Center of Advanced European Studies and Research

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Title DOI
https://doi.org/10.1016/s1474-4422(15)70016-5 Neuroinflammation in Alzheimer's disease
https://doi.org/10.1038/nature11729 NLRP3 is activated in Alzheimer’s disease and contributes to pathology in APP/PS1 mice
https://doi.org/10.1038/nrn.2015.1 Tau in physiology and pathology
https://doi.org/10.15252/embj.201798049 Tau protein liquid–liquid phase separation can initiate tau aggregation
https://doi.org/10.1016/j.matbio.2004.12.004 Isolation of precursor cells (PCs) from human dental follicle of wisdom teeth
https://doi.org/10.1038/s41467-017-00480-0 Liquid–liquid phase separation of the microtubule-binding repeats of the Alzheimer-related protein Tau
https://doi.org/10.1002/jbm.b.30291 Three‐dimensional printing of porous ceramic scaffolds for bone tissue engineering
https://doi.org/10.1038/nmat1593 Combinatorial search of thermoelastic shape-memory alloys with extremely small hysteresis width
https://doi.org/10.1186/s13024-016-0143-y The release and trans-synaptic transmission of Tau via exosomes
https://doi.org/10.1084/jem.20131685 Neuronal activity regulates extracellular tau in vivo
https://doi.org/10.1038/nrn2789 Olfactory signalling in vertebrates and insects: differences and commonalities
https://doi.org/10.1038/nature09769 The CatSper channel mediates progesterone-induced Ca2+ influx in human sperm
https://doi.org/10.1073/pnas.1504081112 Tau stabilizes microtubules by binding at the interface between tubulin heterodimers
https://doi.org/10.1053/jhin.2001.1052 Implant infections: a haven for opportunistic bacteria
https://doi.org/10.1007/s10856-005-4716-5 Hydroxyapatite scaffolds for bone tissue engineering made by 3D printing
https://doi.org/10.1021/la051898e The Effects of Chemisorption on the Luminescence of CdSe Quantum Dots
https://doi.org/10.1021/cr400071f The RNA Polymerase II Carboxy-Terminal Domain (CTD) Code
https://doi.org/10.1021/nl048574f Fabrication and Biocompatibility of Carbon Nanotube-Based 3D Networks as Scaffolds for Cell Seeding and Growth
https://doi.org/10.1371/journal.pone.0060921 Functional Impairment of Microglia Coincides with Beta-Amyloid Deposition in Mice with Alzheimer-Like Pathology
https://doi.org/10.1088/1361-648x/ab6348 The 2020 motile active matter roadmap
https://doi.org/10.1016/j.neuron.2018.07.039 Tau Protein Disrupts Nucleocytoplasmic Transport in Alzheimer’s Disease
https://doi.org/10.1016/j.visres.2016.02.002 Painfree and accurate Bayesian estimation of psychometric functions for (potentially) overdispersed data
https://doi.org/10.1016/j.conb.2021.03.003 A current view on Tau protein phosphorylation in Alzheimer's disease
https://doi.org/10.1186/s40478-017-0488-7 What is the evidence that tau pathology spreads through prion-like propagation?
https://doi.org/10.1038/nchembio.2166 Covalent targeting of remote cysteine residues to develop CDK12 and CDK13 inhibitors
https://doi.org/10.1021/nl049361t Shadow Nanosphere Lithography:  Simulation and Experiment
https://doi.org/10.1038/nature12430 Interactome map uncovers phosphatidylserine transport by oxysterol-binding proteins
https://doi.org/10.1016/j.cell.2014.01.037 Hsp90-Tau Complex Reveals Molecular Basis for Specificity in Chaperone Action
https://doi.org/10.1016/j.insmatheco.2005.05.008 Estimating the tail-dependence coefficient: Properties and pitfalls
https://doi.org/10.1002/smll.200400099 Fabrication of Nanoscale Rings, Dots, and Rods by Combining Shadow Nanosphere Lithography and Annealed Polystyrene Nanosphere Masks
https://doi.org/10.1084/jem.20160933 NLRP3 inflammasome assembly is regulated by phosphorylation of the pyrin domain
https://doi.org/10.7554/elife.23496 Angular velocity integration in a fly heading circuit
https://doi.org/10.1146/annurev.neuro.31.060407.125552 Multifunctional Pattern-Generating Circuits
https://doi.org/10.1016/j.neurobiolaging.2011.11.009 Autophagic degradation of tau in primary neurons and its enhancement by trehalose
https://doi.org/10.1038/nn.4516 Video-rate volumetric functional imaging of the brain at synaptic resolution
