Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Jenifer Plaza‐Sánchez"'
Autor:
Sandra Zazo, Sandra Pérez‐Buira, Nerea Carvajal, Jenifer Plaza‐Sánchez, Rebeca Manso, Nuria Pérez‐González, Carolina Dominguez, Iván Prieto‐Potin, Jaime Rubio, Manuel Dómine, Virginia Lozano, Patricia Mohedano, David Carcedo, Rafael Carias, Federico Rojo
Publikováno v:
Cancer Medicine, Vol 13, Iss 3, Pp n/a-n/a (2024)
Abstract Objective This study aimed to describe the performance of a next‐generation sequencing (NGS) panel for the detection of precise genomic alterations in cancer in Spanish clinical practice. The impact of tumor characteristics was evaluated o
Externí odkaz:
https://doaj.org/article/f005a061fa8f46aca3f748bc4be3e83f
Autor:
Iván Prieto-Potin, Franklin Idrovo, Ana Suárez-Gauthier, María Díaz-Blázquez, Laura Astilleros-Blanco de Córdova, Cristina Chamizo, Sandra Zazo, Nerea Carvajal, Almudena López-Sánchez, Sandra Pérez-Buira, Carmen Laura Aúz-Alexandre, Rebeca Manso, Jenifer Plaza-Sánchez, Virginia de Lucas-López, Nuria Pérez-González, Sara Martín-Valle, Ion Cristóbal, Victoria Casado, Jesús García-Foncillas, Federico Rojo
Publikováno v:
Diagnostics, Vol 12, Iss 8, p 1903 (2022)
Gynecological cancer accounts for an elevated incidence worldwide requiring responsiveness regarding its care. The comprehensive genomic approach agrees with the classification of certain tumor types. We evaluated 49 patients with gynecological tumor
Externí odkaz:
https://doaj.org/article/5997035934bb459c94fd59bc4cba53f2
Autor:
Iván Prieto-Potin, Nerea Carvajal, Jenifer Plaza-Sánchez, Rebeca Manso, Carmen Laura Aúz-Alexandre, Cristina Chamizo, Sandra Zazo, Almudena López-Sánchez, Socorro María Rodríguez-Pinilla, Laura Camacho, Raquel Longarón, Beatriz Bellosillo, Rosa Somoza, Javier Hernández-Losa, Víctor Manuel Fernández-Soria, Ricardo Ramos-Ruiz, Ion Cristóbal, Jesús García-Foncillas, Federico Rojo
Publikováno v:
PeerJ, Vol 8, p e10069 (2020)
Background Next-generation sequencing (NGS) is a high-throughput technology that has become widely integrated in molecular diagnostics laboratories. Among the large diversity of NGS-based panels, the Trusight Tumor 26 (TsT26) enables the detection of
Externí odkaz:
https://doaj.org/article/6a82bc40e8c845f88d8f03973d27e115
Autor:
Ricardo Ramos-Ruiz, Jesús García-Foncillas, Víctor Manuel Fernández-Soria, Raquel Longarón, Laura Camacho, Carmen Laura Aúz-Alexandre, Socorro María Rodríguez-Pinilla, Ion Cristóbal, Cristina Chamizo, Beatriz Bellosillo, Jenifer Plaza-Sánchez, Rebeca Manso, Almudena López-Sánchez, Sandra Zazo, Javier Hernández-Losa, Nerea Carvajal, I. Prieto-Potin, Rosa Somoza, Federico Rojo
Publikováno v:
PeerJ
PeerJ, Vol 8, p e10069 (2020)
PeerJ, Vol 8, p e10069 (2020)
Background Next-generation sequencing (NGS) is a high-throughput technology that has become widely integrated in molecular diagnostics laboratories. Among the large diversity of NGS-based panels, the Trusight Tumor 26 (TsT26) enables the detection of