Advancing Epigenetics Towards Systems Biology

List of EpiGeneSys publications


Information is retrieved from

pubmed

Back to the index page

Group Leader:
Manel Esteller138 Publications.

2016

Associations between whole peripheral blood fatty acids and DNA methylation in humans.

Sci Rep 2016 May 16;6:25867

de la Rocha C, Pérez-Mojica JE, León SZ, Cervantes-Paz B, Tristán-Flores FE, Rodríguez-Ríos D, Molina-Torres J, Ramírez-Chávez E, Alvarado-Caudillo Y, Carmona FJ, Esteller M, Hernández-Rivas R, Wrobel K, Wrobel K, Zaina S, Lund G

View on PubMed

Arachidonic and oleic acid exert distinct effects on the DNA methylome.

Epigenetics 2016 Apr 18;:1-14

Silva-Martínez GA, Rodríguez-Ríos D, Alvarado-Caudillo Y, Vaquero A, Esteller M, Carmona FJ, Moran S, Nielsen FC, Wickström-Lindholm M, Wrobel K, Wrobel K, Barbosa-Sabanero G, Zaina S, Lund G

View on PubMed

Study of breast cancer incidence in patients of lymphangioleiomyomatosis.

Breast Cancer Res Treat 2016 Feb;156(1):195-201

Nuñez O, Román A, Johnson SR, Inoue Y, Hirose M, Casanova Á, de Garibay GR, Herranz C, Bueno-Moreno G, Boni J, Mateo F, Petit A, Climent F, Soler T, Vidal A, Sánchez-Mut JV, Esteller M, López JI, García N, Gumà A, Ortega R, Plà MJ, Campos M, Ansótegui E, Molina-Molina M, Valenzuela C, Ussetti P, Laporta R, Ancochea J, Xaubet A, Pollán M, Pujana MA

View on PubMed

A novel epigenetic signature for early diagnosis in lung cancer.

Clin Cancer Res 2016 Feb 3;

Diaz-Lagares A, Mendez-Gonzalez J, Hervas D, Saigi M, Pajares MJ, Garcia D, Crujeiras AB, Pio R, Montuenga LM, Zulueta J, Nadal E, Rosell A, Esteller M, Sandoval-Del Amor J

View on PubMed

Retraction: A TARBP2 mutation in human cancer impairs microRNA processing and DICER1 function.

Nat Genet 2016 Jan 27;48(2):221

Melo SA, Ropero S, Moutinho C, Aaltonen LA, Yamamoto H, Calin GA, Rossi S, Fernandez AF, Carneiro F, Oliveira C, Ferreira B, Liu CG, Villanueva A, Capella G, Schwartz S Jr, Shiekhattar R, Esteller M

View on PubMed

Epigenomic analysis detects aberrant super-enhancer DNA methylation in human cancer.

Genome Biol 2016 Jan 26;17(1):11

Heyn H, Vidal E, Ferreira HJ, Vizoso M, Sayols S, Gomez A, Moran S, Boque-Sastre R, Guil S, Martinez-Cardus A, Lin CY, Royo R, Sanchez-Mut JV, Martinez R, Gut M, Torrents D, Orozco M, Gut I, Young RA, Esteller M

View on PubMed

Transcriptomic profiling of urine extracellular vesicles reveals alterations of CDH3 in prostate cancer.

Oncotarget 2016 Jan 12;

Royo F, Zuñiga-Garcia P, Torrano V, Loizaga A, Sanchez-Mosquera P, Ugalde-Olano A, González E, Cortazar AR, Palomo L, Fernández-Ruiz S, Lacasa-Viscasillas I, Berdasco M, Sutherland JD, Barrio R, Zabala-Letona A, Martín-Martín N, Arruabarrena-Aristorena A, Valcarcel-Jimenez L, Caro-Maldonado A, Gonzalez-Tampan J, Cachi-Fuentes G, Esteller M, Aransay AM, Unda M, Falcón-Pérez JM, Carracedo A

View on PubMed

IL-4 orchestrates STAT6-mediated DNA demethylation leading to dendritic cell differentiation.

Genome Biol 2016 Jan 13;17(1):4

Vento-Tormo R, Company C, Rodríguez-Ubreva J, de la Rica L, Urquiza JM, Javierre BM, Sabarinathan R, Luque A, Esteller M, Aran JM, Álvarez-Errico D, Ballestar E

View on PubMed

Cancer stem-like cells act at via distinct signaling pathways in promoting late stages of malignant progression.

Cancer Res 2015 Dec 30;

da Silva-Diz V, Simón-Extremera P, Bernat-Peguera A, de Sostoa J, Urpí M, Penin RM, Pérez Sidelnikova D, Bermejo O, Viñals JM, Rodolosse A, Gonzalez-Suarez E, Gómez Moruno A, Pujana MA, Esteller M, Villanueva A, Viñals F, Muñoz P

View on PubMed

2015

Validation of a DNA methylation microarray for 850,000 CpG sites of the human genome enriched in enhancer sequences.

Epigenomics 2015 Dec 17;

Moran S, Arribas C, Esteller M

View on PubMed

Latest publications

2017-06-27

The Histone Acetyltransferase Mst2 Protects Active Chromatin from Epigenetic Silencing by Acetylating the Ubiquitin Ligase Brl1.

Read more
2017-05-26

Proliferation Drives Aging-Related Functional Decline in a Subpopulation of the Hematopoietic Stem Cell Compartment.

Read more
2017-04-30

The impact of rare and low-frequency genetic variants in common disease.

Read more