about
Shearing of the CENP-A dimerization interface mediates plasticity in the octameric centromeric nucleosome.MEDYAN: Mechanochemical Simulations of Contraction and Polarity Alignment in Actomyosin NetworksProtein structure prediction: do hydrogen bonding and water-mediated interactions suffice?Internal modifications in the CENP-A nucleosome modulate centromeric dynamics.High resolution approach to the native state ensemble kinetics and thermodynamics.Theoretical and computational validation of the Kuhn barrier friction mechanism in unfolded proteins.Mechano-chemical feedbacks regulate actin mesh growth in lamellipodial protrusions.Chemically accurate coarse graining of double-stranded DNA.DNA exit ramps are revealed in the binding landscapes obtained from simulations in helical coordinates.Theory of active transport in filopodia and stereocilia.Regulation of the H4 tail binding and folding landscapes via Lys-16 acetylation.Predictive energy landscapes for protein-protein associationComputing free energies of protein conformations from explicit solvent simulations.Hierarchical organization of eglin c native state dynamics is shaped by competing direct and water-mediated interactions.Proteins with weakly funneled energy landscapes challenge the classical structure-function paradigm.Steric Effects Induce Geometric Remodeling of Actin Bundles in FilopodiaElimination of fast variables in chemical Langevin equationsMolecular noise of capping protein binding induces macroscopic instability in filopodial dynamics.Deconstructing the native state: energy landscapes, function, and dynamics of globular proteins.Protein functional landscapes, dynamics, allostery: a tortuous path towards a universal theoretical framework.Protein fluxes along the filopodium as a framework for understanding the growth-retraction dynamics: the interplay between diffusion and active transport.Promiscuous Histone Mis-Assembly Is Actively Prevented by Chaperones.Stochastic Resonance in Protein Folding Dynamics.The Acetylation Landscape of the H4 Histone Tail: Disentangling the Interplay between the Specific and Cumulative Effects.Capsid deformations reveal complex mechano-chemistry.Molecular renormalization group coarse-graining of polymer chains: application to double-stranded DNA.Tunable energy transfer rates via control of primary, secondary, and tertiary structure of a coiled coil peptide scaffold.Interfacial energy conversion in Ru(II) polypyridyl-derivatized oligoproline assemblies on TiO2.Energy landscape analyses of disordered histone tails reveal special organization of their conformational dynamics.Electron-rich rods as building blocks for Sb strips and Te sheets.The physics and bioinformatics of binding and folding-an energy landscape perspective.Role of water mediated interactions in protein-protein recognition landscapes.Polyionic charge density plays a key role in differential recognition of mobile ions by biopolymers.Molecular transport modulates the adaptive response of branched actin networks to an external force.Multiscale stochastic reaction-diffusion modeling: application to actin dynamics in filopodia.Exploring the Free Energy Landscape of Nucleosomes.Reverse-engineering of biochemical reaction networks from spatio-temporal correlations of fluorescence fluctuations.Molecular renormalization group coarse-graining of electrolyte solutions: application to aqueous NaCl and KCl.Stochastic resonant signaling in enzyme cascades.Evolution of complex probability distributions in enzyme cascades.
P50
Q27305245-715E0F4B-D749-45F2-918A-03EBF5FDF39BQ27316439-694DBC9C-99B3-4403-9809-3A38D639DF46Q30390517-61F5BFCD-1260-46CC-BE01-21F56C26B21AQ30843972-2586A237-EDDB-40E5-8C0B-FCA500D2C878Q33370846-A7F8B576-ABB7-4CDF-A399-9EDCD357DE85Q33670312-7B881EEC-DCCF-47AA-BE51-6CB09D4297D8Q33795507-C156032D-E8CB-4F0C-BF99-9B70A0A95995Q34377420-C4727944-29CE-42E5-BB16-E92C2EC7699FQ35559885-DC7F840E-1600-431D-A0C9-210D11A1EE2CQ36079512-42A268E3-A3F8-45E8-A850-D0FF5945A6E5Q36397739-7A4FC587-C78D-41AD-8FB8-45DE7CB0DC3EQ36436864-95E7A480-576A-4AAA-B19F-1FF310E1FE17Q36774555-AB95854A-A2B1-4406-A499-D7E5EAA25AEDQ36825342-BEDA0816-EFD0-4531-8D6E-F833DA6F8F02Q36936200-6E27CB85-7877-43DC-938C-85EB53DB2435Q37081374-60AFC9A3-3B76-4887-A151-060A4237CF21Q37173308-A5EA359A-0DF1-4B61-B6B5-CADB8B70B43DQ37261764-12D6154C-1A45-494E-AD76-35A8B785EC4AQ37488159-4C174EAD-7FBE-4F18-B808-1B0BF36A8EA1Q37785587-CA84A2A1-0AFE-4ABA-BBA1-84E0FDE947B9Q37942764-405A133A-E5A6-4F7E-88BD-B6660CE8B79EQ39563132-78DB91FE-5972-4F85-8410-6A20B738D5B2Q39908280-A7ED250E-86DF-46A6-ABB0-8D7083088E65Q41024071-1A3BCB9C-0ED5-4BF3-9CC3-1BFDECD85CE3Q41948644-C1E2A523-6384-4750-AD0F-14773509B8AAQ42538747-D970B56E-9633-4763-840B-2277B2BCE486Q43634271-94A98428-5514-4A79-BDE4-F0B0483E5AFDQ43676918-FD29DC0E-DF8E-4CFC-A635-6E0C8DFC29D5Q45779631-7531C3F7-C849-4917-BD45-54C18EA868A8Q46348205-F7C904E2-EC9E-47D2-9E96-DFA1A41F8C81Q46353542-ADC20284-D26B-45A4-870E-65579F83BFDEQ46386473-6A1A9C5A-A7A9-4A7D-981A-424E7403A946Q46505001-E49C0944-8C3A-4921-93AE-2CA409D7846CQ47738451-85C2E37A-9A12-4462-B8B7-3DAF18B5A8BBQ51022227-E1C1D539-C07B-46AD-BBC4-3851935818A1Q51703645-367056CD-C119-45BD-838C-D6E562107724Q51720208-19F25AD3-FF3D-4972-8DAE-BDC1E8ED5DDFQ51832438-37A564A4-33D0-439B-9EC7-D4A20B03266CQ51908700-DEF724CC-0E87-4693-910B-BD5294CC6C77Q51910356-F7646D28-3B72-43DB-8DAB-7BE9AA062346
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Garegin A Papoian
@ast
Garegin A Papoian
@en
Garegin A Papoian
@es
Garegin A Papoian
@sl
type
label
Garegin A Papoian
@ast
Garegin A Papoian
@en
Garegin A Papoian
@es
Garegin A Papoian
@sl
prefLabel
Garegin A Papoian
@ast
Garegin A Papoian
@en
Garegin A Papoian
@es
Garegin A Papoian
@sl
P1053
D-6508-2011
P106
P31
P3829
P496
0000-0001-8580-3790
P569
2000-01-01T00:00:00Z