Lista de obras - de La Cruz X - Dominio Público Uruguay

A fast method for the determination of fractional contributions to solvation in proteins.

artículo científico publicado en 2006

A new procedure for constructing peptides into a given Calpha chain.

artículo científico publicado en 1998

A procedure for identifying homologous alternative splicing events

artículo científico publicado en 2007

Alternative splicing mechanisms for the modulation of protein function: conservation between human and other species.

artículo científico publicado en 2004

Alternative splicing of transcription factors' genes: beyond the increase of proteome diversity

scientific article published on 12 July 2009

An atomistic view to the gas phase proteome

artículo científico publicado en 2009

Assessment of blind predictions of the clinical significance of BRCA1 and BRCA2 variants

scientific article published on 23 August 2019

Autoacetylation regulates P/CAF nuclear localization.

artículo científico publicado en 2008

BRCA1- and BRCA2-specific in silico tools for variant interpretation in the CAGI 5 ENIGMA challenge

artículo científico publicado en 2019

Cerebrospinal fluid-derived circulating tumour DNA better represents the genomic alterations of brain tumours than plasma.

artículo científico publicado en 2015

Characterization of disease-associated single amino acid polymorphisms in terms of sequence and structure properties.

artículo científico publicado en 2002

Characterization of structural variability sheds light on the specificity determinants of the interaction between effector domains and histone tails

artículo científico publicado en 2010

Classical molecular interaction potentials: improved setup procedure in molecular dynamics simulations of proteins.

artículo científico publicado en 2001

Clinical and structural impact of mutations affecting the residue Phe367 of FOXP3 in patients with IPEX syndrome.

artículo científico publicado en 2015

Compensated pathogenic variants in coagulation factors VIII and IX present complex mapping between molecular impact and hemophilia severity

artículo científico publicado en 2019

Data Mining of Molecular Dynamic Trajectories of Nucleic Acids

Discrete representations of the protein C alpha chain

artículo científico publicado en 1997

EZH2 regulates neuroepithelium structure and neuroblast proliferation by repressing p21.

artículo científico publicado en 2016

Exploring the Essential Dynamics of B-DNA

artículo científico publicado en 2005

Genome-wide analysis reveals that Smad3 and JMJD3 HDM co-activate the neural developmental program.

artículo científico publicado en 2012

Identification and characterization of a novel splice site mutation in the SERPING1 gene in a family with hereditary angioedema.

artículo científico publicado en 2013

Identification and characterization of the novel point mutation m.3634A>G in the mitochondrial MT-ND1 gene associated with LHON syndrome.

artículo científico publicado en 2016

Investigation of shape variations in the antibody binding site by molecular dynamics computer simulation

artículo científico publicado en 1994

Involvement of chromatin and histone deacetylation in SV40 T antigen transcription regulation.

artículo científico publicado en 2007

Molecular damage in Fabry disease: characterization and prediction of alpha-galactosidase A pathological mutations

artículo científico publicado en 2014

Molecular dynamics study of naturally existing cavity couplings in proteins

artículo científico publicado en 2015

Novel Mutations Causing C5 Deficiency in Three North-African Families.

artículo científico publicado en 2016

PMUT: a web-based tool for the annotation of pathological mutations on proteins.

artículo científico publicado en 2005

Partition of protein solvation into group contributions from molecular dynamics simulations.

artículo científico publicado en 2005

Preservation of protein clefts in comparative models.

artículo científico publicado en 2008

PupasView: a visual tool for selecting suitable SNPs, with putative pathological effect in genes, for genotyping purposes

artículo científico publicado en 2005

Representation of noncovalent interactions in protein structures.

artículo científico publicado en 1992

Scoring by Intermolecular Pairwise Propensities of Exposed Residues (SIPPER): A New Efficient Potential for Protein−Protein Docking

artículo científico publicado en 2011

Sequence-based prediction of pathological mutations

artículo científico publicado en 2004

The (in)dependence of alternative splicing and gene duplication

artículo científico publicado en 2007

The Complementarity Between Protein-Specific and General Pathogenicity Predictors for Amino Acid Substitutions

artículo científico publicado en 2016

The SV40 T antigen modulates CBP histone acetyltransferase activity

artículo científico publicado en 2003

The functional modulation of epigenetic regulators by alternative splicing

artículo científico publicado en 2007

The relationship between gene isoform multiplicity, number of exons and protein divergence

artículo científico publicado en 2013

Toward predicting protein topology: an approach to identifying beta hairpins.

