Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Miguel A. Molina"'
Autor:
Ruth Román-Lladó, Cristina Aguado, Núria Jordana-Ariza, Jaume Roca-Arias, Sonia Rodríguez, Erika Aldeguer, Mónica Garzón-Ibañez, Beatriz García-Peláez, Marta Vives-Usano, Ana Giménez-Capitán, Andrés Aguilar, Alejandro Martinez-Bueno, María Gonzalez Cao, Florencia García-Casabal, Santiago Viteri, Clara Mayo de las Casas, Rafael Rosell, Miguel Angel Molina-Vila
Publikováno v:
Journal of Molecular Pathology; Volume 4; Issue 1; Pages: 57-68
Genetic and drug sensitivity assays on primary cultures are not only of basic but also of translational interest and could eventually aid oncologists in the selection of treatments. However, cancer cells need to be identified and differentiated from
Autor:
Irene Moya, Beatriz García Pelaez, Andrés Aguilar, Laura Berrocal, Santiago Viteri, Maria Gonzalez Cao, Sonia Rodríguez, Marta Vives-Usano, Maria José Catalán, Erika Aldeguer, Francesc Pons, Alejandro Martinez-Bueno, Mónica Garzón Ibañez, Clara Mayo de las Casas, Nuria Jordana, Miguel Angel Molina, Ruth Román Lladó, Juan José García-Mosquera, Rafael Rosell, Carlos Cabrera, Ekaterina Meshoulam
Publikováno v:
Journal of Molecular Pathology
Volume 2
Issue 2
Pages 13-134
Journal of Molecular Pathology, Vol 2, Iss 13, Pp 123-134 (2021)
Volume 2
Issue 2
Pages 13-134
Journal of Molecular Pathology, Vol 2, Iss 13, Pp 123-134 (2021)
Somatic copy number variations (CNV
i.e., amplifications and deletions) have been implicated in the origin and development of multiple cancers and some of these aberrations are designated targets for therapies. Although FISH is still considered
i.e., amplifications and deletions) have been implicated in the origin and development of multiple cancers and some of these aberrations are designated targets for therapies. Although FISH is still considered
Autor:
Marta Vives-Usano, Beatriz García Pelaez, Ruth Román Lladó, Mónica Garzón Ibañez, Erika Aldeguer, Sonia Rodriguez, Andrés Aguilar, Francesc Pons, Santiago Viteri, Carlos Cabrera, Maria José Catalán, Irene Moya, María Gonzalez Cao, Juan José García-Mosquera, Alejandro Martinez-Bueno, Ekaterina Meshoulam, Nuria Jordana, Laura Berrocal, Rafael Rosell, Miguel Angel Molina, Clara Mayo de las Casas
Publikováno v:
Journal of Molecular Pathology, Vol 2, Iss 2, Pp 123-134 (2021)
Somatic copy number variations (CNV; i.e., amplifications and deletions) have been implicated in the origin and development of multiple cancers and some of these aberrations are designated targets for therapies. Although FISH is still considered the
Externí odkaz:
https://doaj.org/article/ca772e98c22442f8b9bdad5c2f30d92d