| P50 | author | Rudolf Krska | Q56860594 |
| | Joseph Strauss | Q41081227 |
| | Michael Sulyok | Q41081251 |
| P2093 | author name string | Gerlinde Wiesenberger | |
| | Norbert Stoppacher | |
| | Yazmid Reyes-Dominguez | |
| | Stefan Boedi | |
| P2860 | cites work | The Heterochromatin Protein 1 family | Q21999710 |
| | Functional mammalian homologues of the Drosophila PEV-modifier Su(var)3-9 encode centromere-associated proteins which complex with the heterochromatin component M31 | Q22009388 |
| | Central role of Drosophila SU(VAR)3-9 in histone H3-K9 methylation and heterochromatic gene silencing | Q24536235 |
| | FGDB: a comprehensive fungal genome resource on the plant pathogen Fusarium graminearum | Q24538334 |
| | Heterochromatin protein 1 is required for the normal expression of two heterochromatin genes in Drosophila | Q24548119 |
| | The chromo shadow domain, a second chromo domain in heterochromatin-binding protein 1, HP1 | Q24623947 |
| | LaeA, a regulator of secondary metabolism in Aspergillus spp | Q24624239 |
| | Trichothecene biosynthesis in Fusarium species: chemistry, genetics, and significance | Q24634648 |
| | Structure of the HP1 chromodomain bound to histone H3 methylated at lysine 9 | Q27638208 |
| | Methylation of histone H3 lysine 9 creates a binding site for HP1 proteins | Q27860456 |
| | Heterochromatic marks are associated with the repression of secondary metabolism clusters in Aspergillus nidulans | Q27976503 |
| | Reduced virulence of Gibberella zeae caused by disruption of a trichothecene toxin biosynthetic gene | Q28611293 |
| | Does heterochromatin protein 1 always follow code? | Q30452367 |
| | Toxicology of mycotoxins | Q33548405 |
| | Putative polyketide synthase and laccase genes for biosynthesis of aurofusarin in Gibberella zeae | Q33754522 |
| | Genomics-driven discovery of PKS-NRPS hybrid metabolites from Aspergillus nidulans | Q42615072 |
| | Novel genes of Fusarium graminearum that negatively regulate deoxynivalenol production and virulence | Q43248737 |
| | Simultaneous determination of 186 fungal and bacterial metabolites in indoor matrices by liquid chromatography/tandem mass spectrometry | Q43294472 |
| | The trichothecene biosynthesis gene cluster of Fusarium graminearum F15 contains a limited number of essential pathway genes and expressed non-essential genes | Q44371544 |
| | Trimethylated lysine 9 of histone H3 is a mark for DNA methylation in Neurospora crassa | Q44393142 |
| | HP1 is essential for DNA methylation in neurospora | Q44766530 |
| | HP1 controls telomere capping, telomere elongation, and telomere silencing by two different mechanisms in Drosophila. | Q45013592 |
| | Identification of a gene cluster responsible for the biosynthesis of aurofusarin in the Fusarium graminearum species complex | Q46420973 |
| | VelB/VeA/LaeA complex coordinates light signal with fungal development and secondary metabolism | Q46537897 |
| | The ability to detoxify the mycotoxin deoxynivalenol colocalizes with a major quantitative trait locus for Fusarium head blight resistance in wheat. | Q46944161 |
| | The biosynthetic pathway for aurofusarin in Fusarium graminearum reveals a close link between the naphthoquinones and naphthopyrones. | Q51723456 |
| | Regulating genes by packaging domains: bits of heterochromatin in euchromatin? | Q52545879 |
| | Role of Drosophila HP1 in euchromatic gene expression. | Q52655216 |
| | Transformation of Trichoderma reesei based on hygromycin B resistance using homologous expression signals. | Q54203124 |
| | Mutations in the fission yeast silencing factors clr4+ and rik1+ disrupt the localisation of the chromo domain protein Swi6p and impair centromere function | Q71821145 |
| | Characterization of a transcriptional activator controlling trichothecene toxin biosynthesis | Q77850187 |
