Frederic Rousseau | Academic Influence

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Frederic Rousseau

Biology

#8739

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#11866

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Molecular Biology

#2466

World Rank

#2505

Historical Rank

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Biology

Frederic Rousseau's Degrees

PhD Molecular Biology University of California, Berkeley
Masters Biochemistry Stanford University
Bachelors Biology University of California, Berkeley

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Why Is Frederic Rousseau Influential?

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According to Wikipedia, See Frédéric Rousseau for the French historian of World War I Frederic Rousseau is a Flemish Belgian molecular biologist and researcher at the KU Leuven . Together with Joost Schymkowitz he is group leader at the VIB Switch Laboratory, KU Leuven. His research interest is on essential cellular processes where functional regulation is governed by protein conformational switches that have to be actively controlled to ensure cell viability

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Frederic Rousseau's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

The FoldX web server: an online force field (2005) (1948)
Prediction of sequence-dependent and mutational effects on the aggregation of peptides and proteins (2004) (1371)
Protein Phase Separation: A New Phase in Cell Biology. (2018) (1096)
Exploring the sequence determinants of amyloid structure using position-specific scoring matrices (2010) (562)
Gain of function of mutant p53 by coaggregation with multiple tumor suppressors. (2011) (444)
Neurotoxicity of Alzheimer's disease Aβ peptides is induced by small changes in the Aβ42 to Aβ40 ratio (2010) (431)
The mechanism of γ-Secretase dysfunction in familial Alzheimer disease (2012) (423)
A comparative study of the relationship between protein structure and beta-aggregation in globular and intrinsically disordered proteins. (2004) (356)
Lipids revert inert Aβ amyloid fibrils to neurotoxic protofibrils that affect learning in mice (2007) (324)
Protein aggregation and amyloidosis: confusion of the kinds? (2006) (322)
Prediction of water and metal binding sites and their affinities by using the Fold-X force field. (2005) (317)
A graphical interface for the FoldX forcefield (2011) (268)
How evolutionary pressure against protein aggregation shaped chaperone specificity. (2006) (241)
SNPeffect 4.0: on-line prediction of molecular and structural effects of protein-coding variants (2011) (228)
PupaSuite: finding functional single nucleotide polymorphisms for large-scale genotyping purposes (2006) (227)
Drosophila screen connects nuclear transport genes to DPR pathology in c9ALS/FTD (2016) (222)
The unfolding story of three-dimensional domain swapping. (2003) (210)
Restricted Location of PSEN2/γ-Secretase Determines Substrate Specificity and Generates an Intracellular Aβ Pool (2016) (208)
Three-dimensional domain swapping in p13suc1 occurs in the unfolded state and is controlled by conserved proline residues (2001) (191)
Structural Basis for Increased Toxicity of Pathological Aβ42:Aβ40 Ratios in Alzheimer Disease* (2011) (187)
Alzheimer’s-Causing Mutations Shift Aβ Length by Destabilizing γ-Secretase-Aβn Interactions (2017) (157)
SNPeffect: a database mapping molecular phenotypic effects of human non-synonymous coding SNPs (2004) (154)
Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease (2008) (149)
Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort (2015) (146)
Progranulin genetic variability contributes to amyotrophic lateral sclerosis (2008) (145)
The culprit behind amyloid beta peptide related neurotoxicity in Alzheimer's disease: oligomer size or conformation? (2010) (140)
Computational design of peptide ligands. (2011) (131)
Redox Proteomics of Protein-bound Methionine Oxidation* (2011) (130)
Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementia (2007) (121)
Recognizing and defining true Ras binding domains II: in silico prediction based on homology modelling and energy calculations. (2005) (117)
Genetic variability in the mitochondrial serine protease HTRA2 contributes to risk for Parkinson disease (2008) (116)
