Lista de obras - Lilia M. Iakoucheva - Dominio Público Uruguay

A Protein Domain-Based Interactome Network for C. elegans Early Embryogenesis

A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex

artículo científico publicado en 2022

A protein domain-based interactome network for C. elegans early embryogenesis

artículo científico publicado en 2008

A proteome-scale map of the human interactome network

artículo científico publicado en 2014

Aberrant mobility phenomena of the DNA repair protein XPA

artículo científico publicado en 2001

Autism-linked Cullin3 germline haploinsufficiency impacts cytoskeletal dynamics and cortical neurogenesis through RhoA signaling

artículo científico publicado en 2021

Combining prediction, computation and experiment for the characterization of protein disorder

artículo científico publicado en 2004

Comprehensive Analyses of Tissue-Specific Networks with Implications to Psychiatric Diseases

artículo científico

Cortical organoids model early brain development disrupted by 16p11.2 copy number variants in autism

artículo científico publicado en 2021

DisProt: a database of protein disorder

artículo científico publicado en 2004

Disease-associated mutations disrupt functionally important regions of intrinsic protein disorder

artículo científico publicado en 2012

Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia

artículo científico publicado en 2011

Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia

artículo científico publicado en 2011

Equilibrium and stop-flow kinetic studies of fluorescently labeled DNA substrates with DNA repair proteins XPA and replication protein A.

artículo científico publicado en 2002

Extended X-ray absorption fine structure evidence for a single metal binding domain in Xenopus laevis nucleotide excision repair protein XPA.

artículo científico publicado en 1999

Flexible nets. The roles of intrinsic disorder in protein interaction networks.

artículo científico publicado en 2005

Frequency and Complexity of De Novo Structural Mutation in Autism

artículo científico publicado en 2016

Full-length isoform transcriptome of the developing human brain provides further insights into autism

scientific article published on 01 August 2021

Functional anthology of intrinsic disorder. 1. Biological processes and functions of proteins with long disordered regions.

artículo científico publicado en 2007

Functional anthology of intrinsic disorder. 2. Cellular components, domains, technical terms, developmental processes, and coding sequence diversities correlated with long disordered regions

artículo científico publicado en 2007

Functional anthology of intrinsic disorder. 3. Ligands, post-translational modifications, and diseases associated with intrinsically disordered proteins.

artículo científico publicado en 2007

Graphlet kernels for prediction of functional residues in protein structures

artículo científico publicado en 2010

Identification, analysis, and prediction of protein ubiquitination sites

artículo científico publicado en 2010

Inferring the molecular and phenotypic impact of amino acid variants with MutPred2

artículo científico publicado en 2020

Intrinsic disorder and functional proteomics

artículo científico publicado en 2006

Intrinsic disorder in cell-signaling and cancer-associated proteins

artículo científico publicado en 2002

Intrinsic disorder is a common feature of hub proteins from four eukaryotic interactomes

artículo científico publicado en 2006

Mapping copy number variation by population-scale genome sequencing

artículo científico publicado en 2011

Microduplications of 16p11.2 are associated with schizophrenia

artículo científico publicado en 2009

Order, Disorder, and Flexibility

artículo científico publicado en 2003

Paternally inherited cis-regulatory structural variants are associated with autism.

artículo científico publicado en 2018

Pathological unfoldomics of uncontrolled chaos: intrinsically disordered proteins and human diseases

artículo científico publicado en 2014

Predicted disorder-to-order transition mutations in IκBα disrupt function

artículo científico publicado en 2014

Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism.

scientific article published on 11 April 2014

Publisher Correction: A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex

artículo científico publicado en 2022

RNA association or phosphorylation of the RS domain prevents aggregation of RS domain-containing proteins

artículo científico publicado en 2007

Serine/arginine-rich splicing factors belong to a class of intrinsically disordered proteins

artículo científico publicado en 2006

Single-molecule conformational dynamics of fluctuating noncovalent DNA-protein interactions in DNA damage recognition.

