About: Ronald Melki

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researcher (ORCID 0000-0003-0000-7096)

Attributes	Values
rdf:type	Item
description	연구원 (ko) 研究者 (ja) 研究者 (zh) onderzoeker (nl) researcher (ORCID 0000-0003-0000-7096) (en)
rdfs:label	Ronald Melki (en) Ronald Melki (fr) Ronald Melki (nl) Ronald Melki (ast)
skos:prefLabel	Ronald Melki (en) Ronald Melki (fr) Ronald Melki (nl) Ronald Melki (ast)
name	Ronald Melki (en) Ronald Melki (fr) Ronald Melki (nl) Ronald Melki (ast)
given name	wds:Q30123639-F0551DA2-934B-40EE-955C-D6277F7FF442
given name	Ronald
instance of	wds:Q30123639-cdd9f5a5-40f7-a686-f2e4-65a5dce53ad5
instance of	Homo sapiens
award received	wds:Q30123639-9BADFCE5-6055-447E-A78C-7AE633C653D0
award received	Cino Del Duca Science Prize
doctoral student	wds:Q30123639-8813E035-A371-4640-9865-F79C17033314
doctoral student	Luc Bousset
occupation	wds:Q30123639-3573390B-B5B3-4C38-A6F8-A5092DF4EA8E
sex or gender	wds:Q30123639-82a3f97f-40ed-158e-1183-2d0da6a0fc1b
VIAF ID	wds:Q30123639-D29B33C4-CD74-474D-B801-1C7BE16A6F6F
Bibliothèque nationale de France ID	wds:Q30123639-F8402954-EB39-4331-9EA0-96F37CDB64AB
IdRef ID	wds:Q30123639-15358237-0085-456F-A1BA-BDCC5FA9AB25
VIAF ID	http://viaf.org/viaf/170493154
Bibliothèque nationale de France ID	http://data.bnf.fr/ark:/12148/cb16275639p#about
IdRef ID	http://www.idref.fr/069798621/id
occupation	Director of Research at CNRS
sex or gender	male
VIAF ID	170493154
Bibliothèque nationale de France ID	16275639p
IdRef ID	069798621
ORCID iD	wds:Q30123639-65729D03-3E19-45B3-B258-FFE8A37CBA8A
ORCID iD	https://orcid.org/0000-0003-0000-7096
ORCID iD	0000-0003-0000-7096
is owl:sameAs of	Ronald Melki
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q30123639
is author of	Cyan fluorescent protein carries a constitutive mutation that prevents its dimerization. More than just trash bins? Potential roles for extracellular vesicles in the vertical and horizontal transmission of yeast prions Sup35p in Its Soluble and Prion States Is Packaged inside Extracellular Vesicles Delaying aging and the aging-associated decline in protein homeostasis by inhibition of tryptophan degradation. Cytoplasmic penetration and persistent infection of mammalian cells by polyglutamine aggregates The ectodomain of the viral receptor YueB forms a fiber that triggers ejection of bacteriophage SPP1 DNA Identification and characterization of a novel human methyltransferase modulating Hsp70 protein function through lysine methylation G51D α-synuclein mutation causes a novel parkinsonian-pyramidal syndrome Structural and functional characterization of two alpha-synuclein strains The cytosolic chaperonin CCT associates to cytoplasmic microtubular structures during mammalian spermiogenesis and to heterochromatin in germline and somatic cells Prion fibrils of Ure2p assembled under physiological conditions contain highly ordered, natively folded modules Biochemical and functional analysis of the assembly of full-length Sup35p and its prion-forming domain Alpha-synuclein transfers from neurons to oligodendrocytes Solid-state NMR sequential assignments of the amyloid core of full-length Sup35p Extensive de novo solid-state NMR assignments of the 33 kDa C-terminal domain of the Ure2 prion Prion-like transmission of protein aggregates in neurodegenerative diseases DNAJB6 is a peptide-binding chaperone which can suppress amyloid fibrillation of polyglutamine peptides at substoichiometric molar ratios. Tunneling nanotube (TNT)-mediated neuron-to neuron transfer of pathological Tau protein assemblies Ectosomes: a new mechanism for non-exosomal secretion of tau protein PhLP3 modulates CCT-mediated actin and tubulin folding via ternary complexes with substrates Transfer of human α-synuclein