about
Viability conditions for a compartmentalized protometabolic system: a semi-empirical approachConsistency Analysis of Genome-Scale Models of Bacterial Metabolism: A Metamodel ApproachThe structural design of glycolysis: an evolutionary approach.A simple self-maintaining metabolic system: robustness, autocatalysis, bistability.The relationship between the error catastrophe, survival of the flattest, and natural selection.Tools-4-Metatool (T4M): online suite of web-tools to process stoichiometric network analysis data from Metatool.Solving gap metabolites and blocked reactions in genome-scale models: application to the metabolic network of Blattabacterium cuenoti.The advantage of arriving first: characteristic times in finite size populations of error-prone replicatorsStoichiometric analysis of self-maintaining metabolisms.Theories of Lethal Mutagenesis: From Error Catastrophe to Lethal Defection.The metabolic productivity of the cell factory.Nature lessons: The whitefly bacterial endosymbiont is a minimal amino acid factory with unusual energetics.Structural analyses of a hypothetical minimal metabolismGeneralization of the theory of transition times in metabolic pathways: a geometrical approach.Metabolic Complementation in Bacterial Communities: Necessary Conditions and Optimality.Transient times in linear metabolic pathways under constant affinity constraints.Network organization of cell metabolism: monosaccharide interconversionCooperative interaction of the C-terminal domain of histone H1 with DNA.Condensation of DNA by the C-terminal domain of histone H1. A circular dichroism study.Influence of the hypercycle on the error threshold: a stochastic approach.From prebiotic chemistry to cellular metabolism--the chemical evolution of metabolism before Darwinian natural selection.Size matters: influence of stochasticity on the self-maintenance of a simple model of metabolic closure.Effect of lethality on the extinction and on the error threshold of quasispecies.Equivalence of branched and unbranched Michaelian pathways concerning periodic signal transmission.METATOOL: for studying metabolic networks.Thermal denaturation profiles of deoxypolynucleotide-destabilizer ligand complexes: semiempirical studies.Thermal denaturation profiles of deoxypolynucleotide-ligand complexes: semiempirical studies.Purification of the histone H1 from the fruit fly Ceratitis capitata. Isolation of a high mobility group (HMG) non-histone protein and aggregation of H1 through a disulphide bridge.Interactions of the high-mobility-group-like Ceratitis capitata C1 proteins with DNA.C1 proteins: a class of high-mobility-group non-histone chromosomal proteins from the fruit fly Ceratitis capitata.Influence of the N- and C-terminal tails on the structure of the globular head of histone H1.Structural studies on histones H1. Circular dichroism and difference spectroscopy of the histones H1 and their trypsin-resistant cores from calf thymus and from the fruit fly Ceratitis capitata.Transition state of the glycolytic pathway under FDP saturating conditions: experimental studies and a theoretical model.Nature lessons: the whitefly bacterial endosymbiont is a minimal amino acid factory with unusual energeticsKinetic analysis of ψ-DNA structure formation induced by histone H1 and its C-terminal domainInteraction of the c-terminal domain of the histone H1 with DNAStudies on evolutionary and selective properties of hypercycles using a Monte Carlo methodChannelling and evolution of metabolismHistones from the fruit fly Ceratitis capitata. Isolation and characterizationModification of the lysine residues of histones H1 and H5: effects on structure and on the binding to chromatin
P50
Q28480846-BE8262AA-5B50-4BDE-9A13-66265DE842FDQ28551270-AF54B572-463A-4004-BC17-8275F9C7A632Q33545427-C36BDEE8-86A0-412C-9C20-FE036499F5C9Q33654162-F2608A06-70D8-4C91-BB69-9A7EFE85289BQ33785372-8110AC6C-90C8-42FA-9A80-DAF3B16477F9Q33893520-D6F38361-5A9B-4051-BD94-CA693A06195BQ35029546-C3B09BC1-8672-48FC-B798-1AC6A6B66E13Q35077947-27FAEAA4-90DC-4130-B659-FD7A17A8673AQ37068176-CFBB9905-23A5-474D-A2F8-43A0980EBD67Q38554400-D27637C1-E589-4DB6-8AE4-4F1272FA18D1Q38560395-F2015EA0-3D1D-453B-9132-B5F8B080B3B8Q39544172-0A1994A9-9EEF-4C12-8FD1-ABCF400B4219Q39649177-B0746A96-840F-40A5-B4D2-BB2BB4DFBD05Q40145273-0A46EDFD-E41B-437E-B7D8-94B0F3DE8821Q41361551-543F46B1-E604-46D4-8C70-40427CD03771Q42134549-60E805AA-1841-4F1C-9F58-66B2D2AD10C0Q42218850-47F28526-9A90-4287-A20F-AA67B21E65C5Q43910521-1A9266C5-DE2C-4802-9AC5-583547DA6E10Q44252124-8DE936ED-24AB-4C1A-BB69-04B734C19E76Q44515775-1B0441A9-A65E-44B9-9A3E-0C9E8E50D865Q46832782-83775079-F060-4E63-8650-9608542F21B9Q47330530-18413A75-E856-4C08-9915-2E48146CEAD5Q51784450-CD31F66F-0017-4623-BF69-CB0087D26A17Q52032413-C02258E5-C955-4A3D-8BBD-3C2197674D53Q52216547-9C6F0A2D-380F-4724-9756-F3A264FE7D00Q52422593-9093070D-1A21-4B74-B428-7C2F6FCEEECCQ52425719-6C03923C-2A77-47D8-AA2B-D9F5AC5DFF5DQ52434395-F6989281-0D98-4922-A1EA-159354B356C2Q52463404-2849D98B-776B-4108-A669-19421C743596Q52521307-270A9D9E-666F-4756-819D-B8B672B0536AQ52531292-C55DD7C0-A79E-415A-981D-2C155E8A2981Q52531964-9E315218-720F-4C4F-A199-C1217458EF22Q52576547-07BC7EBF-1D53-40FB-ACE3-68C80B624200Q58046616-EDD24F8A-4E01-4031-9F36-C502EB17148EQ61456052-CD0F94FA-2687-4ADC-A36D-BE4C33D76747Q61456055-C30015E0-2ED1-4CE2-BC6C-4A3AA1A8E9EBQ61456060-46EF2158-AB62-4459-B228-268A3C2E982BQ67784161-DECCD77F-43D1-4F62-851A-8D7787CE339DQ68870203-9515E2CB-D15C-4812-9DE1-0EF308E6A9E9Q69961556-DC648A2F-1D5F-4A24-9CED-7B7F27C90B0B
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Francisco Montero
@ast
Francisco Montero
@en
Francisco Montero
@es
Francisco Montero
@nl
Francisco Montero
@sl
type
label
Francisco Montero
@ast
Francisco Montero
@en
Francisco Montero
@es
Francisco Montero
@nl
Francisco Montero
@sl
prefLabel
Francisco Montero
@ast
Francisco Montero
@en
Francisco Montero
@es
Francisco Montero
@nl
Francisco Montero
@sl
P1053
G-9850-2015
P106
P21
P31
P3829
P496
0000-0003-2366-3635