Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Marta Bernués"'
Autor:
Marta Bernués, Teresa González, Luis Antonio Corchete, Sandra Santos, Maria Antònia Durán, Bernardo López-Andrade, Laura Lo Riso, Jordi Martínez-Serra, Rafael Ramos, Julio Iglesias, Irina Royo, Jordi Rosell
Cytogenetic studies have played a crucial role in the discovery of genes involved in several diseases. In the field of oncohematology, cytogenetics is still necessary for the classification and prognosis of many diseases. Here we report a new recurre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5e90ac200757e1c088e6d38418f8d19
http://hdl.handle.net/10261/283389
http://hdl.handle.net/10261/283389
Autor:
Jorge Sierra, Salut Brunet, Jose A. Martinez-Climent, Maria Dolors Coll, Jesús M. Hernández, Marta Bernués, Francesc Solé, Francisca Fuentes, Anna Aventin, J. L. M. Duarte, Isabel Granada, Anna Carrió, Montserrat Teixidó, Sı́lvia Casas, Teresa Vallespi
Publikováno v:
Cancer Genetics and Cytogenetics. 153:16-25
A total of 127 adult de novo acute myelocytic leukemia (AML) patients were analyzed by comparative genomic hybridization (CGH) at diagnosis. Conventional cytogenetic analysis (CCA) showed a normal karyotype in 45 cases and an abnormal karyotype in 56
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c73b5fc07620414e8ffae13fc67dc193
https://doi.org/10.1016/j.cancergencyto.2003.12.011
https://doi.org/10.1016/j.cancergencyto.2003.12.011
Publikováno v:
BJU International. 90:332-335
Objective To analyse the DNA methylation status and the loss of heterozygosity (LOH) at the D17S5 locus (17p13.3) in urothelial cancer. Materials and methods DNA methylation was assayed and LOH analysed by Southern blotting in a series of 33 transiti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3aff236828d0151fec024f42e6e003c0
https://doi.org/10.1046/j.1464-410x.2002.02892.x
https://doi.org/10.1046/j.1464-410x.2002.02892.x
Autor:
Marta, Bernués, Maria Antònia, Durán, Guiomar, Puget, Julio, Iglesias, Pilar, Galán, Francisco Javier, Vercher, Joan, Besalduch, Jordi, Rosell
Publikováno v:
Anticancer research. 34(5)
Patients affected by chronic lymphocytic leukemia (CLL) have an increased risk of developing a second cancer. There is not a definitive explanation for this phenomenon, although some hypotheses have been postulated. The aim of the present work was to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::48c0963ef3cb1e314afb48ae447edc87
https://pubmed.ncbi.nlm.nih.gov/24778036
https://pubmed.ncbi.nlm.nih.gov/24778036
Autor:
Gilberto Chéchile, María Rosa Caballín, Marı́a José Ejarque, Antoni Gelabert, Carme Casadevall, Marta Bernués, J. Egozcue, Rosa Miró
Publikováno v:
Cancer Genetics and Cytogenetics. 107:121-124
We performed a study of loss of heterozygosity (LOH) at 3p by restriction fragment length polymorphism analysis in a series of 22 renal tumors. In 11 cases, molecular results could be compared with those of cytogenetic studies. The highest frequency
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6a6dae2ae5d3cebc7ee6b068c1fd521
https://doi.org/10.1016/s0165-4608(98)00090-9
https://doi.org/10.1016/s0165-4608(98)00090-9
Autor:
Ramona, Alfaro, Jordi, Rosell, Maria Antònia, Durán, Guiomar, Puget, Joan, Besalduch, Pilar, Galán, Albert, Vallés, Marta, Bernués
Publikováno v:
Anticancer research. 31(5)
Hyperdiploid multiple myeloma (HMM) is being characterized by the presence of several trisomies and a low incidence of immunoglobulin heavy chain rearrangements. It has not well defined what specific steps are associated with disease progression. We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3d88a8b27022d6a43dc9c62a9be532ac
https://pubmed.ncbi.nlm.nih.gov/21617215
https://pubmed.ncbi.nlm.nih.gov/21617215
Autor:
Maria Antonia Duran, Joan Besalduch, Ángeles Pérez-Granero, Jordi Rosell, Marta Bernués, Ramona Alfaro
Publikováno v:
Leukemia research. 32(1)
Duplication of the long arm of chromosome 1 (1q) has been detected accompanied with other chromosome abnormalities in Myelodysplastic Syndromes (MDS). However, as a sole karyotypic change, it is rarely observed. We present here two patients affected
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ddc1e26228741b2a004b7169873cf3cb
https://pubmed.ncbi.nlm.nih.gov/17509681
https://pubmed.ncbi.nlm.nih.gov/17509681
Autor:
Carlos Caldas, Dolors Colomer, Javier del Rey, Juan Cruz Cigudosa, Jordi Camps, Itziar Salaverria, Rosa Miró, Sílvia Beà, Elias Campo, Jessica C.M. Pole, Marta Bernués, Maria J. Garcia, Lluis Hernández, Esther Prat
Publikováno v:
Leukemia research. 30(8)
Mantle-cell lymphoma (MCL) is genetically characterized by 11q13 chromosomal translocations involving the CCND1 gene. We have characterized five MCL cell lines, JVM-2, GRANTA-519, REC-1, JEKO-1, and NCEB-1, combining metaphase and array comparative g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2781b8e19bb3a951d49560a500f3c3a
https://pubmed.ncbi.nlm.nih.gov/16563503
https://pubmed.ncbi.nlm.nih.gov/16563503
Autor:
María Rosa Caballín, Rosa Miró, M A Rigola, Josep Egozcue, Carme Fuster, Marta Bernués, Antoni Gelabert, Carme Casadevall
Publikováno v:
ResearcherID
Comparative genomic hybridization (CGH) and conventional cytogenetic karyotyping were used to screen for losses and gains of DNA sequences along chromosomes in ten renal tumors (RCC) of different histologic types (clear-cell RCC, papillary RCC, and o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c6c1e3b834bea3bdf4f185c201519dc
https://pubmed.ncbi.nlm.nih.gov/12377413
https://pubmed.ncbi.nlm.nih.gov/12377413
Autor:
Marta Bernués, María Rosa Caballín, Carme Casadevall, M A Rigola, J. Egozcue, Rosa Miró, Antoni Gelabert, Carme Fuster
Publikováno v:
ResearcherID
We used comparative genomic hybridization to analyze 10 primary tumor samples from patients with transitional cell carcinoma of the renal pelvis. The most frequent loss was located at 9q, that is, in 50% of the tumors. Gains of DNA sequences were mos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52bb3187614fd8b096baa7f238f63649
https://pubmed.ncbi.nlm.nih.gov/11408067
https://pubmed.ncbi.nlm.nih.gov/11408067