Publications in OpenAlex of which a co-author is affiliated to this organization
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| Title | DOI |
|---|---|
| https://doi.org/10.1080/20013078.2018.1535750 | Minimal information for studies of extracellular vesicles 2018 (MISEV2018): a position statement of the International Society for Extracellular Vesicles and update of the MISEV2014 guidelines |
| https://doi.org/10.3402/jev.v4.27066 | Biological properties of extracellular vesicles and their physiological functions |
| https://doi.org/10.1002/jev2.12404 | Minimal information for studies of extracellular vesicles (MISEV2023): From basic to advanced approaches |
| https://doi.org/10.1038/s41580-020-0237-9 | Guidelines and definitions for research on epithelial–mesenchymal transition |
| https://doi.org/10.3402/jev.v4.30087 | Applying extracellular vesicles based therapeutics in clinical trials – an ISEV position paper |
| https://doi.org/10.1038/nmeth.4185 | EV-TRACK: transparent reporting and centralizing knowledge in extracellular vesicle research |
| https://doi.org/10.1038/s41568-019-0149-1 | Ferroptosis at the crossroads of cancer-acquired drug resistance and immune evasion |
| https://doi.org/10.1038/s41593-019-0393-4 | A single-cell atlas of mouse brain macrophages reveals unique transcriptional identities shaped by ontogeny and tissue environment |
| https://doi.org/10.3402/jev.v3.24858 | The impact of disparate isolation methods for extracellular vesicles on downstream RNA profiling |
| https://doi.org/10.1038/s41467-020-14766-3 | Trajectory-based differential expression analysis for single-cell sequencing data |
| https://doi.org/10.1093/nar/gky1029 | Vesiclepedia 2019: a compendium of RNA, proteins, lipids and metabolites in extracellular vesicles |
| https://doi.org/10.1126/science.aay3224 | A cell atlas of human thymic development defines T cell repertoire formation |
| https://doi.org/10.1038/s41593-020-00789-y | Single-cell profiling of myeloid cells in glioblastoma across species and disease stage reveals macrophage competition and specialization |
| https://doi.org/10.1016/j.jconrel.2013.08.014 | Electroporation-induced siRNA precipitation obscures the efficiency of siRNA loading into extracellular vesicles |
| https://doi.org/10.1093/nar/gky1031 | LNCipedia 5: towards a reference set of human long non-coding RNAs |
| https://doi.org/10.1136/jitc-2020-001926 | Targeting immunogenic cancer cell death by photodynamic therapy: past, present and future |
| https://doi.org/10.1038/s41467-020-19015-1 | Benchmarking of cell type deconvolution pipelines for transcriptomics data |
| https://doi.org/10.1016/j.jconrel.2021.03.043 | The dawn of mRNA vaccines: The COVID-19 case |
| https://doi.org/10.1136/jitc-2020-001369 | Vaccination with early ferroptotic cancer cells induces efficient antitumor immunity |
| https://doi.org/10.1016/j.celrep.2016.03.037 | Vaccination with Necroptotic Cancer Cells Induces Efficient Anti-tumor Immunity |
| https://doi.org/10.1007/s00431-021-03993-5 | Multisystem inflammatory syndrome in children related to COVID-19: a systematic review |
| https://doi.org/10.1093/nar/gkz445 | MEXPRESS update 2019 |
| https://doi.org/10.1080/20013078.2017.1321455 | A novel community driven software for functional enrichment analysis of extracellular vesicles data |
| https://doi.org/10.1038/s41467-022-31218-2 | Cancer cells dying from ferroptosis impede dendritic cell-mediated anti-tumor immunity |
| https://doi.org/10.15252/emmm.201606271 | Identification of a novel mechanism of blood–brain communication during peripheral inflammation via choroid plexus‐derived extracellular vesicles |
| https://doi.org/10.1016/j.ultrasmedbio.2020.01.002 | Ultrasound-Responsive Cavitation Nuclei for Therapy and Drug Delivery |
| https://doi.org/10.1016/j.nantod.2019.100766 | Three decades of messenger RNA vaccine development |
| https://doi.org/10.1136/gutjnl-2018-317726 | Increased levels of systemic LPS-positive bacterial extracellular vesicles in patients with intestinal barrier dysfunction |
| https://doi.org/10.1016/j.bbcan.2017.06.006 | EMT transcription factors in cancer development re-evaluated: Beyond EMT and MET |
| https://doi.org/10.1016/j.ejpb.2018.05.034 | The proton sponge hypothesis: Fable or fact? |
| https://doi.org/10.1111/j.1751-7915.2011.00308.x | Incorporating a mucosal environment in a dynamic gut model results in a more representative colonization by lactobacilli |
| https://doi.org/10.1038/s41565-021-00976-3 | Photothermal nanofibres enable safe engineering of therapeutic cells |
| https://doi.org/10.1093/bioinformatics/bty019 | Computational deconvolution of transcriptomics data from mixed cell populations |
