| P2093 | author name string | Rahim Mehrabi | |
| | Xinhua Zhao | |
| | Jin-Rong Xu | |
| P2860 | cites work | The genome sequence of the rice blast fungus Magnaporthe grisea | Q22122482 |
| | MAP kinase pathways in the yeast Saccharomyces cerevisiae | Q24548569 |
| | Novel G-protein-coupled receptor-like proteins in the plant pathogenic fungus Magnaporthe grisea | Q24797300 |
| | Regulation of mating and filamentation genes by two distinct Ste12 complexes in Saccharomyces cerevisiae | Q27932174 |
| | The MAPK Hog1p modulates Fps1p-dependent arsenite uptake and tolerance in yeast. | Q27933186 |
| | A third osmosensing branch in Saccharomyces cerevisiae requires the Msb2 protein and functions in parallel with the Sho1 branch | Q27934962 |
| | The Ste5 scaffold allosterically modulates signaling output of the yeast mating pathway. | Q27935451 |
| | Regulation of the yeast Rlm1 transcription factor by the Mpk1 cell wall integrity MAP kinase. | Q27936197 |
| | Protein kinase A operates a molecular switch that governs yeast pseudohyphal differentiation | Q27937159 |
| | Cryptococcus neoformans STE12alpha regulates virulence but is not essential for mating | Q27939881 |
| | Osmotic stress signaling and osmoadaptation in yeasts | Q29617597 |
| | Nonfilamentous C. albicans mutants are avirulent | Q29617839 |
| | Aspergillus nidulans HOG pathway is activated only by two-component signalling pathway in response to osmotic stress | Q30160244 |
| | The ubc2 gene of Ustilago maydis encodes a putative novel adaptor protein required for filamentous growth, pheromone response and virulence | Q30167897 |
| | An ste20 homologue in Ustilago maydis plays a role in mating and pathogenicity. | Q31044238 |
| | Two novel fungal virulence genes specifically expressed in appressoria of the rice blast fungus | Q31108370 |
| | The induction of sexual development and virulence in the smut fungus Ustilago maydis depends on Crk1, a novel MAPK protein | Q33209925 |
| | MgSlt2, a cellular integrity MAP kinase gene of the fungal wheat pathogen Mycosphaerella graminicola, is dispensable for penetration but essential for invasive growth | Q33239732 |
| | Mutations in VMK1, a mitogen-activated protein kinase gene, affect microsclerotia formation and pathogenicity in Verticillium dahliae | Q61464897 |
| | The role of the sakA (Hog1) and tcsB (sln1) genes in the oxidant adaptation of Aspergillus fumigatus | Q61497775 |
| | Targeting antioxidative signal transduction and stress response system: control of pathogenic Aspergillus with phenolics that inhibit mitochondrial function | Q61497784 |
| | A MAP kinase cascade composed of cell type specific and non-specific elements controls mating and differentiation of the fungal pathogen Cryptococcus neoformans | Q62629892 |
| | Osmotic stress-coupled maintenance of polar growth in Aspergillus nidulans | Q62656933 |
| | Magnaporthe grisea pth11p is a novel plasma membrane protein that mediates appressorium differentiation in response to inductive substrate cues | Q73083355 |
| | A role for the MAP kinase gene MKC1 in cell wall construction and morphological transitions in Candida albicans | Q74285641 |
| | CPMK2, an SLT2-homologous mitogen-activated protein (MAP) kinase, is essential for pathogenesis of Claviceps purpurea on rye: evidence for a second conserved pathogenesis-related MAP kinase cascade in phytopathogenic fungi | Q78445893 |
| | Functional studies of the Ssk1p response regulator protein of Candida albicans as determined by phenotypic analysis of receiver domain point mutants | Q79233052 |
| | Hog1p mitogen-activated protein kinase determines acetic acid resistance in Saccharomyces cerevisiae | Q79420008 |
| | The Mep2p ammonium permease controls nitrogen starvation-induced filamentous growth in Candida albicans | Q81631164 |
| | Characterization and complementation of a Fus3/Kss1 type MAPK from Tuber borchii, TBMK | Q83357990 |
| | G-protein beta subunit of Cochliobolus heterostrophus involved in virulence, asexual and sexual reproductive ability, and morphogenesis | Q33559760 |
| | Cellular localization and role of kinase activity of PMK1 in Magnaporthe grisea | Q33559766 |
| | Specialization of the HOG pathway and its impact on differentiation and virulence of Cryptococcus neoformans | Q33768483 |
| | Properties of various Rho1 mutant alleles of Cryptococcus neoformans | Q33791723 |