from the olfactory bulb to interconnected brain regions in mice Toxic effects of amyloid fibrils on cell membranes: the importance of ganglioside GM1. Overexpression of the calpain-specific inhibitor calpastatin reduces human alpha-Synuclein processing, aggregation and synaptic impairment in [A30P]αSyn transgenic mice Oligomerization of the SPP1 scaffolding protein Assembly of the yeast prion Ure2p into protein fibrils. Thermodynamic and kinetic characterization Different roles of two gamma-tubulin isotypes in the cytoskeleton of the Antarctic ciliate Euplotes focardii: remodelling of interaction surfaces may enhance microtubule nucleation at low temperature The conformation of the prion domain of Sup35p in isolation and in the full-length protein Axonal transport and secretion of fibrillar forms of α-synuclein, Aβ42 peptide and HTTExon 1 α-Synuclein propagates from mouse brain to grafted dopaminergic neurons and seeds aggregation in cultured human cells Molecular interaction between the chaperone Hsc70 and the N-terminal flank of huntingtin exon 1 modulates aggregation Fibrillar α-synuclein and huntingtin exon 1 assemblies are toxic to the cells A role for the proteasome in the turnover of Sup35p and in [PSI(+) ] prion propagation. Direct evidence of Parkinson pathology spread from the gastrointestinal tract to the brain in rats Qualitative and quantitative multiplexed proteomic analysis of complex yeast protein fractions that modulate the assembly of the yeast prion Sup35p Molecular chaperones and the assembly of the prion Sup35p, an in vitro study Hsc70 protein interaction with soluble and fibrillar alpha-synuclein Similar and divergent features in mammalian and yeast prions Neuron-to-neuron transmission of α-synuclein fibrils through axonal transport PA700, the regulatory complex of the 26S proteasome, interferes with alpha-synuclein assembly Spreading of a prion domain from cell-to-cell by vesicular transport in Caenorhabditis elegans The yeast prion Ure2p retains its native alpha-helical conformation upon assembly into protein fibrils in vitro The native-like conformation of Ure2p in fibrils assembled under physiologically relevant conditions switches to an amyloid-like conformation upon heat-treatment of the fibrils Unlike twins: an NMR comparison of two α-synuclein polymorphs featuring different toxicity Polyglutamine repeats are associated to specific sequence biases that are conserved among eukaryotes. The cytosolic chaperonin CCT/TRiC and cancer cell proliferation Characterization of monomeric intermediates during VSV glycoprotein structural transition Synthetic lipid vesicles recruit native-like aggregates and affect the aggregation process of the prion Ure2p: insights on vesicle permeabilization and charge selectivity. The yeast prion Ure2p native-like assemblies are toxic to mammalian cells regardless of their aggregation state. An Efficient Procedure for Removal and Inactivation of Alpha-Synuclein Assemblies from Laboratory Materials Swa2p-dependent clathrin dynamics is critical for Flo11p processing and 'Mat' formation in the yeast Saccharomyces cerevisiae Molecular chaperones and the assembly of the prion Ure2p in vitro α-synuclein assemblies sequester neuronal α3-Na+/K+-ATPase and impair Na+ gradient Fibrillar structure and charge determine the interaction of polyglutamine protein aggregates with the cell surface α-Synuclein and huntingtin exon 1 amyloid fibrils bind laterally to the cellular membrane The interaction of Hsc70 protein with fibrillar α-Synuclein and its therapeutic potential in Parkinson's disease Methyl-branched lipids promote the membrane adsorption of α-synuclein by enhancing shallow lipid-packing defects

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