Publications in OpenAlex of which a co-author is affiliated to this organization
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| Title | DOI |
|---|---|
| https://doi.org/10.1371/journal.pone.0112963 | Pilon: An Integrated Tool for Comprehensive Microbial Variant Detection and Genome Assembly Improvement |
| https://doi.org/10.1038/nature11119 | The tomato genome sequence provides insights into fleshy fruit evolution |
| https://doi.org/10.1038/cdd.2008.150 | Classification of cell death: recommendations of the Nomenclature Committee on Cell Death 2009 |
| https://doi.org/10.1128/mmbr.62.3.775-806.1998 | Bacillus thuringiensis and Its Pesticidal Crystal Proteins |
| https://doi.org/10.1038/nprot.2007.324 | Integration of biological networks and gene expression data using Cytoscape |
| https://doi.org/10.1038/cdd.2011.96 | Molecular definitions of cell death subroutines: recommendations of the Nomenclature Committee on Cell Death 2012 |
| https://doi.org/10.1016/j.tplants.2011.03.007 | ROS signaling: the new wave? |
| https://doi.org/10.1093/nar/gkab1113 | JASPAR 2022: the 9th release of the open-access database of transcription factor binding profiles |
| https://doi.org/10.1038/s41580-022-00499-2 | Reactive oxygen species signalling in plant stress responses |
| https://doi.org/10.1038/nature07410 | The Phaeodactylum genome reveals the evolutionary history of diatom genomes |
| https://doi.org/10.1093/nar/gkx1126 | JASPAR 2018: update of the open-access database of transcription factor binding profiles and its web framework |
| https://doi.org/10.1038/nature12211 | The Norway spruce genome sequence and conifer genome evolution |
| https://doi.org/10.1016/j.cell.2009.03.001 | Auxin: A Trigger for Change in Plant Development |
| https://doi.org/10.1038/nature10625 | The Medicago genome provides insight into the evolution of rhizobial symbioses |
| https://doi.org/10.1038/nbt1282 | Genome sequencing and analysis of the versatile cell factory Aspergillus niger CBS 513.88 |
| https://doi.org/10.1105/tpc.110.080788 | TheArabidopsisbHLH Transcription Factors MYC3 and MYC4 Are Targets of JAZ Repressors and Act Additively with MYC2 in the Activation of Jasmonate Responses |
| https://doi.org/10.1038/nrg2600 | The evolutionary significance of ancient genome duplications |
| https://doi.org/10.1038/nature10640 | The genome of Tetranychus urticae reveals herbivorous pest adaptations |
| https://doi.org/10.1371/journal.pone.0001326 | A High Quality Draft Consensus Sequence of the Genome of a Heterozygous Grapevine Variety |
| https://doi.org/10.1128/mmbr.62.3.807-813.1998 | Revision of the Nomenclature for the Bacillus thuringiensis Pesticidal Crystal Proteins |
| https://doi.org/10.1038/s41396-018-0093-1 | Disease-induced assemblage of a plant-beneficial bacterial consortium |
| https://doi.org/10.1016/j.copbio.2019.02.019 | Lignin structure and its engineering |
| https://doi.org/10.1038/nature09016 | The Ectocarpus genome and the independent evolution of multicellularity in brown algae |
| https://doi.org/10.1038/ng.807 | The Arabidopsis lyrata genome sequence and the basis of rapid genome size change |
| https://doi.org/10.1038/328033a0 | Transgenic plants protected from insect attack |
| https://doi.org/10.1039/c5ee00204d | Reductive lignocellulose fractionation into soluble lignin-derived phenolic monomers and dimers and processable carbohydrate pulps |
| https://doi.org/10.1038/347737a0 | Induction of male sterility in plants by a chimaeric ribonuclease gene |
| https://doi.org/10.1016/j.tplants.2018.01.003 | The Pivotal Role of Ethylene in Plant Growth |
| https://doi.org/10.1002/j.1460-2075.1987.tb02537.x | Engineering herbicide resistance in plants by expression of a detoxifying enzyme |
| https://doi.org/10.1038/ncb1754 | The auxin influx carrier LAX3 promotes lateral root emergence |
| https://doi.org/10.1016/j.gde.2015.11.003 | Polyploidy and genome evolution in plants |
| https://doi.org/10.1016/j.copbio.2019.02.018 | Lignin biosynthesis and its integration into metabolism |
| https://doi.org/10.1073/pnas.1019315108 | Obligate biotrophy features unraveled by the genomic analysis of rust fungi |
| https://doi.org/10.1093/gigascience/giw015 | Estimating the total number of phosphoproteins and phosphorylation sites in eukaryotic proteomes |