| | Induction of the Candida albicans filamentous growth program by relief of transcriptional repression: a genome-wide analysis | Q33841447 |
| | A CDC42 homologue in Claviceps purpurea is involved in vegetative differentiation and is essential for pathogenicity | Q33884517 |
| | Mating-type-specific and nonspecific PAK kinases play shared and divergent roles in Cryptococcus neoformans | Q33905126 |
| | A contact-activated kinase signals Candida albicans invasive growth and biofilm development | Q33936541 |
| | Conserved cAMP signaling cascades regulate fungal development and virulence | Q33946381 |
| | Identification and characterization of an SKN7 homologue in Cryptococcus neoformans | Q33946817 |
| | Signal transduction cascades regulating fungal development and virulence. | Q34010291 |
| | White-opaque switching in Candida albicans is controlled by mating-type locus homeodomain proteins and allows efficient mating | Q34144354 |
| | Map kinases in fungal pathogens | Q34198348 |
| | G protein-coupled receptor Gpr4 senses amino acids and activates the cAMP-PKA pathway in Cryptococcus neoformans | Q34325690 |
| | Mating in Candida albicans and the search for a sexual cycle | Q34420674 |
| | A mitogen-activated protein kinase pathway essential for mating and contributing to vegetative growth in Neurospora crassa | Q34576493 |
| | The isolation and characterization of nrc-1 and nrc-2, two genes encoding protein kinases that control growth and development in Neurospora crassa | Q34604356 |
| | The STE12alpha homolog is required for haploid filamentation but largely dispensable for mating and virulence in Cryptococcus neoformans | Q34608349 |
| | TUP1, CPH1 and EFG1 make independent contributions to filamentation in candida albicans | Q34609405 |
| | An STE12 homolog from the asexual, dimorphic fungus Penicillium marneffei complements the defect in sexual development of an Aspergillus nidulans steA mutant. | Q34612036 |
| | A unique fungal two-component system regulates stress responses, drug sensitivity, sexual development, and virulence of Cryptococcus neoformans | Q34698188 |
| | A mitotically inheritable unit containing a MAP kinase module | Q35037293 |
| | Of smuts, blasts, mildews, and blights: cAMP signaling in phytopathogenic fungi | Q35090242 |
| | The Cryptococcus neoformans MAP kinase Mpk1 regulates cell integrity in response to antifungal drugs and loss of calcineurin function | Q35128586 |
| | Cryptococcus neoformans mating and virulence are regulated by the G-protein alpha subunit GPA1 and cAMP. | Q35197981 |
| | Novel mitogen-activated protein kinase MpkC of Aspergillus fumigatus is required for utilization of polyalcohol sugars | Q35216706 |
| | Reduced virulence of Candida albicans MKC1 mutants: a role for mitogen-activated protein kinase in pathogenesis | Q35567860 |
| | Rgs1 regulates multiple Galpha subunits in Magnaporthe pathogenesis, asexual growth and thigmotropism. | Q35629671 |
| | Ste12 transcription factor homologue CpST12 is down-regulated by hypovirus infection and required for virulence and female fertility of the chestnut blight fungus Cryphonectria parasitica | Q35636479 |
| | Melanin biosynthesis in the maize pathogen Cochliobolus heterostrophus depends on two mitogen-activated protein kinases, Chk1 and Mps1, and the transcription factor Cmr1. | Q35690231 |
| | Importance of a developmentally regulated pheromone receptor of Cryptococcus neoformans for virulence | Q35802299 |
| | The response regulator RRG-1 functions upstream of a mitogen-activated protein kinase pathway impacting asexual development, female fertility, osmotic stress, and fungicide resistance in Neurospora crassa | Q35810689 |
| | A walk-through of the yeast mating pheromone response pathway | Q35890686 |
| | Principles of MAP kinase signaling specificity in Saccharomyces cerevisiae. | Q35965868 |
| | Farnesol, a morphogenetic autoregulatory substance in the dimorphic fungus Candida albicans, inhibits hyphae growth through suppression of a mitogen-activated protein kinase cascade | Q44888389 |
| | The Fus3/Kss1 MAP kinase homolog Amk1 regulates the expression of genes encoding hydrolytic enzymes in Alternaria brassicicola | Q44926868 |
| | Fungicide activity through activation of a fungal signalling pathway. | Q45040135 |