Accurate Prediction of DnaK-Peptide Binding via Homology Modelling and Experimental Data (2009) (109)
The Alzheimer Disease Protective Mutation A2T Modulates Kinetic and Thermodynamic Properties of Amyloid-β (Aβ) Aggregation* (2014) (108)
Prediction and Reduction of the Aggregation of Monoclonal Antibodies (2017) (107)
Analysis of Protein Processing by N-terminal Proteomics Reveals Novel Species-specific Substrate Determinants of Granzyme B Orthologs *S (2009) (105)
Variable Glutamine-Rich Repeats Modulate Transcription Factor Activity (2015) (101)
Molecular mechanism of SSR128129E, an extracellularly acting, small-molecule, allosteric inhibitor of FGF receptor signaling. (2013) (98)
A standardized and biocompatible preparation of aggregate-free amyloid beta peptide for biophysical and biological studies of Alzheimer's disease. (2011) (98)
Implications of 3D domain swapping for protein folding, misfolding and function. (2012) (97)
PepX: a structural database of non-redundant protein–peptide complexes (2009) (96)
SNPeffect v2.0: a new step in investigating the molecular phenotypic effects of human non-synonymous SNPs (2006) (95)
Increased Monomerization of Mutant HSPB1 Leads to Protein Hyperactivity in Charcot-Marie-Tooth Neuropathy* (2010) (92)
Protein sequences encode safeguards against aggregation (2009) (83)
Protein aggregation in bacteria: the thin boundary between functionality and toxicity. (2013) (80)
Joint annotation of coding and non-coding single nucleotide polymorphisms and mutations in the SNPeffect and PupaSuite databases (2007) (77)
Protein-peptide interactions adopt the same structural motifs as monomeric protein folds. (2009) (75)
Hsp90 Mediates Membrane Deformation and Exosome Release. (2018) (74)
What Makes a Protein Sequence a Prion? (2015) (70)
Molecular Dissection of FUS Points at Synergistic Effect of Low-Complexity Domains in Toxicity (2018) (67)
Proteome-wide Substrate Analysis Indicates Substrate Exclusion as a Mechanism to Generate Caspase-7 Versus Caspase-3 Specificity* (2009) (66)
A comparative analysis of the aggregation behavior of amyloid‐β peptide variants (2012) (66)
Rational Design of Amyloid-Like Fibrillary Structures for Tailoring Food Protein Techno-Functionality and Their Potential Health Implications. (2018) (62)
A systems biology perspective on protein structural dynamics and signal transduction. (2005) (60)
Observation of signal transduction in three-dimensional domain swapping (2001) (60)
Protein-peptide complex prediction through fragment interaction patterns. (2013) (60)
PrionW: a server to identify proteins containing glutamine/asparagine rich prion-like domains and their amyloid cores (2015) (59)
Reconstruction of Protein Backbones from the BriX Collection of Canonical Protein Fragments (2008) (58)
The folding pathway of the cell-cycle regulatory protein p13suc1: clues for the mechanism of domain swapping. (2000) (53)
Structural hot spots for the solubility of globular proteins (2016) (52)
Post-translational Control of the Temporal Dynamics of Transcription Factor Activity Regulates Neurogenesis (2016) (52)
An Evolutionary Trade-Off between Protein Turnover Rate and Protein Aggregation Favors a Higher Aggregation Propensity in Fast Degrading Proteins (2011) (52)
De novo design of a biologically active amyloid (2016) (51)
BriX: a database of protein building blocks for structural analysis, modeling and design (2010) (51)
WALTZ-DB: a benchmark database of amyloidogenic hexapeptides (2015) (51)
Structure of the Extracellular Domain of Matrix Protein 2 of Influenza A Virus in Complex with a Protective Monoclonal Antibody (2015) (50)
Nuclear inclusion bodies of mutant and wild‐type p53 in cancer: a hallmark of p53 inactivation and proteostasis remodelling by p53 aggregation (2017) (48)
Solubis: a webserver to reduce protein aggregation through mutation. (2016) (47)
Structural Diversity of PDZ–Lipid Interactions (2010) (46)
Exploring the sequence–structure relationship for amyloid peptides (2012) (44)
Genome-Wide Prediction of SH2 Domain Targets Using Structural Information and the FoldX Algorithm (2008) (43)
Characterisation of the BRCT domains of the breast cancer susceptibility gene product BRCA1. (2002) (42)