| https://doi.org/10.1016/j.ejca.2017.01.011 | The rationale of indoleamine 2,3-dioxygenase inhibition for cancer therapy |
| https://doi.org/10.1093/nar/gkw1008 | RNAcentral: a comprehensive database of non-coding RNA sequences |
| https://doi.org/10.1038/s41598-017-02599-y | Confounding factors of ultrafiltration and protein analysis in extracellular vesicle research |
| https://doi.org/10.1007/s00787-017-0952-8 | Emotion regulation across childhood and adolescence: evidence for a maladaptive shift in adolescence |
| https://doi.org/10.1016/j.tig.2017.08.004 | Epithelial-to-Mesenchymal Transition: Epigenetic Reprogramming Driving Cellular Plasticity |
| https://doi.org/10.1186/s40425-019-0826-3 | Immunogenic cell death induced by a new photodynamic therapy based on photosens and photodithazine |
| https://doi.org/10.1038/s41419-022-04851-4 | Which cell death modality wins the contest for photodynamic therapy of cancer? |
| https://doi.org/10.3390/cancers11060838 | The Role of Epithelial-to-Mesenchymal Plasticity in Ovarian Cancer Progression and Therapy Resistance |
| https://doi.org/10.1038/s41596-019-0236-5 | Analyzing bacterial extracellular vesicles in human body fluids by orthogonal biophysical separation and biochemical characterization |
| https://doi.org/10.1111/1541-4337.12567 | Mycotoxin exposure and human cancer risk: A systematic review of epidemiological studies |
| https://doi.org/10.1038/s41556-024-01360-8 | A guideline on the molecular ecosystem regulating ferroptosis |
| https://doi.org/10.1002/jev2.12299 | A compendium of single extracellular vesicle flow cytometry |
| https://doi.org/10.1002/eji.201646347 | Computational methods for trajectory inference from single‐cell transcriptomics |
| https://doi.org/10.1016/j.pharmthera.2015.05.001 | Selective glucocorticoid receptor modulation: New directions with non-steroidal scaffolds |
| https://doi.org/10.3389/fimmu.2020.531491 | IDO Expression in Cancer: Different Compartment, Different Functionality? |
| https://doi.org/10.1073/pnas.1600816113 | pH-degradable imidazoquinoline-ligated nanogels for lymph node-focused immune activation |
| https://doi.org/10.1016/j.addr.2021.02.015 | Opening doors with ultrasound and microbubbles: Beating biological barriers to promote drug delivery |
| https://doi.org/10.3389/fonc.2015.00063 | Cancer-Associated Fibroblasts Connect Metastasis-Promoting Communication in Colorectal Cancer |
| https://doi.org/10.1038/s41523-020-0156-0 | Pitfalls in assessing stromal tumor infiltrating lymphocytes (sTILs) in breast cancer |
| https://doi.org/10.1158/2159-8290.cd-16-0861 | Cross-Cohort Analysis Identifies a TEAD4–MYCN Positive Feedback Loop as the Core Regulatory Element of High-Risk Neuroblastoma |
| https://doi.org/10.1002/smll.201600393 | Identification of Individual Exosome-Like Vesicles by Surface Enhanced Raman Spectroscopy |
| https://doi.org/10.1097/pas.0000000000001119 | Uterine PEComas |
| https://doi.org/10.1038/s41388-018-0281-5 | The cancer-associated microprotein CASIMO1 controls cell proliferation and interacts with squalene epoxidase modulating lipid droplet formation |
| https://doi.org/10.1038/s41580-022-00564-w | Pore-forming proteins as drivers of membrane permeabilization in cell death pathways |
| https://doi.org/10.1111/imr.12583 | Necroptotic cell death in anti‐cancer therapy |
| https://doi.org/10.1038/s41418-020-00658-y | The intrinsic immunogenic properties of cancer cell lines, immunogenic cell death, and how these influence host antitumor immune responses |
| https://doi.org/10.1159/000512218 | Epithelial-Mesenchymal Transition (EMT) as a Therapeutic Target |
| https://doi.org/10.1158/0008-5472.can-17-0524 | Radiotherapy-Activated Cancer-Associated Fibroblasts Promote Tumor Progression through Paracrine IGF1R Activation |
| https://doi.org/10.1002/adma.201803397 | Nanoparticle‐Conjugate TLR7/8 Agonist Localized Immunotherapy Provokes Safe Antitumoral Responses |
| https://doi.org/10.1038/s41587-021-00936-1 | The RNA Atlas expands the catalog of human non-coding RNAs |
| https://doi.org/10.18632/aging.101355 | Exosomal microRNAs derived from colorectal cancer-associated fibroblasts: role in driving cancer progression |
| https://doi.org/10.1038/s41467-019-11182-0 | The generation and use of recombinant extracellular vesicles as biological reference material |
| https://doi.org/10.1002/gcc.22709 | Long noncoding RNA expression profiling in cancer: Challenges and opportunities |
| https://doi.org/10.1080/20013078.2020.1736935 | Unravelling the proteomic landscape of extracellular vesicles in prostate cancer by density‐based fractionation of urine |