| | The G‐beta subunit MGB1 is involved in regulating multiple steps of infection‐related morphogenesis in Magnaporthe grisea | Q45103449 |
| | The Gpmk1 MAP kinase of Fusarium graminearum regulates the induction of specific secreted enzymes | Q45153906 |
| | Fusarium oxysporum G-protein beta subunit Fgb1 regulates hyphal growth, development, and virulence through multiple signalling pathways | Q45180761 |
| | A two-component histidine kinase of the rice blast fungus is involved in osmotic stress response and fungicide action | Q45262658 |
| | A secreted lipase of Fusarium graminearum is a virulence factor required for infection of cereals | Q46447327 |
| | The MAP kinase Mkc1p is activated under different stress conditions in Candida albicans. | Q46633733 |
| | Cell signaling pathways in Paracoccidioides brasiliensis--inferred from comparisons with other fungi | Q46658803 |
| | The importance of the phagocytes' innate response in resolution of the infection induced by a low virulent Candida albicans mutant. | Q46716413 |
| | A downshift in temperature activates the high osmolarity glycerol (HOG) pathway, which determines freeze tolerance in Saccharomyces cerevisiae | Q46863312 |
| | Calcineurin, Mpk1 and Hog1 MAPK pathways independently control fludioxonil antifungal sensitivity in Cryptococcus neoformans | Q46973362 |
| | Expression analysis of PCSTE3, a putative pheromone receptor from the lung pathogenic fungus Pneumocystis carinii | Q47441016 |
| | Two PAK kinase genes, CHM1 and MST20, have distinct functions in Magnaporthe grisea | Q47608558 |
| | MAPK regulation of sclerotial development in Sclerotinia sclerotiorum is linked with pH and cAMP sensing | Q47783969 |
| | The BMP1 gene is essential for pathogenicity in the gray mold fungus Botrytis cinerea | Q47848950 |
| | RAS1 regulates filamentation, mating and growth at high temperature of Cryptococcus neoformans | Q47863650 |
| | Aspergillus SteA (sterile12-like) is a homeodomain-C2/H2-Zn+2 finger transcription factor required for sexual reproduction | Q47863679 |
| | A mitogen-activated protein kinase (MPKA) is involved in polarized growth in the filamentous fungus, Aspergillus nidulans | Q47968910 |
| | G protein alpha subunit genes control growth, development, and pathogenicity of Magnaporthe grisea | Q48042118 |
| | Complementation of Ustilago maydis MAPK mutants by a wheat leaf rust, Puccinia triticina homolog: potential for functional analyses of rust genes | Q48078969 |
| | A highly conserved MAPK-docking site in Mst7 is essential for Pmk1 activation in Magnaporthe grisea | Q48082375 |
| | MgHog1 regulates dimorphism and pathogenicity in the fungal wheat pathogen Mycosphaerella graminicola. | Q48083770 |
| | Multiple upstream signals converge on the adaptor protein Mst50 in Magnaporthe grisea | Q48083934 |
| | Disruption of SRM1, a mitogen-activated protein kinase gene, affects sensitivity to osmotic and ultraviolet stressors in the phytopathogenic fungus Bipolaris oryzae | Q48095350 |
| | A MAP kinase gene, BMK1, is required for conidiation and pathogenicity in the rice leaf spot pathogen Bipolaris oryzae | Q48095866 |
| | Characterization of the ERK homologue CpMK2 from the chestnut blight fungus Cryphonectria parasitica | Q48139567 |
| | A mitogen-activated protein kinase cascade regulating infection-related morphogenesis in Magnaporthe grisea | Q48148021 |
| | Pneumocystis carinii BCK1 functions in a mitogen-activated protein kinase cascade regulating fungal cell-wall assembly | Q48235120 |
| | The Colletotrichum lagenarium Ste12-Like Gene CST1 Is Essential for Appressorium Penetration | Q48246930 |
| | The MAPKK kinase SteC regulates conidiophore morphology and is essential for heterokaryon formation and sexual development in the homothallic fungus Aspergillus nidulans | Q48256556 |
| | A conserved mitogen-activated protein kinase pathway is required for mating in Candida albicans | Q48272020 |
| | SakA MAP kinase is involved in stress signal transduction, sexual development and spore viability in Aspergillus nidulans. | Q48287453 |
| | The biotrophic, non-appressorium-forming grass pathogen Claviceps purpurea needs a Fus3/Pmk1 homologous mitogen-activated protein kinase for colonization of rye ovarian tissue | Q48303186 |
| | The Cryptococcus neoformans STE11alpha gene is similar to other fungal mitogen-activated protein kinase kinase kinase (MAPKKK) genes but is mating type specific | Q48370584 |
