Listar Artículos por autor "Santamaría Ruiz de Azúa, Íñigo"

ABL alternative splicing is quite frequent in normal population - Letter

Santamaría Ruiz de Azúa, Íñigo

; Sánchez Pitiot, Ana Gloria

; Balbín Felechosa, Milagros

(2010)

EGFR l858R mutation may go undetected because of P848l in cis mutation

Santamaría Ruiz de Azúa, Íñigo

; Menéndez, Sofía T.; Balbín Felechosa, Margarita

(2013)

Germ-line mutations in epidermal growth factor receptor (EGFR) are rare but may contribute to oncogenesis: A novel germ-line mutation in EGFR detected in a patient with lung adenocarcinoma

Centeno Ramos, Irene

; Blay Albors, Pilar

; Santamaría Ruiz de Azúa, Íñigo

; Astudillo González, María Aurora

; Sánchez Pitiot, Ana Gloria

; García Osorio, Fernando

; González Arriaga, Patricia

; Iglesias Llaca, Fernando

; Menéndez Rodríguez, María Primitiva

; Tardón García, Adonina

; Pérez Freije, José María

; Balbín Felechosa, Milagros

(BioMed Central, 2011)

Identification of somatic and germ-line DICER1 mutations in pleuropulmonary blastoma, cystic nephroma and rhabdomyosarcoma tumors within a DICER1 syndrome pedigree

Fernández Martínez, Lorena; Villegas, José Antonio; Santamaría Ruiz de Azúa, Íñigo

; Sánchez Pitiot, Ana Gloria

; González Alvarado, María Marta

; Fernández, Soledad; Torres, Héctor; Paredes, Ángeles; Blay Albors, Pilar

; Balbín Felechosa, Milagros

(2017)

Impact of PI3K/AKT/mTOR pathway activation on the prognosis of patients with head and neck squamous cell carcinomas

García Carracedo, Dario

; Villaronga Torres, María de los Ángeles

; Álvarez Teijeiro, Saúl

; Santamaría Ruiz de Azúa, Íñigo

; Allonca Campa, Eva

; Suárez Fernández, Laura

; González Meana, María Victoria

; Balbín Felechosa, Milagros

; Astudillo González, María Aurora

; Martínez Camblor, Pablo

; Rodrigo Tapia, Juan Pablo

; García Pedrero, Juana María

(2016)

Quantifying mutated and unmutated BCR-ABL transcripts confirms suitability of direct sequencing sensitivity in mutation analysis of patients with chronic myeloid leukemia with secondary resistance to tyrosine kinase inhibitors, regardless of ratio values

Santamaría Ruiz de Azúa, Íñigo

; Payer, Ángel R.; Sánchez Pitiot, Ana Gloria

; González Alvarado, María Marta

; Balbín Felechosa, Milagros

(2010)

Residue 826 in the calcium-sensing receptor is implicated in the response to calcium and to R-568 calcimimetic compound

Álvarez Hernández, Daniel; González Suárez, Ignacio; Fernández Martín, José Luis; Rodríguez Fernández, Isabel

; Santamaría Ruiz de Azúa, Íñigo

; Coto García, Eliecer

; Cannata Andía, Jorge Benito

(2010)

A t(1;9) translocation involving CSF3R as a novel mechanism in unclassifiable chronic myeloproliferative neoplasm

Gutiérrez Abril, Jesús

; Santamaría Ruiz de Azúa, Íñigo

; Sánchez Pitiot, Ana Gloria

; Gutiérrez Fernández, Ana Yolanda

; Álvarez Eguiluz, Ángel

; Vicente, José M.; Sanzo Lombardero, María del Carmen

; González Muñiz, S.; Balbín Felechosa, Milagros

; Suárez Puente, Xosé Antón

(2017)

TP53 p.R72P genotype is a marker of poor prognosis in lung cancer

Neumann, Mirko Peter; González Meana, María Victoria

; Sánchez Pitiot, Ana Gloria

; Santamaría Ruiz de Azúa, Íñigo

; Martínez González, María Cristina

; Tardón García, Adonina

; Astudillo González, María Aurora

; Balbín Felechosa, Milagros

(2018)

Transplacental transfer of essential thrombocythemia in monozygotic twins

Valdés Mas, Rafael María

; Gutiérrez Abril, Jesús

; Sánchez Pitiot, Ana Gloria

; Santamaría Ruiz de Azúa, Íñigo

; Álvarez Puente, Diana

; Muñiz Lobato, Sara; Balbín Felechosa, Milagros

; Suárez Puente, Xosé Antón

(2016)

The w/w+ SMART is a useful tool for the evaluation of pesticides

Aguirrezabalaga González, Ignacio; Santamaría Ruiz de Azúa, Íñigo

; Comendador García, Miguel Ángel

(1994)

Listar Artículos por autor "Santamaría Ruiz de Azúa, Íñigo"

ABL alternative splicing is quite frequent in normal population - Letter ﻿

EGFR l858R mutation may go undetected because of P848l in cis mutation ﻿

Germ-line mutations in epidermal growth factor receptor (EGFR) are rare but may contribute to oncogenesis: A novel germ-line mutation in EGFR detected in a patient with lung adenocarcinoma ﻿

Identification of somatic and germ-line DICER1 mutations in pleuropulmonary blastoma, cystic nephroma and rhabdomyosarcoma tumors within a DICER1 syndrome pedigree ﻿

Impact of PI3K/AKT/mTOR pathway activation on the prognosis of patients with head and neck squamous cell carcinomas ﻿

Quantifying mutated and unmutated BCR-ABL transcripts confirms suitability of direct sequencing sensitivity in mutation analysis of patients with chronic myeloid leukemia with secondary resistance to tyrosine kinase inhibitors, regardless of ratio values ﻿

Residue 826 in the calcium-sensing receptor is implicated in the response to calcium and to R-568 calcimimetic compound ﻿

A t(1;9) translocation involving CSF3R as a novel mechanism in unclassifiable chronic myeloproliferative neoplasm ﻿

TP53 p.R72P genotype is a marker of poor prognosis in lung cancer ﻿

Transplacental transfer of essential thrombocythemia in monozygotic twins ﻿

The w/w+ SMART is a useful tool for the evaluation of pesticides ﻿

ABL alternative splicing is quite frequent in normal population - Letter

EGFR l858R mutation may go undetected because of P848l in cis mutation

Germ-line mutations in epidermal growth factor receptor (EGFR) are rare but may contribute to oncogenesis: A novel germ-line mutation in EGFR detected in a patient with lung adenocarcinoma

Identification of somatic and germ-line DICER1 mutations in pleuropulmonary blastoma, cystic nephroma and rhabdomyosarcoma tumors within a DICER1 syndrome pedigree

Impact of PI3K/AKT/mTOR pathway activation on the prognosis of patients with head and neck squamous cell carcinomas

Quantifying mutated and unmutated BCR-ABL transcripts confirms suitability of direct sequencing sensitivity in mutation analysis of patients with chronic myeloid leukemia with secondary resistance to tyrosine kinase inhibitors, regardless of ratio values

Residue 826 in the calcium-sensing receptor is implicated in the response to calcium and to R-568 calcimimetic compound

A t(1;9) translocation involving CSF3R as a novel mechanism in unclassifiable chronic myeloproliferative neoplasm

TP53 p.R72P genotype is a marker of poor prognosis in lung cancer

Transplacental transfer of essential thrombocythemia in monozygotic twins

The w/w+ SMART is a useful tool for the evaluation of pesticides