Listar por autor "Balbín Felechosa, Milagros"

ABL alternative splicing is quite frequent in normal population - Letter

Santamaría Ruiz de Azúa, Íñigo

; Sánchez Pitiot, Ana Gloria

; Balbín Felechosa, Milagros

(2010)

Análisis de haplotipos en familias con alteraciones en genes implicados en cáncer hereditario

Capín Pérez, Raquel

(2014-07)

Association Between Germline Mutations in BRF1, a Subunit of the RNA Polymerase III Transcription Complex, and Hereditary Colorectal Cancer

Bellido, Fernando; Sowada, N.; Mur, P.; Valdés Mas, Rafael María

; Balbín Felechosa, Milagros

; Blay Albors, Pilar

(2018)

Chromosomal changes in sporadic and familial head and neck paragangliomas

Sevilla García, María Agustina

; Hermsen, Mario

; Weiss, Marjan M.; Grimbergen, Anneliese E. M.; Balbín Felechosa, Milagros

; Llorente Pendás, José Luis

; Rodrigo Tapia, Juan Pablo

; Suárez Nieto, Carlos

(2009)

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)

Cloning and sequence of a gene encoding the L7/L12 ribosomal protein equivalent of Streptomyces antibioticus

Parra Fernández, José Francisco

; Blanco Blanco, María Gloria

; Martín Alonso, José Manuel

; Balbín Felechosa, Milagros

; Méndez Fernández, María del Carmen

; Salas Fernández, José Antonio

(1992)

Co-occurrence of mutations in NF1 and other susceptibility genes in pheochromocytoma and paraganglioma

Mellid, Sara; Gil, Eduardo; Letón, Rocío; Balbín Felechosa, Milagros

(2023)

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)

Dinámica de la matriz extracelular de la placa de crecimiento. Patrón de expresión de los colágenos tipo II y X y de la colagenasa-3

Álvarez Piñera, Jesús

(1999-12-14)

Estudio y seguimiento de tumores raros y hematológicos mediante el empleo de técnicas de secuenciación masiva

Álvarez Eguiluz, Ángel

(2023-02-07)

Expresión de los genes estructurales del virus de la gastroenteritis porcina transmisible en saccharomyces cerevisiae

Balbín Felechosa, Milagros

(1990)

Featuring brca1 and brca2 germline mutational landscape from Asturias (north Spain)

Sánchez Pitiot, Ana; Blay, P.; Díaz Navarro, Ander

; Fernández Arrojo, Sara; Romero, R.; Álvarez Eguiluz, Ángel

; Alvarado, M. G.; Álvarez, N.; García Teijido, P.; Fernández, Y.; Palacio, I.; Suárez Puente, Xosé Antón

; Balbín Felechosa, Milagros

(2024)

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)

Germline Mutations in FAN1 Cause Hereditary Colorectal Cancer by Impairing DNA Repair

Seguí, Nuria; Mina, L. B.; Lázaro, Conxi; Valdés Mas, Rafael María

; Balbín Felechosa, Milagros

; Blay Albors, Pilar

; Suárez Puente, Xosé Antón

(2015)

Identification of a signaling Axis HIF-1a/MicroRNA-210/ISCU independent of SDH mutation that defines a subgroup of head and neck paragangliomas

Merlo, Anna

; Bernaldo de Quirós Fernández, Sandra

; Secades Vázquez, Pablo

; Zambrano Andazol, Iriana Penélope

; Balbín Felechosa, Milagros

; Astudillo González, María Aurora

; Scola Yurrita, Bartolomé; Arístegui Ruiz, Miguel; Suárez Nieto, Carlos

; Chiara Romero, María Dolores

(2012)

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)

Mapping the genetic features of T-ALL cases through simplified NGS approach

García Aznar, José María; Alonso, Sara; Uña Iglesias, David de; López de Ugarriza, Paula; Álvarez López, Carmen

; Balbín Felechosa, Milagros

; Bernal del Castillo, Teresa

(2022)

Matrix metalloproteinase Mmp-1a is dispensable for normal growth and fertility in mice and promotes lung cancer progression by modulating inflammatory responses

Fanjul Fernández, Miriam

; Rodríguez Folgueras, Alicia

; Fueyo Silva, Antonio Manuel

; Balbín Felechosa, Milagros

; Fernández Suárez, María

; Fernández García, María de la Soledad

; Shapiro, Steven D.; Pérez Freije, José María

; López Otín, Carlos

(2013)