artículo científico publicado en 2001

Spatiotemporal 16p11.2 protein network implicates cortical late mid-fetal brain development and KCTD13-Cul3-RhoA pathway in psychiatric diseases

artículo científico publicado en 2015

The importance of intrinsic disorder for protein phosphorylation

artículo científico publicado en 2004

Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder

artículo científico publicado en 2018

Two Sample Logo: a graphical representation of the differences between two sets of sequence alignments

artículo científico publicado en 2006

Unfoldomics of human diseases: linking protein intrinsic disorder with diseases

artículo científico publicado en 2009

When loss-of-function is loss of function: assessing mutational signatures and impact of loss-of-function genetic variants.

artículo científico publicado en 2017

Whole-genome sequencing in autism identifies hot spots for de novo germline mutation.

artículo científico publicado en 2012

Widespread Expansion of Protein Interaction Capabilities by Alternative Splicing

artículo científico publicado en 2016

Lista de obras de Lilia M. Iakoucheva

A Protein Domain-Based Interactome Network for C. elegans Early Embryogenesis

A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex

A protein domain-based interactome network for C. elegans early embryogenesis

A proteome-scale map of the human interactome network

Aberrant mobility phenomena of the DNA repair protein XPA

Autism-linked Cullin3 germline haploinsufficiency impacts cytoskeletal dynamics and cortical neurogenesis through RhoA signaling

Combining prediction, computation and experiment for the characterization of protein disorder

Comprehensive Analyses of Tissue-Specific Networks with Implications to Psychiatric Diseases

Cortical organoids model early brain development disrupted by 16p11.2 copy number variants in autism

DisProt: a database of protein disorder

Disease-associated mutations disrupt functionally important regions of intrinsic protein disorder

Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia

Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia

Equilibrium and stop-flow kinetic studies of fluorescently labeled DNA substrates with DNA repair proteins XPA and replication protein A.

Extended X-ray absorption fine structure evidence for a single metal binding domain in Xenopus laevis nucleotide excision repair protein XPA.

Flexible nets. The roles of intrinsic disorder in protein interaction networks.

Frequency and Complexity of De Novo Structural Mutation in Autism

Full-length isoform transcriptome of the developing human brain provides further insights into autism

Functional anthology of intrinsic disorder. 1. Biological processes and functions of proteins with long disordered regions.

Functional anthology of intrinsic disorder. 2. Cellular components, domains, technical terms, developmental processes, and coding sequence diversities correlated with long disordered regions

Functional anthology of intrinsic disorder. 3. Ligands, post-translational modifications, and diseases associated with intrinsically disordered proteins.

Graphlet kernels for prediction of functional residues in protein structures

Identification, analysis, and prediction of protein ubiquitination sites

Inferring the molecular and phenotypic impact of amino acid variants with MutPred2

Intrinsic disorder and functional proteomics

Intrinsic disorder in cell-signaling and cancer-associated proteins

Intrinsic disorder is a common feature of hub proteins from four eukaryotic interactomes

Mapping copy number variation by population-scale genome sequencing

Microduplications of 16p11.2 are associated with schizophrenia

Order, Disorder, and Flexibility

Paternally inherited cis-regulatory structural variants are associated with autism.

Pathological unfoldomics of uncontrolled chaos: intrinsically disordered proteins and human diseases

Predicted disorder-to-order transition mutations in IκBα disrupt function

Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism.

Publisher Correction: A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex

RNA association or phosphorylation of the RS domain prevents aggregation of RS domain-containing proteins

Serine/arginine-rich splicing factors belong to a class of intrinsically disordered proteins

Single-molecule conformational dynamics of fluctuating noncovalent DNA-protein interactions in DNA damage recognition.

Spatiotemporal 16p11.2 protein network implicates cortical late mid-fetal brain development and KCTD13-Cul3-RhoA pathway in psychiatric diseases

The importance of intrinsic disorder for protein phosphorylation

Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder

Two Sample Logo: a graphical representation of the differences between two sets of sequence alignments

Unfoldomics of human diseases: linking protein intrinsic disorder with diseases

When loss-of-function is loss of function: assessing mutational signatures and impact of loss-of-function genetic variants.

Whole-genome sequencing in autism identifies hot spots for de novo germline mutation.

Widespread Expansion of Protein Interaction Capabilities by Alternative Splicing