Zobrazeno 1 - 10
of 116
pro vyhledávání: '"Carles, Besses"'
Autor:
Nicolás Martínez-Calle, Marien Pascual, Raquel Ordoñez, Edurne San José Enériz, Marta Kulis, Estíbaliz Miranda, Elisabeth Guruceaga, Víctor Segura, María José Larráyoz, Beatriz Bellosillo, María José Calasanz, Carles Besses, José Rifón, José I. Martín-Subero, Xabier Agirre, Felipe Prosper
Publikováno v:
Haematologica, Vol 104, Iss 8 (2019)
In this study we interrogated the DNA methylome of myelofibrosis patients using high-density DNA methylation arrays. We detected 35,215 differentially methylated CpG, corresponding to 10,253 genes, between myelofibrosis patients and healthy controls.
Externí odkaz:
https://doaj.org/article/92c068858094471b9449973937dec2fd
Autor:
Nieves Garcia-Gisbert, Sara Garcia-Ávila, Brayan Merchán, Marta Salido, Concepción Fernández-Rodríguez, Joan Gibert, Lierni Fernández-Ibarrondo, Laura Camacho, Marta Lafuente, Raquel Longarón, Blanca Espinet, Patricia Vélez, Ramon M. Pujol, Marcio Andrade-Campos, Leonor Arenillas, Antonio Salar, Xavier Calvo, Carles Besses, Beatriz Bellosillo
Publikováno v:
Blood Advances. 6:3178-3188
Molecular and cytogenetic studies are essential for diagnosis and prognosis in patients with myelodysplastic syndromes (MDSs). Cell-free DNA (cfDNA) analysis has been reported to be a reliable noninvasive approach for detecting molecular abnormalitie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43e1615c3e869303f9b4eebffe4c4a9e
https://doi.org/10.1182/bloodadvances.2021006565
https://doi.org/10.1182/bloodadvances.2021006565
Autor:
Laura, Lo Riso, Gardenia, Vargas-Parra, Gemma, Navarro, Leonor, Arenillas, Lierni, Fernández-Ibarrondo, Beatriz, Robredo, Carmen, Ballester, Bernardo, López, Albert, Perez-Montaña, Antonia, Sampol, Lourdes, Florensa, Carles, Besses, María Antonia, Duran, Beatriz, Bellosillo
Publikováno v:
Genes. 13(10)
Primary familial and congenital polycythemia is a rare disease characterized by an increase in red cell mass that may be due to pathogenic variants in the EPO receptor (iEPOR/i) gene. To date, 33 genetic variants have been reported to be associated.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::63b6d0a65a178fe54a7178c5e0c53566
https://pubmed.ncbi.nlm.nih.gov/36292571
https://pubmed.ncbi.nlm.nih.gov/36292571
Publikováno v:
Blood. 140:3978-3979
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::550646c24b90faa1d9bdd57f91551a53
https://doi.org/10.1182/blood-2022-162714
https://doi.org/10.1182/blood-2022-162714
Autor:
Laura Lo Riso, Gardenia Vargas-Parra, Gemma Navarro, Leonor Arenillas, Lierni Fernández-Ibarrondo, Beatriz Robredo, Carmen Ballester, Bernardo López, Albert Perez-Montaña, Antonia Sampol, Lourdes Florensa, Carles Besses, María Antonia Duran, Beatriz Bellosillo
Publikováno v:
Genes. 13:1686
Primary familial and congenital polycythemia is a rare disease characterized by an increase in red cell mass that may be due to pathogenic variants in the EPO receptor (EPOR) gene. To date, 33 genetic variants have been reported to be associated. We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbc70ea3df4fd53aaf4a3bc8e5f282ea
https://doi.org/10.3390/genes13101686
https://doi.org/10.3390/genes13101686
Autor:
Juan-Carlos Hernández-Boluda, Arturo Pereira, Montse Gómez, Concepción Boqué, Francisca Ferrer-Marín, José-María Raya, Valentín García-Gutiérrez, Ana Kerguelen, Blanca Xicoy, Pere Barba, Jesús Martínez, Elisa Luño, Alberto Alvarez-Larrán, Joaquín Martínez-López, Elisa Arbelo, Carles Besses
Publikováno v:
Haematologica, Vol 99, Iss 4 (2014)
Externí odkaz:
https://doaj.org/article/a31a6ae75bd5428a94102665208c71e1
Autor:
Cristina Pérez, Marien Pascual, José Ignacio Martín-Subero, Beatriz Bellosillo, Victor Segura, Eric Delabesse, Sara Álvarez, María José Larrayoz, José Rifón, Juan Cruz Cigudosa, Carles Besses, María José Calasanz, Nicholas C.P. Cross, Felipe Prósper, Xabier Agirre
Publikováno v:
Haematologica, Vol 98, Iss 9 (2013)
Most DNA methylation studies in classic Philadelphia-negative myeloproliferative neoplasms have been performed on a gene-by-gene basis. Therefore, a more comprehensive methylation profiling is needed to study the implications of this epigenetic marke
Externí odkaz:
https://doaj.org/article/9eeba88cea10444aaafc6a58439ca425
Autor:
Mar García, Beatriz Bellosillo, Blanca Sánchez-González, Francesc García-Payarols, Agustin Seoane, Ana Maria Ferrer, Eva Gimeno, Luis Eugenio Barranco, Ariadna Torner, Francesc Solé, Carles Besses, Sergi Serrano, Antonio Salar
Publikováno v:
PLoS ONE, Vol 7, Iss 12, p e51681 (2012)
PURPOSE: FOXP3+ regulatory T cells (Treg) play an essential role in modulating host responses to tumors and infections. The role of these cells in the pathogenesis of MALT lymphomas remains unknown. The aims of the study were to quantify the number o
Externí odkaz:
https://doaj.org/article/d3761787cd66418ebdbd768a000135f5
Autor:
Ramon Diez-Feijoo, Antonio Salar, Patricia Velez, Concepción Fernández-Rodríguez, Leonor Arenillas, Marcio Andrade, Lierni Fernández-Ibarrondo, Beatriz Bellosillo, Nieves Garcia-Gisbert, Carles Besses, Raquel Longarón, Laura Camacho, Anna Angona, Joan Gibert
Publikováno v:
Blood. 138:3623-3623
Introduction : Hydroxyurea (HU) is the most widely used cytoreductive treatment for patients with essential thrombocythemia (ET) and polycythemia vera (PV) at high risk of thrombosis. It remains unknown whether long-term HU therapy modulates or promo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2860ebcd874d6115ced7d5411521cfbd
https://doi.org/10.1182/blood-2021-150491
https://doi.org/10.1182/blood-2021-150491
Autor:
Brayan Merchan, Sara Garcia-Avila, Marcio Andrade-Campos, Patricia Velez, Concepción Fernández-Rodríguez, Marta Lafuente, Lierni Fernández-Ibarrondo, Beatriz Bellosillo, Antonio Salar, Laura Camacho, Blanca Espinet, Marta Salido, Nieves Garcia-Gisbert, Carles Besses, Raquel Longarón, Xavier Calvo, Leonor Arenillas, Ramon M. Pujol, Joan Gibert
Publikováno v:
Blood. 138:2599-2599
Introduction. Myelodysplastic syndromes (MDS) are clonal heterogeneous disorders in which molecular studies and cytogenetics are essential for diagnosis, classification and prognosis. Cell-free DNA (cfDNA) analysis has been reported as a reliable non
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a15ff454945ff9c4386285d86f4bf37
https://doi.org/10.1182/blood-2021-148297
https://doi.org/10.1182/blood-2021-148297