Aggregating sequences that occur in many proteins constitute weak spots of bacterial proteostasis (2018) (41)
WALTZ-DB 2.0: an updated database containing structural information of experimentally determined amyloid-forming peptides (2019) (41)
Predicting aggregation-prone sequences in proteins. (2014) (39)
Protein aggregation as an antibiotic design strategy (2016) (38)
Molecular Plasticity Regulates Oligomerization and Cytotoxicity of the Multipeptide-length Amyloid-β Peptide Pool* (2012) (38)
Potential human transmission of amyloid β pathology: surveillance and risks (2020) (35)
Highly efficient intercellular spreading of protein misfolding mediated by viral ligand-receptor interactions (2020) (35)
Structure-based machine-guided mapping of amyloid sequence space reveals uncharted sequence clusters with higher solubilities (2020) (34)
Protein design with fragment databases. (2011) (34)
Quantifying information transfer by protein domains: Analysis of the Fyn SH2 domain structure (2008) (34)
Increased Aggregation Is More Frequently Associated to Human Disease-Associated Mutations Than to Neutral Polymorphisms (2015) (33)
Amyloids or prions? That is the question (2015) (33)
The Alzheimer Disease Protective Mutation A2T Modulates Kinetic and Thermodynamic Properties of Amyloid-beta (A beta) Aggregation (2014) (32)
Aggregation prone regions and gatekeeping residues in protein sequences (2013) (32)
Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitability (2019) (31)
Conditions Governing Food Protein Amyloid Fibril Formation. Part II: Milk and Legume Proteins. (2019) (31)
Analysis of the transthyretin-like (TTL) gene family in Ostertagia ostertagi--comparison with other strongylid nematodes and Caenorhabditis elegans. (2008) (30)
α-Galactosidase Aggregation Is a Determinant of Pharmacological Chaperone Efficacy on Fabry Disease Mutants* (2012) (30)
A genome-wide sequence-structure analysis suggests aggregation gatekeepers constitute an evolutionary constrained functional class. (2014) (30)
Stability and folding of the cell cycle regulatory protein, p13(suc1). (1998) (29)
Aggregation gatekeepers modulate protein homeostasis of aggregating sequences and affect bacterial fitness. (2012) (29)
Frizzled 7 and PIP2 binding by syntenin PDZ2 domain supports Frizzled 7 trafficking and signalling (2016) (29)
Intermediates Control Domain Swapping during Folding of p13suc1* (2004) (28)
Conditions Governing Food Protein Amyloid Fibril Formation-Part I: Egg and Cereal Proteins. (2019) (27)
Using structural bioinformatics to investigate the impact of non synonymous SNPs and disease mutations: scope and limitations (2009) (27)
The Dynamic Transition of Persistence toward the Viable but Nonculturable State during Stationary Phase Is Driven by Protein Aggregation (2021) (26)
Domain swapping in p13suc1 results in formation of native-like, cytotoxic aggregates. (2006) (25)
Nanomaterials to avoid and destroy protein aggregates (2020) (24)
Autonomous aggregation suppression by acidic residues explains why chaperones favour basic residues (2020) (24)
The structure of the transition state for folding of domain-swapped dimeric p13suc1. (2002) (24)
Aggregation prone regions and gatekeeping residues in protein sequences. (2012) (23)
Selectivity of aggregation-determining interactions. (2015) (22)
Sequence conservation provides the best prediction of the role of proline residues in p13suc1. (2000) (21)
Folding and association of the human cell cycle regulatory proteins ckshs1 and ckshs2. (2002) (21)
Transcellular Spreading of Tau in Tauopathies (2018) (21)
Structural Basis of the Subcellular Topology Landscape of Escherichia coli (2019) (21)
Reverse engineering synthetic antiviral amyloids (2020) (19)
A guide to studying protein aggregation (2021) (19)
Thermodynamic and Evolutionary Coupling between the Native and Amyloid State of Globular Proteins (2020) (19)
ALS precursor finally shaken into fibrils (2008) (19)
Defective Sec61α1 underlies a novel cause of autosomal dominant severe congenital neutropenia (2020) (19)
Bcl-xL acts as an inhibitor of IP3R channels, thereby antagonizing Ca2+-driven apoptosis (2021) (19)
Sequence-Specific Protein Aggregation Generates Defined Protein Knockdowns in Plants1[OPEN] (2016) (19)
