Search Results - "Renedo, Monica"

Fluorescence in situ hybridization improves the detection of 5q31 deletion in myelodysplastic syndromes without cytogenetic evidence of 5q by Mallo, Mar, Arenillas, Leonor, Espinet, Blanca, Salido, Marta, Hernandez, Jesus M{a}, Lumbreras, Eva, del Rey, Monica, Arranz, Eva, Ramiro, Soraya, Font, Patricia, Gonzalez, Olga, Renedo, Monica, Cervera, Jose, Such, Esperanza, Sanz, Guillermo F, Luno, Elisa, Sanzo, Carmen, Gonzalez, Miriam, Calasanz, Maria Jose, Mayans, Jose, Garcia-Ballesteros, Carlos, Amigo, Victoria, Collado, Rosa, Oliver, Isabel, Carbonell, Felix, Bureo, Encarna, Insunza, Andres, Yanez, Lucrecia, Muruzabal, Maria Jose, Gomez-Beltran, Elena, Andreu, Rafael, Leon, Pilar, Gomez, Valle, Sanz, Angeles, Casasola, Natalia, Moreno, Esperanza, Alegre, Adrian, Martin, Maria Luisa, Pedro, Carmen, Serrano, Sergi, Florensa, Lourdes, Sole, Francesc

“…1 Laboratori de Citogenètica i Biologia Molecular, Laboratori de Citologia Hematològica. Servei de Patologia, IMAS. GRETNHE, IMIM-Hospital del Mar, Barcelona 2…”
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Toward a four-dimensional model of burnout : A multigroup factor-analytic study including depersonalization and cynicism by SALANOVA, Marisa, LLORENS, Susana, GARCIA-RENEDO, Monica, BURRIEL, Raül, BRESO, Edgar, SCHAUFELI, Wilmar B

“…This article investigated whether cynicism and depersonalization are two different dimensions of burnout or whether they maybe collapsed into one construct of…”
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The molecular basis of alkaptonuria by Granadino, Begoña, Fernández-Cañón, José M, De Córdoba, Santiago Rodríguez, De Bernabé, Daniel Beltrán-Valero, Renedo, Mónica, Fernández-Ruiz, Elena, Peñalva, Miguel A

“…Alkaptonuria (AKU) occupies a unique place in the history of human genetics because it was the first disease to be interpreted as a mendelian recessive trait…”
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Phenotypic Aberrations of Myeloid CD34+ Cells in Patients with Myelodysplastic Syndrome (MDS): Clinical Significance and Correlation with Cytogenetics Abnormalities by Subira, Dolores, Font, Patricia, Arranz, Eva, Soraya, Ramiro B, Castanon, Susana, Renedo, Mónica, Blas, Carlos, Garcia B, Maria F., Gonzalez B, Olga, Tomas, José F., Fernandez-Rañada, José M.

“…Expression of abnormal markers in myeloid CD34+ cells of patients with MDS is common, but few immunophenotypic data have been compiled so far. Based on the…”
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Towards a Four-Dimensional Model of Burnout: A Multigroup Factor-Analytic Study Including Depersonalization and Cynicism by Salanova, Marisa, Llorens, Susana, García-Renedo, Mónica, Burriel, Raül, BresÓ, Edgar, Schaufeli, Wilmar B.

“…This article investigated whether cynicism and depersonalization are two different dimensions of burnout or whether they may be collapsed into one construct of…”
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Linear and Whorled Nevoid Hypermelanosis and Axenfeld-Rieger Anomaly: A Novel Association by LLAMAS-VELASCO, Mar, EGUREN, Cristina, ARRANZ, Eva, RENEDO, Monica, DE ARGILA, Diego, GARCIA-DIEZ, Amaro

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Molecular and clinical study of 61 Angelman syndrome patients by Saitoh, S, Harada, N, Jinno, Y, Hashimoto, K, Imaizumi, K, Kuroki, Y, Fukushima, Y, Sugimoto, T, Renedo, M, Wagstaff, J

“…We analyzed 61 Angelman syndrome (AS) patients by cytogenetic and molecular techniques. On the basis of molecular findings, the patients were classified into…”
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Deletion of sequences flanking the t(9;22) breakpoint: a secondary genetic event associated with loss of cytogenetic response to interferon in a Philadelphia‐positive chronic myeloid leukaemia patient by Arranz, Eva, Gil‐Fernández, Juan José, Ramiro, Soraya, Blas, Carlos, Renedo, Mónica, Alegre, Adrián, Escudero, Antonio, Fernández‐Rañada, Jose María

“…We present a Ph‐positive chronic myeloid leukaemia patient who lost a complete cytogenetic response (CCR) of 23 months duration at the time of detection of a…”
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Human KLRF1, a novel member of the killer cell lectin‐like receptor gene family: molecular characterization, genomic structure, physical mapping to the NK gene complex and expression analysis by Roda‐Navarro, Pedro, Arce, Ignacio, Renedo, Mónica, Montgomery, Kate, Kucherlapati, Raju, Fernández‐Ruiz, Elena

“…The human NK gene complex localized on chromosome 12p12.3 – p13.2 codes for several lectin‐like receptor genes expressed by NK cells as well as by other…”
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Linear and whorled nevoid hypermelanosis and Axenfeld-Rieger anomaly: a novel association by Llamas-Velasco, Mar, Eguren, Cristina, Arranz, Eva, Renedo, Monica, de Argila, Diego, García-Díez, Amaro

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A Sequence-Ready Physical Map of the Region Containing the Human Natural Killer Gene Complex on Chromosome 12p12.3–p13.2 by Renedo, Mónica, Arce, Ignacio, Montgomery, Kate, Roda-Navarro, Pedro, Lee, Eunice, Kucherlapati, Raju, Fernández-Ruiz, Elena

“…We developed a sequence-ready physical map of a part of human chromosome 12p12.3–p13.2 where the natural killer gene complex (NKC) is located. The NKC includes…”
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The human natural killer gene complex is located on chromosome 12p12-p13 by Renedo, M, Arce, I, Rodríguez, A, Carretero, M, Lanier, L L, López-Botet, M, Fernández-Ruiz, E

“…Natural killer (NK) cells preferentially express several type II glycoproteins of the calcium-dependent lectin superfamily. The genes coding for these…”
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HumanKLRF1, a novel member of the killer cell lectin-like receptor gene family: molecular characterization, genomic structure, physical mapping to the NK gene complex and expression analysis by Roda-Navarro, Pedro, Arce, Ignacio, Renedo, Mónica, Montgomery, Kate, Kucherlapati, Raju, Fernández-Ruiz, Elena

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