Browse by Author "Barros Angueira, Francisco"

16p11.2 microdeletion associated to early onset benign childhood seizures

2013- Barros Angueira, Francisco; Castro Gago, Manuel; Gómez Lado, María del Carmen; Perez Gay, Laura; Dacruz Álvarez, David [et al.]

A 6q14.1-q15 microdeletion in a male patient with severe autistic disorder, lack of oral language, and dysmorphic features with concomitant presence of a maternally inherited Xp22.31 copy number gain

2015- Quintela, Inés; Fernández Prieto, Montserrat; Gómez Guerrero, Lorena María; Resches, Mariela; Eiris Puñal, Jesús; [et al.]

A maternally inherited 16p13.11-p12.3 duplication concomitant with a de novo SOX5 deletion in a male patient with global developmental delay, disruptive and obsessive behaviors and minor dysmorphic features

2015- Carracedo Álvarez, Ángel; Barros Angueira, Francisco; Castro Gago, Manuel; Eiris Puñal, Jesús; Lago Lestón, Ramón Manuel [et al.]

A novel stop mutation in the vascular endothelial growth factor-C gene (VEGFC) results in Milroy-like disease

2014- Carracedo Álvarez, Ángel; Barros Angueira, Francisco; Couce Pico, María Luz; Balboa Beltran, Emilia; Pérez Muñuzuri, Alejandro; [et al.]

A pharmacogenetics study of TPMT and ITPA genes detects a relationship with side effects and clinical response in patients with inflammatory bowel disease receiving azathioprine

2011- Echarri Piudo, Ana; Castro Alvariño, Javier; Barreiro de Acosta, Manuel; Carracedo Álvarez, Ángel; Barros Angueira, Francisco; [et al.]

A qPCR expression assay of IFI44L gene differentiates viral from bacterial infections in febrile children

2019- Gómez Carballa, Alberto; Cebey López, Miriam; Pardo Seco, Jacobo José; Barral Arca, Ruth; RIVERO CALLE, IRENE; [et al.]

A rare inherited case of 4q deletion detected by GTG and array analyses in a newborn

2011- Barros Angueira, Francisco; Quintas Martínez, María Raquel; Macía Cortiñas, Manuel; Ariza Cobas, Manuela; Míguez Álvarez, Luz; [et al.]

A Xq21.31 duplication without features of Prader-Willi syndrome

2013- Barros Angueira, Francisco; Castro Gago, Manuel; Gómez Lado, María del Carmen; Perez Gay, Laura

Activity of beta2-adrenergic receptor in oral squamous cell carcinoma is mediated by overexpression of the ADRBK2 gene: A pilot study

2012- Pérez Sayáns, Mario; Barros Angueira, Francisco; Gayoso Diz, Pilar; García García, Abel

BCL10 expression is not related to any clinicopathological parameter or prognosis for oral squamous cell carcinomas in Spain

2012- Barros Angueira, Francisco; Gayoso Diz, Pilar; García García, Abel; Suárez Peñaranda, Jose Manuel; Gándara Rey, José Manuel [et al.]

BCL10 expression is unrelated to clinico-pathological parameters or prognoses for oral squamous cell carcinomas

2012- Barros Angueira, Francisco; Gayoso Diz, Pilar; Suárez Peñaranda, Jose Manuel

Candidate genes for azathioprine's efficacy or toxicity in inflammatory bowel disease patients using a exome-wide genotyping analysis

2011- Echarri Piudo, Ana; Castro Alvariño, Javier; Barreiro de Acosta, Manuel; Carracedo Álvarez, Ángel; Barros Angueira, Francisco; [et al.]

Clinical characterization of a male patient with the recently described 8q21.11 microdeletion syndrome

2015- Carracedo Álvarez, Ángel; Barros Angueira, Francisco; Castro Gago, Manuel; Eiris Puñal, Jesús

Comparison of the Cytobrush, dermatological curette and oral CDx brush test as methods for obtaining samples of RNA for molecular analysis of oral cytology

2012- Reboiras-López, MD; Pérez Sayáns, Mario; Somoza Martín, José Manuel; Gayoso Diz, Pilar; Barros Angueira, Francisco; [et al.]

Current trends in miRNAs and their relationship with oral squamous cell carcinoma

2012- Pérez Sayáns, Mario; Barros Angueira, Francisco; Gayoso Diz, Pilar; García García, Abel; Suárez Peñaranda, Jose Manuel [et al.]

Delimiting allelic imbalance of TYMS by allele-specific analysis

2015- Carracedo Álvarez, Ángel; Barros Angueira, Francisco; Balboa Beltran, Emilia; Cruz Guerrero, Raquel

Evolutionary analyses of entire genomes do not support the association of mtdna mutations with ras/mapk pathway syndromes.

2011- Gómez-Carballa, Alberto; Cerezo, María; Balboa Beltrán, Emilia; Heredia Ramírez, Claudia Emilia; Castro Feijoo, Lidia; [et al.]

Exome-wide pharmacogenomic analysis of response to thiopurines in inflammatory bowel disease patients

2015- Echarri Piudo, Ana; Barreiro de Acosta, Manuel; Carracedo Álvarez, Ángel; Barros Angueira, Francisco; Zabala Fernández, William [et al.]

