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Autor:
Inês Crespo, Hermínio Tão, Ana Belen Nieto, Olinda Rebelo, Patrícia Domingues, Ana Luísa Vital, Maria del Carmen Patino, Marcos Barbosa, Maria Celeste Lopes, Catarina Resende Oliveira, Alberto Orfao, María Dolores Tabernero
Publikováno v:
PLoS ONE, Vol 7, Iss 9, p e46088 (2012)
BACKGROUND: Glioblastoma multiforme (GBM) displays multiple amplicons and homozygous deletions that involve relevant pathogenic genes and other genes whose role remains unknown. METHODOLOGY: Single-nucleotide polymorphism (SNP)-arrays were used to de
Externí odkaz:
https://doaj.org/article/f321f4f2408546848241f7b1334a5904
Autor:
Maria do Carmo Lopes, Hermínio Tão, Ana Filipa Guedes, Maria C. Patino-Alonso, Pablo Sousa, María Dolores Tabernero, Olinda Rebelo, María González-Tablas, Ana Luísa Vital, Ana Belen Nieto, Álvaro Otero, Pim J. French, Maria Rosário Almeida, Alberto Orfao, Luis A. Corchete, Marcos Barbosa, Inês Crespo
Publikováno v:
GREDOS: Repositorio Institucional de la Universidad de Salamanca
Universidad de Salamanca (USAL)
Digital.CSIC: Repositorio Institucional del CSIC
Consejo Superior de Investigaciones Científicas (CSIC)
GREDOS. Repositorio Institucional de la Universidad de Salamanca
instname
Digital.CSIC. Repositorio Institucional del CSIC
Oncotarget
Oncotarget, 9(46), 28083-28102. Impact Journals LLC
Universidad de Salamanca (USAL)
Digital.CSIC: Repositorio Institucional del CSIC
Consejo Superior de Investigaciones Científicas (CSIC)
GREDOS. Repositorio Institucional de la Universidad de Salamanca
instname
Digital.CSIC. Repositorio Institucional del CSIC
Oncotarget
Oncotarget, 9(46), 28083-28102. Impact Journals LLC
Several classification systems have been proposed to address genomic heterogeneity of glioblastoma multiforme, but they either showed limited prognostic value and/or are difficult to implement in routine diagnostics. Here we propose a prognostic stra
Autor:
María Dolores Tabernero, Catarina de Oliveira, Pablo Sousa, Álvaro Otero, Cristina Teodosio, Patrícia Domingues, Ana Belen Nieto, Alberto Orfao, Maria do Carmo Lopes, Jesús María Gonçalves
Publikováno v:
Neuropathology and Applied Neurobiology. 41:319-332
Aims Limited information exists about the impact of cytogenetic alterations on the protein expression profiles of individual meningioma cells and their association with the clinicohistopathological characteristics of the disease. The aim of this stud
Publikováno v:
Revista Colombiana de Estadística, Vol 37, Iss 2, Pp 367-397 (2014)
Repositorio UN
Universidad Nacional de Colombia
instacron:Universidad Nacional de Colombia
Repositorio UN
Universidad Nacional de Colombia
instacron:Universidad Nacional de Colombia
A biplot is a graphical representation of two-mode multivariate data based on markers for rows and columns often provided in a two-dimensional space. These markers define parameters that help to interpret goodness of fit, quality of the representatio
Autor:
Maria do Carmo Lopes, Alberto Orfao, Inês Crespo, Hermínio Tão, María Dolores Tabernero, Catarina R. Oliveira, Ana Belen Nieto, Olinda Rebelo, Pim J. French, Ana Luísa Vital
Publikováno v:
Journal of Molecular Diagnostics, 13(6), 634-647. Elsevier Inc.
Glioblastomas are cytogenetically heterogeneous tumors that frequently display alterations of chromosomes 7, 9p, and 10q. We used high-density (500K) single-nucleotide polymorphism arrays to investigate genome-wide copy number alterations and loss of
Autor:
Santiago Muñoz-Criado, Arancha Rodríguez-Caballero, A. López, Carlos E. Pedreira, Ana Belen Nieto, Cristina Teodosio, Wendy G. Nieto, Alberto Orfao, Paulino Fernández-Navarro, Alfonso Romero, Julia Almeida, María Jara-Acevedo
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
Chronic lymphocytic leukemia (CLL) is the most common type of leukemia in the Western world. The disease is typically diagnosed in adults >40 years old, who show an expansion (>5 × 109 cells per l) of clonal B-cells with a unique CD5+, CD23+, B-cell
Autor:
Abel Castrillo, Fernando Gomes, Alberto Orfao, Catarina R. Oliveira, María Tabernero, Ana Luísa Vital, Maria do Carmo Lopes, Hermínio Tão, Olinda Rebelo, Ana Belen Nieto
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
et al.
Despite the increasing knowledge about the genetic alterations and molecular pathways involved in gliomas, few studies have investigated the association between the gene expression profiles (GEP) and both cytogenetics and histopathology o
Despite the increasing knowledge about the genetic alterations and molecular pathways involved in gliomas, few studies have investigated the association between the gene expression profiles (GEP) and both cytogenetics and histopathology o
Autor:
Patrícia Henriques, Domingues, Cristina, Teodósio, Álvaro, Otero, Pablo, Sousa, Jesus Maria, Gonçalves, Ana Belen, Nieto, Maria Celeste, Lopes, Catarina, de Oliveira, Alberto, Orfao, Maria Dolores, Tabernero
Publikováno v:
Neuropathology and applied neurobiology. 41(3)
Limited information exists about the impact of cytogenetic alterations on the protein expression profiles of individual meningioma cells and their association with the clinicohistopathological characteristics of the disease. The aim of this study is
Autor:
Pablo Sousa, Jesús María Gonçalves, Patrícia Domingues, Álvaro Otero, Alberto Orfao, MariaDolores Tabernero, Ana Belen Nieto, María Jara-Acevedo, Arancha Rodríguez Caballero
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
BMC Medical Genetics
instname
BMC Medical Genetics
This is an open-access article distributed under the terms of the Creative Commons Attribution License.
[Background]: Meningioma was the first solid tumor shown to contain a recurrent genetic alteration e.g. monosomy 22/del(22q), NF2 being the m
[Background]: Meningioma was the first solid tumor shown to contain a recurrent genetic alteration e.g. monosomy 22/del(22q), NF2 being the m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24d8a4c90dabd44e547811c33fbd5142
http://hdl.handle.net/10261/85726
http://hdl.handle.net/10261/85726