | ||
Yeast microarrays for genome wide parallel genetic and gene expression analysis | Q24657389 | ||
NRG1 is required for glucose repression of the SUC2 and GAL genes of Saccharomyces cerevisiae | Q24797402 | ||
Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method | Q25938999 | ||
Regulation of mat responses by a differentiation MAPK pathway in Saccharomyces cerevisiae | Q27308564 | ||
Signal integration in the endoplasmic reticulum unfolded protein response | Q27860577 | ||
edgeR: a Bioconductor package for differential expression analysis of digital gene expression data | Q27860819 | ||
Genomic expression programs in the response of yeast cells to environmental changes | Q27860823 | ||
Positioning of cell growth and division after osmotic stress requires a MAP kinase pathway. | Q27930462 | ||
Elements of the yeast pheromone response pathway required for filamentous growth of diploids | Q27930528 | ||
Zinc and the Msc2 zinc transporter protein are required for endoplasmic reticulum function. | Q27930535 | ||
Activation of yeast PBS2 MAPKK by MAPKKKs or by binding of an SH3-containing osmosensor. | Q27930567 | ||
A two-component system that regulates an osmosensing MAP kinase cascade in yeast | Q27930757 | ||
Genetic analysis of the bipolar pattern of bud site selection in the yeast Saccharomyces cerevisiae | Q27930775 | ||
Yeast HOG1 MAP kinase cascade is regulated by a multistep phosphorelay mechanism in the SLN1-YPD1-SSK1 "two-component" osmosensor. | Q27930940 | ||
Glucose depletion causes haploid invasive growth in yeast | Q27931385 | ||
A family of genes required for maintenance of cell wall integrity and for the stress response in Saccharomyces cerevisiae | Q27931403 | ||
The role of CDC28 and cyclins during mitosis in the budding yeast S. cerevisiae | Q27931492 | ||
Regulation of Snf1 kinase. Activation requires phosphorylation of threonine 210 by an upstream kinase as well as a distinct step mediated by the Snf4 subunit | Q27931918 | ||
An osmosensing signal transduction pathway in yeast. | Q27932086 | ||
The filamentous growth MAPK Pathway Responds to Glucose Starvation Through the Mig1/2 transcriptional repressors in Saccharomyces cerevisiae | Q27932392 | ||
Regulation of the Saccharomyces cerevisiae HOG1 mitogen-activated protein kinase by the PTP2 and PTP3 protein tyrosine phosphatases | Q27932501 | ||
Actin recovery and bud emergence in osmotically stressed cells requires the conserved actin interacting mitogen-activated protein kinase kinase kinase Ssk2p/MTK1 and the scaffold protein Spa2p | Q27932526 | ||
MAPK Hog1 closes the S. cerevisiae glycerol channel Fps1 by phosphorylating and displacing its positive regulators. | Q27932780 | ||
Transmembrane mucins Hkr1 and Msb2 are putative osmosensors in the SHO1 branch of yeast HOG pathway. | Q27932838 | ||
Rck2, a member of the calmodulin-protein kinase family, links protein synthesis to high osmolarity MAP kinase signaling in budding yeast | Q27933036 | ||
Remodeling of yeast genome expression in response to environmental changes | Q27933130 | ||
Hog1 mitogen-activated protein kinase (MAPK) interrupts signal transduction between the Kss1 MAPK and the Tec1 transcription factor to maintain pathway specificity | Q27933210 | ||
Stress-induced map kinase Hog1 is part of transcription activation complexes. | Q27933281 | ||
MAP kinases with distinct inhibitory functions impart signaling specificity during yeast differentiation | Q27933379 | ||
The genetic interaction network of CCW12, a Saccharomyces cerevisiae gene required for cell wall integrity during budding and formation of mating projections. | Q27933508 | ||
A Saccharomyces gene family involved in invasive growth, cell-cell adhesion, and mating | Q27933651 | ||
Bakers' yeast, a model for fungal biofilm formation. | Q27933699 | ||
The MEK kinase Ssk2p promotes actin cytoskeleton recovery after osmotic stress | Q27933780 | ||
Hog1 bypasses stress-mediated down-regulation of transcription by RNA polymerase II redistribution and chromatin remodeling | Q27933955 | ||
Coactivation of G protein signaling by cell-surface receptors and an intracellular exchange factor | Q27934014 | ||
Multigenerational cortical inheritance of the Rax2 protein in orienting polarity and division in yeast | Q27934033 | ||
PMI40, an intron-containing gene required for early steps in yeast mannosylation | Q27934052 | ||
Osmotic activation of the HOG MAPK pathway via Ste11p MAPKKK: scaffold role of Pbs2p MAPKK. | Q27934994 | ||
Adaptor functions of Cdc42, Ste50, and Sho1 in the yeast osmoregulatory HOG MAPK pathway. | Q27936208 | ||
