Zobrazeno 1 - 10
of 25
pro vyhledávání: '"J. M. García‐Sagredo"'
Autor:
J. M. García-Sagredo, J. L. Monteagudo
Publikováno v:
Hereditas. 115:9-11
The effects of extremely-low-frequency pulsed magnetic fields on human chromosomes with respect to the capacity of inducing chromosome breakage were studied. After human peripheral lymphocytes were exposed in vitro to pulsed electromagnetic fields at
Autor:
I, Muñoz-Repeto, M J, García, M, Kamieniak, T, Ramón Y Cajal, S, Domingo, A, Cazorla, J, García Donas, S, Hernando Polo, J M, García Sagredo, E, Hernández, C, Lacambra, R, Saez, L, Robles, S, Borrego, J, Prat, J, Palacios, J, Benítez
Publikováno v:
Histology and histopathology. 28(1)
The pathologic and immunohistochemical features of familial epithelial ovarian cancers are not well understood. We have carried out a comprehensive immunohistochemical study of familial ovarian carcinomas from women with and without BRCA1 or BRCA2 mu
Publikováno v:
Environmental Health Perspectives
We exposed human peripheral lymphocytes in vitro to 0.3 and 1 Gy of 60Co gamma rays to evaluate whether the ability and sensitivity to detect chromosomal aberrations by chromosome painting is independent or not to the specific paint probes. To detect
Publikováno v:
Cytometry. 31(2)
The evaluation of an automated system for Fluorescence In Situ Hybridization (FISH) spot counting in interphase nuclei is presented in this paper. Different types of experiments have been performed with samples from known populations. In all of them
Autor:
N, Malpica, C O, de Solórzano, J J, Vaquero, A, Santos, I, Vallcorba, J M, García-Sagredo, F, del Pozo
Publikováno v:
Cytometry. 28(4)
Cluster division is a critical issue in fluorescence microscopy-based analytical cytology when preparation protocols do not provide appropriate separation of objects. Overlooking clustered nuclei and analyzing only isolated nuclei may dramatically in
Autor:
P. A. Benedetti, N. P. Verwoerd, Tommy Gerdes, L.J. van Vliet, J. Vrolijk, Jan Maahr, Jim Piper, Harris Morrison, Peter Lichter, J. Fantes, B. Hemery, Stanislas du Manoir, Damir Sudar, Michel Giollant, J. M. García‐Sagredo, Olli-P. Kallioniemi, Andrew D. Carothers, P. Perry, J. Isola, M. Stark
Publikováno v:
Cytometry, 19 (1)
Recommendations are made for hardware and software capabilities that will permit a level of performance of comparative genomic hybridization (CGH) analysis on metaphase chromosomes that is comparable to the best current practice. Guidelines for inter
Autor:
M T, Ferro, J M, García-Sagredo, M, Resino, E, del Potro, A, Villegas, J, Mediavilla, D, Espinós, C, San Román
Publikováno v:
Cancer genetics and cytogenetics. 78(2)
We describe a family with an inherited fragile chromosome 16 with the concurrence of a constitutional chromosome abnormality, together with neoplastic pathology within the family. The following findings should be pointed out: in relation to the const
Autor:
M, Resino, M T, Ferro, J, García-Laraña, J M, García-Sagredo, P, Cabello, A, López-Yarto, C, San Román
Publikováno v:
Sangre. 39(6)
We report a patient with chronic myelocytic leukaemia (CML) in blastic crisis with a del (7) (p11 p15) in addition to the Philadelphia chromosome. A potential relationship between the presence of this deletion and the therapy in chronic phase is sugg
Autor:
Y, Vázquez-Mazariego, P, Cabello, J M, García-Sagredo, A, López-Yarto, I, Vallcorba, M, Resino, R, Muñoz, I, Pérez, M, Mayayo, M T, Ferro
Publikováno v:
Cancer genetics and cytogenetics. 76(2)
A 51-year-old male patient was diagnosed with Burkitt lymphoma 3 months after cardiac transplantation. The bone marrow karyotype was very complex, and to better define the complex karyotype we used the in situ suppression hybridization technique. Pre
Autor:
P, Cabello, F, Speleman, M T, Ferro, M, Resino, J M, García-Sagredo, C, San Román, M C, Burgaleta
Publikováno v:
Sangre. 37(6)
The non-isotopic in situ hybridization makes it possible the analysis of, both, numeric and structural chromosome aberrations in interphase nuclei. Moreover, this technique is useful for identification of chromosome markers of unknown origin, frequen