https://doi.org/10.1016/j.celrep.2016.10.077 CDK12 Inhibition Reverses De Novo and Acquired PARP Inhibitor Resistance in BRCA Wild-Type and Mutated Models of Triple-Negative Breast Cancer
https://doi.org/10.4161/sgtp.29513 Formins as effector proteins of Rho GTPases
https://doi.org/10.1038/emboj.2013.207 Amyloid‐β oligomers induce synaptic damage via Tau‐dependent microtubule severing by TTLL6 and spastin
https://doi.org/10.1016/j.tins.2014.08.004 Lost after translation: missorting of Tau protein and consequences for Alzheimer disease
https://doi.org/10.1021/nl048950w Layer-by-Layer Assembled Composites from Multiwall Carbon Nanotubes with Different Morphologies
https://doi.org/10.1021/nl0505391 Magnetic Colloidosomes Derived from Nanoparticle Interfacial Self-Assembly
https://doi.org/10.1080/20013078.2018.1528109 Precipitation with polyethylene glycol followed by washing and pelleting by ultracentrifugation enriches extracellular vesicles from tissue culture supernatants in small and large scales
https://doi.org/10.1021/jp048948t Mechanism of Strong Luminescence Photoactivation of Citrate-Stabilized Water-Soluble Nanoparticles with CdSe Cores
https://doi.org/10.1038/nmat1459 From anisotropic photo-fluidity towards nanomanipulation in the optical near-field
https://doi.org/10.1038/s41467-019-10792-y Lysine/RNA-interactions drive and regulate biomolecular condensation
https://doi.org/10.7554/elife.56261 Training deep neural density estimators to identify mechanistic models of neural dynamics
https://doi.org/10.1038/s41592-021-01236-x Deep learning enables fast and dense single-molecule localization with high accuracy
https://doi.org/10.1073/pnas.0912009106 Site-directed spin labeling of a genetically encoded unnatural amino acid
https://doi.org/10.1016/j.ejphar.2005.12.068 Nanomedicine for respiratory diseases
https://doi.org/10.1016/j.bpj.2010.05.015 Hydrodynamics of Sperm Cells near Surfaces
https://doi.org/10.1016/j.aca.2007.09.056 Surface acoustic wave sensors in the bioanalytical field: Recent trends and challenges
https://doi.org/10.1093/nar/gku449 Brd4 activates P-TEFb for RNA polymerase II CTD phosphorylation
https://doi.org/10.1002/anie.200500581 Aligning Au Nanorods by Using Carbon Nanotubes as Templates
https://doi.org/10.1038/emboj.2012.30 The CatSper channel: a polymodal chemosensor in human sperm
https://doi.org/10.1038/emboj.2011.376 Novel diffusion barrier for axonal retention of Tau in neurons and its failure in neurodegeneration
https://doi.org/10.1007/s00791-006-0048-3 AMDiS: adaptive multidimensional simulations
https://doi.org/10.1111/acel.12692 Interplay of pathogenic forms of human tau with different autophagic pathways
https://doi.org/10.1021/ja305470p β-Sheet Core of Tau Paired Helical Filaments Revealed by Solid-State NMR
https://doi.org/10.1038/ncomms8985 Sperm navigation along helical paths in 3D chemoattractant landscapes
https://doi.org/10.1007/s00068-006-6047-8 Biomaterials as Scaffold for Bone Tissue Engineering
https://doi.org/10.1186/s40478-017-0489-6 Atypical, non-standard functions of the microtubule associated Tau protein
https://doi.org/10.1038/ncomms8025 A mechanistic model of tau amyloid aggregation based on direct observation of oligomers
https://doi.org/10.1073/pnas.1212100110 The fuzzy coat of pathological human Tau fibrils is a two-layered polyelectrolyte brush
https://doi.org/10.1016/j.str.2013.10.020 Predictive Atomic Resolution Descriptions of Intrinsically Disordered hTau40 and α-Synuclein in Solution from NMR and Small Angle Scattering
https://doi.org/10.1016/j.biomaterials.2008.06.012 The morphology of anisotropic 3D-printed hydroxyapatite scaffolds
https://doi.org/10.1093/hmg/dds190 Inhibition of tau aggregation in a novel Caenorhabditis elegans model of tauopathy mitigates proteotoxicity
https://doi.org/10.1021/nl801811t Optical and Magnetic Properties of Hexagonal Arrays of Subwavelength Holes in Optically Thin Cobalt Films
https://doi.org/10.1371/journal.pcbi.1006157 Community-based benchmarking improves spike rate inference from two-photon calcium imaging data