The septins: roles in cytokinesis and other processes | Q27936270 | ||
The Hog1 MAPK prevents cross talk between the HOG and pheromone response MAPK pathways in Saccharomyces cerevisiae | Q27936490 | ||
Saccharomyces cerevisiae TEC1 is required for pseudohyphal growth | Q27936711 | ||
Unipolar cell divisions in the yeast S. cerevisiae lead to filamentous growth: regulation by starvation and RAS | Q27936756 | ||
Identification of a developmentally regulated septin and involvement of the septins in spore formation in Saccharomyces cerevisiae | Q27936941 | ||
Combinatorial control required for the specificity of yeast MAPK signaling | Q27937910 | ||
A signaling mucin at the head of the Cdc42- and MAPK-dependent filamentous growth pathway in yeast | Q27938083 | ||
A novel mechanism for regulating activity of a transcription factor that controls the unfolded protein response | Q27938493 | ||
Roles of the Snf1-activating kinases during nitrogen limitation and pseudohyphal differentiation in Saccharomyces cerevisiae | Q27938825 | ||
Transcriptional induction of genes encoding endoplasmic reticulum resident proteins requires a transmembrane protein kinase | Q27938837 | ||
The signaling mucins Msb2 and Hkr1 differentially regulate the filamentation mitogen-activated protein kinase pathway and contribute to a multimodal response. | Q27939105 | ||
Elements of a single MAP kinase cascade in Saccharomyces cerevisiae mediate two developmental programs in the same cell type: mating and invasive growth | Q27939215 | ||
Shedding of the mucin-like flocculin Flo11p reveals a new aspect of fungal adhesion regulation | Q27939435 | ||
The MAPK Hog1 recruits Rpd3 histone deacetylase to activate osmoresponsive genes. | Q27939566 | ||
Adaptor protein Ste50p links the Ste11p MEKK to the HOG pathway through plasma membrane association. | Q27939643 | ||
Properties of Saccharomyces cerevisiae wee1 and its differential regulation of p34CDC28 in response to G1 and G2 cyclins | Q27939854 | ||
Genetic control of bud site selection in yeast by a set of gene products that constitute a morphogenetic pathway | Q27939940 | ||
Rck2 kinase is a substrate for the osmotic stress-activated mitogen-activated protein kinase Hog1. | Q27940318 | ||
MAP kinase and cAMP filamentation signaling pathways converge on the unusually large promoter of the yeast FLO11 gene | Q27940377 | ||
A simple and efficient method for direct gene deletion in Saccharomyces cerevisiae | Q28131603 | ||
Three new dominant drug resistance cassettes for gene disruption in Saccharomyces cerevisiae | Q28131610 | ||
Mechanism of action of tunicamycin on the UDP-GlcNAc:dolichyl-phosphate GlcNAc-1-phosphate transferase | Q41607246 | ||
Two adjacent docking sites in the yeast Hog1 mitogen-activated protein (MAP) kinase differentially interact with the Pbs2 MAP kinase kinase and the Ptp2 protein tyrosine phosphatase | Q41772137 | ||
The Cek1 and Hog1 mitogen-activated protein kinases play complementary roles in cell wall biogenesis and chlamydospore formation in the fungal pathogen Candida albicans. | Q41869795 | ||
Pheromone-induced morphogenesis improves osmoadaptation capacity by activating the HOG MAPK pathway | Q41879786 | ||
Glycosylation defects activate filamentous growth Kss1 MAPK and inhibit osmoregulatory Hog1 MAPK. | Q41920229 | ||
The HOG pathway dictates the short-term translational response after hyperosmotic shock | Q42451574 | ||
Analysis of mitogen-activated protein kinase signaling specificity in response to hyperosmotic stress: use of an analog-sensitive HOG1 allele | Q42559192 | ||
The transcriptional response of yeast to saline stress | Q42623210 | ||
Selective requirement for SAGA in Hog1-mediated gene expression depending on the severity of the external osmostress conditions | Q42738047 | ||
The sequential activation of the yeast HOG and SLT2 pathways is required for cell survival to cell wall stress | Q43069140 | ||
The high osmotic response and cell wall integrity pathways cooperate to regulate transcriptional responses to zymolyase-induced cell wall stress in Saccharomyces cerevisiae | Q43147138 | ||
Multiple mechanisms provide rapid and stringent glucose repression of GAL gene expression in Saccharomyces cerevisiae | Q43181761 | ||
Recruitment of a chromatin remodelling complex by the Hog1 MAP kinase to stress genes. | Q43191422 | ||
Studies on phosphomannose isomerase. II. Characterization as a zinc metalloenzyme | Q44215490 | ||
The Hog1 MAP kinase pathway and the Mec1 DNA damage checkpoint pathway independently control the cellular responses to hydrogen peroxide. | Q45968463 | ||
A yeast protein similar to bacterial two-component regulators | Q46106065 | ||