artículo científico publicado en 2002

Triplex-forming oligonucleotide target sequences in the human genome.

artículo científico publicado en 2004

Use of bioinformatics tools for the annotation of disease-associated mutations in animal models

artículo científico publicado en 2005

Use of surface area computations to describe atom-atom interactions.

artículo científico publicado en 2001

Lista de obras de de La Cruz X

A fast method for the determination of fractional contributions to solvation in proteins.

A new procedure for constructing peptides into a given Calpha chain.

A procedure for identifying homologous alternative splicing events

Alternative splicing mechanisms for the modulation of protein function: conservation between human and other species.

Alternative splicing of transcription factors' genes: beyond the increase of proteome diversity

An atomistic view to the gas phase proteome

Assessment of blind predictions of the clinical significance of BRCA1 and BRCA2 variants

Autoacetylation regulates P/CAF nuclear localization.

BRCA1- and BRCA2-specific in silico tools for variant interpretation in the CAGI 5 ENIGMA challenge

Cerebrospinal fluid-derived circulating tumour DNA better represents the genomic alterations of brain tumours than plasma.

Characterization of disease-associated single amino acid polymorphisms in terms of sequence and structure properties.

Characterization of structural variability sheds light on the specificity determinants of the interaction between effector domains and histone tails

Classical molecular interaction potentials: improved setup procedure in molecular dynamics simulations of proteins.

Clinical and structural impact of mutations affecting the residue Phe367 of FOXP3 in patients with IPEX syndrome.

Compensated pathogenic variants in coagulation factors VIII and IX present complex mapping between molecular impact and hemophilia severity

Data Mining of Molecular Dynamic Trajectories of Nucleic Acids

Discrete representations of the protein C alpha chain

EZH2 regulates neuroepithelium structure and neuroblast proliferation by repressing p21.

Exploring the Essential Dynamics of B-DNA

Genome-wide analysis reveals that Smad3 and JMJD3 HDM co-activate the neural developmental program.

Identification and characterization of a novel splice site mutation in the SERPING1 gene in a family with hereditary angioedema.

Identification and characterization of the novel point mutation m.3634A>G in the mitochondrial MT-ND1 gene associated with LHON syndrome.

Investigation of shape variations in the antibody binding site by molecular dynamics computer simulation

Involvement of chromatin and histone deacetylation in SV40 T antigen transcription regulation.

Molecular damage in Fabry disease: characterization and prediction of alpha-galactosidase A pathological mutations

Molecular dynamics study of naturally existing cavity couplings in proteins

Novel Mutations Causing C5 Deficiency in Three North-African Families.

PMUT: a web-based tool for the annotation of pathological mutations on proteins.

Partition of protein solvation into group contributions from molecular dynamics simulations.

Preservation of protein clefts in comparative models.

PupasView: a visual tool for selecting suitable SNPs, with putative pathological effect in genes, for genotyping purposes

Representation of noncovalent interactions in protein structures.

Scoring by Intermolecular Pairwise Propensities of Exposed Residues (SIPPER): A New Efficient Potential for Protein−Protein Docking

Sequence-based prediction of pathological mutations

The (in)dependence of alternative splicing and gene duplication

The Complementarity Between Protein-Specific and General Pathogenicity Predictors for Amino Acid Substitutions

The SV40 T antigen modulates CBP histone acetyltransferase activity

The functional modulation of epigenetic regulators by alternative splicing

The relationship between gene isoform multiplicity, number of exons and protein divergence

Toward predicting protein topology: an approach to identifying beta hairpins.

Triplex-forming oligonucleotide target sequences in the human genome.

Use of bioinformatics tools for the annotation of disease-associated mutations in animal models

Use of surface area computations to describe atom-atom interactions.