Sequence-dependent Internalization of Aggregating Peptides* (2014) (18)
Processing induced changes in food proteins: amyloid formation during boiling of hen egg white. (2020) (18)
Solubis: optimize your protein (2015) (18)
Hybrid N-glycans on the host protective activation-associated secreted proteins of Ostertagia ostertagi and their importance in immunogenicity. (2008) (18)
Information theoretical quantification of cooperativity in signalling complexes (2009) (17)
Liquid–Liquid Phase Separation Enhances TDP-43 LCD Aggregation but Delays Seeded Aggregation (2021) (15)
Molecular Mechanism of SSR128129E, an Extracellularly Acting, Small-Molecule, Allosteric Inhibitor of FGF Receptor Signaling. (2016) (13)
Heterotypic interactions in amyloid function and disease (2021) (12)
Surfing on protein folding energy landscapes (2002) (12)
Comprehensive subcellular topologies of polypeptides in Streptomyces (2018) (12)
Mechanisms and therapeutic potential of interactions between human amyloids and viruses (2020) (12)
Peptides based on the presenilin‐APP binding domain inhibit APP processing and Aβ production through interfering with the APP transmembrane domain (2012) (11)
Repurposing the Antidepressant Sertraline as SHMT Inhibitor to Suppress Serine/Glycine Synthesis–Addicted Breast Tumor Growth (2020) (11)
Preparation of amorphous solid dispersions by cryomilling: chemical and physical concerns related to APIs and carriers. (2020) (10)
Heterotypic Amyloid β interactions facilitate amyloid assembly and modify amyloid structure (2021) (10)
Protein aggregation: A rescue by chaperones. (2016) (10)
The structural basis for an on–off switch controlling Gβγ-mediated inhibition of TRPM3 channels (2020) (10)
Medin co-aggregates with vascular amyloid-β in Alzheimer’s disease (2022) (9)
Drying mode and hydrothermal treatment conditions govern the formation of amyloid-like protein fibrils in solutions of dried hen egg white (2021) (9)
Entropic Bristles Tune the Seeding Efficiency of Prion-Nucleating Fragments (2020) (9)
MAPRE2 mutations result in altered human cranial neural crest migration, underlying craniofacial malformations in CSC-KT syndrome (2021) (9)
Evaluation of [11C]NMS-E973 as a PET tracer for in vivo visualisation of HSP90 (2019) (8)
Impact of hydrothermal treatment on denaturation and aggregation of water-extractable quinoa (Chenopodium quinoa Willd.) protein (2021) (8)
The dynamic transition of persistence towards the VBNC state during stationary phase is driven by protein aggregation (2021) (8)
Adaption of human antibody λ and κ light chain architectures to CDR repertoires (2019) (8)
Multiple Evolutionary Mechanisms Reduce Protein Aggregation (2009) (8)
SolubiS: Optimizing Protein Solubility by Minimal Point Mutations. (2018) (7)
Heating Wheat Gluten Promotes the Formation of Amyloid-like Fibrils (2021) (7)
Multiple Evolutionary Mechanisms Reduce Protein Aggregation~!2009-04-21~!2009-07-09~!2010-01-02~! (2010) (7)
A structural analysis of amyloid polymorphism in disease: clues for selective vulnerability? (2021) (7)
Motif Discovery with Data Mining in 3D protein Structure Databases: Discovery, Validation and Prediction of the U-Shape zinc binding ("Huf-zinc") Motif (2013) (6)
Differential proteostatic regulation of insoluble and abundant proteins (2019) (6)
PyUUL provides an interface between biological structures and deep learning algorithms (2022) (6)
StAmP-DB: A platform for structures of polymorphic amyloid fibril cores. (2022) (6)
From Binding-Induced Dynamic Effects in SH3 Structures to Evolutionary Conserved Sectors (2016) (6)
In silico prediction of in vitro protein liquid-liquid phase separation experiments outcomes with multi-head neural attention (2021) (6)
Structural Diversity of PDZ—Lipid Interactions (2010) (6)
Assessing computational predictions of the phenotypic effect of cystathionine‐beta‐synthase variants (2019) (6)
Thermodynamic analysis of amyloid fibril structures reveals a common framework for stability in amyloid polymorphs. (2022) (5)
Hydrothermal Treatments Cause Wheat Gluten-Derived Peptides to Form Amyloid-like Fibrils. (2021) (5)
Investigating the mechanism of action of aggregation-inducing antimicrobial Pept-ins. (2020) (5)