| | PTK1, a mitogen-activated-protein kinase gene, is required for conidiation, appressorium formation, and pathogenicity of Pyrenophora teres on barley | Q48379833 |
| | The Pbs2 MAP kinase kinase is essential for the oxidative-stress response in the fungal pathogen Candida albicans. | Q50772221 |
| | Characterization of HOG1 homologue, CpMK1, from Cryphonectria parasitica and evidence for hypovirus-mediated perturbation of its phosphorylation in response to hypertonic stress. | Q51020923 |
| | A class III histidine kinase acts as a novel virulence factor in Botrytis cinerea. | Q51139198 |
| | MAP kinase and cAMP signaling pathways modulate the pH-induced yeast-to-mycelium dimorphic transition in the corn smut fungus Ustilago maydis. | Q51611150 |
| | A screen in Saccharomyces cerevisiae identified CaMCM1, an essential gene in Candida albicans crucial for morphogenesis. | Q52109258 |
| | The Mak2 MAP kinase signal transduction pathway is required for pathogenicity in Stagonospora nodorum. | Q52565253 |
| | Roles of putative His-to-Asp signaling modules HPT-1 and RRG-2, on viability and sensitivity to osmotic and oxidative stresses in Neurospora crassa. | Q52576114 |
| | Independent genetic mechanisms mediate turgor generation and penetration peg formation during plant infection in the rice blast fungus. | Q53635213 |
| | The isolation of FOS-1, a gene encoding a putative two-component histidine kinase from Aspergillus fumigatus. | Q54026697 |
| | Saccharomyces cerevisiae Hog1 protein phosphorylation upon exposure to bacterial endotoxin. | Q54462882 |
| | Identification of OS-2 MAP kinase-dependent genes induced in response to osmotic stress, antifungal agent fludioxonil, and heat shock in Neurospora crassa. | Q54579960 |
| | Distinct signalling pathways coordinately contribute to virulence of Fusarium oxysporum on mammalian hosts | Q56970921 |
| | Independent Signaling Pathways Regulate Cellular Turgor during Hyperosmotic Stress and Appressorium-Mediated Plant Infection by Magnaporthe grisea | Q57362543 |
| | Regulation of the osmoregulatory HOG MAPK cascade in yeast | Q35983907 |
| | Baker's yeast as a tool for the development of antifungal kinase inhibitors--targeting protein kinase C and the cell integrity pathway | Q36282514 |
| | Candida albicans response regulator gene SSK1 regulates a subset of genes whose functions are associated with cell wall biosynthesis and adaptation to oxidative stress | Q36370450 |
| | Two-component signal transduction in human fungal pathogens | Q36399917 |
| | The MAP kinase signal transduction network in Candida albicans. | Q36426498 |
| | Inactivation of the mitogen-activated protein kinase Mps1 from the rice blast fungus prevents penetration of host cells but allows activation of plant defense responses | Q36531836 |
| | A mitogen-activated protein kinase of the corn leaf pathogen Cochliobolus heterostrophus is involved in conidiation, appressorium formation, and pathogenicity: diverse roles for mitogen-activated protein kinase homologs in foliar pathogens. | Q36680610 |
| | Role of a mitogen-activated protein kinase pathway during conidial germination and hyphal fusion in Neurospora crassa | Q37421767 |
| | A mitogen-activated protein kinase that senses nitrogen regulates conidial germination and growth in Aspergillus fumigatus | Q37422080 |
| | Ustilago maydis, model system for analysis of the molecular basis of fungal pathogenicity | Q37766639 |
| | DNA array studies demonstrate convergent regulation of virulence factors by Cph1, Cph2, and Efg1 in Candida albicans | Q38295895 |
| | The G-protein beta subunit GPB1 is required for mating and haploid fruiting in Cryptococcus neoformans | Q39450229 |
| | Discovery of cercosporamide, a known antifungal natural product, as a selective Pkc1 kinase inhibitor through high-throughput screening | Q39601355 |
| | Osmoregulation and fungicide resistance: the Neurospora crassa os-2 gene encodes a HOG1 mitogen-activated protein kinase homologue | Q39649957 |
| | ras2 Controls morphogenesis, pheromone response, and pathogenicity in the fungal pathogen Ustilago maydis | Q39692275 |
| | The Hog1 mitogen-activated protein kinase is essential in the oxidative stress response and chlamydospore formation in Candida albicans. | Q39751926 |
