Navegar por autor "Barros Angueira, Francisco"

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 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

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.]

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.]

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.]

Immunohistochemical localization of C1 subunit of V-ATPase (ATPase C1) in oral squamous cell cancer and normal oral mucosa

2012- Barros Angueira, Francisco; García García, Abel; Antúnez López, José Ramón

LEOPARD syndrome: Clinical characteristics and molecular study

2011- Barros Angueira, Francisco; Balboa Beltran, Emilia; Pombo Arias, Manuel; Cabanas Rodríguez, Paloma; Castro Feijoo, Lidia; [et al.]

Molecular and clinical characterization of a novel nonsense variant in exon 1 of the upf3b gene found in a large spanish basque family (Mrx82)

2019- Tejada, M. I.; Villate, O.; Ibarluzea, N.; de la Hoz, A. B.; Martínez-Bouzas, C.; [et al.]

New genetic associations in thiopurine-related bone marrow toxicity among inflammatory bowel disease patients

2013- Echarri Piudo, Ana; Barreiro de Acosta, Manuel; Carracedo Álvarez, Ángel; Barros Angueira, Francisco; Cruz Guerrero, Raquel; [et al.]

p16(INK4a)/CDKN2 expression and its relationship with oral squamous cell carcinoma is our current knowledge enough?

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

P21Waf1/CIP1 is a poor diagnostic and prognostic marker for OSCC although its expression increases in patients with N1 regional metastasis

2015- Barros Angueira, Francisco

Performance evaluation of deleteriousness prediction methods for intronic SNVs in next generation sequences

2020- Quintas-Rey, R.; Amigo Lechuga, Jorge; Carracedo Álvarez, Ángel; Barros Angueira, Francisco

Pharmacogenetics study of TPMT and ITPA genes in patients with inflammatory bowel disease treated with azathioprine detects relation between ITPase deficiency and clinical response

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

Progressive heterotopic ossification: the arduousness of an accurate diagnosis

2014- Barros Angueira, Francisco; Couce Pico, María Luz; Dosil Gallardo, Silvia; García Magán, Carlos; Fernández Seara, María José [et al.]

Quantitative determination of c-myc facilitates the assessment of prognosis of OSCC patients

2014- Pérez Sayáns, Mario; Suárez Peñaranda, Jose Manuel; Padín-Iruegas, M. E.; Gayoso Diz, Pilar; Reis-De Almeida, M.; [et al.]

The role of p21Waf1/CIP1 as a Cip/Kip type cell-cycle regulator in oral squamous cell carcinoma (Review)

2013- Pérez Sayáns, Mario; Suárez Peñaranda, Jose Manuel; Gayoso Diz, Pilar; Barros Angueira, Francisco; Gándara Rey, José Manuel; [et al.]

The use of CA-IX as a diagnostic method for oral leukoplakia

2015- Pérez Sayáns, Mario; Barros Angueira, Francisco; Gayoso Diz, Pilar; García García, Abel; Suárez Peñaranda, Jose Manuel; [et al.]

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Navegar por autor "Barros Angueira, Francisco"

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 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 ﻿

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 ﻿

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

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

Immunohistochemical localization of C1 subunit of V-ATPase (ATPase C1) in oral squamous cell cancer and normal oral mucosa ﻿

LEOPARD syndrome: Clinical characteristics and molecular study ﻿

Molecular and clinical characterization of a novel nonsense variant in exon 1 of the upf3b gene found in a large spanish basque family (Mrx82) ﻿

New genetic associations in thiopurine-related bone marrow toxicity among inflammatory bowel disease patients ﻿

p16(INK4a)/CDKN2 expression and its relationship with oral squamous cell carcinoma is our current knowledge enough? ﻿

P21Waf1/CIP1 is a poor diagnostic and prognostic marker for OSCC although its expression increases in patients with N1 regional metastasis ﻿

Performance evaluation of deleteriousness prediction methods for intronic SNVs in next generation sequences ﻿

Pharmacogenetics study of TPMT and ITPA genes in patients with inflammatory bowel disease treated with azathioprine detects relation between ITPase deficiency and clinical response ﻿

Progressive heterotopic ossification: the arduousness of an accurate diagnosis ﻿

Quantitative determination of c-myc facilitates the assessment of prognosis of OSCC patients ﻿

The role of p21Waf1/CIP1 as a Cip/Kip type cell-cycle regulator in oral squamous cell carcinoma (Review) ﻿

The use of CA-IX as a diagnostic method for oral leukoplakia ﻿

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 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

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

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

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

Immunohistochemical localization of C1 subunit of V-ATPase (ATPase C1) in oral squamous cell cancer and normal oral mucosa

LEOPARD syndrome: Clinical characteristics and molecular study

Molecular and clinical characterization of a novel nonsense variant in exon 1 of the upf3b gene found in a large spanish basque family (Mrx82)

New genetic associations in thiopurine-related bone marrow toxicity among inflammatory bowel disease patients

p16(INK4a)/CDKN2 expression and its relationship with oral squamous cell carcinoma is our current knowledge enough?

P21Waf1/CIP1 is a poor diagnostic and prognostic marker for OSCC although its expression increases in patients with N1 regional metastasis

Performance evaluation of deleteriousness prediction methods for intronic SNVs in next generation sequences

Pharmacogenetics study of TPMT and ITPA genes in patients with inflammatory bowel disease treated with azathioprine detects relation between ITPase deficiency and clinical response

Progressive heterotopic ossification: the arduousness of an accurate diagnosis

Quantitative determination of c-myc facilitates the assessment of prognosis of OSCC patients

The role of p21Waf1/CIP1 as a Cip/Kip type cell-cycle regulator in oral squamous cell carcinoma (Review)

The use of CA-IX as a diagnostic method for oral leukoplakia