The cellular modifier MOAG-4/SERF drives amyloid formation through charge complementation (2020) (4)
Exposure of a cryptic Hsp70 binding site determines the cytotoxicity of the ALS-associated SOD1-mutant A4V. (2019) (4)
Corrigendum: Exploring the sequence determinants of amyloid structure using position-specific scoring matrices (2010) (4)
Impact of heat and enzymatic treatment on ovalbumin amyloid-like fibril formation and enzyme-induced gelation (2022) (4)
MEA Neurosensor, the Tool for Synaptic Activity Detection: Acute Amyloid- β Oligomers Synaptotoxicity Study (2009) (4)
Targeting S100B with Peptides Encoding Intrinsic Aggregation-Prone Sequence Segments (2021) (4)
Alzheimer’s-causing mutations shift Aβ length by destabilizing γ-secretase-Aβn interactions (2021) (4)
Horizontal gene transfer from human host to HIV-1 reverse transcriptase confers drug resistance and partly compensates for replication deficits. (2014) (4)
The tumor suppressor protein PTEN undergoes amyloid-like aggregation in tumor cells (2020) (3)
Evaluation of [ 11 C ] NMS-E 973 as a PET tracer for in vivo visualisation of HSP 90 (2019) (3)
Bacterial Protein Homeostasis Disruption as a Therapeutic Intervention (2021) (3)
Protein domains as information processing units. (2009) (3)
Heterotypic amyloid interactions: Clues to polymorphic bias and selective cellular vulnerability? (2021) (3)
Protein Homeostasis Database: protein quality control in E.coli (2019) (3)
Brominated phenols as auxin-like molecules (2009) (3)
Variable Glutamine-Rich R epeats Modulate Transcription Factor Activity Graphical (2015) (3)
The effect of mutation on an aggregation-prone protein: An in vivo, in vitro, and in silico analysis (2022) (3)
Protein structure and aggregation: a marriage of necessity ruled by aggregation gatekeepers. (2021) (2)
Mapping the sequence specificity of heterotypic amyloid interactions enables the identification of aggregation modifiers (2022) (2)
The cellular modifier MOAG‐4/SERF drives amyloid formation through charge complementation (2021) (2)
Gene Erosion Can Lead to Gain-of-Function Alleles That Contribute to Bacterial Fitness (2021) (2)
Investigating the Sequence Determinants of the Curling of Amyloid Fibrils Using Ovalbumin as a Case Study. (2022) (2)
Modeling protein-peptide interactions using protein fragments: fitting the pieces? (2010) (2)
Synthetic Pept-Ins as a Generic Amyloid-Like Aggregation-Based Platform for In Vivo PET Imaging of Intracellular Targets (2021) (1)
Exploiting ligand binding domain dimerization for development of novel androgen receptor inhibitors. (2022) (1)
Selective Knockdowns in Maize by Sequence-Specific Protein Aggregation. (2018) (1)
HPMPdb: A machine learning-ready database of protein molecular phenotypes associated to human missense variants (2022) (1)
The A-beta 42/40 ratio is a driver of acute synaptotoxicity and LTP impairment (2010) (1)
EndophilinA-dependent coupling between activity-induced calcium influx and synaptic autophagy is disrupted by a Parkinson-risk mutation (2022) (1)
Progranulin modifies onset age and survival in amyotrophic lateral sclerosis (2007) (1)
Addendum: Exploring the sequence determinants of amyloid structure using position-specific scoring matrices (2010) (1)
Corrigendum to “Hybrid N-glycans on the host protective activation-associated secreted proteins of Ostertagia ostertagi and their importance in immunogenicity” [Mol. Biochem. Parasitol. 161 (1) (2008) 67–71] (2009) (1)
Heterotypic Aβ interactions facilitate amyloid assembly and modify amyloid structure (2021) (1)
Bioavailability and Health Impact of Ingested Amyloid-like Protein Fibrils and their Link with Inflammatory Status: a Need for More Research? (2022) (1)
Surfing on protein folding en (2016) (0)
Crystal structure of the syntenin PDZ1 and PDZ2 tandem in complex with the Frizzled 7 C-terminal fragment and PIP2 (2016) (0)
Amyloid Beta-peptide Length Strongly Affects Aggregation Kinetics (2009) (0)
Reverse engineering synthetic antiviral amyloids (2020) (0)
O2-02-04: Lipids revert inert amyloid fibrils to neurotoxic protofibrils that affect learning in mice (2008) (0)
Biophysical consideration of gamma secretase modulation as potential target for Alzheimer's disease. Consequences of amyloid-beta peptide lenght variation (2011) (0)
