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 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.]

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.]

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

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.]

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.]

Expression of CA-IX is associated with advanced stage tumors and poor survival in oral squamous cell carcinoma patients

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

Genetic study of osteogenesis imperfecta: Two novel mutations in COL1A1 and COL1A2

2014- Leis Trabazo, María Rosaura; Barros Angueira, Francisco; Loidi Fernández, Lourdes; Pombo Arias, Manuel; Cabanas Rodríguez, Paloma; [et al.]

Hypoxia-inducible factors in OSCC

2011- Pérez Sayáns, Mario; Barros Angueira, Francisco; Gayoso Diz, Pilar; García García, Abel; Suárez Peñaranda, Jose Manuel; [et al.]

Interstitial Microdeletions Including the Chromosome Band 4q13.2 and the UBA6 Gene as Possible Causes of Intellectual Disability and Behavior Disorder

2015- Carracedo Álvarez, Ángel; Barros Angueira, Francisco; Fernández Prieto, Montserrat; Castro Gago, Manuel; Gómez Lado, María del Carmen; [et al.]

Microdeleción 16p11.2 asociada a convulsiones benignas de la primera infancia

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

Microdeleción 2q23.1 y hallazgos sindrómicos

2013- Barros Angueira, Francisco; Castro Gago, Manuel; Gómez Lado, María del Carmen; Eiris Puñal, Jesús; Dacruz Álvarez, David; [et al.]

Molecular characterisation and phenotypic description of two patients with reciprocal chromosomal aberrations in the region of the 3q29 microdeletion/microduplication syndromes

2015- Carracedo Álvarez, Ángel; Barros Angueira, Francisco; Castro Gago, Manuel; Perez Gay, Laura; Eiris Puñal, Jesús; [et al.]

Neurofibromatosis without Neurofibromas: Confirmation of a Genotype-Phenotype Correlation and Implications for Genetic Testing.

2011- Carracedo Álvarez, Ángel; Sobrido Gómez, María Jesús; Barros Angueira, Francisco; Campos Balea, Begoña; Quintans Castro, Beatriz; [et al.]

RUNA digital repository

Browse by Author "Barros Angueira, Francisco"

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

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 ﻿

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 ﻿

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

Delimiting allelic imbalance of TYMS by allele-specific analysis ﻿

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

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

Expression of CA-IX is associated with advanced stage tumors and poor survival in oral squamous cell carcinoma patients ﻿

Genetic study of osteogenesis imperfecta: Two novel mutations in COL1A1 and COL1A2 ﻿

Hypoxia-inducible factors in OSCC ﻿

Interstitial Microdeletions Including the Chromosome Band 4q13.2 and the UBA6 Gene as Possible Causes of Intellectual Disability and Behavior Disorder ﻿

Microdeleción 16p11.2 asociada a convulsiones benignas de la primera infancia ﻿

Microdeleción 2q23.1 y hallazgos sindrómicos ﻿

Molecular characterisation and phenotypic description of two patients with reciprocal chromosomal aberrations in the region of the 3q29 microdeletion/microduplication syndromes ﻿

Neurofibromatosis without Neurofibromas: Confirmation of a Genotype-Phenotype Correlation and Implications for Genetic Testing. ﻿

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

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

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

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

Delimiting allelic imbalance of TYMS by allele-specific analysis

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

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

Expression of CA-IX is associated with advanced stage tumors and poor survival in oral squamous cell carcinoma patients

Genetic study of osteogenesis imperfecta: Two novel mutations in COL1A1 and COL1A2

Hypoxia-inducible factors in OSCC

Interstitial Microdeletions Including the Chromosome Band 4q13.2 and the UBA6 Gene as Possible Causes of Intellectual Disability and Behavior Disorder

Microdeleción 16p11.2 asociada a convulsiones benignas de la primera infancia

Microdeleción 2q23.1 y hallazgos sindrómicos

Molecular characterisation and phenotypic description of two patients with reciprocal chromosomal aberrations in the region of the 3q29 microdeletion/microduplication syndromes

Neurofibromatosis without Neurofibromas: Confirmation of a Genotype-Phenotype Correlation and Implications for Genetic Testing.