Matrix metalloproteinase Mmp-1a is dispensable for normal growth and fertility in mice and promotes lung cancer progression by modulating inflammatory responses (vol. 288, pg 1467, 2013). Corrección

Fanjul Fernández, Miriam

; Rodríguez Folgueras, Alicia

; Fueyo Silva, Antonio Manuel

; Balbín Felechosa, Milagros

; Fernández Suárez, María

; Fernández García, María de la Soledad

; Shapiro, Steven D.; Pérez Freije, José María

; López Otín, Carlos

(Amer Soc Biochemistry Molecular Biology INC, 2018-07)

Listar por autor "Balbín Felechosa, Milagros"

ABL alternative splicing is quite frequent in normal population - Letter ﻿

Análisis de haplotipos en familias con alteraciones en genes implicados en cáncer hereditario ﻿

Association Between Germline Mutations in BRF1, a Subunit of the RNA Polymerase III Transcription Complex, and Hereditary Colorectal Cancer ﻿

Chromosomal changes in sporadic and familial head and neck paragangliomas ﻿

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

Cloning and sequence of a gene encoding the L7/L12 ribosomal protein equivalent of Streptomyces antibioticus ﻿

Co-occurrence of mutations in NF1 and other susceptibility genes in pheochromocytoma and paraganglioma ﻿

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

Dinámica de la matriz extracelular de la placa de crecimiento. Patrón de expresión de los colágenos tipo II y X y de la colagenasa-3 ﻿

Estudio y seguimiento de tumores raros y hematológicos mediante el empleo de técnicas de secuenciación masiva ﻿

Expresión de los genes estructurales del virus de la gastroenteritis porcina transmisible en saccharomyces cerevisiae ﻿

Featuring brca1 and brca2 germline mutational landscape from Asturias (north Spain) ﻿

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 ﻿

Germline Mutations in FAN1 Cause Hereditary Colorectal Cancer by Impairing DNA Repair ﻿

Identification of a signaling Axis HIF-1a/MicroRNA-210/ISCU independent of SDH mutation that defines a subgroup of head and neck paragangliomas ﻿

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 ﻿

Mapping the genetic features of T-ALL cases through simplified NGS approach ﻿

Matrix metalloproteinase Mmp-1a is dispensable for normal growth and fertility in mice and promotes lung cancer progression by modulating inflammatory responses ﻿

Matrix metalloproteinase Mmp-1a is dispensable for normal growth and fertility in mice and promotes lung cancer progression by modulating inflammatory responses (vol. 288, pg 1467, 2013). Corrección ﻿

ABL alternative splicing is quite frequent in normal population - Letter

Análisis de haplotipos en familias con alteraciones en genes implicados en cáncer hereditario

Association Between Germline Mutations in BRF1, a Subunit of the RNA Polymerase III Transcription Complex, and Hereditary Colorectal Cancer

Chromosomal changes in sporadic and familial head and neck paragangliomas

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

Cloning and sequence of a gene encoding the L7/L12 ribosomal protein equivalent of Streptomyces antibioticus

Co-occurrence of mutations in NF1 and other susceptibility genes in pheochromocytoma and paraganglioma

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

Dinámica de la matriz extracelular de la placa de crecimiento. Patrón de expresión de los colágenos tipo II y X y de la colagenasa-3

Estudio y seguimiento de tumores raros y hematológicos mediante el empleo de técnicas de secuenciación masiva

Expresión de los genes estructurales del virus de la gastroenteritis porcina transmisible en saccharomyces cerevisiae

Featuring brca1 and brca2 germline mutational landscape from Asturias (north Spain)

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

Germline Mutations in FAN1 Cause Hereditary Colorectal Cancer by Impairing DNA Repair

Identification of a signaling Axis HIF-1a/MicroRNA-210/ISCU independent of SDH mutation that defines a subgroup of head and neck paragangliomas

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

Mapping the genetic features of T-ALL cases through simplified NGS approach

Matrix metalloproteinase Mmp-1a is dispensable for normal growth and fertility in mice and promotes lung cancer progression by modulating inflammatory responses

Matrix metalloproteinase Mmp-1a is dispensable for normal growth and fertility in mice and promotes lung cancer progression by modulating inflammatory responses (vol. 288, pg 1467, 2013). Corrección