| https://doi.org/10.1038/nature10791 | A novel sensor to map auxin response and distribution at high spatio-temporal resolution |
| https://doi.org/10.1126/science.aau6389 | A specialized metabolic network selectively modulates Arabidopsis root microbiota |
| https://doi.org/10.1016/j.cell.2016.08.020 | Domestication and Divergence of Saccharomyces cerevisiae Beer Yeasts |
| https://doi.org/10.1016/j.tplants.2008.12.003 | How relevant are flavonoids as antioxidants in plants? |
| https://doi.org/10.1016/j.tplants.2007.03.012 | Plant dormancy in the perennial context |
| https://doi.org/10.1093/plcell/koaa015 | Polyploidy: an evolutionary and ecological force in stressful times |
| https://doi.org/10.1105/tpc.111.089300 | The JAZ Proteins: A Crucial Interface in the Jasmonate Signaling Cascade |
| https://doi.org/10.1038/cdd.2009.44 | Guidelines for the use and interpretation of assays for monitoring cell death in higher eukaryotes |
| https://doi.org/10.1002/j.1460-2075.1987.tb02538.x | Characterization of the herbicide-resistance gene bar from Streptomyces hygroscopicus |
| https://doi.org/10.1146/annurev-genet-072610-155046 | Variable Tandem Repeats Accelerate Evolution of Coding and Regulatory Sequences |
| https://doi.org/10.1007/978-3-540-87481-2_21 | Robust Feature Selection Using Ensemble Feature Selection Techniques |
| https://doi.org/10.1242/dev.164376 | Reactive oxygen species in plant development |
| https://doi.org/10.1146/annurev-cellbio-101011-155741 | Hormonal Interactions in the Regulation of Plant Development |
| https://doi.org/10.1016/j.tplants.2013.04.006 | Lateral root development in Arabidopsis: fifty shades of auxin |
| https://doi.org/10.1038/cdd.2009.184 | Necroptosis, necrosis and secondary necrosis converge on similar cellular disintegration features |
| https://doi.org/10.1038/s41588-018-0040-0 | Genomes of 13 domesticated and wild rice relatives highlight genetic conservation, turnover and innovation across the genus Oryza |
| https://doi.org/10.1038/s41477-021-00897-y | Plant flavones enrich rhizosphere Oxalobacteraceae to improve maize performance under nitrogen deprivation |
| https://doi.org/10.1016/j.immuni.2019.08.017 | Stellate Cells, Hepatocytes, and Endothelial Cells Imprint the Kupffer Cell Identity on Monocytes Colonizing the Liver Macrophage Niche |
| https://doi.org/10.1038/nature16548 | The genome of the seagrass Zostera marina reveals angiosperm adaptation to the sea |
| https://doi.org/10.1016/j.cell.2018.02.024 | The Soil-Borne Legacy |
| https://doi.org/10.1038/ncomms5767 | Genome dynamics of the human embryonic kidney 293 lineage in response to cell biology manipulations |
| https://doi.org/10.1038/msb.2011.39 | The auxin signalling network translates dynamic input into robust patterning at the shoot apex |
| https://doi.org/10.1038/cdd.2011.36 | Morphological classification of plant cell deaths |
| https://doi.org/10.1038/nature08066 | Subcellular homeostasis of phytohormone auxin is mediated by the ER-localized PIN5 transporter |
| https://doi.org/10.1016/j.tplants.2012.02.003 | Leaf size control: complex coordination of cell division and expansion |
| https://doi.org/10.1016/j.tplants.2004.07.006 | Plant cell factories in the post-genomic era: new ways to produce designer secondary metabolites |
| https://doi.org/10.1038/nbt.1544 | Genome sequence of the recombinant protein production host Pichia pastoris |
| https://doi.org/10.1016/j.copbio.2010.03.002 | More from less: plant growth under limited water |
| https://doi.org/10.1016/j.cell.2018.06.033 | The Chara Genome: Secondary Complexity and Implications for Plant Terrestrialization |
| https://doi.org/10.1038/s41477-018-0188-8 | Fern genomes elucidate land plant evolution and cyanobacterial symbioses |
| https://doi.org/10.1038/nature12221 | Pan genome of the phytoplankton Emiliania underpins its global distribution |
| https://doi.org/10.1186/s40168-017-0241-2 | Structural variability and niche differentiation in the rhizosphere and endosphere bacterial microbiome of field-grown poplar trees |
| https://doi.org/10.1242/dev.057331 | Brassinosteroids control meristem size by promoting cell cycle progression in Arabidopsis roots |
