Preservation of protein clefts in comparative models

por Piedra, David, Lois, Sergi, de la Cruz, Xavier
Publicado 2008

Alternative Splicing of Transcription Factors' Genes: Beyond the Increase of Proteome Diversity

por Talavera, David, Orozco, Modesto, de la Cruz, Xavier
Publicado 2009

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

por Marín, Òscar, Aguirre, Josu, de la Cruz, Xavier
Publicado 2019

Towards a New, Endophenotype-Based Strategy for Pathogenicity Prediction in BRCA1 and BRCA2: In Silico Modeling of the Outcome of HDR/SGE Assays for Missense Variants

por Özkan, Selen, Padilla, Natàlia, de la Cruz, Xavier
Publicado 2021

A procedure for identifying homologous alternative splicing events

por Talavera, David, Hospital, Adam, Orozco, Modesto, de la Cruz, Xavier
Publicado 2007

The functional modulation of epigenetic regulators by alternative splicing

por Lois, Sergio, Blanco, Noemí, Martínez-Balbás, Marian, de la Cruz, Xavier
Publicado 2007

Development of pathogenicity predictors specific for variants that do not comply with clinical guidelines for the use of computational evidence

por de la Campa, Elena Álvarez, Padilla, Natàlia, de la Cruz, Xavier
Publicado 2017

The (In)dependence of Alternative Splicing and Gene Duplication

por Talavera, David, Vogel, Christine, Orozco, Modesto, Teichmann, Sarah A, de la Cruz, Xavier
Publicado 2007

Structural and Computational Characterization of Disease-Related Mutations Involved in Protein-Protein Interfaces

por Navío, Dàmaris, Rosell, Mireia, Aguirre, Josu, de la Cruz, Xavier, Fernández-Recio, Juan
Publicado 2019

Choosing Variant Interpretation Tools for Clinical Applications: Context Matters

por Aguirre, Josu, Padilla, Natàlia, Özkan, Selen, Riera, Casandra, Feliubadaló, Lídia, de la Cruz, Xavier
Publicado 2023

PMut: a web-based tool for the annotation of pathological variants on proteins, 2017 update

por López-Ferrando, Víctor, Gazzo, Andrea, de la Cruz, Xavier, Orozco, Modesto, Gelpí, Josep Ll
Publicado 2017

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

por Conde, Lucía, Vaquerizas, Juan M., Ferrer-Costa, Carles, de la Cruz, Xavier, Orozco, Modesto, Dopazo, Joaquín
Publicado 2005

The Relationship between Gene Isoform Multiplicity, Number of Exons and Protein Divergence

por Morata, Jordi, Béjar, Santi, Talavera, David, Riera, Casandra, Lois, Sergio, de Xaxars, Gemma Mas, de la Cruz, Xavier
Publicado 2013

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

por Valls, Ester, Blanco-García, Noemí, Aquizu, Naiara, Piedra, David, Estarás, Conchi, de la Cruz, Xavier, Martínez-Balbás, Marian A.
Publicado 2007

Molecular Dynamics Study of Naturally Existing Cavity Couplings in Proteins

por Barbany, Montserrat, Meyer, Tim, Hospital, Adam, Faustino, Ignacio, D'Abramo, Marco, Morata, Jordi, Orozco, Modesto, de la Cruz, Xavier
Publicado 2015

EZH2 regulates neuroepithelium structure and neuroblast proliferation by repressing p21

por Akizu, Naiara, García, María Alejandra, Estarás, Conchi, Fueyo, Raquel, Badosa, Carmen, de la Cruz, Xavier, Martínez-Balbás, Marian A.
Publicado 2016

FHLdb: A Comprehensive Database on the Molecular Basis of Familial Hemophagocytic Lymphohistiocytosis

por Viñas-Giménez, Laura, Padilla, Natàlia, Batlle-Masó, Laura, Casals, Ferran, Rivière, Jacques G., Martínez-Gallo, Mónica, de la Cruz, Xavier, Colobran, Roger
Publicado 2020

Case Report: Characterizing the Role of the STXBP2-R190C Monoallelic Mutation Found in a Patient With Hemophagocytic Syndrome and Langerhans Cell Histiocytosis

por Viñas-Giménez, Laura, Rincón, Rafael, Colobran, Roger, de la Cruz, Xavier, Celis, Verónica Paola, Dapena, José Luis, Alsina, Laia, Sayós, Joan, Martínez-Gallo, Mónica
Publicado 2021

Functional consequences of transferrin receptor-2 mutations causing hereditary hemochromatosis type 3

por Joshi, Ricky, Shvartsman, Maya, Morán, Erica, Lois, Sergi, Aranda, Jessica, Barqué, Anna, de la Cruz, Xavier, Bruguera, Miquel, Vagace, José Manuel, Gervasini, Guillermo, Sanz, Cristina, Sánchez, Mayka
Publicado 2015

Lineage specific transcription factors and epigenetic regulators mediate TGFβ-dependent enhancer activation

por Fueyo, Raquel, Iacobucci, Simona, Pappa, Stella, Estarás, Conchi, Lois, Sergio, Vicioso-Mantis, Marta, Navarro, Claudia, Cruz-Molina, Sara, Reyes, José Carlos, Rada-Iglesias, Álvaro, de la Cruz, Xavier, Martínez-Balbás, Marian A
Publicado 2018