Browsing by author "Sánchez Pitiot, Ana Gloria"

ABL alternative splicing is quite frequent in normal population - Letter

Santamaría Ruiz de Azúa, Íñigo

; Sánchez Pitiot, Ana Gloria

; Balbín Felechosa, Milagros

(2010)

Clinical significance and peculiarities of succinate dehydrogenase B and hypoxia inducible factor 1a expression in parasympathetic versus sympathetic paragangliomas

Bernardo Castiñeira, Cristóbal; Sáenz de Santa María Fernández, Inés

; Valdés, Nuria; Astudillo González, María Aurora

; Balbín Felechosa, Milagros

; Sánchez Pitiot, Ana Gloria

; Jiménez Fonseca, Paula

; Suárez Nieto, Carlos

; Chiara Romero, María Dolores

(2018)

Descripción y caracterización de mutaciones hereditarias fundadoras en genes asociados a síndrome de cáncer de mama y ovario familiar en Asturias

Sánchez Pitiot, Ana Gloria

(2024-12-05)

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)

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)

Role of VHL, HIF1A and SDH on the expression of miR-210: implications for tumoral pseudo-hypoxic fate

Merlo, Anna

; Bernardo Castiñeira, Cristóbal; Sáenz de Santa María Fernández, Inés

; Sánchez Pitiot, Ana Gloria

; Balbín Felechosa, Milagros

; Astudillo González, María Aurora

; Suárez Nieto, Carlos

; Chiara Romero, María Dolores

(2017)

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)

Browsing by author "Sánchez Pitiot, Ana Gloria"

ABL alternative splicing is quite frequent in normal population - Letter ﻿

Clinical significance and peculiarities of succinate dehydrogenase B and hypoxia inducible factor 1a expression in parasympathetic versus sympathetic paragangliomas ﻿

Descripción y caracterización de mutaciones hereditarias fundadoras en genes asociados a síndrome de cáncer de mama y ovario familiar en Asturias ﻿

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 ﻿

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 ﻿

Role of VHL, HIF1A and SDH on the expression of miR-210: implications for tumoral pseudo-hypoxic fate ﻿

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 ﻿

ABL alternative splicing is quite frequent in normal population - Letter

Clinical significance and peculiarities of succinate dehydrogenase B and hypoxia inducible factor 1a expression in parasympathetic versus sympathetic paragangliomas

Descripción y caracterización de mutaciones hereditarias fundadoras en genes asociados a síndrome de cáncer de mama y ovario familiar en Asturias

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

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

Role of VHL, HIF1A and SDH on the expression of miR-210: implications for tumoral pseudo-hypoxic fate

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