| https://doi.org/10.1007/s00425-012-1696-9 | Reactive oxygen species and their role in plant defence and cell wall metabolism |
| https://doi.org/10.1016/j.cub.2010.09.007 | A Novel Aux/IAA28 Signaling Cascade Activates GATA23-Dependent Specification of Lateral Root Founder Cell Identity |
| https://doi.org/10.1016/j.tplants.2012.03.001 | Transcriptional machineries in jasmonate-elicited plant secondary metabolism |
| https://doi.org/10.1038/ncomms4606 | The seco-iridoid pathway from Catharanthus roseus |
| https://doi.org/10.1002/ana.22644 | KCNQ2 encephalopathy: Emerging phenotype of a neonatal epileptic encephalopathy |
| https://doi.org/10.1093/nar/gkx1002 | PLAZA 4.0: an integrative resource for functional, evolutionary and comparative plant genomics |
| https://doi.org/10.1016/j.tplants.2010.08.009 | The roots of a new green revolution |
| https://doi.org/10.1038/ng.3149 | The genome sequence of the orchid Phalaenopsis equestris |
| https://doi.org/10.1007/s00425-010-1310-y | Strigolactones affect lateral root formation and root-hair elongation in Arabidopsis |
| https://doi.org/10.1111/j.1365-313x.2012.04946.x | The SAUR19 subfamily of SMALL AUXIN UP RNA genes promote cell expansion |
| https://doi.org/10.1016/j.cell.2010.09.003 | Cell Surface- and Rho GTPase-Based Auxin Signaling Controls Cellular Interdigitation in Arabidopsis |
| https://doi.org/10.1104/pp.113.220921 | The Agony of Choice: How Plants Balance Growth and Survival under Water-Limiting Conditions |
| https://doi.org/10.1105/tpc.109.071316 | Perturbation of Indole-3-Butyric Acid Homeostasis by the UDP-GlucosyltransferaseUGT74E2ModulatesArabidopsisArchitecture and Water Stress Tolerance |
| https://doi.org/10.1111/nph.14586 | Identification of factors required for m 6 A mRNA methylation in Arabidopsis reveals a role for the conserved E3 ubiquitin ligase HAKAI |
| https://doi.org/10.1111/tpj.13801 | The Physcomitrella patens chromosome‐scale assembly reveals moss genome structure and evolution |
| https://doi.org/10.5167/uzh-44099 | Transgenerational adaptation of Arabidopsis to stress requires DNA methylation and the function of Dicer-like proteins |
| https://doi.org/10.1007/s00018-008-8465-8 | The role of the ZEB family of transcription factors in development and disease |
| https://doi.org/10.1016/j.phytochem.2011.12.022 | Oleanolic acid |
| https://doi.org/10.1038/s41586-019-1852-5 | The water lily genome and the early evolution of flowering plants |
| https://doi.org/10.1002/j.1460-2075.1989.tb08368.x | Apidaecins: antibacterial peptides from honeybees. |
| https://doi.org/10.1111/j.1365-3040.2005.01471.x | Induction of systemic resistance in tomato by N‐acyl‐L‐homoserine lactone‐producing rhizosphere bacteria |
| https://doi.org/10.1093/nar/gkx1188 | JASPAR 2018: update of the open-access database of transcription factor binding profiles and its web framework |
| https://doi.org/10.1038/ng.253 | Flowering-time genes modulate meristem determinacy and growth form in Arabidopsis thaliana |
| https://doi.org/10.1016/j.tibtech.2014.03.001 | Nanobody-based products as research and diagnostic tools |
| https://doi.org/10.1104/pp.91.2.694 | Transformation of Brassica napus and Brassica oleracea Using Agrobacterium tumefaciens and the Expression of the bar and neo Genes in the Transgenic Plants |
| https://doi.org/10.1093/jxb/erw080 | Spreading the news: subcellular and organellar reactive oxygen species production and signalling |
| https://doi.org/10.1038/nature10070 | A novel protein family mediates Casparian strip formation in the endodermis |
| https://doi.org/10.1093/aobpla/pls014 | Hydrogen peroxide—a central hub for information flow in plant cells |
| https://doi.org/10.1016/j.copbio.2018.01.014 | Nitrification in agricultural soils: impact, actors and mitigation |
| https://doi.org/10.1038/nature23897 | The Apostasia genome and the evolution of orchids |
| https://doi.org/10.1126/science.1194980 | Arabidopsis Type I Metacaspases Control Cell Death |
| https://doi.org/10.1016/j.cell.2010.09.027 | ABP1 Mediates Auxin Inhibition of Clathrin-Dependent Endocytosis in Arabidopsis |
| https://doi.org/10.1073/pnas.1300127110 | Convergent gene loss following gene and genome duplications creates single-copy families in flowering plants |