Zobrazeno 1 - 10
of 25
pro vyhledávání: '"M. E. Sarasquete"'
Autor:
Maria Luisa Lozano, Luis Javier García-Frade, Ramón García-Sanz, M. del Rey, Rosa Fisac, M. J. Cebeira, Rafael Ramos, José María Bastida, José Ramón González-Porras, C. Aguilera, M. E. Sarasquete, J.M. Hernández-Rivas, Marcos González-Díaz, Emilia Pardal, M. E. Fontecha, B. Pérez, Susana Riesco, Rocío Benito, J. M. Martin-Antorán, Nuria Bermejo, M. C. Mendoza, Carlos Aguilar, María Paz Martínez, M. R. Cardesa, L. A. Silvestre
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
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[Introduction]: Molecular testing of Inherited bleeding coagulation disorders (IBCDs) not only offers confirmation of diagnosis but also aids in genetic counselling, prenatal diagnosis and in certain cases genotype–phenotype correlations are import
Autor:
Josefina Galende, Paloma Bárcena, Diego Alignani, Alfonso García de Coca, Maria-Luz Sanchez, Noemi Puig, Rebeca Cuello, Alberto Orfao, Maria-Victoria Mateos, Luis A. Corchete, María-Belén Vidriales, José L. Alonso, Abelardo Bárez, Bruno Paiva, Cristina Jimenez, Irene Aires-Mejia, Maria-Carmen Montes, Norma C. Gutiérrez, Ramón García-Sanz, Tomás José González-López, José Augusto Evangelho Hernandez, M. E. Sarasquete, Jesús F. San Miguel, Enrique M. Ocio, Fernando Escalante, Magdalena Sierra, José de Jesús Pérez, Emilia Pardal
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
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Although information about the molecular pathogenesis of Waldenström macroglobulinemia (WM) has significantly advanced, the precise cell of origin and the mechanisms behind WM transformation from immunoglobulin-M (IgM) monoclonal gammopathy of undet
Autor:
Ana Balanzategui, Gonzalo R. Ordóñez, Marta González, N. Puig, Miguel Alcoceba, Rocío Corral, M C Chillón, María Isabel Prieto-Conde, Luis Marín, Sara Alonso-Álvarez, Ramón García-Sanz, Carmen Jiménez, María García-Álvarez, Norma C. Gutiérrez, M. E. Sarasquete
Publikováno v:
Blood Cancer Journal
Transformation of Waldenström’s macroglobulinemia (WM) to diffuse large B-cell lymphoma (DLBCL) occurs in up to 10% of patients and is associated with an adverse outcome. Here we performed the first whole-exome sequencing study of WM patients who
Autor:
Ramón García-Sanz, Roberto Maldonado, Marcos González, María García-Álvarez, Carmen Jiménez, Norma C. Gutiérrez, M. Hernández-Ruano, Alicia Antón, M. E. Sarasquete, Isabel Prieto, Miguel Alcoceba, M C Chillón
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
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Chromosome 1q gains and 13q deletions are common cytogenetic aberrations in multiple myeloma (MM) that confer a poor prognosis. There are several techniques for the targeted study of these alterations, but interphase fluorescence in situ hybridizatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::435baab0387e2d9eb6e69b62ff02cf96
http://hdl.handle.net/10261/169073
http://hdl.handle.net/10261/169073
Autor:
M. E. Sarasquete, M.C. Chillón, María Isabel Prieto-Conde, Marcos González-Díaz, M.J. Larrayoz, Norma C. Gutiérrez, T. González-Martínez, M.J. Calasanz, Verónica González-Calle, Miguel Alcoceba, I. Vazquez, R. García-Sanz, Marta Fernandez-Mercado
Publikováno v:
HemaSphere. 3:453
Autor:
J.J. Lahuerta, Luis Marín, Rocío Corral, Ana Balanzategui, Marcos González, Patricia Martín-Jiménez, M. E. Sarasquete, J. Bladé, Miguel Alcoceba, Ramón García-Sanz, Ernesto Pérez-Persona, F.J. Fernandez-Calvo, J F San Miguel, M C Chillón, J M Hernández
Publikováno v:
Tissue Antigens. 71:548-551
The human leukocyte antigen (HLA) system could play an essential role in multiple myeloma (MM) disease control. This report describes the results comparing HLA-DRB1 phenotypic frequencies in 181 MM patients (53 smoldering/indolent MM and 128 symptoma
Autor:
M. E. Sarasquete, M C Chillón, R. López, Magdalena Sierra, J M Hernández, Marcos González, Adriana Armellini, A. Orfao, Miguel Alcoceba, J F San Miguel, Ramón García-Sanz, Marta Megido, M. Fuertes, Ana Balanzategui, J. Fernández-Calvo, Norma C. Gutiérrez
Publikováno v:
British Journal of Haematology. 141:212-215
RAN, ZHX2 and RCBTB2 (CHC1L) expression was evaluated by quantitative real time reverse transcription polymerase chain reaction in plasma cells from 85 monoclonal gammopathies: 58 symptomatic multiple myeloma (MM) (52 untreated, six relapsed), eight
Autor:
Jesús María Hernández-Rivas, J. Rodriguez, Cristina Robledo, Rocío Benito, Carlos Aguilar, María Hernández-Sánchez, Alfonso García de Coca, Marcos González, Eva Lumbreras, Carlos Vicente-Gutierrez, Natalia de las Heras, Ana E. Rodríguez-Vicente, Miguel Alcoceba, José-Ángel Hernández, A Martin, M. E. Sarasquete
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
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Deletion 13q (13q-) is the most common cytogenetic aberration in chronic lymphocytic leukemia (CLL) and is associated with the most favorable prognosis as the sole cytogenetic abnormality. However, it is heterogeneous whereby CLL patients with higher
Autor:
Fermín Sánchez-Guijo, Marcos González, Irena Misiewicz-Krzeminska, Luis Ignacio Sánchez-Abarca, Beatriz Rosón, Silvia Preciado, Sandra Muntión, Javier De Las Rivas, María Díez-Campelo, M. E. Sarasquete, Maria-Consuelo del Cañizo, Teresa L. Ramos
Publikováno v:
PLoS ONE
Digital.CSIC. Repositorio Institucional del CSIC
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PLoS ONE, Vol 11, Iss 2, p e0146722 (2016)
Digital.CSIC. Repositorio Institucional del CSIC
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PLoS ONE, Vol 11, Iss 2, p e0146722 (2016)
Exosomes/microvesicles (MVs) provide a mechanism of intercellular communication. Our hypothesis was that mesenchymal stromal cells (MSC) from myelodysplastic syndrome (MDS) patients could modify CD34 cells properties by MVs. They were isolated from M
Autor:
N. Puig, Quintero J, Rocío Corral, Ramón García-Sanz, Carmen Jiménez, Isabel Conde, Luis Marín, Ana Balanzategui, Jesús F. San-Miguel, M.V. Mateos, Norma C. Gutiérrez, Elena Sebastián, M. E. Sarasquete, Marcos González-Díaz, Miguel Alcoceba, M C Chillón
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
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Multiple myeloma (MM) pathogenesis has been explained for many years by the cancer biology dogma introduced in 1976 by Peter Nowell:1 first, a single plasma cell would be immortalized by an error in the immunoglobulin genes rearrangement process; the