Explore the role that dmet genotyping platform may play in search of genetic polymorphism associated with severe toxicity

2011- Carracedo Álvarez, Ángel; Candamio Folgar, Sonia; López López, Rafael; Barros Angueira, Francisco; Bernárdez Ferrán, Beatriz; [et al.]

Expression of CA IX in dysplasia adjacent to surgical resection margins of oral squamous cell carcinoma

2014- Pérez Sayáns, Mario; Barros Angueira, Francisco; Gayoso Diz, Pilar; García García, Abel; Suárez Peñaranda, Jose Manuel; [et al.]

RUNA digital repository

Browse by Author "Barros Angueira, Francisco"

16p11.2 microdeletion associated to early onset benign childhood seizures ﻿

A 6q14.1-q15 microdeletion in a male patient with severe autistic disorder, lack of oral language, and dysmorphic features with concomitant presence of a maternally inherited Xp22.31 copy number gain ﻿

A maternally inherited 16p13.11-p12.3 duplication concomitant with a de novo SOX5 deletion in a male patient with global developmental delay, disruptive and obsessive behaviors and minor dysmorphic features ﻿

A novel stop mutation in the vascular endothelial growth factor-C gene (VEGFC) results in Milroy-like disease ﻿

A pharmacogenetics study of TPMT and ITPA genes detects a relationship with side effects and clinical response in patients with inflammatory bowel disease receiving azathioprine ﻿

A qPCR expression assay of IFI44L gene differentiates viral from bacterial infections in febrile children ﻿

A rare inherited case of 4q deletion detected by GTG and array analyses in a newborn ﻿

A Xq21.31 duplication without features of Prader-Willi syndrome ﻿

Activity of beta2-adrenergic receptor in oral squamous cell carcinoma is mediated by overexpression of the ADRBK2 gene: A pilot study ﻿

BCL10 expression is not related to any clinicopathological parameter or prognosis for oral squamous cell carcinomas in Spain ﻿

BCL10 expression is unrelated to clinico-pathological parameters or prognoses for oral squamous cell carcinomas ﻿

Candidate genes for azathioprine's efficacy or toxicity in inflammatory bowel disease patients using a exome-wide genotyping analysis ﻿

Clinical characterization of a male patient with the recently described 8q21.11 microdeletion syndrome ﻿

Comparison of the Cytobrush, dermatological curette and oral CDx brush test as methods for obtaining samples of RNA for molecular analysis of oral cytology ﻿

Current trends in miRNAs and their relationship with oral squamous cell carcinoma ﻿

Delimiting allelic imbalance of TYMS by allele-specific analysis ﻿

Evolutionary analyses of entire genomes do not support the association of mtdna mutations with ras/mapk pathway syndromes. ﻿

Exome-wide pharmacogenomic analysis of response to thiopurines in inflammatory bowel disease patients ﻿

Explore the role that dmet genotyping platform may play in search of genetic polymorphism associated with severe toxicity ﻿

Expression of CA IX in dysplasia adjacent to surgical resection margins of oral squamous cell carcinoma ﻿

16p11.2 microdeletion associated to early onset benign childhood seizures

A 6q14.1-q15 microdeletion in a male patient with severe autistic disorder, lack of oral language, and dysmorphic features with concomitant presence of a maternally inherited Xp22.31 copy number gain

A maternally inherited 16p13.11-p12.3 duplication concomitant with a de novo SOX5 deletion in a male patient with global developmental delay, disruptive and obsessive behaviors and minor dysmorphic features

A novel stop mutation in the vascular endothelial growth factor-C gene (VEGFC) results in Milroy-like disease

A pharmacogenetics study of TPMT and ITPA genes detects a relationship with side effects and clinical response in patients with inflammatory bowel disease receiving azathioprine

A qPCR expression assay of IFI44L gene differentiates viral from bacterial infections in febrile children

A rare inherited case of 4q deletion detected by GTG and array analyses in a newborn

A Xq21.31 duplication without features of Prader-Willi syndrome

Activity of beta2-adrenergic receptor in oral squamous cell carcinoma is mediated by overexpression of the ADRBK2 gene: A pilot study

BCL10 expression is not related to any clinicopathological parameter or prognosis for oral squamous cell carcinomas in Spain

BCL10 expression is unrelated to clinico-pathological parameters or prognoses for oral squamous cell carcinomas

Candidate genes for azathioprine's efficacy or toxicity in inflammatory bowel disease patients using a exome-wide genotyping analysis

Clinical characterization of a male patient with the recently described 8q21.11 microdeletion syndrome

Comparison of the Cytobrush, dermatological curette and oral CDx brush test as methods for obtaining samples of RNA for molecular analysis of oral cytology

Current trends in miRNAs and their relationship with oral squamous cell carcinoma

Delimiting allelic imbalance of TYMS by allele-specific analysis

Evolutionary analyses of entire genomes do not support the association of mtdna mutations with ras/mapk pathway syndromes.

Exome-wide pharmacogenomic analysis of response to thiopurines in inflammatory bowel disease patients

Explore the role that dmet genotyping platform may play in search of genetic polymorphism associated with severe toxicity

Expression of CA IX in dysplasia adjacent to surgical resection margins of oral squamous cell carcinoma