A downshift in temperature activates the high osmolarity glycerol (HOG) pathway, which determines freeze tolerance in Saccharomyces cerevisiae | Q46863312 | ||
A conserved mitogen-activated protein kinase pathway is required for mating in Candida albicans | Q48272020 | ||
Bypasses of the antimycin a block of mitochondrial electron transport in relation to ubisemiquinone function. | Q50920269 | ||
A systems-biology analysis of feedback inhibition in the Sho1 osmotic-stress-response pathway. | Q54044321 | ||
Activation of the yeast cell wall integrity MAPK pathway by zymolyase depends on protease and glucanase activities and requires the mucin-like protein Hkr1 but not Msb2. | Q54404891 | ||
Cross-talk and decision making in MAP kinase pathways | Q58028841 | ||
The Saccharomyces cerevisiae Sln1p-Ssk1p two-component system mediates response to oxidative stress and in an oxidant-specific fashion | Q73205031 | ||
Simultaneous detection of mitochondrial respiratory chain activity and reactive oxygen in digitonin-permeabilized cells using flow cytometry | Q73205704 | ||
Negative control of the Mig1p repressor by Snf1p-dependent phosphorylation in the absence of glucose | Q74384683 | ||
The SNF1 kinase complex from Saccharomyces cerevisiae phosphorylates the transcriptional repressor protein Mig1p in vitro at four sites within or near regulatory domain 1 | Q77993773 | ||
MAP kinase pathways | Q81074052 | ||
Global gene deletion analysis exploring yeast filamentous growth | Q84978517 | ||
Sense and sensibility: nutritional response and signal integration in yeast | Q35958180 | ||
Principles of MAP kinase signaling specificity in Saccharomyces cerevisiae. | Q35965868 | ||
The effect of antimycin A on mouse liver inner mitochondrial membrane channel activity | Q36029564 | ||
Sphingolipids regulate the yeast high-osmolarity glycerol response pathway | Q36155090 | ||
The glucose-deprivation network counteracts lapatinib-induced toxicity in resistant ErbB2-positive breast cancer cells | Q36171144 | ||
Loss of the respiratory enzyme citrate synthase directly links the Warburg effect to tumor malignancy. | Q36382575 | ||
MAPK signal specificity: the right place at the right time | Q36444123 | ||
Osmotic stress and the yeast cytoskeleton: phenotype-specific suppression of an actin mutation | Q36531677 | ||
Genetics and genomics of Candida albicans biofilm formation | Q36539594 | ||
Effectors of a developmental mitogen-activated protein kinase cascade revealed by expression signatures of signaling mutants | Q36544126 | ||
Yeast MEK-dependent signal transduction: response thresholds and parameters affecting fidelity | Q36556089 | ||
Candida albicans strains heterozygous and homozygous for mutations in mitogen-activated protein kinase signaling components have defects in hyphal development | Q36690106 | ||
Dysregulated mTORC1 renders cells critically dependent on desaturated lipids for survival under tumor-like stress | Q36902914 | ||
A model fungal gene regulatory mechanism: the GAL genes of Saccharomyces cerevisiae. | Q37064006 | ||
Evidence of a new role for the high-osmolarity glycerol mitogen-activated protein kinase pathway in yeast: regulating adaptation to citric acid stress | Q37277581 | ||
The high-osmolarity glycerol (HOG) and cell wall integrity (CWI) signalling pathways interplay: a yeast dialogue between MAPK routes | Q37773860 | ||
Choosing the right lifestyle: adhesion and development in Saccharomyces cerevisiae | Q37869191 | ||
The regulation of filamentous growth in yeast | Q37973321 | ||
Response to hyperosmotic stress | Q38048770 | ||
Leptin and vascular smooth muscle cells | Q38107983 | ||
Mitogen-activated protein kinase pathways in osteoblasts | Q38110913 | ||
IRE1-dependent activation of AMPK in response to nitric oxide | Q38960360 | ||
Carbon source-dependent phosphorylation of hexokinase PII and its role in the glucose-signaling response in yeast. | Q39583995 | ||
The roles of bud-site-selection proteins during haploid invasive growth in yeast | Q39640754 | ||
Improvement of galactose uptake in Saccharomyces cerevisiae through overexpression of phosphoglucomutase: example of transcript analysis as a tool in inverse metabolic engineering | Q39800927 | ||
The mitogen-activated protein kinase homolog HOG1 gene controls glycerol accumulation in the pathogenic fungus Candida albicans | Q39843038 | ||
Extragenic suppressors of yeast glucose derepression mutants leading to constitutive synthesis of several glucose-repressible enzymes | Q39940956 | ||
A conserved stress-activated protein kinase regulates a core stress response in the human pathogen Candida albicans | Q39968804 | ||