| https://doi.org/10.1016/j.trecan.2019.09.009 | Fibroblasts Fuel Immune Escape in the Tumor Microenvironment |
| https://doi.org/10.1634/theoncologist.2011-0121 | Use of Tamoxifen Before and During Pregnancy |
| https://doi.org/10.1016/j.biomaterials.2016.04.012 | Genipin-crosslinked gelatin microspheres as a strategy to prevent postsurgical peritoneal adhesions: In vitro and in vivo characterization |
| https://doi.org/10.1038/s41419-020-03209-y | Ionizing radiation results in a mixture of cellular outcomes including mitotic catastrophe, senescence, methuosis, and iron-dependent cell death |
| https://doi.org/10.1016/j.jconrel.2016.04.005 | Comparing exosome-like vesicles with liposomes for the functional cellular delivery of small RNAs |
| https://doi.org/10.1038/s43586-023-00240-z | Extracellular vesicle analysis |
| https://doi.org/10.1186/s13059-017-1277-0 | stageR: a general stage-wise method for controlling the gene-level false discovery rate in differential expression and differential transcript usage |
| https://doi.org/10.1016/j.mam.2019.10.005 | Targets, pitfalls and reference materials for liquid biopsy tests in cancer diagnostics |
| https://doi.org/10.1038/nchembio.2261 | Oxidized PEs trigger death |
| https://doi.org/10.1080/20013078.2019.1647027 | Considerations towards a roadmap for collection, handling and storage of blood extracellular vesicles |
| https://doi.org/10.1016/j.addr.2021.113900 | Strategies for controlling the innate immune activity of conventional and self-amplifying mRNA therapeutics: Getting the message across |
| https://doi.org/10.1016/j.immuni.2020.03.019 | Integrated scRNA-Seq Identifies Human Postnatal Thymus Seeding Progenitors and Regulatory Dynamics of Differentiating Immature Thymocytes |
| https://doi.org/10.1080/20013078.2020.1816641 | Towards defining reference materials for measuring extracellular vesicle refractive index, epitope abundance, size and concentration |
| https://doi.org/10.1038/s41598-021-91974-x | Comparison of microsatellite instability detection by immunohistochemistry and molecular techniques in colorectal and endometrial cancer |
| https://doi.org/10.1016/j.stem.2017.08.003 | Mouse Cutaneous Melanoma Induced by Mutant BRaf Arises from Expansion and Dedifferentiation of Mature Pigmented Melanocytes |
| https://doi.org/10.1073/pnas.1906184116 | Homozygous NLRP1 gain-of-function mutation in siblings with a syndromic form of recurrent respiratory papillomatosis |
| https://doi.org/10.1126/scitranslmed.aav7223 | A microRNA-21–mediated SATB1/S100A9/NF-κB axis promotes chronic obstructive pulmonary disease pathogenesis |
| https://doi.org/10.1016/j.jconrel.2017.09.041 | Co-delivery of nucleoside-modified mRNA and TLR agonists for cancer immunotherapy: Restoring the immunogenicity of immunosilent mRNA |
| https://doi.org/10.1158/0008-5472.can-17-2106 | A Novel |
| https://doi.org/10.1136/jitc-2021-003430 | Immunogenic ferroptosis and where to find it? |
| https://doi.org/10.3390/cancers14040902 | Novel Insights on the Use of L-Asparaginase as an Efficient and Safe Anti-Cancer Therapy |
| https://doi.org/10.1016/j.jconrel.2023.03.039 | Continuous freeze-drying of messenger RNA lipid nanoparticles enables storage at higher temperatures |
| https://doi.org/10.1186/s13046-018-0860-x | Anti-inflammatory signaling by mammary tumor cells mediates prometastatic macrophage polarization in an innovative intraductal mouse model for triple-negative breast cancer |
| https://doi.org/10.1186/s12864-020-6721-y | On the utility of RNA sample pooling to optimize cost and statistical power in RNA sequencing experiments |
| https://doi.org/10.1016/j.nantod.2018.10.005 | mRNA therapeutics deliver a hopeful message |
| https://doi.org/10.1093/humrep/dez116 | Plasma miRNAs as biomarkers for endometriosis |
| https://doi.org/10.1016/j.eururo.2019.01.009 | Randomized Phase 1 Trial of Pembrolizumab with Sequential Versus Concomitant Stereotactic Body Radiotherapy in Metastatic Urothelial Carcinoma |
| https://doi.org/10.1016/j.trecan.2021.01.013 | Ferroptosis and Photodynamic Therapy Synergism: Enhancing Anticancer Treatment |
| https://doi.org/10.1016/j.ejca.2021.04.034 | Immune checkpoint inhibitors in treatment of soft-tissue sarcoma: A systematic review and meta-analysis |
| https://doi.org/10.1111/odi.12224 | Microbiota and their role in the pathogenesis of oral mucositis |
| https://doi.org/10.3390/genes8030095 | Influence of microRNAs and Long Non-Coding RNAs in Cancer Chemoresistance |
| https://doi.org/10.1038/s41576-023-00601-0 | The epithelial–mesenchymal plasticity landscape: principles of design and mechanisms of regulation |
| https://doi.org/10.3945/ajcn.2009.28854 | Disposition of soy isoflavones in normal human breast tissue |