| | An unusual MAP kinase is required for efficient penetration of the plant surface by Ustilago maydis | Q39756383 |
| | Guanyl nucleotide exchange factor Sql2 and Ras2 regulate filamentous growth in Ustilago maydis | Q39774488 |
| | The Sho1 adaptor protein links oxidative stress to morphogenesis and cell wall biosynthesis in the fungal pathogen Candida albicans. | Q39890876 |
| | The Fusarium graminearum MAP1 gene is essential for pathogenicity and development of perithecia | Q39938707 |
| | Functional characterization of the MKC1 gene of Candida albicans, which encodes a mitogen-activated protein kinase homolog related to cell integrity | Q40016068 |
| | PKA and MAPK phosphorylation of Prf1 allows promoter discrimination in Ustilago maydis | Q40240145 |
| | Cell wall integrity is dependent on the PKC1 signal transduction pathway in Cryptococcus neoformans. | Q40384960 |
| | Mating and pathogenic development of the Smut fungus Ustilago maydis are regulated by one mitogen-activated protein kinase cascade. | Q40495202 |
| | Fusarium oxysporum as a multihost model for the genetic dissection of fungal virulence in plants and mammals | Q40634702 |
| | Attenuation of the activity of caspofungin at high concentrations against candida albicans: possible role of cell wall integrity and calcineurin pathways. | Q40668367 |
| | The Gbeta-subunit-encoding gene bpp1 controls cyclic-AMP signaling in Ustilago maydis | Q40902857 |
| | The high-mobility-group domain transcription factor Rop1 is a direct regulator of prf1 in Ustilago maydis | Q41095867 |
| | 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 |
| | BcSAK1, a stress-activated mitogen-activated protein kinase, is involved in vegetative differentiation and pathogenicity in Botrytis cinerea | Q42180526 |
| | A mitogen-activated protein kinase pathway modulates the expression of two cellulase genes in Cochliobolus heterostrophus during plant infection. | Q42439156 |
| | Two mitogen-activated protein kinase signalling cascades mediate basal resistance to antifungal plant defensins in Fusarium graminearum. | Q42507405 |
| | Ras1 and Ras2 contribute shared and unique roles in physiology and virulence of Cryptococcus neoformans | Q42667297 |
| | The Slt2-type MAP kinase Bmp3 of Botrytis cinerea is required for normal saprotrophic growth, conidiation, plant surface sensing and host tissue colonization | Q43052612 |
| | The MAP kinase-encoding gene MgFus3 of the non-appressorium phytopathogen Mycosphaerella graminicola is required for penetration and in vitro pycnidia formation. | Q43052644 |
| | Different signalling pathways involving a Galpha protein, cAMP and a MAP kinase control germination of Botrytis cinerea conidia. | Q43433523 |
| | A MAP kinase of the vascular wilt fungus Fusarium oxysporum is essential for root penetration and pathogenesis | Q43544096 |
| | Ras links cellular morphogenesis to virulence by regulation of the MAP kinase and cAMP signalling pathways in the pathogenic fungus Candida albicans | Q43808791 |
| | Mitogen-activated protein kinase Mkp1 of Pneumocystis carinii complements the slt2Delta defect in the cell integrity pathway of Saccharomyces cerevisiae | Q43880922 |
| | The mitogen-activated protein kinase gene MAF1 is essential for the early differentiation phase of appressorium formation in Colletotrichum lagenarium | Q44021360 |
| | A mitogen-activated protein kinase gene (MGV1) in Fusarium graminearum is required for female fertility, heterokaryon formation, and plant infection. | Q44210004 |
| | Mating, conidiation and pathogenicity of Fusarium graminearum, the main causal agent of the head-blight disease of wheat, are regulated by the MAP kinase gpmk1. | Q44403848 |
| | Evidence that the appressorial development in barley powdery mildew is controlled by MAP kinase activity in conjunction with the cAMP pathway | Q44437596 |
| | The sphingolipid pathway regulates Pkc1 through the formation of diacylglycerol in Cryptococcus neoformans | Q44795443 |
| | Lipid-induced filamentous growth in Ustilago maydis | Q44854375 |
| P433 | issue | 10 | |
| P304 | page(s) | 1701-1714 | |
| P577 | publication date | 2007-08-22 | |
| P1433 | published in | Eukaryotic Cell | Q5408685 |
| P1476 | title | Mitogen-activated protein kinase pathways and fungal pathogenesis | |
| P478 | volume | 6 | |