Symmetric cell division in pseudohyphae of the yeast Saccharomyces cerevisiae | Q40366333 | ||
Asymmetrically localized Bud8p and Bud9p proteins control yeast cell polarity and development. | Q40388542 | ||
Transcriptional regulation in the yeast GAL gene family: a complex genetic network | Q40439061 | ||
Cytokine stimulation of energy expenditure through p38 MAP kinase activation of PPARgamma coactivator-1. | Q40763964 | ||
Late phase of the endoplasmic reticulum stress response pathway is regulated by Hog1 MAP kinase | Q40813546 | ||
Glycoprotein biosynthesis in yeast | Q40896550 | ||
Sir2 plays a key role in cell fate determination upon SAPK activation. | Q40900716 | ||
The activity of yeast Hog1 MAPK is required during endoplasmic reticulum stress induced by tunicamycin exposure | Q41192860 | ||
Functional and genomic analyses reveal an essential coordination between the unfolded protein response and ER-associated degradation | Q28131669 | ||
The septin cortex at the yeast mother-bud neck | Q28208432 | ||
Identifying differentially expressed genes using false discovery rate controlling procedures | Q29615200 | ||
Osmotic stress signaling and osmoadaptation in yeasts | Q29617597 | ||
A yeast gene that is essential for release from glucose repression encodes a protein kinase | Q29620532 | ||
Signaling and circuitry of multiple MAPK pathways revealed by a matrix of global gene expression profiles | Q29620701 | ||
N-acetylglucosamine-inducible CaGAP1 encodes a general amino acid permease which co-ordinates external nitrogen source response and morphogenesis in Candida albicans | Q33188344 | ||
The Warburg effect suppresses oxidative stress induced apoptosis in a yeast model for cancer | Q33412131 | ||
An extensive circuitry for cell wall regulation in Candida albicans | Q33530089 | ||
Dimorphism and virulence in Candida albicans | Q33538707 | ||
Glucose repression in yeast | Q33632468 | ||
Roles of the Candida albicans mitogen-activated protein kinase homolog, Cek1p, in hyphal development and systemic candidiasis | Q33754752 | ||
Snf1 protein kinase regulates phosphorylation of the Mig1 repressor in Saccharomyces cerevisiae | Q33781305 | ||
XBP1 promotes triple-negative breast cancer by controlling the HIF1α pathway | Q33926690 | ||
Isogenic strain construction and gene mapping in Candida albicans. | Q33961115 | ||
Synergistic release from glucose repression by mig1 and ssn mutations in Saccharomyces cerevisiae | Q33962945 | ||
Structure and function of enzymes of the Leloir pathway for galactose metabolism | Q33967795 | ||
Genome-wide survey of yeast mutations leading to activation of the yeast cell integrity MAPK pathway: novel insights into diverse MAPK outcomes. | Q33978987 | ||
Signal transduction cascades regulating fungal development and virulence. | Q34010291 | ||
Pheromone response, mating and cell biology | Q34106610 | ||
Pyruvate kinase triggers a metabolic feedback loop that controls redox metabolism in respiring cells | Q34215123 | ||
Intracellular signaling from the endoplasmic reticulum to the nucleus: the unfolded protein response in yeast and mammals | Q34245400 | ||
Regulation of G protein-initiated signal transduction in yeast: paradigms and principles | Q34275492 | ||
Transcriptional control of the GAL/MEL regulon of yeast Saccharomyces cerevisiae: mechanism of galactose-mediated signal transduction | Q34278972 | ||
Cell cycle control of yeast filamentous growth. | Q34455368 | ||
Activation of the Saccharomyces cerevisiae filamentation/invasion pathway by osmotic stress in high-osmolarity glycogen pathway mutants | Q34608075 | ||
The unfolded protein response coordinates the production of endoplasmic reticulum protein and endoplasmic reticulum membrane | Q34673029 | ||
The Hog1 mitogen-activated protein kinase mediates a hypoxic response in Saccharomyces cerevisiae | Q35065482 | ||
Regulation of cell wall biogenesis in Saccharomyces cerevisiae: the cell wall integrity signaling pathway | Q35620450 | ||
Unique and Redundant Roles for HOG MAPK Pathway Components as Revealed by Whole-Genome Expression Analysis | Q35796834 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P4510 | describes a project that uses | ImageJ | Q1659584 |
edgeR | Q113334690 | ||
P433 | issue | 10 | |
P304 | page(s) | e1004734 | |
P577 | publication date | 2014-10-30 | |
P1433 | published in | PLOS Genetics | Q1893441 |
P1476 | title | Metabolic respiration induces AMPK- and Ire1p-dependent activation of the p38-Type HOG MAPK pathway | |
P478 | volume | 10 |
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