Quantifying information transfer by globular proteins (2007) (0)
Author response for "Heterotypic interactions in amyloid function and disease" (2021) (0)
Iconographies supplémentaires de l'article : Defective Sec61?1 underlies a novel cause of autosomal dominant severe congenital neutropenia (2020) (0)
A new generic platform for PET imaging based on 68Ga-labeled Pept-insTM: from infectious disease to cancer imaging (2018) (0)
Sodium glutamate and glutamic acid decarboxylase as alternative for classical chemical leavening in wheat (pan)cake batter systems (2023) (0)
X-ray crystal structure of aggregation-resistant protective antigen of Bacillus anthracis (mutant S559L T576E) (2016) (0)
P3-206: Genetic variability at the progranulin locus contributes to risk for Alzheimer's disease (2008) (0)
Intramolecular H-bond stabilization of a primary hydroxylamine in salen-type metal complexes. (2021) (0)
Evolutionary tuning of heat shock resistance in E. Coli (2020) (0)
Validating the structural information exchange within the domain Fyn SH2 (2010) (0)
Identifying rescuers of misfolding (2017) (0)
Lipid-dependent production of neurotoxic Abeta protofibrils from fibrils (2009) (0)
Information exchange within Src-like SH3 domains: from structure to sector (2011) (0)
PyUUL provides an interface between biological structures and deep learning algorithms (2022) (0)
Aggregating sequences that occur in many proteins constitute weak spots of bacterial proteostasis (2018) (0)
Structural Basis of Information Transfer in Fyn SH2 Domain (2010) (0)
Specificity of allostery networks within the SH3 domain family (2011) (0)
On the evolutionary conservation of the dynamic changes predicted for a collection of SH3 domain structures (2015) (0)
Integrating physics in deep learning algorithms: A force field as a PyTorch module (2023) (0)
Hsp 90 Mediates Membran e Deformation and Exosome Release Graphical Abstract Highlights (2018) (0)
Enhanced therapeutic window for antimicrobial Pept-ins by investigating their structure-activity relationship (2023) (0)
Progress methods for screening for inhibitors of tumor associated protein aggregation (2012) (0)
Experimental identification of intramolecular information exchange within the Fyn SH2 domain (2011) (0)
Biophysical consideration of g-secretase modulation as potential target for Alzheimer's disease (2011) (0)
Exploiting the intrinsic misfolding propensity of the KRAS oncoprotein. (2023) (0)
Secretase dysfunction at the core of Familial Alzheimer disease (2012) (0)
Structure-based machine-guided mapping of amyloid sequence space reveals uncharted sequence clusters with higher solubilities (2020) (0)
Evaluation of [11C]HSP990 as a PET probe for in vivo visualisation of heat shock protein 90 in tumours (2022) (0)
Purposeful induction of aggregation of proteins with cross-beta structure (2008) (0)
Erratum for Mortier and Gayán et al., “Gene Erosion Can Lead to Gain-of-Function Alleles That Contribute to Bacterial Fitness” (2021) (0)
Destabilized γ-Secretase-Aβn interactions cause Alzheimer’s disease, implications for drug discovery (2017) (0)
p53 charged core (2020) (0)
Genetic contribution of PGRN, MAPT, VCP, and CHMP2B to the etiology of frontotemporal dementia (2007) (0)
Seeding, maturation and propagation of amyloid β-peptide aggregates in Alzheimer's disease. (2022) (0)
Aggregation of alpha galactosidase in Fabry disease as a determinant of therapeutic strategy (2010) (0)
Identifying rescuers of misfolding (2017) (0)
De novo missense variants in the E3 ubiquitin ligase adaptor KLHL20 cause a developmental disorder with intellectual disability, epilepsy, and autism spectrum disorder. (2022) (0)
Horizontal gene transfer from human host to HIV-1 reverse transcriptase confers drug resistance and partly compensates for replication de fi cits (2014) (0)
Tau amyloid polymorphism is shaped by local structural propensities of its protein sequence (2022) (0)
Reduced Levels of Misfolded and Aggregated Mutant p53 by Proteostatic Activation (2020) (0)
EXTH-20. SINGLE-CELL DRUG ACTIVITY MAPPING IN GLIOBLASTOMA IDENTIFIES EXTENDED DRUG RESPONSE HETEROGENEITY AND THERAPY-INDUCED CELLULAR PLASTICITY (2021) (0)

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