| | Identification of DIM-7, a protein required to target the DIM-5 H3 methyltransferase to chromatin | Q33929209 |
| | Spotlights on advances in mycotoxin research | Q34109176 |
| | Epigenetic codes for heterochromatin formation and silencing: rounding up the usual suspects | Q34120020 |
| | Functional analysis of the polyketide synthase genes in the filamentous fungus Gibberella zeae (anamorph Fusarium graminearum). | Q34143998 |
| | FfVel1 and FfLae1, components of a velvet-like complex in Fusarium fujikuroi, affect differentiation, secondary metabolism and virulence | Q34341591 |
| | Fungal secondary metabolism - from biochemistry to genomics | Q34472162 |
| | Heterochromatin: new possibilities for the inheritance of structure | Q34563268 |
| | A genetic map of Gibberella zeae (Fusarium graminearum). | Q34614832 |
| | Molecular biology of Fusarium mycotoxins | Q34664585 |
| | The Fusarium graminearum genome reveals a link between localized polymorphism and pathogen specialization | Q34682180 |
| | Tri1 encodes the cytochrome P450 monooxygenase for C-8 hydroxylation during trichothecene biosynthesis in Fusarium sporotrichioides and resides upstream of another new Tri gene | Q34767838 |
| | Tri6 encodes an unusual zinc finger protein involved in regulation of trichothecene biosynthesis in Fusarium sporotrichioides | Q35184264 |
| | Heterochromatin: silence is golden. | Q35599696 |
| | HP1 and the dynamics of heterochromatin maintenance | Q35741016 |
| | Epigenetic regulation by histone methylation and histone variants | Q36022792 |
| | Regulation of secondary metabolism in filamentous fungi | Q36217879 |
| | Heterochromatin protein 1: don't judge the book by its cover! | Q36406941 |
| | Direct interaction between DNA methyltransferase DIM-2 and HP1 is required for DNA methylation in Neurospora crassa | Q36899000 |
| | Molecular and genetic studies of fusarium trichothecene biosynthesis: pathways, genes, and evolution | Q36935157 |
| | Epigenetic regulation of centromeric chromatin: old dogs, new tricks? | Q36981211 |
| | The heterochromatin protein 1 (HP1) family: put away a bias toward HP1. | Q37229600 |
| | Intimate bacterial-fungal interaction triggers biosynthesis of archetypal polyketides in Aspergillus nidulans | Q37321247 |
| | Revisiting the role of heterochromatin protein 1 in DNA repair | Q37487276 |
| | Mobilization and recruitment of HP1: a bimodal response to DNA breakage. | Q37573325 |
| | Metabolic pathways of trichothecenes. | Q37579236 |
| | DNA methylation and the formation of heterochromatin in Neurospora crassa | Q37734874 |
| | The changing faces of HP1: From heterochromatin formation and gene silencing to euchromatic gene expression: HP1 acts as a positive regulator of transcription | Q37832719 |
| | Elements of chromosome structure and function in fission yeast. | Q40406157 |
| | Conserved properties of HP1(Hsalpha). | Q40540453 |
| | The heterochromatin protein 1 prevents telomere fusions in Drosophila | Q40989792 |
| | Chromatin-level regulation of biosynthetic gene clusters | Q41371805 |
| | Heterochromatin is required for normal distribution of Neurospora crassa CenH3. | Q41763284 |
| | Heterochromatin protein 1 (HP1a) positively regulates euchromatic gene expression through RNA transcript association and interaction with hnRNPs in Drosophila | Q41951844 |
| | Nuclear export of the transcription factor NirA is a regulatory checkpoint for nitrate induction in Aspergillus nidulans | Q42060064 |
| P433 | issue | 1 | |
| P921 | main subject | secondary metabolite | Q522244 |
| | Fusarium graminearum | Q103806070 |
| P304 | page(s) | 39-47 | |
| P577 | publication date | 2011-11-11 | |
| P1433 | published in | Fungal Genetics and Biology | Q5509162 |
| P1476 | title | Heterochromatin influences the secondary metabolite profile in the plant pathogen Fusarium graminearum | |
| P478 | volume | 49 | |