S. Lois

发表

Prediction of pathological mutations in proteins: the challenge of integrating sequence conservation and structure stability principles

X. de la Cruz, C. Riera, S. Lois, 2014 .

Characterization of the impact of alternative splicing on protein dynamics: The cases of glutathione S‐transferase and ectodysplasin‐A isoforms

M. Orozco, T. Meyer, M. Barbany, 2012, Proteins.

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

David Talavera, J. Morata, X. de la Cruz, 2013, PloS one.

Preservation of protein clefts in comparative models

Xavier de la Cruz, David Piedra, X. de la Cruz, 2008, BMC Structural Biology.

Molecular damage in Fabry disease: Characterization and prediction of alpha‐galactosidase A pathological mutations

J. Montaner, X. de la Cruz, C. Riera, 2015, Proteins.

The functional modulation of epigenetic regulators by alternative splicing

X. de la Cruz, S. Lois, M. Martínez-Balbás, 2007, BMC Genomics.

The epigenetic landscape of Alu repeats delineates the structural and functional genomic architecture of colon cancer cells

M. Esteller, T. Vavouri, S. Lois, 2016, Genome research.

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

X. de la Cruz, S. Lois, N. Akizu, 2010, Epigenetics.

Identification of Germinal Neurofibromin Hotspots

S. Lois, J. Lacal, J. Triviño, 2022, Biomedicines.

Do protein motifs read the histone code?

X. de la Cruz, S. Lois, M. Martínez-Balbás, 2005, BioEssays : news and reviews in molecular, cellular and developmental biology.

Deconstruction of DNA Methylation Patterns During Myogenesis Reveals Specific Epigenetic Events in the Establishment of the Skeletal Muscle Lineage

I. Cases, S. Lois, M. Peinado, 2015, Stem cells.

Overlapping DNA Methylation Dynamics in Mouse Intestinal Cell Differentiation and Early Stages of Malignant Progression

A. Bigas, S. Lois, M. Peinado, 2015, PloS one.

The histone demethylase PHF8 is a molecular safeguard of the IFNγ response

X. de la Cruz, S. Lois, C. Caelles, 2017, Nucleic acids research.

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

Salvatore Piscuoglio, Xavier de la Cruz, Jordi Rodon, 2015, Nature Communications.

RNA-Seq Perspectives to Improve Clinical Diagnosis

Guillermo Marco-Puche, Sergio Lois, Javier Benítez, 2019, Front. Genet..

Next Generation Cytogenetics in Myeloid Hematological Neoplasms: Detection of CNVs and Translocations

I. Buño, S. Lois, M. Ballesteros, 2021, Cancers.

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

Á. Rada-Iglesias, X. de la Cruz, S. Lois, 2018, Nucleic acids research.

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

X. de la Cruz, S. Lois, R. Colobran, 2014, Clinical immunology.

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

Érica Morán, X. de la Cruz, S. Lois, 2015, Molecular genetics & genomic medicine.

Novel and atypical splicing mutation in a compound heterozygous UNC13D defect presenting in Familial Hemophagocytic Lymphohistiocytosis triggered by EBV infection.

M. Juan, S. Lois, R. Colobran, 2014, Clinical immunology.

Prefoldin-like Bud27 influences the transcription of ribosomal components and ribosome biogenesis in Saccharomyces cerevisiae

S. Lois, J. de la Cruz, J. Triviño, 2020, RNA.