https://doi.org/10.1038/ncomms4505 The structure and substrate specificity of human Cdk12/Cyclin K
https://doi.org/10.1016/s0305-750x(98)00083-7 Russian poverty: Muddling through economic transition with garden plots
https://doi.org/10.1038/s41380-018-0108-3 New role of P2X7 receptor in an Alzheimer’s disease mouse model
https://doi.org/10.1073/pnas.1617249114 Selective entrainment of gamma subbands by different slow network oscillations
https://doi.org/10.1002/adma.200400626 Linear Assemblies of Silica‐Coated Gold Nanoparticles Using Carbon Nanotubes as Templates
https://doi.org/10.1016/j.neuropharm.2010.01.016 Tau protein and tau aggregation inhibitors
https://doi.org/10.1021/la801675d Synthesis of Flexible, Ultrathin Gold Nanowires in Organic Media
https://doi.org/10.1042/bst20120071 Degradation of tau protein by autophagy and proteasomal pathways
https://doi.org/10.15252/embr.201438869 Direct action of endocrine disrupting chemicals on human sperm
https://doi.org/10.1016/j.celrep.2015.12.025 Structural and Functional Analysis of the Cdk13/Cyclin K Complex
https://doi.org/10.1007/s11468-005-9005-0 Drastic Surface Plasmon Mode Shifts in Gold Nanorods Due to Electron Charging
https://doi.org/10.1074/jbc.m113.515445 Extracellular Monomeric Tau Protein Is Sufficient to Initiate the Spread of Tau Protein Pathology
https://doi.org/10.1158/0008-5472.can-09-3155 Y-Box Binding Protein-1 Induces the Expression of CD44 and CD49f Leading to Enhanced Self-Renewal, Mammosphere Growth, and Drug Resistance
https://doi.org/10.1158/0008-5472.can-08-3153 Hyperactivation of the Insulin-like Growth Factor Receptor I Signaling Pathway Is an Essential Event for Cisplatin Resistance of Ovarian Cancer Cells
https://doi.org/10.1126/science.abd4914 Tubulin glycylation controls axonemal dynein activity, flagellar beat, and male fertility
https://doi.org/10.1002/smll.200800923 Periodic Large‐Area Metallic Split‐Ring Resonator Metamaterial Fabrication Based on Shadow Nanosphere Lithography
https://doi.org/10.1016/j.cub.2014.11.065 Complementary Contributions of Spike Timing and Spike Rate to Perceptual Decisions in Rat S1 and S2 Cortex
https://doi.org/10.1074/jbc.m114.611368 Oligomer Formation of Tau Protein Hyperphosphorylated in Cells
https://doi.org/10.1016/s0167-7152(03)00092-0 Elliptical copulas: applicability and limitations
https://doi.org/10.1038/s41467-017-02230-8 Multivalent cross-linking of actin filaments and microtubules through the microtubule-associated protein Tau
https://doi.org/10.1002/anie.202100316 A SARS‐CoV‐2 Spike Binding DNA Aptamer that Inhibits Pseudovirus Infection by an RBD‐Independent Mechanism**
https://doi.org/10.1093/nar/gkv101 Ovarian carcinoma CDK12 mutations misregulate expression of DNA repair genes via deficient formation and function of the Cdk12/CycK complex
https://doi.org/10.1074/jbc.m112.369785 Tau Protein Diffuses along the Microtubule Lattice
https://doi.org/10.1074/jbc.m117.784702 Axodendritic sorting and pathological missorting of Tau are isoform-specific and determined by axon initial segment architecture
https://doi.org/10.1002/anie.201208290 Mechanistic Basis of Phenothiazine‐Driven Inhibition of Tau Aggregation
https://doi.org/10.1021/acs.analchem.5b04509 FLEXITau: Quantifying Post-translational Modifications of Tau Protein in Vitro and in Human Disease
https://doi.org/10.1016/j.tcb.2013.10.004 The computational sperm cell
https://doi.org/10.1063/1.1525056 Measurement of three-dimensional force fields with atomic resolution using dynamic force spectroscopy
https://doi.org/10.1177/0885328210373285 In vitro -Osteoclastic Activity Studies on Surfaces of 3D Printed Calcium Phosphate Scaffolds
https://doi.org/10.1021/bi201857v Interaction of Tau Protein with Model Lipid Membranes Induces Tau Structural Compaction and Membrane Disruption
https://doi.org/10.1016/j.jalz.2016.03.018 Tau: From research to clinical development
https://doi.org/10.1016/j.neuron.2016.10.027 The Impact of Structural Heterogeneity on Excitation-Inhibition Balance in Cortical Networks